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G. Idos · SciRah

Researcher profile · Semantic Scholar

G. Idos

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G. Idos — researcher profile on SciRah

h-index: 14
Works: 66
Citations: 1,517

Most-cited papers

Discovery of common and rare genetic risk variants for colorectal cancer
J. Huyghe, S. Bien, T. Harrison, H. Kang +195 more
2018Nature Genetics479 citations Open access
Semantic Scholar
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and East Asian ancestries
C. Fernández-Rozadilla, M. Timofeeva, Zhi-Shan Chen, P. Law +206 more
2022Nature Genetics204 citations Open access
Semantic Scholar
Genome-wide association study of colorectal cancer identifies six new susceptibility loci
F. Schumacher, S. Schmit, Shuo Jiao, Christopher Edlund +97 more
2015Nature Communications175 citations Open access
Semantic Scholar
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
S. Schmit, Christopher Edlund, F. Schumacher, Jian Gong +179 more
2018Journal of the National Cancer Institute149 citations Open access
Semantic Scholar
Shared heritability and functional enrichment across six solid cancers
Xia Jiang, H. Finucane, F. Schumacher, S. Schmit +329 more
2019Nature Communications104 citations Open access
Semantic Scholar
Increased Yield of Actionable Mutations Using Multi-Gene Panels to Assess Hereditary Cancer Susceptibility in an Ethnically Diverse Clinical Cohort
C. Ricker, Julie O. Culver, K. Lowstuter, D. Sturgeon +6 more
2016Cancer Genetics81 citations Open access
Semantic Scholar
Unexpected CDH1 Mutations Identified on Multigene Panels Pose Clinical Management Challenges.
K. Lowstuter, C. Espenschied, D. Sturgeon, C. Ricker +13 more
2017JCO Precision Oncology50 citations
Semantic Scholar
Multicenter Prospective Cohort Study of the Diagnostic Yield and Patient Experience of Multiplex Gene Panel Testing For Hereditary Cancer Risk
G. Idos, A. Kurian, C. Ricker, D. Sturgeon +25 more
2019JCO Precision Oncology47 citations Open access
Semantic Scholar
Patient communication of cancer genetic test results in a diverse population.
C. Ricker, Rachel Koff, C. Qu, Julie O. Culver +20 more
2018Translational Behavioral Medicine42 citations Open access
Semantic Scholar
Lymphocytic infiltration in stage II microsatellite stable colorectal tumors: A retrospective prognosis biomarker analysis
R. Sanz-Pamplona, Marilena Melas, A. Maoz, S. Schmit +19 more
2020PLoS Medicine36 citations Open access
Semantic Scholar
A novel BAP1 mutation is associated with melanocytic neoplasms and thyroid cancer
K. McDonnell, Gregory T. Gallanis, Kathleen A. Heller, Marilena Melas +5 more
2015Cancer Genetics29 citations Open access
Semantic Scholar
Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes
Zhi-Shan Chen, Xing-Yi Guo, R. Tao, J. Huyghe +201 more
2024Nature Communications18 citations Open access
Semantic Scholar
Differences in Tumor-Associated T cell receptor repertoires between Early-Onset and Average-Onset colorectal cancer.
Ya-Yu Tsai, K. Nair, S. Barot, Shao Xiang +19 more
2024Journal of the National Cancer Institute16 citations
Semantic Scholar
Inhibition of poly(ADP-ribose) polymerase induces synthetic lethality in BRIP1 deficient ovarian epithelial cells
M. Ciccone, C. Adams, C. Bowen, Teena Thakur +10 more
2020Gynecologic Oncology15 citations Open access
Semantic Scholar
Heterozygote advantage at HLA class I and II loci and reduced risk of colorectal cancer
Ya-Yu Tsai, C. Qu, J. Bonner, R. Sanz-Pamplona +16 more
2023Frontiers in Immunology9 citations Open access
Semantic Scholar
Clinical implications of conflicting variant interpretations in the cancer genetics clinic
Elyssa Zukin, Julie O. Culver, Yuxi Liu, Yun-Qi Yang +16 more
2023Genetics in Medicine7 citations Open access
Semantic Scholar
