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Marcela M. França

Observed names: França,Marcela M., MARCELA MOURA FRANÇA, Marcela M Franca, Marcela M França, Marcela M. França, Marcela Moura França
Institution: Unichristus
Observed institutions: Brigham and Women's Hospital, Universidade de São Paulo, Universidade Federal do Ceará, Centre Hospitalier Universitaire Vaudois, Unichristus, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
ORCID: 0009-0000-8689-5316
Observed ORCID: 0009-0000-8689-5316
OpenAlex ID: A5103576972
Novel Heterozygous Nonsense GLI2 Mutations in Patients with Hypopituitarism and Ectopic Posterior Pituitary Lobe without Holoprosencephaly
2010 · Marcela M. França, Alexander A. L. Jorge, et al. · The Journal of Clinical Endocrinology & Metabolism · 135
Role of GLI2 in hypopituitarism phenotype
2015 · Ivo J P Arnhold, Marcela M França, et al. · Journal of Molecular Endocrinology · 74
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Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly
2014 · Kelly A Bear, Benjamin D Solomon, et al. · Journal of Medical Genetics · 72
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FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies
2015 · Fernanda A Correa, Ericka B Trarbach, et al. · Endocrine Connections · 49
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Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center
2014 · Aline P. Otto, Marcela M. França, et al. · Pituitary · 41
Relatively high frequency of non‐synonymous GLI 2 variants in patients with congenital hypopituitarism without holoprosencephaly
2012 · Marcela M. França, Alexander A. L. Jorge, et al. · Clinical Endocrinology · 36
Successful Pregnancies After Adequate Hormonal Replacement in Patients With Combined Pituitary Hormone Deficiencies
2017 · Fernanda A Correa, Paulo H M Bianchi, et al. · Journal of the Endocrine Society · 26
Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency
2011 · Marcela M. França, Alexander A. L. Jorge, et al. · The Journal of Clinical Endocrinology & Metabolism · 24
Prevention of HIV infection among migrant population groups in Northeast Brazil
2004 · Ligia Regina Sansigolo Kerr-Pontes, Fernando González, et al. · Cadernos de Saúde Pública · 24
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GH-Releasing Hormone Receptor Gene: A Novel Splice-Disrupting Mutation and Study of Founder Effects
2012 · Suemi Marui, Ericka B. Trarbach, et al. · Hormone Research in Paediatrics · 22
Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP 1 alterations with three novel mutations
2017 · Joao LO Madeira, Mirian Y Nishi, et al. · Clinical Endocrinology · 16
Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes
2017 · Fernanda A. Correa, Alexander AL Jorge, et al. · Clinical Endocrinology · 15
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD)
2016 · João L O Madeira, Alexander A L Jorge, et al. · European Journal of Endocrinology · 10
Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing
2017 · Fernanda A. Correa, Marcela M. França, et al. · Archives of Endocrinology and Metabolism · 7
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Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort
2014 · Andria C.V. Lido, Marcela M. França, et al. · Growth Hormone & IGF Research · 6
Clarification of intellectual abilities in patients with GLI2 mutations cited by kevelam et al., 2012 Am J med genet part A
2012 · Marcela M. França, Ivo J.P. Arnhold · American Journal of Medical Genetics Part A · 2
Avaliação Do Conhecimento Sobre Diabetes Mellitus Tipo 2 De Adultos Acompanhados No Centro Integrado Em Diabetes E Hipertensão (cidh) Da Rede Estadual De Saúde (sesa/ce)
2026 · Julianna Deusdará Feijó, Maria Thaís Lucena Rodrigues Valente, et al. · Revista Interagir
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A Importância Do Conhecimento E Autocuidado No Diabetes Mellitus Tipo 2
2022 · Maria Thaís Lucena Rodrigues Valente, Priscila Valera Guerra, et al. · Instituto Scientia eBooks
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Coinfecção Hiv-tuberculose: Repercussões E Prognóstico
2022 · BEATRICE ARAÚJO DUARTE, GABRIEL BRAZ DE MENEZES, et al. · Editora Pasteur eBooks
Molecular Analysis of Brazilian Patients With Combined Pituitary Hormone Deficiency (cphd) and Orthotopic Posterior Pituitary Lobe (opp) Reveals 8 Different Prop1 Alterations With Three Novel Mutations
2017 · João Madeira, Mirian Yumie Nishi, et al. · Hormone Research in Paediatrics
GH Deficiency with Advanced Bone Age: GHRH Receptor Mutation Detected by Exome Sequencing Associated to Non-Classical Congenital Adrenal Hyperplasia (CAH)
2015 · Fernanda A. Correa, Marcela M. França, et al. · 54th ESPE Meeting (ESPE 2015)
Copy Number Variants in Patients with Congenital Hypopituitarism Associated with Complex Phenotypes
2015 · Fernanda A. Correa, Marcela M. França, et al. · 54th ESPE Meeting (ESPE 2015)
A Homozygous Point Mutation in the GH1 Promoter ([mdash]161T[gt]C) Leads to Reduced GH Expression in Siblings with Isolated GH Deficiency
2014 · João Madeira, Regina Martin, et al. · 53rd ESPE Meeting
Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients
2013 · Ândria Carla Vito Lido, Marcela M. França, et al. · Hormone Research in Paediatrics
Análise dos genes GHRH e GL12 em pacientes com deficiência de hormônio do crescimento congênita
2012 · Marcela Moura França · Digital Library of Theses and Dissertations (Universidade de São Paulo)
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Works count: 28
Citation count: 559
H-index: 12
I10-index: 13
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