Prof. M.M.A.M. Mannens PhD publications

2020

• Vos Niels, Oussaada Sabrina M., Cooiman Mellody I., Kleinendorst Lotte, ter Horst Kasper W., Hazebroek Eric J., Romijn Johannes A., Serlie Mireille J., Mannens Marcel M. A. M., van Haelst Mieke M. Bariatric Surgery for Monogenic Non-syndromic and Syndromic Obesity Disorders Current diabetes reports 2020;20 (9) [PubMed]
• Struijk Robert B., Dorssers Lambert C. J., Henneman Peter, Rijlaarsdam Martin A., Venema Andrea, Jongejan Aldo, Mannens Marcel M. A. M., Looijenga Leendert H. J., Repping Sjoerd, van Pelt Ans M. M. Comparing genome-scale DNA methylation and CNV marks between adult human cultured ITGA6+ testicular cells and seminomas to assess in vitro genomic stability PLoS ONE 2020;15 (3) [PubMed]
• van der Laan Loes C., Meeks Karlijn A. C., Chilunga Felix P., Agyemang Charles, Venema Andrea, Mannens Marcel M. A. M., Zafarmand Mohammad H., Klipstein-Grobusch Kerstin, Smeeth Liam, Adeyemo Adebowale, Henneman Peter Epigenome-wide association study for perceived discrimination among sub-Saharan African migrants in Europe - the RODAM study Scientific reports 2020;10 (1) [PubMed]
• Aref-Eshghi Erfan, Kerkhof Jennifer, Pedro Victor P., Barat-Houari Mouna, Ruiz-Pallares Nathalie, Andrau Jean-Christophe, Lacombe Didier, van-Gils Julien, Fergelot Patricia, Dubourg Christèle, Cormier-Daire Valerie, Rondeau Sophie, Lecoquierre François, Saugier-Veber Pascale, Nicolas Gaël, Lesca Gaetan, Chatron Nicolas, Sanlaville Damien, Vitobello Antonio, Faivre Laurence, Thauvin-Robinet Christel, Laumonnier Frederic, Raynaud Martine, Alders Mariëlle, Mannens Marcel, Henneman Peter, Hennekam Raoul C., Velasco Guillaume, Francastel Claire, Ulveling Damien, Ciolfi Andrea, Pizzi Simone, Tartaglia Marco, Heide Solveig, Héron Delphine, Mignot Cyril, Keren Boris, Whalen Sandra, Afenjar Alexandra, Bienvenu Thierry, Campeau Philippe M., Rousseau Justine, Levy Michael A., Brick Lauren, Kozenko Mariya, Balci Tugce B., Siu Victoria Mok, Stuart Alan, Kadour Mike, Masters Jennifer Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders American journal of human genetics 2020;106 (3):356-370 [PubMed]
• Verberne Eline A., Faries Sonja, Mannens Marcel M. A. M., Postma Alex V., van Haelst Mieke M. Expanding the phenotype of biallelic RNPC3 variants associated with growth hormone deficiency American journal of medical genetics. Part A 2020;182 (8):1952-1956 [PubMed]
• Chilunga Felix P., Henneman Peter, Requena-Méndez Ana, Meeks Karlijn, Beune Erik, Mannens Marcel M. A. M., Agyemang Charles Hyperuricaemia and its association with 10-year risk of cardiovascular disease among migrant and non-migrant African populations: the RODAM study Tropical medicine & international health 2020;25 (4):496-505 [PubMed]
• Verberne Eline A., Goh Shuxiang, England Jade, van Ginkel Manon, Rafael-Croes Louise, Maas Saskia, Polstra Abeltje, Zarate Yuri A., Bosanko Katherine A., Pechter Kieran B., Bedoukian Emma, Izumi Kosuke, Chaudhry Ayeshah, Robin Nathaniel H., Boothe Megan, Lippa Natalie C., Aggarwal Vimla, de Vivo Darryl C., Lehman Anna, Study Causes, Stockler Sylvia, Bruel Ange-Line, Isidor Bertrand, Lemons Jennifer, Rodriguez-Buritica David F., Richmond Christopher M., Stark Zornitza, Agrawal Pankaj B., Kooy R. Frank, Meuwissen Marije E. C., Koolen David A., Pfundt Rolf, Lieden Agne, Anderlid Britt-Marie, Glatz Dagmar, Mannens Marcel M. A. M., Bakshi Madhura, Mallette Frédérick A., van Haelst Mieke M., Campeau Philippe M. JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome Genetics in medicine 2020 [PubMed]

2019

• Krzyzewska I. M., Maas S. M., Henneman P., Lip K. V. D., Venema A., Baranano K., Chassevent A., Aref-Eshghi E., van Essen A. J., Fukuda T., Ikeda H., Jacquemont M., Kim H. G., Labalme A., Lewis S. M. E., Lesca G., Madrigal I., Mahida S., Matsumoto N., Rabionet R., Rajcan-Separovic E., Qiao Y., Sadikovic B., Saitsu H., Sweetser D. A., Alders M., Mannens M. M. A. M. A genome-wide DNA methylation signature for SETD1B-related syndrome Clinical epigenetics 2019;11 (1):156 [PubMed]
• Cobben Jan Maarten, Krzyzewska Izabela M., Venema Andrea, Mul Adri N., Polstra Abeltje, Postma Alex V., Smigiel Robert, Pesz Karolina, Niklinski Jacek, Chomczyk Monika A., Henneman Peter, Mannens Marcel M. A. M. DNA methylation abundantly associates with fetal alcohol spectrum disorder and its subphenotypes Epigenomics 2019;11 (7):767-785 [PubMed]
• Meeks Karlijn A. C., Henneman Peter, Venema Andrea, Addo Juliet, Bahendeka Silver, Burr Tom, Danquah Ina, Galbete Cecilia, Mannens Marcel M. A. M., Mockenhaupt Frank P., Owusu-Dabo Ellis, Rotimi Charles N., Schulze Matthias B., Smeeth Liam, Spranger Joachim, Zafarmand Mohammad H., Adeyemo Adebowale, Agyemang Charles Epigenome-wide association study in whole blood on type 2 diabetes among sub-Saharan African individuals: Findings from the RODAM study International journal of epidemiology 2019;48 (1):58-70 [PubMed]
• Krzyzewska I. M., Alders M., Maas S. M., Bliek J., Venema A., Henneman P., Rezwan F. I., Lip K. V. D., Mul A. N., Mackay D. J. G., Mannens M. M. A. M. Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics Clinical epigenetics 2019;11 (1) [PubMed]
• Mannens Marcel M. A. M. Klinische implicaties van epigenetische veranderingen Nederlands tijdschrift voor geneeskunde 2019;163 [PubMed]
• Chen Hung-Jen, Li Yim Andrew Y. F., Griffith Guillermo R., de Jonge Wouter J., Mannens Marcel M. A. M., Ferrero Enrico, Henneman Peter, de Winther Menno P. J. Meta-Analysis of in vitro-Differentiated Macrophages Identifies Transcriptomic Signatures That Classify Disease Macrophages in vivo Frontiers in immunology 2019;10 [PubMed]
• Nawijn L., Krzyzewska I. M., van Zuiden M., Henneman P., Koch S. B. J., Mul A. N., Frijling J. L., Veltman D. J., Mannens M. M. A. M., Olff M. Oxytocin receptor gene methylation in male and female PTSD patients and trauma-exposed controls European neuropsychopharmacology 2019;29 (1):147-155 [PubMed]
• Chilunga Felix P, Boateng Daniel, Henneman Peter, Beune Erik, Requena-Méndez Ana, Meeks Karlijn, Smeeth Liam, Addo Juliet, Bahendeka Silver, Danquah Ina, Schulze Matthias B, Klipstein-Grobusch Kerstin, Mannens Marcel M A M, Agyemang Charles Perceived discrimination and stressful life events are associated with cardiovascular risk score in migrant and non-migrant populations: The RODAM study International journal of cardiology 2019;286:169-174 [PubMed]
• Chilunga Felix P., Henneman Peter, Meeks Karlijn Ac, Beune Erik, Requena-Méndez Ana, Smeeth Liam, Addo Juliet, Bahendeka Silver, Danquah Ina, Schulze Matthias B., Spranger Joachim, Owusu-Dabo Ellis, Klipstein-Grobusch Kerstin, Mannens Marcel Mam, Agyemang Charles Prevalence and determinants of type 2 diabetes among lean African migrants and non-migrants: the RODAM study Journal of global health 2019;9 (2):020426 [PubMed]

