Author

Madeleine Richer

UCL Queen Square Institute of NeurologyORCID 0009-0005-4339-4788Unclaimed ORCID profile · follow to get notified of new preprints

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Madeleine Richer1 paper

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Albert Kwaku AkpaluiD· 1 shared Alejandro Martínez-CarrascoiD· 1 shared Alex MedinaiD· 1 shared Alexander A. ZimprichiD· 1 shared Alexis BriceiD· 1 shared Alvaro Hernandez· 1 shared Ana WestenbergeriD· 1 shared Anastasia IllarionovaiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Albert Kwaku AkpaluORCID

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1 paper

Recent·Most cited

Genetic & Genomic Medicinenpj Parkinson s DiseasePeer-reviewedSep 12, 2023

Global Parkinson's Genetics Program (GP2) Complex Network Protocol: Defining the causes of sporadic Parkinson's disease

Clodagh Towns, Madeleine Richer, Simona Jasaityte…·Andrea Quattrone

The paper outlines the protocol for integrating genetic and clinical data from a global cohort of over 150,000 participants to study the genetic causes of sporadic Parkinson's disease.

39 citationstop 2%

humanGWAS summary statistics

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