Mariluce Riegel

3.1k total citations
86 papers, 1.5k citations indexed

About

Mariluce Riegel is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mariluce Riegel has authored 86 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Genetics, 40 papers in Molecular Biology and 30 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mariluce Riegel's work include Genomic variations and chromosomal abnormalities (53 papers), Prenatal Screening and Diagnostics (29 papers) and Chromosomal and Genetic Variations (16 papers). Mariluce Riegel is often cited by papers focused on Genomic variations and chromosomal abnormalities (53 papers), Prenatal Screening and Diagnostics (29 papers) and Chromosomal and Genetic Variations (16 papers). Mariluce Riegel collaborates with scholars based in Switzerland, Brazil and United States. Mariluce Riegel's co-authors include Albert Schinzel, Alessandra Baumer, Roberto Giugliani, Dunja Niedrist, Josef Achermann, Josef Wisser, Sandra Leistner‐Segal, Claudio Castellan, Filippo Pinto e Vairo and Andreas H. Zisch and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Obstetrics and Gynecology and BioMed Research International.

In The Last Decade

Mariluce Riegel

81 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mariluce Riegel Switzerland 21 826 523 434 231 164 86 1.5k
Juan Clinton Llerena Brazil 23 601 0.7× 400 0.8× 346 0.8× 117 0.5× 143 0.9× 112 1.6k
Emmanuelle Lemyre Canada 22 879 1.1× 550 1.1× 276 0.6× 95 0.4× 86 0.5× 52 1.3k
Patricia A. Ward United States 25 1.2k 1.5× 1.0k 2.0× 627 1.4× 152 0.7× 200 1.2× 65 2.5k
Beata Nowakowska Poland 21 741 0.9× 563 1.1× 218 0.5× 197 0.9× 92 0.6× 87 1.5k
Yoshikazu Kuroki Japan 26 1.4k 1.7× 835 1.6× 400 0.9× 159 0.7× 139 0.8× 106 2.2k
G. Shashidhar Pai United States 25 981 1.2× 796 1.5× 450 1.0× 257 1.1× 64 0.4× 55 1.9k
Francesca Forzano Italy 22 675 0.8× 505 1.0× 282 0.6× 92 0.4× 41 0.3× 64 1.4k
Géraldine Viot France 21 647 0.8× 674 1.3× 280 0.6× 82 0.4× 121 0.7× 56 1.4k
Helen Kingston United Kingdom 24 645 0.8× 839 1.6× 161 0.4× 76 0.3× 137 0.8× 63 1.9k
Teresa Mattina Italy 18 839 1.0× 764 1.5× 181 0.4× 172 0.7× 183 1.1× 59 1.4k

Countries citing papers authored by Mariluce Riegel

Since Specialization
Citations

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

Fields of papers citing papers by Mariluce Riegel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mariluce Riegel

