Marianne Schwartz

Paternal Inheritance of Mitochondrial DNA

Marianne Schwartz, John Vissing · New England Journal of Medicine · 2002 · 692 citations

Life Sciences, Genetics, Molecular Genetics +15

Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis

Peter Garred, Tacjana Pressler, Hans O. Madsen et al. · Journal of Clinical Investigation · 1999 · 438 citations · Full text

Life Sciences, Genetics, Microbiology +17

Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia

Koenraad Devriendt, Annette S. Kim, Gert Mathijs et al. · Nature Genetics · 2001 · 436 citations

Life Sciences, Genetics, Molecular Genetics +6

CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders

Bernd Wissinger, Daphne Gamer, Herbert Jägle et al. · The American Journal of Human Genetics · 2001 · 326 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Recombination of Human Mitochondrial DNA

Yevgenya Kraytsberg, Marianne Schwartz, Timothy A. Brown et al. · Science · 2004 · 305 citations

Medicine, Genetics, Molecular Biology +14