Author

Claire Wegel

Indiana University Indianapolis

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· 4 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 5 Approach:statistical model· 4 Research Focus:GWAS / association mapping· 3 Assay:GWAS summary statistics· 3 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Approach:experimental assay· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Andrew SingletoniD· 3 shared Christine KleiniD· 3 shared Cornelis BlauwendraatiD· 3 shared Harutyun MadoeviD· 3 shared Justin Cook SolleiD· 3 shared Kishore Raj KumariD· 3 shared Mike A. NallsiD· 3 shared Ai Huey TaniD· 2 shared

Activity by Year

2019-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Andrew SingletonORCID

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5 papers

Recent·Most cited

Global Perspectives on Returning Genetic Research Results in Parkinson's Disease

Ai Huey Tan, Paula Saffie Awad, Artur Francisco Schumacher Schuh, Shen‐Yang Lim, Harutyun Madoev, Azlina Ahmad‐Annuar, Justin Cook Solle, Claire Wegel, Maria Leila M. Doquenia, Sumit Dey, María Teresa Periñán, Mary B. Makarious, Brian Fiske, Huw R. Morris, Alastair John Noyce, , the Global Parkinson’s Genetics Program (GP2)

This paper surveys global perspectives on returning genetic research results in Parkinson's disease, finding disparities in access, training, and policy practices across countries.

Neurology Genetics · Dec 1, 2024Peer-reviewedGenetic & Genomic Medicine

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

Clodagh Towns, Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar, Alejandro Martínez-Carrasco, Mary B. Makarious, Bradford H. Casey, Dan Vitale, Kristin S. Levine, Hampton L. Leonard, Caroline B. Pantazis, Laurel A. Screven, Dena G. Hernandez, , 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.

npj Parkinson s Disease · Sep 12, 2023Peer-reviewedGenetic & Genomic Medicine

Genetic variants associated with longitudinal cognitive performance in older breast cancer patients and controls

Kelly Nicole Holohan Nudelman, Kwangsik T. Nho, Michael Zhang, Brenna C. McDonald, Wanting Zhai, Brent J. Small, Claire Wegel, Paul B. Jacobsen, Heather Jim, Sunita K. Patel, Deena Mary Atieh Graham, Tim A. Ahles, James C. Root, Tatiana Foroud, Elizabeth Crabb Breen, , the Thinking and Living with Cancer (TLC) Study

This study identifies genetic variants associated with cognitive decline in older breast cancer patients compared to controls using longitudinal cognitive data.

Cancers · May 23, 2023Peer-reviewedGenetic & Genomic Medicine

Global Parkinson's Genetics Program (GP2) Monogenic Network Protocol: Elucidating causative gene variants in hereditary Parkinson's disease

Lara Mariah Lange, Micol Avenali, Melina Ellis, Anastasia Illarionova, Ignacio Juan Keller Sarmiento, Ai Huey Tan, Harutyun Madoev, Caterina Galandra, Johanna Junker, Karisha Roopnarain, Justin Cook Solle, Claire Wegel, Zih‐Hua Fang, Peter Heutink, Kishore Raj Kumar, , the Global Parkinson’s Genetic Program (GP2)

The paper establishes a protocol for whole-genome sequencing to identify genetic causes of Parkinson's disease, focusing on monogenic variants and their clinical implications.

medRxiv · Dec 1, 2022 · PreprintGenetic & Genomic Medicine

Genome-wide association study of Parkinsons disease progression biomarkers in 12 longitudinal patients cohorts

Hirotaka Iwaki, Cornelis Blauwendraat, Hampton L. Leonard, Jonggeol Jeffrey Kim, Ganqiang Liu, Jodi Maple‐Grødem, Jean‐Christophe Corvol, Lasse Pihlstrøm, Marlies van Nimwegen, Samantha J. Hutten, H. Nguyen Khanh-Dung, Jacqueline H. Rick, Shirley W. Eberly, Faraz Faghri, Peggy Auinger, , Mike A. Nalls

This study identifies two genome-wide significant variants associated with Parkinson's disease progression and replicates known risk variants' effects on motor and cognitive decline.

bioRxiv · Mar 27, 2019 · PreprintGenetics