Milena Simioni

423 citations

26 papers · 272 indexed · h-index 9

Co-authors: 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
Topics: Genomic variations and chromosomal abnormalities (18 papers)Congenital heart defects research (9 papers)Chromosomal and Genetic Variations (8 papers)
Cited by: Genetics Molecular Biology
Journals: PLoS ONE Scientific Reports Gene
Partner nations: Brazil United States United Kingdom

In The Last Decade

Milena Simioni

26 papers receiving 257 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Demographic history differences between Hispanics and Brazilians imprint haplotype features 2022 ·G3 Genes Genomes Genetics ·(unknown),(unknown),Rodrigo Secolin,Vera Lúcia Gil‐da‐Silva‐Lopes,Carmen Sílvia Passos Lima,Paulo Henrique Condeixa de França,Amanda Donatti,Gustavo Jacob Lourenço,Tânia Kawasaki de Araujo,Milena Simioni,Íscia Lopes‐Cendes,Fernando Ferreira Costa,Mônica Barbosa de Melo	2
2	Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergence 2019 ·Scientific Reports ·(unknown),(unknown),Vera Lúcia Gil‐da‐Silva‐Lopes,Milena Simioni,Farid Menaa,Marcos André Cavalcanti Bezerra,(unknown),Aderson S. Araújo,Renata Pellegrino,Håkon Håkonarson,Fernando Ferreira Costa,Mônica Barbosa de Melo	7
3	Copy number variation in the susceptibility to systemic lupus erythematosus 2018 ·PLoS ONE ·(unknown),Milena Simioni,(unknown),Fábio R. Torres,(unknown),Melvin M. Bonilla,Tânia Kawasaki de Araujo,Eduardo Antônio Donadi,Vera Lúcia Gil‐da‐Silva‐Lopes,Bernardo Lemos,Aguinaldo Luíz Simões	8
4	A Pure 2-Mb 3q26.2 Duplication Proximal to the Critical Region of 3q Duplication Syndrome 2018 ·Molecular Syndromology ·(unknown),Milena Simioni,Társis Paiva Vieira,Fabíola Paoli Monteiro,Vera Lúcia Gil‐da‐Silva‐Lopes	2
5	Ancestry Informative Marker Panel to Estimate Population Stratification Using Genome‐wide Human Array 2017 ·Annals of Human Genetics ·(unknown),(unknown),Milena Simioni,(unknown),Fábio R. Torres,(unknown),Tânia Kawasaki de Araujo,Vera Lúcia Gil‐da‐Silva‐Lopes,Eduardo Antônio Donadi,Aguinaldo Luíz Simões	14
6	A New Case of the Rare 10q22.3q23.2 Microdeletion Flanked by Low-Copy Repeats 3/4 2017 ·Molecular Syndromology ·(unknown),Milena Simioni,Társis Paiva Vieira,Fabíola Paoli Monteiro,Vera Lúcia Gil‐da‐Silva‐Lopes	4
7	Genomic imbalances in syndromic congenital heart disease 2017 ·Jornal de Pediatria ·(unknown),Milena Simioni,Társis Paiva Vieira,(unknown),Fabíola Paoli Monteiro,Josiane Souza,Agnes Cristina Fett‐Conte,Têmis Maria Félix,Isabella Lopes Monlleó,Vera Lúcia Gil‐da‐Silva‐Lopes	22
8	Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes 2017 ·Molecular Syndromology ·Milena Simioni,François Artiguenave,Vincent Meyer,(unknown),(unknown),Isabella Lopes Monlleó,Andréa Trevas Maciel‐Guerra,Carlos Eduardo Steiner,Vera Lúcia Gil‐da‐Silva‐Lopes	6
9	A Cytogenomic Approach in a Case of Syndromic XY Gonadal Dysgenesis 2016 ·Sexual Development ·Milena Simioni,Isabella Lopes Monlleó,(unknown),(unknown),(unknown),(unknown),(unknown),Maricilda Palandi de Mello,Vera Lúcia Gil‐da‐Silva‐Lopes	1
10	A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population 2015 ·Journal of Cranio-Maxillofacial Surgery ·Tânia Kawasaki de Araujo,Rodrigo Secolin,Têmis Maria Félix,(unknown),(unknown),Isabella Lopes Monlleó,Josiane Souza,Agnes Cristina Fett‐Conte,Erlane Marques Ribeiro,Ana C. Xavier,Adriana Augusto de Rezende,Milena Simioni,Ândrea Ribeiro‐dos‐Santos,Sidney Emanuel Batista dos Santos,Vera Lúcia Gil‐da‐Silva‐Lopes	40
