Décio Brunoni

3.4k total citations
98 papers, 1.8k citations indexed

About

Décio Brunoni is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Décio Brunoni has authored 98 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 28 papers in Cognitive Neuroscience and 21 papers in Molecular Biology. Recurrent topics in Décio Brunoni's work include Autism Spectrum Disorder Research (27 papers), Genomic variations and chromosomal abnormalities (23 papers) and Prenatal Screening and Diagnostics (13 papers). Décio Brunoni is often cited by papers focused on Autism Spectrum Disorder Research (27 papers), Genomic variations and chromosomal abnormalities (23 papers) and Prenatal Screening and Diagnostics (13 papers). Décio Brunoni collaborates with scholars based in Brazil, United States and Canada. Décio Brunoni's co-authors include Ana Beatriz Alvarez Pérez, Chong Ae Kim, Fernando Regla Vargas, Gideon Koren, Lavínia Schüler‐Faccini, Maria Isabel Melaragno, Anne Pastuszak, Juan Clinton Llerena, Leslie Domenici Kulikowski and Vânia D’Almeida and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

Décio Brunoni

93 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Décio Brunoni Brazil	23	555	482	413	305	298	98	1.8k
Stephen R. Braddock United States	25	538 1.0×	525 1.1×	296 0.7×	240 0.8×	302 1.0×	71	1.7k
Arnold L. Christianson South Africa	19	471 0.8×	366 0.8×	435 1.1×	152 0.5×	198 0.7×	52	1.4k
Ingeborg Barišić Croatia	25	525 0.9×	488 1.0×	851 2.1×	710 2.3×	328 1.1×	90	2.2k
Lisa F. Taft United States	12	689 1.2×	553 1.1×	580 1.4×	221 0.7×	418 1.4×	13	1.6k
Faustina Lalatta Italy	24	948 1.7×	714 1.5×	716 1.7×	210 0.7×	214 0.7×	105	1.9k
Juan Clinton Llerena Brazil	23	601 1.1×	400 0.8×	346 0.8×	191 0.6×	237 0.8×	112	1.6k
Helga V. Toriello United States	32	1.4k 2.6×	1.3k 2.8×	707 1.7×	430 1.4×	266 0.9×	97	3.1k
Joseph H. Hersh United States	25	1.3k 2.3×	866 1.8×	554 1.3×	309 1.0×	128 0.4×	82	2.7k
Wendy S. Meschino Canada	29	1.5k 2.7×	758 1.6×	565 1.4×	125 0.4×	247 0.8×	78	3.0k
Sallie B. Freeman United States	20	963 1.7×	812 1.7×	1.2k 2.9×	317 1.0×	756 2.5×	28	2.5k

Countries citing papers authored by Décio Brunoni

Since Specialization

Citations

This map shows the geographic impact of Décio Brunoni'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 Décio Brunoni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Décio Brunoni more than expected).

Fields of papers citing papers by Décio Brunoni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Décio Brunoni. 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 Décio Brunoni. The network helps show where Décio Brunoni may publish in the future.

Co-authorship network of co-authors of Décio Brunoni

This figure shows the co-authorship network connecting the top 25 collaborators of Décio Brunoni. A scholar is included among the top collaborators of Décio Brunoni 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 Décio Brunoni. Décio Brunoni 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

Portolese, Joana, Cristiane Silvestre Paula, Sheila C. Caetano, et al.. (2024). A Normative Model Representing Autistic Individuals Amidst Autism Spectrum Phenotypic Heterogeneity. Brain Sciences. 14(12). 1254–1254. 1 indexed citations

Amato, Cibelle Albuquerque de la Higuera, et al.. (2022). Desempenho motor, competência em leitura, escrita e aritmética no Ensino Fundamental I. Revista Eletrônica de Educação. 16. e4781009–e4781009. 1 indexed citations

Teixeira, María Cristina Triguero Veloz, et al.. (2017). Mismatch between diagnostic reports and special educational needs classification in a public educational system. Arquivos de Neuro-Psiquiatria. 75(4). 244–247. 1 indexed citations

Piazzon, Flávia, S.S. Takeno, Denise Maria Christofolini, et al.. (2012). Cytogenomic characterization of an unexpected 17.6Mb 9p deletion associated to a 14.8Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype. Gene. 496(1). 59–62. 4 indexed citations

