부산대학교 도서관

Felice Capraro; Giancarlo Gualato; Giovanni Agati

Casiraghi, E.; Malchiodi, D.; Trucco, G.; Frasca, M.; Cappelletti, L.; Fontana, T.; Esposito, A.A.; Avola, E.; Jachetti, A.; Reese, J.; Rizzi, A.; Robinson, P.N.; Valentini, G.

IEEE Access Access, IEEE. 8:196299-196325 2020

Avola, D.; Cinque, L.; Emam, E.; Fontana, F.; Luca Foresti, G.; Raoul Marini, M.; Mecca, A.; Pannone, D.

IEEE Access Access, IEEE. 12:125332-125357 2024

Avola, D.; Cinque, L.; Fagioli, A.; Filetti, S.; Grani, G.; Rodola, E.

IEEE Transactions on Circuits and Systems for Video Technology IEEE Trans. Circuits Syst. Video Technol. Circuits and Systems for Video Technology, IEEE Transactions on. 32(5):2527-2534 May, 2022

Avola, D.; Cascio, M.; Cinque, L.; Foresti, G.L.; Massaroni, C.; Rodola, E.

IEEE Transactions on Multimedia IEEE Trans. Multimedia Multimedia, IEEE Transactions on. 22(10):2481-2496 Oct, 2020

D'Avola, D; Lopez-Franco, E; Sangro, B; Paneda, A; Grossios, N; Gil-Farina, I; Benito, A; Twisk, J; Paz, M; Ruiz, J

