Cristina Joana Moreira Marques


AuthID: R-000-JPE

Confirmed Publications: 48



31
TITLE: DNA demethylases: a new epigenetic frontier in drug discovery  Full Text
AUTHORS: Nessa Carey; Joana J Marques ; Wolf Reik;
PUBLISHED: 2011, SOURCE: DRUG DISCOVERY TODAY, VOLUME: 16, ISSUE: 15-16
INDEXED IN: Scopus WOS CrossRef: 39
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
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33
TITLE: Dynamic regulation of 5-hydroxymethylcytosine in mouse ES cells and during differentiation  Full Text
AUTHORS: Gabriella Ficz; Miguel R Branco; Stefanie Seisenberger; Fatima Santos; Felix Krueger; Timothy A Hore; Joana J Marques ; Simon Andrews; Wolf Reik;
PUBLISHED: 2011, SOURCE: NATURE, VOLUME: 473, ISSUE: 7347
INDEXED IN: Scopus WOS CrossRef: 944
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
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35
TITLE: Disease: Adrenal hyperplasia
AUTHORS: Carvalho, B; Marques, CJ ; Carvalho, D ; Barros, A ; Carvalho, F ;
PUBLISHED: 2010, SOURCE: Human Genetics, VOLUME: 127, ISSUE: 4
INDEXED IN: Scopus
IN MY: ORCID | CIÊNCIAVITAE
36
TITLE: Imprinted gene anomalies in sperm
AUTHORS: Marques, CJ ; Sousa, M ;
PUBLISHED: 2010, SOURCE: Paternal Influences on Human Reproductive Success
INDEXED IN: Scopus CrossRef: 1
IN MY: ORCID | CIÊNCIAVITAE
37
TITLE: Methylation defects of imprinted genes in human testicular spermatozoa
AUTHORS: Joana J Marques ; Tania Francisco; Sonia Sousa; Filipa Carvalho ; Alberto Barros ; Mario Sousa ;
PUBLISHED: 2010, SOURCE: FERTILITY AND STERILITY, VOLUME: 94, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 102
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
38
TITLE: Mutational Characterization of Steroid 21-Hydroxylase Gene in Portuguese patients with Congenital Adrenal Hyperplasia
AUTHORS: Marques, CJ ; Pignatelli, D; Carvalho, B; Barcelo, J; Almeida, AC; Fernandes, S; Witchel, SF; Sousa, M ; Oliveira, MJ; Freitas, P ; Fontoura, M ; Carvalho, D ; Barros, A ; Carvalho, F ;
PUBLISHED: 2010, SOURCE: EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, VOLUME: 118, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 9
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
39
TITLE: Novel human pathological mutations. Gene symbol: CYP21A2. Disease: adrenal hyperplasia.
AUTHORS: Carvalho, B; Marques, CJ ; Carvalho, D ; Barros, A ; Carvalho, F ;
PUBLISHED: 2010, SOURCE: Human genetics, VOLUME: 127, ISSUE: 4
INDEXED IN: Scopus
IN MY: ORCID | CIÊNCIAVITAE
40
TITLE: Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia
AUTHORS: Marques, CJ ; Costa, P; Vaz, B; Carvalho, F ; Fernandes, S; Barros, A ; Sousa, M ;
PUBLISHED: 2008, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 14, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 291
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
Page 4 of 5. Total results: 48.

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