Sandra Alves - Concepedia

Author

Sandra Alves

Also Known As

Alves, Sandra, Maria Prata, S ALVES, S Alves, S. Alves, Samuel Carlos Aguiar Alves¹, Samuel Tavares Alves, Sandra Alves, Sara Loize Ponciano Alves, Sebastian Alves

204

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

Universidade do Porto Centro de Genética Clínica National Institute of Health Dr. Ricardo Jorge Hospital de São João Universidade Federal do Rio Grande do Sul

About

Sandra Alves is an author at Universidade do Porto specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	20	548
2	Public Health	4	4	132
3	Natural Sciences	3	3	82
4	Biochemistry	3	3	103
5	Engineering	2	2	36

Sandra Alves

Publications

886

Citations

H-Index

Page 1

	Year	Citations
Prevention of HIV-1 Infection with Early Antiretroviral Therapy for the HPTN 052 Study Team* Myron S. Cohen, Ying Qing Chen, Marybeth McCauley, Hptn 052Early Antiretroviral TherapyTreatment And PreventionHuman RetrovirusAntiviral Therapy	2011	86
Influence of the variable number of tandem repeats located in the promoter region of the thiopurine methyltransferase gene on enzymatic activity Sandra Alves Clinical Pharmacology & Therapeutics	2001	76
Molecular analysis of the <i>GNPTAB </i>and <i>GNPTG </i>genes in 13 patients with mucolipidosis type II or type III – identification of eight novel mutations Marisa Encarnação, Lúcia Lacerda, Romain Da Costa, Clinical Genetics ImmunodeficienciesGeneticsGlycobiologyMucolipidosis Type IiPathology	2009	53
The MTHFR C677T and A1298C Polymorphisms and Susceptibility to Childhood Acute Lymphoblastic Leukemia in Portugal Elisabete Oliveira, Sandra Alves, Sofia Quental, Journal of Pediatric Hematology/Oncology Mixed-phenotype Acute LeukemiaGeneticsEpigenetic ChangeGenetic EpidemiologyHuman Polymorphism	2005	50
The lysosomal storage disorders mucolipidosis type II, type III alpha/beta, and type III gamma: Update on<i>GNPTAB</i>and<i>GNPTG</i>mutations Renata Voltolini Velho, Frederike L. Harms, Tatyana Danyukova, Human Mutation Lysosomal Storage DiseaseGeneticsGlycobiologyPathologyMolecular Genetics	2019	50
Therapeutic strategies based on modified U1 snRNAs and chaperones for Sanfilippo C splicing mutations Liliana Matos, Isaac Canals, Larbi Dridi, Orphanet Journal of Rare Diseases	2014	45
Clinical, biochemical and molecular characterization of Cystinuria in a cohort of 12 patients M. Barbosa, António Lopes, Conceição Mota, Clinical Genetics Slc3a1 GeneMolecular CharacterizationUrologyRenal FunctionType B	2011	42
Molecular characterization of Portuguese patients with mucopolysaccharidosis type II shows evidence that the <i>IDS</i> gene is prone to splicing mutations Sandra Alves, M. Mangas, Maria João Prata, Journal of Inherited Metabolic Disease	2006	41
Do the distribution patterns of polymorphisms at the thiopurine S-methyltransferase locus in sub-Saharan populations need revision? Hints from Cabinda and Mozambique Eugénio Oliveira, Sofia Quental, Sandra Alves, European Journal of Clinical Pharmacology Thiopurine S-methyltransferase LocusAllelic VariantHaplotype DeterminationSub-saharan PopulationsMolecular Ecology	2007	37
Screening of thiopurine S‐methyltransferase mutations by horizontal conformation‐sensitive gel electrophoresis Sandra Alves, Maria João Prata, Fátima Ferreira, Human Mutation GeneticsHuman PolymorphismMolecular BiologyMolecular GeneticsGenomics	2000	31

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