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Cell Reports
|
March 8, 2025
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's disease
Thomas P Spargo, Chloe F Sands, Isabella R Juan, et al.
Brain : a Journal of Neurology
|
February 2, 2026
Mapping the causal chain from genetic risk variants to lipid dysmetabolism in Parkinson's disease
Ruth B De-Paula, Jonggeol Kim, Herve Rhinn, et al.
Biorxiv : the Preprint Server for Biology
|
March 23, 2026
Massive-scale single-nucleus multi-omics identifies novel rare noncoding drivers of Parkinson's disease
Shreya Menon, Adam W Turner, Serena H Chang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 20, 2026
Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorder
Ali H Bereshneh, Kirkland A Wilson, Xueyang Pan, et al.
Brain : a Journal of Neurology
|
November 23, 2019
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
Cornelis Blauwendraat, Xylena Reed, Lynne Krohn, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
February 7, 2022
Adverse Events Reported by Patients With Cancer After Administration of a 2-Dose mRNA COVID-19 Vaccine
Rebecca M Shulman, David S Weinberg, Eric A Ross, et al.
Human Molecular Genetics
|
June 11, 2010
Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals
Jason J Corneveaux, Amanda J Myers, April N Allen, et al.
Genome Biology
|
February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Iris E Jansen, Hui Ye, Sasja Heetveld, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, 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.
Page
of 45
Search research articles
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Showing results (421-430 of 445) with videos related to
Sort By:
Page
of 45
Cell Reports
|
March 8, 2025
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's disease
Thomas P Spargo, Chloe F Sands, Isabella R Juan, et al.
Brain : a Journal of Neurology
|
February 2, 2026
Mapping the causal chain from genetic risk variants to lipid dysmetabolism in Parkinson's disease
Ruth B De-Paula, Jonggeol Kim, Herve Rhinn, et al.
Biorxiv : the Preprint Server for Biology
|
March 23, 2026
Massive-scale single-nucleus multi-omics identifies novel rare noncoding drivers of Parkinson's disease
Shreya Menon, Adam W Turner, Serena H Chang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 20, 2026
Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorder
Ali H Bereshneh, Kirkland A Wilson, Xueyang Pan, et al.
Brain : a Journal of Neurology
|
November 23, 2019
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
Cornelis Blauwendraat, Xylena Reed, Lynne Krohn, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
February 7, 2022
Adverse Events Reported by Patients With Cancer After Administration of a 2-Dose mRNA COVID-19 Vaccine
Rebecca M Shulman, David S Weinberg, Eric A Ross, et al.
Human Molecular Genetics
|
June 11, 2010
Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals
Jason J Corneveaux, Amanda J Myers, April N Allen, et al.
Genome Biology
|
February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Iris E Jansen, Hui Ye, Sasja Heetveld, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, 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.
Page
of 45