Maria Teresa Bassi - Concepedia

Author

Maria Teresa Bassi

Also Known As

Bassi, Maria Teresa, Jin, Meiyan, M BASSI, M Bassi, M T Bassi, M. Bassi, M. T. Bassi, M. Teresa Bassi, M.T Bassi, M.T. Bassi

212

Publications

15.6K

Citations

H-Index

146

Concepts

All Affiliations

IRCCS Eugenio Medea University of Milan Telethon Institute Of Genetics And Medicine Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Vita-Salute San Raffaele University

About

Maria Teresa Bassi is an author at IRCCS Eugenio Medea specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	36	66	5.8K
2	Natural Sciences	14	15	1.1K
3	Health Sciences	3	3	301
4	Engineering	1	1	19
5	Public Health	1	1	24

Maria Teresa Bassi

121

Publications

14.1K

Citations

H-Index

Page 1

	Year	Citations
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) Daniel J. Klionsky, Kotb Abdelmohsen, Akihisa Abe, Autophagy	2016	5.9K
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi, Nature Genetics Rare DiseasesMendelian DisorderGenetic DisorderGeneticsPathology	2012	417
X-linked situs abnormalities result from mutations in ZIC3 Marinella Gebbia, Giovanni Battista Ferrero, Giuseppe Pilia, Nature Genetics Somatic VariantGenetic DisorderMedicineGeneticsX-linked Situs Abnormalities	1997	416
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
SLC7A7, encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance Giuseppe Borsani, Maria Teresa Bassi, Maria Pia Sperandeo, Nature Genetics Putative Permease-related ProteinLysinuric Protein IntoleranceAllergyAutoimmune DiseaseMedicine	1999	263
Cloning of the Gene Encoding a Novel Integral Membrane Protein, Mucolipidin—and Identification of the Two Major Founder Mutations Causing Mucolipidosis Type IV Maria Teresa Bassi, Marta Manzoni, Eugenio Monti, The American Journal of Human Genetics GeneticsPathogenesisPathologyMembrane BiologyMolecular Genetics	2000	252
Characterization and Mutation Analysis of Human LEFTY A and LEFTY B, Homologues of Murine Genes Implicated in Left-Right Axis Development Kenjiro Kosaki, Rika Kosaki, Maria Teresa Bassi, The American Journal of Human Genetics Murine Genes ImplicatedDevelopmental BiologyGenetic DisorderDevelopmental GeneticsGenetics	1999	208
Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome Maria Teresa Bassi, Maria Vittoria Schiaffino, Alessandra Renieri, Nature Genetics CytogeneticsX ChromosomeGeneticsGenetic DisorderMolecular Biology	1995	203
A complex syndrome of left-right axis, central nervous system and axial skeleton defects in<i>Zic3</i>mutant mice Smita M. Purandare, Stephanie M. Ware, Kin Ming Kwan, Development Null MiceNeurological DisorderGeneticsX-linked HeterotaxyEmbryology	2002	178
Agenesis of the Corpus Callosum: Clinical and Genetic Study in 63 Young Patients Maria Francesca Bedeschi, María Clara Bonaglia, Rita Grasso, Pediatric Neurology NeurologyCorpus CallosumGenetic StudyMedicineYoung Patients	2006	170

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