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Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
<i>GCH1</i> p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations
Yi Wen Tay, Andrew Leslie Lee, Jie Ping Schee, et al.
Annals of Neurology
|
March 11, 2011
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease
Alexis Elbaz, Owen A Ross, John P A Ioannidis, et al.
Nature Genetics
|
August 6, 2013
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
Annika Keller, Ana Westenberger, Maria J Sobrido, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 16, 2024
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights from Large-Scale Exome Sequencing
Mirja Thomsen, Fabian Ott, Sebastian Loens, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
The Global Landscape of Genetic Variation in Parkinson's disease: Multi-Ancestry Insights into Established Disease Genes and their Translational Relevance
Lara M Lange, Zih-Hua Fang, Mary B Makarious, et al.
Annals of Clinical and Translational Neurology
|
June 19, 2025
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large-Scale Exome Sequencing
Mirja Thomsen, Fabian Ott, Sebastian Loens, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 28, 2021
A Multi-center Genome-wide Association Study of Cervical Dystonia
Yan V Sun, Chengchen Li, Qin Hui, et al.
Neurobiology of Aging
|
August 22, 2013
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
Michael G Heckman, Alexis Elbaz, Alexandra I Soto-Ortolaza, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 17, 2024
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association Studies
Björn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt, et al.
Nature Genetics
|
September 9, 2025
The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease
Vicente A Yépez, German Demidov, Kornelia Ellwanger, et al.
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of 27
Search research articles
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Showing results (251-260 of 268) with videos related to
Sort By:
Page
of 27
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
<i>GCH1</i> p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations
Yi Wen Tay, Andrew Leslie Lee, Jie Ping Schee, et al.
Annals of Neurology
|
March 11, 2011
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease
Alexis Elbaz, Owen A Ross, John P A Ioannidis, et al.
Nature Genetics
|
August 6, 2013
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
Annika Keller, Ana Westenberger, Maria J Sobrido, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 16, 2024
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights from Large-Scale Exome Sequencing
Mirja Thomsen, Fabian Ott, Sebastian Loens, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
The Global Landscape of Genetic Variation in Parkinson's disease: Multi-Ancestry Insights into Established Disease Genes and their Translational Relevance
Lara M Lange, Zih-Hua Fang, Mary B Makarious, et al.
Annals of Clinical and Translational Neurology
|
June 19, 2025
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large-Scale Exome Sequencing
Mirja Thomsen, Fabian Ott, Sebastian Loens, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 28, 2021
A Multi-center Genome-wide Association Study of Cervical Dystonia
Yan V Sun, Chengchen Li, Qin Hui, et al.
Neurobiology of Aging
|
August 22, 2013
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
Michael G Heckman, Alexis Elbaz, Alexandra I Soto-Ortolaza, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 17, 2024
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association Studies
Björn-Hergen Laabs, Katja Lohmann, Eva-Juliane Vollstedt, et al.
Nature Genetics
|
September 9, 2025
The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease
Vicente A Yépez, German Demidov, Kornelia Ellwanger, et al.
Page
of 27