J Feingold
Impact in
- Genetics top 10%
- Hemoglobinopathies and Related Disorders
- Cleft Lip and Palate Research
- Hematology top 10%
- Iron Metabolism and Disorders
Papers in
-
- Glycosylation and Glycoproteins Research 2
- TGF-β signaling in diseases 2
- Genetics 10
- Genetic Syndromes and Imprinting 3
- Hemoglobinopathies and Related Disorders 2
- Co-authors
- I Emerit (3 shared papers)E May (3 shared papers)Claude Stoll (3 shared papers)E Housset (2 shared papers)J Frézal (4 shared papers)Catherine Bonaïti‐Pellié (4 shared papers)P Sauvage (1 shared paper)Jing Qian (1 shared paper)
In The Last Decade
J Feingold
41 papers receiving 603 citations
Peers
Comparison fields: 5 of 81
- Genetics 112
- Hematology 119
- Genetics 145
- Nutrition and Dietetics 65
- Cardiology and Cardiovascular Medicine 78
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 42 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 78 | |
| 2 | 2001 | 58 | |
| 3 | 1997 | 54 | |
| 4 | 1974 | 48 | |
| 5 | 1981 | 48 | |
| 6 | 1993 | 46 | |
| 7 | 1993 | 37 | |
| 8 | 1976 | 31 | |
| 9 | 1968 | 31 | |
| 10 | Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis? | 1998 | 30 |
| 11 | Chromosomal breakage and scleroderma: studies in family members. | 1976 | 29 |
| 12 | 1994 | 28 | |
| 13 | Statistical study on double paraproteinemias. Evidence for a common cellular origin of both myeloma globulins. | 1975 | 27 |
| 14 | 1986 | 15 | |
| 15 | 1972 | 13 | |
| 16 | Transforming growth factor-alpha: characterization of the BamHI, RsaI, and TaqI polymorphic regions. | 1993 | 13 |
| 17 | 1974 | 9 | |
| 18 | 1997 | 8 | |
| 19 | 1991 | 5 | |
| 20 | [French Society for Human Genetics. "Genetics in Practice" Commission. Core scientific data of use in genetic counseling. Hemochromatosis]. | 1999 | 5 |
About J Feingold
J Feingold is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Hematology and Genetics, having authored 42 papers that have together received 672 indexed citations. Recurring topics across this work include Iron Metabolism and Disorders (5 papers), Prenatal Screening and Diagnostics (4 papers), Genetic Syndromes and Imprinting (3 papers), Ocular Oncology and Treatments (3 papers), Glycosylation and Glycoproteins Research (2 papers), Monoclonal and Polyclonal Antibodies Research (2 papers), Hemoglobinopathies and Related Disorders (2 papers) and TGF-β signaling in diseases (2 papers). The work is most often cited by research in Genetics (112 citations), Hematology (119 citations), Genetics (145 citations), Nutrition and Dietetics (65 citations) and Cardiology and Cardiovascular Medicine (78 citations). J Feingold has collaborated with scholars based in France, Hungary and Australia. Frequent co-authors include I Emerit, E May, Claude Stoll, E Housset, J Frézal, Catherine Bonaïti‐Pellié, P Sauvage, Jing Qian, Corinne Nazaret and M. Broyer. Their work appears in journals such as Human Genetics, Nucleic Acids Research, Journal of Molecular and Cellular Cardiology, Annals of Human Genetics and Biochimie.
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.