Fernanda T. Bellucco

504 total citations
24 papers, 233 citations indexed

About

Fernanda T. Bellucco is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Fernanda T. Bellucco has authored 24 papers receiving a total of 233 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 13 papers in Molecular Biology and 6 papers in Plant Science. Recurrent topics in Fernanda T. Bellucco's work include Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Chromosomal and Genetic Variations (6 papers). Fernanda T. Bellucco is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Chromosomal and Genetic Variations (6 papers). Fernanda T. Bellucco collaborates with scholars based in Brazil, Canada and United States. Fernanda T. Bellucco's co-authors include Maria Isabel Melaragno, Leslie Domenici Kulikowski, Síntia Belangero, Denise Maria Christofolini, Maria Betânia Pereira Toralles, Rodrigo A. Bressan, Marcos Santoro, Jair de Jesus Mari, Ary Gadelha and Marı́lia de Arruda Cardoso Smith and has published in prestigious journals such as PLoS ONE, Psychiatry Research and Schizophrenia Research.

In The Last Decade

Fernanda T. Bellucco

24 papers receiving 209 citations

Peers

Countries citing papers authored by Fernanda T. Bellucco

Since Specialization

Citations

This map shows the geographic impact of Fernanda T. Bellucco'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 T. Bellucco with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fernanda T. Bellucco more than expected).

Fields of papers citing papers by Fernanda T. Bellucco

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fernanda T. Bellucco. 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 T. Bellucco. The network helps show where Fernanda T. Bellucco may publish in the future.

Co-authorship network of co-authors of Fernanda T. Bellucco

This figure shows the co-authorship network connecting the top 25 collaborators of Fernanda T. Bellucco. A scholar is included among the top collaborators of Fernanda T. Bellucco 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 T. Bellucco. Fernanda T. Bellucco 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

