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W. Rubinstein · SciRah

Researcher profile · Semantic Scholar

W. Rubinstein

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W. Rubinstein — researcher profile on SciRah

h-index: 48
Works: 179
Citations: 17K

Most-cited papers

ClinVar: public archive of relationships among sequence variation and human phenotype
M. Landrum, Jennifer M. Lee, George R. Riley, W. Jang +3 more
2013Nucleic Acids Res.3,379 citations Open access
Semantic Scholar
ClinVar: public archive of interpretations of clinically relevant variants
M. Landrum, Jennifer M. Lee, M. Benson, Garth R. Brown +15 more
2015Nucleic Acids Res.2,678 citations Open access
Semantic Scholar
Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
N. Mavaddat, D. Barrowdale, I. Andrulis, S. Domchek +129 more
2011Cancer Epidemiology, Biomarkers and Prevention599 citations Open access
Semantic Scholar
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.
Jun Li, S. Woods, S. Healey, J. Beesley +71 more
2016American Journal of Human Genetics251 citations Open access
Semantic Scholar
Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.
J. Johnston, W. Rubinstein, Flavia M. Facio, David Ng +4 more
2012American Journal of Human Genetics203 citations Open access
Semantic Scholar
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
Karen H. Lu, M. Wood, M. Daniels, C. Burke +13 more
2014Journal of Clinical Oncology202 citations Open access
Semantic Scholar
BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2
Melissa S. Cline, R. Liao, M. Parsons, B. Paten +42 more
2018PLoS Genetics191 citations Open access
Semantic Scholar
The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency
W. Rubinstein, D. Maglott, Jennifer M. Lee, B. Kattman +18 more
2012Nucleic Acids Res.185 citations Open access
Semantic Scholar
Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations for Test Result Reporting
L. Kalman, José A. G. Agúndez, M. L. Appell, J. Black +42 more
2015Clinical pharmacology and therapy158 citations Open access
Semantic Scholar
Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research
T. Manolio, D. Fowler, Lea M. Starita, M. Haendel +27 more
2017Cell105 citations Open access
Semantic Scholar
Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms.
M. de la Hoya, O. Soukarieh, Irene López-Perolio, A. Vega +71 more
2016Human Molecular Genetics94 citations Open access
Semantic Scholar
Family Physicians’ Awareness and Knowledge of the Genetic Information Non-Discrimination Act (GINA)
Amanda L. Laedtke, Suzanne M. O'Neill, W. Rubinstein, Kristen J. Vogel
2012Journal of Genetic Counseling74 citations
Semantic Scholar
Alcohol and Tobacco Lower the Age of Presentation in Sporadic Pancreatic Cancer in a Dose-Dependent Manner: A Multicenter Study
M. Anderson, E. Zolotarevsky, K. Cooper, Simon Sherman +15 more
2012American Journal of Gastroenterology66 citations Open access
Semantic Scholar
Modification of BRCA1-Associated Breast and Ovarian Cancer Risk by BRCA1 Interacting Genes
T. Rebbeck, N. Mitra, S. Domchek, F. Wan +34 more
2011Cancer Research65 citations Open access
Semantic Scholar
Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
F. Couch, M. Gaudet, A. Antoniou, S. Ramus +186 more
2012Cancer Epidemiology, Biomarkers and Prevention63 citations Open access
Semantic Scholar
Family History Assessment
Catharine Wang, Ananda Sen, M. Ruffin, D. Nease +4 more
2012American Journal of Preventive Medicine47 citations Open access
Semantic Scholar
