Most cited papers from Fondazione Stella Maris

Fondazione Stella Maris

What are the most cited papers from Fondazione Stella Maris?

The most cited paper from Fondazione Stella Maris is "Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs" (S Hong Lee et al., 2013), with 2,374 citations. Next come "Functional impact of global rare copy number variation in autism spectrum disorders" (2,073) and "Analysis of shared heritability in common disorders of the brain" (2,056).

Published TypeFieldAccessAuthorsCitations

Showing 50 of 60 papers. Every paper with more than 241 citations is listed.

Most cited papers, sortable by citations and release date
#	Paper
1	Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs S Hong Lee et al. · Nature Genetics Open access370 authors	11 Aug 2013	2,374
2	Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto et al. · Nature Open access177 authors	8 Jun 2010	2,073
3	Analysis of shared heritability in common disorders of the brain Verneri Anttila et al. · Science Open access577 authors	21 Jun 2018	2,056
4	Early, Accurate Diagnosis and Early Intervention in Cerebral Palsy Iona Novak et al. · Archives of Pediatrics and Adolescent Medicine Open access	17 Jul 2017	1,678
5	A developmental and genetic classification for malformations of cortical development: update 2012 Anthony James Barkovich, Renzo Guerrini, Ruben Kuzniecky et al. · Brain Open access	16 Mar 2012	1,109
6	Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders Dalila Pinto et al. · The American Journal of Human Genetics Open access112 authors	24 Apr 2014	1,037
7	Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature Gillian Rice et al. · Nature Genetics Open access	23 Sep 2012	967
8	Terminology and classification of the cortical dysplasias André Palmini, Imad Najm, GIULIANO AVANZINI et al. · Neurology	23 Mar 2004	955
9	Epilepsy in children Renzo Guerrini · The Lancet	Feb 2006	847
10	Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways Colm T. O'Dushlaine et al. · Nature Neuroscience Open access375 authors	19 Jan 2015	807
11	An early marker for neurological deficits after perinatal brain lesions Heinz F.R. Prechtl, Christa Einspieler, Giovanni Cioni et al. · The Lancet Open access	May 1997	742
12	The core Dravet syndrome phenotype Charlotte Dravet · Epilepsia Open access	Apr 2011	638
13	Characterization of human disease phenotypes associated with mutations in TREX1 , RNASEH2A , RNASEH2B , RNASEH2C , SAMHD1 , ADAR , and IFIH1 Yanick Joseph Crow et al. · American Journal of Medical Genetics Part A Open access136 authors	16 Jan 2015	617
14	Association Between ADHD and Obesity: A Systematic Review and Meta-Analysis Samuele Cortese, Carlos Renato Moreira Maia, Diane St. Fleur et al. · American Journal of Psychiatry ReviewOpen access	28 Aug 2015	613
15	Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling Gillian Rice et al. · Nature Genetics Open access	30 Mar 2014	601
16	A genome-wide scan for common alleles affecting risk for autism Richard Anney et al. · Human Molecular Genetics Open access166 authors	27 Jul 2010	594
17	Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study Christopher D. Whelan et al. · Brain Open access	29 Nov 2017	560
18	Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly Karine Poirier et al. · Nature Genetics Open access	21 Apr 2013	517
19	Autism and social robotics: A systematic review Paola Pennisi, Alessandro Tonacci, Gennaro Tartarisco et al. · Autism Research Review	20 Oct 2015	502
20	Elevated fetal steroidogenic activity in autism Simon Baron‐Cohen, Bonnie Auyeung, B Nørgaard‐Pedersen et al. · Molecular Psychiatry Open access	3 Jun 2014	487
21	Early Intervention for Children Aged 0 to 2 Years With or at High Risk of Cerebral Palsy Catherine Morgan et al. · Archives of Pediatrics and Adolescent Medicine Open access	17 May 2021	472
22	Lamotrigine and Seizure Aggravation in Severe Myoclonic Epilepsy Renzo Guerrini, Charlotte Dravet, Pierre Genton et al. · Epilepsia	May 1998	468
23	The qualitative assessment of general movements in preterm, term and young infants — review of the methodology Christa Einspieler, Heinz F.R. Prechtl, Fabrizio Ferrari et al. · Early Human Development	Nov 1997	466
24	Preliminary Experience with a New Sclerosing Foam in the Treatment of Varicose Veins L Tessari, Attilio Cavezzi, Alessandro Frullini · Dermatologic Surgery	2001	453
25	Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders Claire S. Leblond et al. · PLoS Genetics Open access	9 Feb 2012	450
