Israel Gomy

481 total citations
20 papers, 162 citations indexed

About

Israel Gomy is a scholar working on Genetics, Pathology and Forensic Medicine and Cancer Research. According to data from OpenAlex, Israel Gomy has authored 20 papers receiving a total of 162 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Pathology and Forensic Medicine and 5 papers in Cancer Research. Recurrent topics in Israel Gomy's work include Genetic factors in colorectal cancer (7 papers), BRCA gene mutations in cancer (5 papers) and Genomics and Rare Diseases (4 papers). Israel Gomy is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), BRCA gene mutations in cancer (5 papers) and Genomics and Rare Diseases (4 papers). Israel Gomy collaborates with scholars based in Brazil, United States and Sweden. Israel Gomy's co-authors include Maria Del Pilar Estevez-Diz, Mauro Rossi, Caio Robledo D’Angioli Costa Quaio, Dirce Maria Carraro, Chong Ae Kim, Débora Romeo Bertola, Érika Maria Monteiro Santos, José Cláudio Casali da Rocha, Ester A. Barreto and Dalila Lucíola Zanette and has published in prestigious journals such as Journal of Clinical Oncology, International Journal of Cancer and BMC Cancer.

In The Last Decade

Israel Gomy

19 papers receiving 157 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Israel Gomy Brazil 9 61 49 41 38 36 20 162
Brenda Hermsen Netherlands 7 52 0.9× 51 1.0× 130 3.2× 41 1.1× 56 1.6× 16 286
Sophia Peters Germany 8 35 0.6× 67 1.4× 42 1.0× 66 1.7× 46 1.3× 12 178
Iva Petrovchich United States 4 51 0.8× 52 1.1× 118 2.9× 65 1.7× 41 1.1× 8 217
M. Elizabeth McCready Canada 10 25 0.4× 22 0.4× 120 2.9× 80 2.1× 17 0.5× 25 254
Lisa Devlin United Kingdom 9 17 0.3× 38 0.8× 41 1.0× 51 1.3× 53 1.5× 13 232
Karen Ouyang United States 7 54 0.9× 36 0.7× 143 3.5× 113 3.0× 33 0.9× 17 244
Carole Corsini France 8 78 1.3× 38 0.8× 37 0.9× 40 1.1× 18 0.5× 11 165
Lara Rodríguez‐Laguna Spain 8 12 0.2× 34 0.7× 59 1.4× 52 1.4× 25 0.7× 19 154
Susana Sousa Portugal 9 40 0.7× 22 0.4× 47 1.1× 113 3.0× 80 2.2× 28 254
Gaizhi Zhu China 11 21 0.3× 31 0.6× 47 1.1× 78 2.1× 30 0.8× 23 224

Countries citing papers authored by Israel Gomy

Since Specialization
Citations

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

Fields of papers citing papers by Israel Gomy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Israel Gomy

