Author

Justin Cook Solle

Michael J. Fox FoundationORCID 0000-0002-9941-4830Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Organism:human· 6 Research Focus:database / resource· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 3 Research Focus:benchmarking· 2 Approach:experimental assay· 2 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2

Frequent Co-Authors

Christine KleiniD· 5 shared Andrew SingletoniD· 4 shared Cornelis BlauwendraatiD· 4 shared Harutyun MadoeviD· 4 shared Kishore Raj KumariD· 4 shared Mary B. MakariousiD· 4 shared Mike A. NallsiD· 4 shared Zih‐Hua FangiD· 4 shared

Activity by Year

2022-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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5 shared papersGenetic & Genomic Medicine

Christine KleinORCID

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6 papers

Recent·Most cited

Large-scale genetic characterization of Parkinson's disease in the African and African admixed populations

Fulya Akçimen, Kimberly Paquette, Peter Wild Crea, Kathryn Step, Emily Waldo, Mathew J. Koretsky, Paula Saffie Awad, Charles Achoru, Funmilola Taiwo, Simon Izuchukwu Ozomma, Gerald Onwuegbuzie, Marzieh Khani, Spencer M. Grant, Lukman Femi Owolabi, Chiamaka Edith Okereke, , Kamalini Ghosh Galvelis

This study identifies genetic variants associated with Parkinson's disease in African and African admixed populations, highlighting differences from European and Asian populations.

Brain · Oct 7, 2025Peer-reviewedGenetic & Genomic Medicine

The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources

Allison Ann Dilliott, Maria C. Costanzo, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Bradford H. Casey, Quy Hoang, Hirotaka Iwaki, Dongkeun Jang, Jonggeol Jeffrey Kim, Hampton L. Leonard, Kristin S. Levine, Mary B. Makarious, Trang Thi Huyen Nguyen, Guy Armand Rouleau, Andrew Singleton, , Sali M.K. Farhan

The paper introduces the Neurodegenerative Disease Knowledge Portal (NDKP), an open-science platform aggregating genomic datasets for neurodegenerative diseases to enable collaborative analysis and discovery.

Neurology Genetics · Feb 21, 2025Peer-reviewedGenetic & Genomic Medicine

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

Understanding monogenic Parkinson's disease at a global scale

Johanna Junker, Lara Mariah Lange, Eva‐Juliane Vollstedt, Karisha Roopnarain, Maria Leila M. Doquenia, Azlina Ahmad‐Annuar, Micol Avenali, Soraya Bardien, Natascha Bahr, Melina Ellis, Caterina Galandra, Thomas Gasser, Peter Heutink, Anastasia Illarionova, Yuliia Kanana, , the Global Parkinson's Genetics Program (GP2)

This paper combines two global monogenic Parkinson's disease initiatives to create a comprehensive cohort and infrastructure for studying multi-ancestry genetic factors and disease expression.

Movement Disorders · Jul 30, 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

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