Christina Brahe - Concepedia

Author

Christina Brahe

Università Cattolica del Sacro Cuore

Also Known As

C Brahe, C. Brahe, Cecilie C. H. Brahe, Christina Brahe, U. Claussen

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

Università Cattolica del Sacro Cuore Catholic University of America Agostino Gemelli University Polyclinic Bambino Gesù Children's Hospital Leiden University

About

Christina Brahe is an author at Università Cattolica del Sacro Cuore specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	23	1.4K
2	Natural Sciences	3	3	173
3	Health Sciences	2	2	138
4	Humanities	1	1	12
5	Language Studies	1	1	12

Christina Brahe

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
Phenylbutyrate increases SMN expression in vitro: relevance for treatment of spinal muscular atrophy Catia Andreassi, Carla Angelozzi, Francesco Danilo Tiziano, European Journal of Human Genetics Muscle FunctionMolecular PhysiologySkeletal MusclePhysiologyDegenerative Disease	2003	257
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy Eugenio Mercuri, Enrico Bertini, Sonia Messina, Neurology	2006	169
Phenylbutyrate increases SMN gene expression in spinal muscular atrophy patients Christina Brahe, Tiziana Vitali, Francesco Danilo Tiziano, European Journal of Human Genetics Molecular PhysiologyGeneticsPhysiologyDegenerative DiseaseGene Characterization	2004	157
Pilot trial of phenylbutyrate in spinal muscular atrophy Eugenio Mercuri, Enrico Bertini, Sonia Messina, Neuromuscular Disorders Applied PhysiologyRehabilitationSpinal Muscular AtrophySpinal DisorderNeuromusculoskeletal Disorder	2003	134
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
SMT3A,a Human Homologue of theS. cerevisiae SMT3Gene, Maps to Chromosome 21qter and Defines a Novel Gene Family Vincenza Lapenta, Pietro Chiurazzi, Peter J. van der Spek, Genomics ChromatinChromatin StructureNovel Gene FamilyNatural SciencesGenetics	1997	108
Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5. G van der Steege, P.M. Grootscholten, J. M. Cobben, PubMed	1996	93
Frameshift mutation in the survival motor neuron gene in a severe case of SMA type I Christina Brahe Human Molecular Genetics	1996	91
Salbutamol increases SMN mRNA and protein levels in spinal muscular atrophy cells Carla Angelozzi, Federica Borgo, Francesco Danilo Tiziano, Journal of Medical Genetics Amyotrophic Lateral SclerosisSpinal Cord InjuryBiochemistryRelated Smn2 GeneMedicine	2007	89
Apolipoprotein E ε4 Allele Differentiates the Clinical Response to Donepezil in Alzheimer’s Disease Alessandra Bizzarro, Camillo Marra, Adele Acciarri, Dementia and Geriatric Cognitive Disorders NeuropsychologyApoe GenotypeGeneticsNeurochemical BiomarkersAlzheimer ’	2005	85

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