H. Sobol

421 total citations
14 papers, 268 citations indexed

About

H. Sobol is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, H. Sobol has authored 14 papers receiving a total of 268 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in H. Sobol's work include BRCA gene mutations in cancer (10 papers), Nutrition, Genetics, and Disease (6 papers) and Genetic factors in colorectal cancer (2 papers). H. Sobol is often cited by papers focused on BRCA gene mutations in cancer (10 papers), Nutrition, Genetics, and Disease (6 papers) and Genetic factors in colorectal cancer (2 papers). H. Sobol collaborates with scholars based in France, United States and Burkina Faso. H. Sobol's co-authors include François Eisinger, Daniel Birnbaum, Brigitte Bressac–de Paillerets, Michel Longy, Jean‐Marc Guinebretière, Colette Charpin, R Sauvan, T Noguchi, J. Jacquemier and Jean‐Philippe Peyrat and has published in prestigious journals such as International Journal of Cancer, European Journal of Cancer and Genetics in Medicine.

In The Last Decade

H. Sobol

14 papers receiving 259 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
H. Sobol France 7 161 111 86 73 58 14 268
Dominique Stoppa‐Lyonnet France 8 136 0.8× 140 1.3× 57 0.7× 40 0.5× 46 0.8× 17 257
Steven A. Narod Canada 7 308 1.9× 153 1.4× 80 0.9× 85 1.2× 110 1.9× 8 474
Jarosław Dębniak Poland 10 176 1.1× 133 1.2× 55 0.6× 39 0.5× 78 1.3× 25 284
Amal Yussuf United States 11 178 1.1× 92 0.8× 125 1.5× 90 1.2× 95 1.6× 29 322
Sonia Nanda Canada 7 234 1.5× 190 1.7× 108 1.3× 53 0.7× 141 2.4× 8 426
Kristen J. Vogel Postula United States 8 219 1.4× 95 0.9× 112 1.3× 118 1.6× 84 1.4× 13 313
Nicolette M. Chun United States 9 262 1.6× 142 1.3× 119 1.4× 87 1.2× 58 1.0× 24 382
Ashley Woodson United States 9 113 0.7× 90 0.8× 116 1.3× 23 0.3× 76 1.3× 18 242
Salina Chan United States 6 203 1.3× 112 1.0× 144 1.7× 46 0.6× 127 2.2× 9 319
Emily Hallberg United States 2 306 1.9× 165 1.5× 165 1.9× 118 1.6× 104 1.8× 3 398

Countries citing papers authored by H. Sobol

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of H. Sobol

This figure shows the co-authorship network connecting the top 25 collaborators of H. Sobol. A scholar is included among the top collaborators of H. Sobol based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with H. Sobol. H. Sobol is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

14 of 14 papers shown
1.
Julian‐Reynier, Claire, Anne‐Déborah Bouhnik, Christine Lasset, et al.. (2010). Time to prophylactic surgery in BRCA1/2 carriers depends on psychological and other characteristics. Genetics in Medicine. 12(12). 801–807. 30 indexed citations
2.
Tournier, Isabelle, Brigitte Bressac–de Paillerets, H. Sobol, et al.. (2004). Significant contribution of germline BRCA2 rearrangements in male breast cancer families. HAL (Le Centre pour la Communication Scientifique Directe). 7 indexed citations
3.
Eisinger, François, et al.. (2001). PS2 expression in BRCA1-associated breast cancers.. PubMed. 21(4B). 2877–81. 2 indexed citations
4.
Eisinger, François, Alain Brémond, J Dauplat, et al.. (1999). [INSERM-FNCLCC collective expertise. Recommendations for medical management of women with genetic risk of developing breast and/or ovarian cancer].. PubMed. 42(1). 51–64. 5 indexed citations
5.
Allione, Florence, François Eisinger, Patricia Parc, et al.. (1998). Loss of heterozygosity at loci from chromosome arm 22Q in human sporadic breast carcinomas. International Journal of Cancer. 75(2). 181–186. 39 indexed citations
6.
Sobol, H., François Eisinger, R Sauvan, et al.. (1998). [Impact of recent oncogenetic progress on the management of high risk breast cancer patients: the example of BRCA1 and BRCA2 genes].. PubMed. 59(6). 459–64. 1 indexed citations
7.
Eisinger, François, J. Jacquemier, Colette Charpin, et al.. (1998). Mutations at BRCA1: the medullary breast carcinoma revisited.. PubMed. 58(8). 1588–92. 108 indexed citations
8.
Eisinger, François, Alain Brémond, J Dauplat, et al.. (1998). [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].. PubMed. 59(6). 470–84. 2 indexed citations
9.
Sobol, H., Dominique Stoppa‐Lyonnet, J Jacquemier, et al.. (1996). PP-4-6 Germline mutation at BRCA1 affects the histoprognostic grade in hereditary breast cancer. European Journal of Cancer. 32. 28–28. 1 indexed citations
10.
Sobol, H., Brigitte Bressac–de Paillerets, J.P. Peyrat, et al.. (1996). Truncation at conserved terminal regions of BRCA1 protein is associated with highly proliferating hereditary breast cancers.. PubMed. 56(14). 3216–9. 49 indexed citations
11.
Vennin, Philippe, S. Giard, Claire Julian‐Reynier, et al.. (1996). [Attitudes towards screening and prevention of breast and ovarian cancers with hereditary predisposition. Survey by female gynecologists in the north of France].. PubMed. 83(9). 697–702. 4 indexed citations
12.
Bouffet, Éric, Didier Frappaz, H. Sobol, et al.. (1993). Successfull treatment for a metastatic supratentorial malignant rhabdoid tumor. Journal of Neuro-Oncology. 17(1). 65–70. 7 indexed citations
13.
Chabre, Olivier, F Labat-Moleur, François Berthod, et al.. (1992). [Cutaneous lesion associated with multiple endocrine neoplasms type 2A (Sipple's syndrome). An early clinical marker].. PubMed. 21(7). 299–303. 11 indexed citations
14.
Sobol, H., et al.. (1989). Hereditary medullary thyroid carcinoma: genetic annalysis of three related syndromes. Groupe d'Etude des Tumeurs a Calcitonine.. PubMed. 37(3-4). 109–11. 2 indexed citations

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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