Researcher profile · Semantic Scholar

R. L. Dutra

h-index: 10
Works: 28
Citations: 249

Most-cited papers

FGFR4 Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Mouth and Oropharynx
R. L. Dutra, M. D. de Carvalho, M. D. dos Santos, A. M. da Cunha Mercante +5 more
2012PLoS ONE34 citations Open access
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Williams-Beuren Syndrome: A Clinical Study of 55 Brazilian Patients and the Diagnostic Use of MLPA
R. Honjo, R. L. Dutra, E. Furusawa, É. Zanardo +4 more
2015BioMed Research International27 citations Open access
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Congenital Heart Disease as a Warning Sign for the Diagnosis of the 22q11.2 Deletion
M. Grassi, C. M. Jacob, L. Kulikowski, A. Pastorino +6 more
2014Arquivos Brasileiros de Cardiologia25 citations Open access
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Copy number variation in Williams-Beuren syndrome: suitable diagnostic strategy for developing countries
R. L. Dutra, R. Honjo, L. Kulikowski, F. M. Fonseca +4 more
2012BMC Research Notes22 citations Open access
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Investigation of Copy Number Variation in Children with Conotruncal Heart Defects
C. M. R. Campos, É. Zanardo, R. L. Dutra, L. Kulikowski +1 more
2014Arquivos Brasileiros de Cardiologia21 citations Open access
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Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome
É. Zanardo, F. Piazzon, R. L. Dutra, A. T. Dias +6 more
2014Zeitschrift für Induktive Abstammungs- und Vererbungslehre14 citations
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Atypical deletion in Williams-Beuren syndrome critical region detected by MLPA in a patient with supravalvular aortic stenosis and learning difficulty.
R. Honjo, R. L. Dutra, M. Nunes, Israel Gomy +3 more
2012Journal of genetics and genomics = Yi chuan xue bao14 citations
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Cytogenomic delineation and clinical follow-up of 10 Brazilian patients with Pallister-Killian syndrome
Larissa Sampaio de Athayde Costa, Aline C. Zandona-Teixeira, M. Montenegro, A. T. Dias +5 more
2015Molecular Cytogenetics12 citations Open access
Semantic Scholar
Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience
É. Zanardo, R. L. Dutra, F. Piazzon, A. T. Dias +9 more
2017Clinics11 citations Open access
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Assessment of Intellectual and Visuo Spatial Abilities in Children and Adults with Williams Syndrome
Michele Moreira Mika, M. Nunes, R. S. Honjo, R. L. Dutra +7 more
20138 citations Open access
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Post-mortem cytogenomic investigations in patients with congenital malformations.
A. T. Dias, É. Zanardo, R. L. Dutra, F. Piazzon +14 more
2016Experimental and molecular pathology (Print)6 citations
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Subtelomeric Copy Number Variations: The Importance of 4p/4q Deletions in Patients with Congenital Anomalies and Developmental Disability
G. M. Novo-Filho, M. Montenegro, É. Zanardo, R. L. Dutra +7 more
2016Cytogenetic and Genome Research6 citations
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Role of SNAP29, LZTR1 and P2RXL1 genes on immune regulation in a patient with atypical 0.5 Mb deletion in 22q11.2 region.
Diogo Cordeiro de Queiroz Soares, R. L. Dutra, Caio Robledo D'Angioli Costa Quaio, M. Melaragno +3 more
2012Clinical Immunology6 citations
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Corrigendum to “Williams-Beuren Syndrome: A Clinical Study of 55 Brazilian Patients and the Diagnostic Use of MLPA”
R. Honjo, R. L. Dutra, E. Furusawa, É. Zanardo +4 more
2015BioMed Research International5 citations Open access
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Copy number variation in Williams-Beuren syndrome: suitable diagnostic strategy for developing countries
R. L. Dutra, R. Honjo, L. Kulikowski, F. M. Fonseca +4 more
2012BMC Research Notes4 citations Open access
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Rare genomic rearrangement in a boy with Williams–Beuren syndrome associated to XYY syndrome and intriguing behavior
R. L. Dutra, F. Piazzon, É. Zanardo, Thaís V. M. M. Costa +6 more
2015American Journal of Medical Genetics. Part A2 citations
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FGFR4 as a Biomarker in Squamous Cell Cancers of the Mouth and Oropharynx
R. L. Dutra, M. D. dos Santos, S. O. Mendes, G. T. Peterle +2 more
20142 citations Open access
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A Possible Role of Different PTPN Genes in Immune Regulation
C. Quaio, R. L. Dutra, A. S. Brasil, A. Pereira +2 more
2012Scandinavian Journal of Immunology2 citations
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A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability
J. R. M. Ceroni, R. L. Dutra, R. Honjo, J. Llerena +13 more
2018Scientific Reports1 citations Open access
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Investigação da variação no número de cópias gênicas em crianças com defeito cardíaco conotruncal.
Carla Marques, R. Campos, É. Zanardo, R. L. Dutra +3 more
20141 citations
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High frequency of autistic traits in Williams-Beuren patients
M. Nunes, R. Honjo, R. L. Dutra, Vera Alice Alcântara dos Santos Amaral +5 more
20111 citations
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Análise de marcadores moleculares para o diagnóstico da síndrome de Williams-Beuren
R. L. Dutra
20111 citations Open access
Semantic Scholar
Teri Lear, PhD (1951-2016)
P. Ráb, C. F. Yano, S. Lavoué, O. I. Jegede +71 more
2016Cytogenetic and Genome Research0 citations
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Contents Vol. 149, 2016
P. Ráb, C. F. Yano, S. Lavoué, O. I. Jegede +71 more
2016Cytogenetic and Genome Research0 citations Open access
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Stress in children and adolescents with Williams-Beuren syndrome in school age
Vera Alice Alcantara dos Santos Amaral, M. Nunes, R. Honjo, R. L. Dutra +2 more
20130 citations Open access
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Cytogenomic Diagnosis of Congenital Heart Diseases
L. Kulikowski, É. Zanardo, R. L. Dutra, F. Piazzon +9 more
20130 citations
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The role of CNVs in molecular mechanisms for rearrangements in 22q11.2 region diseases
R. L. Dutra, É. Zanardo, F. Piazzon, A. T. Dias +9 more
20130 citations
Semantic Scholar

A. T. Dias

×11

M. Montenegro×11

D. Bertola×10

F. Piazzon×10

G. M. Novo-Filho×8

A. Nascimento×8

Thaís V. M. M. Costa×5

M. Nunes×4