Tianyun Wang - Publications, H-index & Citations

王天云 (Tianyun Wang)

School of Basic Medical Sciences

24H指数

70论文数

3.6K被引数

收录论文 40

发表时间

Lithium chloride in vitro treatment shows potential to rescue the neuronal phenotype caused by WDFY3 haploinsufficiency 氯化锂体外处理显示出挽救由WDFY3单倍剂量不足引起的神经元表型的潜力

Molecular Psychiatry

IF10.1

2026-09-27

OAAI

Moritz J. Paha; Arshi Mustafa; Lyvin Tat; Sandy Richter; Linnaeus Bundalian; Sworadip Chowdhury; Akhil Velluva; Robin-Tobias Jauss; Knut Krohn; Kathleen Schön; Max Holzer; Anna S. Kirstein; Meena Balasubramanian; María Juliana Ballesta-Martínez; Lynne M. Bird; Kirsty Bradshaw; Ange-Line Bruel; Alfredo Brusco; Yanmin Chen; Aurore Garde; Silvia Guarducci; Yoel Gofin; Rachel E. Harrison; Alexis Heidlebaugh; Anna Hurst; Julian A. Martinez-Agosto; Jessica L. Mester; Alistair T. Pagnamenta; Marilena Pantaleo; Andrea Paras; Angela Peron; Tiziana Pisano; Ahna M. Rabani; Marcello Scala; Elena Shukarova-Angelovska; Sui Yang; Slavica Trajkova; Sheila Umayam; Tianyun Wang; Rami Abou Jamra; Johannes R. Lemke; Wieland Kiess; Konstantinos S. Zarbalis; Antje Garten; Diana Le Duc

Effect of clonal hematopoiesis of indeterminate potential on long-term survival in patients with arrhythmias 不确定潜力克隆性造血对心律失常患者长期生存的影响

Journal of Translational Medicine

IF7.5

2026-08-08

OAAI

Lei Ding; Panhui Tian; Fengyuan Yu; Zihan Jiang; Yingjie Qi; Aikai Zhang; Yuandong Liu; Yujing Shen; Hongda Zhang; Min Tang; Tianyun Wang; Junqing Xie

Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorder 单倍型解析的甲基组揭示自闭症谱系障碍中亲源特异性DNA甲基化失衡

Science Advances

IF12.5

2026-06-17

OAAI

Lu Xia; Hailiang Guo; Ruiting Liu; Xue Ren; Shaohuai Han; Xu Huang; Ying Peng; Yan Zhu; Yuanfeng Huang; Zhaowei Jiang; Tengfei Zhu; Tengfei Luo; Zhikun Wang; Xun Zhou; Xiaobo Li; Yanping Zhu; Ting Bai; Qi Tian; Zhiqing Hu; Miaojin Zhou; Qian Jiang; Yidong Shen; Jianjun Ou; Yixiao Zhu; Qiao Zhou; Qian Pan; Tianyun Wang; Hui Guo; Beisha Tang; Zhengmao Hu; Jinchen Li; Kun Xia

Using the linear references from the pangenome to discover missing autism variants 使用来自pangenome的线性参考来发现缺失的自闭症变体

Nature Communications

IF15.7

2026-01-23

OAAI

Yang Sui; Jiadong Lin; Michelle D. Noyes; Youngjun Kwon; Isaac Wong; Nidhi Koundinya; William T. Harvey; Mei Wu; Kendra Hoekzema; Katherine M. Munson; Gage H. Garcia; Jordan Knuth; Julie Wertz; Tianyun Wang; Kelsey Hennick; Druha Karunakaran; Rafael A. Polo Prieto; Rebecca Meyer-Schuman; Fisher Cherry; Davut Pehlivan; Bernhard Suter; Jonas A. Gustafson; Danny E. Miller; Hanna Berk-Rauch; Tomasz J. Nowakowski; Aravinda Chakravarti; Huda Y. Zoghbi; Evan E. Eichler

Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies 研究蛋白酶体ATP酶亚基基因PSMC5在神经发育性蛋白酶体病理学中的神经元作用

