Raquel Boy

741 total citations
25 papers, 264 citations indexed

About

Raquel Boy is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Raquel Boy has authored 25 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Plant Science. Recurrent topics in Raquel Boy's work include Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Chromosomal and Genetic Variations (7 papers). Raquel Boy is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Chromosomal and Genetic Variations (7 papers). Raquel Boy collaborates with scholars based in Brazil, United States and Germany. Raquel Boy's co-authors include Márcia Mattos Gonçalves Pimentel, Cíntia Barros Santos-Rebouças, Ida Vanessa Döederlein Schwartz, Carlos Eduardo Steiner, Angelina Xavier Acosta, Márcia Gonçalves Ribeiro, Taiane Alves Vieira, Fermín Roland Schramm, Chong Ae Kim and Louise L. C. Pinto and has published in prestigious journals such as PLoS ONE, The International Journal of Biochemistry & Cell Biology and Frontiers in Genetics.

In The Last Decade

Raquel Boy

23 papers receiving 257 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raquel Boy Brazil 10 97 85 68 34 31 25 264
Masami Togawa Japan 9 58 0.6× 126 1.5× 118 1.7× 36 1.1× 18 0.6× 16 333
Yann Grattau France 5 100 1.0× 112 1.3× 51 0.8× 45 1.3× 15 0.5× 5 323
Heidi Mateus Colombia 11 119 1.2× 165 1.9× 30 0.4× 18 0.5× 45 1.5× 32 362
Katherine A. White United States 12 67 0.7× 189 2.2× 241 3.5× 44 1.3× 53 1.7× 27 460
Juan Ruiz United States 7 77 0.8× 136 1.6× 126 1.9× 70 2.1× 13 0.4× 23 319
MB Delatycki Australia 10 89 0.9× 37 0.4× 70 1.0× 21 0.6× 12 0.4× 12 377
Anaita Hegde India 10 24 0.2× 58 0.7× 34 0.5× 29 0.9× 31 1.0× 32 240
I. Desguerre France 12 69 0.7× 194 2.3× 26 0.4× 18 0.5× 41 1.3× 37 400
Wakaba Endo Japan 12 108 1.1× 151 1.8× 24 0.4× 15 0.4× 43 1.4× 38 365
Denis Graber France 7 89 0.9× 114 1.3× 83 1.2× 28 0.8× 28 0.9× 10 273

Countries citing papers authored by Raquel Boy

Since Specialization
Citations

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

Fields of papers citing papers by Raquel Boy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raquel Boy

