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Susana Alves Seixas
AuthID:
R-000-GTS
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (20)
Letter (2)
Abstract (1)
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Order:
Year Dsc
Year Asc
Cit. WOS Dsc
IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
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Results:
10
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Confirmed Publications: 23
11
TITLE:
A model to infer the pathogenic significance of CDH1 germline missense variants
Full Text
AUTHORS:
Gianpaolo Suriano
;
Susana Seixas
;
Jorge Rocha
;
Raquel Seruca
;
PUBLISHED:
2006
,
SOURCE:
JOURNAL OF MOLECULAR MEDICINE-JMM,
VOLUME:
84,
ISSUE:
12
INDEXED IN:
Scopus
WOS
CrossRef
:
58
IN MY:
ORCID
|
ResearcherID
12
TITLE:
A model to infer the pathogenic significance of CDH1 germline missense variants
Full Text
AUTHORS:
Suriano, G
;
Seixas, S
;
Rocha, J
;
Seruca, R
;
PUBLISHED:
2006
,
SOURCE:
19th International Workshop on Helicobacter and Related Bacteric in Chronic Digestive Inflammation
in
HELICOBACTER,
VOLUME:
11,
ISSUE:
4
INDEXED IN:
WOS
IN MY:
ResearcherID
13
TITLE:
Lobar brain hemorrhages and white matter changes: Clinical, radiological and laboratorial profiles
AUTHORS:
Luis F Maia
;
Cristiana Vasconcelos
;
Susana Seixas
;
Magalhães, R
;
Manuel Correia
;
PUBLISHED:
2006
,
SOURCE:
CEREBROVASCULAR DISEASES,
VOLUME:
22,
ISSUE:
2-3
INDEXED IN:
Scopus
WOS
CrossRef
:
22
IN MY:
ORCID
|
ResearcherID
14
TITLE:
Microsatellite variation and evolution of human lactase persistence
Full Text
AUTHORS:
Coelho, M
; Luiselli, D; Bertorelle, G;
Lopes, AI
;
Seixas, S
; Destro Bisol, G;
Rocha, J
;
PUBLISHED:
2005
,
SOURCE:
HUMAN GENETICS,
VOLUME:
117,
ISSUE:
4
INDEXED IN:
Scopus
WOS
CrossRef
:
90
IN MY:
ORCID
|
ResearcherID
15
TITLE:
Genetic variation in a compound short tandem repeat/Alu haplotype system at the SB19.3 locus: Properties and interpretation
AUTHORS:
Gaspar, P
;
Seixas, S
;
Rocha, J
;
PUBLISHED:
2004
,
SOURCE:
HUMAN BIOLOGY,
VOLUME:
76,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
:
2
IN MY:
ORCID
|
ResearcherID
16
TITLE:
Influence of apolipoprotein E polymorphism on cardiovascular risk factors in obese children
AUTHORS:
Guerra, A
;
Rego, C
;
Castro, EMB
;
Seixas, S
;
Rocha, J
;
PUBLISHED:
2003
,
SOURCE:
ANNALS OF NUTRITION AND METABOLISM,
VOLUME:
47,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
:
16
IN MY:
ORCID
|
ResearcherID
17
TITLE:
alpha 1-Antitrypsin null alleles: evidence for the recurrence of the L353fsX376 mutation and a novel G -> A transition in position+1 of intron IC affecting normal mRNA splicing. Novel and recurrent PI null mutations
Full Text
AUTHORS:
Seixas, S
; Mendonca, C;
Costa, F
;
Rocha, J
;
PUBLISHED:
2002
,
SOURCE:
CLINICAL GENETICS,
VOLUME:
62,
ISSUE:
2
INDEXED IN:
Scopus
WOS
CrossRef
:
26
IN MY:
ORCID
|
ResearcherID
18
TITLE:
Microsatellite variation and evolution of the human Duffy blood group polymorphism
AUTHORS:
Seixas, S
;
Ferrand, N
;
Rocha, J
;
PUBLISHED:
2002
,
SOURCE:
MOLECULAR BIOLOGY AND EVOLUTION,
VOLUME:
19,
ISSUE:
10
INDEXED IN:
Scopus
WOS
IN MY:
ORCID
|
ResearcherID
19
TITLE:
The peopling of Sao Tome (Gulf of Guinea): Origins of slave settlers and admixture with the Portuguese
AUTHORS:
Tomas, G; Seco, L;
Seixas, S
;
Faustino, P
;
Lavinha, J
;
Rocha, J
;
PUBLISHED:
2002
,
SOURCE:
HUMAN BIOLOGY,
VOLUME:
74,
ISSUE:
3
INDEXED IN:
Scopus
WOS
CrossRef
:
22
IN MY:
ORCID
|
ResearcherID
20
TITLE:
Association between the defective Pro369Ser mutation and in vivo intrahepatic alpha 1-antitrypsin accumulation
AUTHORS:
Seixas, S
;
Lopes, AI
;
Rocha, J
; Silva, L; Salgueiro, C; Salazar de Sousa, J;
Batista, A
;
PUBLISHED:
2001
,
SOURCE:
JOURNAL OF MEDICAL GENETICS,
VOLUME:
38,
ISSUE:
7
INDEXED IN:
Scopus
WOS
CrossRef
:
3
IN MY:
ORCID
|
ResearcherID
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