Matteo Cassina

Matteo Cassina

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Matteo Cassina

Matteo Cassina

Publications by authors named "Matteo Cassina"

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49Publications

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Prevalence and survival of patients with anorectal malformations: A population-based study.

J Pediatr Surg 2019 Oct 16;54(10):1998-2003. Epub 2019 Mar 16.

Pediatric Surgery Unit, Department of Women's and Children's Health, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1016/j.jpedsurg.2019.03.004DOI Listing
October 2019

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

Authors:
Hunna J Watson Zeynep Yilmaz Laura M Thornton Christopher Hübel Jonathan R I Coleman Héléna A Gaspar Julien Bryois Anke Hinney Virpi M Leppä Manuel Mattheisen Sarah E Medland Stephan Ripke Shuyang Yao Paola Giusti-Rodríguez Ken B Hanscombe Kirstin L Purves Roger A H Adan Lars Alfredsson Tetsuya Ando Ole A Andreassen Jessica H Baker Wade H Berrettini Ilka Boehm Claudette Boni Vesna Boraska Perica Katharina Buehren Roland Burghardt Matteo Cassina Sven Cichon Maurizio Clementi Roger D Cone Philippe Courtet Scott Crow James J Crowley Unna N Danner Oliver S P Davis Martina de Zwaan George Dedoussis Daniela Degortes Janiece E DeSocio Danielle M Dick Dimitris Dikeos Christian Dina Monika Dmitrzak-Weglarz Elisa Docampo Laramie E Duncan Karin Egberts Stefan Ehrlich Geòrgia Escaramís Tõnu Esko Xavier Estivill Anne Farmer Angela Favaro Fernando Fernández-Aranda Manfred M Fichter Krista Fischer Manuel Föcker Lenka Foretova Andreas J Forstner Monica Forzan Christopher S Franklin Steven Gallinger Ina Giegling Johanna Giuranna Fragiskos Gonidakis Philip Gorwood Monica Gratacos Mayora Sébastien Guillaume Yiran Guo Hakon Hakonarson Konstantinos Hatzikotoulas Joanna Hauser Johannes Hebebrand Sietske G Helder Stefan Herms Beate Herpertz-Dahlmann Wolfgang Herzog Laura M Huckins James I Hudson Hartmut Imgart Hidetoshi Inoko Vladimir Janout Susana Jiménez-Murcia Antonio Julià Gursharan Kalsi Deborah Kaminská Jaakko Kaprio Leila Karhunen Andreas Karwautz Martien J H Kas James L Kennedy Anna Keski-Rahkonen Kirsty Kiezebrink Youl-Ri Kim Lars Klareskog Kelly L Klump Gun Peggy S Knudsen Maria C La Via Stephanie Le Hellard Robert D Levitan Dong Li Lisa Lilenfeld Bochao Danae Lin Jolanta Lissowska Jurjen Luykx Pierre J Magistretti Mario Maj Katrin Mannik Sara Marsal Christian R Marshall Morten Mattingsdal Sara McDevitt Peter McGuffin Andres Metspalu Ingrid Meulenbelt Nadia Micali Karen Mitchell Alessio Maria Monteleone Palmiero Monteleone Melissa A Munn-Chernoff Benedetta Nacmias Marie Navratilova Ioanna Ntalla Julie K O'Toole Roel A Ophoff Leonid Padyukov Aarno Palotie Jacques Pantel Hana Papezova Dalila Pinto Raquel Rabionet Anu Raevuori Nicolas Ramoz Ted Reichborn-Kjennerud Valdo Ricca Samuli Ripatti Franziska Ritschel Marion Roberts Alessandro Rotondo Dan Rujescu Filip Rybakowski Paolo Santonastaso André Scherag Stephen W Scherer Ulrike Schmidt Nicholas J Schork Alexandra Schosser Jochen Seitz Lenka Slachtova P Eline Slagboom Margarita C T Slof-Op 't Landt Agnieszka Slopien Sandro Sorbi Beata Świątkowska Jin P Szatkiewicz Ioanna Tachmazidou Elena Tenconi Alfonso Tortorella Federica Tozzi Janet Treasure Artemis Tsitsika Marta Tyszkiewicz-Nwafor Konstantinos Tziouvas Annemarie A van Elburg Eric F van Furth Gudrun Wagner Esther Walton Elisabeth Widen Eleftheria Zeggini Stephanie Zerwas Stephan Zipfel Andrew W Bergen Joseph M Boden Harry Brandt Steven Crawford Katherine A Halmi L John Horwood Craig Johnson Allan S Kaplan Walter H Kaye James E Mitchell Catherine M Olsen John F Pearson Nancy L Pedersen Michael Strober Thomas Werge David C Whiteman D Blake Woodside Garret D Stuber Scott Gordon Jakob Grove Anjali K Henders Anders Juréus Katherine M Kirk Janne T Larsen Richard Parker Liselotte Petersen Jennifer Jordan Martin Kennedy Grant W Montgomery Tracey D Wade Andreas Birgegård Paul Lichtenstein Claes Norring Mikael Landén Nicholas G Martin Preben Bo Mortensen Patrick F Sullivan Gerome Breen Cynthia M Bulik

