Eitan Friedman

32.7k citations

484 papers · 17.1k indexed · 1 hit paper · h-index 64

Impact in

Reproductive Medicine top 0.2%
- Ovarian cancer diagnosis and treatment
Genetics top 0.1%
- BRCA gene mutations in cancer

Papers in

Genetics 190
- BRCA gene mutations in cancer 146
Cancer Research 76
- Cancer Genomics and Diagnostics 60

Co-authors: Samuel Gershon Pablo V. Gejman Allen M. Spiegel Lee S. Weinstein Hoau-Yan Wang Maria J. Merino Andrew Shenker Ephrat Levy‐Lahad
Journals: Breast Cancer Research and Treatment (28 papers)Familial Cancer (14 papers)British Journal of Cancer (14 papers)European Journal of Pharmacology (12 papers)Journal of Pharmacology and Experimental Therapeutics (12 papers)
Partner nations: Israel United States Brazil

In The Last Decade

Eitan Friedman

469 papers receiving 16.5k citations

Hit Papers

align trajectories log scale

Activating Mutations of the Stimulatory G Protein in the McCune–Albright Syndrome 1991 · 1.2k citations

Peers

Countries citing papers authored by Eitan Friedman

Since Specialization

Citations

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

Fields of papers citing papers by Eitan Friedman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Eitan Friedman, 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 Eitan Friedman Line = papers co-authored together Eitan Friedman links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Targeted genotyping for recurring variants in cancer susceptibility genes in non‐Ashkenazi Jewish patients with breast cancer diagnosed ≥50 years Cancer ·Rinat Bernstein‐Molho, IA Alakeji, Yael Laitman, Gazim Bižanov, Shurooq M. Abdulkhudhur, Eitan Friedman	2024	0
2	Lessons from the Failure to Complete a Trial of Denosumab in Women With a Pathogenic BRCA1/2 Variant Scheduling Risk-Reducing Salpingo-Oophorectomy Cancer Prevention Research ·Meghna S. Trivedi, Nadir Arber, Eitan Friedman, Judy E. Garber, Kevin Holcomb, Neil S. Horowitz, Jason D. Wright, J. Jack Lee, Lana A. Vornik, Whitney Sanford, Anne Hougaard Hansen, Edward R. Sauter, Eileen Dimond, Brandy M. Heckman‐Stoddard, L Budzyńska, Goli Samimi, Powel H. Brown, Katherine D. Crew	2022	3
3	Variable number tandem repeats (VNTRs) as modifiers of breast cancer risk in carriers of BRCA1 185delAG European Journal of Human Genetics ·Yuan Chun Ding, Aaron W. Adamson, Mehrdad Bakhtiari, Joel Fan, Yang-Mi Lee, Yael Laitman, Jeffrey N. Weitzel, Vineet Bafna, Eitan Friedman, Susan L. Neuhausen	2022	2
4	Ductal Carcinoma In Situ (DCIS) Diagnosed by MRI-Guided Biopsy among BRCA1/BRCA2 Mutation Carriers The Breast Journal ·Oksana Ev. Gudkova, Eitan Friedman, Orit Kaidar‐Person, K. Ya. Faradzheva, B. Hallerbück, Anat Shalmon, Dasuni Nagoda Vithana, Michael Gotlieb, Yael Yagil, David Samoocha, Dana Feldman, Miri Sklair‐Levy	2022	3
5	Germline CDKN1B variant type and site are associated with phenotype in MEN4 Endocrine Related Cancer ·Al- Nawaz, Min Mi hee, Pawel Urbanek, D. W. Barron, Kari Anne Rand, Alona Telerman, Eitan Friedman, Rinat Bernstein‐Molho, Amit Tirosh	2022	14
6	Local microRNA delivery targets Palladin and prevents metastatic breast cancer Nature ·Avital Gilam, Daphna Weissglas‐Volkov, Eitan Friedman, Noam Shomron, João Conde, Hudson Henrique Ferreira [UNESP] Depicoli, Natalie Artzi	2016	1
7	Randomized Controlled Trial of “The Work” Meditation-Based Intervention for BRCA1/2 Mutation Carriers The Journal of Alternative and Complementary Medicine ·Shahar Lev‐Ari, Pierre Morio, Zaved Ahmad, Eitan Friedman	2014	0
8	Missense mutation in the MEN1 gene discovered through whole exome sequencing co-segregates with familial hyperparathyroidism Genetics Research ·Ofer Isakov, Ariana Lisbeth, David Olchovsky, Ilan Shimon, Harry Ostrer, Noam Shomron, Eitan Friedman	2013	8
9	North African Jewish and non-Jewish populations form distinctive, orthogonal clusters Proceedings of the National Academy of Sciences ·Christopher Campbell, Pier Francesco Palamara, Maya Dubrovsky, Laura R. Botigué, Marc Fellous, Gil Atzmon, Carole Oddoux, Alexander Pearlman, Hao Li, Brenna M. Henn, Edward R. Burns, Carlos D. Bustamante, David Comas, Eitan Friedman, Itsik Pe’er, Harry Ostrer	2012	43
10	Effect of BRCA1/2 Mutations on Long-Term Survival of Patients With Invasive Ovarian Cancer: The National Israeli Study of Ovarian Cancer Journal of Clinical Oncology ·Angela Chetrit, Galit Hirsh‐Yechezkel, Yehuda Ben‐David, Flora Lubin, Eitan Friedman, Siegal Sadetzki	2007	242
11	Novel Vasopressin Type 2 ( AVPR2 ) Gene Mutations in Brazilian Nephrogenic Diabetes Insipidus Patients Genetic Testing ·Wolfanga L. Boson, Thaís Della Manna, Durval Damiani, Débora Marques de Miranda, Mônica R. Gadelha, Bernardo Liberman, Humberto Corrêa, Marco Aurélio Romano‐Silva, Eitan Friedman, L Pakotomrivelo, Paulo Ayroza Ribeiro, Luiz Marco	2006	10
12	The P1812A and P25T BRCA1 and the 5164del4 BRCA2 Mutations: Occurrence in High-Risk Non-Ashkenazi Jews Genetic Testing ·Bella Kaufman, Yael Laitman, Marcelo A. Carvalho, P. Mazliak, Federico Gaviria‐Gil, Jamal Zidan, Álvaro N.A. Monteiro, Eitan Friedman	2006	6
13	Mutational Analysis of the hMSH6 Gene in Familial and Early-Onset Colorectal and Endometrial Cancer in Israeli Patients Genetic Testing ·Arié Figer, Anna Kaplan, Ravit Geva, Dov Flex, Michal Yaron, 芹吴, Wataru Ootani, Herma H. Fidder, Eitan Friedman	2002	1
14	Germline mutations in the PTEN gene in Israeli patients with Bannayan–Riley–Ruvalcaba syndrome and women with familial breast cancer Clinical Genetics ·Arié Figer, Alexander Kaplan, Moshe Frydman, Dorit Lev, TJ Zuzak, P. Brücke, Boleslaw Goldman, Eitan Friedman	2002	15
15	Genetic Analysis of Brugada Syndrome in Israel: Two Novel Mutations and Possible Genetic Heterogeneity Genetic Testing ·Etgar Levy‐Nissenbaum, Michael Eldar, Qing Wang, Hadas Lahat, Bernard Belhassen, Gaёtan Le Quang, Eitan Friedman, Elon Pras	2001	13
16	The I1307K APC Polymorphism: Prevalence in Non-Ashkenazi Jews and Evidence for a Founder Effect Genetic Testing ·Rakefet Chen‐Shtoyerman, Eitan Friedman, Arié Figer, Miri Carmel, Martin Wallner, Peter Rath, Herma H. Fidder, Simon Bar–Meir, Livia Theodor	2001	22
17	Genetic Analyses of Male Breast Cancer in Israel Genetic Testing ·Ronit Shiri‐Sverdlov, Iris Barshack, Jessiel Gonçalves De Souza, Ruth Gershoni Baruch, Qinhao Guo, Mark R. Elliott, Meora Feinmesser, Arié Figer, Eitan Friedman	2000	31
18	The Founder Mutations in the BRCA1 , BRCA2 , and ATM Genes in Moroccan Jewish Women with Breast Cancer Genetic Testing ·Yitshak Kreiss, Paul Glasserman, Ruth Gershoni Baruch, Ephrat Levy‐Lahad, Elon Pras, Eitan Friedman	2000	10
19	[Experience at Sheba Hospital in oncogenetic counseling and genetic testing of women with a high risk for breast and ovarian cancer]. PubMed ·Livia Theodor, Ronit Shiri‐Sverdlov, Вероника Александровна Малявина, C.-M. Duval, Y. Xiao, Die Bedeutung von Inter-α-Trypsin-Inhi, Anna Kruglikova, Gilad Ben‐Baruch, Awanis Ghassani Maryono, P. Brücke, Boleslaw Goldman, Eitan Friedman	1998	0
20	Handbook of pharmacology of aging CRC Press eBooks ·David Snyder, Jay Roberts, Eitan Friedman	1996	13