11	8p23.1 Interstitial Deletion in a Patient with Congenital Cardiopathy, Neurobehavioral Disorders, and Minor Signs Suggesting 22q11.2 Deletion Syndrome 2015 ·Journal of Developmental & Behavioral Pediatrics ·(unknown),Fabíola Paoli Monteiro,Milena Simioni,Vera Lúcia Gil‐da‐Silva‐Lopes	7
12	Genotype‐phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: Natural history of a patient and review of the literature 2015 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),(unknown),Milena Simioni,(unknown),(unknown),Carla Rosenberg,Ana Cristina Victorino Krepischi,Simone Appenzeller,Isabella Lopes Monlleó,Vera Lúcia Gil‐da‐Silva‐Lopes	7
13	Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion 2014 ·American Journal of Medical Genetics Part A ·Roberta Santos Guilherme,(unknown),Milena Simioni,Társis Paiva Vieira,Vera Lúcia Gil‐da‐Silva‐Lopes,Chong Ae Kim,Décio Brunoni,Nancy B. Spinner,Laura K. Conlin,Denise Maria Christofolini,Leslie Domenici Kulikowski,Carlos Eduardo Steiner,Maria Isabel Melaragno	15
14	A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversion 2013 ·Gene ·(unknown),Milena Simioni,(unknown),(unknown),Vera Lúcia Gil‐da‐Silva‐Lopes	19
15	Atypical copy number abnormalities in 22q11.2 region: Report of three cases 2013 ·European Journal of Medical Genetics ·(unknown),Társis Paiva Vieira,(unknown),Milena Simioni,(unknown),Josiane Souza,Fabíola Paoli Monteiro,Vera Lúcia Gil‐da‐Silva‐Lopes	14
16	Partial monosomy 21 (q11.2→q21.3) combined with 3p25.3→pter monosomy due to an unbalanced translocation in a patient presenting dysmorphic features and developmental delay 2012 ·Gene ·(unknown),Társis Paiva Vieira,Milena Simioni,Fabíola Paoli Monteiro,Vera Lúcia Gil‐da‐Silva‐Lopes	3
17	A familial case with interstitial 2q36 deletion: Variable phenotypic expression in full and mosaic state 2012 ·European Journal of Medical Genetics ·Érika L. Freitas,Susan Gribble,Milena Simioni,Társis Paiva Vieira,Elena Prigmore,Ana Cristina Victorino Krepischi,Carla Rosenberg,P. Pearson,Débora Gusmão Melo,Vera Lúcia Gil‐da‐Silva‐Lopes	4
18	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 2012 ·American Journal of Medical Genetics Part A ·Milena Simioni,Társis Paiva Vieira,(unknown),Érika L. Freitas,Carla Rosenberg,Cláudia Vianna Maurer‐Morelli,Íscia Lopes‐Cendes,Agnes Cristina Fett‐Conte,Vera Lúcia Gil‐da‐Silva‐Lopes	18
19	Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization 2011 ·American Journal of Medical Genetics Part A ·Érika L. Freitas,Susan Gribble,Milena Simioni,Társis Paiva Vieira,(unknown),(unknown),Elena Prigmore,Ana Cristina Victorino Krepischi,Carla Rosenberg,Károly Szuhai,Arie van Haeringen,Nigel P. Carter,Vera Lúcia Gil‐da‐Silva‐Lopes	8
20	Investigation of the 22q11.2 candidate region in patients with midline facial defects with hypertelorism 2010 ·Journal of Applied Genetics ·Milena Simioni,Érika L. Freitas,Társis Paiva Vieira,Íscia Lopes‐Cendes,Vera Lúcia Gil‐da‐Silva‐Lopes	2

About Milena Simioni

Milena Simioni is a scholar working on Genetics, Genetics and Developmental Biology, having authored 26 papers that have together received 272 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Congenital heart defects research (9 papers) and Chromosomal and Genetic Variations (8 papers). The work is most often cited by research in Genetics (195 citations), Genetics (31 citations) and Molecular Biology (125 citations). Milena Simioni has collaborated with scholars based in Brazil, United States and United Kingdom. Frequent 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. Their work appears in journals such as PLoS ONE, Scientific Reports and Gene.

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