Ben F. Koop

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

The Atlantic salmon genome provides insights into rediploidization

Sigbjørn Lien, Ben F. Koop, Simen R. Sandve et al. · Nature · 2016 · 1.1K citations · Full text

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly

Elena Belloni, Maximilian Muenke, Erich Roessler et al. · Nature Genetics · 1996 · 644 citations

Knockout Mouse, Developmental Biology, Genetics +5

Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

Bech-Hansen Nt, Ben F. Koop, M. B. Mets et al. · Nature Genetics · 1998 · 513 citations

Calcium-channel α1-Subunit Gene, Molecular Neuroscience, Developmental Biology +7

The Complete 685-Kilobase DNA Sequence of the Human β T Cell Receptor Locus

Lee Rowen, Ben F. Koop, Leroy Hood · Science · 1996 · 437 citations