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David Altshuler

Showing results (141-150 of 237) with videos related to

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Nature Genetics|January 24, 2009
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosusRobert R Graham, Chris Cotsapas, Leela Davies, et al.
Science (New York, N.Y.)|May 19, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomesJacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, et al.
The New England Journal of Medicine|January 11, 2008
Association between microdeletion and microduplication at 16p11.2 and autismLauren A Weiss, Yiping Shen, Joshua M Korn, et al.
International Journal of Cancer|August 28, 2007
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohortsDaphne W Bell, Sang H Kim, Andrew K Godwin, et al.
Human Molecular Genetics|April 21, 2009
The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjectsHélène Choquet, Christine Cavalcanti-Proença, Cécile Lecoeur, et al.
Nature Genetics|October 24, 2006
Transferability of tag SNPs in genetic association studies in multiple populationsPaul I W de Bakker, Noël P Burtt, Robert R Graham, et al.
Journal of the American College of Cardiology|July 16, 2011
Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarctionDiego Ardissino, Carlo Berzuini, Piera Angelica Merlini, et al.
The New England Journal of Medicine|December 7, 2020
CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-ThalassemiaHaydar Frangoul, David Altshuler, M Domenica Cappellini, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 2, 2014
Genome Sequencing of Multiple Primary Tumors Reveals a Novel PALB2 VariantKasmintan A Schrader, Kelly L Stratton, Rajmohan Murali, et al.
The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
Pageof 24

Showing results (141-150 of 237) with videos related to

Sort By:
Pageof 24
Nature Genetics|January 24, 2009
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosusRobert R Graham, Chris Cotsapas, Leela Davies, et al.
Science (New York, N.Y.)|May 19, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomesJacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, et al.
The New England Journal of Medicine|January 11, 2008
Association between microdeletion and microduplication at 16p11.2 and autismLauren A Weiss, Yiping Shen, Joshua M Korn, et al.
International Journal of Cancer|August 28, 2007
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohortsDaphne W Bell, Sang H Kim, Andrew K Godwin, et al.
Human Molecular Genetics|April 21, 2009
The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjectsHélène Choquet, Christine Cavalcanti-Proença, Cécile Lecoeur, et al.
Nature Genetics|October 24, 2006
Transferability of tag SNPs in genetic association studies in multiple populationsPaul I W de Bakker, Noël P Burtt, Robert R Graham, et al.
Journal of the American College of Cardiology|July 16, 2011
Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarctionDiego Ardissino, Carlo Berzuini, Piera Angelica Merlini, et al.
The New England Journal of Medicine|December 7, 2020
CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-ThalassemiaHaydar Frangoul, David Altshuler, M Domenica Cappellini, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 2, 2014
Genome Sequencing of Multiple Primary Tumors Reveals a Novel PALB2 VariantKasmintan A Schrader, Kelly L Stratton, Rajmohan Murali, et al.
The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
Pageof 24