Matteo Cassina - Concepedia

Author

Matteo Cassina

Also Known As

Cassina, M., James Mitchell, M Cassina, M. Cassina, Marketa Havlovicova, Matteo Cassina, Mortensen, Preben Bo, Roger Cone, Roland Burghardt

104

Publications

6.1K

Citations

H-Index

Concepts

All Affiliations

University of Padua Città della Speranza Foundation Istituti di Ricovero e Cura a Carattere Scientifico University of North Carolina at Chapel Hill Harvard University

About

Matteo Cassina is an author at University of Padua specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	17	2K
2	Public Health	3	3	87
3	Social Sciences	2	2	1.5K
4	Allergy	1	1	115
5	Biomolecular Engineering	1	1	20

Matteo Cassina

Publications

3.2K

Citations

H-Index

Page 1

	Year	Citations
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders Phil H. Lee, Verneri Anttila, Hyejung Won, Cell PsychiatryPsychiatric DisordersGenetic DisorderGeneticsPsychiatric Genetics	2019	1.4K
Treatment of Hyperthyroidism in Pregnancy and Birth Defects Maurizio Clementi, Elena Di Gianantonio, Matteo Cassina, The Journal of Clinical Endocrinology & Metabolism	2010	156
Pregnancy outcome in women exposed to leflunomide before or during pregnancy Matteo Cassina, Diana L. Johnson, Luther K. Robinson, Arthritis & Rheumatism	2012	128
Genetics of Coenzyme Q10 Deficiency Mara Doimo, María Andrea Desbats, Cristina Cerqua, Molecular Syndromology Primary Coq10 DeficiencyCoenzyme Q10GeneticsGenetic EpidemiologyMolecular Biology	2014	115
Prevalence, characteristics, and survival of children with esophageal atresia: A 32‐year population‐based study including 1,417,724 consecutive newborns Matteo Cassina, Michele Ruol, Riccardo Pertile, Birth Defects Research Part A Clinical and Molecular Teratology	2016	111
Haploinsufficiency of <i>COQ4</i> causes coenzyme Q<sub>10</sub> deficiency Leonardo Salviati, Eva Trevisson, María Hernández, Journal of Medical Genetics	2012	103
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes Silvia Russo, Luciano Calzari, Alessandro Mussa, Clinical Epigenetics	2016	68
Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies Melissa A. Munn‐Chernoff, Emma C. Johnson, Yi‐Ling Chou, Addiction Biology	2020	68
The<i>COQ2</i>genotype predicts the severity of coenzyme Q<sub>10</sub>deficiency María Andrea Desbats, Valeria Morbidoni, Micol Silic‐Benussi, Human Molecular Genetics	2016	66
Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function Luis Vázquez-Fonseca, Mara Doimo, Cristina Calderan, Human Mutation	2017	50

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