This figure shows the co-authorship network connecting the top 25 collaborators of Raquel Boy. A scholar is included among the top collaborators of Raquel Boy 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 Raquel Boy. Raquel Boy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Santos-Rebouças, Cíntia Barros, et al.. (2023). A novel Xp11.22 duplication involving HUWE1 in a male with syndromic intellectual disability and additional neurological findings. European Journal of Medical Genetics. 66(4). 104716–104716. 1 indexed citations
2.
Santos, Jussara Mendonça dos, Raquel Boy, Claudia M.B. Carvalho, et al.. (2021). Molecular and clinical insights into complex genomic rearrangements related to MECP2 duplication syndrome. European Journal of Medical Genetics. 64(12). 104367–104367. 3 indexed citations
3.
Santos-Rebouças, Cíntia Barros, et al.. (2020). Skewed X-Chromosome Inactivation and Compensatory Upregulation of Escape Genes Precludes Major Clinical Symptoms in a Female With a Large Xq Deletion. Frontiers in Genetics. 11. 101–101. 18 indexed citations
4.
Scaini, Giselli, Carolina Fischinger Moura de Souza, Patrícia Fernanda Schuck, et al.. (2018). Evaluation of plasma biomarkers of inflammation in patients with maple syrup urine disease. Journal of Inherited Metabolic Disease. 41(4). 631–640. 15 indexed citations
5.
Velho, Renata Voltolini, Fernanda Sperb‐Ludwig, Angelina Xavier Acosta, et al.. (2017). GNPTAB missense mutations cause loss of GlcNAc-1-phosphotransferase activity in mucolipidosis type II through distinct mechanisms. The International Journal of Biochemistry & Cell Biology. 92. 90–94. 8 indexed citations
6.
Sperb‐Ludwig, Fernanda, Maria Raquel Santos Carvalho, Pablo Augusto de Souza Fonseca, et al.. (2017). Biotinidase deficiency: Genotype-biochemical phenotype association in Brazilian patients. PLoS ONE. 12(5). e0177503–e0177503. 19 indexed citations
7.
Bender, Fernanda, et al.. (2015). Medical Costs Related to Enzyme Replacement Therapy for Mucopolysaccharidosis Types I, II, and VI in Brazil: A Multicenter Study. Value in Health Regional Issues. 8. 99–106. 8 indexed citations
8.
Santos, Jussara Mendonça dos, Flora Tassone, Márcia Gonçalves Ribeiro, et al.. (2015). FindingFMR1mosaicism in Fragile X syndrome. Expert Review of Molecular Diagnostics. 16(4). 501–507. 18 indexed citations
9.
Boy, Raquel, et al.. (2013). Judicialização da saúde e assistência farmacêutica a doenças raras: o exemplo da mucopolissacaridose tipo I no Brasil. 40(131).
10.
Vieira, Gustavo Henrique Apolinário, Jayson Rodriguez, Raquel Boy, et al.. (2011). Differential diagnosis of Smith–Magenis syndrome: 1p36 deletion syndrome. American Journal of Medical Genetics Part A. 155(5). 988–992. 7 indexed citations
11.
Boy, Raquel, Ida Vanessa Döederlein Schwartz, Bárbara Krug, et al.. (2011). Ethical issues related to the access to orphan drugs in Brazil: the case of mucopolysaccharidosis type I. Journal of Medical Ethics. 37(4). 233–239. 14 indexed citations
12.
Vieira, Taiane Alves, Ida Vanessa Döederlein Schwartz, Louise L. C. Pinto, et al.. (2008). Mucopolysaccharidoses in Brazil: What happens from birth to biochemical diagnosis?. American Journal of Medical Genetics Part A. 146A(13). 1741–1747. 61 indexed citations
13.
Santos-Rebouças, Cíntia Barros, et al.. (2005). ARX mutation c.428–451dup (24bp) in a Brazilian family with X-linked mental retardation. European Journal of Medical Genetics. 49(3). 269–275. 8 indexed citations
14.
Boy, Raquel, et al.. (2004). Premature ovarian failure and FRAXA premutation: Positive correlation in a Brazilian survey. American Journal of Medical Genetics Part A. 126A(3). 237–240. 11 indexed citations
15.
Santos-Rebouças, Cíntia Barros, Helle Hjalgrim, Flávia Raquel Gonçalves Carneiro, et al.. (2003). Concurrence of fragile X and Klinefelter syndromes: report of a new case of paternal nondisjunction. Annales de Génétique. 46(1). 53–55. 3 indexed citations
16.
Santos-Rebouças, Cíntia Barros, et al.. (2003). De novo balanced translocation (2;10)(q24;q22) associated with mental retardation. Annales de Génétique. 46(4). 471–473. 4 indexed citations
17.
Boy, Raquel, et al.. (2002). Premature ovarian failure and FMR1 premutation co-segregation in a large Brazilian family. International Journal of Molecular Medicine. 10(2). 231–3. 6 indexed citations
18.
Raskin, Salmo, Hélio A.G. Teive, Francisco Cardoso, et al.. (2000). Huntington disease: DNA analysis in brazilian population. Arquivos de Neuro-Psiquiatria. 58(4). 977–985. 24 indexed citations
19.
Boy, Raquel, et al.. (1998). Chromosome 6q deletion: Report of a new case and review of the literature. Genetics and Molecular Biology. 21(1). 145–149.
20.
Horovitz, Dafne Dain Gandelman, et al.. (1995). Autosomal dominant osteosclerosis type stanescu: The third family. American Journal of Medical Genetics. 57(4). 605–609. 2 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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