Kelly D F Hagman (Kelly D Farwell Hagman, Kelly D Farwell)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2015-2022
Publications (10 Years): 8

Top Topics

Human Immunodeficiency Virus

Dna Methylation

Genome Wide Identification

Top Venues

Molecular genetics & genomic medicine

Genetics in medicine : official journal of the American College of Medical Genetics

Journal of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Meghan C Towne, Mari Rossi, Bess Wayburn, Jennifer M Huang, Kelly Radtke, Wendy Alcaraz, Kelly D F Hagman, Deepali N Shinde
Diagnostic testing laboratories are valuable partners for disease gene discovery: 5-year experience with GeneMatcher. Human mutation 43 (6) (2022)
Zöe Powis, Kelly D F Hagman, Kirsten Blanco, Margaret Au, John M Graham, Kathryn Singh, Natalie Gallant, Linda M Randolph, Meghan C Towne, Jesse Hunter, Deepali N Shinde, Erika Palmaer, Brian Schoenfeld, Sha Tang
When moments matter: Finding answers with rapid exome sequencing. Molecular genetics & genomic medicine 8 (2) (2019)
Tricia N Zion, Bess Wayburn, Sourat Darabi, Devon Lamb Thrush, Erica D Smith, Tami Johnston, Brissa Martin, Kelly D F Hagman, Melissa Parra, Christian Antolik
Clinical validity assessment of genes for inclusion in multi-gene panel testing: A systematic approach. Molecular genetics & genomic medicine 7 (5) (2019)
Zöe Powis, Meghan C Towne, Kelly D F Hagman, Kirsten Blanco, Erika Palmaer, Andrew Castro, Samin A Sajan, Kelly Radtke, Timothy J Feyma, Kali Juliette, Sha Tang, Christos Sidiropoulos
Clinical diagnostic exome sequencing in dystonia: Genetic testing challenges for complex conditions. Clinical genetics 97 (2) (2019)
Wenbo Mu, Bing Li, Sitao Wu, Jefferey Chen, Divya Sain, Dong Xu, Mary Helen Black, Rachid Karam, Katrina Gillespie, Kelly D F Hagman, Lucia Guidugli, Melissa Pronold, Aaron Elliott, Hsiao-Mei Lu
Detection of structural variation using target captured next-generation sequencing data for genetic diagnostic testing. Genetics in medicine : official journal of the American College of Medical Genetics 21 (7) (2018)
Nancy Niguidula, Christina Alamillo, Elizabeth C Chao, Zöe Powis, Julie S Cohen, Kelly D F Hagman
Clinical whole-exome sequencing results impact medical management. Molecular genetics & genomic medicine 6 (6) (2018)
Kelly D F Hagman, Deepali N Shinde, Cameron Mroske, Erica D Smith, Kelly Radtke, Elizabeth C Chao, Dima El-Khechen, Zöe Powis, Elizabeth C Chao, Wendy A Alcaraz, Katherine L Helbig, Samin A Sajan, Mari Rossi, Hsiao-Mei Lu, Robert Huether, Shuwei Li, Sitao Wu, Mark E Nunes, Sha Tang
Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases. Genetics in medicine : official journal of the American College of Medical Genetics 19 (2) (2016)
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin, Gregory M Cooper, Soma Das, Joshua L Deignan, Michael O Dorschner, James P Evans, Arezou A Ghazani, Katrina A B Goddard, Michele C Gornick, Kelly D F Hagman, Tina Hambuch, Madhuri Hegde, Lucia A Hindorff, Ingrid A Holm, Gail P Jarvik, Amy Knight Johnson, Lindsey Mighion, Massimo Morra, Sharon E Plon, Sumit Punj, Carolyn Sue Richards, Avni Santani, Brian H Shirts, Nancy B Spinner, Sha Tang, Karen E Weck, Susan M Wolf, Yaping Yang, Michael J Bamshad
A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories. Genetics in medicine : official journal of the American College of Medical Genetics 19 (5) (2016)
Zöe Powis, Kelly D F Hagman, Christina L Alamillo, Sha Tang
Diagnostic exome sequencing for patients with a family history of consanguinity: over 38% of positive results are not autosomal recessive pattern. Journal of human genetics 61 (2) (2015)