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TITLE: Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders
AUTHORS: Sanchis Juan, Alba; Megy, Karyn; Stephens, Jonathan; Ricaurte, Camila Armirola; Dewhurst, Eleanor; Low, Kayyi; French, Courtney E.; Grozeva, Detelina; Stirrups, Kathleen; Erwood, Marie; McTague, Amy; Penkett, Christopher J.; Shamardina, Olga; Tuna, Salih; Daugherty, Louise C.; Gleadall, Nicholas; Duarte, Sofia T.; Hedrera Fernandez, Antonio; Vogt, Julie; Ambegaonkar, Gautam; Chitre, Manali; Josifova, Dragana; Kurian, Manju A.; Parker, Alasdair; Rankin, Julia; Reid, Evan; Wakeling, Emma; Wassmer, Evangeline; NIHR BioResource, F. Lucy; Raymond, F. Lucy; Carss, Keren J.; ...More
PUBLISHED: 2023, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 110, ISSUE: 8
INDEXED IN: Scopus WOS
2
TITLE: Combination treatment of COVID-19 associated herpes zoster scar with 1540 nm and 755 nm picosecond lasers: a case report
AUTHORS: Alpalhao, Miguel; Duarte, Sofia; Correia, Isabel; Filipe, Paulo;
PUBLISHED: 2022, SOURCE: JOURNAL OF COSMETIC AND LASER THERAPY
INDEXED IN: WOS
3
TITLE: Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking
AUTHORS: Robert Behne; Julian Teinert; Miriam Wimmer; Angelica D'Amore; Alexandra K Davies; Joseph M Scarrott; Kathrin Eberhardt; Barbara Brechmann; Ivy Pin Fang Chen; Elizabeth D Buttermore; Lee Barrett; Sean Dwyer; Teresa Chen; Jennifer Hirst; Antje Wiesener; Devorah Segal; Andrea Martinuzzi; Sofia T Duarte; James T Bennett; Thomas Bourinaris; Henry Houlden; Agathe Roubertie; Filippo M Santorelli; Margaret Robinson; Mimoun Azzouz; Jonathan O Lipton; Georg H H Borner; Mustafa Sahin; Darius Ebrahimi Fakhari; ...More
PUBLISHED: 2020, SOURCE: HUMAN MOLECULAR GENETICS, VOLUME: 29, ISSUE: 2
INDEXED IN: Scopus WOS
4
TITLE: Structural analysis of pathogenic missense mutations in GABRA2 and identification of a novel de novo variant in the desensitization gate
AUTHORS: Alba Sanchis Juan; Marcia A Hasenahuer; James A Baker; Amy McTague; Katy Barwick; Manju A Kurian; Sofia T Duarte; Keren J Carss; Janet Thornton; Lucy L Raymond;
PUBLISHED: 2020, SOURCE: MOLECULAR GENETICS & GENOMIC MEDICINE, VOLUME: 8, ISSUE: 7
INDEXED IN: Scopus WOS
5
TITLE: Impairment of adenosinergic system in Rett syndrome: Novel therapeutic target to boost BDNF signalling  Full Text
AUTHORS: Miranda Lourenco, C; Duarte, ST; Palminha, C; Gaspar, C; Rodrigues, TM; Magalhaes Cardoso, T; Rei, N; Colino Oliveira, M; Gomes, R; Ferreira, S; Rosa, J; Xapelli, S; Armstrong, J; Garcia Cazorla, A; Correia de Sa, P ; Sebastiao, AM; Diogenes, MJ;
PUBLISHED: 2020, SOURCE: NEUROBIOLOGY OF DISEASE, VOLUME: 145
INDEXED IN: WOS CrossRef: 8
6
TITLE: De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures
AUTHORS: Yoko Ito; Keren J Carss; Sofia T Duarte; Taila Hartley; Boris Keren; Manju A Kurian; Isabelle Marey; Perinne Charles; Carla Mendonca; Caroline Nava; Rolph Pfundt; Alba Sanchis Juan; Hans van Bokhoven; Anthony van Essen; Conny van Ravenswaaij Arts; Kym M Boycott; Kristin D Kernohan; Sarah Dyack; Lucy L Raymond;
PUBLISHED: 2018, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 103, ISSUE: 1
INDEXED IN: WOS
7
TITLE: Loss of hierarchical imprinting regulation at the Prader-Willi/Angelman syndrome locus in human iPSCs
AUTHORS: Duarte Polvora Brandao; Mariana Joaquim; Ines Godinho; Domenico Aprile; Ana Rita Alvaro; Isabel Onofre; Ana Claudia Raposo; Luis Pereira de Almeida; Sofia T Duarte; Simao T da Rocha;
PUBLISHED: 2018, SOURCE: HUMAN MOLECULAR GENETICS, VOLUME: 27, ISSUE: 23
INDEXED IN: WOS
10
TITLE: INTERSTITIAL LUNG DISEASE IN SCLERODERMA PORTUGUESE PATIENTS
AUTHORS: Sousa, SI; Duarte, A; Cordeiro, I; Teixeira, L; Canas da Silva, JC; Cordeiro, A; Santos, MJ;
PUBLISHED: 2016, SOURCE: Annual European Congress of Rheumatology (EULAR) in ANNALS OF THE RHEUMATIC DISEASES, VOLUME: 75
INDEXED IN: WOS
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