Enrika Bartels

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association

Pawaree Saisawat, Stefan Kohl, Alina C. Hilger et al. · Kidney International · 2013 · 128 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy

Markus Draaken, Heiko Reutter, Charlotte Schramm et al. · European Journal of Medical Genetics · 2010 · 123 citations

Medicine, Molecular Genetics, Urology +9

Research perspectives in the etiology of congenital anorectal malformations using data of the International Consortium on Anorectal Malformations: evidence for risk factors across different populations

Charlotte H. W. Wijers, Ivo de Blaauw, Carlo Marcelis et al. · Pediatric Surgery International · 2010 · 70 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL‐like association and analysis of <i>EFNB2</i> in patients with anorectal malformations

Gabriel C. Dworschak, Markus Draaken, Carlo Marcelis et al. · American Journal of Medical Genetics Part A · 2013 · 66 citations

Life Sciences, Genetics, Molecular Genetics +17

De novo microduplication at 22q11.21 in a patient with VACTERL association

Charlotte Schramm, Markus Draaken, Enrika Bartels et al. · European Journal of Medical Genetics · 2010 · 60 citations

Life Sciences, Genetics, Molecular Genetics +11