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Nature
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November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Nature Genetics
|
March 6, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Seung Hoan Choi, Sean J Jurgens, Ling Xiao, et al.
Nature
|
April 12, 2023
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
Joshua S Weinstock, Jayakrishnan Gopakumar, Bala Bharathi Burugula, et al.
Nature Genetics
|
August 29, 2022
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility
Aleksejs Sazonovs, Christine R Stevens, Guhan R Venkataraman, et al.
Molecular Psychiatry
|
February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Nature Genetics
|
March 6, 2025
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Carolina Roselli, Ida Surakka, Morten S Olesen, et al.
Nature Communications
|
September 1, 2022
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
William J Young, Najim Lahrouchi, Aaron Isaacs, et al.
Nature Communications
|
May 23, 2020
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ioanna Ntalla, Lu-Chen Weng, James H Cartwright, et al.
Nature Genetics
|
June 13, 2018
Multi-ethnic genome-wide association study for atrial fibrillation
Carolina Roselli, Mark D Chaffin, Lu-Chen Weng, et al.
Nature
|
October 19, 2007
Genome-wide detection and characterization of positive selection in human populations
Pardis C Sabeti, Patrick Varilly, Ben Fry, et al.
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of 81
Search research articles
Search
Showing results (791-800 of 803) with videos related to
Sort By:
Page
of 81
Nature
|
November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Nature Genetics
|
March 6, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Seung Hoan Choi, Sean J Jurgens, Ling Xiao, et al.
Nature
|
April 12, 2023
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis
Joshua S Weinstock, Jayakrishnan Gopakumar, Bala Bharathi Burugula, et al.
Nature Genetics
|
August 29, 2022
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility
Aleksejs Sazonovs, Christine R Stevens, Guhan R Venkataraman, et al.
Molecular Psychiatry
|
February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Nature Genetics
|
March 6, 2025
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Carolina Roselli, Ida Surakka, Morten S Olesen, et al.
Nature Communications
|
September 1, 2022
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
William J Young, Najim Lahrouchi, Aaron Isaacs, et al.
Nature Communications
|
May 23, 2020
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ioanna Ntalla, Lu-Chen Weng, James H Cartwright, et al.
Nature Genetics
|
June 13, 2018
Multi-ethnic genome-wide association study for atrial fibrillation
Carolina Roselli, Mark D Chaffin, Lu-Chen Weng, et al.
Nature
|
October 19, 2007
Genome-wide detection and characterization of positive selection in human populations
Pardis C Sabeti, Patrick Varilly, Ben Fry, et al.
Page
of 81