Yael Goldberg

2.9k total citations
76 papers, 1.4k citations indexed

About

Yael Goldberg is a scholar working on Pathology and Forensic Medicine, Genetics and Cancer Research. According to data from OpenAlex, Yael Goldberg has authored 76 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Pathology and Forensic Medicine, 28 papers in Genetics and 26 papers in Cancer Research. Recurrent topics in Yael Goldberg's work include Genetic factors in colorectal cancer (35 papers), Cancer Genomics and Diagnostics (24 papers) and BRCA gene mutations in cancer (19 papers). Yael Goldberg is often cited by papers focused on Genetic factors in colorectal cancer (35 papers), Cancer Genomics and Diagnostics (24 papers) and BRCA gene mutations in cancer (19 papers). Yael Goldberg collaborates with scholars based in Israel, United States and Netherlands. Yael Goldberg's co-authors include Chrystelle Colas, Tamar Peretz, Katharina Wimmer, Martine Muleris, Laurence Brugières, Clara Ruíz-Ponte, Hans F. A. Vasen, Christian P. Kratz, Alex Duval and Natacha Entz‐Werlé and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Gastroenterology and Cancer Research.

In The Last Decade

Yael Goldberg

73 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yael Goldberg Israel 19 735 470 465 459 404 76 1.4k
Chrystelle Colas France 23 1.1k 1.5× 556 1.2× 577 1.2× 573 1.2× 358 0.9× 72 1.7k
Olivier Caron France 23 746 1.0× 657 1.4× 1.0k 2.2× 842 1.8× 721 1.8× 72 2.4k
Swen Weßendorf Germany 19 665 0.9× 299 0.6× 521 1.1× 624 1.4× 325 0.8× 31 1.6k
Stéphanie Baert‐Desurmont France 15 376 0.5× 421 0.9× 596 1.3× 419 0.9× 412 1.0× 38 1.2k
Denisa Ilenčíková Slovakia 15 438 0.6× 257 0.5× 301 0.6× 227 0.5× 190 0.5× 40 851
Ana Novokmet Canada 11 161 0.2× 444 0.9× 582 1.3× 472 1.0× 355 0.9× 15 1.3k
Carsten Schwäenen Germany 19 420 0.6× 362 0.8× 663 1.4× 377 0.8× 347 0.9× 25 1.4k
Debra M. Lillington United Kingdom 27 640 0.9× 386 0.8× 1.2k 2.5× 631 1.4× 361 0.9× 50 3.0k
Patrick R. Benusiglio France 15 263 0.4× 352 0.7× 652 1.4× 515 1.1× 345 0.9× 38 1.3k
Inga Vater Germany 21 701 1.0× 304 0.6× 594 1.3× 377 0.8× 139 0.3× 35 1.6k

Countries citing papers authored by Yael Goldberg

Since Specialization
Citations

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

Fields of papers citing papers by Yael Goldberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yael Goldberg

