Ana Catarina Alves

medical researcher

Ana Catarina Alves is …
instance of (P31):
humanQ5

External links are
P7893CIÊNCIAVITAE ID3E16-21FB-4B19
P6178Dimensions author ID01362471173.54
P496ORCID iD0000-0003-3157-7542
P3829Publons author ID1360003
P1053ResearcherIDK-6455-2014
P1153Scopus author ID55676862500

P69educated atUniversity of LisbonQ1122926
Independente UniversityQ2492346
P108employerNational Institute of Health Dr. Ricardo JorgeQ6041414
University of the Basque CountryQ1232428
P735given nameAnaQ482671
AnaQ482671
P106occupationresearcherQ1650915
P21sex or genderfemaleQ6581072

Reverse relations

author (P50)
Q35409900Advantages and versatility of fluorescence-based methodology to characterize the functionality of LDLR and class mutation assignment
Q61988935Analysis of publicly available LDLR, APOB, and PCSK9 variants associated with familial hypercholesterolemia: application of ACMG guidelines and implications for familial hypercholesterolemia diagnosis
Q37716374Cardiovascular risk assessment of dyslipidemic children: analysis of biomarkers to identify monogenic dyslipidemia.
Q50632268Cardiovascular risk profile of high school students: a cross-sectional study.
Q61988938Characterization of the First PCSK9 Gain of Function Homozygote
Q38845770Clinical and molecular aspects of familial hypercholesterolemia in Ibero-American countries.
Q52804842Familial hypercholesterolaemia in Portugal.
Q90439216Functional Analysis of LDLR (Low-Density Lipoprotein Receptor) Variants in Patient Lymphocytes to Assess the Effect of Evinacumab in Homozygous Familial Hypercholesterolemia Patients With a Spectrum of LDLR Activity
Q47893397Genetic diagnosis of familial hypercholesterolaemia: the importance of functional analysis of potential splice-site mutations.
Q92195954Genomics of familial hypercholesterolaemia
Q35920600Hepatitis B and C prevalence in Portugal: disparity between the general population and high-risk groups.
Q44751613How good is controlled attenuation parameter and fatty liver index for assessing liver steatosis in general population: correlation with ultrasound
Q45326595Hypercholesterolemia--a disease with expression from childhood.
Q51756675In vitro functional characterization of missense mutations in the LDLR gene.
Q39124388Low-density lipoprotein receptor mutational analysis in diagnosis of familial hypercholesterolemia
Q50649200Lysosomal acid lipase deficiency: A hidden disease among cohorts of familial hypercholesterolemia?
Q38801930Mutational analysis and genotype-phenotype relation in familial hypercholesterolemia: The SAFEHEART registry
Q48181942Mutational analysis of a cohort with clinical diagnosis of familial hypercholesterolemia: considerations for genetic diagnosis improvement.
Q60310655No Evidence for Lower Levels of Serum Vitamin D in the Presence of Hepatic Steatosis. A Study on the Portuguese General Population
Q39062979Novel functional APOB mutations outside LDL-binding region causing familial hypercholesterolaemia
Q36353492Structural analysis of APOB variants, p.(Arg3527Gln), p.(Arg1164Thr) and p.(Gln4494del), causing Familial Hypercholesterolaemia provides novel insights into variant pathogenicity
Q92361445The familial hypercholesterolaemia phenotype: Monogenic familial hypercholesterolaemia, polygenic hypercholesterolaemia and other causes
Q35572016The importance of an integrated analysis of clinical, molecular, and functional data for the genetic diagnosis of familial hypercholesterolemia.
Q42912037Update of the Portuguese Familial Hypercholesterolaemia Study

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