Wu Huidan - Central South University

基本信息

Career Trajectory

Bio

Wu Huidan currently works at the State Key Laboratory of Medical Genetics, Central South University. Wu does research in Molecular Biology, Bioinformatics and Genetics. Their most recent publication is 'Peer Review File'.

Research Interests

Papers共 17 篇Author StatisticsCo-AuthorSimilar Experts

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SLC39A5 Dysfunction Impairs Extracellular Matrix Synthesis in High Myopia Pathogenesis

Shanshan Dong,Qi Tian,Tengfei Zhu,Kangli Wang, Ganting Lei,Yanling Liu,Haofeng Xiong,Lu Shen,Meng Wang,Rongjuan Zhao,Huidan Wu,Bin Li,Qiumeng Zhang, Yujun Yao,Hui Guo,Kun Xia,Lu Xia,Zhengmao Hu

Journal of Cellular and Molecular Medicine（2021）

Cited10Views0WOSBibtex

Mutation Pattern and Genotype-Phenotype Correlations of SETD2 in Neurodevelopmental Disorders

Meilin Chen,Yingting Quan,Guiqin Duan,Huidan Wu,Ting Bai,Yazhe Wang, Shimin Zhou,Jianjun Ou,Yidong Shen,Zhengmao Hu,Kun Xia,Hui Guo

European journal of medical genetics（2021）

Cited4Views0WOSBibtex

NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism

Hui Guo,Qiumeng Zhang,Rujia Dai,Bin Yu,Kendra Hoekzema,Jieqiong Tan,Senwei Tan,Xiangbin Jia,Wendy K. Chung,Rebecca Hernan,Fowzan S. Alkuraya,Ahood Alsulaiman,Mohammad A. Al-Muhaizea,Gaetan Lesca,Linda Pons,Audrey Labalme,Linda Laux,Emily Bryant,Natasha J. Brown,Elena Savva,Samantha Ayres,Dhamidhu Eratne,Hilde Peeters,Frederic Bilan, Lucile Letienne-Cejudo,Brigitte Gilbert-Dussardier,Inge-Lore Ruiz-Arana, Jenny Meylan Merlini,Alexia Boizot,Lucia Bartoloni,Federico Santoni,Danielle Karlowicz,Marie McDonald,Huidan Wu,Zhengmao Hu,Guodong Chen,Jianjun Ou,Charlotte Brasch-Andersen,Christina R. Fagerberg, Inken Dreyer,Anne Chun-hui Tsai,Valerie Slegesky,Rose B. McGee,Brina Daniels,Elizabeth A. Sellars,Lori A. Carpenter,Bradley Schaefer,Maria J. Guillen Sacoto,Amber Begtrup,Rhonda E. Schnur,Sumit Punj,Ingrid M. Wentzensen,Lindsay Rhodes,Qian Pan,Raphael A. Bernier,Chao Chen,Evan E. Eichler,Kun Xia

American journal of human genetics（2020）

Cited15Views0WOSBibtex

Genotype and Phenotype Correlations for TBL1XR1 in Neurodevelopmental Disorders

Yingting Quan,Qiumeng Zhang,Meilin Chen,Huidan Wu,Jianjun Ou,Yidong Shen,Kuokuo Li,Guanglei Xun,Jingping Zhao,Zhengmao Hu,Kun Xia,Hui Guo

Journal of Molecular Neuroscience（2020）

Cited6Views0WOSBibtex

Excess of RALGAPB De Novo Variants in Neurodevelopmental Disorders

Abid Ali Shah, Ge Zhang,Kuokuo Li,Chenbin Liu, Ashafaque Ahmad Kanhar,Meng Wang,Yingting Quan,Huidan Wu,Lu Shen,Rizwan Khan,Guodong Chen,Jianjun Ou,Zhengmao Hu,Kun Xia,Hui Guo

European Journal of Medical Genetics（2020）

Cited2Views0WOSBibtex

Large-scale Targeted Sequencing Identifies Risk Genes for Neurodevelopmental Disorders

