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Acta Neuropathologica
|
August 29, 2019
The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion
Zeran Li, Fabiana H G Farias, Umber Dube, et al.
NPJ Parkinson'S Disease
|
July 8, 2023
Proteome wide association studies of LRRK2 variants identify novel causal and druggable proteins for Parkinson's disease
Bridget Phillips, Daniel Western, Lihua Wang, et al.
Acta Neuropathologica Communications
|
November 20, 2020
Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease
Laura Ibanez, Jorge A Bahena, Chengran Yang, et al.
Nature Genetics
|
November 11, 2024
Genetic architecture of cerebrospinal fluid and brain metabolite levels and the genetic colocalization of metabolites with human traits
Ciyang Wang, Chengran Yang, Daniel Western, et al.
Research Square
|
June 19, 2023
Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and informs causal proteins for Alzheimer's disease
Carlos Cruchaga, Dan Western, Jigyasha Timsina, et al.
Science Translational Medicine
|
July 5, 2023
Proteomics of brain, CSF, and plasma identifies molecular signatures for distinguishing sporadic and genetic Alzheimer's disease
Yun Ju Sung, Chengran Yang, Joanne Norton, et al.
The Lancet. Neurology
|
May 13, 2026
Identification of genetic modifiers of autosomal dominant Alzheimer's disease: a genome-wide association study
Maulikkumar Patel, Wei Feng, Nicole S Mckay, et al.
Molecular Neurodegeneration
|
January 3, 2024
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer's disease
Lihua Wang, Niko-Petteri Nykänen, Daniel Western, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 12, 2026
CSF turnover reshapes biomarker interpretation in neurodegeneration studies
Pablo García-González, Raquel Puerta, Jonas Dehairs, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 27, 2026
Human CSF proteogenomics links genetic variation to neurodegenerative disease proteins
Raquel Puerta, Pablo Garcia-Gonzalez, Itziar de Rojas, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 49) with videos related to
Sort By:
Page
of 5
Acta Neuropathologica
|
August 29, 2019
The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion
Zeran Li, Fabiana H G Farias, Umber Dube, et al.
NPJ Parkinson'S Disease
|
July 8, 2023
Proteome wide association studies of LRRK2 variants identify novel causal and druggable proteins for Parkinson's disease
Bridget Phillips, Daniel Western, Lihua Wang, et al.
Acta Neuropathologica Communications
|
November 20, 2020
Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease
Laura Ibanez, Jorge A Bahena, Chengran Yang, et al.
Nature Genetics
|
November 11, 2024
Genetic architecture of cerebrospinal fluid and brain metabolite levels and the genetic colocalization of metabolites with human traits
Ciyang Wang, Chengran Yang, Daniel Western, et al.
Research Square
|
June 19, 2023
Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and informs causal proteins for Alzheimer's disease
Carlos Cruchaga, Dan Western, Jigyasha Timsina, et al.
Science Translational Medicine
|
July 5, 2023
Proteomics of brain, CSF, and plasma identifies molecular signatures for distinguishing sporadic and genetic Alzheimer's disease
Yun Ju Sung, Chengran Yang, Joanne Norton, et al.
The Lancet. Neurology
|
May 13, 2026
Identification of genetic modifiers of autosomal dominant Alzheimer's disease: a genome-wide association study
Maulikkumar Patel, Wei Feng, Nicole S Mckay, et al.
Molecular Neurodegeneration
|
January 3, 2024
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer's disease
Lihua Wang, Niko-Petteri Nykänen, Daniel Western, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 12, 2026
CSF turnover reshapes biomarker interpretation in neurodegeneration studies
Pablo García-González, Raquel Puerta, Jonas Dehairs, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 27, 2026
Human CSF proteogenomics links genetic variation to neurodegenerative disease proteins
Raquel Puerta, Pablo Garcia-Gonzalez, Itziar de Rojas, et al.
Page
of 5