Guilherme, Roberta Santos, S.S. Takeno, Renata Pellegrino, et al.. (2012). Twenty-year cytogenetic and molecular follow-up of a patient with ring chromosome 15: a case report. Journal of Medical Case Reports. 6(1). 283–283. 20 indexed citations

Paula, Cristiane Silvestre, Rosane Lowenthal, Eduardo Yoshio Nakano, et al.. (2009). Instrumento para rastreamento dos casos de Transtorno Invasivo do Desenvolvimento. Brazilian Journal of Psychiatry. 31(1). 1 indexed citations

Dathe, Katarina, Klaus Kjaer, Anja Brehm, et al.. (2009). Duplications Involving a Conserved Regulatory Element Downstream of BMP2 Are Associated with Brachydactyly Type A2. The American Journal of Human Genetics. 84(4). 483–492. 120 indexed citations

Brunoni, Décio, et al.. (2009). Genotype-phenotype correlation in Brazillian Rett syndrome patients. Arquivos de Neuro-Psiquiatria. 67(3a). 577–584. 7 indexed citations

Orsati, Fernanda Tebexreni, José Salomão Schwartzman, Décio Brunoni, Tatiana Pontrelli Mecca, & Elizeu Coutinho de Macedo. (2008). NOVAS POSSIBILIDADES NA AVALIAÇÃO NEUROPSICOLÓGICA DOS TRANSTORNOS INVASIVOS DO DESENVOLVIMENTO: ANÁLISE DOS MOVIMENTOS OCULARES. SHILAP Revista de lepidopterología. 3 indexed citations

10.

Kulikowski, Leslie Domenici, Denise Maria Christofolini, Marı́lia de Arruda Cardoso Smith, et al.. (2008). Pure duplication 1q41‐qter: Further delineation of trisomy 1q syndromes. American Journal of Medical Genetics Part A. 146A(20). 2663–2667. 22 indexed citations

11.

Sobreira, Nara, Mirlene Cecília Soares Pinho Cernach, Décio Brunoni, & Ana Beatriz Alvarez Pérez. (2008). Complex toe syndactyly with characteristic facial phenotype: A new syndrome?. American Journal of Medical Genetics Part A. 146A(13). 1725–1728. 3 indexed citations

12.

Christofolini, Denise Maria, Maisa Yoshimoto, Jeremy A. Squire, et al.. (2006). Hydrocephaly, penoscrotal transposition, and digital anomalies associated with de novo pseudodicentric rearranged chromosome 13 characterized by classical cytogenetic methods and mBAND analysis. American Journal of Medical Genetics Part A. 140A(12). 1321–1325. 8 indexed citations

13.

Takeno, S.S., et al.. (2004). Duplication 4p and deletion 4p (Wolf–Hirschhorn syndrome) due to complementary gametes from a 3:1 segregation of a maternal balanced t(4;13)(p16;q11) translocation. American Journal of Medical Genetics Part A. 129A(2). 180–183. 5 indexed citations

14.

Kavamura, Maria Inês, Maria Grazia Pomponi, Marcella Zollino, et al.. (2003). PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndrome. European Journal of Human Genetics. 11(1). 64–68. 22 indexed citations

15.

Pallos, Débora, Patricia Hart, José Roberto Cortelli, et al.. (2001). Novel COL1A1 mutation (G599C) associated with mild osteogenesis imperfecta and dentinogenesis imperfecta. Archives of Oral Biology. 46(5). 459–470. 39 indexed citations

16.

Pérez, Ana Beatriz Alvarez, et al.. (1999). Identification of 8 new mutations in Brazilian families with Marfan syndrome. Human Mutation. 13(1). 84–84. 11 indexed citations

17.

Pastuszak, Anne, Lavínia Schüler‐Faccini, Fernando Regla Vargas, et al.. (1998). Use of Misoprostol during Pregnancy and Möbius' Syndrome in Infants. New England Journal of Medicine. 338(26). 1881–1885. 177 indexed citations

18.

Erwenne, Clélia Maria, et al.. (1988). Bilateral retinoblastoma associated with 13q− mosaicism. Cancer Genetics and Cytogenetics. 32(2). 169–175. 17 indexed citations

19.

Brunoni, Décio, et al.. (1987). Duplication 2q31qter due to a maternal (2;14) translocation. Revista brasileira de genetica. 10(2). 253–260. 1 indexed citations

20.

Brunoni, Décio. (1986). Alto risco genético: aspectos neonatais. 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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