Murray Feingold
Impact in
- Developmental Biology top 0.5%
- Congenital limb and hand anomalies
- Genetics top 1%
- Craniofacial Disorders and Treatments
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Ocular Disorders and Treatments
- Genetic and rare skin diseases.
Papers in
- Genetics 86
- Craniofacial Disorders and Treatments 35
- Genomics and Rare Diseases 29
- Connective tissue disorders research 11
- Genetic and rare skin diseases. 10
- Genomic variations and chromosomal abnormalities 8
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- Congenital limb and hand anomalies 21
- Co-authors
- Sydney S. Gellis (51 shared papers)William H. Bossert (1 shared paper)Leonard Atkins (3 shared papers)JULES L. BAUM (1 shared paper)Louis Bartoshesky (3 shared papers)H. Eugene Hoyme (2 shared papers)Laurie H. Seaver (2 shared papers)Marilyn J. Bull (7 shared papers)
- Journals
- Archives of Pediatrics and Adolescent Medicine (16 papers)The Journal of Pediatrics (9 papers)New England Journal of Medicine (8 papers)PEDIATRICS (6 papers)The American Journal of Human Genetics (4 papers)
- Partner nations
- United StatesNetherlandsUnited Kingdom
In The Last Decade
Murray Feingold
140 papers receiving 3.4k citations
Peers
Comparison fields: 5 of 114
- Developmental Biology 307
- Genetics 1.7k
- Pediatrics, Perinatology and Child Health 243
- Genetics 140
- Otorhinolaryngology 85
Countries citing papers authored by Murray Feingold
This map shows the geographic impact of Murray Feingold's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Murray Feingold with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Murray Feingold more than expected).
Fields of papers citing papers by Murray Feingold
This network shows the impact of papers produced by Murray Feingold. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Murray Feingold. The network helps show where Murray Feingold may publish in the future.
Co-authors
The 25 scholars most cited alongside Murray Feingold, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 160 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 211 | |
| 2 | 2011 | 194 | |
| 3 | 1998 | 181 | |
| 4 | 2003 | 181 | |
| 5 | Normal values for selected physical parameters: an aid to syndrome delineation. | 1974 | 168 |
| 6 | 1971 | 142 | |
| 7 | 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. | 1996 | 142 |
| 8 | 1998 | 142 | |
| 9 | 1973 | 127 | |
| 10 | 1998 | 126 | |
| 11 | 1977 | 109 | |
| 12 | 1973 | 105 | |
| 13 | 1978 | 88 | |
| 14 | 2011 | 84 | |
| 15 | 2012 | 79 | |
| 16 | 1966 | 76 | |
| 17 | 2013 | 64 | |
| 18 | 1978 | 62 | |
| 19 | Mucolipidosis III (pseudo-Hurler polydystrophy): Clinical and laboratory studies in a series of 12 patients. | 1975 | 59 |
| 20 | 1969 | 58 |
About Murray Feingold
Murray Feingold is a scholar working on Genetics, Developmental Biology, Clinical Biochemistry, Surgery and Pediatrics, Perinatology and Child Health, having authored 160 papers that have together received 3.9k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (35 papers), Genomics and Rare Diseases (29 papers), Congenital limb and hand anomalies (21 papers), Connective tissue disorders research (11 papers), Down syndrome and intellectual disability research (10 papers), Genetic and rare skin diseases. (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Metabolism and Genetic Disorders (7 papers). The work is most often cited by research in Developmental Biology (307 citations), Genetics (1.7k citations), Pediatrics, Perinatology and Child Health (243 citations), Genetics (140 citations) and Otorhinolaryngology (85 citations). Murray Feingold has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include Sydney S. Gellis, William H. Bossert, Leonard Atkins, JULES L. BAUM, Louis Bartoshesky, H. Eugene Hoyme, Laurie H. Seaver, Marilyn J. Bull, Jürgen W. Spranger and Jules G. Leroy. Their work appears in journals such as Archives of Pediatrics and Adolescent Medicine, The Journal of Pediatrics, New England Journal of Medicine, PEDIATRICS and The American Journal of Human Genetics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.