#	Work	Indexed citations
1	Fold-back mechanism originating inv-dup-del rearrangements in chromosomes 13 and 15 2023 ·Chromosome Research ·(unknown), (unknown), (unknown), Vera Ayres Meloni, Eny Maria Goloni‐Bertollo, Fernanda T. Bellucco, Maria Isabel Melaragno	1
2	Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion Syndrome 2022 ·Cytogenetic and Genome Research ·(unknown), (unknown), (unknown), Ana Beatriz Alvarez Pérez, (unknown), Vera Ayres Meloni, Fernanda T. Bellucco, Maria Isabel Melaragno	1
3	Mechanisms of structural chromosomal rearrangement formation 2022 ·Molecular Cytogenetics ·(unknown), (unknown), Fernanda T. Bellucco, Maria Isabel Melaragno	50
4	Antibody indexes in COVID-19 convalescent plasma donors: Unanswered questions 2021 ·Clinics ·T.C. Bonetti, Flávia Roche Moreira Latini, (unknown), Marcelo Cunio Machado Fonseca, Fúlvio A. Scorza, (unknown), Fernanda T. Bellucco, (unknown), (unknown), Manoel João Batista Castelo Girão	1
5	Serologic evidence of West Nile virus and Saint Louis encephalitis virus in horses from Southern Brazil 2021 ·Brazilian Journal of Microbiology ·Matheus Nunes Weber, Ana Cristina Sbaraini Mósena, (unknown), (unknown), (unknown), Débora Regina Lopes dos Santos, Renata da Fontoura Budaszewski, (unknown), (unknown), (unknown), Fernanda T. Bellucco, (unknown), (unknown), Laura H. V. G. Gil, Mauro Riegert Borba, Luís Gustavo Corbellini, Cláudio Wageck Canal	4
6	Partial 5p Gain and 15q Loss in Three Patients from a Family with a t(5;15)(p13.3;q26.3) Translocation 2020 ·Cytogenetic and Genome Research ·Fernanda T. Bellucco, (unknown), (unknown), Maria Isabel Melaragno	2
7	Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literature 2019 ·Molecular Genetics & Genomic Medicine ·Fernanda T. Bellucco, Cláudia Berlim de Mello, Vera Ayres Meloni, Maria Isabel Melaragno	6
8	DGCR2 influences cortical thickness through a mechanism independent of schizophrenia pathogenesis 2019 ·Psychiatry Research ·Síntia Belangero, Vanessa Ota, Ary Gadelha, (unknown), (unknown), Cristiano Noto, Denise Maria Christofolini, Fernanda T. Bellucco, Marcos Santoro, Diego R. Mazzotti, André Zugman, Maria Isabel Melaragno, Marı́lia de Arruda Cardoso Smith, Renata Pellegrino, Håkon Håkonarson, Quirino Cordeiro, Patricia Moretti, Rodrigo A. Bressan, Jair de Jesus Mari, Andrea Parolin Jackowski	3
9	Deletion of Chromosome 13 due to Different Rearrangements and Impact on Phenotype 2019 ·Molecular Syndromology ·Fernanda T. Bellucco, (unknown), Roberta Santos Guilherme, (unknown), Ana Beatriz Alvarez Pérez, Vera Ayres Meloni, Maria Isabel Melaragno	8
10	Complex Small Supernumerary Marker Chromosome Leading to Partial 4q/21q Duplications: Clinical Implication and Review of the Literature 2018 ·Cytogenetic and Genome Research ·Fernanda T. Bellucco, (unknown), (unknown), Ana Beatriz Alvarez Pérez, Maria Isabel Melaragno	3
11	PRODH Polymorphisms, Cortical Volumes and Thickness in Schizophrenia 2014 ·PLoS ONE ·Vanessa Ota, Fernanda T. Bellucco, Ary Gadelha, Marcos Santoro, Cristiano Noto, Denise Maria Christofolini, (unknown), (unknown), Ândrea Ribeiro‐dos‐Santos, Sidney Emanuel Batista dos Santos, Jair de Jesus Mari, Marı́lia de Arruda Cardoso Smith, Maria Isabel Melaragno, Rodrigo A. Bressan, João Ricardo Sato, Andrea Parolin Jackowski, Síntia Belangero	12
12	ZDHHC8 gene may play a role in cortical volumes of patients with schizophrenia 2013 ·Schizophrenia Research ·Vanessa Ota, Ary Gadelha, (unknown), Marcos Santoro, Denise Maria Christofolini, Fernanda T. Bellucco, (unknown), Gustavo L. Ottoni, Diogo R. Lara, Jair de Jesus Mari, Maria Isabel Melaragno, Marı́lia de Arruda Cardoso Smith, Rodrigo A. Bressan, Síntia Belangero, Andrea Parolin Jackowski	20
13	DRD1 rs4532 polymorphism: A potential pharmacogenomic marker for treatment response to antipsychotic drugs 2012 ·Schizophrenia Research ·Vanessa Ota, Letícia Spíndola, Ary Gadelha, (unknown), Marcos Santoro, Denise Maria Christofolini, Fernanda T. Bellucco, Ândrea Ribeiro‐dos‐Santos, Sidney Emanuel Batista dos Santos, Jair de Jesus Mari, Maria Isabel Melaragno, Rodrigo A. Bressan, Marı́lia de Arruda Cardoso Smith, Síntia Belangero	26
14	Wide Clinical Variability in Cat Eye Syndrome Patients: Four Non-Related Patients and Three Patients from the Same Family 2012 ·Cytogenetic and Genome Research ·Síntia Belangero, (unknown), Fernanda T. Bellucco, Denise Maria Christofolini, Leslie Domenici Kulikowski, Roberta Santos Guilherme, (unknown), (unknown), Flávia Piazzon, Mirlene Cecília Soares Pinho Cernach, Maria Isabel Melaragno	16
15	Trisomy 16q21 → qter: Seven‐year follow‐up of a girl with unusually long survival 2010 ·American Journal of Medical Genetics Part A ·(unknown), Fernanda T. Bellucco, (unknown), Renata Pellegrino, Lília Maria de Azevedo Moreira, Maria Betânia Pereira Toralles, Leslie Domenici Kulikowski, Maria Isabel Melaragno	4
16	Cytogenetic molecular delineation of a terminal 18q deletion suggesting neo-telomere formation 2010 ·European Journal of Medical Genetics ·Leslie Domenici Kulikowski, Maisa Yoshimoto, Fernanda T. Bellucco, Síntia Belangero, Denise Maria Christofolini, (unknown), (unknown), Marı́lia de Arruda Cardoso Smith, Jeremy A. Squire, Maria Isabel Melaragno	3
17	Investigating 22q11.2 Deletion and Other Chromosomal Aberrations in Fetuses With Heart Defects Detected by Prenatal Echocardiography 2010 ·Pediatric Cardiology ·Fernanda T. Bellucco, Síntia Belangero, (unknown), (unknown), (unknown), Lílian Maria Lopes, Marco Antônio Borges Lopes, Marcelo Zugaib, Mirlene Cecília Soares Pinho Cernach, Maria Isabel Melaragno	16
18	Subtelomeric rearrangements and copy number variations in people with intellectual disabilities 2010 ·Journal of Intellectual Disability Research ·Denise Maria Christofolini, Marco A. Ramos, Leslie Domenici Kulikowski, Fernanda T. Bellucco, Síntia Belangero, Décio Brunoni, Maria Isabel Melaragno	9
19	A rare case of trisomy 15pter‐q21.2 due to a de novo marker chromosome 2010 ·American Journal of Medical Genetics Part A ·(unknown), Denise Maria Christofolini, Leslie Domenici Kulikowski, Síntia Belangero, Fernanda T. Bellucco, Monica Castro Varela, Célia Priszkulnik Koiffmann, Maisa Yoshimoto, Jeremy A. Squire, (unknown), (unknown), Maria Isabel Melaragno	6
20	Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation 2008 ·Human Genetics ·(unknown), Fernanda T. Bellucco, Leslie Domenici Kulikowski, Maria Betânia Pereira Toralles, Maria Isabel Melaragno	24

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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