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Raíssa Carneiro Rezende

Observed names: Alexander A L Jorge, R C Rezende, Raissa C Rezende, Raissa C. Rezende, Raissa Carneiro Rezende, Raissa Rezende, Raíssa C Rezende, Raíssa C. Rezende, Raíssa Rezende, Rezende RC, Rezende, R, Rezende, Raissa C., Rezende, Raíssa Carneiro
ORCID: 0000-0002-7207-5576
Observed ORCID: 0000-0002-7207-5576
OpenAlex ID: A5002329561
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and Puberty
2023 · Katie Duckett, Alice Williamson, et al. · The Journal of Clinical Endocrinology & Metabolism · 18
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Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature
2022 · Nathalia Liberatoscioli Menezes Andrade, Mariana Ferreira de Assis Funari, et al. · Endocrine Connections · 18
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Idiopathic Short Stature: What to Expect from Genomic Investigations
2023 · Nathalia Liberatoscioli Menezes Andrade, Laurana Polli Cellin, et al. · Endocrines · 13
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Adult Height of Patients with SHOX Haploinsufficiency with or without GH Therapy: A Real-World Single-Center Study
2022 · Naiara C.B. Dantas, Mariana F.A. Funari, et al. · Hormone Research in Paediatrics · 12
Diagnostic yield of genetic testing in children with short stature: a systematic review
2026 · Renata C Scalco, Jan W Schoones, et al. · European Journal of Endocrinology · 9
Contributions of Common Genetic Variants to Constitutional Delay of Puberty and Idiopathic Hypogonadotropic Hypogonadism
2024 · Margaret F Lippincott, Evan C Schafer, et al. · The Journal of Clinical Endocrinology & Metabolism · 8
Delayed Puberty Phenotype Observed in Noonan Syndrome Is More Pronounced in Girls than Boys
2022 · Raissa C. Rezende, Renata Maria Noronha, et al. · Hormone Research in Paediatrics · 8
DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders
2025 · Ivana Lessel, Anja Baresic, et al. · The American Journal of Human Genetics · 7
Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders
2023 · Raissa Carneiro Rezende, Nathalia Liberatoscioli Menezes de Andrade, et al. · The Journal of Pediatrics · 6
Clinical Characteristics of Children with THRA Mutations: Variable Phenotype and Good Response to Recombinant Human Growth Hormone Therapy
2024 · Nathalia L.M. Andrade, Raissa C. Rezende, et al. · Hormone Research in Paediatrics · 5
Nano-plastics Impair GnRH Neuron Migration and Neuroendocrine Function: Emerging Players in the Pathogenesis of Reproductive Disorders
2026 · Federica Amoruso, Alyssa Julia Jennifer Paganoni, et al. · Small · 3
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Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability
2023 · Naiara C B Dantas, Mariana F A Funari, et al. · European Journal of Endocrinology · 3
Avaliação do conhecimento e hábitos de fotoproteção entre crianças e seus cuidadores na cidade de Porto Alegre, Brasil
2014 · Raquel Bonfá, Gabriela Mynarski Martins-Costa, et al. · Redalyc (Universidad Autónoma del Estado de México) · 3
Severe hypercalcemia caused by repeated mineral oil injections: a case report
2023 · Raissa Carneiro Rezende, Isabella Carvalho Oliveira, et al. · Archives of Endocrinology and Metabolism · 2
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Artigo Original Avaliação do conhecimento e hábitos de fotoproteção entre crianças e seus cuida dores na cidade de Porto Alegre, Brasil Evaluation of the knowledge and photoprotection habits of children and their caregivers in the city of Porto Alegre, Brazil
2014 · Raquel Bonfá, Gabriela Mynarski Martins-Costa, et al. · 1
Growth and Growth Factors
2026 · Annalisa Deodati, Valentina Pampanini, et al. · Yearbook of pediatric endocrinology
Diagnostic yield of genetic testing in children with short stature: a systematic review
2026 · Scalco RC, Schoones JW, et al. · Yearbook of pediatric endocrinology
Genetic testing in “Mild Growth Hormone Deficiency”
2026 · Andrew Dauber, Alexander A L Jorge, et al. · European Journal of Endocrinology
Non‐ RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome
2025 · Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, et al. · American Journal of Medical Genetics Part A
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SAT-195 Exome Sequencing of Patients with Syndromic Tall Stature Reveals Novel Candidate Genes
2025 · Gabriela Jeesoo Kim, Edoarda Vasco de Albuquerque Albuquerque, et al. · Journal of the Endocrine Society
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OR03-03 Whole Exome Sequencing (WES) in a Large Prospective Cohort of Idiopathic Short Stature (ISS): New Genes Implicated in the ISS Phenotype
2025 · Laurana de Polli Cellin, Nathalia Liberatoscioli Menezes de Andrade, et al. · Journal of the Endocrine Society
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Exome sequencing of patients with syndromic tall stature reveals four novel candidate genes
2025 · Gabriela Jeesoo Kim, Edoarda Vasco de Albuquerque Albuquerque, et al. · Endocrine Connections
Deleterious variants in intolerant genes reveal new candidates for self-limited delayed puberty
2025 · Raíssa C Rezende, Wen He, et al. · European Journal of Endocrinology
DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders
2025 · Kubisch, Christian, Cogne, Benjamin, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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New candidate genes for constitutional delay of growth and puberty identified through whole-exome sequencing
2025 · Rezende, Raíssa Carneiro · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Works count: 34
Citation count: 116
H-index: 7
I10-index: 4
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