Nature Communications

IF15.7

2025-11-26

OAAI

Sébastien Küry; Janelle E. Stanton; Geeske M. van Woerden; Amélie Bosc-Rosati; Tzung-Chien Hsieh; Lise Bray; Marielle Oloudé; Cory Rosenfelt; Marie Pier Scott-Boyer; Victoria Most; Tianyun Wang; Jonas J. Papendorf; Charlotte de Konink; Wallid Deb; Virginie Vignard; Maja Studencka-Turski; Thomas Besnard; Anna M. Hajdukowicz; Franziska G. Thiel; Sophie Wolfgramm; Laëtitia Florenceau; Silvestre Cuinat; Sylvain Marsac; Yann Verrès; Audrey Dangoumau; Léa Poirier; Ingrid M. Wentzensen; Annabelle Tuttle; Cara Forster; Johanna Striesow; Richard Golnik; Damara Ortiz; Laura Jenkins; Jill A. Rosenfeld; Alban Ziegler; Clara Houdayer; Dominique Bonneau; Erin Torti; Amber Begtrup; Kristin G. Monaghan; Sureni V. Mullegama; Catharina M. L. Nienke Volker-Touw; Koen L. I. van Gassen; Renske Oegema; Mirjam S. de Pagter; Katharina Steindl; Anita Rauch; Ivan Ivanovski; Kimberly McDonald; Emily Boothe; Andrew Dauber; Janice Baker; Noelle Andrea V. Fabie; Raphael A. Bernier; Tychele N. Turner; Siddharth Srivastava; Kira A. Dies; Lindsay C. Swanson; Carrie Costin; Alali Abdulrazak; Rebekah K. Jobling; John Pappas; Rachel Rabin; Dmitriy Niyazov; Anne Chun-Hui Tsai; Karen Kovak; David B. Beck; May Christine V. Malicdan; David R. Adams; Lynne Wolfe; Rebecca D. Ganetzky; Colleen C. Muraresku; Davit Babikyan; Zdeněk Sedláček; Miroslava Hančárová; Andrew T. Timberlake; Hind Al Saif; Berkley Nestler; Kayla King; MJ Hajianpour; Gregory Costain; D’Arcy Prendergast; Chumei Li; David Geneviève; Antonio Vitobello; Arthur Sorlin; Christophe Philippe; Tamar Harel; Ori Toker; Ataf Sabir; Derek Lim; Mark J. Hamilton; Lisa J. Bryson; Elaine Cleary; Sacha Weber; Trevor L. Hoffman; Anna M. Cueto-González; Eduardo F. Tizzano; David Gómez-Andrés; Marta Codina-Solà; Athina Ververi; Efterpi Pavlidou; Alexandros Lambropoulos; Kyriakos Garganis; Marlène Rio; Jonathan Levy; Sarah J. Langas; Anne M. McRae; Mathieu K. Lessard; Maria Daniela D’Agostino; Isabelle De Bie; Meret Wegler; Rami Abou Jamra; Susanne B. Kamphausen; Viktoria Bothe; Lorraine Potocki; Eric Olinger; Yves Sznajer; Elsa Wiame; Michelle L. Thompson; Molly C. Schroeder; Catherine Gooch; Raphael A. Smith; Arti Pandya; Larissa M. Busch; Uwe Völker; Elke Hammer; Kristian Wende; Benjamin Cogné; Bertrand Isidor; Jens Meiler; Clémentine Ripoll; Stéphanie Bigou; Frédéric Laumonnier; Peter W. Hildebrand; Evan E. Eichler; Kirsty McWalter; Peter M. Krawitz; Florence Roux-Dalvai; Ype Elgersma; Julien Marcoux; Marie-Pierre Bousquet; Arnaud Droit; Jeremie Poschmann; Andreas M. Grabrucker; Francois V. Bolduc; Stéphane Bézieau; Frédéric Ebstein; Elke Krüger

