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Papers共 56 篇Author StatisticsCo-AuthorSimilar Experts

By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选
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MARK2 Variants Cause Autism Spectrum Disorder Via the Downregulation of WNT/β-catenin Signaling Pathway
Maolei Gong, Jiayi Li, Zailong Qin, Matheus Vernet Machado Bressan Wilke, Yijun Liu, Qian Li, Haoran Liu, Chen Liang, Joel A Morales-Rosado, Ana S A Cohen,Susan S Hughes,Bonnie R Sullivan, Valerie Waddell, Marie-José H van den Boogaard, Richard H van Jaarsveld,Ellen van Binsbergen, Koen L van Gassen,Tianyun Wang,Susan M Hiatt,Michelle D Amaral,Whitley V Kelley, Jianbo Zhao, Weixing Feng,Changhong Ren, Yazhen Yu,Nicole J Boczek,Matthew J Ferber,Carrie Lahner, Sherr Elliott, Yiyan Ruan, Cyril Mignot, Boris Keren,Hua Xie,Xiaoyan Wang, Bernt Popp, Christiane Zweier,Juliette Piard,Christine Coubes, Frederic Tran Mau-Them,Hana Safraou,A Micheil Innes,Julie Gauthier,Jacques L Michaud, Daniel C Koboldt, Odent Sylvie,Marjolaine Willems, Wen-Hann Tan, Benjamin Cogne,Claudine Rieubland, Dominique Braun,Scott Douglas McLean,Konrad Platzer,Pia Zacher,Henry Oppermann, Lucie Evenepoel, Pierre Blanc, Laïla El Khattabi,Neshatul Haque, Nikita R Dsouza,Michael T Zimmermann,Raul Urrutia, Eric W Klee,Yiping Shen, Hongzhen Du, Leonard Rappaport, Chang-Mei Liu,Xiaoli Chen
American journal of human genetics (2024)
Cited0Views0WOSBibtex
0
0
Deleterious, Protein-Altering Variants in the Transcriptional Coregulator ZMYM3 in 27 Individuals with a Neurodevelopmental Delay Phenotype
Susan M. Hiatt,Slavica Trajkova,Matteo Rossi Sebastiano,E. Christopher Partridge,Fatima E. Abidi,Ashlyn Anderson,Muhammad Ansar,Stylianos E. Antonarakis,Azadeh Azadi,Ruxandra Bachmann-Gagescu,Andrea Bartuli,Caroline Benech,Jennifer L. Berkowitz,Michael J. Betti,Alfredo Brusco,Ashley Cannon,Giulia Caron,Yanmin Chen,Meagan E. Cochran,Tanner F. Coleman,Molly M. Crenshaw,Laurence Cuisset,Cynthia J. Curry,Hossein Darvish,Serwet Demirdas,Maria Descartes,Jessica Douglas,David A. Dyment,Houda Zghal Elloumi,Giuseppe Ermondi,Marie Faoucher,Emily G. Farrow,Stephanie A. Felker,Heather Fisher,Anna C. E. Hurst,Pascal Joset,Melissa A. Kelly,Stanislav Kmoch, Benjamin R. Leadem,Michael J. Lyons,Marina Macchiaiolo,Martin Magner,Giorgia Mandrile,Francesca Mattioli,Megan McEown,Sarah K. Meadows,Livija Medne,Naomi J. L. Meeks,Sarah Montgomery, Melanie P. Napier,Marvin Natowicz,Kimberly M. Newberry,Marcello Niceta,Lenka Noskova,Catherine B. Nowak,Amanda G. Noyes,Matthew Osmond,Eloise J. Prijoles,Jada Pugh,Verdiana Pullano,Chloe Quelin,Simin Rahimi-Aliabadi,Anita Rauch,Sylvia Redon,Alexandre Reymond,Caitlin R. Schwager,Elizabeth A. Sellars,Angela E. Scheuerle, Elena Shukarova-Angelovska,Cara Skraban,Elliot Stolerman,Bonnie R. Sullivan,Marco Tartaglia,Isabelle Thiffault,Kevin Uguen,Luis A. Umana,Yolande van Bever,Saskia N. van der Crabben,Marjon A. van Slegtenhorst,Quinten Waisfisz,Camerun Washington,Lance H. Rodan,Richard M. Myers,Gregory M. Cooper
American journal of human genetics（2023）
Cited4Views0WOSBibtex
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Author Statistics

#Papers: 56

#Citation: 2159

H-Index: 19

G-Index: 29

Sociability: 7

Diversity: 2

Activity: 23

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