I Magyar

Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness

Christina Zeitz, Barbara Kloeckener‐Gruissem, U. Förster et al. · The American Journal of Human Genetics · 2006 · 181 citations · Full text

Medicine, Genetics, Molecular Genetics +9

Lopinavir-ritonavir and hydroxychloroquine for critically ill patients with COVID-19: REMAP-CAP randomized controlled trial

Yaseen M. Arabi, Anthony Gordon, Lennie Derde et al. · Intensive Care Medicine · 2021 · 100 citations · Full text

Pharmacy, Infectious Diseases, Pharmacotherapy +9

Large genomic fibrillin-1 (FBN1) gene deletions provide evidence for true haploinsufficiency in Marfan syndrome

Gábor Mátyás, Sira Alonso, Andrea Patrignani et al. · Human Genetics · 2007 · 90 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Double-Blind Multicenter Study of Paroxetine and Amitriptyline in Depressed Inpatients

Hans‐Jürgen Möller, Horst Berzewski, F Eckmann et al. · Pharmacopsychiatry · 1993 · 48 citations

Medicine, Pharmacology, Pharmacotherapy +16

Alterations of the 5′Untranslated Region of<i>SLC16A12</i>Lead to Age-Related Cataract

Jurian Zuercher, John Neidhardt, I Magyar et al. · Investigative Ophthalmology & Visual Science · 2010 · 47 citations

Life Sciences, Genetics, Molecular Genetics +13