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Author Details

Wendy S Rubinstein
CancerLinQ LLC, American Society of Clinical Oncology
1987
95
43
PMIDPaper TitleJournal TitlePublished Year
35015861Quantitating and assessing interoperability between electronic health records.J Am Med Inform Assoc2022
35639494Encoding laboratory testing data: case studies of the national implementation of HHS requirements and related standards in five laboratories.J Am Med Inform Assoc2022
35015861Quantitating and assessing interoperability between electronic health records.J Am Med Inform Assoc2022
35639494Encoding laboratory testing data: case studies of the national implementation of HHS requirements and related standards in five laboratories.J Am Med Inform Assoc2022
34264612Pharmacogenetic Gene-Drug Associations: FDA Perspective on What Physicians Need to Know.Am Fam Physician2021
33910935The FDA Oncology Center of Excellence Scientific Collaborative: Charting a Course for Applied Regulatory Science Research in Oncology.Clin Cancer Res2021
34264612Pharmacogenetic Gene-Drug Associations: FDA Perspective on What Physicians Need to Know.Am Fam Physician2021
33563634Impact of Broadening Trial Eligibility Criteria for Patients with Advanced Non-Small Cell Lung Cancer: Real-World Analysis of Select ASCO-<i>Friends</i> Recommendations.Clin Cancer Res2021
33910935The FDA Oncology Center of Excellence Scientific Collaborative: Charting a Course for Applied Regulatory Science Research in Oncology.Clin Cancer Res2021
33563634Impact of Broadening Trial Eligibility Criteria for Patients with Advanced Non-Small Cell Lung Cancer: Real-World Analysis of Select ASCO-<i>Friends</i> Recommendations.Clin Cancer Res2021
33104389Development of CancerLinQ, a Health Information Learning Platform From Multiple Electronic Health Record Systems to Support Improved Quality of Care.JCO Clin Cancer Inform2020
33104389Development of CancerLinQ, a Health Information Learning Platform From Multiple Electronic Health Record Systems to Support Improved Quality of Care.JCO Clin Cancer Inform2020
30566370CancerLinQ: Cutting the Gordian Knot of Interoperability.J Oncol Pract2019
32923847Next-Generation Sequencing and the Clinical Oncology Workflow: Data Challenges, Proposed Solutions, and a Call to Action.JCO Precis Oncol2019
30566370CancerLinQ: Cutting the Gordian Knot of Interoperability.J Oncol Pract2019
32923847Next-Generation Sequencing and the Clinical Oncology Workflow: Data Challenges, Proposed Solutions, and a Call to Action.JCO Precis Oncol2019
30586411BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2.PLoS Genet2018
30586411BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2.PLoS Genet2018
28340351Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research.Cell2017
28340351Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research.Cell2017
27008870Combined genetic and splicing analysis of BRCA1 c.[594-2A&gt;C; 641A&gt;G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms.Hum Mol Genet2016
27008870Combined genetic and splicing analysis of BRCA1 c.[594-2A&gt;C; 641A&gt;G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms.Hum Mol Genet2016
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
26942283A Clinical Service to Support the Return of Secondary Genomic Findings in Human Research.Am J Hum Genet2016
26479518Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting.Clin Pharmacol Ther2016
26582918ClinVar: public archive of interpretations of clinically relevant variants.Nucleic Acids Res2016
27579472Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard.Appl Clin Inform2016
26479518Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting.Clin Pharmacol Ther2016
26582918ClinVar: public archive of interpretations of clinically relevant variants.Nucleic Acids Res2016
27579472Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard.Appl Clin Inform2016
26942283A Clinical Service to Support the Return of Secondary Genomic Findings in Human Research.Am J Hum Genet2016
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
24946156Evidence synthesis and guideline development in genomic medicine: current status and future prospects.Genet Med2015
25901453Impact of family history assessment on communication with family members and health care providers: A report from the Family Healthwareâ¿¢ Impact Trial (FHITr).Prev Med2015
24946156Evidence synthesis and guideline development in genomic medicine: current status and future prospects.Genet Med2015
25901453Impact of family history assessment on communication with family members and health care providers: A report from the Family Healthwareâ¿¢ Impact Trial (FHITr).Prev Med2015
24234437ClinVar: public archive of relationships among sequence variation and human phenotype.Nucleic Acids Res2014
24234437ClinVar: public archive of relationships among sequence variation and human phenotype.Nucleic Acids Res2014
24493721American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.J Clin Oncol2014
24493721American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.J Clin Oncol2014
23193275The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency.Nucleic Acids Res2013
23193275The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency.Nucleic Acids Res2013
21927977Family physicians' awareness and knowledge of the Genetic Information Non-Discrimination Act (GINA).J Genet Couns2012
22703879Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.Am J Hum Genet2012
22351618Common 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.Cancer Epidemiol Biomarkers Prev2012
22929760Alcohol and tobacco lower the age of presentation in sporadic pancreatic cancer in a dose-dependent manner: a multicenter study.Am J Gastroenterol2012
22430266Breast and ovarian cancer risk and risk reduction in Jewish BRCA1/2 mutation carriers.J Clin Oncol2012
22729394A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers.Cancer Epidemiol Biomarkers Prev2012
22992357Family history assessment: impact on disease risk perceptions.Am J Prev Med2012
22257420Health beliefs among individuals at increased familial risk for type 2 diabetes: implications for prevention.Diabetes Res Clin Pract2012
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Mia M Gaudet
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Mary Beth Terry
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Esther M John
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Louise Izatt
Guy's and St Thomas' NHS Foundation Trust
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Ana Osorio
Familial Cancer Clinical Unit, Spanish National Cancer Research Centre
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Noralane M Lindor
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Susan J Ramus
School of Clinical Medicine, University of NSW Sydney, Lowy Cancer Research Centre
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Jan Lubinski
Pomeranian Medical University
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Release 1.2