Emanuele Bellacchio - Concepedia

Author

Emanuele Bellacchio

Bambino Gesù Children's Hospital ORCID

Also Known As

Bellacchio, E., E Bellacchio, E. Bellacchio, Emanuele BELLACCHIO, Emanuele Bellacchio, Emanuele Bellacchio (258331)

167

Publications

5.1K

Citations

H-Index

152

Concepts

All Affiliations

Bambino Gesù Children's Hospital Istituti di Ricovero e Cura a Carattere Scientifico Sapienza University of Rome Casa Sollievo della Sofferenza Università Cattolica del Sacro Cuore

About

Emanuele Bellacchio is an author at Bambino Gesù Children's Hospital specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	40	2.5K
2	Engineering	8	9	515
3	Natural Sciences	8	8	739
4	Arts	2	2	43
5	Health Sciences	1	1	20

Emanuele Bellacchio

Publications

4.6K

Citations

H-Index

Page 1

	Year	Citations
Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism Laura Silvestri, Viviana Caputo, Emanuele Bellacchio, Human Molecular Genetics MitophagyPink1 MutantsGeneticsMitochondrial TargetingMolecular Biology	2005	443
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome Enza Maria Valente, Jennifer L. Silhavy, Francesco Brancati, Nature Genetics Developmental BiologyMendelian DisorderJoubert SyndromeGenetic DisorderGenetics	2006	400
Absence of Mn-Centered Oxidation in the S<sub>2</sub>→ S<sub>3</sub>Transition: Implications for the Mechanism of Photosynthetic Water Oxidation Johannes Messinger, John H. Robblee, Uwe Bergmann, Journal of the American Chemical Society	2001	303
Template-Imprinted Chiral Porphyrin Aggregates Emanuele Bellacchio, Rosaria Lauceri, Sergio Gurrieri, Journal of the American Chemical Society Inorganic ChemistryChemical EngineeringChemical MeasurementEngineeringDonut Icon	1998	152
NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome Alessandro De Luca, Irene Bottillo, Anna Sárközy, The American Journal of Human Genetics Neurobiology Of DiseaseMendelian DisorderGenetic DisorderMedicinePathology	2005	151
<i>AHI1</i> gene mutations cause specific forms of Joubert syndrome–related disorders Enza Maria Valente, Francesco Brancati, Jennifer L. Silhavy, Annals of Neurology	2006	138
Familial transposition of the great arteries caused by multiple mutations in laterality genes Alessandro De Luca, Anna Sárközy, Federica Consoli, Heart	2009	137
Calcium EXAFS Establishes the Mn-Ca Cluster in the Oxygen-Evolving Complex of Photosystem II Roehl M. Cinco, Karen L. McFarlane Holman, John H. Robblee, Biochemistry	2002	131
Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome Francesco Brancati, Paola Fortugno, Irene Bottillo, The American Journal of Human Genetics Developmental BiologyGenetic DisorderPathogenesisPathologyDegenerative Disease	2010	120
Chiral H- and J-Type Aggregates of <i>meso</i>-Tetrakis(4-sulfonatophenyl)porphine on α-Helical Polyglutamic Acid Induced by Cationic Porphyrins Roberto Purrello, Luigi Monsù Scolaro, Emanuele Bellacchio, Inorganic Chemistry Derivative (Chemistry)Chemical MeasurementEngineeringBiochemistryCationic Porphyrins	1998	113

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