Author

Alexander Hsieh

Columbia UniversityORCID 0000-0003-4227-1952Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Approach:matrix factorization· 1

Frequent Co-Authors

Wendy K. ChungiD· 2 shared Yufeng SheniD· 2 shared Ahmad S. Chatha· 1 shared Akhila BalasubramanianiD· 1 shared Alexies Camba· 1 shared Ali S. FatemiiD· 1 shared Alpha Amatya· 1 shared Amanda C. GulsrudiD· 1 shared

Activity by Year

2019-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Wendy K. ChungORCID

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2 papers

Recent·Most cited

Geneticsnpj Genomic MedicinePeer-reviewedAug 23, 2019

Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes

Pamela Feliciano, Xueya Zhou, Irina Astrovskaya…·Brenda Hauf

The paper reports exome sequencing of 457 ASD families, identifying 10.4% with known ASD genes and 3.4% with possibly associated variants, and provides statistical support for 34 ASD risk genes using the TADA framework.

247 citationstop 1%

humanwhole-exome sequencing

𝕏 PostBluesky

BioinformaticsbioRxivPreprintAug 13, 2019

Early post-zygotic mutations contribute to congenital heart disease

Alexander Hsieh, Sarah U. Morton, Jon A. L. Willcox…·Yufeng Shen

The paper identifies mosaic mutations in blood and cardiac tissue from CHD patients, finding 1% of cases have detectable mosaic variants that may contribute to congenital heart disease.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky