Publications by authors named "Wendy McKinnon"

29Publications

Risk for breast cancer and management of unaffected individuals with non-BRCA hereditary breast cancer.

Breast J 2020 08 2;26(8):1528-1534. Epub 2020 Aug 2.

DFCI, Harvard, Boston, Massachusetts, USA.

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August 2020

Cancer Risks Associated With Germline Pathogenic Variants: An International Study of 524 Families.

Authors:
Xin Yang Goska Leslie Alicja Doroszuk Sandra Schneider Jamie Allen Brennan Decker Alison M Dunning James Redman James Scarth Inga Plaskocinska Craig Luccarini Mitul Shah Karen Pooley Leila Dorling Andrew Lee Muriel A Adank Julian Adlard Kristiina Aittomäki Irene L Andrulis Peter Ang Julian Barwell Jonine L Bernstein Kristie Bobolis Åke Borg Carl Blomqvist Kathleen B M Claes Patrick Concannon Adeline Cuggia Julie O Culver Francesca Damiola Antoine de Pauw Orland Diez Jill S Dolinsky Susan M Domchek Christoph Engel D Gareth Evans Florentia Fostira Judy Garber Lisa Golmard Ellen L Goode Stephen B Gruber Eric Hahnen Christopher Hake Tuomas Heikkinen Judith E Hurley Ramunas Janavicius Zdenek Kleibl Petra Kleiblova Irene Konstantopoulou Anders Kvist Holly Laduca Ann S G Lee Fabienne Lesueur Eamonn R Maher Arto Mannermaa Siranoush Manoukian Rachel McFarland Wendy McKinnon Alfons Meindl Kelly Metcalfe Nur Aishah Mohd Taib Jukka Moilanen Katherine L Nathanson Susan Neuhausen Pei Sze Ng Tu Nguyen-Dumont Sarah M Nielsen Florian Obermair Kenneth Offit Olufunmilayo I Olopade Laura Ottini Judith Penkert Katri Pylkäs Paolo Radice Susan J Ramus Vilius Rudaitis Lucy Side Rachel Silva-Smith Valentina Silvestri Anne-Bine Skytte Thomas Slavin Jana Soukupova Carlo Tondini Alison H Trainer Gary Unzeitig Lydia Usha Thomas van Overeem Hansen James Whitworth Marie Wood Cheng Har Yip Sook-Yee Yoon Amal Yussuf George Zogopoulos David Goldgar John L Hopper Georgia Chenevix-Trench Paul Pharoah Sophia H L George Judith Balmaña Claude Houdayer Paul James Zaki El-Haffaf Hans Ehrencrona Marketa Janatova Paolo Peterlongo Heli Nevanlinna Rita Schmutzler Soo-Hwang Teo Mark Robson Tuya Pal Fergus Couch Jeffrey N Weitzel Aaron Elliott Melissa Southey Robert Winqvist Douglas F Easton William D Foulkes Antonis C Antoniou Marc Tischkowitz

J Clin Oncol 2020 03 16;38(7):674-685. Epub 2019 Dec 16.

Department of Medical Genetics, NIHR Cambridge Biomedical Research Centre, and Cancer Research UK Cambridge Centre, University of Cambridge, Cambridge, United Kingdom.

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March 2020

Colorectal Carcinomas With Isolated Loss of PMS2 Staining by Immunohistochemistry.

Arch Pathol Lab Med 2018 Apr 16;142(4):523-528. Epub 2018 Jan 16.

From the Departments of Pathology (Drs Alpert, Setia, Xiao, and Hart) and Medicine (Dr Kupfer), University of Chicago, Chicago, Illinois; the Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania (Dr Reetesh Pai); the Department of Pathology, Brigham and Womens Hospital, Boston, Massachusetts (Dr Srivastava); the Departments of Medicine (Ms McKinnon) and Pathology and Laboratory Medicine (Dr Wilcox), University of Vermont Medical Center, Burlington; the Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York (Dr Yantiss); the Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles (Drs Arcega and Wang); the Department of Pathology, Yale-New Haven Hospital, New Haven, Connecticut (Dr Robert); the Department of Pathology, Cleveland Clinic, Cleveland, Ohio (Drs Liu and Rish Pai); the Department of Pathology, University of Alabama, Birmingham (Dr Zhao); the Department of Pathology, University of Washington, Seattle (Dr Westerhoff); and the Departments of Internal Medicine (Ms Hampel) and Pathology (Dr Frankel), The Ohio State University Wexner Medical Center, Columbus. Dr Rish Pai is now with the Department of Laboratory Medicine and Pathology, Mayo Clinic, Scottsdale, Arizona. Dr Liu is now with the Department of Pathology, University of Florida, Gainesville. Dr Zhao is now with the Department of Pathology, Brigham and Womens Hospital, Boston, Massachusetts. Dr Westerhoff is now with the Department of Pathology, University of Michigan, Ann Arbor.