JOURNAL OF HEPATOLOGY. 65(4):776-783

Jensen M; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Smolen C; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Tyryshkina A; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Pizzo L; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Sun J; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Noss S; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Banerjee D; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Oetjens M; Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA 17837, USA.; Shimelis H; Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA 17837, USA.; Taylor CM; Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA 17837, USA.; Pounraja VK; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Song H; Department of Statistics, Pennsylvania State University, University Park, PA 16802, USA.; Rohan L; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; Huber E; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.; El Khattabi L; Paris Brain Institute, Sorbonne Université, Inserm U1127, CNRS UMR 7225, Hôpital Pitié Salpêtrière, 75013 Paris, France.; van de Laar I; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, 3000 Rotterdam, the Netherlands.; Tadros R; Department of Experimental Cardiology, Amsterdam University Medical Center, University of Amsterdam, 1081 Amsterdam, the Netherlands.; Bezzina CR; Department of Experimental Cardiology, Amsterdam University Medical Center, University of Amsterdam, 1081 Amsterdam, the Netherlands.; van Slegtenhorst M; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, 3000 Rotterdam, the Netherlands.; Kammeraad J; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, 3000 Rotterdam, the Netherlands.; Prontera P; Medical Genetics Unit, Hospital Santa Maria della Misericordia, 06156 Perugia, Italy.; Caberg JH; Centre Hospitalier Universitaire de Liège, Domaine Universitaire du Sart Tilman, 4000 Liège, Belgium.; Fraser H; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PL, UK.; Banka S; Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PL, UK; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Central Manchester University Hospitals, NHS Foundation Trust Manchester Academic Health Sciences Centre, Manchester M13 9WL, UK.; Van Dijck A; Department of Medical Genetics, University and University Hospital Antwerp, 2650 Edegem, Belgium.; Schwartz C; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Voorhoeve E; Department of Human Genetics, Amsterdam Reproduction & Development Research Institute, Amsterdam UMC, Vrije Universiteit Amsterdam, 1105 AZ Amsterdam, the Netherlands.; Callier P; Laboratoire de Genetique Chromosomique et Moleculaire, CHU Dijon, 21000 Dijon, France.; Mosca-Boidron AL; Laboratoire de Genetique Chromosomique et Moleculaire, CHU Dijon, 21000 Dijon, France.; Marle N; Laboratoire de Genetique Chromosomique et Moleculaire, CHU Dijon, 21000 Dijon, France.; Lefebvre M; Laboratoire de Genetique Chromosomique et Moleculaire, CHU Dijon, 21000 Dijon, France.; Pope K; Bruce Lefroy Centre, Murdoch Children's Research Institute, Parkville, VIC 3052, Australia.; Snell P; Bruce Lefroy Centre, Murdoch Children's Research Institute, Parkville, VIC 3052, Australia.; Boys A; Bruce Lefroy Centre, Murdoch Children's Research Institute, Parkville, VIC 3052, Australia.; Lockhart PJ; Bruce Lefroy Centre, Murdoch Children's Research Institute, Parkville, VIC 3052, Australia; Department of Paediatrics, University of Melbourne, Parkville, VIC 3010, Australia.; Ashfaq M; Department of Pediatrics, McGovern Medical School, University of Texas Health Science Center, Houston, TX 77030, USA.; McCready E; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON L8S 4L8, Canada.; Nowacyzk M; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON L8S 4L8, Canada.; Castiglia L; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Galesi O; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Avola E; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Mattina T; Section of Clinical Biochemistry and Medical Genetics, Department of Biomedical and Biotechnological Sciences, University of Catania School of Medicine, 95131 Catania, Italy.; Fichera M; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy; Section of Clinical Biochemistry and Medical Genetics, Department of Biomedical and Biotechnological Sciences, University of Catania School of Medicine, 95131 Catania, Italy.; Bruccheri MG; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Mandarà GML; Medical Genetics, ASP Ragusa, 97100 Ragusa, Italy.; Mari F; Medical Genetics Unit of the General Hospital of Siena, University of Siena, 53100 Siena, Italy.; Privitera F; Medical Genetics Unit of the General Hospital of Siena, University of Siena, 53100 Siena, Italy.; Longo I; Medical Genetics Unit of the General Hospital of Siena, University of Siena, 53100 Siena, Italy.; Curró A; Medical Genetics Unit of the General Hospital of Siena, University of Siena, 53100 Siena, Italy.; Renieri A; Medical Genetics Unit of the General Hospital of Siena, University of Siena, 53100 Siena, Italy.; Keren B; Department of Genetics, Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, Sorbonne University, 75013 Paris, France.; Charles P; Department of Genetics, Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, Sorbonne University, 75013 Paris, France.; Cuinat S; Medical Genetics Department, CHU Nantes, 44093 Nantes, France.; Nizon M; Medical Genetics Department, CHU Nantes, 44093 Nantes, France.; Pichon O; Medical Genetics Department, CHU Nantes, 44093 Nantes, France.; Bénéteau C; Medical Genetics Department, CHU Nantes, 44093 Nantes, France.; Stoeva R; Department of Medical Genetics, Le Mans Hospital, 72037 Le Mans, France.; Martin-Coignard D; Department of Medical Genetics, Le Mans Hospital, 72037 Le Mans, France.; Blesson S; Department of Genetics, Bretonneau University Hospital, 37000 Tours, France.; Le Caignec C; Department of Medical Genetics, CHU Toulouse, 31300 Toulouse, France; Toulouse Neuro Imaging Center, Inserm, UPS, Université de Toulouse, 31300 Toulouse, France.; Mercier S; Medical Genetics Department, CHU Nantes, 44093 Nantes, France.; Vincent M; Medical Genetics Department, CHU Nantes, 44093 Nantes, France.; Martin CL; Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA 17837, USA.; Mannik K; Institute of Genomics, University of Tartu, 50090 Tartu, Estonia; Health2030 Genome Center, Fondation Campus Biotech, 1202 Geneva, Switzerland.; Reymond A; Center for Integrative Genomics, Faculty of Biology and Medicine, University of Lausanne, 1015 Lausanne, Switzerland.; Faivre L; Center for Rare Diseases and Reference Developmental Anomalies and Malformation Syndromes, CHU Dijon, 21000 Dijon, France.; Sistermans E; Department of Human Genetics, Amsterdam Reproduction & Development Research Institute, Amsterdam UMC, Vrije Universiteit Amsterdam, 1105 AZ Amsterdam, the Netherlands.; Kooy RF; Department of Medical Genetics, University and University Hospital Antwerp, 2650 Edegem, Belgium.; Amor DJ; Bruce Lefroy Centre, Murdoch Children's Research Institute, Parkville, VIC 3052, Australia; Department of Paediatrics, University of Melbourne, Parkville, VIC 3010, Australia.; Romano C; Research Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy; Section of Clinical Biochemistry and Medical Genetics, Department of Biomedical and Biotechnological Sciences, University of Catania School of Medicine, 95131 Catania, Italy.; Andrieux J; Institut de Genetique Medicale, Hopital Jeanne de Flandre, CHRU de Lille, 59000 Lille, France.; Girirajan S; Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA. Electronic address: sxg47@psu.edu.

Publisher: Cell Press Country of Publication: United States NLM ID: 0413066 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-4172 (Electronic) Linking ISSN: 00928674 NLM ISO Abbreviation: Cell Subsets: MEDLINE

Jacob Long; Laura Mezei; Lira Souza-Gonzaga; Trent E. Johnson; Armando Corsi; Sue Bastian

OENO One, Vol 57, Iss 4 (2023)

Maurizio Avola; Anna Cortese

Quaderni di Sociologia, Vol 58, Pp 7-40 (2012)

Calì F; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Department of Medicine and Surgery, Kore University of Enna, 94100 Enna, Italy.; Treccarichi S; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Vinci M; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Avola E; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Musumeci A; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Ragalmuto A; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Costanza C; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Greco D; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Brancato D; Department of Biological, Geological and Environmental Sciences, University of Catania, 95124 Catania, Italy.; Federico C; Department of Biological, Geological and Environmental Sciences, University of Catania, 95124 Catania, Italy.; Città S; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Di Blasi FD; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Saccone S; Department of Biological, Geological and Environmental Sciences, University of Catania, 95124 Catania, Italy.; Scudieri P; Medical Genetics Unit, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genoa, 16147 Genoa, Italy.; Zara F; Medical Genetics Unit, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genoa, 16147 Genoa, Italy.; Elia M; Oasi Research Institute-IRCCS, 94018 Troina, Italy.; Department of Medicine and Surgery, Kore University of Enna, 94100 Enna, Italy.

Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE

G. Russo; E. Ponzo; M. Avola; G. Morabito; G. Danna; V. Fascetto; G. Mancuso

Microbiologia Medica, Vol 38, Iss 1 (2023)

Tianyun Wang; Kendra Hoekzema; Davide Vecchio; Huidan Wu; Arvis Sulovari; Bradley P. Coe; Madelyn A. Gillentine; Amy B. Wilfert; Luis A. Perez-Jurado; Malin Kvarnung; Yoeri Sleyp; Rachel K. Earl; Jill A. Rosenfeld; Madeleine R. Geisheker; Lin Han; Bing Du; Chris Barnett; Elizabeth Thompson; Marie Shaw; Renee Carroll; Kathryn Friend; Rachael Catford; Elizabeth E. Palmer; Xiaobing Zou; Jianjun Ou; Honghui Li; Hui Guo; Jennifer Gerdts; Emanuela Avola; Giuseppe Calabrese; Maurizio Elia; Donatella Greco; Anna Lindstrand; Ann Nordgren; Britt-Marie Anderlid; Geert Vandeweyer; Anke Van Dijck; Nathalie Van der Aa; Brooke McKenna; Miroslava Hancarova; Sarka Bendova; Marketa Havlovicova; Giovanni Malerba; Bernardo Dalla Bernardina; Pierandrea Muglia; Arie van Haeringen; Mariette J. V. Hoffer; Barbara Franke; Gerarda Cappuccio; Martin Delatycki; Paul J. Lockhart; Melanie A. Manning; Pengfei Liu; Ingrid E. Scheffer; Nicola Brunetti-Pierri; Nanda Rommelse; David G. Amaral; Gijs W. E. Santen; Elisabetta Trabetti; Zdeněk Sedláček; Jacob J. Michaelson; Karen Pierce; Eric Courchesne; R. Frank Kooy; The SPARK Consortium; Magnus Nordenskjöld; Corrado Romano; Hilde Peeters; Raphael A. Bernier; Jozef Gecz; Kun Xia; Evan E. Eichler

Nature Communications, Vol 11, Iss 1, Pp 1-13 (2020)

Bojan Losic; Amanda J. Craig; Carlos Villacorta-Martin; Sebastiao N. Martins-Filho; Nicholas Akers; Xintong Chen; Mehmet E. Ahsen; Johann von Felden; Ismail Labgaa; Delia DʹAvola; Kimaada Allette; Sergio A. Lira; Glaucia C. Furtado; Teresa Garcia-Lezana; Paula Restrepo; Ashley Stueck; Stephen C. Ward; Maria I. Fiel; Spiros P. Hiotis; Ganesh Gunasekaran; Daniela Sia; Eric E. Schadt; Robert Sebra; Myron Schwartz; Josep M. Llovet; Swan Thung; Gustavo Stolovitzky; Augusto Villanueva

Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)

Laura V. Mezei; Trent E. Johnson; Steven Goodman; Cassandra Collins; Sue Bastian

OENO One, Vol 55, Iss 2 (2021)

Saliba T; Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.; Rotzinger D; Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.; Vietti-Violi N; Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.; Avola E; Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.

Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101467888 Publication Model: eCollection Cited Medium: Print ISSN: 1930-0433 (Print) Linking ISSN: 19300433 NLM ISO Abbreviation: Radiol Case Rep Subsets: PubMed not MEDLINE

Mitchell E; Douglas A; Kjaegaard S; Callewaert B; Vanlander A; Janssens S; Lawson Yuen A; Skinner C; Failla P; Alberti A; Avola E; FICHERA, Marco; Kibaek M; Digilio MC; Hannibal MC; den Hollander NS; Bizzarri V; Renieri A; Mencarelli MA; Fitzgerald T; Piazzolla S; van Oudenhove E; Romano C; Schwartz C; Eichler EE; Slavotinek A; Escobar L; Rajan D; Crolla J; Carter N; Hodge JC; Mefford HC

Mitchell, E, Douglas, A, Kjaegaard, S, Callewaert, B, Vanlander, A, Janssens, S, Yuen, A L, Skinner, C, Failla, P, Alberti, A, Avola, E, Fichera, M, Kibæk, M, Digilio, M C, Hannibal, M C, den Hollander, N S, Bizzarri, V, Renieri, A, Mencarelli, M A, Fitzgerald, T, Piazzolla, S, van Oudenhove, E, Romano, C, Schwartz, C, Eichler, E E, Slavotinek, A, Escobar, L, Rajan, D, Crolla, J, Carter, N, Hodge, J C & Mefford, H C 2015, ' Recurrent duplications of 17q12 associated with variable phenotypes ', American Journal of Medical Genetics. Part A, vol. 167, no. 12, pp. 3038-3045 . https://doi.org/10.1002/ajmg.a.37351

Cazzulani, Elena; Bigica, Michele; Avola, Tiziana; Campisi, Sebastiano

Rendiconti Lincei. Scienze Fisiche e Naturali. :1-29