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论文共 112 篇作者统计合作学者相似作者

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AUTS2-related Syndrome: Insights from a Large European Cohort
Lorenzo Loberti,Loredaria Adamo,Enrica Antolini, Giulia Casamassima,Anne Destrèe,Nicola Brunetti-Pierri,David Genevieve, Philippe Christophe,Christine Coubes,Hilde Van Esch,Theresia Herget,Fanny Kortüm,Jasmin Lisfeld, Anna Charlotte Möllring,Martin Zenker,Jonathan Levy,Laurence Perrin,Anne-Claude Tabet,Anna Maruani,Arthur Sorlin,Daniel Stieber, Lucas Herissant, Karin Dahan,Lorenzo Sinibaldi,Rossella Capolino,Maria Lisa Dentici,Bruno Dallapiccola,Antonio Novelli,Livia Garavelli,Stefano Giuseppe Caraffi,Gianluca Piatelli,Irene Valenzuela,Maria Cristina Digilio,Roseline Caumes,Cordula Knopp,Karolina Chwiałkowska,Aleksandra Jezela-Stanek, Miroslaw Kwasniewski, Urszula Korotko, Ewelina Gorzałczyńska,Roberto Canitano,Salvatore Grosso,Elisa Rahikkala, Larissa Mattern,Miriam Elbracht,Orsetta Zuffardi,Valentina Caputo, Benedetta Toschi,Gea Beunders,Lisette Leeuwen,Mariet W Elting,Liselot van der Laan, Marjoleine F Broekema,Alexander J Groffen, Jiddeke M van de Kamp, Mieke M van Haelst,Marielle Alders, Salvatore Pietro Mauro, Francesca De Razza, Dora Varvara, Johanna Kick,Harald Gaspar,Dominique Braun,Eva Lausberg, Andrea Maier,Valentin Ruault,Rita Genesio,Marco Tartaglia,Rossella Tita,Mirella Bruttini,Ilaria Longo,Margherita Baldassarri,Maria Antonietta Mencarelli,Alessandra Renieri,Anna Maria Pinto
Genetics in medicine official journal of the American College of Medical Geneticspp.101375-101375, (2025)
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Role of Pediatric Nephrologist in Williams Syndrome: Care from Childhood to Adulthood
Arianna Moroni,Hector Rios, Carmen Larramendi, Amaia Lasa,Irene Valenzuela, Ferran Roses,Paola Dolader,Maria Gema Ariceta Iraola
crossref（2025）
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Cryptic Rearrangement in an Apparently Balanced Translocation: the Role of Molecular Cytogenetic Techniques
Mar Xuncla, Natalia Rey,Neus Castells,Alberto Plaja,Irene Valenzuela Palafoll,Anna Maria Cueto-Gonzalez, Maria Serrano, Pedro Antonio Martinez, Lourdes Trobo, Maria Angels Rigola,Elena Garcia-Arumi,Eduardo Tizzano
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 276-276
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Mutations in the U2 Snrna Genernu2-2Pcause a Severe Neurodevelopmental Disorder with Prominent Epilepsy
Daniel Greene, Koenraad De Wispelaere, Jon Lees, Andrea Katrinecz, Sonia Pascoal, Emma Hales,Marta Codina-Sola,Irene Valenzuela, Eduardo F Tizzano, Giles Atton,Deirdre Donnelly,Nicola Foulds,Joanna Jarvis,Shane McKee, Michael O'Donoghue,Mohnish Suri,Pradeep Vasudevan, Kathy Stirrups, Natasha P Morgan,Kathleen Freson,Andrew D Mumford,Ernest Turro
crossref（2024）
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作者统计

#Papers: 111

#Citation: 662

H-Index: 14

G-Index: 23

Sociability: 7

Diversity: 2

Activity: 42

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