Author

Yavuz Bayram

Children's Hospital of PhiladelphiaORCID 0000-0001-7350-6027Unclaimed 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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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:statistical model· 1

Frequent Co-Authors

Ada HamoshiD· 2 shared Claudia M.B. CarvalhoiD· 2 shared David L. ValleiD· 2 shared Eric BoerwinkleiD· 2 shared James R. LupskiiD· 2 shared Jennifer Ellen PoseyiD· 2 shared Nara Lygia de Macena SobreiraiD· 2 shared Richard A. GibbsiD· 2 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Ada HamoshORCID

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2 papers

Recent·Most cited

GenomicsGenetics in Medicine OpenPeer-reviewedJan 1, 2024

The impact of the Turkish (TK) population variome on the genomic architecture of rare disease traits

Zeynep Coban‐Akdemir, Xiaofei Song, Francisco C. Ceballos…·James R. Lupski

The paper analyzes the Turkish population's variome to understand its impact on rare disease traits, finding that long ROHs and inbreeding contribute to recessive diseases.

12 citations

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedFeb 8, 2022

Centers for Mendelian Genomics: A decade of facilitating gene discovery

Samantha M. Baxter, Jennifer Ellen Posey, Nicole J. Lake…·Kurt N. Hetrick

The paper describes the role of the Centers for Mendelian Genomics in advancing gene discovery through data sharing, collaboration, and resource development over the past decade.

72 citations

humanwhole-exome sequencing

𝕏 PostBluesky