Evolutionary divergence in CTCF-mediated chromatin topology drives transcriptional innovation in humans CTCF介导的染色质拓扑结构的进化分歧驱动人类的转录创新

NATURE COMMUNICATIONS

IF15.7

2025-03-26

OAAI

Wu, Xia; Xiong, Dan; Liu, Rong; Lai, Xingqiang; Tian, Yuhan; Xie, Ziying; Chen, Li; Hu, Lanqi; Duan, Jingjing; Gao, Xinyu; Zeng, Xian; Dong, Wei; Xu, Ting; Fu, Fang; Yang, Xin; Cheng, Xinlai; Plewczynski, Dariusz; Kim, Minji; Xin, Wenjun; Wang, Tianyun; Xiang, Andy Peng; Tang, Zhonghui

Characterizing executive functioning and associated behaviors in individuals with dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) syndrome 具有双特异性酪氨酸磷酸化调节激酶1A (DYRK1A) 综合征的个体的执行功能和相关行为的特征

FRONTIERS IN NEUROSCIENCE

IF3.2

2025-01-07

OAAI

Rea, Hannah M.; Webb, Sara Jane; Kurtz-Nelson, Evangeline C.; Hudac, Caitlin M.; Bernier, Raphael A.; Miles, Conor; Earl, Rachel; Whiting, Alana; Eayrs, Curtis; Johansson, Margaret; Wang, Tianyun; Eichler, Evan E.; Neuhaus, Emily

MARK2 variants cause autism spectrum disorder via the downregulation of WNT/b-catenin signaling pathway

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2024-11-01

OAAI

Gong, Maolei; Li, Jiayi; Qin, Zailong; Wilke, Matheus Vernet Machado Bressan; Liu, Yijun; Li, Qian; Liu, Haoran; Liang, Chen; Morales-Rosado, Joel A.; Cohen, Ana S. A.; Hughes, Susan S.; Sullivan, Bonnie R.; Waddell, Valerie; van den Boogaard, Marie-Jose H.; van Jaarsveld, Richard H.; van Binsbergen, Ellen; van Gassen, Koen L.; Wang, Tianyun; Hiatt, Susan M.; Amaral, Michelle D.; Kelley, Whitley, V; Zhao, Jianbo; Feng, Weixing; Ren, Changhong; Yu, Yazhen; Boczek, Nicole J.; Ferber, Matthew J.; Lahner, Carrie; Elliott, Sherr; Ruan, Yiyan; Mignot, Cyril; Keren, Boris; Xie, Hua; Wang, Xiaoyan; Popp, Bernt; Zweier, Christiane; Piard, Juliette; Coubes, Christine; Mau-Them, Frederic Tran; Safraou, Hana; Innes, A. Micheil; Gauthier, Julie; Michaud, Jacques L.; Koboldt, Daniel C.; Sylvie, Odent; Willems, Marjolaine; Tan, Wen-Hann; Cogne, Benjamin; Rieubland, Claudine; Braun, Dominique; Mclean, Scott Douglas; Platzer, Konrad; Zacher, Pia; Oppermann, Henry; Evenepoel, Lucie; Blanc, Pierre; El Khattabi, Laila; Haque, Neshatul; Dsouza, Nikita R.; Zimmermann, Michael T.; Urrutia, Raul; Klee, Eric W.; Shen, Yiping; Du, Hongzhen; Rappaport, Leonard; Liu, Chang-Mei; Chen, Xiaoli

Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder CUL3中的功能丧失变体导致综合征性神经发育障碍

