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论文共 504 篇作者统计合作学者相似作者

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O48: International Consortium on Newborn Sequencing (icons) Consensus Guidelines for Gene Selection in Genomic Newborn Screening Programs
Nina Gold, Julie Yeo, Derek Ansel, Mei Baker,Jorune Balciuniene, Jonathan Berg,François Boemer,Wendy Chung,Heidi Cope, David Eckstein, Nicolas Encina,Laurence Faivre,Alessandra Ferlini,Judit Garcia-Villoria,Michael Gelb, Jose Manuel Gonzalez De Aledo Castillo, Katie Golden-Grant, Thomas Minten, Richard Parad,Nidhi Shah,Zornitza Stark, Kristen Sund, Petros Tsipouras, Meekai To,Lilian Downie
Genetics in Medicine Open (2025): 102421
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Characterization of a Novel FLI1 Mutation in a Family with Thrombocytopenia and Other Congenital Malformations
Daniele Ammeti,Serena Barozzi,Alessandro Pecci, Melania Eva Zanchetta, Edward Cesnik,Alessandra Ferlini, Mariabeatrice Sanchini, Laura Verga,Valeria Bozzi,Fabio Corsolini, Michela Faleschini,Anna Savoia,Stefania Bigoni
Haematologica (2025)
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MECP2 Mrna Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and in Situ RNA Mapping
Martina Mietto, Silvia Montanari, Maria Sofia Falzarano, Elisa Manzati,Paola Rimessi, Marina Fabris,Rita Selvatici,Francesca Gualandi,Marcella Neri, Fernanda Fortunato, Miryam Rosa Stella Foti,Stefania Bigoni, Marco Gessi,Marcella Vacca,Silvia Torelli,Joussef Hayek,Alessandra Ferlini
Biomoleculesno. 5 (2025)
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Data-driven Consideration of Genetic Disorders for Global Genomic Newborn Screening Programs
Thomas Minten, Sarah Bick, Sophia Adelson, Nils Gehlenborg,Laura M Amendola,François Boemer,Alison J Coffey, Nicolas Encina,Alessandra Ferlini, Janbernd Kirschner, Bianca E Russell,Laurent Servais,Kristen L Sund,Ryan J Taft, Petros Tsipouras,Hana Zouk, ICoNS Gene List Contributors,David Bick, International Consortium on Newborn Sequencing (ICoNS),Robert C Green,Nina B Gold
Genetics in medicine official journal of the American College of Medical Geneticsno. 7 (2025): 101443-101443
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TREAT: Systematic and Inclusive Selection Process of Genes for Genomic Newborn Screening As Part of the Screen4Care Project
Christina Saier, Stefaan Sansen, Joanne Berghout, Kathrin Freyler, Moshe Einhorn, Yaron Einhorn,Leslie Matalonga,Sergi Beltran,Antonio Novelli,Rita Selvatici, Fernanda Fortunato, Silvia Montanari, Maria Martinez-Fresno,Gulcin Gumus,Emanuele Agolini, Nicolas Garnier,Alessandra Ferlini, Enrico Bertini,Janbernd Kirschner
Orphanet Journal of Rare Diseasesno. 1 (2025): 1-9
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作者统计

#Papers: 505

#Citation: 14026

H-Index: 63

G-Index: 106

Sociability: 8

Diversity: 4

Activity: 40

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