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Eloísa Sá Moreira
Observed names:
E S Moreira,
E de Sá Moreira,
E. Moreira,
E. S. Moreira,
E.S. Moreira,
ES Moreira,
Eloisa S. Moreira,
Eloisa Sa Moreira,
Eloísa S. Moreira
show all 9
Observed institutions:
Leiden University,
Universidade de São Paulo,
Universidade Estadual de Campinas (UNICAMP),
Kantar Health (Brazil),
Genethon (France),
Fleury S.A. (Brazil),
Newcastle University,
Universidade Federal de São Paulo
show all 8
OpenAlex ID:
A5057625052
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin
2000
·
Eloisa S. Moreira
, Tim J. Wiltshire
, et al.
·
Nature Genetics
·
335
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.
1996
·
E M McNally
, M R Passos-Bueno
, et al.
·
PubMed Central
·
156
The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome
2001
·
Anamaria A. Camargo
, Helena P. B. Samaia
, et al.
·
Proceedings of the National Academy of Sciences
·
139
The Seventh Form of Autosomal Recessive Limb-Girdle Muscular Dystrophy Is Mapped to 17q11-12
1997
·
Eloisa S. Moreira
, Mariz Vainzof
, et al.
·
The American Journal of Human Genetics
·
132
Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G
1999
·
Maria Rita Passos-Bueno
, Mariz Vainzof
, et al.
·
American Journal of Medical Genetics
·
105
A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma.
2001
·
P Iughetti
, O Suzuki
, et al.
·
PubMed
·
84
Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies
2001
·
Mariz Vainzof
, Louise V. B. Anderson
, et al.
·
Journal of Molecular Neuroscience
·
84
A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
1995
·
M. R. P. Bueno
, E. S. Moreira
, et al.
·
Human Molecular Genetics
·
65
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.
1996
·
M R Passos-Bueno
, E S Moreira
, et al.
·
Journal of Medical Genetics
·
57
PDF
Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations
2003
·
E S Moreira
, M Vainzof
, et al.
·
Journal of Medical Genetics
·
55
PDF
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.
1998
·
E S Moreira
, M Vainzof
, et al.
·
Journal of Medical Genetics
·
52
PDF
Confirmation of the 2p Locus for the Mild Autosomal Recessive Limb-Girdle Muscular Dystrophy Gene (LGMD2B) in Three Families Allows Refinement of the Candidate Region
1995
·
M.Rita Passos-Bueno
, Ramaisa Bashir
, et al.
·
Genomics
·
40
HTR1B and HTR2C in autism spectrum disorders in Brazilian families
2008
·
G.M. Orabona
, K. Griesi-Oliveira
, et al.
·
Brain Research
·
34
Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in Autism Spectrum Disorder Brazilian Individuals with and without Epilepsy
2014
·
Danielle P. Moreira
, Karina Griesi-Oliveira
, et al.
·
PLoS ONE
·
31
PDF
Partial α‐sarcoglycan deficiency with retention of the dystrophin‐glycoprotein complex in a LGMD2D family
2000
·
Mariz Vainzof
, Eloisa S. Moreira
, et al.
·
Muscle & Nerve
·
27
Deficiency of α-Actinin-3 (ACTN3) Occurs in Different Forms of Muscular Dystrophy
1997
·
M. Vainzof
, C. Costa
, et al.
·
Neuropediatrics
·
27
Acute promyelocytic leukemia with t(15;17): frequency of additional clonal chromosome abnormalities and FLT3 mutations
2008
·
Maria De Lourdes Chauffaille
, Daniela Borri
, et al.
·
Leukemia & lymphoma/Leukemia and lymphoma
·
22
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin–glycoprotein complex
1999
·
M Vainzof
, ES Moreira
, et al.
·
European Journal of Human Genetics
·
22
Does the P172H mutation at the TM4SF2 gene cause X‐linked mental retardation?
2003
·
Carlos Magno da Costa Maranduba
, Eloísa Sá Moreira
, et al.
·
American Journal of Medical Genetics Part A
·
20
Impact of C4, C4A and C4B gene copy number variation in the susceptibility, phenotype and progression of systemic lupus erythematosus
2019
·
Kaline Medeiros Costa Pereira
, Sandro Perazzio
, et al.
·
Revista Brasileira de Reumatologia
·
18
PDF
Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH)
2016
·
Eloisa S. Moreira
, Isabela M.W. Silva
, et al.
·
Research in Autism
·
12
PDF
Factors associated with the intensity of liver fibrosis in renal transplant patients with hepatitis B virus infection
2007
·
Carla A.L. Matos
, Renata M. Perez
, et al.
·
European Journal of Gastroenterology & Hepatology
·
12
Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR
2008
·
C.B. Moysés
, E.S. Moreira
, et al.
·
Brazilian Journal of Medical and Biological Research
·
11
Corrigendum to “HTR1B and HTR2C in Autism Spectrum Disorder in Brazilian families” [Brain Res. 1250 (2009) 14–19]
2009
·
G.M. Orabona
, K. Griesi-Oliveira
, et al.
·
Brain Research
·
1
Acute Promyelocytic Leukemia with T(15;17): Frequency of Additional Clonal Chromosome Abnormalities and FLT3
2008
·
Maria L. Chauffaille
, Rodrigo Proto Siqueira
, et al.
·
Blood
·
1
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Works count:
38
Citation count:
1,542
H-index:
19
I10-index:
23
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