Roberto Militerni

3.3k total citations
30 papers, 1.9k citations indexed

About

Roberto Militerni is a scholar working on Cognitive Neuroscience, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Roberto Militerni has authored 30 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Cognitive Neuroscience, 16 papers in Genetics and 9 papers in Psychiatry and Mental health. Recurrent topics in Roberto Militerni's work include Autism Spectrum Disorder Research (19 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Child Nutrition and Feeding Issues (8 papers). Roberto Militerni is often cited by papers focused on Autism Spectrum Disorder Research (19 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Child Nutrition and Feeding Issues (8 papers). Roberto Militerni collaborates with scholars based in Italy, Norway and United States. Roberto Militerni's co-authors include Carmela Bravaccio, Antonio M. Persico, Raun D. Melmed, Cindy Schneider, Roberto Sacco, Maurizio Elia, Simona Trillo, Antonio Pascotto, Alessandro Frolli and Mark T. Palermo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Biological Psychiatry and Molecular Psychiatry.

In The Last Decade

Roberto Militerni

30 papers receiving 1.8k citations

Peers

Roberto Militerni

GENET

PMH

Cynthia A. Molloy United States

Michael Chez United States

Lijie Wu China

Roberto Sacco Italy

Jessica A. Hellings United States

Raffaella Tancredi Italy

Veronica J. Hinton United States

Rudimar dos Santos Riesgo Brazil

Kathleen Angkustsiri United States

Thayne L. Sweeten United States

Cynthia A. Molloy United States

Roberto Militerni

1.3k ×1.2

505 ×0.7

GENET

847 ×1.6

PMH

206 ×0.4

403 ×1.8

Citations per year, relative to Roberto Militerni Roberto Militerni (= 1×) peers Cynthia A. Molloy

Countries citing papers authored by Roberto Militerni

Since Specialization

Citations

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

Fields of papers citing papers by Roberto Militerni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberto Militerni

This figure shows the co-authorship network connecting the top 25 collaborators of Roberto Militerni. A scholar is included among the top collaborators of Roberto Militerni 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 Roberto Militerni. Roberto Militerni 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

Esposito, Maria, Francesca Gimigliano, Maria Rosaria Barillari, et al.. (2017). Pediatric selective mutism therapy: a randomized controlled trial. European Journal of Physical and Rehabilitation Medicine. 53(5). 643–650. 12 indexed citations

Gentile, Ivan, Emanuela Zappulo, Roberto Militerni, et al.. (2013). Etiopathogenesis of autism spectrum disorders: Fitting the pieces of the puzzle together. Medical Hypotheses. 81(1). 26–35. 36 indexed citations

Napolioni, Valerio, Federica Lombardi, Roberto Sacco, et al.. (2010). Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes. European Journal of Human Genetics. 19(3). 353–359. 39 indexed citations

Sacco, Roberto, Paolo Curatolo, Barbara Manzi, et al.. (2010). Principal pathogenetic components and biological endophenotypes in autism spectrum disorders. Autism Research. 3(5). 237–252. 81 indexed citations

Magistris, Laura de, V. Familiari, Antonio Pascotto, et al.. (2010). Alterations of the Intestinal Barrier in Patients With Autism Spectrum Disorders and in Their First‐degree Relatives. Journal of Pediatric Gastroenterology and Nutrition. 51(4). 418–424. 398 indexed citations

Muscarella, Lucia Anna, Vito Guarnieri, Roberto Sacco, et al.. (2010). Candidate gene study of HOXB1 in autism spectrum disorder. Molecular Autism. 1(1). 9–9. 6 indexed citations

Lintas, Carla, Roberto Sacco, Krassimira Garbett, et al.. (2008). Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression. Molecular Psychiatry. 14(7). 705–718. 57 indexed citations

Sacco, Roberto, Roberto Militerni, Alessandro Frolli, et al.. (2007). Clinical, Morphological, and Biochemical Correlates of Head Circumference in Autism. Biological Psychiatry. 62(9). 1038–1047. 84 indexed citations

Sacco, Roberto, Jörg Hager, Francis Rousseau, et al.. (2007). Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1. BMC Medical Genetics. 8(1). 11–11. 45 indexed citations

10.

Campbell, Jerry L., James S. Sutcliffe, Philip J. Ebert, et al.. (2006). A genetic variant that disrupts MET transcription is associated with autism. Proceedings of the National Academy of Sciences. 103(45). 16834–16839. 310 indexed citations

11.

D’Amelio, Marcello, Irene Ricci, Roberto Sacco, et al.. (2005). Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions. Molecular Psychiatry. 10(11). 1006–1016. 94 indexed citations

12.

Bellini, Giulia, Carmela Bravaccio, Antonella Gagliano, et al.. (2005). No Evidence for Association Between Dyslexia and <I>DYX1C1</I> Functional Variants in a Group of Children and Adolescents From Southern Italy. Journal of Molecular Neuroscience. 27(3). 311–314. 50 indexed citations

13.

Persico, Antonio M., Leonardo D’Agruma, Leopoldo Zelante, et al.. (2004). Enhanced APOE2 transmission rates in families with autistic probands. Psychiatric Genetics. 14(2). 73–82. 25 indexed citations

14.

Militerni, Roberto, et al.. (2002). Repetitive behaviors in autistic disorder.. European Child & Adolescent Psychiatry. 11(5). 210–218. 166 indexed citations

15.

Mazzei, R., F. L. Conforti, A. Magariello, et al.. (2002). A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis. Journal of Neurology. 249(10). 1398–1400. 14 indexed citations

16.

Persico, Antonio M., Tiziana Pascucci, Stefano Puglisi‐Allegra, et al.. (2002). Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children. Molecular Psychiatry. 7(7). 795–800. 46 indexed citations

17.

Persico, Antonio M., Chris Stodgell, Leopoldo Zelante, et al.. (2002). The HOXA1 G allele may be associated with dysmorphism in autism. 478. 1 indexed citations

18.

Persico, Antonio M., Roberto Militerni, Carmela Bravaccio, et al.. (2001). No association between the 4G/5G polymorphism of the plasminogen activator inhibitor-1 gene promoter and autistic disorder. Psychiatric Genetics. 11(2). 99–103. 10 indexed citations

19.

Militerni, Roberto, et al.. (1999). Intellectual outcome at 12 years of age in congenital hypothyroidism. European Journal of Endocrinology. 141(2). 105–110. 60 indexed citations

20.

Maio, Sara, et al.. (1995). Prognostic factors in the intellectual development at 7 years of age in children with congenital hypothyroidism. Journal of Endocrinological Investigation. 18(10). 774–779. 18 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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