Ben F. Koop - Concepedia

Author

Ben F. Koop

University of Victoria ORCID

Also Known As

B F Koop, B KOOP, B Koop, B. C. Koop, B. F Koop, B. F. KOOP, B. F. Koop, B. Koop, B.F Koop, B.F. KOOP

360

Publications

19.9K

Citations

H-Index

203

Concepts

All Affiliations

University of Victoria Simon Fraser University Fisheries and Oceans Canada Norwegian University of Life Sciences University of Washington

About

Ben F. Koop is an author at University of Victoria specializing in medicine, genetics, and biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	50	107	10.4K
2	Natural Sciences	35	62	4.1K
3	Engineering	10	10	401
4	Public Health	7	7	433
5	Health Sciences	2	2	113

Ben F. Koop

208

Publications

18K

Citations

H-Index

Page 1

	Year	Citations
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency Angela Brooks‐Wilson, Michel Marcil, Susanne M. Clee, Nature Genetics Mendelian DisorderDisease MechanismGenetic DisorderMedicineGenetics	1999	1.7K
The Atlantic salmon genome provides insights into rediploidization Sigbjørn Lien, Ben F. Koop, Simen R. Sandve, Nature	2016	1.1K
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly Elena Belloni, Maximilian Muenke, Erich Roessler, Nature Genetics Knockout MouseDevelopmental BiologyGeneticsMorphogenesisMedicine	1996	644
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, Nature Genetics Calcium-channel α1-Subunit GeneMolecular NeuroscienceDevelopmental BiologyOphthalmologyGenetic Disorder	1998	513
The Complete 685-Kilobase DNA Sequence of the Human β T Cell Receptor Locus Lee Rowen, Ben F. Koop, Leroy Hood Science	1996	437
Embryonic ε and γ globin genes of a prosimian primate (Galago crassicaudatus) Danilo A. Tagle, Ben F. Koop, Morris Goodman, Journal of Molecular Biology BiologyDevelopmental BiologyDevelopmental GeneticsGeneticsGalago Crassicaudatus	1988	365
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness N. Torben Bech‐Hansen, Margaret J. Naylor, Tracy A. Maybaum, Nature Genetics Ocular DiseaseDevelopmental BiologyOphthalmologyPathologyPediatric Ophthalmology	2000	349
Development and Application of a Salmonid EST Database and cDNA Microarray: Data Mining and Interspecific Hybridization Characteristics Matthew L. Rise, Kristian R. von Schalburg, Gordon D. Brown, Genome Research	2004	318
Cell death attenuation by `Usurpin', a mammalian DED-caspase homologue that precludes caspase-8 recruitment and activation by the CD-95 (Fas, APO-1) receptor complex Dita Rasper, John P. Vaillancourt, Vicky M. Houtzager, Cell Death and Differentiation Cell Death AttenuationSignal TransductionSignaling PathwayCell InteractionApoptosis	1998	315
Sex-dependent dominance maintains migration supergene in rainbow trout Devon E. Pearse, Nicola J. Barson, Torfinn Nome, Nature Ecology & Evolution	2019	304

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