2018

• Li Yim Andrew Y F, de Bruyn Jessica R, Duijvis Nicolette W, Sharp Catriona, Ferrero Enrico, de Jonge Wouter J, Wildenberg Manon E, Mannens Marcel M A M, Buskens Christianne J, D'Haens Geert R, Henneman Peter, Te Velde Anje A A distinct epigenetic profile distinguishes stenotic from non-inflamed fibroblasts in the ileal mucosa of Crohn's disease patients PLoS ONE 2018;13 (12):e0209656 [PubMed]
• Ferrer Christina M., Alders Marielle, Postma Alex V., Park Seonmi, Klein Mark A., Cetinbas Murat, Pajkrt Eva, Glas Astrid, van Koningsbruggen Silvana, Christoffels Vincent M., Mannens Marcel M. A. M., Knegt Lia, Etchegaray Jean-Pierre, Sadreyev Ruslan I., Denu John M., Mostoslavsky Gustavo, van Maarle Merel C., Mostoslavsky Raul An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality Genes & development 2018;32 (5-6):373-388 [PubMed]
• Stalman Susanne E., Solanky Nita, Ishida Miho, Alemán-Charlet Cristina, Abu-Amero Sayeda, Alders Marielle, Alvizi Lucas, Baird William, Demetriou Charalambos, Henneman Peter, James Chela, Knegt Lia C., Leon Lydia J., Mannens Marcel M. A. M., Mul Adi N., Nibbering Nicole A., Peskett Emma, Rezwan Faisal I., Ris-Stalpers Carrie, van der Post Joris A. M., Kamp Gerdine A., Plötz Frans B., Wit Jan M., Stanier Philip, Moore Gudrun E., Hennekam Raoul C. Genetic Analyses in Small for Gestational Age Newborns Journal of clinical endocrinology and metabolism 2018;103 (3):917-925 [PubMed]
• Krzyzewska Izabela M., Ensink Judith B. M., Nawijn Laura, Mul Adri N., Koch Saskia B., Venema Andrea, Shankar Vinod, Frijling Jessie L., Veltman Dirk J., Lindauer Ramon J. L., Olff Miranda, Mannens Marcel M. A. M., van Zuiden Mirjam, Henneman Peter Genetic variant in CACNA1C is associated with PTSD in traumatized police officers European journal of human genetics 2018;26 (2):247-257 [PubMed]
• Jansen Philip R., Petrus Nicole C. M., Venema Andrea, Posthuma Danielle, Mannens Marcel M. A. M., Sprikkelman Aline B., Henneman Peter Higher Polygenetic Predisposition for Asthma in Cow's Milk Allergic Children Nutrients 2018;10 (11) [PubMed]
• Henneman Peter, Bouman Arjan, Mul Adri, Knegt Lia, van der Kevie-Kersemaekers Anne-Marie, Zwaveling-Soonawala Nitash, Meijers-Heijboer Hanne E. J., Paul van Trotsenburg A. S., Mannens Marcel M. Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates PLoS ONE 2018;13 (3) [PubMed]

2017

• Chatzispyrou Iliana A., Alders Marielle, Guerrero-Castillo Sergio, Zapata Perez Ruben, Haagmans Martin A., Mouchiroud Laurent, Koster Janet, Ofman Rob, Baas Frank, Waterham Hans R., Spelbrink Johannes N., Auwerx Johan, Mannens Marcel M., Houtkooper Riekelt H., Plomp Astrid S. A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome Human molecular genetics 2017;26 (13):2541-2550 [PubMed]
• Meeks Karlijn A. C., Henneman Peter, Venema Andrea, Burr Tom, Galbete Cecilia, Danquah Ina, Schulze Matthias B., Mockenhaupt Frank P., Owusu-Dabo Ellis, Rotimi Charles N., Addo Juliet, Smeeth Liam, Bahendeka Silver, Spranger Joachim, Mannens Marcel M. A. M., Zafarmand Mohammad H., Agyemang Charles, Adeyemo Adebowale An epigenome-wide association study in whole blood of measures of adiposity among Ghanaians: the RODAM study Clinical epigenetics 2017;9:103 [PubMed]
• van de Meerakker Judith B. A. Genetic aspects of congenital heart defects 2017. 184p. ISBN 9789462997547. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Moorman A. F. M.; Co-supervisors: Mannens M. M. A. M., Postma A. V.)
• van Herpe Filip, Waterham Hans R., Adams Christopher J., Mannens Marcel, Bikker Hennie, Vaz Frédéric M., Cassiman David NTCP deficiency and persistently raised bile salts: an adult case Journal of inherited metabolic disease 2017;40 (3):313-315 [PubMed]
• Vermeer Alexa M. C., Janssen Anneloes, Boorsma Peter C., Mannens Marcel M. A. M., Wilde Arthur A. M., Christiaans Imke Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathy Amyloid : the international journal of experimental and clinical investigation 2017;24 (2):87-91 [PubMed]
• Jansweijer Joeri A., Nieuwhof Karin, Russo Francesco, Hoorntje Edgar T., Jongbloed Jan D. H., Lekanne Deprez Ronald H., Postma Alex V., Bronk Marieke, van Rijsingen Ingrid A. W., de Haij Simone, Biagini Elena, van Haelst Paul L., van Wijngaarden Jan, van den Berg Maarten P., Wilde Arthur A. M., Mannens Marcel M. A. M., de Boer Rudolf A., van Spaendonck-Zwarts Karin Y., van Tintelen J. Peter, Pinto Yigal M. Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy European journal of heart failure 2017;19 (4):512-521 [PubMed]

2016

• Petrus Nicole C. M., Henneman Peter, Venema Andrea, Mul Adri, van Sinderen Femke, Haagmans Martin, Mook Olaf, Hennekam Raoul C., Sprikkelman Aline B., Mannens Marcel Cow's milk allergy in Dutch children: an epigenetic pilot survey Clinical and translational allergy 2016;6:16 [PubMed]
• Eggermann Katja, Bliek Jet, Brioude Frédéric, Algar Elizabeth, Buiting Karin, Russo Silvia, Tümer Zeynep, Monk David, Moore Gudrun, Antoniadi Thalia, Macdonald Fiona, Netchine Irène, Lombardi Paolo, Soellner Lukas, Begemann Matthias, Prawitt Dirk, Maher Eamonn R., Mannens Marcel, Riccio Andrea, Weksberg Rosanna, Lapunzina Pablo, Grønskov Karen, Mackay Deborah J. G., Eggermann Thomas EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome European journal of human genetics 2016;24 (10):1377-1387 [PubMed]
• Henneman Peter, Petrus Nicole C. M., Venema Andrea, van Sinderen Femke, van der Lip Karin, Hennekam Raoul C., Mannens Marcel, Sprikkelman Aline B. Genetic susceptibility for cow's milk allergy in Dutch children: the start of the allergic march? Clinical and translational allergy 2016;6:7 [PubMed]
• Mannens Marcel, Temple I. Karen, Brioude Frédéric IGF2, H19, CDKN1C and KCNQ1OT1 and the Beckwith-Wiedemann Syndromein: Robert P. Erickson, Anthony J. Wynshaw-Boris, editors. Epstein’s inborn errors of development. Oxford University Press; 2016. p. 965-971, ISBN 9780199934522
• Li Yim Andrew Y. F., Duijvis Nicolette W., Zhao Jing, de Jonge Wouter J., D'Haens Geert R. A. M., Mannens Marcel M. A. M., Mul Adri N. P. M., te Velde Anje A., Henneman Peter Peripheral blood methylation profiling of female Crohn's disease patients Clinical epigenetics 2016;8:65 [PubMed]
• Maas Saskia M., Vansenne Fleur, Kadouch Daniel J. M., Ibrahim Abdulla, Bliek Jet, Hopman Saskia, Mannens Marcel M., Merks Johannes H. M., Maher Eamonn R., Hennekam Raoul C. Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups American journal of medical genetics. Part A 2016;170 (9):2248-2260 [PubMed]
• Eggermann Thomas, Brioude Frédéric, Russo Silvia, Lombardi Maria P., Bliek Jet, Maher Eamonn R., Larizza Lidia, Prawitt Dirk, Netchine Irène, Gonzales Marie, Grønskov Karen, Tümer Zeynep, Monk David, Mannens Marcel, Chrzanowska Krystyna, Walasek Malgorzata K., Begemann Matthias, Soellner Lukas, Eggermann Katja, Tenorio Jair, Nevado Julián, Moore Gudrun E., Mackay Deborah Jg, Temple Karen, Gillessen-Kaesbach Gabriele, Ogata Tsutomu, Weksberg Rosanna, Algar Elizabeth, Lapunzina Pablo Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling European journal of human genetics 2016;24 (6):784-793 [PubMed]
• Rump Patrick, Jazayeri Omid, van Dijk-Bos Krista K., Johansson Lennart F., van Essen Anthonie J., Verheij Johanna B. G. M., Veenstra-Knol Hermine E., Redeker Egbert J. W., Mannens Marcel M. A. M., Swertz Morris A., Alizadeh Behrooz Z., van Ravenswaaij-Arts Conny M. A., Sinke Richard J., Sikkema-Raddatz Birgit Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly BMC medical genomics 2016;9 (1):7 [PubMed]

