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论文共 39 篇作者统计合作学者相似作者

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Large-scale Evaluation of Outcomes Following a Genetic Diagnosis in Children with Severe Developmental Disorders
Harriet Copeland,Karen J Low,Sarah Wynn, Ayesha Ahmed, Victoria Arthur,Meena Balasubramanian, Katya Bennett,Jonathan Berg,Marta Bertoli,Lisa Bryson, Catrin Bucknall,Jamie Campbell,Kate Chandler,Jaynee Chauhan, Amy Clarkson, Rachel Coles, Hector Conti,Philandra Costello, Tessa Coupar, Amy Craig,John Dean, Amy Dillon,Abhijit Dixit, Kathryn Drew,Jacqueline Eason,Francesca Forzano,Nicky Foulds,Alice Gardham,Neeti Ghali,Andrew Green, William Hanna,Rachel Harrison, Mairead Hegarty,Jenny Higgs,Muriel Holder,Rachel Irving,Vani Jain,Katie Johnson, Rachel Jolley,Wendy Jones,Gabriela Jones,Shelagh Joss, Ruta Kalinauskiene, Farah Kanini,Karl Kavanagh, Mahmudur Khan,Naz Khan,Emma Kivuva,Nayana Lahiri, Neeta Lakhani,Anne Lampe,Sally Ann Lynch,Sahar Mansour, Alice Marsden, Hannah Massey,Shane McKee,Shehla Mohammed,Swati Naik, Mithushanaa Nesarajah,Ruth Newbury-Ecob, Fiona Osborne,Michael J Parker,Jenny Patterson,Caroline Pottinger,Matina Prapa,Katrina Prescott, Shauna Quinn,Jessica A Radley,Sarah Robart,Alison Ross,Giulia Rosti,Francis Sansbury,Ajoy Sarkar,Claire Searle,Nora Shannon,Debbie Shears,Sarah Smithson,Helen Stewart,Mohnish Suri,Shereen Tadros, Rachel Theobald, Rhian Thomas, Olga Tsoulaki,Pradeep Vasudevan, Maribel Verdesoto,Emma Vittery, Sinead Whyte,Emily Woods,Thomas Wright,David Zocche,Helen V Firth,Caroline F Wright,the DDD Study
Genetics in Medicine Open (2024)
引用0浏览0引用
0
0
Brain Monoamine Vesicular Transport Disease Caused by Homozygous SLC18A2 Variants: A Study in 42 Affected Individuals
Ken Saida, Reza Marootain,Toru Sengoku,Tadahiro Mitani,Alistair T. Pagnamenta,Dana Marafi,Maha S. Zaki,Thomas J. O'Brian,Ehsan Ghayoor Karimiani,Rauan Kaiyrzhanov, Marina Takizawa,Sachiko Ohori,Huey Yin Leong,Gulsen Akay,Hamid Galehdari,Mina Zamani, Ratna Romy,Christopher J. Carroll,Mehran Beiraghi Toosi,Farah Ashrafzadeh,Shima Imannezhad,Hadis Malek,Najmeh Ahangari,Hoda Tomoum,Vykuntaraju K. Gowda,Varunvenkat M. Srinivasan,David Murphy,Natalia Dominik,Hasnaa M. Elbendary,Karima Rafat,Sanem Yilmaz,Seda Kanmaz,Mine Serin, Deepa Krishnakumar,Alice Gardham, Anna Maw, Tekki Sreenivasa Rao,Sarah Alsubhi,Myriam Srour,Daniela Buhas,Tamison Jewett, Rachel E. Goldberg,Hanan Shamseldin,Eirik Frengen,Doriana Misceo,Petter Stromme,Jose Ricardo Magliocco Ceroni,Chong Ae Kim,Gozde Yesil,Esma Sengenc,Serhat Guler,Mariam Hull,Mered Parnes,Dilek Aktas,Banu Anlar,Yavuz Bayram,Davut Pehlivan,Jennifer E. Posey, Shahryar Alayi, Seyed Ali Madani Manshadi,Hamad Alzaidan,Mohammad Al-Owain,Lama Alabdi,Ferdous Abdulwahab,Futoshi Sekiguchi,Kohei Hamanaka,Atsushi Fujita,Yuri Uchiyama,Takeshi Mizuguchi,Satoko Miyatake,Noriko Miyake,Reem M. Elshafie,Kamran Salayev,Ulviyya Guliyeva,Fowzan S. Alkuraya,Joseph G. Gleeson,Kristin G. Monaghan,Katherine G. Langley, Hui Yang,Mahsa Motavaf, Saeid Safari,Mozhgan Alipour,Kazuhiro Ogata,Andre E. X. Brown,James R. Lupski,Henry Houlden,Naomichi Matsumoto
Genetics in medicine（2023）
引用7浏览0WOS引用
7
0
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作者统计

#Papers: 40

#Citation: 395

H-Index: 8

G-Index: 19

Sociability: 7

Diversity: 2

Activity: 12

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