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Sofia Dória Príncipe dos Santos Cerveira
AuthID:
R-000-K7H
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (36)
Abstract (19)
Review (3)
Editorial Material (1)
Letter (1)
Note (1)
Year Start - End:
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Order:
Year Dsc
Year Asc
Cit. WOS Dsc
IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
Title Asc
Title Dsc
Results:
10
20
30
40
50
Confirmed Publications: 61
21
TITLE:
Altered expression of epigenetic regulators and imprinted genes in human placenta and fetal tissues from second trimester spontaneous pregnancy losses
AUTHORS:
Sara Vasconcelos
;
Ramalho C
;
Joana Marques, CJ
;
Sofia Doria
;
PUBLISHED:
2019
,
SOURCE:
EPIGENETICS,
VOLUME:
14,
ISSUE:
12
INDEXED IN:
Scopus
WOS
CrossRef
:
18
IN MY:
ORCID
22
TITLE:
Chromosome 18p11.31p11.23 Triplication
Full Text
AUTHORS:
Vera Lima
; Joel Pinto; Francisco Valente; Cristina Godinho; Sergio Castedo; Alberto Barros;
Sofia Doria
;
PUBLISHED:
2019
,
SOURCE:
MOLECULAR CYTOGENETICS,
VOLUME:
12
INDEXED IN:
WOS
IN MY:
ORCID
23
TITLE:
Epigenetic modifications could contribute for second trimester pregnancy spontaneous losses
Full Text
AUTHORS:
Sara Vasconcelos
;
Ramalho C
;
Joana Marques
;
Sofia Doria
;
PUBLISHED:
2019
,
SOURCE:
22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH)
in
MEDICINE,
VOLUME:
98,
ISSUE:
26
INDEXED IN:
WOS
IN MY:
ORCID
24
TITLE:
Identification of Copy Number Variation by array CGH in Portuguese Children Diagnosed with Autism Spectrum Disorders
Full Text
AUTHORS:
Sidonie Monteiro; Joel Pinto; Miguel Leao;
Sofia Doria
;
PUBLISHED:
2019
,
SOURCE:
MOLECULAR CYTOGENETICS,
VOLUME:
12
INDEXED IN:
WOS
IN MY:
ORCID
25
TITLE:
Identification of Copy Number Variation by Array-CGH in Portuguese Children and Adolescents Diagnosed with Autism Spectrum Disorders
AUTHORS:
Monteiro, S; Pinto, J;
Mira Coelho, AM
;
Leao, M
;
Doria, S
;
PUBLISHED:
2019
,
SOURCE:
NEUROPEDIATRICS,
VOLUME:
50,
ISSUE:
6
INDEXED IN:
WOS
CrossRef
:
5
IN MY:
ORCID
26
TITLE:
Reproductive success of assisted reproductive technology in couples with chromosomal abnormalities
Full Text
AUTHORS:
Ana Rita Jesus
; Sandra Silva Soares; Joaquina Silva;
Milton Severo
;
Alberto Barros
;
Sofia Doria
;
PUBLISHED:
2019
,
SOURCE:
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS,
VOLUME:
36,
ISSUE:
7
INDEXED IN:
Scopus
WOS
CrossRef
:
8
IN MY:
ORCID
27
TITLE:
Success evaluation of Assisted Reproductive Technology in couples with chromosomal abnormalities
Full Text
AUTHORS:
Ana Rita Jesus
;
Sandra Soares
; Joaquina Silva;
Alberto Barros
;
Sofia Doria
;
PUBLISHED:
2019
,
SOURCE:
22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH)
in
MEDICINE,
VOLUME:
98,
ISSUE:
26
INDEXED IN:
WOS
IN MY:
ORCID
28
TITLE:
Neonatal dilated cardiomyopathy
AUTHORS:
Soares, P; Rocha, G; Pissarra, S;
Soares, H
;
Flor de Lima, F
;
Costa, S
; Moura, C;
Doria, S
; Guimaraes, H;
PUBLISHED:
2017
,
SOURCE:
REVISTA PORTUGUESA DE CARDIOLOGIA,
VOLUME:
36,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
:
17
IN MY:
ORCID
29
TITLE:
Chromosome mis-segregation and cytokinesis failure in trisomic human cells
AUTHORS:
Joshua M Nicholson; Joana C Macedo; Aaron J Mattingly;
Darawalee Wangsa
; Jordi Camps;
Vera Lima
;
Ana M Gomes
;
Sofia Doria
; Thomas Ried;
Elsa Logarinho
; Daniela Cimini;
PUBLISHED:
2015
,
SOURCE:
ELIFE,
VOLUME:
4,
ISSUE:
MAY
INDEXED IN:
Scopus
WOS
CrossRef
:
83
IN MY:
ORCID
30
TITLE:
Intellectual disability and overgrowthA new case of 19p13.13 microdeletion syndrome with digital abnormalities
Full Text
AUTHORS:
Rita Jorge; Carmen Silva; Sofia Agueda;
Sofia Doria
;
Miguel Leao
;
PUBLISHED:
2015
,
SOURCE:
AMERICAN JOURNAL OF MEDICAL GENETICS PART A,
VOLUME:
167,
ISSUE:
11
INDEXED IN:
Scopus
WOS
CrossRef
:
7
IN MY:
ORCID
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