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

All Works

20 of 20 papers shown
1.
Golan, Maya Aharoni, Lior H. Katz, Ido Laish, et al.. (2025). Raising the Age for Starting Colonoscopy to 35 Years for Individuals With path_MSH6 Carriers May Lead to Missed Opportunities for Detecting Advanced Neoplasia in a Notable Percentage of Carriers. The American Journal of Gastroenterology. 121(1). 205–211. 2 indexed citations
2.
Yerushalmi, Rinat, Shani Paluch–Shimon, Lior Soussan‐Gutman, et al.. (2024). BRCA1/2 mutation carriers vs the general breast cancer population (N = 799,986): 21-gene assay-based molecular characterization. Breast Cancer Research and Treatment. 206(1). 67–76.
3.
Tschernichovsky, Roi, Daniel A. Goldstein, Elizabeth Dudnik, et al.. (2023). Correlations between pathogenic variants in DNA repair genes and anticancer treatment efficacy in stage IV non‐small cell lung cancer: A large real‐world cohort and review of the literature. Thoracic Cancer. 14(17). 1589–1596. 3 indexed citations
4.
Katz, Lior H., Rachel Gingold‐Belfer, Ido Laish, et al.. (2022). Phenotypic diversity among juvenile polyposis syndrome patients from different ethnic background. Hereditary Cancer in Clinical Practice. 20(1). 2–2. 4 indexed citations
5.
Michaeli, Orli, Ayelet Erez, Shai Izraeli, et al.. (2021). Di‐genic inheritance of germline POLE and PMS2 pathogenic variants causes a unique condition associated with pediatric cancer predisposition. Clinical Genetics. 101(4). 442–447. 10 indexed citations
6.
Shamai, Sivan, Hana Strul, Guy Rosner, et al.. (2021). Abdominal Desmoid: Course, Severe Outcomes, and Unique Genetic Background in a Large Local Series. Cancers. 13(15). 3673–3673. 5 indexed citations
7.
Laish, Ido, Yael Goldberg, Eitan Friedman, et al.. (2021). Genetic testing for assessment of lynch syndrome in young patients with polyps. Digestive and Liver Disease. 53(12). 1640–1646. 1 indexed citations
8.
Halpern, Naama, Albert Grinshpun, Ben Boursi, et al.. (2020). <p>Clinical Characteristics and Prognosis of Gastric Cancer Patients with <em>BRCA 1/2</em> Germline Mutations: Report of Ten Cases and a Literature Review</p>. OncoTargets and Therapy. Volume 13. 11637–11644. 7 indexed citations
9.
Goldberg, Yael, Rony Cohen, Rivka Friedland, et al.. (2019). The great mimicker: Phenotypic overlap between constitutional mismatch repair deficiency and Tuberous Sclerosis complex. Clinical Genetics. 97(2). 296–304. 6 indexed citations
10.
Valle, Laura, Richarda M. de Voer, Yael Goldberg, et al.. (2019). Update on genetic predisposition to colorectal cancer and polyposis. Molecular Aspects of Medicine. 69. 10–26. 116 indexed citations
11.
Tamary, Hannah, Nadav Sahar, Noam Zevit, et al.. (2018). Endoscopic findings and esophageal cancer incidence among Fanconi Anemia patients participating in an endoscopic surveillance program. Digestive and Liver Disease. 51(2). 242–246. 10 indexed citations
12.
Halpern, Naama, Yael Goldberg, Luna Kadouri, et al.. (2017). Clinical course and outcome of patients with high-level microsatellite instability cancers in a real-life setting: a retrospective analysis. OncoTargets and Therapy. Volume 10. 1889–1896. 17 indexed citations
13.
Maya, Idit, Reuven Sharony, Shiri Yacobson, et al.. (2017). When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations. Genetics in Medicine. 20(1). 128–131. 46 indexed citations
14.
Vasen, Hans F. A., Franck Bourdeaut, Odile Cabaret, et al.. (2014). Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D). Journal of Medical Genetics. 51(5). 283–293. 142 indexed citations
15.
Wimmer, Katharina, Irene Slavc, Yael Goldberg, et al.. (2010). Brain tumors in constitutional mismatch repair deficiency syndrome: four new families with biallelic pms2 mutations. Neuro-Oncology. 12(6). 1 indexed citations
16.
Sagi, Michal, Yael Goldberg, Dani Bercovich, et al.. (2010). Two BRCA1/2 founder mutations in Jews of Sephardic origin. Familial Cancer. 10(1). 59–63. 18 indexed citations
17.
Goldberg, Yael, Rinnat M. Porat, Inbal Kedar, et al.. (2009). An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC. Familial Cancer. 9(2). 141–150. 21 indexed citations
18.
Cordero, Dwight R., Yael Goldberg, Donald Basel, et al.. (2006). Prenatal Sonographic Diagnosis of Grebe Syndrome. Journal of Ultrasound in Medicine. 25(1). 115–118. 1 indexed citations
19.
Goldberg, Yael, et al.. (1996). Neurofibromatosis Type 1—An Update and Review for the Primary Pediatrician. Clinical Pediatrics. 35(11). 545–561. 24 indexed citations
20.
Mevorach, Dror, et al.. (1996). Antiphospholipid Syndrome Manifested by Ischemic Stroke in a Patient with Crohn's Disease. Journal of Clinical Gastroenterology. 22(2). 141–143. 17 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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