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April 2018

Randomized Noninferiority Trial of Telephone vs In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer: A 12-Month Follow-Up.

JNCI Cancer Spectr 2017 Sep 22;1(1):pkx002. Epub 2017 Sep 22.

Georgetown Lombardi Comprehensive Cancer Center (MKI, HS, BNP, RN, MS, TD, GH, KG, CI, MDS) and Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research (MKI, HS, BNP, KG, CI, MDS), Georgetown University, Washington, DC; Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY (HBV, JH); Department of Psychology, Reykjavik University, Reykjavik, Iceland (HBV); School of Medicine, University of Maryland, Baltimore, MD (RN); National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD (MS); Cancer Genetic Counseling Program, Inova Translational Medicine Institute, Inova Health System, Falls Church, VA (TD); NextGxDx, Inc, Franklin, TN (GH); Familial Cancer Program of the Vermont Cancer Center, University of Vermont College of Medicine, Burlington, VT (MW, WM); Center for Cancer Genetics and Prevention, Dana-Farber Cancer Institute-Harvard Medical School, Boston, MA (JG, SM); Center for Cancer Risk Assessment, Massachusetts General Hospital Cancer Center, Boston, MA (SM); Carol G. Simon Cancer Center, Atlantic Health Services, Summit, NJ (JH); University of Utah School of Medicine and Huntsman Cancer Institute, Salt Lake City, UT (AYK); Cancer Control and Population Sciences, University of New Mexico Cancer Center, Albuquerque, NM (AYK).

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September 2017

Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program.

Fam Cancer 2017 01;16(1):159-166

Department of Medicine and University of Vermont Cancer Center, University of Vermont College of Medicine, 89 Beaumont Ave, Given E214, Burlington, VT, 05405, USA.

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January 2017

Universal Versus Targeted Screening for Lynch Syndrome: Comparing Ascertainment and Costs Based on Clinical Experience.

Dig Dis Sci 2016 10 6;61(10):2887-2895. Epub 2016 Jul 6.

Hematology/Oncology Division, Department of Medicine, University of Vermont College of Medicine, Given Suite E214, 89 Beaumont Avenue, Burlington, VT, 05405, USA.

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October 2016

Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer.

Fam Cancer 2016 10;15(4):529-39

Department of Oncology, Lombardi Comprehensive Cancer Center, Jess and Mildred Fisher Center for Hereditary Cancer and Clinical Genomics Research, Georgetown University Medical Center, 3300 Whitehaven Street, NW, Suite 4100, Washington, DC, 20007, USA.

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October 2016

Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling.

Genet Med 2015 Jun 18;17(6):467-75. Epub 2014 Sep 18.

Department of Oncology, Cancer Prevention and Control Program and Fisher Center for Familial Cancer Research, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

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June 2015

Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer.

J Clin Oncol 2014 Mar 21;32(7):618-26. Epub 2014 Jan 21.

Marc D. Schwartz, Beth N. Peshkin, Jeanne Mandelblatt, Rachel Nusum, An-Tsun Huang, Yaojen Chang, Kristi Graves, Claudine Isaacs, George Luta, Sarah Kelleher, Kara-Grace Leventhal, Patti Vegella, Angie Tong, and Lesley King, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC; Heiddis B. Valdimarsdottir, Mount Sinai School of Medicine, New York, NY; Marie Wood and Wendy McKinnon, Familial Cancer Program of the Vermont Cancer Center, University of Vermont College of Medicine, Burlington, VT; Judy Garber and Shelley McCormick, Dana-Farber Cancer Institute-Harvard Medical School, Boston, MA; and Anita Y. Kinney, University of Utah School of Medicine and Huntsman Cancer Institute, Salt Lake City, UT.

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March 2014

The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype.

Eur J Hum Genet 2014 May 2;22(5):617-24. Epub 2013 Oct 2.

1] Adult Cancer Program, Lowy Cancer Research Centre, Prince of Wales Clinical School, University of New South Wales, Sydney, NSW, Australia [2] Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.

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May 2014

Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individuals.

Fam Cancer 2009 24;8(4):363-9. Epub 2009 May 24.

Familial Cancer Program of the Vermont Cancer Center, University of Vermont College of Medicine, Burlington, VT 05401, USA.

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January 2010