Daniel Cohen
Impact in
Papers in
- Genetics 81
- Genetic Associations and Epidemiology 46
- Genomic variations and chromosomal abnormalities 27
- Diabetes and associated disorders 12
- Genetic Mapping and Diversity in Plants and Animals 9
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- Hereditary Neurological Disorders 11
- Co-authors
- Denis Le Paslier (28 shared papers)Philippe Froguel (18 shared papers)Jean Weissenbach (10 shared papers)Philippe Millasseau (5 shared papers)Jean B. Dausset (34 shared papers)Olivier Clermont (3 shared papers)Suzie Lefebvre (3 shared papers)Lydie Bürglen (3 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (15 papers)Genomics (14 papers)Immunogenetics (9 papers)Nature Genetics (6 papers)Cell (6 papers)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Daniel Cohen
149 papers receiving 20.8k citations
Daniel Cohen's Hit Papers
Peers
Comparison fields: 5 of 157
- Genetics 3.1k
- Aging 398
- Genetics 5.3k
- Pathology and Forensic Medicine 2k
- Molecular Biology 4.5k
Countries citing papers authored by Daniel Cohen
This map shows the geographic impact of Daniel Cohen'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 Daniel Cohen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Cohen more than expected).
Fields of papers citing papers by Daniel Cohen
This network shows the impact of papers produced by Daniel Cohen. 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 Daniel Cohen. The network helps show where Daniel Cohen may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel Cohen, 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 151 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Identification and characterization of a spinal muscular atrophy-determining gene Hit paper breakdown → | 1995 | 3338 |
| 2 | Identification of the von Hippel-Lindau Disease Tumor Suppressor Gene Hit paper breakdown → | 1993 | 2387 |
| 3 | Identification and characterization of the familial adenomatous polyposis coli gene Hit paper breakdown → | 1991 | 2337 |
| 4 | Genetic associations with human longevity at the APOE and ACE loci Hit paper breakdown → | 1994 | 952 |
| 5 | Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A Hit paper breakdown → | 1995 | 840 |
| 6 | Genetic and physiological data implicating the new human gene G72 and the gene for d -amino acid oxidase in schizophrenia Hit paper breakdown → | 2002 | 702 |
| 7 | Identification of deletion mutations and three new genes at the familial polyposis locus Hit paper breakdown → | 1991 | 661 |
| 8 | Familial Hyperglycemia Due to Mutations in Glucokinase -- Definition of a Subtype of Diabetes Mellitus Hit paper breakdown → | 1993 | 600 |
| 9 | The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules Hit paper breakdown → | 1991 | 586 |
| 10 | Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus Hit paper breakdown → | 1992 | 503 |
| 11 | Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus Hit paper breakdown → | 1992 | 498 |
| 12 | 1990 | 480 | |
| 13 | 1994 | 436 | |
| 14 | 1990 | 352 | |
| 15 | 1993 | 347 | |
| 16 | 1990 | 332 | |
| 17 | 1994 | 315 | |
| 18 | 1992 | 307 | |
| 19 | 1998 | 297 | |
| 20 | 1994 | 281 |
About Daniel Cohen
Daniel Cohen is a scholar working on Genetics, Cellular and Molecular Neuroscience, Transplantation, Molecular Biology and Surgery, having authored 151 papers that have together received 22.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (46 papers), Genomic variations and chromosomal abnormalities (27 papers), Pancreatic function and diabetes (14 papers), Diabetes and associated disorders (12 papers), Hereditary Neurological Disorders (11 papers), vaccines and immunoinformatics approaches (9 papers), Genetic Mapping and Diversity in Plants and Animals (9 papers) and Muscle Physiology and Disorders (8 papers). The work is most often cited by research in Genetics (3.1k citations), Aging (398 citations), Genetics (5.3k citations), Pathology and Forensic Medicine (2k citations) and Molecular Biology (4.5k citations). Daniel Cohen has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Denis Le Paslier, Philippe Froguel, Jean Weissenbach, Philippe Millasseau, Jean B. Dausset, Olivier Clermont, Suzie Lefebvre, Lydie Bürglen, Philippe Burlet and Gilberto Velho. Their work appears in journals such as Proceedings of the National Academy of Sciences, Genomics, Immunogenetics, Nature Genetics and Cell.
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.