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Jill S. Dolinsky · SciRah

Researcher profile · Semantic Scholar

Jill S. Dolinsky

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Jill S. Dolinsky — researcher profile on SciRah

h-index: 26
Works: 97
Citations: 3,978

Most-cited papers

Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer
F. Couch, H. Shimelis, Chun-Ling Hu, S. Hart +14 more
2017JAMA Oncology580 citations Open access
Semantic Scholar
Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families.
Xin Yang, Goska Leslie, Alicja Doroszuk, S. Schneider +115 more
2019Journal of Clinical Oncology371 citations Open access
Semantic Scholar
Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients
H. LaDuca, A. Stuenkel, Jill S. Dolinsky, S. Keiles +10 more
2014Genetics in Medicine357 citations Open access
Semantic Scholar
Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing
H. Shimelis, H. LaDuca, Chun-Ling Hu, S. Hart +25 more
2018Journal of the National Cancer Institute291 citations Open access
Semantic Scholar
Clinical Laboratories Collaborate to Resolve Differences in Variant Interpretations Submitted to ClinVar
S. Harrison, Jill S. Dolinsky, A. K. Knight Johnson, T. Pesaran +6 more
2017Genetics in Medicine233 citations Open access
Semantic Scholar
A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients
H. LaDuca, E. Polley, Amal Yussuf, Lily Hoang +17 more
2019Genetics in Medicine197 citations Open access
Semantic Scholar
Association of Breast and Ovarian Cancers With Predisposition Genes Identified by Large-Scale Sequencing
Hsiao-Mei Lu, Shuwei Li, M. Black, Shela Lee +13 more
2019JAMA Oncology171 citations Open access
Semantic Scholar
Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D
Xin Yang, Hong-Lin Song, Goska Leslie, C. Engel +57 more
2020Journal of the National Cancer Institute165 citations Open access
Semantic Scholar
Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results
Mary Pritzlaff, P. Summerour, R. McFarland, Shuwei Li +7 more
2016Breast Cancer Research and Treatment145 citations Open access
Semantic Scholar
Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls
J. Lilyquist, H. LaDuca, E. Polley, Brigette Tippin Davis +6 more
2017Gynecologic Oncology134 citations Open access
Semantic Scholar
Somatic TP53 variants frequently confound germline testing results
J. Weitzel, Elizabeth C. Chao, Bita Nehoray, Lily R. Van Tongeren +14 more
2017Genetics in Medicine112 citations Open access
Semantic Scholar
Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2.
L. Minion, Jill S. Dolinsky, D. Chase, Charles L. M. Dunlop +2 more
2014Gynecologic Oncology111 citations Open access
Semantic Scholar
The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort
Chun-Ling Hu, E. Polley, S. Yadav, J. Lilyquist +9 more
2020Journal of the National Cancer Institute103 citations Open access
Semantic Scholar
Guidelines an
S. Hart, E. Polley, Amal Yussuf, S. Yadav +9 more
201991 citations
Semantic Scholar
Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing
H. Rana, R. Gelman, H. LaDuca, R. McFarland +6 more
2018Journal of the National Cancer Institute84 citations Open access
Semantic Scholar
Prospective study of germline genetic testing in incident cases of pancreatic adenocarcinoma
R. Brand, E. Borazanci, V. Speare, Beth Dudley +23 more
2018Cancer83 citations Open access
Semantic Scholar
Assessment of Diagnostic Outcomes of RNA Genetic Testing for Hereditary Cancer
R. Karam, B. Conner, H. LaDuca, K. McGoldrick +21 more
2019JAMA Network Open69 citations Open access
Semantic Scholar
Multigene Hereditary Cancer Panels Reveal High-Risk Pancreatic Cancer Susceptibility Genes
Chun-Ling Hu, H. LaDuca, H. Shimelis, E. Polley +11 more
2018JCO Precision Oncology55 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
Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast
