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论文共 13 篇作者统计合作学者相似作者

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Mutation-specific Pathophysiological Mechanisms Define Different Neurodevelopmental Disorders Associated with SATB1 Dysfunction
Joery den Hoed,Elke de Boer,Norine Voisin,Alexander J. M. Dingemans,Nicolas Guex,Laurens Wiel,Christoffer Nellaker,Shivarajan M. Amudhavalli,Siddharth Banka,Frederique S. Bena,Bruria Ben-Zeev,Vincent R. Bonagura,Ange-Line Bruel,Theresa Brunet,Han G. Brunner,Hui B. Chew,Jacqueline Chrast,Loreta Cimbalistiene,Hilary Coon, Emmanuelle C. Delot,Florence Demurger,Anne-Sophie Denomme-Pichon,Christel Depienne,Dian Donnai,David A. Dyment,Orly Elpeleg,Laurence Faivre,Christian Gilissen,Leslie Granger,Benjamin Haber,Yasuo Hachiya,Yasmin Hamzavi Abedi, Jennifer Hanebeck,Jayne Y. Hehir-Kwa,Brooke Horist,Toshiyuki Itai,Adam Jackson,Rosalyn Jewell,Kelly L. Jones,Shelagh Joss,Hirofumi Kashii,Mitsuhiro Kato,Anja A. Kattentidt-Mouravieva,Fernando Kok,Urania Kotzaeridou,Vidya Krishnamurthy,Vaidutis Kucinskas,Alma Kuechler,Alinoe Lavillaureix,Pengfei Liu,Linda Manwaring,Naomichi Matsumoto,Benoit Mazel,Kirsty McWalter,Vardiella Meiner,Mohamad A. Mikati,Satoko Miyatake,Takeshi Mizuguchi, Lip H. Moey,Shehla Mohammed,Hagar Mor-Shaked,Hayley Mountford,Ruth Newbury-Ecob,Sylvie Odent,Laura Orec,Matthew Osmond,Timothy B. Palculict,Michael Parker,Andrea K. Petersen,Rolph Pfundt,Egle Preiksaitiene,Kelly Radtke,Emmanuelle Ranza,Jill A. Rosenfeld,Teresa Santiago-Sim,Caitlin Schwager,Margje Sinnema,Lot Snijders Blok,Rebecca C. Spillmann,Alexander P. A. Stegmann,Isabelle Thiffault,Linh Tran,Adi Vaknin-Dembinsky,Juliana H. Vedovato-dos-Santos,Samantha A. Schrier Vergano,Eric Vilain,Antonio Vitobello,Matias Wagner,Androu Waheeb,Marcia Willing,Britton Zuccarelli,Usha Kini,Dianne F. Newbury,Tjitske Kleefstra,Alexandre Reymond,Simon E. Fisher,Lisenka E. L. M. Vissers
American journal of human genetics（2021）
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作者统计

#Papers: 13

#Citation: 500

H-Index: 5

G-Index: 8

Sociability: 5

Diversity: 2

Activity: 8

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