Kate Shane

Predictors of risk-reducing surgery intentions following genetic counseling for hereditary breast and ovarian cancer.

Authors:

Mary Kathleen Ladd Beth N Peshkin Leigha Senter Shari Baldinger Claudine Isaacs Hannah Segal Samantha Philip Chloe Phillips Kate Shane Aimee Martin Veronique Weinstein Robert Pilarski Joanne Jeter Kevin Sweet Bonnie Hatten Elisabeth J Wurtmann Shanda Phippen Della Bro Marc D Schwartz

Transl Behav Med 2020 05;10(2):337-346

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.

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May 2020

12q14 microdeletion associated with HMGA2 gene disruption and growth restriction.

Authors:

Fadel Alyaqoub Robert E Pyatt Andrea Bailes Amanda Brock Carol Deeg Aimee McKinney Caroline Astbury Shalini Reshmi Kate P Shane Devon Lamb Thrush Annemarie Sommer Julie M Gastier-Foster

Am J Med Genet A 2012 Nov 14;158A(11):2925-30. Epub 2012 Sep 14.

Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, Ohio 43205, USA.

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November 2012

Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.

Authors:

Nils Krone Nicole Reisch Jan Idkowiak Vivek Dhir Hannah E Ivison Beverly A Hughes Ian T Rose Donna M O'Neil Raymon Vijzelaar Matthew J Smith Fiona MacDonald Trevor R Cole Nicolai Adolphs John S Barton Edward M Blair Stephen R Braddock Felicity Collins Deborah L Cragun Mehul T Dattani Ruth Day Shelley Dougan Miriam Feist Michael E Gottschalk John W Gregory Michaela Haim Rachel Harrison Ann Haskins Olney Berthold P Hauffa Peter C Hindmarsh Robert J Hopkin Petr E Jira Marlies Kempers Michiel N Kerstens Mohamed M Khalifa Birgit Köhler Dominique Maiter Shelly Nielsen Stephen M O'Riordan Christian L Roth Kate P Shane Martin Silink Nike M M L Stikkelbroeck Elizabeth Sweeney Maria Szarras-Czapnik John R Waterson Lori Williamson Michaela F Hartmann Norman F Taylor Stefan A Wudy Ewa M Malunowicz Cedric H L Shackleton Wiebke Arlt

J Clin Endocrinol Metab 2012 Feb 7;97(2):E257-67. Epub 2011 Dec 7.

Centre for Endocrinology, Diabetes, and Metabolism, School of Clinical and Experimental Medicine, University of Birmingham, Birmingham B15 2TT, UK.

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February 2012

Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalities.

Am J Hum Genet 2010 Mar 4;86(3):454-61. Epub 2010 Mar 4.

Signature Genomic Laboratories, Spokane, WA 99207, USA.

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March 2010

Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.

Hum Mol Genet 2009 Apr 3;18(8):1377-83. Epub 2009 Feb 3.

Signature Genomic Laboratories, LLC, Spokane, WA 99207, USA.

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April 2009

Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.

Am J Hum Genet 2008 Jul 19;83(1):106-11. Epub 2008 Jun 19.

Program in Genetics & Genomic Biology and The Centre for Applied Genomics, Hospital for Sick Children, Toronto, ON M5G 1L7, Canada.

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July 2008

Publications by authors named "Kate Shane"

Predictors of risk-reducing surgery intentions following genetic counseling for hereditary breast and ovarian cancer.

Authors:

12q14 microdeletion associated with HMGA2 gene disruption and growth restriction.

Authors:

Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.

Authors:

Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalities.

Authors:

Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.

Authors:

Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.

Authors: