Author

Joe Glessner

Children's Hospital of Philadelphia

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· 3

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Adam X. MaihoferiD· 2 shared Aiden Peter CorviniD· 2 shared Allison E. AielloiD· 2 shared Ananda B. AmstadteriD· 2 shared Andreas J. ForstneriD· 2 shared Arianna Di FlorioiD· 2 shared Astrid DempfleiD· 2 shared Barbara FrankeiD· 2 shared

Activity by Year

2023-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Adam X. MaihoferORCID

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3 papers

Recent·Most cited

A cross-disorder analysis of CNVs finds novel loci and dose-dependent relationships of genes to psychiatric traits

Omar Shanta, Marieke Klein, Molly Sacks, Jeffrey R. MacDonald, Adam X. Maihofer, Mohammad Mehdi Ahangari, Worrawat Engchuan, Bhooma Thiruvahindrapuram, James Guevara, Oanh Hong, Guillaume Huguet, Ida Elken Sønderby, Maria Kalyuzhny, Mark J. Adams, Rolf Adolfsson, , Annette M. Hartmann

The paper identifies novel CNV loci and dose-dependent gene effects across six psychiatric disorders using genome-wide analysis.

medRxiv · Jul 11, 2025 · PreprintGenetic & Genomic Medicine

Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effects

Worrawat Engchuan, Omar Shanta, Kuldeep Kumar, Jeffrey R. MacDonald, Bhooma Thiruvahindrapuram, Omar Hamdan, Marieke Klein, Adam X. Maihofer, James Guevara, Oanh Hong, Guillaume Huguet, Molly Sacks, Mohammad Mehdi Ahangari, Rayssa M.M.W. Feitosa, Kara Han, , Michael Foster Green

The paper identifies shared and divergent genetic mechanisms across psychiatric disorders using gene-set burden analysis of copy number variants.

medRxiv · Jul 11, 2025 · PreprintGenetic & Genomic Medicine

Clinical consequences of a polygenic predisposition to benign lower white blood cell counts

Jonathan D. Mosley, John P. Shelley, Alyson L. Dickson, Jacy Zanussi, Laura L. Daniel, Neil S. Zheng, Lisa A. Bastarache, Wei‐Qi Wei, Mingjian Shi, Gail Pairitz Jarvik, Elisabeth A. Rosenthal, Atlas Khan, Alborz Sherafati, Iftikhar J. Kullo, Theresa L. Walunas, , Vivian K. Kawai

This study investigates the clinical consequences of a genetic predisposition to lower white blood cell counts using a polygenic score and finds associations with bone marrow biopsy outcomes and treatment responses.

medRxiv · Aug 20, 2023 · PreprintGenetic & Genomic Medicine