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论文共 356 篇作者统计合作学者相似作者

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The Contribution of De Novo Coding Mutations to Meningomyelocele
Yoo-Jin Jiny Ha, Ashna Nisal, Isaac Tang,Chanjae Lee, Ishani Jhamb, Cassidy Wallace, Robyn Howarth, Sarah Schroeder, Keng Ioi Vong, Naomi Meave, Fiza Jiwani, Chelsea Barrows, Sangmoon Lee, Nan Jiang,Arzoo Patel, Krisha Bagga, Niyati Banka, Liana Friedman, Francisco A Blanco,Seyoung Yu, Soeun Rhee, Hui Su Jeong,Isaac Plutzer, Michael B Major,Béatrice Benoit,Christian Poüs,Caleb Heffner,Zoha Kibar, Gyang Markus Bot,Hope Northrup,Kit Sing Au, Madison Strain,Allison E Ashley-Koch,Richard H Finnell, Joan T Le,Hal S Meltzer, Camila Araujo, Helio R Machado,Roger E Stevenson, Anna Yurrita,Sara Mumtaz, Awais Ahmed, Mulazim Hussain Khara, Osvaldo M Mutchinick, José Ramón Medina-Bereciartu,Friedhelm Hildebrandt,Gia Melikishvili,Ahmed I Marwan,Valeria Capra, Mahmoud M Noureldeen, Aida M S Salem,Mahmoud Y Issa,Maha S Zaki,Libin Xu, Ji Eun Lee, Donghyuk Shin,Anna Alkelai,Alan R Shuldiner,Stephen F Kingsmore,Stephen A Murray,Heon Yung Gee,W Todd Miller,Kimberley F Tolias,John B Wallingford, Spina Bifida Sequencing Consortium, Sangwoo Kim,Joseph G Gleeson
Natureno. 8062 (2025): 419-426
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Inherited Deficiency of DIAPH1 Identifies a DNA Double Strand Break Repair Pathway Regulated by Γ-Actin
Beth L Woodward, Sudipta Lahiri, Anoop S Chauhan, Marcos Rios Garcia, Lucy E Goodley, Thomas L Clarke, Mohinder Pal,Angelo Agathanggelou, Satpal S Jhujh, Anil N Ganesh, Fay M Hollins, Valentina Galassi Deforie,Reza Maroofian,Stephanie Efthymiou, Andrea Meinhardt, Christopher G Mathew,Michael A Simpson,Heather C Mefford, Eissa A Faqeih,Sergio D Rosenzweig,Stefano Volpi, Gigliola Di Matteo, Caterina Cancrini, Annarita Scardamaglia,Fiona Shackley, E Graham Davies,Shahnaz Ibrahim, Peter D Arkwright,Maha S Zaki,Tatjana Stankovic, A Malcolm R Taylor, Antonina J Mazur,Nataliya Di Donato,Henry Houlden,Eli Rothenberg, Grant S Stewart
Nature communicationsno. 1 (2025): 4491-4491
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Bi-allelic Pathogenic Variants in TRMT1 Disrupt Trna Modification and Induce a Neurodevelopmental Disorder
Stephanie Efthymiou, Cailyn P Leo, Chenghong Deng,Sheng-Jia Lin,Reza Maroofian, Renee Lin, Irem Karagoz, Kejia Zhang,Rauan Kaiyrzhanov, Annarita Scardamaglia, Daniel Owrang, Valentina Turchetti, Friederike Jahnke, Kevin Huang,Cassidy Petree, Anna V Derrick, Mark I Rees,Javeria Raza Alvi,Tipu Sultan,Chumei Li, Marie-Line Jacquemont, Frederic Tran-Mau-Them, Maria Valenzuela-Palafoll, Rich Sidlow,Grace Yoon, Michelle M Morrow, Deanna Alexis Carere, Mary O'Connor, Julie Fleischer, Erica H Gerkes,Chanika Phornphutkul,Bertrand Isidor, Clotilde Rivier-Ringenbach, Christophe Philippe,Semra Hiz Kurul,Didem Soydemir,Bulent Kara,Deniz Sunnetci-Akkoyunlu, Viktoria Bothe,Konrad Platzer,Dagmar Wieczorek, Margarete Koch-Hogrebe, Nils Rahner,Ann-Charlotte Thuresson,Hans Matsson,Carina Frykholm, Sevcan Tuğ Bozdoğan,Atil Bisgin,Nicolas Chatron,Gaetan Lesca, Sara Cabet,Zeynep Tümer, Tina D Hjortshøj,Gitte Rønde,Thorsten Marquardt,Janine Reunert,Erum Afzal,Mina Zamani, Reza Azizimalamiri,Hamid Galehdari, Pardis Nourbakhsh, Niloofar Chamanrou, Seo-Kyung Chung,Mohnish Suri,Paul J Benke,Maha S Zaki,Joseph G Gleeson,Daniel G Calame,Davut Pehlivan, Halil I Yilmaz,Alper Gezdirici, Aboulfazl Rad, Iman Sabri Abumansour,Gabriela Oprea, Muhammed Burak Bereketoğlu, Guillaume Banneau,Sophie Julia,Jawaher Zeighami, Saeed Ashoori,Gholamreza Shariati,Alireza Sedaghat, Alihossein Sabri,Mohammad Hamid, Sahere Parvas, Tajul Arifin Tajudin,Uzma Abdullah,Shahid Mahmood Baig, Wendy K Chung, Olga O Glazunova,Sigaudy Sabine,Huma Arshad Cheema,Giovanni Zifarelli,Peter Bauer, Jai Sidpra,Kshitij Mankad,Barbara Vona, Andrew E Fry,Gaurav K Varshney,Henry Houlden,Dragony Fu
American journal of human genetics（2025）
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作者统计

#Papers: 358

#Citation: 9246

H-Index: 47

G-Index: 85

Sociability: 8

Diversity: 3

Activity: 108

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