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Alberto Manuel Barros da Silva
AuthID:
R-000-KE6
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (162)
Abstract (67)
Review (10)
Editorial Material (6)
Proceedings Paper (5)
Note (4)
Letter (4)
Correction (3)
Book Chapter (2)
Article in Press (1)
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Order:
Year Dsc
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Cit. WOS Dsc
IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
Title Asc
Title Dsc
Results:
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Confirmed Publications: 264
141
TITLE:
Y-chromosome detection in turner syndrome
AUTHORS:
Ventura, V;
Doria, S
; Fernandes, S;
Barros, A
;
PUBLISHED:
2011
,
SOURCE:
27th Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology
in
HUMAN REPRODUCTION,
VOLUME:
26
INDEXED IN:
WOS
IN MY:
ResearcherID
142
TITLE:
Aneuploidies detection in miscarriages and fetal deaths using multiplex ligation-dependent probe amplification: an alternative for speeding up results?
Full Text
AUTHORS:
Berta Carvalho
;
Sofia Doria
;
Ramalho C
;
Otilia Brandao
;
Mario Sousa
;
Alexandra Matias
;
Alberto Barros
;
Filipa Carvalho
;
PUBLISHED:
2010
,
SOURCE:
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY,
VOLUME:
153,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
:
21
IN MY:
ORCID
|
ResearcherID
143
TITLE:
Application of touch FISH in the study of mosaic tetraploidy and maternal cell contamination in pregnancy losses
Full Text
AUTHORS:
Sofia Doria
;
Vera Lima
;
Berta Carvalho
; Maria Lina Moreira;
Mario Sousa
;
Alberto Barros
;
Filipa Carvalho
;
PUBLISHED:
2010
,
SOURCE:
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS,
VOLUME:
27,
ISSUE:
11
INDEXED IN:
Scopus
WOS
CrossRef
:
10
IN MY:
ORCID
|
ResearcherID
144
TITLE:
Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens
AUTHORS:
Viktoria Havasi;
Steven M Rowe
;
Peter N Kolettis
;
Didem Dayangac
; Ahmet Sahin;
Ana Grangeia
;
Filipa Carvalho
;
Alberto Barros
;
Mario Sousa
;
Lluis Bassas
; Teresa Casals; Eric J Sorscher;
PUBLISHED:
2010
,
SOURCE:
FERTILITY AND STERILITY,
VOLUME:
94,
ISSUE:
6
INDEXED IN:
Scopus
WOS
CrossRef
:
17
IN MY:
ORCID
|
ResearcherID
145
TITLE:
CFTR mRNA transcripts quantification in infertile CAVD patients
AUTHORS:
Sousa, L; Grangeia, A;
Carvalho, F
; Sousa, M;
Barros, A
;
PUBLISHED:
2010
,
SOURCE:
26th Annual Meeting of ESHRE
in
HUMAN REPRODUCTION,
VOLUME:
25
INDEXED IN:
WOS
IN MY:
ResearcherID
146
TITLE:
DEMETHYLATION OF THE CODING REGION IS PIVOTAL FOR TRANSCRIPTION OF THE HUMAN TESTIS-SPECIFIC PDHA2 GENE
Full Text
AUTHORS:
Pinheiro, A; Faustino, I; Silva, MJ; Silva, J; Sa, R; Sousa, M;
Barros, A
; Almeida, IT; Rivera, I;
PUBLISHED:
2010
,
SOURCE:
JOURNAL OF INHERITED METABOLIC DISEASE,
VOLUME:
33
INDEXED IN:
WOS
IN MY:
ResearcherID
147
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
148
TITLE:
Gene expression pattern of IGF2, PHLDA2, PEG10 and CDKN1C imprinted genes in spontaneous miscarriages or fetal deaths
AUTHORS:
Sofia Doria
;
Mario Sousa
;
Susana Fernandes
;
Ramalho C
;
Otilia Brandao
;
Alexandra Matias
;
Alberto Barros
;
Filipa Carvalho
;
PUBLISHED:
2010
,
SOURCE:
EPIGENETICS,
VOLUME:
5,
ISSUE:
5
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
|
ResearcherID
149
TITLE:
Gene expression pattern ofIGF2,PHLDA2,PEG10andCDKN1Cimprinted genes in spontaneous miscarriages or fetal deaths
AUTHORS:
Sofia Dória
;
Mário Sousa
;
Susana Fernandes
;
Ramalho C
;
Otília Brandão
;
Alexandra Matias
;
Alberto Barros
; Filipa Carvalho;
PUBLISHED:
2010
,
SOURCE:
Epigenetics,
VOLUME:
5,
ISSUE:
5
INDEXED IN:
CrossRef
:
41
IN MY:
ORCID
150
TITLE:
Human testis-specific PDHA2 gene: Methylation status of a CpG island in the open reading frame correlates with transcriptional activity
Full Text
AUTHORS:
Ana Pinheiro; Ines Faustino;
Maria Joao Silva
; Joaquina Silva;
Rosalia Sa
;
Mario Sousa
;
Alberto Barros
;
Isabel Tavares de Almeida
;
Isabel Rivera
;
PUBLISHED:
2010
,
SOURCE:
MOLECULAR GENETICS AND METABOLISM,
VOLUME:
99,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
:
10
IN MY:
ORCID
|
ResearcherID
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