Author

Simon Xu

Simons Foundation

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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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Alex LashiD· 2 shared A Jarratt· 1 shared A Raven· 1 shared Abha R. GuptaiD· 1 shared Addie Luo· 1 shared Adriana MuñoziD· 1 shared Adrienne L. AdamsiD· 1 shared Ai Nhu Nguyen· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersBioinformatics

Alex LashORCID

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2 papers

Recent·Most cited

The Genotype and Phenotypes in Families (GPF) platform manages the large and complex data at SFARI

Liubomir Chorbadjiev, Murat Cokol, Zohar Weinstein, Kevin Y. Shi, Chris Fleisch, Nikolay Dimitrov, Svetlin Mladenov, Simon Xu, Jake Hall, Steven Ford, Yoon-ha Lee, Boris Yamrom, Steven Marks, Adriana Muñoz, Alex Lash, , Ivan H. Iossifov

The GPF platform manages and analyzes large family genotypic and phenotypic data for autism research, enabling variant analysis and secure data sharing.

bioRxiv · Feb 8, 2024 · PreprintBioinformatics

Integrating de novo and inherited variants in over 42,607 autism cases identifies mutations in new moderate risk genes

Xueya Zhou, Pamela Feliciano, Chang Shu, Tianyun Wang, Irina Astrovskaya, Jacob B. Hall, Joseph U. Obiajulu, Jessica R. Wright, Shwetha Canchi Murali, Simon Xu, Leo Brueggeman, Taylor Thomas, Olena Marchenko, Christopher Fleisch, Sarah D. Barns, , Catherine A. Edmonson

The paper identifies 60 new moderate risk genes for autism by integrating de novo and inherited variants across 42,607 cases and 236,000 controls.

Nature Genetics · Aug 18, 2022Peer-reviewedGenetic & Genomic Medicine