H. Sobol
Impact in
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- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
- Breast Cancer Treatment Studies
Papers in
- Genetics 11
- BRCA gene mutations in cancer 10
- Nutrition, Genetics, and Disease 6
- Dermatological and Skeletal Disorders 1
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- Chromatin Remodeling and Cancer 2
- Mechanisms of cancer metastasis 1
- DNA Repair Mechanisms 1
- Co-authors
- François Eisinger (9 shared papers)Daniel Birnbaum (5 shared papers)Brigitte Bressac–de Paillerets (3 shared papers)Michel Longy (3 shared papers)T Noguchi (1 shared paper)Colette Charpin (1 shared paper)J. Jacquemier (2 shared papers)Jean‐Marc Guinebretière (1 shared paper)
- Journals
- Genetics in Medicine (1 paper)Journal of Neuro-Oncology (1 paper)International Journal of Cancer (1 paper)European Journal of Cancer (1 paper)PubMed (9 papers)
- Partner nations
- FranceUnited StatesLuxembourg
In The Last Decade
H. Sobol
14 papers receiving 259 citations
Peers
Comparison fields: 5 of 42
- Genetics 161
- Cancer Research 86
- Pathology and Forensic Medicine 73
- Reproductive Medicine 28
- Oncology 58
Countries citing papers authored by H. Sobol
This map shows the geographic impact of H. Sobol'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 H. Sobol with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H. Sobol more than expected).
Fields of papers citing papers by H. Sobol
This network shows the impact of papers produced by H. Sobol. 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 H. Sobol. The network helps show where H. Sobol may publish in the future.
Co-authors
The 25 scholars most cited alongside H. Sobol, 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 | Mutations at BRCA1: the medullary breast carcinoma revisited. | 1998 | 108 |
| 2 | Truncation at conserved terminal regions of BRCA1 protein is associated with highly proliferating hereditary breast cancers. | 1996 | 49 |
| 3 | 1998 | 39 | |
| 4 | 2010 | 30 | |
| 5 | [Cutaneous lesion associated with multiple endocrine neoplasms type 2A (Sipple's syndrome). An early clinical marker]. | 1992 | 11 |
| 6 | 1993 | 7 | |
| 7 | Significant contribution of germline BRCA2 rearrangements in male breast cancer families | 2004 | 7 |
| 8 | [INSERM-FNCLCC collective expertise. Recommendations for medical management of women with genetic risk of developing breast and/or ovarian cancer]. | 1999 | 5 |
| 9 | [Attitudes towards screening and prevention of breast and ovarian cancers with hereditary predisposition. Survey by female gynecologists in the north of France]. | 1996 | 4 |
| 10 | PS2 expression in BRCA1-associated breast cancers. | 2001 | 2 |
| 11 | Hereditary medullary thyroid carcinoma: genetic annalysis of three related syndromes. Groupe d'Etude des Tumeurs a Calcitonine. | 1989 | 2 |
| 12 | [INSERM-FNCLCC collective expert's report. Recommendations for management of women having a genetic risk of developing breast and/or ovarian cancer. National Federation of Centers of the Fight Against Cancer]. | 1998 | 2 |
| 13 | 1996 | 1 | |
| 14 | [Impact of recent oncogenetic progress on the management of high risk breast cancer patients: the example of BRCA1 and BRCA2 genes]. | 1998 | 1 |
About H. Sobol
H. Sobol is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Oncology and Dermatology, having authored 14 papers that have together received 268 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Nutrition, Genetics, and Disease (6 papers), Genetic factors in colorectal cancer (2 papers), Chromatin Remodeling and Cancer (2 papers), Dermatological and Skeletal Disorders (1 paper), Cancer-related Molecular Pathways (1 paper), Mechanisms of cancer metastasis (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Genetics (161 citations), Cancer Research (86 citations), Pathology and Forensic Medicine (73 citations), Reproductive Medicine (28 citations) and Oncology (58 citations). H. Sobol has collaborated with scholars based in France, United States and Luxembourg. Frequent co-authors include François Eisinger, Daniel Birnbaum, Brigitte Bressac–de Paillerets, Michel Longy, T Noguchi, Colette Charpin, J. Jacquemier, Jean‐Marc Guinebretière, Jean‐Philippe Peyrat and R Sauvan. Their work appears in journals such as Genetics in Medicine, Journal of Neuro-Oncology, International Journal of Cancer, European Journal of Cancer and PubMed.
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.