| A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 DA Van Heel, L Franke, KA Hunt, R Gwilliam, A Zhernakova, M Inouye, ... Nature genetics 39 (7), 827-829, 2007 | 854 | 2007 |
| Newly identified genetic risk variants for celiac disease related to the immune response KA Hunt, A Zhernakova, G Turner, GAR Heap, L Franke, M Bruinenberg, ... Nature genetics 40 (4), 395-402, 2008 | 853 | 2008 |
| Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. JT Den Dunnen, PM Grootscholten, E Bakker, LA Blonden, HB Ginjaar, ... American journal of human genetics 45 (6), 835, 1989 | 696 | 1989 |
| Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect AJ Monsuur, PIW Bakker, BZ Alizadeh, A Zhernakova, MR Bevova, ... Nature genetics 37 (12), 1341-1344, 2005 | 322 | 2005 |
| Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy MH Hofker, MC Wapenaar, N Goor, E Bakker, GJB van Ommen, ... Human genetics 70, 148-156, 1985 | 246 | 1985 |
| Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitisAn unusual case of ascites MC Wapenaar, AJ Monsuur, AA van Bodegraven, RK Weersma, ... Gut 57 (4), 463-467, 2008 | 209 | 2008 |
| A gene from the Xp22. 3 region shares homology with voltage-gated chloride channels MA Slegtenhorst, M T. Bassl, G Borsanil, MC Wapenaar, GB Ferrero, ... Human molecular genetics 3 (4), 547-552, 1994 | 130 | 1994 |
| A deletion hot spot in the Duchenne muscular dystrophy gene MC Wapenaar, T Kievits, KA Hart, S Abbs, LAJ Blonden, JT Den Dunnen, ... Genomics 2 (2), 101-108, 1988 | 129 | 1988 |
| A microarray screen for novel candidate genes in coeliac disease pathogenesis B Diosdado, MC Wapenaar, L Franke, KJ Duran, MJ Goerres, M Hadithi, ... Gut 53 (7), 944-951, 2004 | 110 | 2004 |
| A high resolution deletion map of human chromosome Xp22 L Schaefer, GB Ferrero, A Grillo, MT Bassi, EJ Roth, MC Wapenaar, ... Nature genetics 4 (3), 272-279, 1993 | 109 | 1993 |
| Effect of pirfenidone on cough in patients with idiopathic pulmonary fibrosis MJG van Manen, SS Birring, C Vancheri, V Vindigni, E Renzoni, ... European Respiratory Journal 50 (4), 2017 | 106 | 2017 |
| The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility MC Wapenaar, MJ Van Belzen, JH Fransen, AF Sarasqueta, ... Journal of autoimmunity 23 (2), 183-190, 2004 | 90 | 2004 |
| Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease AM Szperl, MR Golachowska, M Bruinenberg, R Prekeris, ... Journal of pediatric gastroenterology and nutrition 52 (3), 307-313, 2011 | 87 | 2011 |
| The X chromosome shows less genetic variation at restriction sites than the autosomes. MH Hofker, MI Skraastad, AA Bergen, MC Wapenaar, E Bakker, ... American journal of human genetics 39 (4), 438, 1986 | 83 | 1986 |
| High resoluation deletion breakpoint mapping in the DMD gene by whole cosmid hybridization LAJ Blonden, JT Dunnen, HMB Paassen, MC Wapenaar, ... Nucleic acids research 17 (14), 5611-5621, 1989 | 75 | 1989 |
| Characterization ofCxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil α-helical domains L de Conciliis, A Marchitiello, MC Wapenaar, G Borsani, S Giglio, ... Genomics 51 (2), 243-250, 1998 | 73 | 1998 |
| Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort SS Amundsen, AJ Monsuur, MC Wapenaar, BA Lie, J Ek, ... Human immunology 67 (4-5), 341-345, 2006 | 72 | 2006 |
| Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomes T Kievits, P Devilee, J Wiegant, MC Wapenaar, CJ Cornelisse, ... Cytometry: The Journal of the International Society for Analytical Cytology …, 1990 | 71 | 1990 |
| A home monitoring program including real-time wireless home spirometry in idiopathic pulmonary fibrosis: a pilot study on experiences and barriers CC Moor, M Wapenaar, JR Miedema, JJM Geelhoed, PP Chandoesing, ... Respiratory Research 19, 1-5, 2018 | 67 | 2018 |
| The SPINK gene family and celiac disease susceptibility MC Wapenaar, AJ Monsuur, J Poell, R van ‘t Slot, JWR Meijer, GA Meijer, ... Immunogenetics 59, 349-357, 2007 | 66 | 2007 |