S. Yadav, Chun-Ling Hu, K. Nathanson, J. Weitzel +38 more
2021Journal of Clinical Oncology47 citations Open access
Semantic Scholar
Breast cancer risk is similar for CHEK2 founder and non-founder mutation carriers.
T. Leedom, H. LaDuca, R. McFarland, Shuwei Li +2 more
2016Cancer Genetics46 citations Open access
Semantic Scholar
Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort
Hong-Yan Li, H. LaDuca, T. Pesaran, Elizabeth C. Chao +9 more
2019Genetics in Medicine45 citations Open access
Semantic Scholar
Diagnosing hereditary cancer predisposition in men with prostate cancer
Mary Pritzlaff, Yuan Tian, P. Reineke, A. Stuenkel +8 more
2020Genetics in Medicine43 citations Open access
Semantic Scholar
Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer
S. Yadav, H. LaDuca, E. Polley, Chun-Ling Hu +14 more
2020Journal of the National Cancer Institute36 citations Open access
Semantic Scholar
Mutation prevalence tables for hereditary cancer derived from multi-gene panel testing
S. Hart, E. Polley, Amal Yussuf, S. Yadav +8 more
2019Human Mutation32 citations Open access
Semantic Scholar
Risk of Late-Onset Breast Cancer in Genetically Predisposed Women
N. Boddicker, Chun-Ling Hu, J. Weitzel, P. Kraft +47 more
2021Journal of Clinical Oncology30 citations Open access
Semantic Scholar
Genotype–phenotype associations among panel-based TP53+ subjects
H. Rana, J. Clifford, Lily Hoang, H. LaDuca +7 more
2019Genetics in Medicine25 citations Open access
Semantic Scholar
A rare TP53 mutation predominant in Ashkenazi Jews confers risk of multiple cancers
J. Powers, E. Pinto, T. Barnoud, Jessica C. Leung +32 more
2020Cancer Research22 citations Open access
Semantic Scholar
Suggested application of HER2+ breast tumor phenotype for germline TP53 variant classification within ACMG/AMP guidelines
Cristina Fortuno, J. Mester, T. Pesaran, J. Weitzel +14 more
2020Human Mutation22 citations Open access
Semantic Scholar
Quality of Clinician-Reported Cancer History When Ordering Genetic Testing.
H. LaDuca, R. McFarland, S. Gutierrez, Amal Yussuf +7 more
2018JCO Clinical Cancer Informatics22 citations
Semantic Scholar
p53 major hotspot variants are associated with poorer prognostic features in hereditary cancer patients.
Cristina Fortuno, T. Pesaran, Jill S. Dolinsky, Amal Yussuf +4 more
2019Cancer Genetics17 citations
Semantic Scholar
Prevalence of germline variants in inflammatory breast cancer
H. Rana, R. Sacca, C. Drogan, S. Gutierrez +7 more
2019Cancer17 citations Open access
Semantic Scholar
Family communication and patient distress after germline genetic testing in individuals with pancreatic ductal adenocarcinoma
M. L. Peters, Lindsey Stobie, Beth Dudley, E. Karloski +11 more
2019Cancer17 citations Open access
Semantic Scholar
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations
A. Safonov, Tomoki T. Nomakuchi, Elizabeth C. Chao, Carrie Horton +23 more
2025Nature Communications14 citations Open access
Semantic Scholar
Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C
Chun-Ling Hu, Anil Belur Nagaraj, H. Shimelis, G. Montalban +40 more
2023Cancer Research14 citations Open access
Semantic Scholar
An updated quantitative model to classify missense variants in the TP53 gene: A novel multifactorial strategy
Cristina Fortuno, T. Pesaran, Jill S. Dolinsky, Amal Yussuf +5 more
2021Human Mutation14 citations Open access
Semantic Scholar
Genotype-phenotype correlations among TP53 carriers: Literature review and analysis of probands undergoing multi-gene panel testing and single-gene testing.
Cristina Fortuno, T. Pesaran, J. Mester, Jill S. Dolinsky +4 more
2020Cancer Genetics14 citations
Semantic Scholar
Pretest Video Education Versus Genetic Counseling for Patients With Prostate Cancer: ProGen, A Multisite Randomized Controlled Trial
H. Rana, Jill E. Stopfer, M. Weitz, L. Kipnis +30 more
