Mara Cavallin

574 total citations
13 papers, 185 citations indexed

About

Mara Cavallin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Cell Biology. According to data from OpenAlex, Mara Cavallin has authored 13 papers receiving a total of 185 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Cell Biology. Recurrent topics in Mara Cavallin's work include Fetal and Pediatric Neurological Disorders (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). Mara Cavallin is often cited by papers focused on Fetal and Pediatric Neurological Disorders (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). Mara Cavallin collaborates with scholars based in France, Italy and Netherlands. Mara Cavallin's co-authors include Nadia Bahi‐Buisson, Nathalie Boddaert, Jamel Chelly, Karine Poirier, Annie Laquerrière, Jelena Martinović, Rita Garbelli, Laura Tassi, Anna Maria Buccoliero and Stéphanie Valence and has published in prestigious journals such as Journal of Neuropathology & Experimental Neurology, Journal of Medical Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Mara Cavallin

13 papers receiving 182 citations

Peers

Mara Cavallin

GENET

PPCH

CMN

Kristin Petras United States

Chloe Stutterd Australia

Abdelhafid Natiq Morocco

Marisol Mirabelli-Badenier Italy

Kim Doheny United States

Leanne Moynihan United Kingdom

Emilie Landais France

Aurélie Toussaint France

Simone Gana Italy

Marie Laure Moutard France

Kristin Petras United States

Mara Cavallin

141 ×1.4

189 ×2.6

GENET

80 ×1.6

PPCH

35 ×0.9

33 ×1.3

CMN

Citations per year, relative to Mara Cavallin Mara Cavallin (= 1×) peers Kristin Petras

Countries citing papers authored by Mara Cavallin

Since Specialization

Citations

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

Fields of papers citing papers by Mara Cavallin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mara Cavallin

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

All Works

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13 of 13 papers shown

Cetica, Valentina, et al.. (2024). Double gonosomal mosaicism as an unusual hereditary mechanism in familial GRIN2A-related disorder. Journal of Medical Genetics. 61(10). 999–1002. 1 indexed citations

Liccioli, Giulia, Gabriele Simonini, Federico Melani, et al.. (2020). Hypersensitivity to Rituximab in Children. Pharmacology. 106(5-6). 341–344. 1 indexed citations

Guerrini, Renzo, Mara Cavallin, Tommaso Pippucci, et al.. (2020). Is Focal Cortical Dysplasia/Epilepsy Caused by Somatic MTOR Mutations Always a Unilateral Disorder?. Neurology Genetics. 7(1). e540–e540. 22 indexed citations

Cavallin, Mara, Tjitske Kleefstra, Lonneke de Boer, et al.. (2018). Mutations in TBR1 gene leads to cortical malformations and intellectual disability. European Journal of Medical Genetics. 61(12). 759–764. 21 indexed citations

Deloison, B., P. Sonigo, A. Millischer, et al.. (2018). Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome. European Journal of Medical Genetics. 61(12). 773–782. 12 indexed citations

Cavallin, Mara, Marie Hully, Nathalie Boddaert, et al.. (2018). TLE1, a key player in neurogenesis, a new candidate gene for autosomal recessive postnatal microcephaly. European Journal of Medical Genetics. 61(12). 729–732. 7 indexed citations

Cavallin, Mara, Laurent Salomon, Christine Bole, et al.. (2018). Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria and growth restriction. European Journal of Medical Genetics. 61(12). 755–758. 7 indexed citations

Cavallin, Mara, Manuèle Miné, Nathalie Boddaert, et al.. (2018). Further refinement of COL4A1 and COL4A2 related cortical malformations. European Journal of Medical Genetics. 61(12). 765–772. 23 indexed citations

Cavallin, Mara, A. Millischer, Despina Moshous, et al.. (2017). Prenatal and postnatal presentations of corpus callosum agenesis with polymicrogyria caused by EGP5 mutation. American Journal of Medical Genetics Part A. 173(3). 706–711. 10 indexed citations

10.

Laquerrière, Annie, Mara Cavallin, Françoise Chapon, et al.. (2017). Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 Mutations. Journal of Neuropathology & Experimental Neurology. 76(3). 195–205. 16 indexed citations

11.

Cavallin, Mara, Emilia K. Bijlsma, Sébastien Moutton, et al.. (2016). Recurrent KIF2A mutations are responsible for classic lissencephaly. Neurogenetics. 18(2). 73–79. 21 indexed citations

12.

Poirier, Karine, Jelena Martinović, A. Laquérrière, et al.. (2015). Rare ACTG1 variants in fetal microlissencephaly. European Journal of Medical Genetics. 58(8). 416–418. 22 indexed citations

13.

Laquerrière, Annie, Marie Gonzalès, Yoann Saillour, et al.. (2015). De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathy. European Journal of Medical Genetics. 59(4). 249–256. 22 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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