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Tianyun Wang (王天云)
Tianyun Wang (王天云)
Assistant Professor, Peking University
Verified email at pku.edu.cn - Homepage
Title
Cited by
Cited by
Year
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
HAF Stessman, BO Xiong, BP Coe, T Wang, K Hoekzema, M Fenckova, ...
Nature genetics 49 (4), 515-526, 2017
5142017
De novo genic mutations among a Chinese autism spectrum disorder cohort
T Wang, H Guo, B Xiong, HAF Stessman, H Wu, BP Coe, TN Turner, Y Liu, ...
Nature communications 7 (1), 13316, 2016
3472016
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
P Feliciano, X Zhou, I Astrovskaya, TN Turner, T Wang, L Brueggeman, ...
NPJ genomic medicine 4 (1), 19, 2019
1912019
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ...
Nature communications 10 (1), 3094, 2019
1872019
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
MR Geisheker, G Heymann, T Wang, BP Coe, TN Turner, HAF Stessman, ...
Nature neuroscience 20 (8), 1043-1051, 2017
1712017
Disruption of POGZ is associated with intellectual disability and autism spectrum disorders
HAF Stessman, MH Willemsen, M Fenckova, O Penn, A Hoischen, ...
The American Journal of Human Genetics 98 (3), 541-552, 2016
1672016
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
T Wang, K Hoekzema, D Vecchio, H Wu, A Sulovari, BP Coe, ...
Nature communications 11 (1), 4932, 2020
1432020
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
X Zhou, P Feliciano, C Shu, T Wang, I Astrovskaya, JB Hall, JU Obiajulu, ...
Nature genetics 54 (9), 1305-1319, 2022
1412022
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model
H Guo, T Wang, H Wu, M Long, BP Coe, H Li, G Xun, J Ou, B Chen, ...
Molecular autism 9, 1-12, 2018
1392018
Targeted long-read sequencing identifies missing disease-causing variation
DE Miller, A Sulovari, T Wang, H Loucks, K Hoekzema, KM Munson, ...
The American Journal of Human Genetics 108 (8), 1436-1449, 2021
1292021
SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia
H Guo, X Jin, T Zhu, T Wang, P Tong, L Tian, Y Peng, L Sun, A Wan, ...
Journal of medical genetics 51 (8), 518-525, 2014
1182014
Recent ultra-rare inherited variants implicate new autism candidate risk genes
AB Wilfert, TN Turner, SC Murali, PH Hsieh, A Sulovari, T Wang, BP Coe, ...
Nature genetics 53 (8), 1125-1134, 2021
922021
Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders
J Li, L Wang, H Guo, L Shi, K Zhang, M Tang, S Hu, S Dong, Y Liu, ...
Molecular psychiatry 22 (9), 1282-1290, 2017
912017
Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia
H Guo, P Tong, Y Liu, L Xia, T Wang, Q Tian, Y Li, Y Hu, Y Zheng, X Jin, ...
Genetics in Medicine 17 (4), 300-306, 2015
792015
Homozygous loss‐of‐function mutation of the LEPREL1 gene causes severe non‐syndromic high myopia with early‐onset cataract
H Guo, P Tong, Y Peng, T Wang, Y Liu, J Chen, Y Li, Q Tian, Y Hu, ...
Clinical genetics 86 (6), 575-579, 2014
682014
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females
FC Radio, K Pang, A Ciolfi, MA Levy, A Hernández-García, L Pedace, ...
The American Journal of Human Genetics 108 (3), 502-516, 2021
622021
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort
H Guo, Y Peng, Z Hu, Y Li, G Xun, J Ou, L Sun, Z Xiong, Y Liu, T Wang, ...
Scientific reports 7 (1), 44155, 2017
622017
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
MA Gillentine, T Wang, K Hoekzema, J Rosenfeld, P Liu, H Guo, CN Kim, ...
Genome medicine 13, 1-26, 2021
602021
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders
H Guo, E Bettella, PC Marcogliese, R Zhao, JC Andrews, TJ Nowakowski, ...
Nature communications 10 (1), 4679, 2019
562019
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome
MA Cousin, BA Creighton, KA Breau, RC Spillmann, E Torti, S Dontu, ...
Nature genetics 53 (7), 1006-1021, 2021
432021
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