谷歌浏览器插件
订阅小程序
在清言上使用
VIPCreated with Sketch.
研究兴趣

论文共 334 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选
时间
引用量
主题
期刊级别
合作者
合作机构
Exome Copy Number Variant (CNV) Detection, Analysis, and Curation from 6,678 Families with Undiagnosed Rare Genetic Disease
Gabrielle Lemire,Kathryn Russell,Samantha Baxter,Katherine Chao, Emily Evangelista, Moriel Singer-Berk, Alba Sanchis-Juan,Emily Groopman,Isaac Wong,Stephanie DiTroia,Eleina England,Julia Goodrich,Lynn Pais,Christina Austintse, Emily O'Heir,Hana Snow, Ikeoluwa A. Osei-Owusu,Jack Fu,Daniel MacArthur,Heidi Rehm,Michael Talkowski, Harrison Brand, Anne O'Donnell-Luria
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 45-45
引用0浏览0引用
0
0
Digenic Inheritance Involving a Muscle Specific Protein Kinase and the Giant Titin Protein Causes a Skeletal Muscle Myopathy
Ana Töpf, Dan Cox,Irina T. Zaharieva,Valeria Di Leo,Jaakko Sarparanta,Per Harald Jonson,Ian M. Sealy,Andrei Smolnikov,Richard J. White,Anna Vihola,Marco Savarese,Munise Merteroglu,Neha Wali,Kristen M. Laricchia,Cristina Venturini,Bas Vroling,Sarah L. Stenton,Beryl B. Cummings,Elizabeth Harris,Chiara Marini-Bettolo,Jordi Diaz-Manera, Matt Henderson,Rita Barresi,Jennifer Duff,Eleina M. England, Jane Patrick, Sundos Al-Husayni,Valerie Biancalana,Alan H. Beggs,Istvan Bodi,Shobhana Bommireddipalli,Carsten G. Bönnemann,Anita Cairns, Mei-Ting Chiew,Kristl G. Claeys,Sandra T. Cooper,Mark R. Davis,Sandra Donkervoort,Corrie E. Erasmus,Mahmoud R. Fassad,Casie A. Genetti,Carla Grosmann,Heinz Jungbluth,Erik-Jan Kamsteeg,Xavière Lornage,Wolfgang N. Löscher,Edoardo Malfatti,Adnan Manzur,Pilar Martí,Tiziana E. Mongini,Nuria Muelas,Atsuko Nishikawa,Anne O’Donnell-Luria,Narumi Ogonuki,Gina L. O’Grady,Emily O’Heir,Stéphanie Paquay,Rahul Phadke,Beth A. Pletcher,Norma B. Romero,Meyke Schouten, Snehal Shah,Izelle Smuts,Yves Sznajer,Giorgio Tasca,Robert W. Taylor,Allysa Tuite,Peter Van den Bergh,Grace VanNoy,Nicol C. Voermans,Julia V. Wanschitz,Elizabeth Wraige, Kimihiko Yoshimura,Emily C. Oates,Osamu Nakagawa,Ichizo Nishino,Jocelyn Laporte,Juan J. Vilchez,Daniel G. MacArthur,Anna Sarkozy,Heather J. Cordell,Bjarne Udd,Elisabeth M. Busch-Nentwich,Francesco Muntoni,Volker Straub
NATURE GENETICS（2024）
引用0浏览0WOSNATURE引用
0
0
Neurodevelopmental Disorder Caused by Deletion of CHASERR , a Lncrna Gene
Vijay S Ganesh, Kevin Riquin,Nicolas Chatron, Esther Yoon, Kay-Marie Lamar,Miriam C Aziz,Pauline Monin, Melanie C O'Leary, Julia K Goodrich, Kiran V Garimella,Eleina England,Ben Weisburd, François Aguet,Carlos A Bacino, David R Murdock, Hongzheng Dai,Jill A Rosenfeld, Lisa T Emrick,Shamika Ketkar, Yael Sarusi,Damien Sanlaville, Saima Kayani, Brian Broadbent, Alisée Pengam,Bertrand Isidor,Stéphane Bezieau, Benjamin Cogné,Daniel G MacArthur,Igor Ulitsky, Gemma L Carvill, Anne O'Donnell-Luria
The New England journal of medicineno. 16 (2024): 1511-1518
引用0浏览0WOS引用
0
0
加载更多
作者统计

#Papers: 337

#Citation: 39396

H-Index: 74

G-Index: 198

Sociability: 9

Diversity: 3

Activity: 241

  • 合作者
  • 学生
  • 导师
暂无相似学者，你可以通过学者研究领域进行搜索筛选
数据免责声明
页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn