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Anja Ernst

Observed names: A Ernst, A. Ernst, Ernst, Anja
ORCID: 0000-0001-5120-9259
Observed ORCID: 0000-0001-5120-9259
OpenAlex ID: A5033399129
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
2019 · Morten K Herlin, Vang Q Le, et al. · Human Reproduction · 65
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The polymorphism rs3024505 proximal to IL-10 is associated with risk of ulcerative colitis and Crohns disease in a Danish case-control study
2010 · Vibeke Andersen, Anja Ernst, et al. · BMC Medical Genetics · 62
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Cyclooxygenase-2, multidrug resistance 1, and breast cancer resistance protein gene polymorphisms and inflammatory bowel disease in the Danish population
2008 · Mette Østergaard, Anja Ernst, et al. · Scandinavian Journal of Gastroenterology · 36
ECEL1 mutation causes fetal arthrogryposis multiplex congenita
2015 · N. Dohrn, V.Q. Le, et al. · American Journal of Medical Genetics Part A · 29
Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population
2007 · Anja Ernst, Bent Jacobsen, et al. · Scandinavian Journal of Gastroenterology · 28
Four weeks of ledipasvir/sofosbuvir and ribavirin with or without pegylated interferon for chronic hepatitis C in non-cirrhotic people who inject drugs. A randomized trial
2017 · Anne L.H. Øvrehus, Henrik Krarup, et al. · Journal of Hepatology · 27
Cyclooxygenase-2 (COX-2) polymorphisms and risk of inflammatory bowel disease in a Scottish and Danish case–control study
2010 · Vibeke Andersen, Elaine Nimmo, et al. · Inflammatory Bowel Diseases · 27
Direct acting antiviral treatment of chronic hepatitis C in Denmark: factors associated with and barriers to treatment initiation
2018 · Christina Sølund, Sofie Hallager, et al. · Scandinavian Journal of Gastroenterology · 25
Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease
2021 · Wen-Qiang Zheng, Signe Vandal Pedersen, et al. · Human Molecular Genetics · 23
A systematic review on concurrent aneuploidy screening and preimplantation genetic testing for hereditary disorders: What is the prevalence of aneuploidy and is there a clinical effect from aneuploidy screening?
2020 · Christian Liebst Frisk Toft, Hans Jakob Ingerslev, et al. · Acta Obstetricia Et Gynecologica Scandinavica · 20
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National data on the early clinical use of non‐invasive prenatal testing in public and private healthcare in Denmark 2013–2017
2020 · Ida C. B. Lund, Olav B. Petersen, et al. · Acta Obstetricia Et Gynecologica Scandinavica · 18
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Global evolutionary analysis of chronic hepatitis C patients revealed significant effect of baseline viral resistance, including novel non‐target sites, for DAA‐based treatment and retreatment outcome
2020 · Ulrik Fahnøe, Martin S. Pedersen, et al. · Journal of Viral Hepatitis · 13
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Genetic variants of glutathione S-transferases μ, θ, and π display no susceptibility to inflammatory bowel disease in the Danish population
2010 · Anja Ernst, Vibeke Andersen, et al. · Scandinavian Journal of Gastroenterology · 13
Mitochondrial Disease Caused by a Novel Homozygous Mutation (Gly106del) in the SCO1 Gene
2019 · Ninna Brix, Janni Majgaard Jensen, et al. · Neonatology · 12
Cell-based non-invasive prenatal testing for monogenic disorders: confirmation of unaffected fetuses following preimplantation genetic testing
2021 · Christian Liebst Frisk Toft, Hans Jakob Ingerslev, et al. · Journal of Assisted Reproduction and Genetics · 10
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Feasibility and early clinical impact of precision medicine for late-stage cancer patients in a regional public academic hospital
2023 · Morten Ladekarl, Anne Krogh Nøhr, et al. · Acta Oncologica · 9
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De novo KAT6B Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome
2016 · Malene Lundsgaard, Vang Q. Le, et al. · Molecular Syndromology · 9
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The PHF6 Mutation c.1A>G; pM1V Causes Börjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys
2015 · Anja Ernst, Vang Q. Le, et al. · Molecular Syndromology · 9
Longer survival with precision medicine in late-stage cancer patients
2025 · C.K. Mapendano, A.K. Nøhr, et al. · ESMO Open · 7
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Scrotal Paget's Disease Associated With Human Epidermal Growth Factor Receptor 2–Overexpressing Metastatic Apocrine Carcinoma With Complete Response to Paclitaxel, Trastuzumab, and Pertuzumab
2023 · Kinga Nowicka-Matus, Giedrius Salkus, et al. · JCO Precision Oncology · 6
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A Danish national effort of BRCA1/2 variant classification
2017 · Inge Søkilde Pedersen, Ane Y. Schmidt, et al. · Acta Oncologica · 6
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Assessment of heterogeneity between European Populations: a Baltic and Danish replication case-control study of SNPs from a recent European ulcerative colitis genome wide association study
2011 · Vibeke Andersen, Anja Ernst, et al. · BMC Medical Genetics · 6
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Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public Healthcare
2025 · Ida Vogel, Lotte Andreasen, et al. · Prenatal Diagnosis · 5
Common polymorphisms in the microsomal epoxide hydrolase and N-acetyltransferase 2 genes in association with inflammatory bowel disease in the Danish population
2011 · Anja Ernst, Vibeke Andersen, et al. · European Journal of Gastroenterology & Hepatology · 4
THU-193-4 week treatment for hepatitis C: A randomized controlled trial (4RIBC)
2019 · Lone Wulff Madsen, Anne Ovrehus, et al. · Journal of Hepatology · 3
Works count: 54
Citation count: 480
H-index: 13
I10-index: 15
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