2015

• Vrijenhoek Terry, Kraaijeveld Ken, Elferink Martin, de Ligt Joep, Kranendonk Elcke, Santen Gijs, Nijman Isaac J., Butler Derek, Claes Godelieve, Costessi Adalberto, Dorlijn Wim, van Eyndhoven Winfried, Halley Dicky J. J., van den Hout Mirjam C. G. N., van Hove Steven, Johansson Lennart F., Jongbloed Jan D. H., Kamps Rick, Kockx Christel E. M., de Koning Bart, Kriek Marjolein, Lekanne Dit Deprez Ronald, Lunstroo Hans, Mannens Marcel, Mook Olaf R., Nelen Marcel, Ploem Corrette, Rijnen Marco, Saris Jasper J., Sinke Richard, Sistermans Erik, van Slegtenhorst Marjon, Sleutels Frank, van der Stoep Nienke, van Tienhoven Marianne, Vermaat Martijn, Vogel Maartje, Waisfisz Quinten, Marjan Weiss Janneke, van den Wijngaard Arthur, van Workum Wilbert, Ijntema Helger, van der Zwaag Bert, van Ijcken Wilfred F. J., den Dunnen Johan, Veltman Joris A., Hennekam Raoul, Cuppen Edwin Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects European journal of human genetics 2015;23 (9):1142-1150 [PubMed]
• Vrijenhoek Terry, Kraaijeveld Ken, Elferink Martin, de Ligt Joep, Kranendonk Elcke, Santen Gijs, Nijman Isaac J., Butler Derek, Claes Godelieve, Costessi Adalberto, Dorlijn Wim, van Eyndhoven Winfried, Halley Dicky J. J., van den Hout Mirjam C. G. N., van Hove Steven, Johansson Lennart F., Jongbloed Jan D. H., Kamps Rick, Kockx Christel E. M., de Koning Bart, Kriek Marjolein, Lekanne Dit Deprez Ronald, Lunstroo Hans, Mannens Marcel, Mook Olaf R., Nelen Marcel, Ploem Corrette, Rijnen Marco, Saris Jasper J., Sinke Richard, Sistermans Erik, van Slegtenhorst Marjon, Sleutels Frank, van der Stoep Nienke, van Tienhoven Marianne, Vermaat Martijn, Vogel Maartje, Waisfisz Quinten, Weiss Janneke Marjan, van den Wijngaard Arthur, van Workum Wilbert, Ijntema Helger, van der Zwaag Bert, van Ijcken Wilfred F. J., den Dunnen Johan T., Veltman Joris A., Hennekam Raoul, Cuppen Edwin Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects (vol 23, pg 1142, 2015) European journal of human genetics 2015;23 (9):1270 [PubMed]
• Maas Saskia M., Shaw Adam C., Bikker Hennie, Lüdecke Hermann-Josef, van der Tuin Karin, Badura-Stronka Magdalena, Belligni Elga, Biamino Elisa, Bonati Maria Teresa, Carvalho Daniel R., Cobben JanMaarten, de Man Stella A., den Hollander Nicolette S., Di Donato Nataliya, Garavelli Livia, Grønborg Sabine, Herkert Johanna C., Hoogeboom A. Jeannette M., Jamsheer Aleksander, Latos-Bielenska Anna, Maat-Kievit Anneke, Magnani Cinzia, Marcelis Carlo, Mathijssen Inge B., Nielsen Maartje, Otten Ellen, Ousager Lilian B., Pilch Jacek, Plomp Astrid, Poke Gemma, Poluha Anna, Posmyk Renata, Rieubland Claudine, Silengo Margharita, Simon Marleen, Steichen Elisabeth, Stumpel Connie, Szakszon Katalin, Polonkai Edit, van den Ende Jenneke, van der Steen Antony, van Essen Ton, van Haeringen Arie, van Hagen Johanna M., Verheij Joke B. G. M., Mannens Marcel M., Hennekam Raoul C. Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome European journal of medical genetics 2015;58 (5):279-292 [PubMed]
• Meeks Karlijn A. C., Stronks Karien, Beune Erik J. A. J., Adeyemo Adebowale, Henneman Peter, Mannens Marcel M. A. M., Nicolaou Mary, Peters Ron J. G., Rotimi Charles N., Snijder Marieke B., Agyemang Charles Prevalence of type 2 diabetes and its association with measures of body composition among African residents in the Netherlands--The HELIUS study Diabetes research and clinical practice 2015;110 (2):137-146 [PubMed]
• Fernando Febilla, Keijser Remco, Henneman Peter, van der Kevie-Kersemaekers Anne-Marie F., Mannens Marcel Mam, van der Post Joris Am, Afink Gijs B., Ris-Stalpers Carrie The idiopathic preterm delivery methylation profile in umbilical cord blood DNA BMC genomics 2015;16 (1):736 [PubMed]

2014

• Eggermann Thomas, Algar Elizabeth, Lapunzina Pablo, Mackay Deborah, Maher Eamonn R., Mannens Marcel, Netchine Irène, Prawitt Dirk, Riccio Andrea, Temple I. Karen, Weksberg Rosanna Clinical utility gene card for: Beckwith-Wiedemann Syndrome European journal of human genetics 2014;22 (3):10.1038/ejhg.2013.132 [PubMed]
• Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J.E., Michels M., Postema P. G., Majoor-Krakauer D., Van Den Wijngaard A., Mannens M. M.A.M., Van Tintelen J. P., Van Langen I. M., Wilde A. A.M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlandsin: Founder Mutations in Inherited Cardiac Diseases in the Netherlands. Bohn Stafleu von Loghum; 2014. p. 37-42, ISBN 9036807042; 9789036807043
• Alders Mariëlle, Al-Gazali Lihadh, Cordeiro Isabelle, Dallapiccola Bruno, Garavelli Livia, Tuysuz Beyhan, Salehi Faranak, Haagmans Martin A., Mook Olaf R., Majoie Charles B., Mannens Marcel M., Hennekam Raoul C. Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome Human genetics 2014;133 (9):1161-1167 [PubMed]
• Alders Mariëlle, Maas Saskia M., Kadouch Daniël J. M., van der Lip Karin, Bliek Jet, van der Horst Chantal M. A. M., Mannens Marcel M. A. M. Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood European journal of medical genetics 2014;57 (6):293-297 [PubMed]
• Postma A. V., Alders M., Sylva M., Bilardo C. M., Pajkrt E., van Rijn R. R., Schulte-Merker S., Bulk S., Stefanovic S., Ilgun A., Barnett P., Mannens M. M. A. M., Moorman A. F. M., Oostra R. J., van Maarle M. C. Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal Journal of medical genetics 2014;51 (2):90-97 [PubMed]
• Cordeddu Viviana, Redeker Bert, Stellacci Emilia, Jongejan Aldo, Fragale Alessandra, Bradley Ted E. J., Anselmi Massimiliano, Ciolfi Andrea, Cecchetti Serena, Muto Valentina, Bernardini Laura, Azage Meron, Carvalho Daniel R., Espay Alberto J., Male Alison, Molin Anna-Maja, Posmyk Renata, Battisti Carla, Casertano Alberto, Melis Daniela, van Kampen Antoine, Baas Frank, Mannens Marcel M., Bocchinfuso Gianfranco, Stella Lorenzo, Tartaglia Marco, Hennekam Raoul C. Mutations in ZBTB20 cause Primrose syndrome Nature genetics 2014;46 (8):815-817 [PubMed]
• Agyemang Charles, Beune Erik, Meeks Karlijn, Owusu-Dabo Ellis, Agyei-Baffour Peter, Aikins Ama de-Graft, Dodoo Francis, Smeeth Liam, Addo Juliet, Mockenhaupt Frank P., Amoah Stephen K., Schulze Matthias B., Danquah Ina, Spranger Joachim, Nicolaou Mary, Klipstein-Grobusch Kerstin, Burr Tom, Henneman Peter, Mannens Marcel M., van Straalen Jan P., Bahendeka Silver, Zwinderman A. H., Kunst Anton E., Stronks Karien Rationale and cross-sectional study design of the Research on Obesity and type 2 Diabetes among African Migrants: the RODAM study BMJ open 2014;4 (3):e004877 [PubMed]

