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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 12, 2019
Variant classification changes over time in BRCA1 and BRCA2
Chloe Mighton, George S Charames, Marina Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 19, 2015
VisCap: inference and visualization of germ-line copy-number variants from targeted clinical sequencing data
Trevor J Pugh, Sami S Amr, Mark J Bowser, et al.
BMC Genomics
|
October 8, 2010
Dynamic, mating-induced gene expression changes in female head and brain tissues of Drosophila melanogaster
Justin E Dalton, Tanvi S Kacheria, Simon Rv Knott, et al.
The Journal of Molecular Diagnostics : JMD
|
May 17, 2025
Path to Health Equity and Improved Outcomes through Inclusive Sex and Gender Data Collection in Genomic Testing
Marco L Leung, Ina Amarillo, Danielle Jordan, et al.
Journal of the American Medical Informatics Association : JAMIA
|
August 26, 2025
Electronic health records-based algorithms to screen for U.S. Centers for Disease Control and Prevention tier 1 genetic diseases: a scoping review
William R Harris, Marianna S Hernandez, Khanh N H Ngo, et al.
The Journal of Molecular Diagnostics : JMD
|
January 6, 2019
A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing-Detected Variants with an Orthogonal Method in Clinical Genetic Testing
Stephen E Lincoln, Rebecca Truty, Chiao-Feng Lin, et al.
Vox Sanguinis
|
June 23, 2020
Overcoming the challenges of interpreting complex and uncommon RH alleles from whole genomes
Justin B L Halls, Sunitha Vege, Daimon P Simmons, et al.
American Journal of Human Genetics
|
February 12, 2011
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy
Daniel M Jordan, Adam Kiezun, Samantha M Baxter, et al.
Journal of Personalized Medicine
|
August 26, 2022
The Evolution of a Large Biobank at Mass General Brigham
Natalie T Boutin, Samantha B Schecter, Emma F Perez, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 13, 2017
A curated gene list for reporting results of newborn genomic sequencing
Ozge Ceyhan-Birsoy, Kalotina Machini, Matthew S Lebo, et al.
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of 7
Search research articles
Search
Showing results (21-30 of 69) with videos related to
Sort By:
Page
of 7
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 12, 2019
Variant classification changes over time in BRCA1 and BRCA2
Chloe Mighton, George S Charames, Marina Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 19, 2015
VisCap: inference and visualization of germ-line copy-number variants from targeted clinical sequencing data
Trevor J Pugh, Sami S Amr, Mark J Bowser, et al.
BMC Genomics
|
October 8, 2010
Dynamic, mating-induced gene expression changes in female head and brain tissues of Drosophila melanogaster
Justin E Dalton, Tanvi S Kacheria, Simon Rv Knott, et al.
The Journal of Molecular Diagnostics : JMD
|
May 17, 2025
Path to Health Equity and Improved Outcomes through Inclusive Sex and Gender Data Collection in Genomic Testing
Marco L Leung, Ina Amarillo, Danielle Jordan, et al.
Journal of the American Medical Informatics Association : JAMIA
|
August 26, 2025
Electronic health records-based algorithms to screen for U.S. Centers for Disease Control and Prevention tier 1 genetic diseases: a scoping review
William R Harris, Marianna S Hernandez, Khanh N H Ngo, et al.
The Journal of Molecular Diagnostics : JMD
|
January 6, 2019
A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing-Detected Variants with an Orthogonal Method in Clinical Genetic Testing
Stephen E Lincoln, Rebecca Truty, Chiao-Feng Lin, et al.
Vox Sanguinis
|
June 23, 2020
Overcoming the challenges of interpreting complex and uncommon RH alleles from whole genomes
Justin B L Halls, Sunitha Vege, Daimon P Simmons, et al.
American Journal of Human Genetics
|
February 12, 2011
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy
Daniel M Jordan, Adam Kiezun, Samantha M Baxter, et al.
Journal of Personalized Medicine
|
August 26, 2022
The Evolution of a Large Biobank at Mass General Brigham
Natalie T Boutin, Samantha B Schecter, Emma F Perez, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 13, 2017
A curated gene list for reporting results of newborn genomic sequencing
Ozge Ceyhan-Birsoy, Kalotina Machini, Matthew S Lebo, et al.
Page
of 7