Development of CancerLinQ, a Health Information Learning Platform From Multiple Electronic Health Record Systems to Support Improved Quality of Care.
D. Potter, Raven Brothers, Andrej Kolacevski, J. Koskimaki +8 more
2020JCO Clinical Cancer Informatics44 citations Open access
Semantic Scholar
Medical Genetics Summaries
V. Pratt, H. McLeod, W. Rubinstein, L. Dean +2 more
201243 citations
Semantic Scholar
Challenges to Using Big Data in Cancer
S. Sweeney, Hisham Hamadeh, Natalie Abrams, S. Adam +26 more
2023Cancer Research42 citations Open access
Semantic Scholar
Next-Generation Sequencing and the Clinical Oncology Workflow: Data Challenges, Proposed Solutions, and a Call to Action.
J. R. Conway, J. Warner, W. Rubinstein, Robert S. Miller
2019JCO Precision Oncology42 citations Open access
Semantic Scholar
Breast and ovarian cancer risk and risk reduction in Jewish BRCA1/2 mutation carriers.
B. Finkelman, W. Rubinstein, S. Friedman, T. Friebel +27 more
2012Journal of Clinical Oncology39 citations Open access
Semantic Scholar
Health beliefs among individuals at increased familial risk for type 2 diabetes: Implications for prevention,
J. Dorman, R. Valdez, Tie-Bin Liu, Catharine Wang +5 more
2012Diabetes Research and Clinical Practice36 citations Open access
Semantic Scholar
A Clinical Service to Support the Return of Secondary Genomic Findings in Human Research.
Andrew J. Darnell, H. Austin, D. Bluemke, R. Cannon +11 more
2016American Journal of Human Genetics35 citations Open access
Semantic Scholar
Impact of Broadening Trial Eligibility Criteria for Patients with Advanced Non–Small Cell Lung Cancer: Real-World Analysis of Select ASCO-Friends Recommendations
R. Harvey, S. Bruinooge, L. Chen, E. Garrett-Mayer +11 more
2021Clinical Cancer Research32 citations
Semantic Scholar
A non-synonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers
Yuan C. Ding, L. McGuffog, S. Healey, E. Friedman +157 more
2012Cancer Epidemiology, Biomarkers and Prevention25 citations Open access
Semantic Scholar
Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard
Bret S. E. Heale, C. Overby, G. Del Fiol, W. Rubinstein +7 more
2016Applied Clinical Informatics23 citations Open access
Semantic Scholar
Impact of Family History Assessment on Communication with Family Members and Health Care Providers: A report from the Family Healthware™ Impact Trial (FHITr)
Catharine Wang, Ananda Sen, M. Plegue, M. Ruffin +22 more
2015Preventive Medicine21 citations Open access
Semantic Scholar
Case Studies for Overcoming Challenges in Using Big Data in Cancer
S. Sweeney, Hisham Hamadeh, Natalie Abrams, S. Adam +26 more
2023Cancer Research20 citations Open access
Semantic Scholar
Components of family history associated with women's disease perceptions for cancer: A report from the Family Healthware™ Impact Trial
W. Rubinstein, Suzanne M. O'Neill, N. Rothrock, E. Starzyk +6 more
2011Genetics in Medicine20 citations Open access
Semantic Scholar
Real-world outcomes of patients with advanced non-small cell lung cancer (aNSCLC) and autoimmune disease (AD) receiving immune checkpoint inhibitors (ICIs).
S. Khozin, M. Walker, M. Jun, L. Chen +9 more
2019Journal of Clinical Oncology18 citations
Semantic Scholar
Genetic Variation in IGF2 and HTRA1 and Breast Cancer Risk among BRCA1 and BRCA2 Carriers
S. Neuhausen, S. Brummel, Yuan C. Ding, L. Steele +20 more
2011Cancer Epidemiology, Biomarkers and Prevention18 citations Open access
Semantic Scholar
Encoding laboratory testing data: case studies of the national implementation of HHS requirements and related standards in five laboratories