Tianyun Wang,Kendra Hoekzema,Davide Vecchio,Huidan Wu,Arvis Sulovari,Bradley P. Coe,Madelyn A. Gillentine,Amy B. Wilfert,Luis A. Perez-Jurado,Malin Kvarnung,Yoeri Sleyp,Rachel K. Earl,Jill A. Rosenfeld,Madeleine R. Geisheker,Lin Han,Bing Du,Chris Barnett,Elizabeth Thompson,Marie Shaw,Renee Carroll,Kathryn Friend,Rachael Catford,Elizabeth E. Palmer,Xiaobing Zou,Jianjun Ou,Honghui Li,Hui Guo,Jennifer Gerdts,Emanuela Avola,Giuseppe Calabrese,Maurizio Elia,Donatella Greco,Anna Lindstrand,Ann Nordgren,Britt-Marie Anderlid,Geert Vandeweyer,Anke Van Dijck,Nathalie Van der Aa,Brooke McKenna,Miroslava Hancarova,Sarka Bendova,Marketa Havlovicova,Giovanni Malerba,Bernardo Dalla Bernardina,Pierandrea Muglia,Arie van Haeringen,Mariette J. V. Hoffer,Barbara Franke,Gerarda Cappuccio,Martin Delatycki,Paul J. Lockhart,Melanie A. Manning,Pengfei Liu,Ingrid E. Scheffer,Nicola Brunetti-Pierri,Nanda Rommelse,David G. Amaral,Gijs W. E. Santen,Elisabetta Trabetti,Zdeněk Sedláček,Jacob J. Michaelson,Karen Pierce,Eric Courchesne,R. Frank Kooy, John Acampado,Magnus Nordenskjöld,Corrado Romano,Hilde Peeters,Raphael A. Bernier,Jozef Gecz,Kun Xia,Evan E. Eichler

Nature communicationsno. 1 (2020)

Cited5Views0WOSNATUREBibtex

Biallelic Loss-of-function Variants in NEMF Cause Central Nervous System Impairment and Axonal Polyneuropathy

Ahmed Ashfaque,Wang Meng,Bergant Gaber,Maroofian Reza,Zhao Rongjuan,Nashabat Marwan,Alswaid Abdulrahman, Beetz Christian, Qin Yan,Zhu Tengfei,Tian Qi,Xia Lu,Wu Huidan,Shen Lu,Dong Shanshan,Yang Xinyi,Liu Cenying,Ma Linya,Zhang Qiumeng,Khan Rizwan,Shah Abid Ali, Central South University,University of Ljubljana,Writzl Karin,Peterlin Borut, Hunan Key Laboratory of Animal Models for Human Diseases,Malik Sajid

Human Genetics（2020）

Cited10Views0WOSBibtex

AMPA Receptor GluA2 Subunit Defects Are a Cause of Neurodevelopmental Disorders

Vincenzo Salpietro,Christine L. Dixon,Hui Guo,Oscar D. Bello,Jana Vandrovcova,Stephanie Efthymiou,Reza Maroofian,Gali Heimer,Lydie Burglen,Stephanie Valence,Erin Torti,Moritz Hacke,Julia Rankin,Huma Tariq,Estelle Colin,Vincent Procaccio,Pasquale Striano,Kshitij Mankad,Andreas Lieb, Sharon Chen,Laura Pisani,Conceicao Bettencourt,Roope Männikkö,Andreea Manole,Alfredo Brusco,Enrico Grosso,Giovanni Battista Ferrero,Judith Armstrong-Moron,Sophie Gueden,Omer Bar-Yosef,Michal Tzadok,Kristin G. Monaghan,Teresa Santiago-Sim,Richard E. Person,Megan T. Cho,Rebecca Willaert,Yongjin Yoo,Jong-Hee Chae,Yingting Quan,Huidan Wu,Tianyun Wang,Raphael A. Bernier,Kun Xia,Alyssa Blesson,Mahim Jain,Mohammad M. Motazacker,Bregje Jaeger,Amy L. Schneider,Katja Boysen,Alison M. Muir,Candace T. Myers,Ralitza H. Gavrilova,Lauren Gunderson,Laura Schultz-Rogers,Eric W. Klee,David Dyment,Matthew Osmond,Mara Parellada,Cloe Llorente,Javier Gonzalez-Peñas,Angel Carracedo,Arie Van Haeringen,Claudia Ruivenkamp,Caroline Nava,Delphine Heron,Rosaria Nardello,Michele Iacomino,Carlo Minetti,Aldo Skabar,Antonella Fabretto,Michael G. Hanna,Miquel Raspall-Chaure,Michael Chez,Anne Tsai,Emily Fassi,Marwan Shinawi,John N. Constantino,Rita De Zorzi,Sara Fortuna,Fernando Kok,Boris Keren,Dominique Bonneau,Murim Choi,Bruria Benzeev,Federico Zara,Heather C. Mefford,Ingrid E. Scheffer,Jill Clayton-Smith,Alfons Macaya,James E. Rothman,Evan E. Eichler,Dimitri M. Kullmann,Henry Houlden

Nature communications（2019）

Cited0Views0WOSNATUREBibtex

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