Giovanni Neri - Concepedia

Author

Giovanni Neri

Università Cattolica del Sacro Cuore

Also Known As

G Neri, G. NERI, G. Neri, GIOVANNI NERI, Giovanni Neri

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Università Cattolica del Sacro Cuore University of Modena and Reggio Emilia University of Chieti-Pescara Centro di Riferimento Oncologico Catholic University of America

About

Giovanni Neri is an author at Università Cattolica del Sacro Cuore specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	1.3K
2	Cell Biology	3	3	366
3	Public Health	2	2	27
4	Social Sciences	2	2	118
5	Natural Sciences	1	1	264

Giovanni Neri

Publications

3.1K

Citations

H-Index

Page 1

	Year	Citations
Molecular alterations of the <i>AKT</i>2 oncogene in ovarian and breast carcinomas Alfonso Bellacosa, Daniela De Feo, Andrew K. Godwin, International Journal of Cancer	1995	836
p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation Hans van Bokhoven, Ben C.J. Hamel, Mike Bamshad, The American Journal of Human Genetics Eec SyndromeDevelopmental BiologyGenetic DisorderGeneticsPathology	2001	376
MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1 Alfonso Bellacosa, Lucia Cicchillitti, Filippo Schepis, Proceedings of the National Academy of Sciences ChromatinGenome InstabilityNatural SciencesGeneticsEpigenetic Change	1999	264
Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister‐Killian syndrome): Report of 11 cases James F. Reynolds, Art Daniel, Thaddeus E. Kelly, American Journal of Medical Genetics	1987	140
Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy Christina Brahe, Stefania Zappata, Giovanni Neri, The Lancet Rare DiseasesMendelian DisorderGenetic DisorderGeneticsGenetic Epidemiology	1995	119
A case of Beckwith–Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus Marcella Zollino, Daniela Orteschi, Giuseppe Marangi, Journal of Medical Genetics	2009	101
Further delineation of a syndrome of cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, coloboma, and hepatic fibrosis Alain Verloès, C Lambotte, Giovanni Neri, American Journal of Medical Genetics	1989	88
A New Susceptibility Locus for Migraine with Aura in the 15q11-q13 Genomic Region Containing Three GABA-A Receptor Genes Luisa Russo, Paolo Mariotti, Eugenio Sangiorgi, The American Journal of Human Genetics Cluster HeadacheNeurophysiologyMedicineNeurologyNeuroscience	2005	87
Simpson‐Golabi‐Behmel syndrome: An X‐linked encephalo‐trophoschisis syndrome Giovanni Neri, R. Marini, Marco Cappa, American Journal of Medical Genetics Neurological DisorderDiagnosisPathologyMild Intellectual ImpairmentGolabi‐rosen Syndrome	1988	80
Survival analysis in families affected by hereditary non-polyposis colorectal cancer Antonio Percesepe, Piero Benatti, Luca Roncucci, International Journal of Cancer Family MedicineCancer RiskCancer EpidemiologyMedicineEpidemiology Of Cancer	1997	77

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