Concepedia

Murray Feingold

MF

Statistics

Publications

64

Citations

4.1K

H-Index

34

Active since

1963

Affiliations

National Center on Birth Defects and Developmental Disabilities(Current)

Tufts University

Tufts Medical Center

Tufts Children's Hospital

Harvard University

Murray Feingold is an author at National Center on Birth Defects and Developmental Disabilities specializing in human genetics, genetics, and genetic disorders.

Publications per year

1963–2016

64

Publications

64

Novel HOXA13 Mutations and the Phenotypic Spectrum of Hand-Foot-Genital Syndrome

Frances R. Goodman, Chiara Bacchelli, Angela F. Brady et al. · The American Journal of Human Genetics · 2000 · 264 citations · Full text

, , +12

Mutations in the pre-replication complex cause Meier-Gorlin syndrome

Louise S. Bicknell, Ernie M.H.F. Bongers, Andrea Leitch et al. · Nature Genetics · 2011 · 251 citations · Full text

, , +6

Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis

Sandra Hanks, Sarah Adams, Jenny Douglas et al. · The American Journal of Human Genetics · 2003 · 241 citations · Full text

, , +12

Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations

William A. Paznekas, Michael L. Cunningham, Timothy D. Howard et al. · The American Journal of Human Genetics · 1998 · 221 citations · Full text

, , +17

Normal values for selected physical parameters: an aid to syndrome delineation.

Murray Feingold, William H. Bossert · PubMed · 1974 · 197 citations

, , +5

1–5 of 64