J Feingold

888 citations
42 papers · 695 indexed · h-index 15

Impact in

  • Genetics top 10%
    • Hemoglobinopathies and Related Disorders
    • Cleft Lip and Palate Research
    • Craniofacial Disorders and Treatments
  • Hematology top 10%
    • Iron Metabolism and Disorders

Papers in

J Feingold

42 papers receiving 625 citations

Peers

J Feingold
Comparison fields: 5 of 88
  • Genetics 121
  • Hematology 126
  • Genetics 152
  • Nutrition and Dietetics 72
  • Molecular Biology 287
Replace Leena Peltonen with:
Leena Peltonen Finland
Takeshi Ninchoji Japan
Angela D’Elia Italy
Nora Butta Spain
Shiqiao Ye United States
Chun‐Ming Pan China
Patrice Eydoux Canada
Emanuele Cotroneo United Kingdom
Sophie Valleix France
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Citations per field
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Citations per year

Countries citing papers authored by J Feingold

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

Border = papers with J Feingold Line = papers co-authored together J Feingold links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1
Carrier frequency of 550delA mutation of CAPN3 gene in Croatia
20021
2
Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?
199830
3 199754
4 199778
5 19978
6 19963
7 199428
8 199337
9 199346
10
Transforming growth factor-alpha: characterization of the BamHI, RsaI, and TaqI polymorphic regions.
199313
11 199123
12 19915
13
The Quest of the Sons
19891
14 198148
15
Desferrioxamine utilisation for the quantitation of iron excess. Study of 24 patients having idiopathic haemochromatosis.
19782
16
[Risk of recurrence of several congenital malformations: anencephaly, spina bifida, cleft palate and cleft lip].
19763
17
[Prevalence of etinoblastoma in the Midi-Pyrenées area].
19753
18 197448
19
[Genetics of blood uric acid levels: study of 3 Amerindian tribes of Upper French Guyana].
19722
20
Gènes majeurs, gènes modificateurs et effets du milieu dans la myopathie de Duchenne de Boulogne.
19714

About J Feingold

J Feingold is a scholar working on Hematology, Aging, Genetics, Genetics and Pediatrics, Perinatology and Child Health, having authored 42 papers that have together received 695 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), Chronic Lymphocytic Leukemia Research (2 papers), Skin and Cellular Biology Research (2 papers) and Genetic Neurodegenerative Diseases (2 papers). The work is most often cited by research in Genetics (121 citations), Hematology (126 citations), Genetics (152 citations), Nutrition and Dietetics (72 citations) and Molecular Biology (287 citations). J Feingold has collaborated with scholars based in France, South Africa and Australia. Frequent co-authors include I Emerit, E May, Claude Stoll, E Housset, J Frézal, Catherine Bonaïti‐Pellié, Jing Qian, P Sauvage, M. Broyer and Tamara Sarkisian. Their work appears in journals such as Human Genetics, JNCI Journal of the National Cancer Institute, Annals of Human Genetics, Journal of Molecular and Cellular Cardiology and Brain.

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.

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