This figure shows the co-authorship network connecting the top 25 collaborators of Israel Gomy. A scholar is included among the top collaborators of Israel Gomy 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 Israel Gomy. Israel Gomy 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.
Altmayer, Stephan, et al.. (2024). Baseline surveillance in Li Fraumeni syndrome using whole-body MRI: a systematic review and updated meta-analysis. European Radiology. 35(2). 643–651. 4 indexed citations
2.
Gomy, Israel, Alexander Gusev, Bruce E. Johnson, et al.. (2021). Germline Testing Data Validate Inferences of Mutational Status for Variants Detected From Tumor-Only Sequencing. JCO Precision Oncology. 5(5). 1749–1757. 9 indexed citations
3.
Bychkovsky, Brittany, Tianyu Li, Nabihah Tayob, et al.. (2021). Identification and management of pathogenic mutations in BRCA1, BRCA2, and PALB2 in a tumor-only genomic testing program.. Journal of Clinical Oncology. 39(15_suppl). 10528–10528. 1 indexed citations
4.
Pérez, Ana Beatriz Alvarez, Vânia D’Almeida, Cláudia Berlim de Mello, et al.. (2020). Clinical and molecular evaluation of 13 Brazilian patients with Gomez‐López‐Hernández syndrome. American Journal of Medical Genetics Part A. 185(4). 1047–1058. 3 indexed citations
5.
Gomy, Israel. (2019). Modern Medical Genetics and Genomics. IntechOpen eBooks. 4 indexed citations
6.
Gomy, Israel & Maria Del Pilar Estevez-Diz. (2016). Hereditary cancer risk assessment: insights and perspectives for the Next-Generation Sequencing era. Genetics and Molecular Biology. 39(2). 184–188. 8 indexed citations
7.
Villacis, Rolando André Rios, Israel Gomy, Érika Maria Monteiro Santos, et al.. (2015). Contribution of rare germline copy number variations and common susceptibility loci in Lynch syndrome patients negative for mutations in the mismatch repair genes. International Journal of Cancer. 138(8). 1928–1935. 13 indexed citations
8.
Borlot, Felippe, Paula Ricci Arantes, Caio Robledo D’Angioli Costa Quaio, et al.. (2014). Mucopolysaccharidosis type IVA: Evidence of primary and secondary central nervous system involvement. American Journal of Medical Genetics Part A. 164(5). 1162–1169. 12 indexed citations
9.
Gomy, Israel & Maria Del Pilar Estevez-Diz. (2013). Hereditary cancer risk assessment: essential tools for a better approach. Hereditary Cancer in Clinical Practice. 11(1). 16–16. 7 indexed citations
10.
Dominguez–Valentin, Mev, Felipe Cavalcanti Carneiro da Silva, Érika Maria Monteiro Santos, et al.. (2012). Evaluation of MLH1 I219V polymorphism in unrelated South American individuals suspected of having Lynch syndrome.. PubMed. 32(10). 4347–51. 5 indexed citations
11.
Santos, Érika Maria Monteiro, Mev Dominguez–Valentin, Samuel Aguiar, et al.. (2012). Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries. BMC Cancer. 12(1). 64–64. 9 indexed citations
12.
13.
Quaio, Caio Robledo D’Angioli Costa, Tatiana Ferreira de Almeida, Lílian Maria José Albano, et al.. (2012). A clinical follow-up of 35 Brazilian patients with Prader-Willi Syndrome. Clinics. 67(8). 917–921. 4 indexed citations
14.
Gomy, Israel, et al.. (2012). Molecular Pathogenesis of Renal Cell Carcinoma: A Review. InTech eBooks. 2 indexed citations
15.
Dominguez–Valentin, Mev, Felipe Cavalcanti Carneiro da Silva, Érika Maria Monteiro Santos, et al.. (2011). Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals. Familial Cancer. 10(4). 641–647. 20 indexed citations
16.
Quaio, Caio Robledo D’Angioli Costa, Maria Lúcia Carneiro Vieira, Gabriela Nunes Leal, et al.. (2011). Report of a Large Brazilian Family With a Very Attenuated Form of Hunter Syndrome (MPS II). JIMD Reports. 125–128. 16 indexed citations
17.
Gomy, Israel, Greice Andreotti de Molfetta, Ester A. Barreto, et al.. (2010). Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation. Familial Cancer. 9(4). 635–642. 18 indexed citations
18.
Pfeifer, Luzia Iara, et al.. (2010). Three-year-old child with meroacrania – Neurological signs. Brain and Development. 33(1). 86–89. 3 indexed citations
19.
Gomy, Israel, et al.. (2008). Two new Brazilian patients with Gómez–López‐Hernández syndrome: Reviewing the expanded phenotype with molecular insights. American Journal of Medical Genetics Part A. 146A(5). 649–657. 15 indexed citations
20.
Peres, Luíz César, et al.. (2004). Splenopancreatic Field Abnormality is Not Unique to Trisomy 13. Pediatric and Developmental Pathology. 7(1). 91–94. 9 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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