Fernanda A. Correa

440 total citations
21 papers, 268 citations indexed

About

Fernanda A. Correa is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics and Molecular Biology. According to data from OpenAlex, Fernanda A. Correa has authored 21 papers receiving a total of 268 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Endocrinology, Diabetes and Metabolism, 11 papers in Genetics and 10 papers in Molecular Biology. Recurrent topics in Fernanda A. Correa's work include Growth Hormone and Insulin-like Growth Factors (12 papers), Genetic Syndromes and Imprinting (4 papers) and Sexual Differentiation and Disorders (4 papers). Fernanda A. Correa is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (12 papers), Genetic Syndromes and Imprinting (4 papers) and Sexual Differentiation and Disorders (4 papers). Fernanda A. Correa collaborates with scholars based in Brazil, United States and Argentina. Fernanda A. Correa's co-authors include Alexander A.L. Jorge, Ivo J.P. Arnhold, Luciani R. Carvalho, Berenice B. Mendonça, Marcela M. França, Everlayny F. Costalonga, Carla Rosenberg, Ana O. Hoff, Silvia Souza da Costa and Ana Pinheiro Machado Canton and has published in prestigious journals such as BMC Genomics, Molecular and Cellular Endocrinology and Clinical Endocrinology.

In The Last Decade

Fernanda A. Correa

21 papers receiving 261 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Fernanda A. Correa Brazil	11	169	106	91	51	23	21	268
Dinesh Giri United Kingdom	9	125 0.7×	74 0.7×	77 0.8×	76 1.5×	13 0.6×	45	266
Annalisa Calcagno Italy	9	184 1.1×	65 0.6×	88 1.0×	59 1.2×	33 1.4×	12	308
Everlayny F. Costalonga Brazil	13	229 1.4×	200 1.9×	165 1.8×	49 1.0×	48 2.1×	22	421
Abdulsalam Abu‐Libdeh Israel	10	75 0.4×	115 1.1×	187 2.1×	66 1.3×	23 1.0×	25	338
Daniela Choukair Germany	10	72 0.4×	70 0.7×	76 0.8×	34 0.7×	28 1.2×	32	217
Quentin Thomas France	5	90 0.5×	116 1.1×	114 1.3×	24 0.5×	12 0.5×	17	278
Concepción Páramo Spain	7	269 1.6×	42 0.4×	47 0.5×	39 0.8×	22 1.0×	10	315
Gilberto K. Furuzawa Brazil	9	96 0.6×	74 0.7×	116 1.3×	68 1.3×	8 0.3×	14	222
Matthias Viemann Germany	7	160 0.9×	80 0.8×	217 2.4×	40 0.8×	12 0.5×	10	269
Mirta Miras Argentina	11	241 1.4×	115 1.1×	145 1.6×	16 0.3×	67 2.9×	27	363

Countries citing papers authored by Fernanda A. Correa

Since Specialization

Citations

This map shows the geographic impact of Fernanda A. Correa's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Fernanda A. Correa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fernanda A. Correa more than expected).

Fields of papers citing papers by Fernanda A. Correa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fernanda A. Correa. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Fernanda A. Correa. The network helps show where Fernanda A. Correa may publish in the future.

Co-authorship network of co-authors of Fernanda A. Correa

This figure shows the co-authorship network connecting the top 25 collaborators of Fernanda A. Correa. A scholar is included among the top collaborators of Fernanda A. Correa based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Fernanda A. Correa. Fernanda A. Correa is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Irshad, Saba, Ambrin Fatima, Fernanda A. Correa, et al.. (2024). Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism. BMC Genomics. 25(1). 787–787. 1 indexed citations

Toyoshima, Marcos Tadashi Kakitani, Priscilla Cukier, Aline Santos Damascena, et al.. (2023). Fructosamine and glycated hemoglobin as biomarkers of glycemic control in people with type 2 diabetes mellitus and cancer (GlicoOnco study). Clinics. 78. 100240–100240. 4 indexed citations

Correa, Fernanda A., et al.. (2021). Hormone resistance and short stature: A journey through the pathways of hormone signaling. Molecular and Cellular Endocrinology. 536. 111416–111416. 2 indexed citations

