Michael R. Hayden

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

Angela Brooks‐Wilson, Michel Marcil, Susanne M. Clee et al. · Nature Genetics · 1999 · 1.7K citations

Mendelian Disorder, Disease Mechanism, Genetic Disorder +13

Loss of Huntingtin-Mediated BDNF Gene Transcription in Huntington's Disease

Chiara Zuccato, Andrea Ciammola, Dorotea Rigamonti et al. · Science · 2001 · 1.3K citations

Neurodegenerative Diseases, Wild-type Huntingtin Activity, Bdnf Production +12

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

Susan E. Andrew, Y. Paul Goldberg, Berry Kremer et al. · Nature Genetics · 1993 · 1.1K citations

Genetic Disorder, Genetics, Molecular Biology +8

Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines

Alexander Panov, Claire‐Anne Gutekunst, Blair R. Leavitt et al. · Nature Neuroscience · 2002 · 1K citations

Mitochondrial Function, Mitochondrial Dynamic, Genetics +7

Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

George Papanikolaou, Mark Samuels, E H Ludwig et al. · Nature Genetics · 2003 · 976 citations · Full text

Juvenile Hemochromatosis, Heme Homeostasis, Iron Metabolism +8