About Eitan Friedman

Eitan Friedman is a scholar working on Genetics, Cancer Research, Reproductive Medicine, Cellular and Molecular Neuroscience and Pathology and Forensic Medicine, having authored 484 papers that have together received 17.1k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (146 papers), Cancer Genomics and Diagnostics (60 papers), DNA Repair Mechanisms (59 papers), Neurotransmitter Receptor Influence on Behavior (47 papers), Neuroscience and Neuropharmacology Research (42 papers), Genetic factors in colorectal cancer (42 papers), Ovarian cancer diagnosis and treatment (38 papers) and Receptor Mechanisms and Signaling (36 papers). The work is most often cited by research in Reproductive Medicine (1.6k citations), Genetics (5.1k citations), Cellular and Molecular Neuroscience (3.1k citations), Cancer Research (2.4k citations) and Oncology (3.3k citations). Eitan Friedman has collaborated with scholars based in Israel, United States and Brazil. Frequent co-authors include Samuel Gershon, Pablo V. Gejman, Allen M. Spiegel, Lee S. Weinstein, Hoau-Yan Wang, Maria J. Merino, Andrew Shenker, Ephrat Levy‐Lahad, H Y Wang and Steven A. Narod. Their work appears in journals such as Breast Cancer Research and Treatment, Familial Cancer, British Journal of Cancer, European Journal of Pharmacology and Journal of Pharmacology and Experimental Therapeutics.

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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