Murray Feingold
- Developmental Biology top 2%
- Genetics top 1%
- Craniofacial Disorders and Treatments 13
- Cleft Lip and Palate Research 10
- Genetic and rare skin diseases. 5
- Connective tissue disorders research 4
- Otorhinolaryngology top 5%
- Physiology top 5%
- Urology top 5%
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- Metabolism and Genetic Disorders 7
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- Tracheal and airway disorders 6
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- Congenital Anomalies and Fetal Surgery 5
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- Biomedical Research and Pathophysiology 4
- Co-authors
- William H. BossertJules BaumLouis BartosheskySydney S. GellisMarilyn J. BullJürgen W. SprangerJohn M. OpitzJules G. Leroy
- Journals
- The Journal of Pediatrics (9 papers)PEDIATRICS (6 papers)New England Journal of Medicine (5 papers)
- Partner nations
- United StatesUnited KingdomSpain
In The Last Decade
Murray Feingold
102 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 118
- Developmental Biology 161
- Genetics 1.2k
- Otorhinolaryngology 78
- Physiology 76
- Urology 100
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 33 | |
| 2 | 2015 | 37 | |
| 3 | 2011 | 64 | |
| 4 | 2008 | 0 | |
| 5 | 2006 | 14 | |
| 6 | 2005 | 9 | |
| 7 | 2000 | 189 | |
| 8 | 1998 | 160 | |
| 9 | 1996 | 1 | |
| 10 | 1993 | 2 | |
| 11 | 1988 | 41 | |
| 12 | Genetics and birth defects in clinical practice | 1983 | 1 |
| 13 | 1983 | 26 | |
| 14 | Picture of the month. Metaphyseal chondrodysplasia, Schmid type. | 1980 | 2 |
| 15 | Picture of the month. Nager's syndrome (Nager's acrofacial dystosis) | 1978 | 11 |
| 16 | Picture of the month: hemangiomas with osteolysis (Gorham's disease, vanishing bone disease). | 1978 | 4 |
| 17 | 1978 | 84 | |
| 18 | 1971 | 128 | |
| 19 | 1970 | 0 | |
| 20 | 1969 | 14 |
About Murray Feingold
Murray Feingold is a scholar working on Developmental Biology, Genetics and Clinical Biochemistry, having authored 111 papers that have together received 2.6k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (13 papers), Cleft Lip and Palate Research (10 papers), Metabolism and Genetic Disorders (7 papers), Tracheal and airway disorders (6 papers), Genetic and rare skin diseases. (5 papers), Congenital Anomalies and Fetal Surgery (5 papers), Connective tissue disorders research (4 papers) and Biomedical Research and Pathophysiology (4 papers). The work is most often cited by research in Developmental Biology (161 citations), Genetics (1.2k citations) and Otorhinolaryngology (78 citations). Murray Feingold has collaborated with scholars based in United States, United Kingdom and Spain. Frequent co-authors include William H. Bossert, Jules Baum, Louis Bartoshesky, Sydney S. Gellis, Marilyn J. Bull, Jürgen W. Spranger, John M. Opitz, Jules G. Leroy, Allen C. Crocker and Ethylin Wang Jabs. Their work appears in journals such as The Journal of Pediatrics, PEDIATRICS, New England Journal of Medicine, The American Journal of Human Genetics and Journal of Medical 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.