Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression von Fu, Jingyuan, Wolfs, Marcel G M, Deelen, Patrick, Westra, Harm-Jan, Fehrmann, Rudolf S N, Te Meerman, Gerard J, Buurman, Wim A, Rensen, Sander S M, Groen, Harry J M, Weersma, Rinse K, van den Berg, Leonard H, Veldink, Jan, Ophoff, Roel A, Snieder, Harold, van Heel, David, Jansen, Ritsert C, Hofker, Marten H, Wijmenga, Cisca, Franke, Lude

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Evidence based selection of housekeeping genes von de Jonge, Hendrik J M, Fehrmann, Rudolf S N, de Bont, Eveline S J M, Hofstra, Robert M W, Gerbens, Frans, Kamps, Willem A, de Vries, Elisabeth G E, van der Zee, Ate G J, te Meerman, Gerard J, ter Elst, Arja

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Survival-related profile, pathways, and transcription factors in ovarian cancer von Crijns, Anne P G, Fehrmann, Rudolf S N, de Jong, Steven, Gerbens, Frans, Meersma, Gert Jan, Klip, Harry G, Hollema, Harry, Hofstra, Robert M W, te Meerman, Gerard J, de Vries, Elisabeth G E, van der Zee, Ate G J

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Gene expression analysis identifies global gene dosage sensitivity in cancer von Fehrmann, Rudolf S N, Karjalainen, Juha M, Krajewska, Małgorzata, Westra, Harm-Jan, Maloney, David, Simeonov, Anton, Pers, Tune H, Hirschhorn, Joel N, Jansen, Ritsert C, Schultes, Erik A, van Haagen, Herman H H B M, de Vries, Elisabeth G E, te Meerman, Gerard J, Wijmenga, Cisca, van Vugt, Marcel A T M, Franke, Lude

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Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA von Fehrmann, Rudolf S N, Jansen, Ritsert C, Veldink, Jan H, Westra, Harm-Jan, Arends, Danny, Bonder, Marc Jan, Fu, Jingyuan, Deelen, Patrick, Groen, Harry J M, Smolonska, Asia, Weersma, Rinse K, Hofstra, Robert M W, Buurman, Wim A, Rensen, Sander, Wolfs, Marcel G M, Platteel, Mathieu, Zhernakova, Alexandra, Elbers, Clara C, Festen, Eleanora M, Trynka, Gosia, Hofker, Marten H, Saris, Christiaan G J, Ophoff, Roel A, van den Berg, Leonard H, van Heel, David A, Wijmenga, Cisca, Te Meerman, Gerard J, Franke, Lude

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A "late-but-fitter revertant cell" explains the high frequency of revertant mosaicism in epidermolysis bullosa von van den Akker, Peter C, Pasmooij, Anna M G, Joenje, Hans, Hofstra, Robert M W, Te Meerman, Gerard J, Jonkman, Marcel F

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PLS3 Mutations in X-Linked Osteoporosis with Fractures von van Dijk, Fleur S, Zillikens, M. Carola, Micha, Dimitra, Riessland, Markus, Marcelis, Carlo L.M, de Die-Smulders, Christine E, Milbradt, Janine, Franken, Anton A, Harsevoort, Arjan J, Lichtenbelt, Klaske D, Pruijs, Hans E, Rubio-Gozalbo, M. Estela, Zwertbroek, Rolf, Moutaouakil, Youssef, Egthuijsen, Jaqueline, Hammerschmidt, Matthias, Bijman, Renate, Semeins, Cor M, Bakker, Astrid D, Everts, Vincent, Klein-Nulend, Jenneke, Campos-Obando, Natalia, Hofman, Albert, te Meerman, Gerard J, Verkerk, Annemieke J.M.H, Uitterlinden, André G, Maugeri, Alessandra, Sistermans, Erik A, Waisfisz, Quinten, Meijers-Heijboer, Hanne, Wirth, Brunhilde, Simon, Marleen E.H, Pals, Gerard

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CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3 von Leotti, Vanessa B., Vries, Jeroen J., Oliveira, Camila M., Mattos, Eduardo P., Te Meerman, Gerard J., Brunt, Ewout R., Kampinga, Harm H., Jardim, Laura B., Verbeek, Dineke S.

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Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model von Alves, Maria M., Sribudiani, Yunia, Brouwer, Rutger W.W., Amiel, Jeanne, Antiñolo, Guillermo, Borrego, Salud, Ceccherini, Isabella, Chakravarti, Aravinda, Fernández, Raquel M., Garcia-Barcelo, Maria-Mercè, Griseri, Paola, Lyonnet, Stanislas, Tam, Paul K., van IJcken, Wilfred F.J., Eggen, Bart J.L., te Meerman, Gerard J., Hofstra, Robert M.W.

