Anja Ernst

Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome. A case report

Morten Krogh Herlin, Vang Quy Le, Allan Thomas Højland et al. · Human Reproduction · 2019 · 69 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The polymorphism rs3024505 proximal to IL-10 is associated with risk of ulcerative colitis and Crohns disease in a Danish case-control study

Vibeke Andersen, Anja Ernst, Jane Christensen et al. · BMC Medical Genetics · 2010 · 63 citations · Full text

Life Sciences, Immunology, Molecular Genetics +17

Cyclooxygenase-2, multidrug resistance 1, and breast cancer resistance protein gene polymorphisms and inflammatory bowel disease in the Danish population

Mette Østergaard, Anja Ernst, Rodrigo Labouriau et al. · Scandinavian Journal of Gastroenterology · 2008 · 37 citations

Life Sciences, Genetics, Molecular Genetics +15

<i>ECEL1</i> mutation causes fetal arthrogryposis multiplex congenita

Niclas Dohrn, Vang Quy Le, Astrid Petersen et al. · American Journal of Medical Genetics Part A · 2015 · 28 citations

Life Sciences, Genetics, Molecular Genetics +16

Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population

Anja Ernst, Bent Ascanius Jacobsen, Mette Østergaard et al. · Scandinavian Journal of Gastroenterology · 2007 · 26 citations

Life Sciences, Genetics, Molecular Genetics +16