J Feingold
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Hemoglobinopathies and Related Disorders
- Genetic Associations and Epidemiology
-
- Genetic Neurodegenerative Diseases
Papers in
- Genetics 35
- Genetic Associations and Epidemiology 8
- Hemoglobinopathies and Related Disorders 8
- Genomics and Rare Diseases 8
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- Sexual Differentiation and Disorders 7
- Co-authors
- Marion Leboyer (9 shared papers)Philip Gorwood (12 shared papers)Alexis Brice (6 shared papers)E Bois (10 shared papers)N Feingold (6 shared papers)M Guilloud-Bataille (6 shared papers)Dominique Hillaire (5 shared papers)Marie‐Louise Briard (7 shared papers)
- Journals
- Journal of Medical Genetics (6 papers)Human Genetics (6 papers)European Psychiatry (4 papers)Clinical Genetics (4 papers)American Journal of Tropical Medicine and Hygiene (2 papers)
- Partner nations
- FranceTunisiaRepublic of the Congo
In The Last Decade
J Feingold
112 papers receiving 2.3k citations
Peers
Comparison fields: 5 of 121
- Genetics 866
- Cellular and Molecular Neuroscience 438
- Cognitive Neuroscience 395
- Genetics 201
- Psychiatry and Mental health 234
Countries citing papers authored by J Feingold
This map shows the geographic impact of J 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 J Feingold with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J Feingold more than expected).
Fields of papers citing papers by J Feingold
This network shows the impact of papers produced by J 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 J Feingold. The network helps show where J Feingold may publish in the future.
Co-authors
The 25 scholars most cited alongside J 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 115 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 385 | |
| 2 | 1996 | 140 | |
| 3 | A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage. | 1991 | 126 |
| 4 | 1998 | 99 | |
| 5 | 1998 | 93 | |
| 6 | 1995 | 76 | |
| 7 | 1982 | 73 | |
| 8 | 1992 | 71 | |
| 9 | Penetrance of familial hypertrophic cardiomyopathy. | 1997 | 67 |
| 10 | EGEA (Epidemiological study on the Genetics and Environment of Asthma, bronchial hyperresponsiveness and atopy)-- descriptive characteristics. | 1999 | 63 |
| 11 | Segregation analysis detects a major gene controlling blood infection levels in human malaria. | 1992 | 60 |
| 12 | 2007 | 57 | |
| 13 | 1976 | 45 | |
| 14 | 1998 | 43 | |
| 15 | Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France. | 1988 | 41 |
| 16 | 1999 | 37 | |
| 17 | 1996 | 36 | |
| 18 | 2001 | 35 | |
| 19 | 1976 | 35 | |
| 20 | 2000 | 32 |
About J Feingold
J Feingold is a scholar working on Genetics, Molecular Biology, Genetics, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 115 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (8 papers), Hemoglobinopathies and Related Disorders (8 papers), Genomics and Rare Diseases (8 papers), Iron Metabolism and Disorders (8 papers), Genetic Neurodegenerative Diseases (8 papers), Sexual Differentiation and Disorders (7 papers), Cystic Fibrosis Research Advances (6 papers) and Neonatal Health and Biochemistry (6 papers). The work is most often cited by research in Genetics (866 citations), Cellular and Molecular Neuroscience (438 citations), Cognitive Neuroscience (395 citations), Genetics (201 citations) and Psychiatry and Mental health (234 citations). J Feingold has collaborated with scholars based in France, Tunisia and Republic of the Congo. Frequent co-authors include Marion Leboyer, Philip Gorwood, Alexis Brice, E Bois, N Feingold, M Guilloud-Bataille, Dominique Hillaire, Marie‐Louise Briard, Lionel Van Maldergem and Christiane Penet. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, European Psychiatry, Clinical Genetics and American Journal of Tropical Medicine and Hygiene.
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.