Wendy Sue Rubinstein, MD

Unless otherwise indicated, this information has been self-reported and has not been verified by the Board of Medicine.

University Of Pittsburgh School Of Medicine - Pittsburgh PA
Rank: Assistant Professor
Years: 1996-2001

Northwestern University, Feinberg School of Medicine - Chicago IL
Rank: Assistant Professor
Years: 2002-2008

Northwestern University, Feinberg School of Medicine - Chicago IL
Rank: Associate Professor
Years: 2008-2009

University of Chicago Pritzker School of Medicine - Chicago IL
Rank: Associate Professor
Years: 2009-2011

None Reported

The NIH Genetic Testing Registry: A new, centralized database of genetic tests to enable access to comprehensive information and improve transparency
Nucleic Acids Research
41:D925-D935
Date: 01 2013
www.ncbi.nlm.nih.gov/pmc/articles/PMC3531155/

ClinVar: public archive of relationships among sequence variation and human phenotype
Nucleic Acids Research
42:980–D985.
Date: 01 2014
www.ncbi.nlm.nih.gov/pmc/articles/PMC3965032/

American Society of Clinical Oncology Expert Statement: Collection and Use of a Cancer Family History for Oncology Providers
Journal of Clinical Oncology
2(8):833-840
Date: 03 2014
www.ncbi.nlm.nih.gov/pmc/articles/PMC3940540/

ClinVar: public archive of interpretations of clinically relevant variants
Nucleic Acids Research
44:D862–D868
Date: 01 2016
www.ncbi.nlm.nih.gov/pmc/articles/PMC4702865/

Database resources of the National Center for Biotechnology Information
Nucleic Acids Research
44(D1):D7-D19
Date: 01 2016
www.ncbi.nlm.nih.gov/pmc/articles/PMC4702911/

Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations for Test Result Reporting
Clinical Pharmacology & Therapeutics
99(2):172-185
Date: 02 2016
www.ncbi.nlm.nih.gov/pmc/articles/PMC4724253/

A clinical service to support the return of secondary genomic findings in human research
The American Journal of Human Genetics
98:435-441
Date: 03 2016
www.sciencedirect.com/science/article/pii/S0002929716000161

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
Human Molecular Genetics
25:2256-2268
Date: 03 2016
academic.oup.com/hmg/article/25/11/2256/2446205

Point mutations in exon 1B of APC reveal gastric adenocarcinoma and proximal polyposis of the stomach as a familial adenomatous polyposis variant.
American Journal of Human Genetics
98(5):830-842
Date: 05 2016
www.ncbi.nlm.nih.gov/pmc/articles/PMC4863475/

Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research
Cell
169(1):6-12
Date: 03 2017
www.ncbi.nlm.nih.gov/pmc/articles/PMC5511379/