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Melissa Machado Viana

Observed names: M. M. Viana, MELISSA MACHADO VIANA, MM Viana
ORCID: 0000-0002-1573-4176
Observed ORCID: 0000-0002-1573-4176
OpenAlex ID: A5089114407
Familial suicide behaviour: association with probands suicide attempt characteristics and 5‐HTTLPR polymorphism
2004 · H. Correa, A. C. Campi‐Azevedo, et al. · Acta Psychiatrica Scandinavica · 32
Investigation of A218C tryptophan hydroxylase polymorphism: association with familial suicide behavior and proband's suicide attempt characteristics
2005 · M. M. Viana, L. A. De Marco, et al. · Genes Brain & Behavior · 30
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Ocular Features in 16 Brazilian Patients with Williams-Beuren Syndrome
2014 · Melissa Machado Viana, Maria Frasson, et al. · Ophthalmic Genetics · 19
Analysis of T102C 5HT2A Polymorphism in Brazilian Psychiatric Inpatients: Relationship with Suicidal Behavior
2002 · H. Correa, L. De Marco, et al. · Cellular and Molecular Neurobiology · 18
Oral findings in Williams-Beuren syndrome
2017 · SBP Ferreira, MM Viana, et al. · Medicina oral, patología oral y cirugía bucal · 16
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A New Case of Keratoconus Associated with Williams-Beuren Syndrome
2012 · Melissa Machado Viana, Maria Frasson, et al. · Ophthalmic Genetics · 11
High‐level mosaic monosomy 21 in a 13‐year‐old girl: Case report and review of the literature
2021 · Melissa Machado Viana, Gabrielle Sousa Vianna, et al. · American Journal of Medical Genetics Part A · 4
Phenotype of Williams–Beuren syndrome in Brazilian patients: Comments on the article by Patil et al. [2012] and discussion of variable phenotypes in distinct populations
2013 · Melissa Machado Viana, Martin Stofanko, et al. · American Journal of Medical Genetics Part A · 4
Psiconeuroendocrinologia e comportamento suicida
2005 · Humberto Corrêa, Melissa Machado Viana, et al. · Jornal Brasileiro de Psiquiatria · 1
Teleinterconsulta médica no cuidado de crianças com suspeita de doenças raras: relato de experiência de um estudo piloto no Brasil durante a pandemia de COVID-19
2022 · Lívia Maria Ferreira Sobrinho, Melissa Machado Viana, et al. · Latin American Journal of Telehealth
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Website para informação sobre doenças raras de origem genética: primeiro passo para telegenética em Minas Gerais, Brasil
2021 · Lívia Maria Ferreira Sobrinho, Letícia Lima Leão, et al. · Latin American Journal of Telehealth
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Williams-beuren Syndrome and Oral Findings
2019 · RODRIGO SOARES DE ANDRADE, SHIRLENE BARBOSA PIMENTEL FERREIRA, et al. · Oral Surgery Oral Medicine Oral Pathology and Oral Radiology
Oral Manifestations of Williams-Beuren Syndrome
2018 · Shirlene Barbosa Pimentel Ferreira, Melissa Machado Viana, et al. · Oral Surgery Oral Medicine Oral Pathology and Oral Radiology
Regarding Camurati-Engelmann Disease
2018 · Melissa Machado Viana, Sabrina Versuti Nunes, et al. · Clinics in Orthopedic Surgery
Regarding Camurati-Engelmann Disease: To the Editor
2018 · Melissa Machado Viana, Sabrina Versuti Nunes, et al. · Clinics in Orthopedic Surgery
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Contribuição do fenótipo para o diagnóstico de síndromes de microdeleções por meio de metodologia adequada à realidade brasileira
2013 · Melissa Machado Viana · Americanae (AECID Library)
A Comparison of Visual Acuity Loss in Patients With Different Stages of Stargardt Disease
2006 · L.S. Kim, G. A. Fishman, et al. · Investigative Ophthalmology & Visual Science
Works count: 17
Citation count: 135
H-index: 6
I10-index: 6
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