Breast Cancer MRI Screening of Patients After Multiplex Gene Panel Testing
L. Naghi, Julie O. Culver, Charité Ricker, D. Sturgeon +15 more
2025JAMA Network Open6 citations
Semantic Scholar
Germline genetic regulation of the colorectal tumor immune microenvironment
S. Schmit, Ya-Yu Tsai, J. Bonner, R. Sanz-Pamplona +21 more
2024BMC Genomics6 citations Open access
Semantic Scholar
Publisher Correction: Shared heritability and functional enrichment across six solid cancers
Xia Jiang, H. Finucane, F. Schumacher, S. Schmit +329 more
2019Nature Communications6 citations Open access
Semantic Scholar
Correction: Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci
F. Schumacher, S. Schmit, Shuo Jiao, Christopher Edlund +97 more
2015Nature Communications6 citations Open access
Semantic Scholar
Safety of multiplex gene testing for inherited cancer risk: Interim analysis of a clinical trial.
A. Kurian, G. Idos, Julie O. Culver, C. Ricker +16 more
20165 citations
Semantic Scholar
Family communication of cancer genetic test results in an ethnically diverse population: a qualitative exploration of more than 200 patients
Rachel Hodan, M. Picus, C. Stanclift, K. Ormond +4 more
2024Journal of Community Genetics3 citations Open access
Semantic Scholar
Statistical methods for Mendelian models with multiple genes and cancers
Jane W. Liang, G. Idos, C. Hong, S. Gruber +2 more
2021Genetic Epidemiology3 citations Open access
Semantic Scholar
Yield of multiplex panel testing compared to expert opinion and validated prediction models.
G. Idos, A. Kurian, C. Ricker, D. Sturgeon +16 more
20163 citations
Semantic Scholar
Promoting breast cancer screening after multiplex genetic panel testing (MGPT) and genetic counseling.
G. Idos, A. Kurian, C. Ricker, D. Sturgeon +15 more
20182 citations
Semantic Scholar
Inactivation of the Tumor Suppressor BRCA1 Interacting Protein C-terminal Helicase 1 (BRIP1) Gene Confers Increased Susceptibility to Platinum Antineoplastic Agents and Augments the Synergistic Response to Poly (ADP-ribose) Polymerase (PARP) Inhibition in Ovarian Epithelial Cells
M. Ciccone, C. Ricker, Julie O. Culver, A. Maoz +4 more
20162 citations
Semantic Scholar
“The GI Gap” in Genetic Testing for Inherited Susceptibility to Cancer: 1402
G. Idos, A. Kurian, K. McDonnell, C. Ricker +16 more
20152 citations
Semantic Scholar
Clinical implications of con ﬂ icting variant interpretations in the cancer genetics clinic
Elyssa Zukin, Julie O. Culver, Yuxi Liu, Yunqi Yang +17 more
2 citations
Semantic Scholar
O06: Penetrance and prevalence of CDKN2A pathogenic variants in a large institutional cohort: Scrutinizing the common p.Ile49Thr variant
L. Gima, Christina Fujii, Michael Restrepo, Christina Rybak +9 more
2024Genetics in Medicine Open1 citations Open access
Semantic Scholar
Abstract PD14-03: PD14-03 Reappraising the Fanconi Anemia DNA repair pathway in breast cancer risk and precision intervention: Insights and opportunities from the City of Hope INSPIRE study
L. Kruper, K. McDonnell, J. Bonner, K. Tsang +9 more
2023Cancer Research1 citations
Semantic Scholar
Abstract P051: The INSPIRE Study (Implementing Next-generation Sequencing for Precision Intervention and Risk Evaluation): scaling return of genomic results
Ilana Solomon, H. Hampel, K. McDonnell, K. Blazer +18 more
2023Cancer Prevention Research1 citations
Semantic Scholar
Germline mutational landscape of non-highly penetrant Fanconi anemia genes unveiled from sequencing of 5,044 patients with solid tumor cancer.
K. McDonnell, C. Hong, J. Bonner, S. Lindsey +6 more
2022Journal of Clinical Oncology1 citations Open access
Semantic Scholar
Evaluation of Lynch syndrome risk models in a multicenter diverse population.
Jenny Lu, Stephen Knapp, Gubidxa Gutierrez Seymour, Cathy Wang +9 more
2022Journal of Clinical Oncology1 citations
