Milena Simioni

423 total citations
26 papers, 272 citations indexed

About

Milena Simioni is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Milena Simioni has authored 26 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 15 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Milena Simioni's work include Genomic variations and chromosomal abnormalities (18 papers), Congenital heart defects research (9 papers) and Chromosomal and Genetic Variations (8 papers). Milena Simioni is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Congenital heart defects research (9 papers) and Chromosomal and Genetic Variations (8 papers). Milena Simioni collaborates with scholars based in Brazil, United States and United Kingdom. Milena Simioni's co-authors include Vera Lúcia Gil‐da‐Silva‐Lopes, Társis Paiva Vieira, Isabella Lopes Monlleó, Tânia Kawasaki de Araujo, Fabíola Paoli Monteiro, Cláudia Vianna Maurer‐Morelli, Agnes Cristina Fett‐Conte, Josiane Souza, Têmis Maria Félix and Ana C. Xavier and has published in prestigious journals such as PLoS ONE, Scientific Reports and Gene.

In The Last Decade

Milena Simioni

26 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
Milena Simioni Brazil 9 195 125 37 33 31 26 272
Koen Devriendt Belgium 9 137 0.7× 205 1.6× 31 0.8× 61 1.8× 11 0.4× 13 290
Cinthya Zepeda‐Mendoza United States 9 92 0.5× 122 1.0× 23 0.6× 32 1.0× 20 0.6× 23 230
G R Jalali United Kingdom 9 163 0.8× 213 1.7× 46 1.2× 54 1.6× 27 0.9× 13 431
Társis Paiva Vieira Brazil 11 226 1.2× 197 1.6× 74 2.0× 36 1.1× 19 0.6× 52 344
Eriko Nishi Japan 9 84 0.4× 113 0.9× 40 1.1× 47 1.4× 23 0.7× 32 252
Michal Klysik United States 7 147 0.8× 234 1.9× 25 0.7× 11 0.3× 13 0.4× 9 380
Heide Seidel Germany 14 192 1.0× 182 1.5× 36 1.0× 32 1.0× 19 0.6× 24 337
A Mavrou Greece 9 104 0.5× 172 1.4× 20 0.5× 26 0.8× 23 0.7× 16 290
Alison Colley Australia 9 129 0.7× 229 1.8× 32 0.9× 30 0.9× 17 0.5× 15 350
Julie Sillibourne United Kingdom 6 126 0.6× 149 1.2× 14 0.4× 17 0.5× 24 0.8× 6 301

Countries citing papers authored by Milena Simioni

Since Specialization
Citations

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

Fields of papers citing papers by Milena Simioni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Milena Simioni

This figure shows the co-authorship network connecting the top 25 collaborators of Milena Simioni. A scholar is included among the top collaborators of Milena Simioni 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 Milena Simioni. Milena Simioni 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.
Secolin, Rodrigo, Vera Lúcia Gil‐da‐Silva‐Lopes, Carmen Sílvia Passos Lima, et al.. (2022). Demographic history differences between Hispanics and Brazilians imprint haplotype features. G3 Genes Genomes Genetics. 12(7). 2 indexed citations
2.
Gil‐da‐Silva‐Lopes, Vera Lúcia, Milena Simioni, Farid Menaa, et al.. (2019). Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergence. Scientific Reports. 9(1). 7 indexed citations
3.
Simioni, Milena, Fábio R. Torres, Melvin M. Bonilla, et al.. (2018). Copy number variation in the susceptibility to systemic lupus erythematosus. PLoS ONE. 13(11). e0206683–e0206683. 8 indexed citations
4.
Simioni, Milena, et al.. (2018). A Pure 2-Mb 3q26.2 Duplication Proximal to the Critical Region of 3q Duplication Syndrome. Molecular Syndromology. 9(4). 197–204. 2 indexed citations
5.
Simioni, Milena, Fábio R. Torres, Tânia Kawasaki de Araujo, et al.. (2017). Ancestry Informative Marker Panel to Estimate Population Stratification Using Genome‐wide Human Array. Annals of Human Genetics. 81(6). 225–233. 14 indexed citations
6.
Simioni, Milena, et al.. (2017). A New Case of the Rare 10q22.3q23.2 Microdeletion Flanked by Low-Copy Repeats 3/4. Molecular Syndromology. 8(3). 161–167. 4 indexed citations
7.
Simioni, Milena, Társis Paiva Vieira, Fabíola Paoli Monteiro, et al.. (2017). Genomic imbalances in syndromic congenital heart disease. Jornal de Pediatria. 93(5). 497–507. 22 indexed citations
8.
Simioni, Milena, François Artiguenave, Vincent Meyer, et al.. (2017). Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes. Molecular Syndromology. 8(4). 187–194. 6 indexed citations
9.
Simioni, Milena, et al.. (2016). A Cytogenomic Approach in a Case of Syndromic XY Gonadal Dysgenesis. Sexual Development. 10(1). 23–27. 1 indexed citations
10.
Araujo, Tânia Kawasaki de, Rodrigo Secolin, Têmis Maria Félix, et al.. (2015). A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population. Journal of Cranio-Maxillofacial Surgery. 44(1). 16–20. 40 indexed citations
11.
Monteiro, Fabíola Paoli, et al.. (2015). 8p23.1 Interstitial Deletion in a Patient with Congenital Cardiopathy, Neurobehavioral Disorders, and Minor Signs Suggesting 22q11.2 Deletion Syndrome. Journal of Developmental & Behavioral Pediatrics. 36(7). 544–548. 7 indexed citations
12.
Simioni, Milena, Carla Rosenberg, Ana Cristina Victorino Krepischi, et al.. (2015). Genotype‐phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: Natural history of a patient and review of the literature. American Journal of Medical Genetics Part A. 170(3). 766–772. 7 indexed citations
13.
Guilherme, Roberta Santos, Milena Simioni, Társis Paiva Vieira, et al.. (2014). Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion. American Journal of Medical Genetics Part A. 164(7). 1659–1665. 15 indexed citations
14.
Simioni, Milena, et al.. (2013). A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversion. Gene. 523(2). 192–194. 19 indexed citations
15.
Vieira, Társis Paiva, et al.. (2013). Atypical copy number abnormalities in 22q11.2 region: Report of three cases. European Journal of Medical Genetics. 56(9). 515–520. 14 indexed citations
16.
17.
Freitas, Érika L., Susan Gribble, Milena Simioni, et al.. (2012). A familial case with interstitial 2q36 deletion: Variable phenotypic expression in full and mosaic state. European Journal of Medical Genetics. 55(11). 660–665. 4 indexed citations
18.
Simioni, Milena, Társis Paiva Vieira, Érika L. Freitas, et al.. (2012). Insertional translocation of 15q25‐q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia. American Journal of Medical Genetics Part A. 158A(11). 2905–2910. 18 indexed citations
19.
Freitas, Érika L., Susan Gribble, Milena Simioni, et al.. (2011). Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization. American Journal of Medical Genetics Part A. 155(11). 2754–2761. 8 indexed citations
20.
Simioni, Milena, Érika L. Freitas, Társis Paiva Vieira, Íscia Lopes‐Cendes, & Vera Lúcia Gil‐da‐Silva‐Lopes. (2010). Investigation of the 22q11.2 candidate region in patients with midline facial defects with hypertelorism. Journal of Applied Genetics. 51(2). 219–221. 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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