Dina Marek

Point Mutation in the HCN4 Cardiac Ion Channel Pore Affecting Synthesis, Trafficking, and Functional Expression Is Associated With Familial Asymptomatic Sinus Bradycardia

Eyal Nof, David Luria, Dovrat Brass et al. · Circulation · 2007 · 178 citations

Natural Sciences, Cardiology, Genetics +17

Deleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome

Almogit Abu, Moshe Frydman, Dina Marek et al. · The American Journal of Human Genetics · 2008 · 139 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis

Abraham Zlotogorski, Dina Marek, Liran Horev et al. · Journal of Investigative Dermatology · 2006 · 97 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

Acute Lymphoblastic Leukemia in Early Childhood as the Presenting Sign of Ataxia-Telangiectasia Variant

Bella Bielorai, Tamar Fisher, Dalia Waldman et al. · Pediatric Hematology and Oncology · 2013 · 39 citations

Medicine, Hematology, Oncology +17

Mapping of a Gene Causing Brittle Cornea Syndrome in Tunisian Jews to 16q24

Almogit Abu, Moshe Frydman, Dina Marek et al. · Investigative Ophthalmology & Visual Science · 2006 · 27 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12