Author

Andrew Polyak

Pennsylvania State University

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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Genomics· 2

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:differential expression· 1 Organism:human· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Santhosh GirirajaniD· 2 shared Alessandra RenieriiD· 1 shared Alexandre ReymondiD· 1 shared Anke Van DijckiD· 1 shared Anne‐Laure Mosca‐BoidroniD· 1 shared Arjun KrishnaniD· 1 shared Aurora CurròiD· 1 shared Bertrand IsidoriD· 1 shared

Activity by Year

2015-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Santhosh GirirajanORCID

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2 papers

Recent·Most cited

Rare variants in the genetic background modulate the expressivity of neurodevelopmental disorders

Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill Anne Rosenfeld, Katrin Männik, Arjun Krishnan, Elizabeth McCready, Olivier Pichon, Cédric Le Caignec, Anke Van Dijck, Kate Pope, Els Voorhoeve, Jieun Yoon, Paweł Stankiewicz, Sau Wai Cheung, , Santhosh Girirajan

The paper shows that rare secondary mutations in functionally intolerant genes affect the expressivity of neurodevelopmental disorders in individuals with primary mutations.

Genetics in Medicine · Sep 5, 2018Peer-reviewedGenomics

The impact of comorbidity of intellectual disability on estimates of autism prevalence among children enrolled in US special education

Andrew Polyak, Richard M Kubina, Santhosh Girirajan

This paper examines how comorbidity with intellectual disability affects autism prevalence estimates among US special education children, finding a 331% increase in autism prevalence linked to diagnostic recategorization.

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · Oct 1, 2015Peer-reviewedGenomics