Sofia Dória Príncipe dos Santos Cerveira


AuthID: R-000-K7H

Confirmed Publications: 79



11
TITLE: Kidney Failure Secondary to Hereditary Xanthinuria due to a Homozygous Deletion of the XDH Gene in the Absence of Overt Kidney Stone Disease
AUTHORS: Goncalves, Pedro Lisboa; Diniz, Hugo; Tavares, Isabel; Doria, Sofia ; Dong, Juan; Kyriss, McKenna; Fairbanks, Lynette; Oliveira, JP;
PUBLISHED: 2024, SOURCE: NEPHRON, VOLUME: 148, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 1 Unpaywall
IN MY: ORCID | CIÊNCIAVITAE
12
TITLE: Syncytiotrophoblast Markers Are Downregulated in Placentas from Idiopathic Stillbirths  Full Text
AUTHORS: Vasconcelos, Sara; Moustakas, Ioannis; Branco, Miguel R.; Guimaraes, Susana; Canicais, Carla; van der Helm, Talia; Ramalho C; Marques, Cristina Joana ; Lopes, Susana M. Chuva de Sousa; Doria, Sofia ;
PUBLISHED: 2024, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 25, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 1 Unpaywall
IN MY: ORCID | CIÊNCIAVITAE
13
TITLE: X-chromosome inactivation pattern and telomere length in recurrent pregnancy loss
AUTHORS: Vaz, Diane; Vasconcelos, Sara; Canicais, Carla; Costa, Beatriz; Ramalho C; Marques, Joana; Doria, Sofia ;
PUBLISHED: 2024, SOURCE: REPRODUCTIVE BIOLOGY, VOLUME: 24, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | CIÊNCIAVITAE
14
TITLE: ARE X-CHROMOSOME INACTIVATION PATTERN AND TELOMERE LENGTH UNDERLYING RECURRENT PREGNANCY LOSS?  Full Text
AUTHORS: Vaz, Diane; Vasconcelos, Sara; Canicais, Carla; Costa, Beatriz; Ramalho, Carla; Marques, Joana ; Doria, Sofia ;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
15
16
TITLE: Copy number variations on chromosome 2: impact on human phenotype, a cross-sectional study
AUTHORS: Beatriz Sousa; Ana Grangeia ; Joel Pinto ; Helena Santos; Sofia Dória ;
PUBLISHED: 2023, SOURCE: Porto Biomedical Journal, VOLUME: 8, ISSUE: 1
INDEXED IN: CrossRef
IN MY: ORCID | CIÊNCIAVITAE
17
TITLE: Klinefelter syndrome: The characterization of the clinical and sociological features of 51 patients
AUTHORS: Mendonca, Fernando ; Souto, Selma ; Doria, Sofia ; Carvalho, Davide ;
PUBLISHED: 2023, SOURCE: REVISTA INTERNACIONAL DE ANDROLOGIA, VOLUME: 21, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID | CIÊNCIAVITAE
18
TITLE: Severe KIDAR syndrome caused by deletion in the AP1B1 gene: Report of a teenage patient and systematic review of the literature
AUTHORS: Vasconcelos, Alice P.; Nogueira, Ana; Matos, Pedro; Pinto, Joel ; Pinho, Maria Joao; Fernandes, Susana; Doria, Sofia ; Carla Pinto Moura ;
PUBLISHED: 2023, SOURCE: EUROPEAN JOURNAL OF MEDICAL GENETICS, VOLUME: 66, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | CIÊNCIAVITAE
19
TITLE: The role of DNA hydroxymethylation and TET enzymes in placental development and pregnancy outcome  Full Text
AUTHORS: Vasconcelos, Sara; Canicais, Carla; Lopes, Susana M. Chuva de Sousa; Marques, C. Joana ; Doria, Sofia ;
PUBLISHED: 2023, SOURCE: CLINICAL EPIGENETICS, VOLUME: 15, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 7 Unpaywall
IN MY: ORCID | CIÊNCIAVITAE
20
TITLE: Clinical Findings on Chromosome Copy Number Variations
AUTHORS: Leitao, Filipa; Grangeia, Ana ; Pinto, Joel ; Passas, Armanda; Doria, Sofia ;
PUBLISHED: 2022, SOURCE: NEUROPEDIATRICS, VOLUME: 53, ISSUE: 04
INDEXED IN: Scopus WOS CrossRef: 2
IN MY: ORCID | CIÊNCIAVITAE
Page 2 of 8. Total results: 79.

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