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Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping von Vermeulen, Carlo, Geeven, Geert, de Wit, Elzo, Verstegen, Marjon J.A.M., Jansen, Rumo P.M., van Kranenburg, Melissa, de Bruijn, Ewart, Pulit, Sara L., Kruisselbrink, Evelien, Shahsavari, Zahra, Omrani, Davood, Zeinali, Fatemeh, Najmabadi, Hossein, Katsila, Theodora, Vrettou, Christina, Patrinos, George P., Traeger-Synodinos, Joanne, Splinter, Erik, Beekman, Jeffrey M., Kheradmand Kia, Sima, te Meerman, Gerard J., Ploos van Amstel, Hans Kristian, de Laat, Wouter

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MixupMapper: correcting sample mix-ups in genome-wide datasets increases power to detect small genetic effects von Westra, Harm-Jan, Jansen, Ritsert C., Fehrmann, Rudolf S. N., te Meerman, Gerard J., van Heel, David, Wijmenga, Cisca, Franke, Lude

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Current smoking-specific gene expression signature in normal bronchial epithelium is enhanced in squamous cell lung cancer von Boelens, Mirjam C, van den Berg, Anke, Fehrmann, Rudolf SN, Geerlings, Marie, de Jong, Wouter K, te Meerman, Gerard J, Sietsma, Hannie, Timens, Wim, Postma, Dirkje S, Groen, Harry JM

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NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing von Johansson, Lennart F, de Weerd, Hendrik A, de Boer, Eddy N, van Dijk, Freerk, Te Meerman, Gerard J, Sijmons, Rolf H, Sikkema-Raddatz, Birgit, Swertz, Morris A

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Familial Aggregation between the 14th and 21st Century and Type 2 Diabetes Risk in an Isolated Dutch Population von de Visser, Kees L, Landman, Gijs W D, Kleefstra, Nanne, Meyboom-de Jong, Betty, de Visser, Wim, te Meerman, Gerard J, Bilo, Henk J G

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Serum chemokine levels in Hodgkin lymphoma patients: highly increased levels of CCL17 and CCL22 von Niens, Marijke, Visser, Lydia, Nolte, Ilja M., Van Der Steege, Gerrit, Diepstra, Arjan, Cordano, Pablo, Jarrett, Ruth F., Te Meerman, Gerard J., Poppema, Sibrand, Van Den Berg, Anke

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Periconceptional folic acid associated with an increased risk of oral clefts relative to non-folate related malformations in the Northern Netherlands: a population based case-contr... von Rozendaal, Anna M., van Essen, Anthonie J., te Meerman, Gerard J., Bakker, Marian K., van der Biezen, Jan J., Goorhuis-Brouwer, Sieneke M., Vermeij-Keers, Christl, de Walle, Hermien E. K.

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CLMP Is Required for Intestinal Development, and Loss-of-Function Mutations Cause Congenital Short-Bowel Syndrome von Van Der Werf, Christine S, Wabbersen, Tara D, Hsiao, Nai–Hua, Paredes, Joana, Etchevers, Heather C, Kroisel, Peter M, Tibboel, Dick, Babarit, Candice, Schreiber, Richard A, Hoffenberg, Edward J, Vekemans, Michel, Zeder, Sirkka L, Ceccherini, Isabella, Lyonnet, Stanislas, Ribeiro, Ana S, Seruca, Raquel, te Meerman, Gerard J, van Ijzendoorn, Sven C.D, Shepherd, Iain T, Verheij, Joke B.G.M, Hofstra, Robert M.W

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HLA Class II Expression by Hodgkin Reed-Sternberg Cells Is an Independent Prognostic Factor in Classical Hodgkin's Lymphoma von DIEPSTRA, Arjan, VAN IMHOFF, Gustaaf W, POPPEMA, Sibrand, KARIM-KOS, Henrike E, VAN DEN BERG, Anke, TE MEERMAN, Gerard J, NIENS, Marijke, NOLTE, Ilja M, BASTIAANNET, Esther, SCHAAPVELD, Michael, VELLENGA, Edo

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HLA-A02 is associated with a reduced risk and HLA-A01 with an increased risk of developing EBV+ Hodgkin lymphoma von Niens, Marijke, Jarrett, Ruth F., Hepkema, Bouke, Nolte, Ilja M., Diepstra, Arjan, Platteel, Mathieu, Kouprie, Niels, Delury, Craig P., Gallagher, Alice, Visser, Lydia, Poppema, Sibrand, te Meerman, Gerard J., van den Berg, Anke

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Lamin A/C-Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation von Hoorntje, Edgar T, Bollen, Ilse A, Barge-Schaapveld, Daniela Q, van Tienen, Florence H, te Meerman, Gerard J, Jansweijer, Joeri A, van Essen, Anthonie J, Volders, Paul G, Constantinescu, Alina A, van den Akker, Peter C, van Spaendonck-Zwarts, Karin Y, Oldenburg, Rogier A, Marcelis, Carlo L, van der Smagt, Jasper J, Hennekam, Eric A, Vink, Aryan, Bootsma, Marianne, Aten, Emmelien, Wilde, Arthur A, van den Wijngaard, Arthur, Broers, Jos L, Jongbloed, Jan D, van der Velden, Jolanda, van den Berg, Maarten P, van Tintelen, J Peter

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