Danilovic, Debora Lúcia Seguro, Luciana Audi Castroneves, Cláudia Kimie Suemoto, et al.. (2020). Is There a Difference Between Minimal and Gross Extension into the Strap Muscles for the Risk of Recurrence in Papillary Thyroid Carcinomas?. Thyroid. 30(7). 1008–1016. 33 indexed citations

Correa, Fernanda A., Mirian Yumie Nishi, Alexander A.L. Jorge, et al.. (2019). Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery. Archives of Endocrinology and Metabolism. 63(2). 167–174. 14 indexed citations

Vasques, Gabriela A., et al.. (2019). Update on new GH-IGF axis genetic defects. Archives of Endocrinology and Metabolism. 63(6). 608–617. 12 indexed citations

Correa, Fernanda A., et al.. (2019). Quality of Life and Coping in Multiple Endocrine Neoplasia Type 2. Journal of the Endocrine Society. 3(6). 1167–1174. 6 indexed citations

Correa, Fernanda A., Alexander A.L. Jorge, Mariana F.A. Funari, et al.. (2019). Probably Pathogenic Variants in New Candidate Genes in Patients with Pituitary Stalk Interruption Syndrome (PSIS) Revealed by Whole-Exome Sequencing. 1 indexed citations

Nishi, Mirian Yumie, Anna Benedetti, Marcela M. França, et al.. (2017). Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations. Clinical Endocrinology. 87(6). 725–732. 10 indexed citations

10.

Correa, Fernanda A., Ana Pinheiro Machado Canton, Silvia Souza da Costa, et al.. (2017). Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes. Clinical Endocrinology. 88(3). 425–431. 11 indexed citations

11.

Correa, Fernanda A., Marcela M. França, Qing Fang, et al.. (2017). Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing. Archives of Endocrinology and Metabolism. 61(6). 633–636. 5 indexed citations

12.

Correa, Fernanda A., Marcela M. França, Dani Ejzenberg, et al.. (2017). Successful Pregnancies After Adequate Hormonal Replacement in Patients With Combined Pituitary Hormone Deficiencies. Journal of the Endocrine Society. 1(10). 1322–1330. 15 indexed citations

13.

Jorge, Alexander A.L., Regina Matsunaga Martin, Luciana Ribeiro Montenegro, et al.. (2016). A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD). European Journal of Endocrinology. 175(2). K7–K15. 2 indexed citations

14.

Correa, Fernanda A., Ericka Barbosa Trarbach, Cíntia Tusset, et al.. (2015). FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies. Endocrine Connections. 4(2). 100–107. 33 indexed citations

15.

Canton, Ana Pinheiro Machado, Silvia Souza da Costa, Débora Romeo Bertola, et al.. (2014). Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. European Journal of Endocrinology. 171(2). 253–262. 37 indexed citations

16.

França, Marcela M., Fernanda A. Correa, Luciani R. Carvalho, et al.. (2014). Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort. Growth Hormone & IGF Research. 24(5). 180–186. 2 indexed citations

17.

França, Marcela M., Fernanda A. Correa, Everlayny F. Costalonga, et al.. (2014). 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. Pituitary. 18(4). 561–567. 25 indexed citations

18.

França, Marcela M., Alexander A.L. Jorge, Luciani R. Carvalho, et al.. (2012). Relatively high frequency of non‐synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly. Clinical Endocrinology. 78(4). 551–557. 27 indexed citations

19.

Carnier, June, Aline de Piano, Priscila de Lima Sanches, et al.. (2010). The role of orexigenic and anorexigenic factors in an interdisciplinary weight loss therapy for obese adolescents with symptoms of eating disorders. International Journal of Clinical Practice. 64(6). 784–790. 16 indexed citations

20.

Correa, Fernanda A. & Tânia A.S.S. Bachega. (2003). Avaliação dos critérios diagnósticos hormonais da forma não clássica da deficiência da 21-hidroxilase através do estudo molecular do gene CYP21A2. Arquivos Brasileiros de Endocrinologia & Metabologia. 47(5). 622–631. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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