Nat Genet 2019 08 15;51(8):1207-1214. Epub 2019 Jul 15.

Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

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http://dx.doi.org/10.1038/s41588-019-0439-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779477PMC
August 2019

The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromas.

Mol Genet Genomic Med 2019 05 6;7(5):e616. Epub 2019 Mar 6.

Department of Women's and Children's Health, Clinical Genetics Unit, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1002/mgg3.616DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503065PMC
May 2019

Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive cases.

Eur J Obstet Gynecol Reprod Biol 2018 Feb 7;221:23-27. Epub 2017 Dec 7.

Clinical Genetics Unit, Department of Women's and Children's Health, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1016/j.ejogrb.2017.12.012DOI Listing
February 2018

Natural history of optic pathway gliomas in a cohort of unselected patients affected by Neurofibromatosis 1.

J Neurooncol 2017 Sep 2;134(2):279-287. Epub 2017 Jun 2.

Clinical Genetics Unit, Department of Woman and Child Health, University of Padova, Via Giustiniani 3, 35128, Padova, Italy.

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http://dx.doi.org/10.1007/s11060-017-2517-6DOI Listing
September 2017

A synonymous splicing mutation in the SF3B4 gene segregates in a family with highly variable Nager syndrome.

Eur J Hum Genet 2017 02 14;25(3):371-375. Epub 2016 Dec 14.

Department of Woman and Child Health, Clinical Genetics Unit, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1038/ejhg.2016.176DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315512PMC
February 2017

Human teratogens and genetic phenocopies. Understanding pathogenesis through human genes mutation.

Eur J Med Genet 2017 Jan 14;60(1):22-31. Epub 2016 Sep 14.

Clinical Genetics Unit, Department of Women's and Children's Health, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1016/j.ejmg.2016.09.011DOI Listing
January 2017

Clinical and genetic correlates of decision making in anorexia nervosa.

J Clin Exp Neuropsychol 2016 29;38(3):327-37. Epub 2015 Dec 29.

a Department of Neurosciences: DNS ; University of Padova , Padua , Italy.

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http://dx.doi.org/10.1080/13803395.2015.1112878DOI Listing
November 2016

Response to: Papetti et al., "The crucial role of FBXO28 in the pathogenesis of the 1q41q42 microdeletion syndrome".

Authors:
Matteo Cassina

Am J Med Genet A 2016 Nov 13;170(11):3054. Epub 2016 May 13.

Clinical Genetics Unit, Department of Women's and Children's Health, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1002/ajmg.a.37742DOI Listing
November 2016

The COQ2 genotype predicts the severity of coenzyme Q10 deficiency.

Hum Mol Genet 2016 10 4;25(19):4256-4265. Epub 2016 Aug 4.

