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Sayonara Gonzalez

Observed names: S M de Carvalho Gonzalez, S. Maria de Carvalho Gonzalez, Sayonara Maria de Carvalho Gonzalez, Sayonara Maria de Carvalho Gonzalez
ORCID: 0000-0002-9140-1963
Observed ORCID: 0000-0002-9140-1963
OpenAlex ID: A5089157565
Characterization of a Smad Motif Similar to Drosophila Mad in the Mouse Msx 1 Promoter
2002 · Cristina E. Alvarez Martinez, Renata Binato, et al. · Biochemical and Biophysical Research Communications · 31
Pregnancy-induced hypertension, preterm birth, and cord blood adipokine levels
2020 · Elizabeth Soares da Silva Magalhães, Maria Dalva Barbosa Baker Méio, et al. · European Journal of Pediatrics · 23
Novel and Recurrent Mutations in the FGFR3 Gene and Double Heterozygosity Cases in a Cohort of Brazilian Patients with Skeletal Dysplasia
2018 · Maria E.S. Gomes, Thatiane Y. Kanazawa, et al. · Molecular Syndromology · 19
miRNA Genetic Variants Alter Their Secondary Structure and Expression in Patients With RASopathies Syndromes
2019 · Joseane Biso de Carvalho, Guilherme Loss de Morais, et al. · Frontiers in Genetics · 17
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Structural and Functional Analysis of Mouse Msx1 Gene Promoter: Sequence Conservation with Human MSX1 Promoter Points at Potential Regulatory Elements
1998 · Sayonara Maria de Carvalho Gonzalez, Louis H. Ferland, et al. · DNA and Cell Biology · 15
Identification of Novel and Recurrent RMRP Variants in a Series of Brazilian Patients with Cartilage-Hair Hypoplasia: McKusick Syndrome
2019 · Maria E. Gomes, Luiza Calatrava Paternostro, et al. · Molecular Syndromology · 12
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RASopathy Cohort of Patients Enrolled in a Brazilian Reference Center for Rare Diseases: A Novel Familial LZTR1 Variant and Recurrent Mutations
2022 · Natana Chaves Rabelo, Maria Eduarda Gomes, et al. · The Application of Clinical Genetics · 11
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Venous anomalies in hypoplastic posterior fossa: unsolved questions
2021 · T. Protzenko, A. Bellas, et al. · Child s Nervous System · 9
Identification of a founder effect involving n.197C>T variant in RMRP gene associated to cartilage-hair hypoplasia syndrome in Brazilian patients
2024 · Maria Eduarda Gomes, Fernanda Kehdy, et al. · Scientific Reports · 7
Conserved transcription factor binding sites suggest an activator basal promoter and a distal inhibitor in the galanin gene promoter in mouse ES cells
2014 · Sayonara Gonzalez, Renata Binato, et al. · Gene · 5
Autosomal recessive primary microcephaly in sibs in time of Zika epidemic: a Case Report
2025 · Julia V. Almeida, Bianca Barbosa Abdala, et al. · Frontiers in Genetics · 3
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High-Resolution Melting Analysis for Rapid Detection of Mutations in Patients with FGFR3 -Related Skeletal Dysplasias
2021 · Fernanda Rolemberg G. Riba, Maria E.S. Gomes, et al. · Genetic Testing and Molecular Biomarkers · 1
Five-year outcomes of next-generation sequencing implementation at a Brazilian public health system reference centre for rare diseases
2026 · Natana Chaves Rabelo, Maria Eduarda Gomes, et al. · Frontiers in Genetics
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Challenges in cephalometric landmark identification in syndromic craniosynostoses: the role of 3D multislice computed tomography
2026 · Michelle Protzenko, Cesar Augusto Vianna de Araújo, et al. · Journal Archives of Health
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Contributing Factors for Angle's Class III Phenotype in Crouzon Syndrome.
2026 · M Protzenko, C A Viana de Araújo, et al. · PubMed
Análise cefalométrica comparativa nas craniossinostoses sindrômicas
2026 · Michelle Protzenko, Cesar Augusto Viana de Araújo, et al. · Revista da Academia Brasileira de Odontologia
Unilateral buphthalmos in a patient with short stature: a rare case of dual recessive disorders
2026 · Juan Clinton Llerena, Maria Eduarda Gomes, et al. · Revista Brasileira de Oftalmologia
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REACT Congress Program 2018
2018 · Anne Ronan, Gemma Poke, et al. · Molecular Syndromology
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Works count: 18
Citation count: 153
H-index: 8
I10-index: 7
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