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Association of a rare variant of the TNFSF13B gene with susceptibility to Rheumatoid Arthritis and Systemic Lupus Erythematosus.

González-Serna, David, Ortiz-Fernández, Lourdes, Vargas, Sofía, García, Antonio, Raya, Enrique, Fernández-Gutierrez, Benjamín, López-Longo, Francisco Javier, Balsa, Alejandro, González-Álvaro, Isidoro, Narvaez, Javier, Gómez-Vaquero, Carmen, Sabio, José Mario, García-Portales, Rosa, González-Escribano, María Francisca, Tolosa, Carles, Carreira, Patricia, Kiemeney, Lambertus, Coenen, Marieke J H, Witte, Torsten, Schneider, Matthias, González-Gay, Miguel Ángel, Martín, Javier
2018

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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

Hinney, A, Kesselmeier, M, Jall, S, Volckmar, A-L, Föcker, M, Antel, J, Heid, I M, Winkler, T W, Grant, S F A, Guo, Y, Bergen, A W, Kaye, W, Berrettini, W, Hakonarson, H, Herpertz-Dahlmann, B, de Zwaan, M, Herzog, W, Ehrlich, S, Zipfel, S, Egberts, K M, Adan, R, Brandys, M, van Elburg, A, Boraska Perica, V, Franklin, C S, Tschöp, M H, Zeggini, E, Bulik, C M, Collier, D, Scherag, A, Müller, T D, Hebebrand, J, Hottenga, J.J., Willemsen, Gonneke, Boomsma, D.I., van Beijsterveldt, C.E.M., Middeldorp, C.M., de Geus, Eco
Veröffentlicht in: Hinney , A , Kesselmeier , M , Jall , S , Volckmar , A-L , Föcker , M , Antel , J , Heid , I M , Winkler , T W , Grant , S F A , Guo , Y , Bergen , A W , Kaye , W , Berrettini , W , Hakonarson , H , Herpertz-Dahlmann , B , de Zwaan , M , Herzog , W , Ehrlich , S , Zipfel , S , Egberts , K M , Adan , R , Brandys , M , van Elburg , A , Boraska Perica , V , Franklin , C S , Tschöp , M H , Zeggini , E , Bulik , C M , Collier , D , Scherag , A , Müller , T D , Hebebrand , J , GCAN , Hottenga , J J , Willemsen , G , Boomsma , D I , van Beijsterveldt , C E M , Middeldorp , C M & de Geus , E 2017 , ' Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index ' , Molecular Psychiatry , vol. 22 , no. 2 , pp. 192-201 . https://doi.org/10.1038/mp.2016.71;
2017

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Cardiovascular risk associated with interactions among polymorphisms in genes from the renin-angiotensin, bradykinin, and fibrinolytic systems

Bentley, JP, Asselbergs, FW, Coffey, CS, Hebert, PR, Moore, JH, Hillege, HL, van Gilst, WH
2010

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EPHX1 polymorphisms do not modify esophageal carcinoma susceptibility in Dutch Caucasians.

Dura, Polat, Bregitha, Caro V V, Te Morsche, Rene H M, Roelofs, Hennie M J, Kristinsson, Jon O, Wobbes, Theo, Witteman, Ben J M, Tan, Adriaan C I T L, Drenth, Joost P H, Peters, Wilbert H M
2013

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Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.

Styrkarsdottir, Unnur, Thorleifsson, Gudmar, Helgadottir, Hafdis T, Bomer, Nils, Metrustry, Sarah, Bierma-Zeinstra, S, Strijbosch, Annelieke M, Evangelou, Evangelos, Hart, Deborah, Beekman, Marian, Jonasdottir, Aslaug, Sigurdsson, Asgeir, Eiriksson, Finnur F, Thorsteinsdottir, Margret, Frigge, Michael L, Kong, Augustine, Gudjonsson, Sigurjon A, Magnusson, Olafur T, Masson, Gisli, Hofman, Albert, Arden, Nigel K, Ingvarsson, Thorvaldur, Lohmander, Stefan, Kloppenburg, Margreet, Rivadeneira, Fernando, Nelissen, Rob G H H, Spector, Tim, Uitterlinden, Andre, Slagboom, P Eline, Thorsteinsdottir, Unnur, Jonsdottir, Ingileif, Valdes, Ana M, Meulenbelt, Ingrid, van Meurs, Joyce, Jonsson, Helgi, Stefansson, Kari
2014

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Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2.

