Author

William Wallace

BioMarin (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

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

A. LinderholmiD· 1 shared Adrián Muñoz‐BarreraiD· 1 shared Alicia LjungdahliD· 1 shared Amy Stockwell· 1 shared Andrew Gordon NicholsoniD· 1 shared Arthur WüsteriD· 1 shared Avner SchlessingeriD· 1 shared Ayodeji AdegunsoyeiD· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. LinderholmORCID

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Author profile →

2 papers

Recent·Most cited

PCSK6 and Survival in Idiopathic Pulmonary Fibrosis

Justin M. Oldham, Richard J. Allen, Jose Miguel Lorenzo-Salazar, Philip L. Molyneaux, Shwu‐Fan Ma, Chitra Joseph, John S. Kim, Beatriz Guillén‐Guío, Tamara Hernández-Beeftink, Jonathan A. Kropski, Yong Huang, Cathryn T. Lee, Ayodeji Adegunsoye, Janelle Vu Pugashetti, A. Linderholm, , Imre Noth

The paper identifies four novel genetic variants associated with IPF survival, including a PCSK6 variant, and suggests PCSK6 as a prognostic biomarker and therapeutic target.

American Journal of Respiratory and Critical Care Medicine · Feb 13, 2023Peer-reviewedGenetic & Genomic Medicine

Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1/GAT-1 variants

Dina Buitrago Silva, Marena I. Trinidad, Alicia Ljungdahl, Jezrael L. Revalde, Geoffrey Y. Berguig, William Wallace, Cory S. Patrick, Lorenzo Bomba, Michelle R. Arkin, Shan Dong, Karol Estrada, Keino Hutchinson, Jonathan H. LeBowitz, Avner Schlessinger, Katrine M. Johannesen, , Arthur Wüster

The paper investigates the functional consequences of SLC6A1 variants, finding haploinsufficiency underlies neurodevelopmental phenotypes and identifying missense residues sensitive to substitution.

medRxiv · Mar 9, 2022 · PreprintGenetic & Genomic Medicine