Raja A. Cholan, G. Pappas, Greg Rehwoldt, A. Sills +9 more
2022J. Am. Medical Informatics Assoc.13 citations Open access
Semantic Scholar
Impact of broadening clinical trial eligibility criteria for advanced non-small cell lung cancer patients: Real-world analysis.
R. Harvey, W. Rubinstein, G. Ison, S. Khozin +13 more
2019Journal of Clinical Oncology12 citations
Semantic Scholar
Clozapine Therapy and CYP2D6, CYP1A2, and CYP3A4 Genotypes
V. Pratt, H. McLeod, W. Rubinstein, S. Scott +3 more
201610 citations
Semantic Scholar
Real-world prevalence of autoimmune disease (AD) among patients (pts) receiving immune checkpoint inhibitors (ICI) in ASCO’s CancerLinQ database.
L. Chen, M. Walker, Jizu Zhi, G. Komatsoulis +9 more
2019Journal of Clinical Oncology9 citations
Semantic Scholar
Quantitating and assessing interoperability between electronic health records
E. Bernstam, J. Warner, J. Krauss, E. Ambinder +4 more
2022J. Am. Medical Informatics Assoc.8 citations Open access
Semantic Scholar
Pharmacogenetic Gene-Drug Associations: FDA Perspective on What Physicians Need to Know.
W. Rubinstein, M. Pacanowski
2021American Family Physician8 citations
Semantic Scholar
CancerLinQ: Cutting the Gordian Knot of Interoperability.
W. Rubinstein
2019Journal of Oncology Practice6 citations Open access
Semantic Scholar
Irinotecan Therapy and UGT1A1 Genotype -- Medical Genetics Summaries
Pratt, H. McLeod, W. Rubinstein, L. Dean +2 more
20126 citations
Semantic Scholar
Azathioprine Therapy and TPMT Genotype -- Medical Genetics Summaries
Pratt, H. McLeod, W. Rubinstein, L. Dean +2 more
20125 citations
Semantic Scholar
P1.01-105 US Real-World Management of EGFR-Mutated Advanced NSCLC: Prescribing and Attrition Data from First-To-Second-Line Treatment
K. Reckamp, J. Nieva, A. Taylor, B. Thakrar +5 more
2019Journal of Thoracic Oncology4 citations Open access
Semantic Scholar
Warfarin Therapy and VKORC1 and CYP Genotype -- Medical Genetics Summaries
V. Pratt, McLeod Hl, W. Rubinstein, Scott Sa +3 more
20124 citations
Semantic Scholar
Metoprolol Therapy and CYP2D6 Genotype -- Medical Genetics Summaries
Pratt, H. McLeod, W. Rubinstein, L. Dean +2 more
20124 citations
Semantic Scholar
NCI and ASCO CancerLinQ collaboration to advance quality of cancer care and surveillance.
D. Rivera, W. Rubinstein, Nicola C Schussler, M. Charlton +9 more
2019Journal of Clinical Oncology3 citations
Semantic Scholar
Family History and Health Risk Assessment
W. Rubinstein
20133 citations
Semantic Scholar
Atomoxetine Therapy and CYP2D6 Genotype -- Medical Genetics Summaries
Pratt, H. McLeod, W. Rubinstein, L. Dean +2 more
20123 citations
Semantic Scholar
Methylenetetrahydrofolate Reductase Deficiency -- Medical Genetics Summaries
V. Pratt, McLeod Hl, W. Rubinstein, Scott Sa +3 more
20123 citations
Semantic Scholar
Capecitabine Therapy and DPYD Genotype -- Medical Genetics Summaries
V. Pratt, H. McLeod, W. Rubinstein, S. Scott +3 more
20123 citations
Semantic Scholar
Real-world characteristics and outcomes of patients with advanced non-small cell lung cancer (aNSCLC) receiving immune checkpoint inhibitor.
S. Khozin, Jizu Zhi, M. Jun, L. Chen +9 more
2019Journal of Clinical Oncology2 citations
Semantic Scholar
Quantifying interoperability: An analysis of oncology practice electronic health record data variability.
E. Bernstam, J. Warner, J. Krauss, E. Ambinder +4 more
2019Journal of Clinical Oncology2 citations
Semantic Scholar

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