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TITLE: Development and Validation of a Mathematical Model to Predict the Complexity of FMR1 Allele Combinations  Full Text
AUTHORS: Rodrigues, B; Vale Fernandes, E ; Maia, N; Santos, F; Marques, I; Santos, R; Nogueira, AJA; Jorge, P ;
PUBLISHED: 2020, SOURCE: FRONTIERS IN GENETICS, VOLUME: 11
INDEXED IN: Scopus WOS CrossRef Handle
12
TITLE: Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4–BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature
AUTHORS: Natália Oliva-Teles ; Maria Chiara de Stefano; Louise Gallagher; Severin Rakic; Paula Jorge ; Goran Cuturilo; Silvana Markovska-Simoska; Isabella Borg; Jeanne Wolstencroft; Zeynep Tümer; Adrian J Harwood; Yllka Kodra; David Skuse;
PUBLISHED: 2020, SOURCE: International Journal of Environmental Research and Public Health, VOLUME: 17, ISSUE: 24
INDEXED IN: CrossRef: 2
13
TITLE: Two Compound Heterozygous Variants inSNX14Cause Stereotypies and Dystonia in Autosomal Recessive Spinocerebellar Ataxia 20  Full Text
AUTHORS: Maia, N; Soares, G; Silva, C; Marques, I ; Rodrigues, B; Santos, R; Melo Pires, M; de Brouwer, AP; Temudo, T; Jorge, P ;
PUBLISHED: 2020, SOURCE: FRONTIERS IN GENETICS, VOLUME: 11
INDEXED IN: Scopus WOS CrossRef: 2
14
TITLE: Usher syndrome and Nebulin-associated myopathy in a single patient due to variants in MYO7A and NEB
AUTHORS: Maia, N; Soares, AR ; Fortuna, AM; Marques, I ; Goncalves, A ; Santos, R; Pires, MM ; de Brouwer, APM; Jorge, P ;
PUBLISHED: 2020, SOURCE: CLINICAL CASE REPORTS, VOLUME: 8, ISSUE: 12
INDEXED IN: Scopus WOS CrossRef
15
TITLE: Gordon Holmes syndrome due to compound heterozygosity of two new PNPLA6 variants – A diagnostic challenge
AUTHORS: Salgado, P; Carvalho, R; Brandão, AF; Jorge, P ; Ramos, C; Dias, D; Alonso, I; Magalhães, M;
PUBLISHED: 2019, SOURCE: eNeurologicalSci, VOLUME: 14
INDEXED IN: Scopus CrossRef: 9
16
TITLE: EGGS, Oranges and other technological devices in science dissemination
AUTHORS: Celina P Leão ; Filomena Soares ; João Sena Esteves; Paula Jorge ;
PUBLISHED: 2016, SOURCE: ASME International Mechanical Engineering Congress and Exposition, Proceedings (IMECE), VOLUME: 5
INDEXED IN: Scopus CrossRef: 1 Handle
17
TITLE: Erratum to: Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect  Full Text
AUTHORS: Noura Bougacha-Elleuch; Nadia Charfi; Nabil Miled; Houda Bouhajja; Neila Belguith; Mouna Mnif; Paula Jorge ; Nessrine Chikhrouhou; Hammadi Ayadi; Mongia Hachicha; Mohamed Abid;
PUBLISHED: 2015, SOURCE: European Journal of Pediatrics - Eur J Pediatr, VOLUME: 174, ISSUE: 12
INDEXED IN: CrossRef
18
TITLE: Erratum to: Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect(Eur J Pediatr, (2015), 174, 1491-1501, Doi:10.1007/s00431-015-2550-4)
AUTHORS: Bougacha Elleuch, N; Charfi, N; Miled, N; Bouhajja, H; Belguith, N; Mnif, M; Jorge, P ; Chikhrouhou, N; Ayadi, H; Hachicha, M; Abid, M;
PUBLISHED: 2015, SOURCE: European Journal of Pediatrics, VOLUME: 174, ISSUE: 12
INDEXED IN: Scopus
19
TITLE: Unraveling the pathogenesis of ARX polyalanine tract variants using a clinical and molecular interfacing approach
AUTHORS: Marques, I ; Sa, MJ; Soares, G; Mota, MD; Pinheiro, C; Aguiar, L; Amado, M; Soares, C; Calado, A; Dias, P; Sousa, AB; Fortuna, AM; Santos, R; Howell, KB; Ryan, MM; Leventer, RJ; Sachdev, R; Catford, R; Friend, K; Mattiske, TR; Shoubridge, C; Jorge, P ; ...More
PUBLISHED: 2015, SOURCE: MOLECULAR GENETICS & GENOMIC MEDICINE, VOLUME: 3, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 20
20
TITLE: A 26-Year Experience in Chorionic Villus Sampling Prenatal Genetic Diagnosis
AUTHORS: Paula Jorge ; Maria Mota-Freitas; Rosário Santos; Maria Silva; Gabriela Soares; Ana Fortuna;
PUBLISHED: 2014, SOURCE: Journal of Clinical Medicine, VOLUME: 3, ISSUE: 3
INDEXED IN: CrossRef: 3
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