Keith Fichter

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

Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

Michel Marcil, Angela Brooks‐Wilson, Susanne M. Clee et al. · The Lancet · 1999 · 357 citations

Abc 1, Mendelian Disorder, Familial Hdl Deficiency +12

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

Angela Brooks‐Wilson, Michel Marcil, Susanne M. Clee et al. · Max Planck Institute for Plasma Physics · 1999 · 81 citations

Genetic Analysis, Mendelian Disorder, Genetic Disorder +12

Cloning and Characterization of Three Novel Genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the Juvenile Amyotrophic Lateral Sclerosis (ALS2) Critical Region at Chromosome 2q33–q34: Candidate Genes for ALS2

Yoshiko Yanagisawa, Jennifer Skaug, Keith Fichter et al. · Genomics · 2001 · 50 citations

Neurodegenerative Diseases, Candidate Genes, Amyotrophic Lateral Sclerosis +8

HIP12 is a non-proapoptotic member of a gene family including HIP1, an interacting protein with huntingtin

Vikramjit Chopra, Martina Metzler, Dita Rasper et al. · Mammalian Genome · 2000 · 44 citations

Protein Function, Signaling Pathway, Medicine +10