Anticipation and phenotype in familial intracranial aneurysms

af Ruigrok, Y, Rinkel, G, Wijmenga, C, van Gijn, J
Udgivet 2004

Defining the genetic contribution of type 2 diabetes mellitus

af van Tilburg, J., van Haeften, T. W, Pearson, P., Wijmenga, C.
Udgivet 2001

Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes

af de Bie, P, Muller, P, Wijmenga, C, Klomp, L W J
Udgivet 2007

Linkage analysis localises a Kartagener syndrome gene to a 3.5 cM region on chromosome 15q24–25

af Geremek, M, Ziętkiewicz, E, Diehl, S R, Alizadeh, B Z, Wijmenga, C, Witt, M
Udgivet 2006

Type 2 Diabetes Mellitus: New Genetic Insights will Lead to New Therapeutics

af Wolfs, M.G.M, Hofker, M.H, Wijmenga, C, van Haeften, T.W.
Udgivet 2009

Core binding factor beta-smooth muscle myosin heavy chain chimeric protein involved in acute myeloid leukemia forms unusual nuclear rod-like structures in transformed NIH 3T3 cells...

af Wijmenga, C, Gregory, P E, Hajra, A, Schröck, E, Ried, T, Eils, R, Liu, P P, Collins, F S
Udgivet 1996

Dutch patients with glycogen storage disease type II show common ancestry for the 525delT and del exon 18 mutations

af Ausems, M., ten, B, Sandkuijl, L., Kroos, M., Bardoel, A., Roumelioti, K., Reuser, A., Sinke, R., Wijmenga, C.
Udgivet 2001

Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphrodite.

af Giltay, J C, Brunt, T, Beemer, F A, Wit, J M, van Amstel, H K, Pearson, P L, Wijmenga, C
Udgivet 1998

High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families.

af Zatz, M, Marie, S K, Passos-Bueno, M R, Vainzof, M, Campiotto, S, Cerqueira, A, Wijmenga, C, Padberg, G, Frants, R
Udgivet 1995

Genetic mapping of the dentinogenesis imperfecta type II locus.

af Crosby, A H, Scherpbier-Heddema, T, Wijmenga, C, Altherr, M R, Murray, J C, Buetow, K H, Dixon, M J
Udgivet 1995

Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases.

af Bakker, E, Van der Wielen, M J, Voorhoeve, E, Ippel, P F, Padberg, G W, Frants, R R, Wijmenga, C
Udgivet 1996

Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).

af Mills, K A, Buetow, K H, Xu, Y, Ritty, T M, Mathews, K D, Bodrug, S E, Wijmenga, C, Balazs, I, Murray, J C
Udgivet 1992

Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter

af Wijmenga, C., Sandkuijl, L. A., Moerer, P., van der Boorn, N., Bodrug, S. E., Ray, P. N., Brouwer, O. F., Murray, J. C., van Ommen, G. J. B., Padberg, G. W., Frants, R. R.
Udgivet 1992

OR7-002 – Pyrin 577 mutations in dominant autoinflammation

af Stoffels, M, Szperl, A, Simon, A, Netea, MG, Plantinga, TS, van Deuren, M, Kamphuis, S, Lachmann, H, Cuppen, E, Kloosterman, WP, Frenkel, J, van Diemen, CC, Wijmenga, C, van Gijn, M, van der Meer, JW
Udgivet 2013

Lack of association of MYO9B genetic variants with coeliac disease in a British cohort

af Hunt, K A, Monsuur, A J, McArdle, W L, Kumar, P J, Travis, S P L, Walters, J R F, Jewell, D P, Strachan, D P, Playford, R J, Wijmenga, C, van Heel, D A
Udgivet 2006

A microarray screen for novel candidate genes in coeliac disease pathogenesis

af Diosdado, B, Wapenaar, M C, Franke, L, Duran, K J, Goerres, M J, Hadithi, M, Crusius, J B A, Meijer, J W R, Duggan, D J, Mulder, C J J, Holstege, F C P, Wijmenga, C
Udgivet 2004

Association of the TGF-β receptor genes with abdominal aortic aneurysm

af Baas, A F, Medic, J, van 't Slot, R, de Kovel, C G, Zhernakova, A, Geelkerken, R H, Kranendonk, S E, van Sterkenburg, S M, Grobbee, D E, Boll, A P, Wijmenga, C, Blankensteijn, J D, Ruigrok, Y M
Udgivet 2010

A combination of fecal calprotectin and human beta-defensin 2 facilitates diagnosis and monitoring of inflammatory bowel disease

af Gacesa, R., Vich Vila, A., Collij, V., Mujagic, Z., Kurilshikov, A., Voskuil, M.D., Festen, E.A.M., Wijmenga, C., Jonkers, D.M.A.E., Dijkstra, G., Fu, J., Zhernakova, A., Imhann, F., Weersma, R.K.
Udgivet i Gut Microbes (2021)

Determining the association between adipokine expression in multiple tissues and phenotypic features of non-alcoholic fatty liver disease in obesity

af Wolfs, M G M, Gruben, N, Rensen, S S, Verdam, F J, Greve, J W, Driessen, A, Wijmenga, C, Buurman, W A, Franke, L, Scheja, L, Koonen, D P Y, Shiri-Sverdlov, R, van Haeften, T W, Hofker, M H, Fu, J
Udgivet i Nutr Diabetes (2015)

Localization of the ICF syndrome to chromosome 20 by homozygosity mapping.

af Wijmenga, C, van den Heuvel, L P, Strengman, E, Luyten, J A, van der Burgt, I J, de Groot, R, Smeets, D F, Draaisma, J M, van Dongen, J J, De Abreu, R A, Pearson, P L, Sandkuijl, L A, Weemaes, C M
Udgivet 1998