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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 14, 2021
Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants
Adam H Buchanan, Kandamurugu Manickam, Michelle N Meyer, et al.
Circulation
|
May 15, 2023
Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease
Yiyi Zhang, Jacqueline S Dron, Brandon K Bellows, 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.
JAMA Cardiology
|
January 31, 2024
Familial Hypercholesterolemia Variant and Cardiovascular Risk in Individuals With Elevated Cholesterol
Yiyi Zhang, Jacqueline S Dron, Brandon K Bellows, et al.
Genome Medicine
|
June 28, 2022
Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations
Tian Ge, Marguerite R Irvin, Amit Patki, et al.
JAMA Network Open
|
January 16, 2019
Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants
Kandamurugu Manickam, Adam H Buchanan, Marci L B Schwartz, et al.
Science (New York, N.Y.)
|
December 24, 2016
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
Frederick E Dewey, Michael F Murray, John D Overton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 3, 2023
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change
Heidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
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Search research articles
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Showing results (61-70 of 69) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 69 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 14, 2021
Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants
Adam H Buchanan, Kandamurugu Manickam, Michelle N Meyer, et al.
Circulation
|
May 15, 2023
Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease
Yiyi Zhang, Jacqueline S Dron, Brandon K Bellows, 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.
JAMA Cardiology
|
January 31, 2024
Familial Hypercholesterolemia Variant and Cardiovascular Risk in Individuals With Elevated Cholesterol
Yiyi Zhang, Jacqueline S Dron, Brandon K Bellows, et al.
Genome Medicine
|
June 28, 2022
Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations
Tian Ge, Marguerite R Irvin, Amit Patki, et al.
JAMA Network Open
|
January 16, 2019
Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants
Kandamurugu Manickam, Adam H Buchanan, Marci L B Schwartz, et al.
Science (New York, N.Y.)
|
December 24, 2016
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
Frederick E Dewey, Michael F Murray, John D Overton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 3, 2023
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change
Heidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Page
of 7