João Manuel da Silva Gonçalves


AuthID: R-000-73J

Confirmed Publications: 10



1
TITLE: Identification of SOX3 as an XX male sex reversal gene in mice and humans
AUTHORS: Edwina Sutton; James Hughes; Stefan White; Ryohei Sekido; Jacqueline Tan; Valerie Arboleda; Nicholas Rogers; Kevin Knower; Lynn Rowley; Helen Eyre; Karine Rizzoti; Dale McAninch; Joao Goncalves ; Jennie Slee; Erin Turbitt; Damien Bruno; Henrik Bengtsson; Vincent Harley; Eric Vilain; Andrew Sinclair; Robin Lovell Badge; Paul Thomas; ...More
PUBLISHED: 2011, SOURCE: JOURNAL OF CLINICAL INVESTIGATION, VOLUME: 121, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
2
3
TITLE: Genetic Dissection of the AZF Regions of the Human Y Chromosome: Thriller or Filler for Male (In) fertility?
AUTHORS: Paulo Navarro Costa ; Carlos E Plancha; Joao Goncalves ;
PUBLISHED: 2010, SOURCE: JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, VOLUME: 2010
INDEXED IN: Scopus WOS
4
TITLE: Incorrect DNA methylation of the DAZL promoter CpG island associates with defective human sperm(dagger)
AUTHORS: Paulo Navarro Costa ; Paulo Nogueira; Marta Carvalho; Fernanda Leal; Isabel Cordeiro; Carlos Calhaz Jorge; Joao Goncalves ; Carlos E Plancha;
PUBLISHED: 2010, SOURCE: HUMAN REPRODUCTION, VOLUME: 25, ISSUE: 10
INDEXED IN: Scopus WOS
5
TITLE: The AZFc region of the Y chromosome: at the crossroads between genetic diversity and male infertility
AUTHORS: Paulo Navarro Costa ; Joao Goncalves ; Carlos E Plancha;
PUBLISHED: 2010, SOURCE: HUMAN REPRODUCTION UPDATE, VOLUME: 16, ISSUE: 5
INDEXED IN: Scopus WOS
6
TITLE: Characterizing partial AZFc deletions of the Y chromosome with amplicon-specific sequence markers  Full Text
AUTHORS: Paulo Navarro Costa ; Luisa Pereira ; Cintia Alves; Leonor Gusmao ; Carmen Proenca; Pedro Marques Vidal; Tiago Rocha; Sonia C Correia; Sonia Jorge; Antonio Neves; Ana P Soares; Joaquim Nunes; Carlos Calhaz Jorge; Amorim, Antonio ; Carlos E Plancha; Joao Goncalves ;
PUBLISHED: 2007, SOURCE: BMC GENOMICS, VOLUME: 8, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 25
IN MY: ORCID
7
TITLE: Congenital adrenal hyperplasia: Focus on the molecular basis of 21-hydroxylase deficiency
AUTHORS: Goncalves, J ; Friaes, A; Moura, L;
PUBLISHED: 2007, SOURCE: Expert Reviews in Molecular Medicine, VOLUME: 9, ISSUE: 11
INDEXED IN: Scopus
8
TITLE: No evidence for an mtDNA role in sperm motility: Data from complete sequencing of asthenozoospermic males
AUTHORS: Luisa Pereira ; Joao Goncalves ; Ricardo Franco Duarte; Julia Silva; Tiago Rocha; Christiane Arnold; Martin Richards; Vincent Macaulay;
PUBLISHED: 2007, SOURCE: MOLECULAR BIOLOGY AND EVOLUTION, VOLUME: 24, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 50
IN MY: ORCID
9
TITLE: CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions  Full Text
AUTHORS: Friaes, A; Rego, AT; Aragues, JM; Moura, LF; Mirante, A; Mascarenhas, MR ; Kay, TT; Lopes, LA; Rodrigues, JC; Guerra, S; Dias, T; Teles, AG; Goncalves, J ;
PUBLISHED: 2006, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 88, ISSUE: 1
INDEXED IN: Scopus WOS
10
TITLE: Human mtDNA haplogroups and reduced male fertility: real association or hidden population substructuring. mtDNA and oligozoospermia  Full Text
AUTHORS: Pereira, L ; Goncalves, J ; Goios, A ; Rocha, T; Amorim, Antonio ;
PUBLISHED: 2005, SOURCE: INTERNATIONAL JOURNAL OF ANDROLOGY, VOLUME: 28, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 27
IN MY: ORCID

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