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Brain : a Journal of Neurology
|
March 27, 2026
Quantitative pathology and APOE genotype reveal dementia risk and progression in Lewy body disease
Hemanth R Nelvagal, Nancy Chiraki, Toby Curless, et al.
Nature Communications
|
February 27, 2020
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
Sebastian Guelfi, Karishma D'Sa, Juan A Botía, et al.
NPJ Parkinson'S Disease
|
May 25, 2019
Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset
Kimberley J Billingsley, Ines A Barbosa, Sara Bandrés-Ciga, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 21, 2023
Investigation of the genetic aetiology of Lewy body diseases with and without dementia
Lesley Wu, Raquel Real, Alejandro Martinez, et al.
Brain : a Journal of Neurology
|
January 9, 2023
Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia
Zhongbo Chen, Arianna Tucci, Valentina Cipriani, et al.
The Lancet. Neurology
|
December 20, 2020
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
Edwin Jabbari, Shunsuke Koga, Rebecca R Valentino, et al.
Plos Genetics
|
September 18, 2023
eQTL Catalogue 2023: New datasets, X chromosome QTLs, and improved detection and visualisation of transcript-level QTLs
Nurlan Kerimov, Ralf Tambets, James D Hayhurst, et al.
Nature Genetics
|
November 19, 2013
Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome
Sérgio B Sousa, Dagan Jenkins, Estelle Chanudet, et al.
Neurobiology of Disease
|
March 22, 2012
Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain
Dena G Hernandez, Mike A Nalls, Matthew Moore, et al.
Biorxiv : the Preprint Server for Biology
|
April 17, 2023
Systematic visualisation of molecular QTLs reveals variant mechanisms at GWAS loci
Nurlan Kerimov, Ralf Tambets, James D Hayhurst, et al.
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Search research articles
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Showing results (91-100 of 176) with videos related to
Sort By:
Page
of 18
Brain : a Journal of Neurology
|
March 27, 2026
Quantitative pathology and APOE genotype reveal dementia risk and progression in Lewy body disease
Hemanth R Nelvagal, Nancy Chiraki, Toby Curless, et al.
Nature Communications
|
February 27, 2020
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
Sebastian Guelfi, Karishma D'Sa, Juan A Botía, et al.
NPJ Parkinson'S Disease
|
May 25, 2019
Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset
Kimberley J Billingsley, Ines A Barbosa, Sara Bandrés-Ciga, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 21, 2023
Investigation of the genetic aetiology of Lewy body diseases with and without dementia
Lesley Wu, Raquel Real, Alejandro Martinez, et al.
Brain : a Journal of Neurology
|
January 9, 2023
Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia
Zhongbo Chen, Arianna Tucci, Valentina Cipriani, et al.
The Lancet. Neurology
|
December 20, 2020
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
Edwin Jabbari, Shunsuke Koga, Rebecca R Valentino, et al.
Plos Genetics
|
September 18, 2023
eQTL Catalogue 2023: New datasets, X chromosome QTLs, and improved detection and visualisation of transcript-level QTLs
Nurlan Kerimov, Ralf Tambets, James D Hayhurst, et al.
Nature Genetics
|
November 19, 2013
Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome
Sérgio B Sousa, Dagan Jenkins, Estelle Chanudet, et al.
Neurobiology of Disease
|
March 22, 2012
Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain
Dena G Hernandez, Mike A Nalls, Matthew Moore, et al.
Biorxiv : the Preprint Server for Biology
|
April 17, 2023
Systematic visualisation of molecular QTLs reveals variant mechanisms at GWAS loci
Nurlan Kerimov, Ralf Tambets, James D Hayhurst, et al.
Page
of 18