Author

William M. McMahon

University of Utah

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 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Cathy L. BarriD· 3 shared Cathy L. BudmaniD· 3 shared Daniëlle C. CathiD· 3 shared Dongmei YuiD· 3 shared James Frederick LeckmaniD· 3 shared Andrea DietrichiD· 2 shared Andreas HartmanniD· 2 shared Barbara J. CoffeyiD· 2 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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Curved chords = mutual co-authorship

3 shared papersGenetic & Genomic Medicine

Cathy L. BarrORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genome-Wide Association Analysis of Tic Disorders Reveals 6 Independent Risk Loci and Highlights Tic-Associated Cell Types and Brain Circuitry

Dongmei Yu, Nora I. Strom, Zachary F. Gerring, Apostolia Topaloudi, Matthew Halvorsen, Sudhanshu Shekhar, Tyne W. Miller‐Fleming, Miao Tang, Luz M Porras, Franjo Ivankovic, Behrang Mahjani, Teemu Palviainen, Elizabeth C. Corfield, Christos Androutsos, Alan Apter, , Pablo Mir

This study identifies six genome-wide significant risk loci for tic disorders and links genetic risk to specific brain cell types and circuits.

medRxiv · Apr 13, 2026 · PreprintGenetic & Genomic Medicine

Distinct patterns of de novo coding variants contribute to Tourette Syndrome etiology

Lingyu Zhan, Dongmei Yu, Franjo Ivankovic, Maria Niarchou, Laura Domènech, Cathy L. Barr, Fortu Benarroch, Cathy L. Budman, Daniëlle C. Cath, Nelson B. Freimer, Helena Garrido, Marco A. Grados, Varda Gross‐Tsur, Luis Diego Herrera-Amighetti, Robert A. King, , Roel A. Ophoff

This study identifies distinct rare de novo coding variants associated with Tourette Syndrome, highlighting loss-of-function mutations and novel candidate genes.

bioRxiv · Nov 4, 2025 · PreprintNeuroscience

Synaptic processes and immune-related pathways implicated in Tourette Syndrome

Fotis Tsetsos, Dongmei Yu, Jae Hoon Sul, Alden Y. Huang, Cornelia Illmann, Lisa Osiecki, Sabrina Michelle Darrow, Matthew E. Hirschtritt, Erica Greenberg, Kirsten Müller‐Vahl, Manfred Stuhrmann, Yves Dion, Guy Armand Rouleau, Harald N. Aschauer, Mara Stamenkovic, , Harald Aschauer

This study identifies gene sets associated with Tourette Syndrome using genome-wide data, highlighting synaptic and immune-related pathways.

Translational Psychiatry · Jan 18, 2021Peer-reviewedGenetic & Genomic Medicine