ANNALS OF NEUROLOGY

IF7.7

2024-09-20

PREAI

Blackburn, Patrick R.; Ebstein, Frederic; Hsieh, Tzung-Chien; Motta, Marialetizia; Radio, Francesca Clementina; Herkert, Johanna C.; Rinne, Tuula; Thiffault, Isabelle; Rapp, Michele; Alders, Mariel; Maas, Saskia; Gerard, Benedicte; Smol, Thomas; Vincent-Delorme, Catherine; Cogne, Benjamin; Isidor, Bertrand; Vincent, Marie; Bachmann-Gagescu, Ruxandra; Rauch, Anita; Joset, Pascal; Ferrero, Giovanni Battista; Ciolfi, Andrea; Husson, Thomas; Guerrot, Anne-Marie; Bacino, Carlos; Macmurdo, Colleen; Thompson, Stephanie S.; Rosenfeld, Jill A.; Faivre, Laurence; Mau-Them, Frederic Tran; Deb, Wallid; Vignard, Virginie; Agrawal, Pankaj B.; Madden, Jill A.; Goldenberg, Alice; Lecoquierre, Francois; Zech, Michael; Prokisch, Holger; Necpal, Jan; Jech, Robert; Winkelmann, Juliane; Koprusakova, Monika Turcanova; Konstantopoulou, Vassiliki; Younce, John R.; Shinawi, Marwan; Mighton, Chloe; Fung, Charlotte; Morel, Chantal F.; Lerner-Ellis, Jordan; Ditroia, Stephanie; Barth, Magalie; Bonneau, Dominique; Krapels, Ingrid; Stegmann, Alexander P. A.; van Der Schoot, Vyne; Brunet, Theresa; Bussmann, Cornelia; Mignot, Cyril; Zampino, Giuseppe; Wortmann, Saskia B.; Mayr, Johannes A.; Feichtinger, Rene G.; Courtin, Thomas; Ravelli, Claudia; Keren, Boris; Ziegler, Alban; Hasadsri, Linda; Pichurin, Pavel N.; Klee, Eric W.; Grand, Katheryn; Sanchez-Lara, Pedro A.; Krueger, Elke; Bezieau, Stephane; Klinkhammer, Hannah; Krawitz, Peter Michael; Eichler, Evan E.; Tartaglia, Marco; Kuery, Sebastien; Wang, Tianyun

Embryonic origin of two ASD subtypes of social symptom severity: the larger the brain cortical organoid size, the more severe the social symptoms 两种ASD亚型社会症状严重程度的胚胎起源: 大脑皮层类器官大小越大，社会症状越严重

MOLECULAR AUTISM

IF5.5

2024-05-25

OAAI

Courchesne, Eric; Taluja, Vani; Nazari, Sanaz; Aamodt, Caitlin M.; Pierce, Karen; Duan, Kuaikuai; Stophaeros, Sunny; Lopez, Linda; Barnes, Cynthia Carter; Troxel, Jaden; Campbell, Kathleen; Wang, Tianyun; Hoekzema, Kendra; Eichler, Evan E.; Nani, Joao V.; Pontes, Wirla; Sanchez, Sandra Sanchez; Lombardo, Michael V.; de Souza, Janaina S.; Hayashi, Mirian A. F.; Muotri, Alysson R.

The role of copy number variants in the genetic architecture of common familial epilepsies