2013

• van de Meerakker Judith B. A., Christiaans Imke, Barnett Phil, Lekanne Deprez Ronald H., Ilgun Aho, Mook Olaf R. F., Mannens Marcel M. A. M., Lam Jan, Wilde Arthur A. M., Moorman Antoon F. M., Postma Alex V. A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH 2013;1833 (4):833-839 [PubMed]
• Weterings A. A. W., van Rijsingen I. A. W., Plomp A. S., Zwinderman A. H., Lekanne Deprez R. H., Mannens M. M., van den Bergh Weerman M. A., van der Wal A. C., Pinto-Sietsma S. J. A novel lamin A/C mutation in a Dutch family with premature atherosclerosis Atherosclerosis 2013;229 (1):169-173 [PubMed]
• Huisman Sylvia A., Redeker Egbert J. W., Maas Saskia M., Mannens Marcel M., Hennekam Raoul C. M. High rate of mosaicism in individuals with Cornelia de Lange syndrome Journal of medical genetics 2013;50 (5):339-344 [PubMed]
• Mook Olaf R. F., Haagmans Martin A., Soucy Jean-François, van de Meerakker Judith B. A., Baas Frank, Jakobs Marja E., Hofman Nynke, Christiaans Imke, Lekanne Deprez Ronald H., Mannens Marcel M. A. M. Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnostics Journal of medical genetics 2013;50 (9):614-626 [PubMed]
• Joustra S. D., Schoenmakers N., Persani L., Campi I., Bonomi M., Radetti G., Beck-Peccoz P., Zhu H., Davis T. M. E., Sun Y., Corssmit E. P., Appelman-Dijkstra N. M., Heinen C. A., Pereira A. M., Varewijck A. J., Janssen J. A. M. J. L., Endert E., Hennekam R. C., Lombardi M. P., Mannens M. M. A. M., Bak B., Bernard D. J., Breuning M. H., Chatterjee K., Dattani M. T., Oostdijk W., Biermasz N. R., Wit J. M., van Trotsenburg A. S. P. The IGSF1 deficiency syndrome: characteristics of male and female patients Journal of clinical endocrinology and metabolism 2013;98 (12):4942-4952 [PubMed]
• Hofman Nynke, Tan Hanno L., Alders Mariëlle, Kolder Iris, de Haij Simone, Mannens Marcel M. A. M., Lombardi Maria Paola, Lekanne Deprez Ronald H., van Langen Irene, Wilde Arthur A. M. Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience Circulation 2013;128 (14):1513-1521 [PubMed]

2012

• Hollak C. E. M., de Sonnaville E. S. V., Cassiman D., Linthorst G. E., Groener J. E., Morava E., Wevers R. A., Mannens M., Aerts J. M. F. G., Meersseman W., Akkerman E., Niezen-Koning K. E., Mulder M. F., Visser G., Wijburg F. A., Lefeber D., Poorthuis B. J. H. M. Acid sphingomyelinase (Asm) deficiency patients in The Netherlands and Belgium: Disease spectrum and natural course in attenuated patients Molecular genetics and metabolism 2012;107 (3):526-533 [PubMed]

2011

• Biegstraaten M., van Schaik I. N., Aerts J. M. F. G., Langeveld M., Mannens M. M. A. M., Bour L. J., Sidransky E., Tayebi N., Fitzgibbon E., Hollak C. E. M. A monozygotic twin pair with highly discordant Gaucher phenotypes Blood cells, molecules & diseases 2011;46 (1):39-41 [PubMed]
• van de Meerakker Judith B. A., van Engelen Klaartje, Mathijssen Inge B., Lekanne dit Deprez Ronald H., Lam Jan, Wilde Arthur A. M., Baars Marieke J. H., Mannens Marcel M. A. M., Mulder Barbara J. M., Moorman Antoon F. M., Postma Alex V. A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q European journal of human genetics 2011;19 (7):820-826 [PubMed]
• Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J. E., Michels M., Postema P. G., Majoor-Krakauer D., van den Wijngaard A., Mannens M. M. A. M., van Tintelen J. P., van Langen I. M., Wilde A. A. M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands Netherlands heart journal 2011;19 (Suppl. S):32-37
• Mannens M., Smeets E. Introduction to molecular geneticsin: H. F. Baars, J. J. van der Smagt, P. A. F. M. Doevendans, editors. Clinical Cardiogenetics. London: Springer-Verlag; 2011. p. 3-21, ISBN 9781849964708
• Christiaans Imke, Birnie Erwin, Bonsel Gouke J., Mannens Marcel M. A. M., Michels Michelle, Majoor-Krakauer Daniëlle, Dooijes Dennis, van Tintelen J. Peter, van den Berg Maarten P., Volders Paul G. A., Arens Yvonne H., van den Wijngaard Arthur, Atsma Douwe E., Helderman-van den Enden Apollonia T. J. M., Houweling Arjan C., de Boer Karin, van der Smagt Jasper J., Hauer Richard N. W., Marcelis Carlo L. M., Timmermans Janneke, van Langen Irene M., Wilde Arthur A. M. Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy European heart journal 2011;32 (9):1161-1170 [PubMed]
• Lombardi Maria Paola, Bulk Saskia, Celli Jacopo, Lampe Anne, Gabbett Michael T., Ousager Lillian Bomme, van der Smagt Jasper J., Soller Maria, Stattin Eva-Lena, Mannens Marcel A. M. M., Smigiel Robert, Hennekam Raoul C. Mutation update for the PORCN gene Human mutation 2011;32 (7):723-728 [PubMed]
• Nof Eyal, Belhassen Bernard, Arad Michael, Bhuiyan Zahurul A., Antzelevitch Charles, Rosso Raphael, Fogelman Rami, Luria David, El-Ani Dalia, Mannens Marcel M. A. M., Viskin Sami, Eldar Michael, Wilde Arthur A. M., Glikson Michael Postpacing abnormal repolarization in catecholaminergic polymorphic ventricular tachycardia associated with a mutation in the cardiac ryanodine receptor gene Heart rhythm 2011;8 (10):1546-1552 [PubMed]
• van den Wijngaard A., Volders P., van Tintelen J. P., Jongbloed J. D. H., van den Berg M. P., Lekanne Deprez R. H., Mannens M. M. A. M., Hofmann N., Slegtenhorst M., Dooijes D., Michels M., Arens Y., Jongbloed R., Smeets B. J. M. Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy Netherlands heart journal 2011;19 (7-8):344-351 [PubMed]

2010

• Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J. E., Michels M., Postema P. G., Majoor-Krakauer D., van den Wijngaard A., Mannens M. M. A. M., van Tintelen J. P., van Langen I. M., Wilde A. A. M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands Netherlands heart journal 2010;18 (5):248-254 [PubMed]
• van Kuilenburg André B. P., Meijer Judith, Mul Adri N. P. M., Meinsma Rutger, Schmid Veronika, Dobritzsch Doreen, Hennekam Raoul C. M., Mannens Marcel M. A. M., Kiechle Marion, Etienne-Grimaldi Marie-Christine, Klümpen Heinz-Josef, Maring Jan Gerard, Derleyn Veerle A., Maartense Ed, Milano Gérard, Vijzelaar Raymon, Gross Eva Intragenic deletions and a deep intronic mutation affecting pre-mRNA splicing in the dihydropyrimidine dehydrogenase gene as novel mechanisms causing 5-fluorouracil toxicity Human genetics 2010;128 (5):529-538 [PubMed]
• Kuipers Remko, van den Bergh Tom, Joosten Henk-Jan, Lekanne dit Deprez Ronald H., Mannens Marcel M. A. M., Schaap Peter J. Novel tools for extraction and validation of disease-related mutations applied to fabry disease Human mutation 2010;31 (9):1026-1032 [PubMed]

