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  1. Tianyun Wang (王天云) Assistant Professor, Peking University. Verified email at pku.edu.cn - Homepage. Medical genetics Neurodevelopmental disorders. Title. Sort. Sort by citations Sort by year Sort by title. Cited by.

  2. Nov 15, 2022 · Tianyun Wang 1 2 3 , Chang N Kim 4 , Trygve E Bakken 5 , Madelyn A Gillentine 1 , Barbara Henning 1 , Yafei Mao 1 6 , Christian Gilissen 7 ; SPARK Consortium 8 ; Tomasz J Nowakowski 4 9 10 , Evan E Eichler 1 11. Affiliations. 1 Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195.

  3. Wang TIANYUN | Cited by 2,215 | of State Key Laboratory of Medical Genetics of China, Changsha | Read 77 publications | Contact Wang TIANYUN

  4. Oct 1, 2020 · Tianyun Wang 1 , Kendra Hoekzema 1 , Davide Vecchio 2 3 , Huidan Wu 4 , Arvis Sulovari 1 , Bradley P Coe 1 , Madelyn A Gillentine 1 , Amy B Wilfert 1 , Luis A Perez-Jurado 5 6 7 , Malin Kvarnung 8 9 , Yoeri Sleyp 10 , Rachel K Earl 11 , Jill A Rosenfeld 12 13 , Madeleine R Geisheker 1 , Lin Han 4 , Bing Du 4 , Chris Barnett 5 14 , Elizabeth ...

    • Tianyun Wang, Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe, Madelyn A....
    • 2020
  5. Sep 16, 2021 · Integrated gene analyses of de novo mutations from 46,612 trios with autism and developmental disorders Tianyun Wang , Chang Kim , Trygve E. Bakken , Madelyn A. Gillentine , Barbara Henning , Yafei Mao , Christian Gilissen , The SPARK Consortium , Tomasz J. Nowakowski , Evan E. Eichler

    • Tianyun Wang, Chang Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao, Christ...
    • 2021
  6. Jun 21, 2021 · PMID: 34148555. Reflections on the genetics-first approach to advancements in molecular genetic and neurobiological research on neurodevelopmental disorders. Anne B. Arnett, 1,2 Tianyun Wang, 3 Evan E. Eichler, 3,4 and Raphael A. Bernier 1. Author information Article notes Copyright and License information PMC Disclaimer. Associated Data.

  7. Jun 21, 2021 · The genetics-first approach to research on NDDs has advanced the identification of critical protein function pathways and temporospatial expression patterns, expanding the impact of this research beyond individuals with single-gene mutations to the broader population of patients with NDDs.

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