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论文共 15 篇作者统计合作学者相似作者

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Disruption of RFX Family Transcription Factors Causes Autism, Attention-Deficit/hyperactivity Disorder, Intellectual Disability, and Dysregulated Behavior
Holly K. Harris,Tojo Nakayama,Jenny Lai,Boxun Zhao, Nikoleta Argyrou,Cynthia S. Gubbels,Aubrie Soucy,Casie A. Genetti,Victoria Suslovitch,Lance H. Rodan,George E. Tiller,Gaetan Lesca,Karen W. Gripp,Reza Asadollahi,Ada Hamosh,Carolyn D. Applegate,Peter D. Turnpenny,Marleen E. H. Simon,Catharina M. L. Volker-Touw,Koen L. I. van Gassen,Ellen van Binsbergen,Rolph Pfundt,Thatjana Gardeitchik,Bert B. A. de Vries,LaDonna L. Immken,Catherine Buchanan,Marcia Willing,Tomi L. Toler,Emily Fassi,Laura Baker,Fleur Vansenne, Xiadong Wang,Julian L. Ambrus Jr.,Madeleine Fannemel,Jennifer E. Posey,Emanuele Agolini,Antonio Novelli,Anita Rauch,Paranchai Boonsawat,Christina R. Fagerberg,Martin J. Larsen,Maria Kibaek,Audrey Labalme,Alice Poisson,Katelyn K. Payne,Laurence E. Walsh,Kimberly A. Aldinger,Jorune Balciuniene,Cara Skraban,Christopher Gray,Jill Murrell,Caleb P. Bupp,Giulia Pascolini,Paola Grammatico,Martin Broly,Sébastien Küry,Mathilde Nizon,Iqra Ghulam Rasool,Muhammad Yasir Zahoor,Cornelia Kraus,André Reis,Muhammad Iqbal,Kevin Uguen,Severine Audebert-Bellanger,Claude Ferec,Sylvia Redon,Janice Baker, Yunhong Wu, Guiseppe Zampino, Steffan Syrbe,Ines Brosse,Rami Abou Jamra,William B. Dobyns,Lilian L. Cohen,Anne Blomhoff,Cyril Mignot,Boris Keren,Thomas Courtin,Pankaj B. Agrawal,Alan H. Beggs,Timothy W. Yu
Genetics in Medicineno. 6 (2021): 1028-1040
引用29浏览0WOS引用
29
0
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）
引用0浏览0WOSNATURE引用
0
0
Widening of the Genetic and Clinical Spectrum of Lamb–Shaffer Syndrome, a Neurodevelopmental Disorder Due to SOX5 Haploinsufficiency
Ash Zawerton,Cyril Mignot,Ashley Sigafoos,Patrick R. Blackburn,Abdul Haseeb,Kirsty McWalter,Shoji Ichikawa,Caroline Nava,Boris Keren,Perrine Charles,Isabelle Marey,Anne-Claude Tabet,Jonathan Levy,Laurence Perrin,Andreas Hartmann,Gaetan Lesca,Caroline Schluth-Bolard,Pauline Monin,Sophie Dupuis-Girod,Maria J. Guillen Sacoto,Rhonda E. Schnur,Zehua Zhu,Alice Poisson,Salima El Chehadeh,Yves Alembik,Ange-Line Bruel,Daphné Lehalle,Sophie Nambot,Sébastien Moutton,Sylvie Odent,Sylvie Jaillard,Christèle Dubourg,Yvonne Hilhorst-Hofstee,Tina Barbaro-Dieber,Lucia Ortega,Elizabeth J. Bhoj,Diane Masser-Frye,Lynne M. Bird,Kristin Lindstrom,Keri M. Ramsey,Vinodh Narayanan,Emily Fassi,Marcia Willing,Trevor Cole,Claire G. Salter,Rhoda Akilapa,Anthony Vandersteen,Natalie Canham,Patrick Rump,Erica H. Gerkes,Jolien S. Klein Wassink-Ruiter,Emilia Bijlsma,Mariëtte J. V. Hoffer,Marcelo Vargas, Antonina Wojcik,Florian Cherik,Christine Francannet,Jill A. Rosenfeld,Keren Machol,Daryl A. Scott,Carlos A. Bacino,Xia Wang,Gary D. Clark,Marta Bertoli,Simon Zwolinski,Rhys H. Thomas,Ela Akay,Richard C. Chang, Rebekah Bressi,Rossana Sanchez Russo,Myriam Srour,Laura Russell,Anne-Marie E. Goyette,Lucie Dupuis,Roberto Mendoza-Londono,Catherine Karimov,Maries Joseph,Mathilde Nizon,Benjamin Cogné,Alma Kuechler,Amélie Piton,Eric W. Klee,Véronique Lefebvre,Karl J. Clark,Christel Depienne
Genetics in Medicine（2019）
引用22浏览0WOS引用
22
0
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作者统计

#Papers: 15

#Citation: 687

H-Index: 12

G-Index: 12

Sociability: 6

Diversity: 2

Activity: 1

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