Semantic Scholar
Extending models via gradient boosting: An application to Mendelian models
Theodore Huang, G. Idos, C. Hong, S. Gruber +2 more
2021Annals of Applied Statistics1 citations Open access
Semantic Scholar
Cancer risk and overall survival in APC I1307K carriers.
S. Gruber, J. Bonner, F. Lejbkowicz, S. Schmit +12 more
20201 citations
Semantic Scholar
A likelihood‐based approach to assessing frequency of pathogenicity among variants of unknown significance in susceptibility genes
Yun-Qi Yang, C. Hong, Jane W. Liang, S. Gruber +3 more
2020Statistics in Medicine1 citations
Semantic Scholar
Preventive surgery after multiplex genetic panel testing (MGPT).
G. Idos, A. Kurian, C. Ricker, D. Sturgeon +16 more
2019Journal of Clinical Oncology1 citations
Semantic Scholar
777 Optimizing the Threshold for Genetic Testing for Colorectal Cancer Syndromes
L. Naghi, Kellie Spector, J. Haisman, A. Kurian +19 more
20161 citations
Semantic Scholar
Genetic variation and regulation of MICA alters natural killer cell-mediated immunosurveillance in early-onset colorectal cancer.
H. M. McGee, J. Bonner, C. Egelston, Yu-Bo Fu +15 more
2026Journal of Clinical Oncology0 citations
Semantic Scholar
Provider perceptions and insights on polygenic risk scores for colorectal cancer: A qualitative study
Shenazar Esmundo, N. Cáceres, Charité Ricker, G. Idos +7 more
2025Journal of Genetic Counseling0 citations
Semantic Scholar
Sex differences in the colorectal tumor immune microenvironment.
Elizabeth Seitz, Ya-Yu Tsai, Marilena Melas, S. Lindsey +9 more
2025Journal of Clinical Oncology0 citations Open access
Semantic Scholar
Variant‐Specific Mendelian Risk Prediction Model
Julie A. Dias, Eunchan Bae, Theodore Huang, Jinbo Chen +5 more
2025Statistics in Medicine0 citations
Semantic Scholar
Editorial: Hereditary colorectal cancer syndromes and risk assessment in the era of precision medicine
K. McDonnell, G. Rennert, G. Idos
2024Frontiers in Oncology0 citations Open access
Semantic Scholar
Genetic Variation and Regulation of MICA Alters Natural Killer Cell-Mediated Immunosurveillance in Early-Onset Colorectal Cancer
H. M. McGee, J. Bonner, C. Egelston, Y. Fu +44 more
2024medRxiv0 citations Open access
Semantic Scholar
Sa1168 PREVALENCE AND PENETRANCE OF SPINK1 PATHOGENIC VARIANTS: A BURDEN TO PATIENTS AND PROVIDERS
Kathryn Reyes, J. Alcántara, A. Chitre, Christina Fujii +11 more
2024Gastroenterology0 citations
Semantic Scholar
Universal germline testing for cancer susceptibility and actionable noncancer disorders among 19,842 patients: Initial findings from the City of Hope INSPIRE study.
S. Gray, Ilana Solomon, Heather Hampel, Michael García +16 more
2024Journal of Clinical Oncology0 citations Open access
Semantic Scholar
Healthcare utilization among individuals diagnosed with lynch syndrome through a universal germline genetic testing program.
H. Hampel, Ilana Solomon, Michael García, Marilan Luong +15 more
2023Journal of Clinical Oncology0 citations
Semantic Scholar
Differences in tumor-associated T cell receptor repertoires between young-onset and average-onset colorectal cancer.
S. Schmit, Ya-Yu Tsai, K. Nair, S. Barot +15 more
2023Journal of Clinical Oncology0 citations Open access
Semantic Scholar
Abstract P6-02-07: Uptake of Breast Cancer MRI Screening in Patients After Multiplex Gene Panel Testing
L. Naghi, C. Ricker, D. Sturgeon, Julie O. Culver +14 more
2023Cancer Research0 citations Open access
Semantic Scholar
Healthcare utilization among individuals diagnosed with hereditary breast-ovarian cancer syndrome through a universal germline genetic testing program.
S. Gray, H. Hampel, Ilana Solomon, Michael García +15 more
2023Journal of Clinical Oncology0 citations
Semantic Scholar

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