Marco Seri - Concepedia

Author

Marco Seri

Also Known As

Domenico Berardi, Elena Maestrini, Franck Schürhoff, M SERI, M Seri, M. Seri, MARCO SERI, Marco Seri, Michelangelo Fiorentino, Seri

353

Publications

12.5K

Citations

H-Index

162

Concepts

All Affiliations

University of Bologna IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola Istituto Giannina Gaslini Istituti di Ricovero e Cura a Carattere Scientifico University of Pavia

About

Marco Seri is an author at University of Bologna specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	38	83	6K
2	Public Health	5	5	313
3	Natural Sciences	4	4	103
4	Arts	2	2	33
5	Engineering	1	1	54

Marco Seri

165

Publications

10.8K

Citations

H-Index

Page 1

	Year	Citations
Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene Alison J. Coffey, Robert A. Brooksbank, Oliver Brandau, Nature Genetics Host ResponseSh2-domain Encoding GeneMolecular VirologyPathogenesisImmunology	1998	754
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease Giovanni Romeo, Patrizia Ronchetto, Yin Luo, Nature Somatic VariantPoint MutationsMendelian DisorderGenetic DisorderReceptor Tyrosine Kinase	1994	702
MYH9-Related Disease Marco Seri, Alessandro Pecci, Filomena Di Bari, Medicine Mild MacrothrombocytopeniaAutoimmune DiseaseMendelian DisorderGenetic DisorderGenetics	2003	307
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families Patrizia Noris, Silverio Perrotta, Marco Seri, Blood	2011	288
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population Elisa Benetti, Rossella Tita, Ottavia Spiga, European Journal of Human Genetics	2020	267
EXCAVATOR: detecting copy number variants from whole-exome sequencing data Alberto Magi, Lorenzo Tattini, Ingrid Cifola, Genome biology	2013	238
Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease. János Sümegi, Dali Huang, Árpád Lányi, PubMed	2000	236
RET mutations in exons 13 and 14 of FMTC patients. Alessandra Bolino, Isabelle Schuffenecker, Yin Luo, PubMed	1995	222
Loss of function effect of RET mutations causing Hirschsprung disease Barbara Pasini, Maria Grazia Borrello, Angela Greco, Nature Genetics Gene TherapiesRet MutationsGenetic DisorderGeneticsPathology	1995	217
Mutations in the 5′ UTR of ANKRD26, the Ankirin Repeat Domain 26 Gene, Cause an Autosomal-Dominant Form of Inherited Thrombocytopenia, THC2 Tommaso Pippucci, Anna Savoia, Silverio Perrotta, The American Journal of Human Genetics ThrombopoiesisAutoimmune DiseaseGenetic DisorderGeneticsHematology	2011	217

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