Most cited papers from IRCCS Eugenio Medea

IRCCS Eugenio Medea

What are the most cited papers from IRCCS Eugenio Medea?

The most cited paper from IRCCS Eugenio Medea is "Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)" (Daniel J. Klionsky et al., 2016), with 6,023 citations. Next come "Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1" (2,743) and "Factors Influencing Children’s Eating Behaviours" (1,260).

Published TypeFieldAccessAuthorsCitations

Showing 50 of 60 papers. Every paper with more than 248 citations is listed.

Most cited papers, sortable by citations and release date
#	Paper
1	Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) Daniel J. Klionsky et al. · Autophagy Open access2,467 authors	2 Jan 2016	6,023
2	Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1 Daniel J. Klionsky et al. · Autophagy Open access2,930 authors	2 Jan 2021	2,743
3	Factors Influencing Children’s Eating Behaviours Silvia Scaglioni, Valentina De Cosmi, Valentina Ciappolino et al. · Nutrients Open access	31 May 2018	1,260
4	Human cingulate cortex and autonomic control: converging neuroimaging and clinical evidence Hugo Critchley, Christopher J. Mathias, Oliver Josephs et al. · Brain Open access	5 Sep 2003	1,217
5	Characterizing the RNA targets and position-dependent splicing regulation by TDP-43 James R. Tollervey, Tomaž Curk, Boris Rogelj et al. · Nature Neuroscience Open access	27 Feb 2011	1,213
6	Calorie Restriction Promotes Mitochondrial Biogenesis by Inducing the Expression of eNOS Enzo Nisoli, Cristina Tonello, Annalisa Cardile et al. · Science	13 Oct 2005	1,110
7	Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group for the ENIGMA Bipolar Disorder Working Group et al. · Molecular Psychiatry Open access124 authors	2 May 2017	838
8	Molecular Evolution of Human Coronavirus Genomes Diego Forni, Rachele Cagliani, Mario Salvatore Clerici et al. · Trends in Microbiology ReviewOpen access	19 Oct 2016	793
9	Developmental trajectory of number acuity reveals a severe impairment in developmental dyscalculia Manuela Piazza, Andrea Facoetti, Anna Noemi Trussardi et al. · Cognition	12 Apr 2010	746
10	Aging-Dependent Large Accumulation of Point Mutations in the Human mtDNA Control Region for Replication Yuichi Michikawa, Franca Mazzucchelli, Nereo Bresolin et al. · Science	22 Oct 1999	730
11	Signatures of Environmental Genetic Adaptation Pinpoint Pathogens as the Main Selective Pressure through Human Evolution Matteo Fumagalli, Manuela Sironi, Uberto Pozzoli et al. · PLoS Genetics Open access	3 Nov 2011	630
12	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
13	A cultural effect on brain function Eraldo Paulesu, Eamon J. P. McCrory, Ferruccio Fazio et al. · Nature Neuroscience	2000	600
14	A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures Andrew J. Sharp et al. · Nature Genetics Open access	17 Feb 2008	595
15	Acid sphingomyelinase activity triggers microparticle release from glial cells Fabio Bianco, Cristiana Perrotta, Luisa Novellino et al. · The EMBO Journal Open access	19 Mar 2009	595
16	A Causal Link between Visual Spatial Attention and Reading Acquisition Sandro Franceschini, Simone Gori, Milena Ruffino et al. · Current Biology Open access	5 Apr 2012	537
17	Action Video Games Make Dyslexic Children Read Better Sandro Franceschini, Simone Gori, Milena Ruffino et al. · Current Biology Open access	28 Feb 2013	529
18	Homotypic fusion of ER membranes requires the dynamin-like GTPase Atlastin Genny Orso, Diana Pendin, Song Liu et al. · Nature	26 Jul 2009	487
19	Testing the 8-Syndrome Structure of the Child Behavior Checklist in 30 Societies Masha Y. Ivanova et al. · Journal of Clinical Child & Adolescent Psychology	17 Jul 2007	427
20	De novo mutations in ATP1A3 cause alternating hemiplegia of childhood Erin L. Heinzen et al. · Nature Genetics Open access	29 Jul 2012	427
21	Taxonomy of the order Bunyavirales: update 2019 Abulikemu Abudurexiti et al. · Archives of Virology Open access103 authors	7 May 2019	406
22	Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements Sabrina Giglio, Karl W. Broman, Naomichi Matsumoto et al. · The American Journal of Human Genetics Open access	Apr 2001	399
23	Behavioral and Emotional Problems Reported by Parents of Children Ages 6 to 16 in 31 Societies Leslie A. Rescorla et al. · Journal of Emotional and Behavioral Disorders Open access	Jul 2007	398
24	Disorders of cognitive and affective development in cerebellar malformations Alessandro Tavano, Roberto Grasso, Chiara Gagliardi et al. · Brain	14 Sep 2007	383
25	Human circulating AC133+ stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle Yvan Torrente, M. Belicchi, Maurilio Sampaolesi et al. · Journal of Clinical Investigation Open access	15 Jul 2004	370
26	Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients Manuela De Gregori et al. · Journal of Medical Genetics Open access	31 Aug 2007	359