2009

• Bliek Jet Aberrant genomic imprinting in chromosome 11p15-associated congenital growth disorders: consequences for DNA-diagnostics 2009. 201p. ISBN 9789036737739. [UvA Dissertations Online] University of Amsterdam. (Supervisors: Leschot N. J., Westerveld A.; Co-supervisor: Mannens M. M. A. M.)
• Bhuiyan Zahurul A., Al-Shahrani Safar, Al-Khadra Ayman S., Al-Ghamdi Saleh, Al-Khalaf Khalaf, Mannens Marcel M. A. M., Wilde Arthur A. M., Momenah Tarek S. Clinical and Genetic Analysis of Long QT Syndrome in Children from Six Families in Saudi Arabia: Are They Different? Pediatric cardiology 2009;30 (4):490-501 [PubMed]
• Bhuiyan Zahurul A. Clinical and genetic spectrum of hereditary cardiac arrhythmia syndromes 2009. 327p. ISBN 9789090243184. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisor: Mannens M. M. A. M.)
• Bhuiyan Zahurul A., Jongbloed Jan D. H., van der Smagt Jasper, Lombardi Paola M., Wiesfeld Ans C. P., Nelen Marcel, Schouten Meyke, Jongbloed Roselie, Cox Moniek G. P. J., van Wolferen Marleen, Rodriguez Luz M., van Gelder Isabelle C., Bikker Hennie, Suurmeijer Albert J. H., van den Berg Maarten P., Mannens Marcel M. A. M., Hauer Richard N. W., Wilde Arthur A. M., van Tintelen J. Peter Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients Results From a Multicenter Study Circulation. Cardiovascular genetics 2009;2 (5):418-U22 [PubMed]
• Alders Marielle, Bliek Jet, van der Lip Karin, van der Bogaard Ruud, Mannens Marcel Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis European journal of human genetics 2009;17 (4):467-473 [PubMed]
• Alders Marielle, Koopmann Tamara T., Christiaans Imke, Postema Pieter G., Beekman Leander, Tanck Michael W. T., Zeppenfeld Katja, Loh Peter, Koch Karel T., Demolombe Sophie, Mannens Marcel M. A. M., Bezzina Connie R., Wilde Arthur A. M. Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation American journal of human genetics 2009;84 (4):468-476 [PubMed]
• Bliek Jet, Verde Gaetano, Callaway Jonathan, Maas Saskia M., de Crescenzo Agostina, Sparago Angela, Cerrato Flavia, Russo Silvia, Ferraiuolo Serena, Rinaldi Maria Michela, Fischetto Rita, Lalatta Faustina, Giordano Lucio, Ferrari Paola, Cubellis Maria Vittoria, Larizza Lidia, Temple I. Karen, Mannens Marcel M. A. M., Mackay Deborah J. G., Riccio Andrea Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome European journal of human genetics 2009;17 (5):611-619 [PubMed]
• Bliek Jet, Alders Marielle, Maas Saskia M., Oostra Roelof-Jan, Mackay Deborah M., van der Lip Karin, Callaway Johnatan L., Brooks Alice, van 't Padje Sandra, Westerveld Andries, Leschot Nico J., Mannens Marcel M. A. M. Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells European journal of human genetics 2009;17 (12):1625-1634 [PubMed]
• de Fost M., Langeveld M., Franssen R., Hutten B. A., Groener J. E. M., de Groot E., Mannens M. M., Bikker H., Aerts J. M. F. G., Kastelein J. J. P., Hollak C. E. M. Low HDL cholesterol levels in type I Gaucher disease do not lead to an increased risk of cardiovascular disease Atherosclerosis 2009;204 (1):267-272 [PubMed]
• Alders Marielle, Hogan Benjamin M., Gjini Evisa, Salehi Faranak, Al-Gazali Lihadh, Hennekam Eric A., Holmberg Eva E., Mannens Marcel M. A. M., Mulder Margot F., Offerhaus G. Johan A., Prescott Trine E., Schroor Eelco J., Verheij Joke B. G. M., Witte Merlijn, Zwijnenburg Petra J., Vikkula Mikka, Schulte-Merker Stefan, Hennekam Raoul C. Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans Nature genetics 2009;41 (12):1272-1274 [PubMed]
• Bliek J., Snijder S., maas S. M., Polstra A., van der Lip K., Alders M., Knegt A. C., Mannens M. M. A. M. Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regions European journal of medical genetics 2009;52 (6):404-408 [PubMed]
• Medeiros-Domingo Argelia, Bhuiyan Zahurul A., Tester David J., Hofman Nynke, Bikker Hennie, van Tintelen J. Peter, Mannens Marcel M. A. M., Wilde Arthur A. M., Ackerman Michael J. The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome A Comprehensive Open Reading Frame Mutational Analysis Journal of the American College of Cardiology 2009;54 (22):2065-2074 [PubMed]

2008

• Bhuiyan Zahurul A., Momenah Tarek S., Amin Ahmad S., Al-Khadra Ayman S., Alders Marielle, Wilde Arthur A. M., Mannens Marcel M. A. M. An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome Progress in biophysics and molecular biology 2008;98 (2-3):319-327 [PubMed]
• Bliek Jet, Maas Saskia, Alders Mariel, Merks Johannes H. M., Mannens Marcel Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia Journal of pediatrics 2008;153 (1):95-100 [PubMed]
• Gijsbers Antoinet C. J., D'haene Barbara, Hilhorst-Hofstee Yvonne, Mannens Marcel, Albrecht Beate, Seidel Joerg, Witt David R., Maisenbacher Melissa K., Loeys Bart, van Essen Ton, Bakker Egbert, Hennekam Raoul, Breuning Martijn H., de Baere Elfride, Ruivenkamp Claudia A. L. Identification of copy number variants associated with BPES-like phenotypes Human genetics 2008;124 (5):489-498 [PubMed]
• Redeker Egbert J. W., de Visser Annette S. H., Bergen Arthur A. B., Mannens Marcel M. A. M. Multiplex ligation-dependent probe amplification (MLPA) enhances the molecular diagnosis of aniridia and related disorders Molecular vision 2008;14 (97-99):836-840 [PubMed]
• Bhuiyan Zahurul A., Momenah Tarek S., Gong Qiuming, Amin Ahmad S., Ghamdi Saleh Al, Carvalho Julene S., Homfray Tessa, Mannens Marcel M. A. M., Zhou Zhengfeng, Wilde Arthur A. M. Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation Heart rhythm 2008;5 (4):553-561 [PubMed]

2007

• Bhuiyan Zahurul A., Hamdan Mohamed A., Shamsi Eman T. A., Postma Alex V., Mannens Marcel M. A. M., Wilde Arthur A. M., Al-Gazali Lihadh A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22 Journal of cardiovascular electrophysiology 2007;18 (10):1060-1066 [PubMed]
• Hofman Nynke, Wilde Arthur A. M., Kääb Stefan, van Langen Irene M., Tanck Michael W. T., Mannens Marcel M. A. M., Hinterseer Martin, Beckmann Britt-Maria, Tan Hanno L. Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? European heart journal 2007;28 (5):575-580 [PubMed]
• Koopmann Tamara T., Beekman Leander, Alders Marielle, Meregalli Paola G., Mannens Marcel M. A. M., Moorman Antoon F. M., Wilde Arthur A. M., Bezzina Connie R. Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort Heart rhythm 2007;4 (6):752-755 [PubMed]
• Bhuiyan Zahurul A., van den Berg Maarten P., van Tintelen J. Peter, Bink-Boelkens Margreet T. E., Wiesfeld Ans C. P., Alders Marielle, Postma Alex V., van Langen Irene, Mannens Marcel M. A. M., Wilde Arthur A. M. Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features Circulation 2007;116 (14):1569-1576 [PubMed]
• Vrouwe Mischa G., Elghalbzouri-Maghrani Elhaam, Meijers Matty, Schouten Peter, Godthelp Barbara C., Bhuiyan Zahurul A., Redeker Egbert J., Mannens Marcel M., Mullenders Leon H. F., Pastink Albert, Darroudi Firouz Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair Human molecular genetics 2007;16 (12):1478-1487 [PubMed]
• Bhuiyan Zahurul A., Stewart Helen, Redeker Egbert J., Mannens Marcel M. A. M., Hennekam Raoul C. M. Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange syndrome European journal of human genetics 2007;15 (4):505-508 [PubMed]
• Vedder A. C., Linthorst G. E., van Breemen M. J., Groener J. E. M., Bemelman F. J., Strijland A., Mannens M. M. A. M., Aerts J. M. F. G., Hollak C. E. M. The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levels Journal of inherited metabolic disease 2007;30 (1):68-78 [PubMed]

2006

• Kannankeril Prince J., Bhuiyan Zahurul A., Darbar Dawood, Mannens Marcel M. A. M., Wilde Arthur A. M., Roden Dan M. Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family Heart rhythm 2006;3 (8):939-944 [PubMed]
• Bhuiyan Z. A., Klein M., Hammond P., van Haeringen A., Mannens M. M. A. M., van Berckelaer-Onnes I., Hennekam R. C. M. Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience Journal of medical genetics 2006;43 (7):568-575 [PubMed]
• Bliek Jet, Terhal Paulien, van den Bogaard Marie-José, Maas Saskia, Hamel Ben, Salieb-Beugelaar Georgette, Simon Marleen, Letteboer Tom, van der Smagt Jasper, Kroes Hester, Mannens Marcel Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype American journal of human genetics 2006;78 (4):604-614 [PubMed]
• Koopmann Tamara T., Alders Marielle, Jongbloed Roselie J., Guerrero Silvia, Mannens Marcel M. A. M., Wilde Arthur A. M., Bezzina Connie R. Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies Heart rhythm 2006;3 (1):52-55 [PubMed]
• Lombardi M. P., Redeker E. J. W., van Gent D. H. M., Smeele K. L., Weerdesteijn R., Mannens M. M. A. M. Molecular genetic testing for familial hypercholesterolemia in the Netherlands: a stepwise screening strategy enhances the mutation detection rate Genetic testing 2006;10 (2):77-84 [PubMed]
• Florijn Ralph J., Loves Willem, Maillette de Buy Wenniger-Prick Liesbeth J. J. M., Mannens Marcel M. A. M., Tijmes Nel, Brooks Simon P., Hardcastle Alison J., Bergen Arthur A. B. New mutations in the NHS gene in Nance-Horan Syndrome families from the Netherlands European journal of human genetics 2006;14 (9):986-990 [PubMed]
• van Tintelen J. Peter, Entius Mark M., Bhuiyan Zahurul A., Jongbloed Roselie, Wiesfeld Ans C. P., Wilde Arthur A. M., van der Smagt Jasper, Boven Ludolf G., Mannens Marcel M. A. M., van Langen Irene M., Hofstra Robert M. W., Otterspoor Luuk C., Doevendans Pieter A. F. M., Rodriguez Luz-Maria, van Gelder Isabelle C., Hauer Richard N. W. Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy Circulation 2006;113 (13):1650-1658 [PubMed]

