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Medrxiv : the Preprint Server for Health Sciences
|
November 21, 2023
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations
Sara Bandres-Ciga, Faraz Faghri, Elisa Majounie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 16, 2024
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations
Sara Bandres-Ciga, Faraz Faghri, Elisa Majounie, et al.
Genome Medicine
|
November 30, 2017
Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience
Perry G Ridge, Celeste M Karch, Simon Hsu, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 26, 2024
Understanding monogenic Parkinson's disease at a global scale
Johanna Junker, Lara M Lange, Eva-Juliane Vollstedt, et al.
Plos Genetics
|
May 10, 2008
A genome-wide association study identifies protein quantitative trait loci (pQTLs)
David Melzer, John R B Perry, Dena Hernandez, et al.
Plos Genetics
|
June 27, 2009
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
Maja Bucan, Brett S Abrahams, Kai Wang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 30, 2023
<i>MAPT</i> allele and haplotype frequencies in Nigerian Africans: population distribution and association with Parkinson's disease risk and age at onset
Olaitan Okunoye, Oluwadamilola Ojo, Oladunni Abiodun, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, et al.
American Journal of Human Genetics
|
March 5, 2016
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Suzanne Lesage, Valérie Drouet, Elisa Majounie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 27, 2020
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease
Alexey A Shadrin, Sören Mucha, David Ellinghaus, et al.
Page
of 29
Search research articles
Search
Showing results (231-240 of 286) with videos related to
Sort By:
Page
of 29
Medrxiv : the Preprint Server for Health Sciences
|
November 21, 2023
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations
Sara Bandres-Ciga, Faraz Faghri, Elisa Majounie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 16, 2024
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations
Sara Bandres-Ciga, Faraz Faghri, Elisa Majounie, et al.
Genome Medicine
|
November 30, 2017
Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resilience
Perry G Ridge, Celeste M Karch, Simon Hsu, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 26, 2024
Understanding monogenic Parkinson's disease at a global scale
Johanna Junker, Lara M Lange, Eva-Juliane Vollstedt, et al.
Plos Genetics
|
May 10, 2008
A genome-wide association study identifies protein quantitative trait loci (pQTLs)
David Melzer, John R B Perry, Dena Hernandez, et al.
Plos Genetics
|
June 27, 2009
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
Maja Bucan, Brett S Abrahams, Kai Wang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 30, 2023
<i>MAPT</i> allele and haplotype frequencies in Nigerian Africans: population distribution and association with Parkinson's disease risk and age at onset
Olaitan Okunoye, Oluwadamilola Ojo, Oladunni Abiodun, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, et al.
American Journal of Human Genetics
|
March 5, 2016
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Suzanne Lesage, Valérie Drouet, Elisa Majounie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 27, 2020
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease
Alexey A Shadrin, Sören Mucha, David Ellinghaus, et al.
Page
of 29