2023JCO Oncology Practice13 citations Open access
Semantic Scholar
Pathogenic Variants in Cancer Susceptibility Genes Predispose to Ductal Carcinoma In Situ of the Breast
Huai-Zhi Huang, Ronan E. Couch, R. Karam, Chun-Ling Hu +38 more
2024Clinical Cancer Research11 citations Open access
Semantic Scholar
Polygenic risk score for breast cancer in high-risk women.
M. Black, Shuwei Li, H. LaDuca, Jefferey Chen +8 more
20189 citations
Semantic Scholar
Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing
H. Shimelis, H. LaDuca, Chun-Ling Hu, S. Hart +28 more
20188 citations
Semantic Scholar
Suspected clonal hematopoiesis as a natural functional assay of TP53 germline variant pathogenicity.
Cristina Fortuno, K. McGoldrick, T. Pesaran, Jill S. Dolinsky +6 more
2021Genetics in Medicine7 citations Open access
Semantic Scholar
DIAGNOSTIC EXOME SEQUENCING IN PEDIATRIC PATIENTS WITH CONGENITAL HEART DISEASE
Z. Powis, D. Thrush, Brigette Tippin Davis, Jill S. Dolinsky
20167 citations Open access
Semantic Scholar
Case–case analysis addressing ascertainment bias for multigene panel testing implicates BRCA1 and PALB2 in endometrial cancer
S. Johnatty, T. Pesaran, Jill S. Dolinsky, Amal Yussuf +4 more
2021Human Mutation6 citations Open access
Semantic Scholar
Challenges and approaches to calibrating patient phenotype as evidence for cancer gene variant classification under ACMG/AMP guidelines.
Cristina Fortuno, K. Michailidou, M. Parsons, Jill S. Dolinsky +12 more
2024Human Molecular Genetics5 citations Open access
Semantic Scholar
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations
A. Safonov, Tomoki T. Nomakuchi, Elizabeth C. Chao, Carrie Horton +12 more
2023medRxiv5 citations Open access
Semantic Scholar
Association of Family Cancer History With Pathogenic Variants in Specific Breast Cancer Susceptibility Genes.
A. Kurian, P. Abrahamse, K. Ward, A. Hamilton +9 more
2021JCO Precision Oncology5 citations Open access
Semantic Scholar
A randomized controlled trial of video-education or in-person genetic counseling for men with prostate cancer (ProGen).
H. Rana, J. Stopfer, N. Petrucelli, Diane R. Koeller +16 more
2020Journal of Clinical Oncology5 citations
Semantic Scholar
Human Mutation
Cristina Fortuno, T. Pesaran, Jill S. Dolinsky, Amal Yussuf +4 more
20204 citations
Semantic Scholar
Racial and ethnic differences in the results of multigene panel testing of inherited cancer predisposition genes in breast cancer patients.
S. Yadav, H. LaDuca, E. Polley, H. Shimelis +14 more
2019Journal of Clinical Oncology3 citations
Semantic Scholar

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H. LaDuca×30
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H. LaDuca — researcher profile on SciRah
T. Pesaran×24
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T. Pesaran — researcher profile on SciRah
F. Couch×21
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F. Couch — researcher profile on SciRah
Amal Yussuf×21
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Amal Yussuf — researcher profile on SciRah

×20

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D. Goldgar — researcher profile on SciRah

Elizabeth C. Chao×19

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Elizabeth C. Chao — researcher profile on SciRah

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E. Polley — researcher profile on SciRah

Chun-Ling Hu×15

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Chun-Ling Hu — researcher profile on SciRah

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S. Hart — researcher profile on SciRah

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Jie Na — researcher profile on SciRah

H. Shimelis×11

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H. Shimelis — researcher profile on SciRah

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V. Speare — researcher profile on SciRah