Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis

per Alders, Marielle, Bliek, Jet, vd Lip, Karin, vd Bogaard, Ruud, Mannens, Marcel
Publicat 2009

Expanding the phenotype of biallelic RNPC3 variants associated with growth hormone deficiency

per Verberne, Eline A., Faries, Sonja, Mannens, Marcel M. A. M., Postma, Alex V., van Haelst, Mieke M.
Publicat a Am J Med Genet A (2020)

Multiplex ligation-dependent probe amplification (MLPA) enhances the molecular diagnosis of aniridia and related disorders

per Redeker, Egbert J.W., de Visser, Annette S.H., Bergen, Arthur A.B., Mannens, Marcel M.A.M.
Publicat 2008

Higher Polygenetic Predisposition for Asthma in Cow’s Milk Allergic Children

per Jansen, Philip R., Petrus, Nicole C. M., Venema, Andrea, Posthuma, Danielle, Mannens, Marcel M. A. M., Sprikkelman, Aline B., Henneman, Peter
Publicat a Nutrients (2018)

Genetic susceptibility for cow’s milk allergy in Dutch children: the start of the allergic march?

per Henneman, Peter, Petrus, Nicole C. M., Venema, Andrea, van Sinderen, Femke, van der Lip, Karin, Hennekam, Raoul C., Mannens, Marcel, Sprikkelman, Aline B.
Publicat a Clin Transl Allergy (2016)

Clinical utility gene card for: Beckwith–Wiedemann Syndrome

per Eggermann, Thomas, Algar, Elizabeth, Lapunzina, Pablo, Mackay, Deborah, Maher, Eamonn R, Mannens, Marcel, Netchine, Irène, Prawitt, Dirk, Riccio, Andrea, Temple, I Karen, Weksberg, Rosanna
Publicat 2014

Cow’s milk allergy in Dutch children: an epigenetic pilot survey

per 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
Publicat a Clin Transl Allergy (2016)

Recurrent Intrauterine Fetal Loss due to Near Absence of HERG: Clinical and Functional Characterization of a Homozygous Non-sense HERG mutation

per Bhuiyan, Zahurul A., Momenah, Tarek S., Gong, Qiuming, Amin, A. S., Al Ghamdi, Saleh, Carvalho, Julene S., Homfray, Tessa, Mannens, Marcel M.A.M., Zhou, Zhengfeng, Wilde, Arthur A. M.
Publicat 2008

The idiopathic preterm delivery methylation profile in umbilical cord blood DNA

per 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
Publicat a BMC Genomics (2015)

Hypomethylation of the H19 Gene Causes Not Only Silver-Russell Syndrome (SRS) but Also Isolated Asymmetry or an SRS-Like Phenotype

per 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
Publicat 2006

Comprehensive Open Reading Frame Mutational Analysis of the RYR2-Encoded Ryanodine Receptor/Calcium Channel in Patients Diagnosed Previously with Either Catecholaminergic Polymorph...

per 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.
Publicat 2009

Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates

per Henneman, Peter, Bouman, Arjan, Mul, Adri, Knegt, Lia, van der Kevie-Kersemaekers, Anne-Marie, Zwaveling-Soonawala, Nitash, Meijers-Heijboer, Hanne E. J., van Trotsenburg, A. S. Paul, Mannens, Marcel M.
Publicat a PLoS One (2018)

Meta-Analysis of in vitro-Differentiated Macrophages Identifies Transcriptomic Signatures That Classify Disease Macrophages in vivo

per 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.
Publicat a Front Immunol (2019)

Clinical and community genetics services in the Dutch Caribbean

per Verberne, Eline A., Ecury-Goossen, Ginette M., Manshande, Meindert E., Ponson-Wever, Maria, de Vroomen, Maartje, Tilanus, Martijn, Mannens, Marcel M. A. M., Henneman, Lidewij, van Haelst, Mieke M.
Publicat a J Community Genet (2021)

Comparing genome-scale DNA methylation and CNV marks between adult human cultured ITGA6+ testicular cells and seminomas to assess in vitro genomic stability

per 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.
Publicat a PLoS One (2020)

Bariatric Surgery for Monogenic Non-syndromic and Syndromic Obesity Disorders

per 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.
Publicat a Curr Diab Rep (2020)

Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells

per 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 MAM
Publicat 2009

Epigenome-wide association study for perceived discrimination among sub-Saharan African migrants in Europe - the RODAM study

per 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
Publicat a Sci Rep (2020)

Whole-Genome DNA Methylation Profiling of CD14+ Monocytes Reveals Disease Status and Activity Differences in Crohn’s Disease Patients

per Li Yim, Andrew Y.F., Duijvis, Nicolette W., Ghiboub, Mohammed, Sharp, Catriona, Ferrero, Enrico, Mannens, Marcel M.A.M., D’Haens, Geert R., de Jonge, Wouter J., te Velde, Anje A., Henneman, Peter
Publicat a J Clin Med (2020)

Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation

per 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.
Publicat 2009