2005

• Smits Jeroen P. P., Koopmann Tamara T., Wilders Ronald, Veldkamp Marieke W., Opthof Tobias, Bhuiyan Zahir A., Mannens Marcel M. A. M., Balser Jeffrey R., Tan Hanno L., Bezzina Connie R., Wilde Arthur A. M. A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families Journal of molecular and cellular cardiology 2005;38 (6):969-981 [PubMed]
• Tycko B., Mannens M. M. A. M. Beckwith-Wiedemann syndromein: L. B. Jorde, P. F. R. Little, M. J. Dunn, editors. Encyclopedia of genetics, genomics, proteomics and bioinformatics 1. S.l.: Wiley; 2005. p. 259-ev
• Postma A. V., Denjoy I., Kamblock J., Alders M., Lupoglazoff J.-M., Vaksmann G., Dubosq-Bidot L., Sebillon P., Mannens M. M. A. M., Guicheney P., Wilde A. A. M. Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients Journal of medical genetics 2005;42 (11):863-870 [PubMed]
• van der Velde E. T., Vander Velde E. T., Vriend J. W. J., Mannens M. M. A. M., Uiterwaal C. S. P. M., Brand R., Mulder Barbara J. M. CONCOR, an initiative towards a national registry and DNA-bank of patients with congenital heart disease in the Netherlands: Rationale, design, and first results European journal of epidemiology 2005;20 (6):549-557 [PubMed]
• van der Velde E. T., Vriend J. W. J., Mannens M. M. A. M., Uiterwaal C. S. P. M., Brand R., Mulder B. J. M. CONCOR, an initiative towards a national registry and DNA-bank of patients with congenital heart disease in the Netherlands: Rationale, design, and frst results (vol 20, pg 549, 2005) European journal of epidemiology 2005;20 (10):885
• Wilde A. A. M., van Langen I. M., Mannens M. M. A. M., Waalewijn R. A., Maes A. Plotseling overlijden op jonge leeftijd en het belang van moleculair-pathologisch onderzoek Nederlands tijdschrift voor geneeskunde 2005;149 (29):1601-1604 [PubMed]
• Verkerk Arie O., Wilders Ronald, Schulze-Bahr Eric, Beekman Leander, Bhuiyan Zahurul A., Bertrand Jessica, Eckardt Lars, Lin Dongxin, Borggrefe Martin, Breithardt Günter, Mannens Marcel M. A. M., Tan Hanno L., Wilde Arthur A. M., Bezzina Connie R. Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome Cardiovascular research 2005;68 (3):441-453 [PubMed]

2004

• Leschot N. J., Mannens M. M. A. M. De zorgwekkende gevolgen van het octrooieren van humane genen voor de gezondheidszorg en het wetenschappelijk onderzoek in Nederland Nederlands tijdschrift voor geneeskunde 2004;148 (35):1712-1715 [PubMed]
• Hu Xiaofeng, Plomp Astrid, Gorgels Theo, Brink Jacoline Ten, Loves Willem, Mannens Marcel, de Jong Paulus T. V. M., Bergen Arthur A. B. Efficient molecular diagnostic strategy for ABCC6 in pseudoxanthoma elasticum Genetic testing 2004;8 (3):292-300 [PubMed]
• Bliek Jet, Gicquel Christine, Maas Saskia, Gaston Véronique, Le Bouc Yves, Mannens Marcel Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS) Journal of pediatrics 2004;145 (6):796-799 [PubMed]
• Bellocq Chloé, van Ginneken Antoni C. G., Bezzina Connie R., Alders Mariel, Escande Denis, Mannens Marcel M. A. M., Baró Isabelle, Wilde Arthur A. M. Mutation in the KCNQ1 gene leading to the short QT-interval syndrome Circulation 2004;109 (20):2394-2397 [PubMed]

2003

• Bezzina Connie R., Verkerk Arie O., Busjahn Andreas, Jeron Andreas, Erdmann Jeanette, Koopmann Tamara T., Bhuiyan Zahurul A., Wilders Ronald, Mannens Marcel M. A. M., Tan Hanno L., Luft Friedrich C., Schunkert Heribert, Wilde Arthur A. M. A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization Cardiovascular research 2003;59 (1):27-36 [PubMed]
• Groenewegen W. Antoinette, Bezzina Connie R., van Tintelen J. Peter, Hoorntje Theo M., Mannens Marcel M. A. M., Wilde Arthur A. M., Jongsma Habo J., Rook Martin B. A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics Cardiovascular research 2003;57 (4):1072-1078 [PubMed]
• Gianotten Judith, van der Veen Fulco, Alders Mariëlle, Leschot Nico J., Tanck Michael W. T., Land Jolande A., Kremer Jan A. M., Hoefsloot Lies H., Mannens Marcel M., Lombardi M. Paola, Hoffer Mariëtte J. V. Chromosomal region 11p15 is associated with male factor subfertility Molecular human reproduction 2003;9 (10):587-592 [PubMed]
• Bezzina Connie R., Rook Martin B., Groenewegen W. Antoinette, Herfst Lucas J., van der Wal Allard C., Lam Jan, Jongsma Habo J., Wilde Arthur A. M., Mannens Marcel M. A. M. Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system Circulation research 2003;92 (2):159-168 [PubMed]
• Postma A. V. Genetics aspects of cardiac arrythmia syndromes 2003. 162p. ISBN 9789090170916. [UvA Dissertations Online] University of Amsterdam. (Supervisor: Wilde A. A. M.; Co-supervisors: Moorman A. F. M., Mannens M. M. A. M.)
• Alders Marielle, Jongbloed Roselie, Deelen Wout, van den Wijngaard Arthur, Doevendans Pieter, ten Cate Folkert, Regitz-Zagrosek Vera, Vosberg Hans Peter, van Langen Irene, Wilde Arthur, Dooijes Dennis, Mannens Marcel The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands European heart journal 2003;24 (20):1848-1853 [PubMed]

2002

• Postma Alex V., Denjoy Isabelle, Hoorntje Theo M., Lupoglazoff Jean-Marc, Da Costa Antoine, Sebillon Pascale, Mannens Marcel M. A. M., Wilde Arthur A. M., Guicheney Pascale Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia Circulation research 2002;91 (8):E21-E26 [PubMed]
• Breugem Corstiaan C., Alders Marielle, Salieb-Beugelaar Georgette B., Mannens Marcel M. A. M., van der Horst Chantal M., Hennekam Raoul C. M. A locus for hereditary capillary malformations mapped on chromosome 5q Human genetics 2002;110 (4):343-347 [PubMed]
• Mannens M. M. A. M. Beckwith-Wiedemann syndromein: C. D. M. Fletcher, K. K. Unni, F. Mertens, editors. Pathology & Genetics. Tumours of soft tissue and bone. S.l.: WHO Classification of tumours; 2002. p. 354-355

2001

• Bliek J., maas S. M., Ruijter J. M., Hennekam R. C., Alders M., Westerveld A., Mannens M. M. Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS Human molecular genetics 2001;10 (5):467-476 [PubMed]