This figure shows the co-authorship network connecting the top 25 collaborators of Mariluce Riegel. A scholar is included among the top collaborators of Mariluce Riegel 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 Mariluce Riegel. Mariluce Riegel 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.
Poswar, Fabiano de Oliveira, et al.. (2020). Candidate Genes Associated With Neurological Findings in a Patient With Trisomy 4p16.3 and Monosomy 5p15.2. Frontiers in Genetics. 11. 561–561. 3 indexed citations
2.
Vieira, Taiane Alves, Carolina Fischinger Moura de Souza, Lavínia Schüler‐Faccini, et al.. (2019). Information and Diagnosis Networks – tools to improve diagnosis and treatment for patients with rare genetic diseases. Genetics and Molecular Biology. 42(1 suppl 1). 155–164. 10 indexed citations
3.
Moreira, Lília Maria de Azevedo, et al.. (2019). Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome. SHILAP Revista de lepidopterología. 2019(1). 7250838–7250838. 2 indexed citations
4.
Giugliani, Roberto, Fabiano de Oliveira Poswar, Cláudia Vanzella, et al.. (2018). Intrathecal/Intracerebroventricular enzyme replacement therapy for the mucopolysaccharidoses: efficacy, safety, and prospects. Expert Opinion on Orphan Drugs. 6(7). 403–411. 12 indexed citations
5.
Riegel, Mariluce, et al.. (2017). Chromosomal Structural Rearrangements: Characterizing Interstitial Deletions and Duplications in The Clinical Practice. 2 indexed citations
6.
Giugliani, Roberto, Filippo Pinto e Vairo, Francyne Kubaski, et al.. (2017). Neurological manifestations of lysosomal disorders and emerging therapies targeting the CNS. The Lancet Child & Adolescent Health. 2(1). 56–68. 37 indexed citations
7.
Karam, Simone de Menezes, Aluísio J. D. Barros, Alícia Matijasevich, et al.. (2016). Intellectual Disability in a Birth Cohort: Prevalence, Etiology, and Determinants at the Age of 4 Years. Public Health Genomics. 19(5). 290–297. 21 indexed citations
8.
Riegel, Mariluce, et al.. (2014). Molecular cytogenetic evaluation of chromosomal microdeletions: the experience of a public hospital in Southern Brazil. Clinical & Biomedical Research. 34(4). 357–365. 1 indexed citations
9.
Leite, Júlio César Loguercio, et al.. (2014). Microarray-based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances. Jornal de Pediatria. 91(1). 59–67. 14 indexed citations
10.
Schinzel, Albert, Mariluce Riegel, Alessandra Baumer, et al.. (2013). Long‐term follow‐up of four patients with langer–giedion syndrome: Clinical course and complications. American Journal of Medical Genetics Part A. 161(9). 2216–2225. 26 indexed citations
11.
12.
Zech, Nicolas H., Josef Wisser, Giancarlo Natalucci, et al.. (2008). Monochorionic‐diamniotic twins discordant in gender from a naturally conceived pregnancy through postzygotic sex chromosome loss in a 47,XXY zygote. Prenatal Diagnosis. 28(8). 759–763. 43 indexed citations
13.
Bartholdi, Deborah, Sandra P. Toelle, Bernhard Steiner, et al.. (2008). Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: Description in a boy with partial trisomy 10q and monosomy 4q and review of the literature. European Journal of Medical Genetics. 51(2). 113–123. 15 indexed citations
14.
Bauersfeld, Urs, et al.. (2007). The Fate of Children with Microdeletion 22q11.2 Syndrome and Congenital Heart Defect: Clinical Course and Cardiac Outcome. Pediatric Cardiology. 29(1). 76–83. 35 indexed citations
15.
Riegel, Mariluce, Josef Wisser, Alessandra Baumer, & Albert Schinzel. (2006). Postzygotic isochromosome formation as a cause for false‐negative results from chorionic villus chromosome examinations. Prenatal Diagnosis. 26(3). 221–225. 22 indexed citations
16.
Utermann, Barbara, Mariluce Riegel, Dru F. Leistritz, et al.. (2006). Pre‐ and postnatal findings in trisomy 17 mosaicism. American Journal of Medical Genetics Part A. 140A(15). 1628–1636. 17 indexed citations
17.
Riegel, Mariluce, et al.. (2005). Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21. European Journal of Medical Genetics. 48(2). 167–174. 15 indexed citations
18.
Czakó, Márta, Mariluce Riegel, Éva Morava, Albert Schinzel, & György Kosztolányi. (2002). Patient with rheumatoid arthritis and MCA/MR syndrome due to unbalanced der(18) transmission of a paternal translocation t(18;20)(p11.1;p11.1). American Journal of Medical Genetics. 108(3). 226–228. 21 indexed citations
19.
Röthlisberger, Benno, Krystyńa Chrzańowska, Damina Balmer, Mariluce Riegel, & Albert Schinzel. (2000). A supernumerary marker chromosome originating from two different regions of chromosome 18. Journal of Medical Genetics. 37(2). 121–124. 10 indexed citations
20.
Kozlov, Serguei, Mariluce Riegel, Jochen Kinter, et al.. (1999). Assignment<footref rid="foot01"><sup>1</sup></footref> of the gene encoding the neuronal multidomain serine protease neurotrypsin (PRSS12) to human chromosome band 4q25→q26 by in situ hybridization. Cytogenetic and Genome Research. 84(1-2). 107–108. 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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