Author

Renqian Du

Baylor College of Medicine

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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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Haowei DuiD· 2 shared James R. LupskiiD· 2 shared Jennifer Ellen PoseyiD· 2 shared Shalini N. JhangianiiD· 2 shared Shen GuiD· 2 shared Tomasz GambiniD· 2 shared Zeynep Coban‐AkdemiriD· 2 shared Ada HamoshiD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Haowei DuORCID

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2 papers

Recent·Most cited

Centers for Mendelian Genomics: A decade of facilitating gene discovery

Samantha M. Baxter, Jennifer Ellen Posey, Nicole J. Lake, Nara Lygia de Macena Sobreira, Jessica X. Chong, Steven G. Buyske, Elizabeth Blue, Lisa Helbling Chadwick, Zeynep Coban‐Akdemir, Kimberly Floy Doheny, Colleen P. Davis, Monkol Lek, Christopher Wellington, Shalini N. Jhangiani, Mark Gerstein, , 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.

Genetics in Medicine · Feb 8, 2022Peer-reviewedGenetic & Genomic Medicine

Integrated Sequencing & Array Comparative Genomic Hybridization in Familial Parkinson’s Disease

Laurie A. Robak, Renqian Du, Bo Yuan, Shen Gu, Isabel Alfradique‐Dunham, Vismaya Kondapalli, Evelyn Hinojosa, Amanda Stillwell, Emily Young, Chaofan Zhang, Xiaofei Song, Haowei Du, Tomasz Gambin, Shalini N. Jhangiani, Zeynep Coban‐Akdemir, , Joshua M Shulman

The paper combines exome sequencing and array-based comparative genomic hybridization to identify genetic risk factors in familial Parkinson’s disease, finding novel SNVs and CNVs.

bioRxiv · Nov 11, 2019 · PreprintGenetics