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论文共 9 篇作者统计合作学者相似作者

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Expanded Phenotypic Spectrum of Neurodevelopmental and Neurodegenerative Disorder Bryant-Li-Bhoj Syndrome with 38 Additional Individuals
Dana E. Layo-Carris,Emily E. Lubin,Annabel K. Sangree,Kelly J. Clark,Emily L. Durham,Elizabeth M. Gonzalez, Sarina Smith,Rajesh Angireddy, Xiao Min Wang, Erin Weiss,Roberto Mendoza-Londono,Lucie Dupuis,Nadirah Damseh,Danita Velasco,Irene Valenzuela,Marta Codina-Sola,Catherine Ziats, Jaclyn Have,Katie Clarkson,Dora Steel,Manju Kurian,Katy Barwick, Diana Carrasco,Aditi I. Dagli,M. J. M. Nowaczyk,Miroslava Hancarova,Sarka Bendova,Darina Prchalova,Zdenek Sedlacek, Alica Baxova,Catherine Bearce Nowak,Jessica Douglas,Wendy K. Chung,Nicola Longo,Konrad Platzer,Chiara Kloeckner,Luisa Averdunk,Dagmar Wieczorek,Ilona Krey,Christiane Zweier,Andre Reis,Tugce Balci,Marleen Simon,Hester Y. Kroes,Antje Wiesener,Georgia Vasileiou,Nikolaos M. Marinakis,Danai Veltra,Christalena Sofocleous,Konstantina Kosma,Joanne Traeger Synodinos, Konstantinos A. Voudris,Marie-Laure Vuillaume,Paul Gueguen,Nicolas Derive,Estelle Colin, Clarisse Battault,Billie Au,Martin Delatycki,Mathew Wallis,Lyndon Gallacher,Fatma Majdoub,Noor Smal,Sarah Weckhuysen,An-Sofie Schoonjans,R. Frank Kooy,Marije Meuwissen,Benjamin T. Cocanougher,Kathryn Taylor,Carolyn E. Pizoli,Marie T. McDonald, Philip James,Elizabeth R. Roeder,Rebecca Littlejohn,Nicholas A. Borja,Willa Thorson, Kristine King,Radka Stoeva,Manon Suerink,Esther Nibbeling, Stephanie Baskin, Gwenael L. E. Guyader,Julie Kaplan,Candace Muss,Deanna Alexis Carere,Elizabeth J. K. Bhoj,Laura M. Bryant
EUROPEAN JOURNAL OF HUMAN GENETICS (2024)
引用0浏览0WOSNATURE引用
0
0
Rare Deleterious Mutations of HNRNP Genes Result in Shared Neurodevelopmental Disorders
Gillentine Madelyn A.,Wang Tianyun,Hoekzema Kendra, Baylor College of Medicine,Liu Pengfei, Central South University, Weill Institute for Neurosciences, University of California at San Francisco,De Vries Bert B. A.,Vissers Lisenka E. L. M., Karolinska University Hospital, South Australian Health and Medical Research Institute,Iascone Maria,Cereda Anna,Scatigno Agnese,Maitz Silvia,Zanni Ginevra,Bertini Enrico,Zweier Christiane,Schuhmann Sarah,Wiesener Antje, Seattle Children’s Autism Center,Torti Erin, Texas Children’s Hospital,Anselm Irina,Srivastava Siddharth,Atwal Paldeep,Bacino Carlos A.,Bhat Gifty,Cobian Katherine, Rady Children’s Hospital San Diego, Rady Children’s Institute for Genomic Medicine,Callewaert Bert,Petit Florence,Mathieu Sophie,Afenjar Alexandra,Christensen Celenie K.,White Kerry M.,Elpeleg Orly, Ben-Gurion University of the Negev,Fagerberg Christina,Brasch-Andersen Charlotte,Hansen Lars Kjærsgaard,Feyma Timothy, The University of Missouri-Kansas City, School of Medicine, Children’s Mercy Kansas City, Center for Pediatric Genomic Medicine,Sullivan Bonnie,Yan Shuang,Keller Kory,Keren Boris,Mignot Cyril,Kooy Frank,Meuwissen Marije,Basinger Alice,Kukolich Mary, Philips Meredith,Ortega Lucia,Drummond-Borg Margaret,Lauridsen Mathilde,Sorensen Kristina, BC Children’s Hospital and BC Women’s Hospital, Sunny Hill Health Centre for Children,Levy Paul,Lessel Davor,Lotze Timothy, UPMC Children’s Hospital of Pittsburgh,Sebastian Jessica,Vento Jodie,Vats Divya, Benman L. Manace,Mckee Shane, Brotman Baty Institute for Precision Medicine,Muss Candace,Pappas John,Peeters Hilde,Romano Corrado,Elia Maurizio,Galesi Ornella,Simon Marleen E. H.,van Gassen Koen L. I.,Simpson Kara,Stratton Robert,Syed Sabeen,Thevenon Julien,Palafoll Irene Valenzuela, Université Bourgogne Franche-Comté,Xia Kun, Howard Hughes Medical Institute, University of Washington
Genome Medicine（2021）
引用42浏览0WOS引用
42
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作者统计

#Papers: 10

#Citation: 108

H-Index: 4

G-Index: 4

Sociability: 6

Diversity: 1

Activity: 15

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