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American Journal of Human Genetics
|
February 1, 2023
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly
Margaux Serey-Gaut, Marisol Cortes, Periklis Makrythanasis, et al.
The Journal of Allergy and Clinical Immunology
|
April 19, 2021
Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency
Stefano Vavassori, Janet Chou, Laura Eva Faletti, et al.
Acta Neuropathologica Communications
|
April 26, 2023
Large multi-ethnic genetic analyses of amyloid imaging identify new genes for Alzheimer disease
Muhammad Ali, Derek B Archer, Priyanka Gorijala, et al.
Journal of the American College of Cardiology
|
March 8, 2023
Virtual Care Team Guided Management of Patients With Heart Failure During Hospitalization
Ankeet S Bhatt, Anubodh S Varshney, Alea Moscone, et al.
Human Mutation
|
October 25, 2019
Missense variants in TAF1 and developmental phenotypes: challenges of determining pathogenicity
Hanyin Cheng, Simona Capponi, Emma Wakeling, et al.
Brain : a Journal of Neurology
|
May 13, 2022
Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease
Jaclyn M Eissman, Logan Dumitrescu, Emily R Mahoney, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 30, 2023
Novel <i>CYP1B1-RMDN2</i> Alzheimer's disease locus identified by genome-wide association analysis of cerebral tau deposition on PET
Kwangsik Nho, Shannon L Risacher, Liana Apostolova, et al.
Nature Communications
|
September 20, 2024
CYP1B1-RMDN2 Alzheimer's disease endophenotype locus identified for cerebral tau PET
Kwangsik Nho, Shannon L Risacher, Liana G Apostolova, et al.
Molecular Psychiatry
|
October 9, 2019
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry
Tim B Bigdeli, Giulio Genovese, Penelope Georgakopoulos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 23, 2024
Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort
Kerith-Rae Dias, Rupendra Shrestha, Deborah Schofield, et al.
Page
of 59
Search research articles
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Showing results (571-580 of 587) with videos related to
Sort By:
Page
of 59
American Journal of Human Genetics
|
February 1, 2023
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly
Margaux Serey-Gaut, Marisol Cortes, Periklis Makrythanasis, et al.
The Journal of Allergy and Clinical Immunology
|
April 19, 2021
Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency
Stefano Vavassori, Janet Chou, Laura Eva Faletti, et al.
Acta Neuropathologica Communications
|
April 26, 2023
Large multi-ethnic genetic analyses of amyloid imaging identify new genes for Alzheimer disease
Muhammad Ali, Derek B Archer, Priyanka Gorijala, et al.
Journal of the American College of Cardiology
|
March 8, 2023
Virtual Care Team Guided Management of Patients With Heart Failure During Hospitalization
Ankeet S Bhatt, Anubodh S Varshney, Alea Moscone, et al.
Human Mutation
|
October 25, 2019
Missense variants in TAF1 and developmental phenotypes: challenges of determining pathogenicity
Hanyin Cheng, Simona Capponi, Emma Wakeling, et al.
Brain : a Journal of Neurology
|
May 13, 2022
Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease
Jaclyn M Eissman, Logan Dumitrescu, Emily R Mahoney, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 30, 2023
Novel <i>CYP1B1-RMDN2</i> Alzheimer's disease locus identified by genome-wide association analysis of cerebral tau deposition on PET
Kwangsik Nho, Shannon L Risacher, Liana Apostolova, et al.
Nature Communications
|
September 20, 2024
CYP1B1-RMDN2 Alzheimer's disease endophenotype locus identified for cerebral tau PET
Kwangsik Nho, Shannon L Risacher, Liana G Apostolova, et al.
Molecular Psychiatry
|
October 9, 2019
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry
Tim B Bigdeli, Giulio Genovese, Penelope Georgakopoulos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 23, 2024
Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort
Kerith-Rae Dias, Rupendra Shrestha, Deborah Schofield, et al.
Page
of 59