Elsa Reich

891 total citations
22 papers, 644 citations indexed

About

Elsa Reich is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Elsa Reich has authored 22 papers receiving a total of 644 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Reproductive Medicine. Recurrent topics in Elsa Reich's work include BRCA gene mutations in cancer (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Ovarian cancer diagnosis and treatment (3 papers). Elsa Reich is often cited by papers focused on BRCA gene mutations in cancer (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Ovarian cancer diagnosis and treatment (3 papers). Elsa Reich collaborates with scholars based in United States, Switzerland and France. Elsa Reich's co-authors include Neil Risch, Joseph G. McCarthy, Maximilian Muenke, Sahan V. Rannan‐Eliya, Shih‐hsin Kan, Navaratnam Elanko, Jackie Cook, Alain Verloès, Elaine H. Zackai and David Johnson and has published in prestigious journals such as Journal of Clinical Oncology, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Elsa Reich

22 papers receiving 615 citations

Peers

Elsa Reich

GENET

PPCH

ONCOL

SURGE

M Shohat Israel

Stavit A. Shalev Israel

Sophia Kitsiou‐Tzeli Greece

Rena E. Falk United States

Indira B. Taylor United Kingdom

Roberto Lala Italy

Tracy Dudding Australia

Violetta Anastasiadou Cyprus

M Stefanova Germany

Huw Dorkins United Kingdom

M Shohat Israel

Elsa Reich

387 ×1.2

GENET

329 ×1.1

134 ×1.4

PPCH

64 ×0.9

ONCOL

88 ×1.3

SURGE

Citations per year, relative to Elsa Reich Elsa Reich (= 1×) peers M Shohat

Countries citing papers authored by Elsa Reich

Since Specialization

Citations

This map shows the geographic impact of Elsa Reich'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 Elsa Reich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elsa Reich more than expected).

Fields of papers citing papers by Elsa Reich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elsa Reich. 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 Elsa Reich. The network helps show where Elsa Reich may publish in the future.

Co-authorship network of co-authors of Elsa Reich

This figure shows the co-authorship network connecting the top 25 collaborators of Elsa Reich. A scholar is included among the top collaborators of Elsa Reich 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 Elsa Reich. Elsa Reich is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Reich, Elsa, et al.. (2019). Attenuated familial adenomatous polyposis (AFAP) in a patient associated with a novel mutation in APC. BMJ Case Reports. 12(11). e231232–e231232. 1 indexed citations

Safra, Tamar, Maria Ornella Nicoletto, Tara Berman, et al.. (2013). BRCA mutations and outcome in epithelial ovarian cancer (EOC): experience in ethnically diverse groups. Annals of Oncology. 24. viii63–viii68. 27 indexed citations

Kwa, Maryann, et al.. (2013). Ovarian Cancer in BRCA Mutation Carriers: Improved Outcome After Intraperitoneal (IP) Cisplatin. Annals of Surgical Oncology. 21(5). 1468–1473. 26 indexed citations

Safra, Tamar, et al.. (2012). BRCA mutations and outcome in epithelial ovarian cancer (EOC): Experience in ethnically diverse groups.. Journal of Clinical Oncology. 30(15_suppl). 5078–5078. 1 indexed citations

Adams, Sylvia, Elsa Reich, Yongzhao Shao, et al.. (2011). Expression of cancer testis antigens in human BRCA-associated breast cancers: potential targets for immunoprevention?. Cancer Immunology Immunotherapy. 60(7). 999–1007. 26 indexed citations

Valenzuela, Cristian D., Harvey G. Moore, William C. Huang, et al.. (2009). Three synchronous primary carcinomas in a patient with HNPCC associated with a novel germline mutation in MLH1: Case report. World Journal of Surgical Oncology. 7(1). 94–94. 3 indexed citations

Chanan‐Khan, Asher, et al.. (2003). T-cell clonality and myelodysplasia without chromosomal fragility in a patient with features of Seckel syndrome.. PubMed. 88(5). ECR14–ECR14. 13 indexed citations

Kan, Shih‐hsin, Navaratnam Elanko, David Johnson, et al.. (2002). Genomic Screening of Fibroblast Growth-Factor Receptor 2 Reveals a Wide Spectrum of Mutations in Patients with Syndromic Craniosynostosis. The American Journal of Human Genetics. 70(2). 472–486. 177 indexed citations

Mailman, Matthew, Ying Huang, Robert B. Chadwick, et al.. (2001). Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome. Human Genetics. 108(2). 109–115. 36 indexed citations

10.

Oddoux, Carole, Elsa Reich, Felicia B. Axelrod, et al.. (1995). Prenatal diagnostic testing for familial dysautonomia using linked genetic markers. Prenatal Diagnosis. 15(9). 817–826. 9 indexed citations

11.

Robin, Nathaniel H., George Feldman, Peter Lorenz, et al.. (1994). REPORTS. Human Molecular Genetics. 3(12). 2153–2158. 40 indexed citations

12.

Perle, Mary Ann, et al.. (1994). Cerebral myelin deficiency in teenage girls with the 18q- syndrome. Pediatric Neurology. 11(2). 145–145. 1 indexed citations

13.

Heimler, Audrey, et al.. (1992). American Board of Medical Genetics restructuring: make an informed decision.. PubMed. 51(5). v–vii. 3 indexed citations

14.

Sica, R. E. P., Marcela Panizza, Elsa Reich, & Jorge Correale. (1989). Modifications of the N1-P1 component of the somatosensory evoked potential in humans after partial limb amputation as a manifestation of central nervous system remodeling.. PubMed. 28(5). 227–31. 5 indexed citations

15.

Benn, Peter, et al.. (1987). Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection.. PubMed. 70(3 Pt 2). 449–52. 4 indexed citations

16.

Risch, Neil, et al.. (1987). Spontaneous mutation and parental age in humans.. PubMed. 41(2). 218–48. 196 indexed citations

17.

McGlynn, F, et al.. (1987). Laparoscopic treatment of tubal pregnancy. International Journal of Gynecology & Obstetrics. 25(6). 490–490. 26 indexed citations

18.

Wishnick, Marcia, et al.. (1983). Möbius syndrome and limb abnormalities with dominant inheritance. Ophthalmic Paediatrics and Genetics. 2(2). 77–81. 15 indexed citations

19.

Verma, Rama Shanker, et al.. (1982). GTG banding is not sufficient for the localization of breakpoints in translocations.. PubMed. 34(135-36). 175–80. 5 indexed citations

20.

Reich, Elsa, et al.. (1978). Recognition in adult patients of malformations induced by folic-acid antagonists.. PubMed. 14(6B). 139–60. 15 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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