Silvestri, V, Barrowdale, D, Mulligan, AM, Neuhausen, SL, Fox, S, Karlan, BY, Mitchell, G, James, P, Thull, DL, Zorn, KK, Carter, NJ, Nathanson, KL, Domchek, SM, Rebbeck, TR, Ramus, SJ, Nussbaum, RL, Olopade, OI, Rantala, J, Yoon, S-Y, Caligo, MA, Spugnesi, L, Bojesen, A, Pedersen, IS, Thomassen, M, Jensen, UB, Toland, AE, Senter, L, Andrulis, IL, Glendon, G, Hulick, PJ, Imyanitov, EN, Greene, MH, Mai, PL, Singer, CF, Rappaport-Fuerhauser, C, Kramer, G, Vijai, J, Offit, K, Robson, M, Lincoln, A, Jacobs, L, Machackova, E, Foretova, L, Navratilova, M, Vasickova, P, Couch, FJ, Hallberg, E, Ruddy, KJ, Sharma, P, Kim, S-W, kConFab Investigators,, Teixeira, MR, Pinto, P, Montagna, M, Matricardi, L, Arason, A, Johannsson, OT, Barkardottir, RB, Jakubowska, A, Lubinski, J, Izquierdo, A, Pujana, MA, Balmaña, J, Diez, O, Ivady, G, Papp, J, Olah, E, Kwong, A, Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON),, Nevanlinna, H, Aittomäki, K, Perez Segura, P, Caldes, T, Van Maerken, T, Poppe, B, Claes, KBM, Isaacs, C, Elan, C, Lasset, C, Stoppa-Lyonnet, D, Barjhoux, L, Belotti, M, Meindl, A, Gehrig, A, Sutter, C, Engel, C, Niederacher, D, Steinemann, D, Hahnen, E, Kast, K, Arnold, N, Varon-Mateeva, R, Wand, D, Godwin, AK, Evans, DG, Frost, D, Perkins, J, Adlard, J, Izatt, L, Platte, R, Eeles, R, Ellis, S, EMBRACE,, Hamann, U, Garber, J, Fostira, F, Fountzilas, G, Pasini, B, Giannini, G, Rizzolo, P, Russo, A, Cortesi, L, Papi, L, Varesco, L, Palli, D, Zanna, I, Savarese, A, Radice, P, Manoukian, S, Peissel, B, Barile, M, Bonanni, B, Viel, A, Pensotti, V, Tommasi, S, Peterlongo, P, Weitzel, JN, Osorio, A, Benitez, J, McGuffog, L, Healey, S, Gerdes, A-M, Ejlertsen, B, Hansen, TVO, Steele, L, Ding, YC, Tung, N, Janavicius, R, Goldgar, DE, Buys, SS, Daly, MB, Bane, A, Terry, MB, John, EM, Southey, M, Easton, DF, Chenevix-Trench, G, Antoniou, AC, Ottini, L
2018

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Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.

Rosso, S.M. (Sonia), Donker Kaat, L. (Laura), Baks, T. (Timo), Joosse, M. (Marijke), Koning, I. (Inge) de, Pijnenburg, Y.A.L. (Yolande), Jong, D. (Danielle) de, Dooijes, D. (Dennis), Kamphorst, W. (Wouter), Ravid, R. (Rivka), Niermeijer, M.F. (Martinus), Verheij, F. (Fop), Kremer, H.P., Scheltens, P. (Philip), Duijn, C.M. (Cornelia) van, Heutink, P. (Peter), Swieten, J.C. (John) van
2003

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Project MinE : study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

Project Mine Als Sequencing Consortium, Mine Als Sequencing Consortium, Pulit, Sara L., Dekker, Annelot M., Al Khleifat, Ahmad, Brands, William J., Iacoangeli, Alfredo, Kenna, Kevin P., Kavak, Ersen, Kooyman, Maarten, McLaughlin, Russell L., Middelkoop, Bas, Moisse, Matthieu, Schellevis, Raymond D., Shatunov, Aleksey, Sproviero, William, Tazelaar, Gijs H.P., van der Spek, Rick A.A., van Doormaal, Perry T.C., van Eijk, Kristel R., van Vugt, Joke, Basak, A. Nazli, Blair, Ian P., Glass, Jonathan D., Hardiman, Orla, Hide, Winston, Landers, John E., Mora, Jesus S., Morrison, Karen E., Newhouse, Stephen, Robberecht, Wim, Shaw, Christopher E., Shaw, Pamela J., van Damme, Philip, van Es, Michael A., Wray, Naomi R., Al-Chalabi, Ammar, van Den Berg, Leonard H., Veldink, Jan H.
2018

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A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the Netherlands

Vaessen, N. (Norbert), Houwing-Duistermaat, J.J. (Jeanine), Rademaker, T.A.M. (Tessa), Testers, L., Batstra, M.R. (Manou), Sandkuijl, L.A. (Lodewijk), Duijn, C.M. (Cornelia) van, Oostra, B.A. (Ben), Snijders, P.J.L.M. (Pieter), Heutink, P. (Peter)
2002

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Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

Project Mine Als Sequencing Consortium, Mine Als Sequencing Consortium, Pulit, Sara L., Dekker, Annelot M., Al Khleifat, Ahmad, Brands, William J., Iacoangeli, Alfredo, Kenna, Kevin P., Kavak, Ersen, Kooyman, Maarten, McLaughlin, Russell L., Middelkoop, Bas, Moisse, Matthieu, Schellevis, Raymond D., Shatunov, Aleksey, Sproviero, William, Tazelaar, Gijs H.P., van der Spek, Rick A.A., van Doormaal, Perry T.C., van Eijk, Kristel R., van Vugt, Joke, Basak, A. Nazli, Blair, Ian P., Glass, Jonathan D., Hardiman, Orla, Hide, Winston, Landers, John E., Mora, Jesus S., Morrison, Karen E., Newhouse, Stephen, Robberecht, Wim, Shaw, Christopher E., Shaw, Pamela J., van Damme, Philip, van Es, Michael A., Wray, Naomi R., Al-Chalabi, Ammar, van Den Berg, Leonard H., Veldink, Jan H.
2018