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Yalda Jamshidi

Showing results (51-60 of 75) with videos related to

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JCI Insight|October 11, 2019
KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization patternAlexander Teumer, Teresa Trenkwalder, Thorsten Kessler, et al.
Plos Medicine|June 22, 2016
Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization StudyBram P Prins, Ali Abbasi, Anson Wong, et al.
Nature Genetics|March 28, 2026
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosityHye In Kim, Christopher DeBoever, Klaudia Walter, et al.
Annals of Neurology|April 26, 2022
Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic ParaplegiaDaniel G Calame, Isabella Herman, Reza Maroofian, et al.
Human Molecular Genetics|September 1, 2016
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African AmericansDaniel S Evans, Christy L Avery, Mike A Nalls, et al.
European Journal of Human Genetics : EJHG|January 26, 2019
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traitsJessica van Setten, Niek Verweij, Hamdi Mbarek, et al.
The Journal of Clinical Investigation|October 14, 2025
Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathyNatalia Dominik, Stephanie Efthymiou, Christopher J Record, et al.
Human Molecular Genetics|July 20, 2010
Genome-wide association analysis identifies multiple loci related to resting heart rateMark Eijgelsheim, Christopher Newton-Cheh, Nona Sotoodehnia, et al.
Brain : a Journal of Neurology|November 11, 2023
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disordersRauan Kaiyrzhanov, Aboulfazl Rad, Sheng-Jia Lin, et al.
American Journal of Human Genetics|August 2, 2020
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function EffectsAndreea Manole, Stephanie Efthymiou, Emer O'Connor, et al.
Pageof 8

Showing results (51-60 of 75) with videos related to

Sort By:
Pageof 8
JCI Insight|October 11, 2019
KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization patternAlexander Teumer, Teresa Trenkwalder, Thorsten Kessler, et al.
Plos Medicine|June 22, 2016
Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization StudyBram P Prins, Ali Abbasi, Anson Wong, et al.
Nature Genetics|March 28, 2026
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosityHye In Kim, Christopher DeBoever, Klaudia Walter, et al.
Annals of Neurology|April 26, 2022
Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic ParaplegiaDaniel G Calame, Isabella Herman, Reza Maroofian, et al.
Human Molecular Genetics|September 1, 2016
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African AmericansDaniel S Evans, Christy L Avery, Mike A Nalls, et al.
European Journal of Human Genetics : EJHG|January 26, 2019
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traitsJessica van Setten, Niek Verweij, Hamdi Mbarek, et al.
The Journal of Clinical Investigation|October 14, 2025
Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathyNatalia Dominik, Stephanie Efthymiou, Christopher J Record, et al.
Human Molecular Genetics|July 20, 2010
Genome-wide association analysis identifies multiple loci related to resting heart rateMark Eijgelsheim, Christopher Newton-Cheh, Nona Sotoodehnia, et al.
Brain : a Journal of Neurology|November 11, 2023
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disordersRauan Kaiyrzhanov, Aboulfazl Rad, Sheng-Jia Lin, et al.
American Journal of Human Genetics|August 2, 2020
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function EffectsAndreea Manole, Stephanie Efthymiou, Emer O'Connor, et al.
Pageof 8