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Journal of Personalized Medicine
|
December 24, 2021
Defining the Critical Components of Informed Consent for Genetic Testing
Kelly E Ormond, Maia J Borensztein, Miranda L G Hallquist, et al.
Genome Medicine
|
April 30, 2021
Application of a framework to guide genetic testing communication across clinical indications
Miranda L G Hallquist, Eric P Tricou, Kelly E Ormond, et al.
Human Mutation
|
October 13, 2018
ClinGen's GenomeConnect registry enables patient-centered data sharing
Juliann M Savatt, Danielle R Azzariti, W Andrew Faucett, et al.
JAMA Psychiatry
|
December 11, 2014
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions
Andres Moreno-De-Luca, David W Evans, K B Boomer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 7, 2018
Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background
Kelly E Ormond, Miranda L G Hallquist, Adam H Buchanan, et al.
Health Affairs (Project Hope)
|
May 8, 2018
Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience
Marc S Williams, Adam H Buchanan, F Daniel Davis, et al.
American Journal of Human Genetics
|
August 14, 2018
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort
Marci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 8, 2013
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future
Omri Gottesman, Helena Kuivaniemi, Gerard Tromp, et al.
Journal of Medical Genetics
|
October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 21, 2017
Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants
Adam H Buchanan, Kandamurugu Manickam, Michelle N Meyer, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
Journal of Personalized Medicine
|
December 24, 2021
Defining the Critical Components of Informed Consent for Genetic Testing
Kelly E Ormond, Maia J Borensztein, Miranda L G Hallquist, et al.
Genome Medicine
|
April 30, 2021
Application of a framework to guide genetic testing communication across clinical indications
Miranda L G Hallquist, Eric P Tricou, Kelly E Ormond, et al.
Human Mutation
|
October 13, 2018
ClinGen's GenomeConnect registry enables patient-centered data sharing
Juliann M Savatt, Danielle R Azzariti, W Andrew Faucett, et al.
JAMA Psychiatry
|
December 11, 2014
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions
Andres Moreno-De-Luca, David W Evans, K B Boomer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 7, 2018
Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background
Kelly E Ormond, Miranda L G Hallquist, Adam H Buchanan, et al.
Health Affairs (Project Hope)
|
May 8, 2018
Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience
Marc S Williams, Adam H Buchanan, F Daniel Davis, et al.
American Journal of Human Genetics
|
August 14, 2018
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort
Marci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 8, 2013
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future
Omri Gottesman, Helena Kuivaniemi, Gerard Tromp, et al.
Journal of Medical Genetics
|
October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 21, 2017
Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants
Adam H Buchanan, Kandamurugu Manickam, Michelle N Meyer, et al.
Page
of 4