EPILEPSIA

IF6.6

2024-01-20

PREAI

Fuerte, Edith P. Almanza; Nguyen, John; Mehaffey, Michelle; Sulovari, Arvis; Wang, Tianyun; Galey, Miranda; Miller, Danny E.; Eichler, Evan E.; Mefford, Heather C.; Abou-Khalil, Bassel; Afawi, Zaid Afawi; Allen, Andrew S.; Amrom, Dina; Andermann, Eva; Bautista, Jocelyn F.; Bellows, Susannah T.; Berkovic, Samuel F.; Bluvstein, Judith; Boro, Alexis; Burgess, Rosemary; Cascino, Gregory D.; Chung, Seo-Kyung; Consalvo, Damian; Cossette, Patrick; Crompton, Douglas E.; Crumrine, Patricia; Curtis, Sarah W.; Delanty, Norman; Devinsky, Orrin; Dlugos, Dennis; Ellis, Colin A.; Epstein, Michael P.; Fiol, Miguel; Fountain, Nathan B.; Freyer, Catharine; Friedman, Dan; Geller, Eric B.; Glauser, Tracy; Glynn, Simon; Goldstein, David B.; Gravel, Micheline; Haas, Kevin; Harris, Rebekah V.; Haut, Sheryl; Heinzen, Erin L.; Helmers, Sandra; Henry, Olivia J.; Joshi, Sucheta; Kirsch, Heidi E.; Kivity, Sara; Knowlton, Robert C.; Kossoff, Eric; Kuzniecky, Ruben; Loeb, Rebecca; Lowenstein, Daniel H.; Marson, Anthony G.; McCormack, Mark; McGuire, Shannon M.; McKenna, Kevin; Motika, Paul V.; Mullen, Saul A.; Novotny, Edward J.; O'Brien, Terence J.; Oliver, Karen L.; Ottman, Ruth; Paolicchi, Juliann M.; Parent, Jack M.; Park, Kristen L.; Paterson, Sarah J.; Petrovski, Slave; Pickrell, William O.; Poduri, Annapurna; Rees, Mark I.; Sadleir, Lynette G.; Scheffer, Ingrid E.; Shellhaas, Renee A.; Sherr, Elliott H.; Shih, Jerry J.; Shinnar, Shlomo; Singh, Rani K.; Sirven, Joseph; Smith, Michael C.; Smith, Philip E. M.; Sperling, Michael R.; Sullivan, Joseph; Thio, Liu Lin; Thomas, Rhys H.; Venkat, Anu; Vining, Eileen P. G.; Von Allmen, Gretchen K.; Weisenberg, Judith; Widdess-Walsh, Peter; Winawer, Melodie R.

Genetic Ablation of GIGYF1, Associated With Autism, Causes Behavioral and Neurodevelopmental Defects in Zebrafish and Mice

BIOLOGICAL PSYCHIATRY

IF9

2023-11-01

OAAI

Ding, Zijiao; Huang, Guiyang; Wang, Tianyun; Duan, Weicheng; Li, Hua; Wang, Yirong; Jia, Huiting; Yang, Ziqian; Wang, Kang; Chu, Xufeng; Kurtz-Nelson, Evangeline C.; Ahlers, Kaitlyn; Earl, Rachel K.; Han, Yunyun; Feliciano, Pamela; Chung, Wendy K.; Eichler, Evan E.; Jiang, Man; Xiong, Bo

Polygenic adaptation leads to a higher reproductive fitness of native Tibetans at high altitude

CURRENT BIOLOGY

IF7.5

2023-10-01

OAAI

He, Yaoxi; Guo, Yongbo; Zheng, Wangshan; Yue, Tian; Zhang, Hui; Wang, Bin; Feng, Zhanying; Cui, Chaoying; Liu, Kai; Zhou, Bin; Zeng, Xuerui; Li, Liya; Wang, Tianyun; Wang, Yong; Zhang, Chao; Xu, Shuhua; Qi, Xuebin; Su, Bing

Case report: A novel frameshift mutation in BRSK2 causes autism in a 16-year old Chinese boy

FRONTIERS IN PSYCHIATRY

IF3.2

2023-08-21

OAAI

Hu, Yu; Li, Miao; Shen, Yanmei; Wang, Tianyun; Liu, Qiwei; Lu, Zhonghua; Wang, Hong; Luo, Xuerong; Yang, Lixin

Characterizing the autism spectrum phenotype in DYRK1A-related syndrome

AUTISM RESEARCH

IF5.6

2023-07-27

PREAI

Kurtz-Nelson, Evangeline C.; Rea, Hannah M.; Petriceks, Aiva C.; Hudac, Caitlin M.; Wang, Tianyun; Earl, Rachel K.; Bernier, Raphael A.; Eichler, Evan E.; Neuhaus, Emily

PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production

SCIENCE TRANSLATIONAL MEDICINE

IF14.6

2023-05-31

OAAI

Ebstein, Frederic; Kuery, Sebastien; Most, Victoria; Rosenfelt, Cory; Scott-Boyer, Marie-Pier; van Woerden, Geeske M.; Besrard, Thomas; Papendorf, Jonas Johannes; Studencka-Turski, Maja; Wang, Tianyun; Hsieh, Tzung-Chien; Golnik, Richard; Baldridge, Dustin; Forster, Cara; de Konink, Charlotte; Teurlings, Selina M. W.; Vignard, Virginie; van Jaarsveld, Richard H.; Ades, Lesley; Cogne, Benjamin; Mignot, Cyril; Deb, Wallid; Jongmans, Marjolijn C. J.; Cole, F. Sessions; van den Boogaard, Marie-Jose H.; Wambach, Jennifer A.; Wegner, Daniel J.; Yang, Sandra; Hannig, Vickie; Brault, Jennifer Ann; Zadeh, Neda; Bennetts, Bruce; Keren, Boris; Gelineau, Anne-Claire; Powis, Zoee; Towne, Meghan; Bachman, Kristine; Seeley, Andrea; Beck, Anita E.; Morrison, Jennifer; Westman, Rachel; Averill, Kelly; Brunet, Theresa; Haasters, Judith; Carter, Melissa T.; Osmond, Matthew; Wheeler, Patricia G.; Forzano, Francesca; Mohammed, Shehla; Trakadis, Yannis; Accogli, Andrea; Harrison, Rachel; Guo, Yiran; Hakonarson, Hakon; Rondeau, Sophie; Baujat, Genevieve; Barcia, Giulia; Feichtinger, Rene Guenther; Mayr, Johannes Adalbert; Preisel, Martin; Laumonnier, Frederic; Kallinich, Tilmann; Knaus, Alexej; Isidor, Bertrand; Krawitz, Peter; Voelker, Uwe; Hammer, Elke; Droit, Arnaud; Eichler, Evan E.; Elgersma, Ype; Hildebrand, Peter W.; Bolduc, Francois; Krueger, Elke; Bezieau, Stephane

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders 来自自闭症和发育障碍的46,612三人组的从头变体的整合基因分析

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2022-11-11

OAAI

Wang, Tianyun; Kim, Chang N.; Bakken, Trygve E.; Gillentine, Madelyn A.; Henning, Barbara; Mao, Yafei; Gilissen, Christian; Nowakowski, Tomasz J.; Eichler, Evan E.

Estimating the Prevalence of De Novo Monogenic Neurodevelopmental Disorders from Large Cohort Studies

BIOMEDICINES

IF3.9

2022-11-09

OAAI

Gillentine, Madelyn A.; Wang, Tianyun; Eichler, Evan E.

A predictive ensemble classifier for the gene expression diagnosis of ASD at ages 1 to 4 years

MOLECULAR PSYCHIATRY

IF10.1

2022-10-20

OAAI

Bao, Bokan; Zahiri, Javad; Gazestani, Vahid H.; Lopez, Linda; Xiao, Yaqiong; Kim, Raphael; Wen, Teresa H.; Chiang, Austin W. T.; Nalabolu, Srinivasa; Pierce, Karen; Robasky, Kimberly; Wang, Tianyun; Hoekzema, Kendra; Eichler, Evan E.; Lewis, Nathan E.; Courchesne, Eric

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes 在42,607自闭症病例中整合de novo和遗传变异可确定新的中等风险基因的突变

NATURE GENETICS

IF31.8

2022-08-18

148

OAAI

Zhou, Xueya; Feliciano, Pamela; Shu, Chang; Wang, Tianyun; Astrovskaya, Irina; Hall, Jacob B.; Obiajulu, Joseph U.; Wright, Jessica R.; Murali, Shwetha C.; Xu, Simon Xuming; Brueggeman, Leo; Thomas, Taylor R.; Marchenko, Olena; Fleisch, Christopher; Barns, Sarah D.; Snyder, LeeAnne Green; Han, Bing; Chang, Timothy S.; Turner, Tychele N.; Harvey, William T.; Nishida, Andrew; O'Roak, Brian J.; Geschwind, Daniel H.; Michaelson, Jacob J.; Volfovsky, Natalia; Eichler, Evan E.; Shen, Yufeng; Chung, Wendy K.

研究方向