Leopoldo Zelante - Concepedia

Author

Leopoldo Zelante

Istituti di Ricovero e Cura a Carattere Scientifico

Also Known As

Heckbert, Susan R, L Zelante, L. Zelante, LEOPOLDO ZELANTE, Leopoldo Zelante, Massimo Carella

220

Publications

12.9K

Citations

H-Index

164

Concepts

All Affiliations

Istituti di Ricovero e Cura a Carattere Scientifico Casa Sollievo della Sofferenza Nuovo Ospedale San Giovanni di Dio University of Bari Aldo Moro Bambino Gesù Children's Hospital

About

Leopoldo Zelante is an author at Istituti di Ricovero e Cura a Carattere Scientifico specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	36	74	6.5K
2	Arts	6	6	671
3	Education	2	2	140
4	Health Sciences	2	2	116
5	Engineering	1	1	29

Leopoldo Zelante

133

Publications

11.6K

Citations

H-Index

Page 1

	Year	Citations
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome Laura Crisponi, Manila Deiana, Angela Loi, Nature Genetics Transcriptional RegulationDevelopmental BiologyGenetic DisorderGeneticsPathogenesis	2001	974
Connexin-26 mutations in sporadic and inherited sensorineural deafness Xavier Estivill, Paolo Fortina, Saul Surrey, The Lancet	1998	642
Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans Leopoldo Zelante Human Molecular Genetics	1997	623
Mutations of SURF-1 in Leigh Disease Associated with Cytochrome c Oxidase Deficiency Valeria Tiranti, Konstanze Hoertnagel, Rosalba Carrozzo, The American Journal of Human Genetics Mendelian DisorderDisease MechanismGenetic DisorderGeneticsOxidase Deficiency	1998	525
Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine Marı́a Julia Calonge, Paolo Gasparini, Miguel Chillón, Nature Genetics BiologyNatural SciencesGeneticsBiochemical GeneticsMolecular Biology	1994	377
Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients Manuela De Gregori, Roberto Ciccone, Pamela Magini, Journal of Medical Genetics	2007	354
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder Antonio M. Persico, Leonardo D’Agruma, Nunzia Maiorano, Molecular Psychiatry Reelin Gene AllelesDevelopmental BiologySyndromic AutismGenetic DisorderGenetics	2001	337
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT Lídia Feliubadaló, Mariona Font, Jesús Purroy, Nature Genetics GeneticsBiochemical GeneticsMolecular BiologyMolecular GeneticsGenomics	1999	329
Positional cloning of the Fanconi anaemia group A gene Sinoula Apostolou, S.A. Whitmore, Joanna Crawford, Nature Genetics BiologyGeneticsGene StructureGenome StructureGenetic Mechanism	1996	294
Comparison between SLC3A1 and SLC7A9 Cystinuria Patients and Carriers Luca Dello Strologo, Elon Pras, C. Pontesilli, Journal of the American Society of Nephrology	2002	277

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