27	International Consensus Based Review and Recommendations for Minimum Reporting Standards in Research on Transcutaneous Vagus Nerve Stimulation (Version 2020) Adam Donald Farmer et al. · Frontiers in Human Neuroscience Open access	23 Mar 2021	358
28	Controlling Memory Impairment in Elderly Adults Using Virtual Reality Memory Training: A Randomized Controlled Pilot Study Gabriele Optale, Cosimo Urgesi, Valentina Busato et al. · Neurorehabilitation and neural repair Open access	24 Nov 2009	333
29	Microvesicles released from microglia stimulate synaptic activity via enhanced sphingolipid metabolism Flavia Antonucci, Elena Turola, Loredana Riganti et al. · The EMBO Journal Open access	13 Jan 2012	333
30	Extra-large letter spacing improves reading in dyslexia Marco Zorzi, Chiara Barbiero, Andrea Facoetti et al. · Proceedings of the National Academy of Sciences Open access	4 Jun 2012	332
31	Fronto-limbic brain structures in suicidal and non-suicidal female patients with major depressive disorder Emel Serap Monkul, J. P. Hatch, María Aparecida Nicoletti et al. · Molecular Psychiatry Open access	5 Sep 2002	330
32	CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders Bernd Wissinger et al. · The American Journal of Human Genetics Open access	Oct 2001	329
33	Disruption of the ProSAP2 Gene in a t(12;22)(q24.1;q13.3) Is Associated with the 22q13.3 Deletion Syndrome María Clara Bonaglia, Roberto Giorda, Renato Borgatti et al. · The American Journal of Human Genetics Open access	Aug 2001	329
34	Evolutionary insights into host–pathogen interactions from mammalian sequence data Manuela Sironi, Rachele Cagliani, Diego Forni et al. · Nature Reviews Genetics ReviewOpen access	18 Mar 2015	323
35	A different vision of dyslexia: Local precedence on global perception Sandro Franceschini, Sara Bertoni, Tiziana Gianesini et al. · Scientific Reports Open access	6 Dec 2017	318
36	Definitions and classification of malformations of cortical development: practical guidelines Mariasavina Severino, Ana Filipa Geraldo, Norbert Utz et al. · Brain Open access	11 May 2020	311
37	The Bilingual Brain: Cerebral Representation of Languages Franco Fabbro · Brain and Language	Nov 2001	305
38	Multisensory Spatial Attention Deficits Are Predictive of Phonological Decoding Skills in Developmental Dyslexia Andrea Facoetti, Anna Noemi Trussardi, Milena Ruffino et al. · Journal of Cognitive Neuroscience	14 Apr 2009	301
39	2020 taxonomic update for phylum Negarnaviricota (Riboviria: Orthornavirae), including the large orders Bunyavirales and Mononegavirales Jens H. Kuhn et al. · Archives of Virology Open access229 authors	4 Sep 2020	298
40	Low-grade glioma surgery in eloquent areas: volumetric analysis of extent of resection and its impact on overall survival. A single-institution experience in 190 patients Tamara Ius, Miriam Isola, Riccardo Budai et al. · Journal of neurosurgery	5 Oct 2012	297
41	Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy. Makoto Yoneda, Anne Chomyn, Andrea Martinuzzi et al. · Proceedings of the National Academy of Sciences Open access	Dec 1992	294
42	Visual-Spatial Attention in Developmental Dyslexia Andrea Facoetti, P PAGANONI, Massimo Turatto et al. · Cortex	2000	285
43	Preschool Psychopathology Reported by Parents in 23 Societies: Testing the Seven-Syndrome Model of the Child Behavior Checklist for Ages 1.5–5 Masha Y. Ivanova et al. · Journal of the American Academy of Child & Adolescent Psychiatry Open access	12 Nov 2010	285
44	Different underlying neurocognitive deficits in developmental dyslexia: A comparative study Deny Menghini, Alessandra Finzi, Mariagrazia Benassi et al. · Neuropsychologia	12 Nov 2009	278
45	HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment Claudia Colussi et al. · Proceedings of the National Academy of Sciences Open access	Dec 2008	277
46	Identification of a Primitive Brain–Derived Neural Stem Cell Population Based on Aldehyde Dehydrogenase Activity Stefania Paola Corti, Federica Locatelli, Dimitra A. Papadimitriou et al. · Stem Cells	18 Nov 2005	276
47	Autophagy as a new therapeutic target in Duchenne muscular dystrophy Clara De Palma, Federica Morisi, Stefania Cheli et al. · Cell Death and Disease Open access	15 Nov 2012	275
48	Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy John R. Guy, Xiaoping Qi, Francesco Pallotti et al. · Annals of Neurology	11 Oct 2002	274
49	Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2 Marcella Zollino, Rosetta Lecce, Rita Fischetto et al. · The American Journal of Human Genetics Open access	Mar 2003	271
50	Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation Sabrina Giglio, Vladimiro Calvari, Giuliana Gregato et al. · The American Journal of Human Genetics Open access	Aug 2002	266

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.