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Author Details

Mike A Nalls
Center for Alzheimer's and Related Dementias, National Institutes of Health
2007
374
100
PMIDPaper TitleJournal TitlePublished Year
37886468Lack of genetic evidence for NLRP3-inflammasome involvement in Parkinson's disease pathogenesis.medRxiv2024
37886468Lack of genetic evidence for NLRP3-inflammasome involvement in Parkinson's disease pathogenesis.medRxiv2024
36669485Virus exposure and neurodegenerative disease risk across national biobanks.Neuron2023
37606627Artificial intelligence for dementia genetics and omics.Alzheimers Dement2023
38014237Human brain single nucleus cell type enrichments in neurodegenerative diseases.Res Sq2023
37729920A fully automated FAIMS-DIA mass spectrometry-based proteomic pipeline.Cell Rep Methods2023
37577689Human brain single nucleus cell type enrichments in neurodegenerative diseases.medRxiv2023
37577533Divergent patterns of healthy aging across human brain regions at single-cell resolution reveal links to neurodegenerative disease.bioRxiv2023
37986980NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations.medRxiv2023
37986827Sleep disturbances as risk factors for neurodegeneration later in life.medRxiv2023
38076854The non-coding <i>GBA1</i> rs3115534 variant is associated with REM sleep behavior disorder in Nigerians.medRxiv2023
37704671Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).NPJ Parkinsons Dis2023
37034649Multi-ancestry genome-wide study in &gt;2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37409055Application of Aligned-UMAP to longitudinal biomedical studies.Patterns (N Y)2023
37090536Analysis of rare Parkinson's disease variants in millions of people.Res Sq2023
37398408Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed Populations.medRxiv2023
37398091Genome-wide meta-analysis of CSF biomarkers in Alzheimer's disease and Parkinson's disease cohorts.medRxiv2023
36950378The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism.Cell Genom2023
37198259Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease.Mol Psychiatry2023
37192343Genetic risk factor clustering within and across neurodegenerative diseases.Brain2023
36871034The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data.NPJ Parkinsons Dis2023
36695634Genome-Wide Analysis of Structural Variants in Parkinson Disease.Ann Neurol2023
36869417Polygenic Parkinson's Disease Genetic Risk Score as Risk Modifier of Parkinsonism in Gaucher Disease.Mov Disord2023
36747793Mis-spliced transcripts generate de novo proteins in TDP-43-related ALS/FTD.bioRxiv2023
37369645Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).NPJ Parkinsons Dis2023
37225742Author Correction: The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data.NPJ Parkinsons Dis2023
36669485Virus exposure and neurodegenerative disease risk across national biobanks.Neuron2023
37539664Genome-Wide Meta-Analysis of Cerebrospinal Fluid Biomarkers in Alzheimer's Disease and Parkinson's Disease Cohorts.Mov Disord2023
37494933Parallel CRISPR-Cas9 screens identify mechanisms of PLIN2 and lipid droplet regulation.Dev Cell2023
37163045Creating the Pick's disease International Consortium: Association study of <i>MAPT</i> H2 haplotype with risk of Pick's disease.medRxiv2023
37099244Evaluating the harmonisation potential of diverse cohort datasets.Eur J Epidemiol2023
38076854The non-coding <i>GBA1</i> rs3115534 variant is associated with REM sleep behavior disorder in Nigerians.medRxiv2023
38014237Human brain single nucleus cell type enrichments in neurodegenerative diseases.Res Sq2023
37704671Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).NPJ Parkinsons Dis2023
37986980NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations.medRxiv2023
37986827Sleep disturbances as risk factors for neurodegeneration later in life.medRxiv2023
37577689Human brain single nucleus cell type enrichments in neurodegenerative diseases.medRxiv2023
37577533Divergent patterns of healthy aging across human brain regions at single-cell resolution reveal links to neurodegenerative disease.bioRxiv2023
37606627Artificial intelligence for dementia genetics and omics.Alzheimers Dement2023
37539664Genome-Wide Meta-Analysis of Cerebrospinal Fluid Biomarkers in Alzheimer's Disease and Parkinson's Disease Cohorts.Mov Disord2023
37729920A fully automated FAIMS-DIA mass spectrometry-based proteomic pipeline.Cell Rep Methods2023
37494933Parallel CRISPR-Cas9 screens identify mechanisms of PLIN2 and lipid droplet regulation.Dev Cell2023
37192343Genetic risk factor clustering within and across neurodegenerative diseases.Brain2023
37090536Analysis of rare Parkinson's disease variants in millions of people.Res Sq2023
36950378The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism.Cell Genom2023
37409055Application of Aligned-UMAP to longitudinal biomedical studies.Patterns (N Y)2023
37369645Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).NPJ Parkinsons Dis2023
37034649Multi-ancestry genome-wide study in &gt;2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37099244Evaluating the harmonisation potential of diverse cohort datasets.Eur J Epidemiol2023
37398408Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed Populations.medRxiv2023
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James G Wilson
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Alexander Teumer
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Thomas H Mosley
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Nicholas J Wareham
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Alexis Brice
Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS
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Paul M Ridker
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Release 1.2