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Stacey B Gabriel

Showing results (121-130 of 133) with videos related to

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Molecular Psychiatry|October 23, 2019
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Molecular Psychiatry|August 16, 2018
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Science (New York, N.Y.)|January 3, 2015
Mosquito genomics. Highly evolvable malaria vectors: the genomes of 16 Anopheles mosquitoesDaniel E Neafsey, Robert M Waterhouse, Mohammad R Abai, et al.
Nature Genetics|August 29, 2022
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibilityAleksejs Sazonovs, Christine R Stevens, Guhan R Venkataraman, et al.
Nature|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, et al.
Nature|October 19, 2007
Genome-wide detection and characterization of positive selection in human populationsPardis C Sabeti, Patrick Varilly, Ben Fry, et al.
Nature|October 19, 2007
A second generation human haplotype map of over 3.1 million SNPs, Kelly A Frazer, Dennis G Ballinger, et al.
Nature Genetics|March 14, 2023
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease riskNick Shrine, Abril G Izquierdo, Jing Chen, et al.
Nature Genetics|February 10, 2009
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants, Sekar Kathiresan, Benjamin F Voight, et al.
Pageof 14

Showing results (121-130 of 133) with videos related to

Sort By:
Pageof 14
Molecular Psychiatry|October 23, 2019
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Molecular Psychiatry|August 16, 2018
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Science (New York, N.Y.)|January 3, 2015
Mosquito genomics. Highly evolvable malaria vectors: the genomes of 16 Anopheles mosquitoesDaniel E Neafsey, Robert M Waterhouse, Mohammad R Abai, et al.
Nature Genetics|August 29, 2022
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibilityAleksejs Sazonovs, Christine R Stevens, Guhan R Venkataraman, et al.
Nature|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, et al.
Nature|October 19, 2007
Genome-wide detection and characterization of positive selection in human populationsPardis C Sabeti, Patrick Varilly, Ben Fry, et al.
Nature|October 19, 2007
A second generation human haplotype map of over 3.1 million SNPs, Kelly A Frazer, Dennis G Ballinger, et al.
Nature Genetics|March 14, 2023
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease riskNick Shrine, Abril G Izquierdo, Jing Chen, et al.
Nature Genetics|February 10, 2009
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants, Sekar Kathiresan, Benjamin F Voight, et al.
Pageof 14