2000

• Aalfs C. M., Salieb-Beugelaar G. B., Wanders R. J., Mannens M. M., Wijburg F. A. A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basis Human mutation 2000;16 (1):18-22 [PubMed]
• Wilde A. A. M., Mannens M. M. A. M., Alders M., van der Lip K., Hoorntje T. M., Sreeram N., van Tintelen P., van der Wal A. A knockout may not always be a knockout - Response Circulation 2000;102 (18):E122-E122
• Steenman M. J., Zijlstra N., Kruitbosch D. L., Wiesmeijer C., Larizza L., Voûte P. A., Westerveld A., Mannens M. M. Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors Cytogenetics and cell genetics 2000;88 (3-4):289-295 [PubMed]
• Leschot N. J., Mannens M. M. De ontrafeling van het humane genoom: een mijlpaal, geen eindstreep Nederlands tijdschrift voor geneeskunde 2000;144 (23):1093-1096 [PubMed]
• Alders M., Ryan A., Hodges M., Bliek J., Feinberg A. P., Privitera O., Westerveld A., Little P. F., Mannens M. Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome American journal of human genetics 2000;66 (5):1473-1484 [PubMed]
• Steenman M., Westerveld A., Mannens M. Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways Genes, chromosomes & cancer 2000;28 (1):1-13 [PubMed]
• Postma A. V., Bezzina C. R., de Vries J. F., Wilde A. A., Moorman A. F., Mannens M. M. Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3 Human genetics 2000;106 (6):614-619 [PubMed]
• van den Bogaard R., Fijen C. A., Schipper M. G., de Galan L., Kuijper E. J., Mannens M. M. Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies European journal of human genetics 2000;8 (7):513-518 [PubMed]
• Lombardi M. P., Redeker E. J., Defesche J. C., Kamerling S. W., Trip M. D., Mannens M. M., Havekes L. M., Kastelein J. J. Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The Netherlands Clinical genetics 2000;57 (2):116-124 [PubMed]

1999

• Bezzina C., Veldkamp M. W., van den Berg M. P., Postma A. V., Rook M. B., Viersma J. W., van Langen I. M., Tan-Sindhunata G., Bink-Boelkens M. T., van der Hout A. H., Mannens M. M., Wilde A. A. A single Na(+) channel mutation causing both long-QT and Brugada syndromes Circulation research 1999;85 (12):1206-1213 [PubMed]
• Schott J. J., Alshinawi C., Kyndt F., Probst V., Hoorntje T. M., Hulsbeek M., Wilde A. A., Escande D., Mannens M. M., Le Marec H. Cardiac conduction defects associate with mutations in SCN5A Nature genetics 1999;23 (1):20-21 [PubMed]
• Steenman M., Tomlinson G., Westerveld A., Mannens M. Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma Cytogenetics and cell genetics 1999;86 (2):157-161 [PubMed]
• Mannens M., Alders M. Genomic imprinting: concept and clinical consequences Annals of medicine 1999;31 (1):4-11 [PubMed]
• Hoorntje T., Alders M., van Tintelen P., van der Lip K., Sreeram N., van der Wal A., Mannens M., Wilde A. Homozygous premature truncation of the HERG protein : the human HERG knockout Circulation 1999;100 (12):1264-1267 [PubMed]
• Rook M. B., Bezzina Alshinawi C., Groenewegen W. A., van Gelder I. C., van Ginneken A. C., Jongsma H. J., Mannens M. M., Wilde A. A. Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome Cardiovascular research 1999;44 (3):507-517 [PubMed]
• Fijen C. A., van den Bogaard R., Schipper M., Mannens M., Schlesinger M., Nordin F. G., Dankert J., Daha M. R., Sjöholm A. G., Truedsson L., Kuijper E. J. Properdin deficiency: molecular basis and disease association Molecular immunology 1999;36 (13-14):863-867 [PubMed]
• Gaudray P., Carle G. F., Gerhard D. S., Gessler M., Mannens M. M., Athanasiou M., Bliek J., Calender A., Debelenko L. V., Devignes M., Evans G. A., Favier R., Forbes S., Gaudray G., Gawin B., Gordon M., Grimmond S., Grossfeld P., Harris J., Hattori M., Hosoda F., Hummerich H., James M., Kalla J., Katsanis N. Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998. Nice, France, May 2-5, 1998 Cytogenetics and cell genetics 1999;86 (3-4):167-186 [PubMed]

1998

• Demolombe S., Baró I., Péréon Y., Bliek J., Mohammad-Panah R., Pollard H., Morid S., Mannens M., Wilde A., Barhanin J., Charpentier F., Escande D. A dominant negative isoform of the long QT syndrome 1 gene product Journal of biological chemistry 1998;273 (12):6837-6843 [PubMed]
• Speleman F., van den Berg E., Dhooge C., Oosterhuis W., Redeker B., de Potter C. R., Tamminga R. Y., van Roy N., Mannens M. Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma Genes, chromosomes & cancer 1998;21 (3):265-269 [PubMed]
• Henderson H. E., Bijvoet S. M., Mannens M. A., Bruin T., Erkelens D. W., Hayden M. R., Kastelein J. J. Ile225Thr loop mutation in the lipoprotein lipase (LPL) gene is a de novo event American journal of medical genetics 1998;78 (4):313-316 [PubMed]
• van Langen I. M., Wilde A. A., Mannens M. A. Plotselinge dood bij jonge mensen door aritmogene rechterventrikeldysplasie Nederlands tijdschrift voor geneeskunde 1998;142 (13):739-740 [PubMed]
• Boot R. G., Renkema G. H., Verhoek M., Strijland A., Bliek J., de Meulemeester T. M., Mannens M. M., Aerts J. M. The human chitotriosidase gene. Nature of inherited enzyme deficiency Journal of biological chemistry 1998;273 (40):25680-25685 [PubMed]

1997

• Steenman M., Redeker B., de Meulemeester M., Wiesmeijer K., Voûte P. A., Westerveld A., Slater R., Mannens M. Comparative genomic hybridization analysis of Wilms tumors Cytogenetics and cell genetics 1997;77 (3-4):296-303 [PubMed]
• Nesbit M. A., Hodges M. D., Campbell L., de Meulemeester T. M., Alders M., Rodrigues N. R., Talbot K., Theodosiou A. M., Mannens M. A., Nakamura Y., Little P. F., Davies K. E. Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2 Genomics 1997;42 (2):284-294 [PubMed]
• Boot R. G., Hollak C. E., Verhoek M., Sloof P., Poorthuis B. J., Kleijer W. J., Wevers R. A., van Oers M. H., Mannens M. M., Aerts J. M., van Weely S. Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic value Human mutation 1997;10 (5):348-358 [PubMed]
• Oudejans C., Westerman B., van Elk E., Könst A., Mulders M., Alders M., van Vugt J., van Wijk I., Mannens M. Growth regulation of extraembryonic tissues. The effect of genomic imprinting on development of the placenta European journal of obstetrics, gynecology, and reproductive biology 1997;75 (1):29-32 [PubMed]
• Wilde A. A., Mannens M. M. Iatrogene collaps; is die te voorkomen? Nederlands tijdschrift voor geneeskunde 1997;141 (16):796-797 [PubMed]
• Mannens M., Wilde A. KVLQT1, the rhythm of imprinting Nature genetics 1997;15 (2):113-115 [PubMed]
• Alders M., Hodges M., Hadjantonakis A. K., Postmus J., van Wijk I., Bliek J., de Meulemeester M., Westerveld A., Guillemot F., Oudejans C., Little P., Mannens M. The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts Human molecular genetics 1997;6 (6):859-867 [PubMed]

1996

• Fijen C. A., van den Bogaard R., Daha M. R., Dankert J., Mannens M., Kuijper E. J. Carrier detection by microsatellite haplotyping in 10 properdin type 1-deficient families European journal of clinical investigation 1996;26 (10):902-906 [PubMed]
• Alders M., Bliek J., Redeker B., Ryan A., Feinberg A., Westerveld A., Little P., Mannens M. Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors Medical and pediatric oncology 1996;27 (5):495-497 [PubMed]
• Mannens M., Alders M., Redeker B., Bliek J., Steenman M., Wiesmeyer C., de Meulemeester M., Ryan A., Kalikin L., Voûte T., de Kraker J., Hoovers J., Slater R., Feinberg A., Little P., Westerveld A. Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors Medical and pediatric oncology 1996;27 (5):490-494 [PubMed]
• Shows T. B., Alders M., Bennett S., Burbee D., Cartwright P., Chandrasekharappa S., Cooper P., Courseaux A., Davies C., Devignes M. D., Devilee P., Elliott R., Evans G., Fantes J., Garner H., Gaudray P., Gerhard D. S., Gessler M., Higgins M., Hummerich H., James M., Lagercrantz J., Litt M., Little P., Mannens M., Munroe D., Nowak N., O'Brien S., Parker N., Perlin M., Reid L., Richard C., Sawicki M., Swallow D., Thakker R., van Heyningen V., van Schothorst E., Vorechovsky I., Wadelius C., Weber B., Zabel B. Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996 Cytogenetics and cell genetics 1996;74 (1-2):1-56 [PubMed]
• de Meulemeester M., Vink A., Jakobs M., Hermsen M., Steenman M., Slater R., Dietrich A., Mannens M. The application of microwave denaturation in comparative genomic hybridization Genetic analysis 1996;13 (5):129-133 [PubMed]

