Publications by authors named "Denae M Golden"

4Publications

Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar.

Authors:
Erin R Riggs Tristan Nelson Andrew Merz Todd Ackley Brian Bunke Christin D Collins Morag N Collinson Yao-Shan Fan McKinsey L Goodenberger Denae M Golden Linda Haglund-Hazy Danijela Krgovic Allen N Lamb Zoe Lewis Guang Li Yajuan Liu Jeanne Meck Whitney Neufeld-Kaiser Cassandra K Runke Jennifer N Sanmann Dimitri J Stavropoulos Emma Strong Meng Su Marwan K Tayeh Nadja Kokalj Vokac Erik C Thorland Erica Andersen Christa L Martin

Hum Mutat 2018 11;39(11):1650-1659

Autism & Developmental Medicine Institute, Geisinger, Danville, PA, USA.

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November 2018

Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray.

Authors:
Jennifer N Sanmann Diane L Pickering Denae M Golden Jadd M Stevens Thomas E Hempel Pamela A Althof Michele L Wiggins Lois J Starr Bhavana J Davé Warren G Sanger

Genet Med 2015 Nov 15;17(11):875-9. Epub 2015 Jan 15.

Human Genetics Laboratory, Munroe-Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha, Nebraska, USA.

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November 2015

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

Authors:
Erin B Kaminsky Vineith Kaul Justin Paschall Deanna M Church Brian Bunke Dawn Kunig Daniel Moreno-De-Luca Andres Moreno-De-Luca Jennifer G Mulle Stephen T Warren Gabriele Richard John G Compton Amy E Fuller Troy J Gliem Shuwen Huang Morag N Collinson Sarah J Beal Todd Ackley Diane L Pickering Denae M Golden Emily Aston Heidi Whitby Shashirekha Shetty Michael R Rossi M Katharine Rudd Sarah T South Arthur R Brothman Warren G Sanger Ramaswamy K Iyer John A Crolla Erik C Thorland Swaroop Aradhya David H Ledbetter Christa L Martin

Genet Med 2011 Sep;13(9):777-84

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

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September 2011

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.

Authors:
Daniel Moreno-De-Luca Jennifer G Mulle Erin B Kaminsky Stephan J Sanders Scott M Myers Margaret P Adam Amy T Pakula Nancy J Eisenhauer Kim Uhas LuAnn Weik Lisa Guy Melanie E Care Chantal F Morel Charlotte Boni Bonnie Anne Salbert Ashadeep Chandrareddy Laurie A Demmer Eva W C Chow Urvashi Surti Swaroop Aradhya Diane L Pickering Denae M Golden Warren G Sanger Emily Aston Arthur R Brothman Troy J Gliem Erik C Thorland Todd Ackley Ram Iyer Shuwen Huang John C Barber John A Crolla Stephen T Warren Christa L Martin David H Ledbetter

Am J Hum Genet 2010 Nov 4;87(5):618-30. Epub 2010 Nov 4.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.

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November 2010