26	Functional implications of cross-orientation inhibition of cortical visual cells. I. Neurophysiological evidence Maria Concetta Morrone, David C. Burr, Lamberto Maffei · Proceedings of the Royal Society B Biological Sciences	22 Oct 1982	434
27	Preterm and early postterm motor behaviour in low-risk premature infants Giovanni Cioni, Heinz F.R. Prechtl · Early Human Development	Sep 1990	423
28	Theory of Production: A Long-Period Analysis. Christopher Bliss, Heinz Dieter Kurz, Neri Salvadori · The Economic Journal	Nov 1996	421
29	A cortical area that responds specifically to optic flow, revealed by fMRI Maria Concetta Morrone, Michela Tosetti, Domenico Montanaro et al. · Nature Neuroscience	Dec 2000	399
30	Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex Volney L. Sheen, Vijay S Ganesh, Meral Topçu et al. · Nature Genetics Open access	30 Nov 2003	398
31	Sulfasalazine in the treatment of spondylarthropathy Maxime Dougados, Sjef van der Linden, Marjatta Leirisalo‐Repo et al. · Arthritis & Rheumatism	May 1995	389
32	Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations Elena Parrini · Brain	10 May 2006	368
33	Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms Temistocle Lo Giudice, Federica Lombardi, Filippo Maria Santorelli et al. · Experimental Neurology Open access	19 Jun 2014	356
34	Intraneural stimulation elicits discrimination of textural features by artificial fingertip in intact and amputee humans Calogero Maria Oddo, Staniša Raspopović, Fiorenzo Artoni et al. · eLife Open access	7 Mar 2016	341
35	Attentional Skills During the First 6 Months of Age in Autism Spectrum Disorder Sandra Maestro, Filippo Muratori, Maria Cristina Cavallaro et al. · Journal of the American Academy of Child & Adolescent Psychiatry	Oct 2002	336
36	Mutations of ARX are associated with striking pleiotropy and consistent genotype–phenotype correlation Mitsuhiro Kato et al. · Human Mutation	9 Jan 2004	332
37	European guidelines for sclerotherapy in chronic venous disorders Eberhard Rabe, F. X. Breu, Attilio Cavezzi et al. · Phlebology The Journal of Venous Disease	5 Apr 2013	320
38	Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation Agatino Battaglia, H. Eugene Hoyme, Bruno Dallapiccola et al. · PEDIATRICS	Feb 2008	313
39	Interactive Technologies for Autistic Children: A Review Sofiane Boucenna, Antonio Narzisi, Elodie Tilmont et al. · Cognitive Computation	16 May 2014	307
40	Handle the Autism Spectrum Condition during Coronavirus (COVID-19) Stay at Home Period: Ten Tips for Helping Parents and Caregivers of Young Children Antonio Narzisi · Brain Sciences Open access	Apr 2020	301
41	Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets Merel C. Postema et al. · Nature Communications Open access	31 Oct 2019	300
42	Qualitative changes of general movements in preterm infants with brain lesions Fabrizio Ferrari, Giovanni Cioni, Heinz F.R. Prechtl · Early Human Development Open access	Sep 1990	290
43	Benign familial neonatal‐infantile seizures: Characterization of a new sodium channelopathy Samuel Frank Berkovic, Sarah E. Heron, Lucio Giordano et al. · Annals of Neurology	21 Mar 2004	282
44	Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism Ghayda Mirzaa et al. · JAMA Neurology Open access	9 May 2016	281
45	The genetics of Dravet syndrome Carla Marini, Ingrid Eileen Scheffer, Rima Nabbout et al. · Epilepsia	Apr 2011	277
46	Cramped Synchronized General Movements in Preterm Infants as an Early Marker for Cerebral Palsy Fabrizio Ferrari, Giovanni Cioni, Christa Einspieler et al. · Archives of Pediatrics and Adolescent Medicine Open access	May 2002	272
47	Is hemiplegic cerebral palsy equivalent to amblyopia of the corticospinal system? J A Eyre, Martin J. Smith, Lyvia Dabydeen et al. · Annals of Neurology	19 Apr 2007	269
48	Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders Autism Spectrum Disorder et al. · JAMA Psychiatry Open access304 authors	26 Aug 2020	267
49	The Hippocampus, Neurotrophic Factors and Depression Gabriele Masi, Paola Brovedani · CNS Drugs	Nov 2011	262
50	tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia Birgit Susanne Budde et al. · Nature Genetics	17 Aug 2008	260

Citations are OpenAlex's own counts, from its 2026-09-23 snapshot, so the ranking can differ from Google Scholar or Web of Science. A paper is listed for an institution when any of its authors gave it as an affiliation; retracted papers and papers whose citation count cannot be traced to citing works are left out, and a preprint and the article it became are shown once. Release dates are OpenAlex's: where a source gave only a month or a year, that is what is shown. How the lists are chosen.