Gregory A. Meyers

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Publications

Citations

1.2K

H-Index

Active since

1995

Affiliations

Virginia Commonwealth University Medical Center(Current)

Johns Hopkins Medicine

Johns Hopkins University

New York University

Virginia BioTechnology Research Park

Gregory A. Meyers is an author at Virginia Commonwealth University Medical Center specializing in life sciences, genetic disorders, and molecular genetics.

Publications per year

1995–1999

Publications

Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans

Gregory A. Meyers, Seth J. Orlow, Ian R. Munro et al. · Nature Genetics · 1995 · 393 citations

Life Sciences, Genetics, Molecular Genetics +11

Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.

Woojin Park, Christiane Theda, Nancy E. Maestri et al. · PubMed · 1995 · 262 citations

Life Sciences, Genetics, Molecular Genetics +14

Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability

W.-J. Park, Gregory A. Meyers, Xun Li et al. · Human Molecular Genetics · 1995 · 173 citations

Life Sciences, Genetics, Molecular Genetics +17

FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing.

Gregory A. Meyers, David A. Day, Rosalie Goldberg et al. · PubMed · 1996 · 170 citations

Life Sciences, Genetics, Molecular Genetics +13

Mutations in the Human Biotinidase Gene That Cause Profound Biotinidase Deficiency in Symptomatic Children: Molecular, Biochemical, and Clinical Analysis

Robert J. Pomponio, Jeanne Hymes, Thomas Reynolds et al. · Pediatric Research · 1997 · 84 citations

Life Sciences, Genetics, Molecular Genetics +13

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