Clinical Genetics Unit, Department of Woman and Child Health, University of Padova, Padova, Italy

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http://dx.doi.org/10.1093/hmg/ddw257DOI Listing
October 2016

Prevalence, characteristics, and survival of children with esophageal atresia: A 32-year population-based study including 1,417,724 consecutive newborns.

Birth Defects Res A Clin Mol Teratol 2016 Jul 2;106(7):542-8. Epub 2016 Mar 2.

Clinical Genetics Unit, Department of Women's and Children's Health, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1002/bdra.23493DOI Listing
July 2016

Functional connectivity correlates of response inhibition impairment in anorexia nervosa.

Psychiatry Res Neuroimaging 2016 Jan 2;247:9-16. Epub 2015 Dec 2.

Psychiatric Clinic, Department of Neurosciences, University of Padova, Via Giustiniani 3, 35128 Padova, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.pscychresns.2015.11.008DOI Listing
January 2016

FBXO28 is a critical gene of the 1q41q42 microdeletion syndrome.

Am J Med Genet A 2015 Jun 21;167(6):1418-20. Epub 2015 Apr 21.

Clinical Genetics Unit, Department of Women's and Children's Health, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1002/ajmg.a.37033DOI Listing
June 2015

Multigram synthesis and in vivo efficacy studies of a novel multitarget anti-Alzheimer's compound.

Molecules 2015 Mar 10;20(3):4492-515. Epub 2015 Mar 10.

Laboratori de Química Farmacèutica (Unitat Associada al CSIC), Facultat de Farmàcia and Institut de Biomedicina (IBUB), Universitat de Barcelona, Av. Joan XXIII, 27-31, Barcelona E-08028, Spain.

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http://dx.doi.org/10.3390/molecules20034492DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272704PMC
March 2015

Forkhead box G1 gene haploinsufficiency: an emerging cause of dyskinetic encephalopathy of infancy.

Neuropediatrics 2015 Feb 7;46(1):56-64. Epub 2015 Jan 7.

Child Neurology Unit, Department of Woman's and Child's Health, University Hospital of Padua, Padua, Italy.

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http://www.thieme-connect.de/DOI/DOI?10.1055/s-0034-1395345
Publisher Site
http://dx.doi.org/10.1055/s-0034-1395345DOI Listing
February 2015

A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus.

JIMD Rep 2014 25;17:13-21. Epub 2014 Jul 25.

Laboratory of Diagnosis and Therapy of Lysosomal Disorders, Department of Women's and Children's Health, University of Padova, Padova, Italy.

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http://link.springer.com/10.1007/8904_2014_317
Publisher Site
http://dx.doi.org/10.1007/8904_2014_317DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241202PMC
November 2014

First-trimester exposure to metformin and risk of birth defects: a systematic review and meta-analysis.

Hum Reprod Update 2014 Sep-Oct;20(5):656-69. Epub 2014 May 25.

Teratology Information Service, Clinical Genetics Unit, Department of Women's and Children's Health, University of Padova, Padova, Italy

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http://dx.doi.org/10.1093/humupd/dmu022DOI Listing
October 2014

Genetics of coenzyme q10 deficiency.

Mol Syndromol 2014 Jul;5(3-4):156-62

Clinical Genetics Unit, Department of Woman and Child Health, University of Padova, and IRP Città della Speranza, Padova, Italy.

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http://dx.doi.org/10.1159/000362826DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112527PMC
July 2014

14q12 duplication including FOXG1: is there a common age-dependent epileptic phenotype?

Brain Dev 2014 May 6;36(5):402-7. Epub 2013 Jul 6.

Pediatric Neurology Unit, Department of Women's and Children's Health, University of Padua, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.braindev.2013.06.008DOI Listing
May 2014

Pregnancy outcome in women exposed to antiepileptic drugs: teratogenic role of maternal epilepsy and its pharmacologic treatment.

Reprod Toxicol 2013 Aug 13;39:50-7. Epub 2013 Apr 13.

Teratology Information Service, Clinical Genetics Unit, Department of Woman and Child Health, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1016/j.reprotox.2013.04.002DOI Listing
August 2013

Eating-induced epileptic spasms in a boy with MECP2 duplication syndrome: insights into pathogenesis of genetic epilepsies.

