Nicole C. Meyer

A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

John N. Feder, Andreas Gnirke, Zenta Tsuchihashi et al. · Nature Genetics · 1996 · 3.7K citations

Life Sciences, Genetics, Molecular Genetics +12

Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein

Matthew R. Avenarius, Michael S. Hildebrand, Yuzhou Zhang et al. · The American Journal of Human Genetics · 2009 · 280 citations · Full text

Medicine, Genetics, Molecular Genetics +13

Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome

Fengxiao Bu, Tara Maga, Nicole C. Meyer et al. · Journal of the American Society of Nephrology · 2013 · 238 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Branchio-oto-renal syndrome: The mutation spectrum in<i>EYA1</i>and its phenotypic consequences

Eugene H. Chang, Maithilee Menezes, Nicole C. Meyer et al. · Human Mutation · 2004 · 227 citations

Life Sciences, Genetics, Molecular Genetics +17

Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement

Sanjeev Sethi, Fernando C. Fervenza, Yuzhou Zhang et al. · Kidney International · 2012 · 203 citations · Full text

Medicine, Immunology, Pathology +14