Concepedia

W G Pearce

WG

Statistics

Publications

25

Citations

1.5K

H-Index

19

Active since

1965

Affiliations

University of Alberta(Current)

University of Calgary

Alberta Children's Hospital

Nagoya University

Oregon Health & Science University

W G Pearce is an author at University of Alberta specializing in medicine, human genetics, and genetics.

Publications per year

1965–2001

25

Publications

25

Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly

Alan J. Mears, Tim Jordan, Farideh Mirzayans et al. · The American Journal of Human Genetics · 1998 · 328 citations · Full text

, , +11

Mutation of the PAX6 gene in patients with autosomal dominant keratitis.

Farideh Mirzayans, W G Pearce, Ian M. MacDonald et al. · PubMed · 1995 · 147 citations

, , +8

Mutation in the RIEG1 Gene in Patients with Iridogoniodysgenesis Syndrome

Stephen C. Kulak, K. Kozlowski, Elena V. Semina et al. · Human Molecular Genetics · 1998 · 123 citations

, , +17

Diagnostic and genetical aspects of tuberous sclerosis.

N C Nevin, W G Pearce · Journal of Medical Genetics · 1968 · 108 citations · Full text

, , +7

A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

Kym M. Boycott, Tracy A. Maybaum, MARGARET NAYLOR et al. · Human Genetics · 2001 · 102 citations

, , +9

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