1995

• Fantes J. A., Oghene K., Boyle S., Danes S., Fletcher J. M., Bruford E. A., Williamson K., Seawright A., Schedl A., Hanson I., Zehetner G., Bhogal R., Lehrach H., Gregory S., Williams J., Little P. F. R., Sellar G. C., Hoovers J., Mannens M., Weissenbach J., Junien C., van Heyningen V., Bickmore W. A. A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1 Genomics 1995;25 (2):447-461 [PubMed]
• Fantes J., Redeker B., Breen M., Boyle S., Brown J., Fletcher J., Jones S., Bickmore W., Fukushima Y., Mannens M. Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype Human molecular genetics 1995;4 (3):415-422 [PubMed]
• Austruy E., Candon S., Henry I., Gyapay G., Tournade M. F., Mannens M., Callen D., Junien C., Jeanpierre C. Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis Genes, chromosomes & cancer 1995;14 (4):285-294 [PubMed]
• Fijen C. A., Derkx B. H., Kuijper E. J., Mannens M., Poort S. R., Peters M., Daha M. R., Dankert J. Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiency Clinical and experimental immunology 1995;102 (2):290-296 [PubMed]
• Aalfs C. M., Hoovers J. M., Nieste-Otter M. A., Mannens M. M., Hennekam R. C., Leschot N. J. Further delineation of the partial proximal trisomy 10q syndrome Journal of medical genetics 1995;32 (12):968-971 [PubMed]
• Hoovers J. M., Kalikin L. M., Johnson L. A., Alders M., Redeker B., Law D. J., Bliek J., Steenman M., Benedict M., Wiegant J., Lengauer C., Taillon-Miller P., Schlessinger D., Edwards M. C., Elledge S. J., Ivens A., Westerveld A., Little P., Mannens M., Feinberg A. P. Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments Proceedings of the National Academy of Sciences of the United States of America 1995;92 (26):12456-12460 [PubMed]
• Redeker E., Alders M., Hoovers J. M., Richard C. W., Westerveld A., Mannens M. Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3 Cytogenetics and cell genetics 1995;68 (3-4):222-225 [PubMed]

1994

• Redeker E., Hoovers J. M., Alders M., van Moorsel C. J., Ivens A. C., Gregory S., Kalikin L., Bliek J., de Galan L., van den Bogaard R., Visser J., van der Voort R., Feinberg A. P., Little P. F. R., Westerveld A., Mannens M. An integrated physical map of 210 markers assigned to the short arm of human chromosome 11 Genomics 1994;21 (3):538-550 [PubMed]
• Mannens M., Hoovers J. M., Redeker E., Verjaal M., Feinberg A. P., Little P., Boavida M., Coad N., Steenman M., Bliek J. Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia European journal of human genetics 1994;2 (1):3-23 [PubMed]

1993

• Caron H., van Sluis P., van Hoeve M., de Kraker J., Bras J., Slater R., Mannens M., Voûte P. A., Westerveld A., Versteeg R. Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification Nature genetics 1993;4 (2):187-190 [PubMed]
• Caron H., van Sluis P., van Hoeve M., de Kraker J., Bras J., Slater R., Mannens M., Voûte P. A., Westerveld A., Versteeg R. Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification [Correction] Nature genetics 1993;4 (4):431-431
• Fukushima Y., Hoovers J., Mannens M., Wakui K., Ohashi H., Ohno T., Ueoka Y., Niikawa N. Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization Human genetics 1993;91 (3):205-209 [PubMed]
• Little M. H., Williamson K. A., Mannens M., Kelsey A., Gosden C., Hastie N. D., van Heyningen V. Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion Human molecular genetics 1993;2 (3):259-264 [PubMed]
• Hoovers J. M., Redeker E., Speleman F., Höppener J. W., Bhola S., Bliek J., van Roy N., Leschot N. J., Westerveld A., Mannens M. High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members Genomics 1993;15 (3):525-529 [PubMed]
• Henry I., Hoovers J., Barichard F., Berthéas M. F., Puech A., Prieur F., Gessler M., Bruns G., Mannens M., Junien C. Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family Genes, chromosomes & cancer 1993;7 (1):57-62 [PubMed]
• Henry I., van Heyningen V., Puech A., Scrable H., Augereau P., Boehm T., Rabbitts T., Mannens M., Rochefort H., Jones C. Reassessment of breakpoints in chromosome 11p15 Cytogenetics and cell genetics 1993;62 (1):52-53 [PubMed]
• Henry I., Puech A., Riesewijk A., Ahnine L., Mannens M., Beldjord C., Bitoun P., Tournade M. F., Landrieu P., Junien C. Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event European journal of human genetics 1993;1 (1):19-29 [PubMed]
• Redeker E., van Moorsel C. J., Feinberg A., Mannens M. TaqI and RsaI polymorphisms in the H19 gene (D11S813E) Human molecular genetics 1993;2 (6):823 [PubMed]
• Mannens M., Hoovers J. M., Bleeker-Wagemakers E. M., Mäntyjärvi M., Tuppurainen K. The importance of DNA analysis in sporadic aniridia Acta ophthalmologica 1993;71 (6):841-845 [PubMed]

1992

• Slater R. M., Mannens M. M. Cytogenetics and molecular genetics of Wilms' tumor of childhood Cancer genetics and cytogenetics 1992;61 (2):111-121 [PubMed]
• Hoovers J. M., Mannens M., John R., Bliek J., van Heyningen V., Porteous D. J., Leschot N. J., Westerveld A., Little P. F. High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered Genomics 1992;12 (2):254-263 [PubMed]
• Hoovers J. M., Dietrich A. J., Mannens M. M. Imprinting and Beckwith-Wiedemann syndrome Lancet 1992;339 (8803):1228 [PubMed]
• Junien C., van Heyningen V., Evans G., Little P., Mannens M. Report of the second chromosome 11 workshop Genomics 1992;12 (3):620-625 [PubMed]
• Heding I. J., Ivens A. C., Wilson J., Strivens M., Gregory S., Hoovers J. M., Mannens M., Redeker B., Porteous D., van Heyningen V. The generation of ordered sets of cosmid DNA clones from human chromosome region 11p Genomics 1992;13 (1):89-94 [PubMed]
• van den Ouweland A. M., Verdijk M., Mannens M. M., van Oost B. A. The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumor Human genetics 1992;90 (1-2):144-146 [PubMed]

1991

• Speleman F., Mannens M., Redeker B., Vercruyssen M., van Oostveldt P., Leroy J., Slater R. Characterization of a de novo duplication of 11p14----p13, using fluorescent in situ hybridization and southern hybridization Cytogenetics and cell genetics 1991;56 (3-4):129-131 [PubMed]
• Devilee P., van den Broek M., Mannens M., Slater R., Cornelisse C. J., Westerveld A., Khan P. M. Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhood International journal of cancer. Journal international du cancer 1991;47 (6):817-821 [PubMed]
• Verbraak F. D., Mannens M. A., Redeker E. J., Saunders G. F., Bleeker-Wagemakers E. M. DNA diagnosis in a family with autosomal dominant aniridia Ophthalmic paediatrics and genetics 1991;12 (4):165-170 [PubMed]
• Mannens M., Hoovers J. M., Bleeker-Wagemakers E. M., Redeker E., Bliek J., Overbeeke-Melkert M., Saunders G., Williams B., van Heyningen V., Junien C. The distal region of 11p13 and associated genetic diseases Genomics 1991;11 (2):284-293 [PubMed]

1990

• Mannens M., Devilee P., Bliek J., Mandjes I., de Kraker J., Heyting C., Slater R. M., Westerveld A. Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11 Cancer research 1990;50 (11):3279-3283 [PubMed]

1989

• Bout A., Hoovers J. M., Bakker E., Mannens M. M., Geurts van Kessel A., Westerveld A., Tager J. M., Benne R. Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23 Cytogenetics and cell genetics 1989;52 (3-4):147-150 [PubMed]
• Mannens M., Bleeker-Wagemakers E. M., Bliek J., Hoovers J., Mandjes I., van Tol S., Frants R. R., Heyting C., Westerveld A., Slater R. M. Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family Cytogenetics and cell genetics 1989;52 (1-2):32-36 [PubMed]

1988

• Mannens M., Slater R. M., Heyting C., Bliek J., de Kraker J., Coad N., de Pagter-Holthuizen P., Pearson P. L. Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours Human genetics 1988;81 (1):41-48 [PubMed]
• de Ronde A., Mannens M., Slater R. M., Hoovers J., Heyting C., Bleeker-Wagemakers E. M., Leschot N. J., van Strien A., Sol C. J., ter Schegget J. Morphological transformation by early region human polyomavirus BK DNA of human fibroblasts with deletions in the short arm of one chromosome 11 Journal of general virology 1988;69 (2):467-471 [PubMed]

1987

• Mannens M., Slater R. M., Heyting C., Geurts van Kessel A., Goedde-Salz E., Frants R. R., van Ommen G. J., Pearson P. L. Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions Human genetics 1987;75 (2):180-187 [PubMed]