Author

Emily A. Malouf

University of WashingtonORCID 0000-0002-9068-8720Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Angela M. Zou· 1 shared Annie CheniD· 1 shared Asha Pathak· 1 shared Brian H. ShirtsiD· 1 shared Darwin Tsinajinne· 1 shared Fuki Marie HisamaiD· 1 shared He FangiD· 1 shared Jailanie KaganovskyiD· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenomics

Angela M. Zou

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2 papers

Recent·Most cited

Diagnostic yield of genetic screening in a diverse, community-ascertained cohort

Nandana D. Rao, Jailanie Kaganovsky, Emily A. Malouf, Sandy Coe, Jenna Huey, Darwin Tsinajinne, Sajida Hassan, Kristine M. King, Stephanie Malia Fullerton, Annie Chen, Brian H. Shirts

This study evaluates the diagnostic yield and enrollment rates of population genetic screening in a diverse cohort, finding 2.6% actionable genetic findings but challenges in recruitment and sample collection.

medRxiv · Dec 20, 2022 · PreprintGenetic & Genomic Medicine

Deletion of FUNDC2 and CMC4 on chromosome Xq28 is sufficient to cause hypergonadotropic hypogonadism in men

Xinxian Deng, He Fang, Asha Pathak, Angela M. Zou, Whitney Neufeld‐Kaiser, Emily A. Malouf, R. Alan Failor, Fuki Marie Hisama, Yajuan J. Liu

This study identifies a deletion of FUNDC2 and CMC4 on Xq28 as sufficient to cause hypergonadotropic hypogonadism in men by disrupting apoptosis, inflammation, and FSH regulation.

Frontiers in Genetics · Sep 22, 2020Peer-reviewedGenomics