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Author Details

Robin L Bennett
University of Washington
1992
76
29
PMIDPaper TitleJournal TitlePublished Year
36524987Words matter: The language of difference in human genetics.Genet Med2023
36519192Both sides now: Changing a long-standing pedigree tradition of men on the left and women on the right.J Genet Couns2023
36106433Practice resource-focused revision: Standardized pedigree nomenclature update centered on sex and gender inclusivity: A practice resource of the National Society of Genetic Counselors.J Genet Couns2022
35628017Socioeconomic Status and Interest in Genetic Testing in a US-Based Sample.Healthcare (Basel)2022
34309119Genetic counseling and screening of consanguineous couples and their offspring practice resource: Focused Revision.J Genet Couns2021
33649579Taking an antiracist posture in scientific publications in human genetics and genomics.Genet Med2021
34216551Targeted long-read sequencing identifies missing disease-causing variation.Am J Hum Genet2021
32232917Assessing transgender and gender non-conforming pedigree nomenclature in current genetic counselors' practice: The case for geometric inclusivity.J Genet Couns2020
31883735Simultaneous germline and somatic sequencing in ovarian carcinoma: mutation rate and impact on clinical decision-making.Gynecol Oncol2020
30327540Trends over 42 years in the Adult Medical Genetics Clinic at the University of Washington.Genet Med2019
31582006Family Health History: The First Genetic Test in Precision Medicine.Med Clin North Am2019
31317629Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests.J Genet Couns2019
31400517Clinical exome sequencing vs. usual care for hereditary colorectal cancer diagnosis: A pilot comparative effectiveness study.Contemp Clin Trials2019
29075947National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions.J Genet Couns2018
30267214Rare loss of function variants in candidate genes and risk of colorectal cancer.Hum Genet2018
29052810Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.J Genet Couns2018
28617418Medical genetics and genomics education: how do we define success? Where do we focus our resources?Genet Med2017
26845104Improving performance of multigene panels for genomic analysis of cancer predisposition.Genet Med2016
26589312Novel Report of Phosphoserine Phosphatase Deficiency in an Adult with Myeloneuropathy and Limb Contractures.JIMD Rep2016
26480326Initiation of universal tumor screening for Lynch syndrome in colorectal cancer patients as a model for the implementation of genetic information into clinical oncology practice.Cancer2016
26637299Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome.J Genet Couns2016
27819239Biochemical and imaging surveillance in Li-Fraumeni syndrome.Lancet Oncol2016
27422780Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational Tool.J Genet Couns2016
26888760Erratum to: Novel Report of Phosphoserine Phosphatase Deficiency in an Adult with Myeloneuropathy and Limb Contractures.JIMD Rep2016
26739839Developing a Model of Advanced Training to Promote Career Advancement for Certified Genetic Counselors: An Investigation of Expanded Skills, Advanced Training Paths, and Professional Opportunities.J Genet Couns2016
25394175A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.Genet Med2015
25637381Actionable exomic incidental findings in 6503 participants: challenges of variant classification.Genome Res2015
24997220Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes.Contemp Clin Trials2014
23619277A mosaic PTEN mutation causing Cowden syndrome identified by deep sequencing.Genet Med2013
24055113Actionable, pathogenic incidental findings in 1,000 participants' exomes.Am J Hum Genet2013
23860966Fabry disease practice guidelines: recommendations of the National Society of Genetic Counselors.J Genet Couns2013
23907645Recommendations for returning genomic incidental findings? We need to talk!Genet Med2013
22134580Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors.J Genet Couns2012
22734033Germline mutation in MSH6 associated with multiple malignant neoplasms in a patient With Muir-Torre syndrome.J Clin Oncol2012
22797890Genetic counseling and testing for FMR1 gene mutations: practice guidelines of the national society of genetic counselors.J Genet Couns2012
22810887The family medical history as a tool in preconception consultation.J Community Genet2012
22446623A self-administered family history questionnaire improves identification of women who warrant referral to genetic counseling for hereditary cancer risk.Gynecol Oncol2012
22658618ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.J Mol Diagn2012
21555946Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report.Genet Med2011
21811163Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: variant reclassification and surgical decisions.Genet Med2011
20160979Will knowledge of gene-based colorectal cancer disease risk influence quality of life and screening behavior? Findings from a population-based study.Public Health Genomics2010
19466581Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individuals.Fam Cancer2009
19788769Adjusting to pancreatic cancer: perspectives from first-degree relatives.Palliat Support Care2009
18792771Standardized human pedigree nomenclature: update and assessment of the recommendations of the National Society of Genetic Counselors.J Genet Couns2008
17575505Indications for genetic referral: a guide for healthcare providers.Genet Med2007
16761103A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.J Genet Couns2006
15959648Genetic evaluation and counseling of couples with recurrent miscarriage: recommendations of the National Society of Genetic Counselors.J Genet Couns2005
16047089Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors.J Genet Couns2005
15331243The family medical history.Prim Care2004
15604628Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors.J Genet Couns2004
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Collaborators

Gail P Jarvik
University of Washington Medical Center
Co-authored papers 11
Wylie Burke
The Heart Institute, Cincinnati Children's Hospital Medical Center
Co-authored papers 10
Fuki M Hisama
University of Washington
Co-authored papers 10
Brian H Shirts
Institute for Public Health Genetics, University of Washington
Co-authored papers 9
Colin C Pritchard
University of Washington, USA Brotman Baty Institute for Precision Medicine
Co-authored papers 8
Laura M Amendola
Illumina Inc.
Co-authored papers 8
Deborah A Nickerson
University of Washington
Co-authored papers 6
Tom Walsh
University of Washington
Co-authored papers 6
Michael O Dorschner
University of Washington
Co-authored papers 6
Elisabeth A Rosenthal
University of Washington Medical Center
Co-authored papers 5
William M Grady
. Fred Hutchinson Cancer Center
Co-authored papers 5
Carlos J Gallego
University of Washington
Co-authored papers 5
Wendy H Raskind
University of Washington School of Medicine
Co-authored papers 5
Arno G Motulsky
University of Washington
Co-authored papers 5
Thomas D Bird
University of Washington School of Medicine
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Martha Horike-Pyne
University of Washington School of Medicine
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Kathleen A Leppig
Kaiser Permanente Washington
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Emily H Turner
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Allyn McConkie-Rosell
Duke University School of Medicine and Duke Health System
Co-authored papers 3
Stephanie M Fullerton
University of Washington School of Medicine
Co-authored papers 3
Michael J Bamshad
University of Washington
Co-authored papers 3
David L Veenstra
University of Washington
Co-authored papers 3
Mary-Claire King
University of Washington
Co-authored papers 3
Susan Brown Trinidad
University of Washington
Co-authored papers 2
Kyle B Brothers
Norton Children's Research Institute Affiliated with the University of Louisville
Co-authored papers 2
Benjamin S Wilfond
University of Washington School of Medicine.
Co-authored papers 2
Holly K Tabor
Stanford Center for Biomedical Ethics (SCBE), Stanford University
Co-authored papers 2
Mildred K Cho
Center for Biomedical Ethics, Stanford University School of Medicine
Co-authored papers 2
Ming K Lee
University of Washington
Co-authored papers 2
Patrick J Heagerty
University of Washington
Co-authored papers 2
Release 1.2