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Breast Cancer Research and Treatment
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April 4, 2014
Long-term risk of medical conditions associated with breast cancer treatment
Deirdre A Hill, Nora K Horick, Claudine Isaacs, et al.
American Journal of Human Genetics
|
January 10, 2025
Design and implementation of an action plan for justice, equity, diversity, and inclusion within the Clinical Genome Resource
Alice B Popejoy, Deborah I Ritter, Danielle Azzariti, et al.
JAMA
|
July 14, 2011
Clinically relevant changes in family history of cancer over time
Argyrios Ziogas, Nora K Horick, Anita Y Kinney, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 17, 2016
Germline Analysis from Tumor-Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings
Bryce A Seifert, Julianne M O'Daniel, Krunal Amin, et al.
Neurology. Genetics
|
February 9, 2018
Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders
Gloria T Haskell, Michael C Adams, Zheng Fan, et al.
Patient Education and Counseling
|
January 23, 2023
Question prompt lists and caregiver question asking in pediatric specialty appointments: A randomized controlled trial
Margaret Waltz, Haoyang Yan, R Jean Cadigan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 17, 2012
Exploring concordance and discordance for return of incidental findings from clinical sequencing
Robert C Green, Jonathan S Berg, Gerard T Berry, et al.
Trials
|
June 15, 2021
Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial
Brooke S Staley, Laura V Milko, Margaret Waltz, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2016
Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing
Michael C Leo, Carmit McMullen, Benjamin S Wilfond, et al.
The Journal of Pediatrics
|
March 11, 2019
An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening
Laura V Milko, Julianne M O'Daniel, Daniela M DeCristo, et al.
Page
of 17
Search research articles
Search
Showing results (121-130 of 168) with videos related to
Sort By:
Page
of 17
Breast Cancer Research and Treatment
|
April 4, 2014
Long-term risk of medical conditions associated with breast cancer treatment
Deirdre A Hill, Nora K Horick, Claudine Isaacs, et al.
American Journal of Human Genetics
|
January 10, 2025
Design and implementation of an action plan for justice, equity, diversity, and inclusion within the Clinical Genome Resource
Alice B Popejoy, Deborah I Ritter, Danielle Azzariti, et al.
JAMA
|
July 14, 2011
Clinically relevant changes in family history of cancer over time
Argyrios Ziogas, Nora K Horick, Anita Y Kinney, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 17, 2016
Germline Analysis from Tumor-Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings
Bryce A Seifert, Julianne M O'Daniel, Krunal Amin, et al.
Neurology. Genetics
|
February 9, 2018
Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders
Gloria T Haskell, Michael C Adams, Zheng Fan, et al.
Patient Education and Counseling
|
January 23, 2023
Question prompt lists and caregiver question asking in pediatric specialty appointments: A randomized controlled trial
Margaret Waltz, Haoyang Yan, R Jean Cadigan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 17, 2012
Exploring concordance and discordance for return of incidental findings from clinical sequencing
Robert C Green, Jonathan S Berg, Gerard T Berry, et al.
Trials
|
June 15, 2021
Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial
Brooke S Staley, Laura V Milko, Margaret Waltz, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2016
Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing
Michael C Leo, Carmit McMullen, Benjamin S Wilfond, et al.
The Journal of Pediatrics
|
March 11, 2019
An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening
Laura V Milko, Julianne M O'Daniel, Daniela M DeCristo, et al.
Page
of 17