Epileptic Disord 2012 Dec;14(4):414-7

Department of Women's and Children's Health, University of Padua, Padua, Italy.

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http://dx.doi.org/10.1684/epd.2012.0546DOI Listing
December 2012

Genetic susceptibility to teratogens: state of the art.

Reprod Toxicol 2012 Sep 1;34(2):186-91. Epub 2012 Jun 1.

Teratology Information Service, Clinical Genetics Unit, Department of Woman and Child Health, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1016/j.reprotox.2012.05.004DOI Listing
September 2012

Pharmacologic treatment of hyperthyroidism during pregnancy.

Birth Defects Res A Clin Mol Teratol 2012 Aug 18;94(8):612-9. Epub 2012 Apr 18.

Teratology Information Service, Clinical Genetics Unit, Department of Women's and Children's Health, University of Padova, Padova, Italy.

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http://doi.wiley.com/10.1002/bdra.23012
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http://dx.doi.org/10.1002/bdra.23012DOI Listing
August 2012

Congenital pulmonary airway malformation (CPAM) [congenital cystic adenomatoid malformation] associated with tracheoesophageal fistula and agensesis of the corpus callosum.

Fetal Pediatr Pathol 2012 Jun 13;31(3):169-75. Epub 2012 Mar 13.

Department of Medical Diagnostic Sciences & Special Therapies, Surgical Pathology & Cytopathology Unit, University of Padua, Padua, Italy.

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http://dx.doi.org/10.3109/15513815.2012.659392DOI Listing
June 2012

Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A.

Seizure 2011 Dec 3;20(10):813-6. Epub 2011 Sep 3.

Pediatric Neurology and Clinical Neurophysiology Unit, Department of Pediatrics, University of Padova, Italy.

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http://dx.doi.org/10.1016/j.seizure.2011.07.008DOI Listing
December 2011

First trimester diclofenac exposure and pregnancy outcome.

Reprod Toxicol 2010 Nov 10;30(3):401-4. Epub 2010 May 10.

Servizio di Informazione Teratologica, Genetica Clinica, Department of Pediatrics, University of Padova, Padova, Italy.

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http://dx.doi.org/10.1016/j.reprotox.2010.04.010DOI Listing
November 2010

Migraine therapy during pregnancy and lactation.

Expert Opin Drug Saf 2010 Nov;9(6):937-48

University of Padova, Department of Pediatrics, Clinical Genetics Unit, via Giustiniani 3, Padua, Italy.

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http://dx.doi.org/10.1517/14740338.2010.505601DOI Listing
November 2010

Treatment of hyperthyroidism in pregnancy and birth defects.

J Clin Endocrinol Metab 2010 Nov 28;95(11):E337-41. Epub 2010 Jul 28.

Servizio di Informazione Teratologica, Genetica Clinica, Department of Pediatrics, University of Padova, Padova, Italy.

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https://academic.oup.com/jcem/article-lookup/doi/10.1210/jc.
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http://dx.doi.org/10.1210/jc.2010-0652DOI Listing
November 2010

Age estimation from the rib by components method analysis in white males.

Am J Forensic Med Pathol 2010 Mar;31(1):27-33

Department of Forensic Medicine, University of Brescia, Piazzale Spedali Civili 1, 25123, Brescia, Italy.

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http://dx.doi.org/10.1097/paf.0b013e3181c0e7a5DOI Listing
March 2010

Therapy of inflammatory bowel diseases in pregnancy and lactation.

Expert Opin Drug Saf 2009 Nov;8(6):695-707

University of Padova, Genetica Clinica ed Epidemiologica, Dipartimento di Pediatria, Italy.

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http://dx.doi.org/10.1517/14740330903357463DOI Listing
November 2009

Medications in pregnancy and lactation.

Obstet Gynecol 2009 Jul;114(1):166

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http://dx.doi.org/10.1097/AOG.0b013e3181ac7b14DOI Listing
July 2009