Kelly D Farwell Hagman - Ambry Genetics

基本信息

浏览量：0

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 32 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Recommendations for Next-Generation Sequencing Germline Variant Confirmation A Joint Report of the Association for Molecular Pathology and National Society of Genetic Counselors

Kristy R. Crooks,Kelly D. Farwell Hagman,Diana Mandelker,Avni Santani,Ryan J. Schmidt,Robyn L. Temple-Smolkin,Stephen E. Lincoln

The Journal of Molecular Diagnosticsno. 7 (2023): 411-427

引用0浏览0WOS引用

Recommendations for Next-Generation Sequencing Germline Variant Confirmation

Kristy Crooks,Kelly D. Farwell Hagman,Diana Mandelker,Avni Santani,Ryan J. Schmidt,Robyn Temple-Smolkin,Stephen E. Lincoln

The Journal of molecular diagnostics/The journal of molecular diagnosticsno. 7 (2023): 411-427

引用0浏览0引用

Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices

Julie Stefka,Dima El-Khechen,Taylor Cain,Kirsten Blanco,Benjamin Feldmann,Meghan C. Towne,Kelly D. Farwell Hagman

JOURNAL OF GENETIC COUNSELING（2022）

引用1浏览0WOS引用

Diagnostic testing laboratories are valuable partners for disease gene discovery: 5-year experience with GeneMatcher

Meghan C. Towne,Mari Rossi,Bess Wayburn, Jennifer M. Huang,Kelly Radtke,Wendy Alcaraz,Kelly D. Farwell Hagman,Deepali N. Shinde

HUMAN MUTATIONno. 6 (2022): 772-781

引用3浏览0WOS引用

Facing The Challenge Of Genetic Counselors' Need For Rapid Continuing Education About Genomic Technologies

Kelly D Farwell Hagman, Devon Lamb Thrush, Samantha Freeze, Darnelle L Dorsainville,Jennifer Eichmeyer,Kimberly C Banks

JOURNAL OF GENETIC COUNSELING（2020）

引用7浏览0WOS引用

Points to consider when assessing relationships (or suspecting misattributed relationships) during family-based clinical genomic testing: a statement of the American College of Medical Genetics and Genomics (ACMG)

Joshua L. Deignan,Elizabeth Chao,Jennifer L. Gannon,Henry T. Greely,Kelly D. Farwell Hagman,Rong Mao,Scott Topper

Genetics in Medicine（2020）

引用8浏览0WOS引用

Detection of Structural Variation Using Target Captured Next-Generation Sequencing Data for Genetic Diagnostic Testing

Wenbo Mu,Bing Li,Sitao Wu,Jefferey Chen,Divya Sain,Dong Xu,Mary Helen Black,Rachid Karam,Katrina Gillespie,Kelly D. Farwell Hagman,Lucia Guidugli,Melissa Pronold,Aaron Elliott,Hsiao-Mei Lu

Genetics in medicine（2019）

引用23浏览0WOS引用

A retrospective review of multiple findings in diagnostic exome sequencing: half are distinct and half are overlapping diagnoses

Erica D. Smith,Kirsten Blanco,Samin A. Sajan,Jesse M. Hunter,Deepali N. Shinde,Bess Wayburn,Mari Rossi,Jennifer Huang,Cathy A. Stevens,Candace Muss,Wendy Alcaraz,Kelly D. Farwell Hagman,Sha Tang,Kelly Radtke

Genetics in Medicine（2019）

引用55浏览0WOS引用

Clinical Validity Assessment of Genes for Inclusion in Multi‐gene Panel Testing: A Systematic Approach

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

Molecular genetics & genomic medicine（2019）

引用3浏览0WOS引用

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn