Author

Paul Cannon

23andMe (United States)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 2

Signature Assays, Organisms & Methods

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Assay:GWAS summary statistics· 4 Organism:human· 4 Approach:statistical model· 4 Research Focus:GWAS / association mapping· 2 Research Focus:differential expression· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Karl HeilbroniD· 4 shared Andrew SingletoniD· 3 shared Alastair John NoyceiD· 2 shared Artur Francisco Schumacher SchuhiD· 2 shared Carlos Roberto de Mello RiederiD· 2 shared Cornelis BlauwendraatiD· 2 shared Edward A. FoniD· 2 shared Hampton L. LeonardiD· 2 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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Focal author (center)Selected co-authorORCID co-authorUnlinked name

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4 shared papersGenetic & Genomic Medicine

Karl HeilbronORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Multi-ancestry genome-wide meta-analysis in Parkinson's disease

Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, Michelle Mulan Lian, Karl Heilbron, Stella W. Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Paul Cannon, Daniella Coker, Gabriel Cuéllar-Partida, , Piu Chan

This paper conducts a multi-ancestry genome-wide meta-analysis of Parkinson's disease, identifying 78 independent loci and 23 genes associated with PD risk.

Nature Genetics · Dec 28, 2023Peer-reviewedGenetic & Genomic Medicine

Characterizing the genetic architecture of Parkinson's disease in Latinos

Douglas P. Loesch, Andréa R. V. R. Horimoto, Karl Heilbron, Elif Irem Sarihan, Miguel Inca‐Martinez, Emily Mason, Mario Cornejo‐Olivas, Luis Torres, Pilar Mazzetti, Carlos Cosentino, Elison H. Sarapura‐Castro, Andrea Rivera‐Valdivia, Ángel C. Medina, Elena Diéguez, Víctor E. Raggio, , Ignacio Fernandez Mata

This study conducts the first GWAS of Parkinson's disease in Latinos, identifies SNCA as significant, and finds genetic overlap with Europeans.

Annals of Neurology · Jul 6, 2021Peer-reviewedGenetic & Genomic Medicine

Fine-mapping of SNCA in REM sleep behavior disorder and overt synucleinopathies

Lynne Krohn, Richard Y. J. Wu, Karl Heilbron, Jennifer A. Ruskey, Sandra B. Laurent, Cornelis Blauwendraat, Armaghan Alam, Isabelle Arnulf, Michele T.M. Hu, Yves A Dauvilliers, Birgit Högl, Mathias Toft, Kari Anne Bjørnarå, Ambra Stefani, Evi Holzknecht, , Ziv Gan‐Or

This study identifies SNCA risk variants specific to RBD and overt synucleinopathies, finding distinct associations and opposite effects at the 3' end of SNCA.

Annals of Neurology · Jan 24, 2020Peer-reviewedGenetics

Genetic modifiers of risk and age at onset in GBA associated Parkinson disease and Lewy body dementia

Cornelis Blauwendraat, Xylena Reed, Lynne Krohn, Karl Heilbron, Sara Bandrés‐Ciga, Manuela M. X. Tan, Jesse Raphael Gibbs, Dena G. Hernandez, Ravindran Kumaran, Rebekah G. Langston, Luis Bonet‐Ponce, Roy N. Alcalay, Sharon Hassin‐Baer, Lior Greenbaum, Hirotaka Iwaki, , Andrew Singleton

The paper identifies genetic modifiers of risk and age at onset in GBA-associated Parkinson disease and Lewy body dementia using large case-control datasets and genome-wide association studies.

Brain · Oct 23, 2019Peer-reviewedGenetics