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Lista de obras de Philippa Talmud

A common restriction fragment length polymorphism of the human apolipoprotein E gene and its relationship to type III hyperlipidaemia

artículo científico publicado en 1987

A common single-nucleotide variant in T is strongly associated with chordoma

artículo científico publicado en 2012

A gene-centric study of common carotid artery remodelling

artículo científico publicado en 2012

A postulated phylogenetic tree for the human apolipoprotein B gene: Unpredicted haplotypes are associated with elevated apo B levels

article

A proposal to redefine familial combined hyperlipidaemia - Third workshop on FCHL held in Barcelona from 3 to 5 May 2001, during the Scientific Sessions of the European Society for Clinical Investigation

artículo científico publicado en 2002

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

artículo científico publicado en 2014

A systematic review and meta-analysis of 130,000 individuals shows smoking does not modify the association of APOE genotype on risk of coronary heart disease

artículo científico publicado en 2014

ADIPOQ gene polymorphism rs1501299 interacts with fibre intake to affect adiponectin concentration in children: the GENe-Diet Attica Investigation on childhood obesity

artículo científico publicado en 2009

ANGPTL4 E40K and T266M: effects on plasma triglyceride and HDL levels, postprandial responses, and CHD risk

artículo científico publicado en 2008

ANGPTL4 variants E40K and T266M are associated with lower fasting triglyceride levels in Non-Hispanic White Americans from the Look AHEAD Clinical Trial

artículo científico publicado en 2011

APOA5 Ala315>Val, identified in patients with severe hypertriglyceridemia, is a common mutation with no major effects on plasma lipid levels

artículo científico publicado en 2008

APOA5 gene variants, lipoprotein particle distribution, and progression of coronary heart disease: results from the LOCAT study

artículo científico publicado en 2004

APOA5 variants predispose hyperlipidemic patients to atherogenic dyslipidemia and subclinical atherosclerosis

artículo científico publicado en 2015

APOE polymorphism, socioeconomic status and cognitive function in mid-life--the Whitehall II longitudinal study.

scientific article published on 15 July 2005

APOE, CETP and LPL genes show strong association with lipid levels in Greek children

artículo científico publicado en 2009

APOE/C1/C4/C2 gene cluster genotypes, haplotypes and lipid levels in prospective coronary heart disease risk among UK healthy men

artículo científico publicado en 2010

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis

artículo científico publicado en 2016

Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations.

artículo científico publicado en 2007

Angiotensin converting enzyme gene polymorphism and the course of angiographically defined coronary artery disease

article

Angiotensin-converting-enzyme gene insertion/deletion polymorphism and response to physical training

scientific article published in The Lancet

Apo B versus cholesterol in estimating cardiovascular risk and in guiding therapy: report of the thirty-person/ten-country panel.

artículo científico publicado en 2006

Apolipoprotein A-V, triglycerides and risk of coronary artery disease: the prospective Epic-Norfolk Population Study

artículo científico publicado en 2006

Apolipoprotein AIV Gene Variant S347 Is Associated With Increased Risk of Coronary Heart Disease and Lower Plasma Apolipoprotein AIV Levels

article

Apolipoprotein B gene polymorphisms, lipoproteins and coronary atherosclerosis: A study of young myocardial infarction survivors and healthy population-based individuals

article

Apolipoprotein B gene variants are involved in the determination of serum cholesterol levels: a study in normo- and hypelipidaemic individuals

article

Apolipoprotein E genotype, cardiovascular biomarkers and risk of stroke: systematic review and meta-analysis of 14,015 stroke cases and pooled analysis of primary biomarker data from up to 60,883 individuals

artículo científico publicado en 2013

Apolipoprotein E4 and coronary heart disease in middle-aged men who smoke: a prospective study

scientific article published in The Lancet

Apolipoproteins C-I and C-III inhibit lipoprotein lipase activity by displacement of the enzyme from lipid droplets

scientific article published on 11 October 2013

Application of statistical and functional methodologies for the investigation of genetic determinants of coronary heart disease biomarkers: lipoprotein lipase genotype and plasma triglycerides as an exemplar.

artículo científico publicado en 2010

Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

artículo científico publicado en 2014

Association between the Ala379Val variant of the lipoprotein associated phospholipase A2 and risk of myocardial infarction in the north and south of Europe

artículo científico publicado en 2003

Association between the LPL-D9N mutation in the lipoprotein lipase gene and plasma lipid traits in myocardial infarction survivors from the ECTIM study

article

Association of TERC and OBFC1 haplotypes with mean leukocyte telomere length and risk for coronary heart disease

scientific article published on 12 December 2013

Association of telomere length with type 2 diabetes, oxidative stress and UCP2 gene variation

artículo científico publicado en 2009

Binding of low density lipoproteins to lipoprotein lipase is dependent on lipids but not on apolipoprotein B.

artículo científico publicado en 2001

Blood pressure loci identified with a gene-centric array

artículo científico publicado en 2011

C-reactive protein and coronary heart disease: predictive test or therapeutic target?

artículo científico publicado en 2008

Candidate gene genotypes, along with conventional risk factor assessment, improve estimation of coronary heart disease risk in healthy UK men.

artículo científico publicado en 2006

Candidate-Gene Studies of the Atherogenic Lipoprotein Phenotype: A Sib-Pair Linkage Analysis of DZ Women Twins ⬇️

artículo científico publicado el 1 de febrero de 1998

Cardiovascular GO annotation initiative year 1 report: why cardiovascular GO?

artículo científico

Cardiovascular disease risk prediction using genetic information (gene scores): is it really informative?

scientific article published on April 2008

Causal relevance of blood lipid fractions in the development of carotid atherosclerosis: Mendelian randomization analysis

artículo científico publicado en 2012

Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk

artículo científico publicado en 2012

Cholesteryl ester transfer protein TaqIB variant, high-density lipoprotein cholesterol levels, cardiovascular risk, and efficacy of pravastatin treatment: individual patient meta-analysis of 13,677 subjects.

artículo científico publicado en 2005

Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men.

artículo científico publicado en 2008

Circulating methylarginine levels and the decline in renal function in patients with chronic kidney disease are modulated by DDAH1 polymorphisms

artículo científico publicado en 2009

Collaborative meta-analysis of individual participant data from observational studies of Lp-PLA2 and cardiovascular diseases

artículo científico publicado en 2007

Commentary on the paper by Gustavsson et al. entitled ‘Interaction of apolipoprotein E genotype with smoking and physical inactivity on coronary heart disease risk in men and women’ ⬇️

artículo científico publicado el 3 de noviembre de 2011

Common variants in the TCF7L2 gene and predisposition to type 2 diabetes in UK European Whites, Indian Asians and Afro-Caribbean men and women

article

Common variants of apolipoprotein A-IV differ in their ability to inhibit low density lipoprotein oxidation

artículo científico publicado en 2007

Common variation in the gene for apolipoprotein B modulates postprandial lipoprotein metabolism: a hypothesis generating study

artículo científico publicado en 1995

Common variation in the lipoprotein lipase gene: effects on plasma lipids and risk of atherosclerosis.

artículo científico publicado en 1997

Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration

artículo científico publicado en 2011

Contents

artículo científico publicado en 1999

Contribution of APOA5 gene variants to plasma triglyceride determination and to the response to both fat and glucose tolerance challenges

artículo científico publicado en 2003

Coronary heart disease risk prediction in the era of genome-wide association studies: current status and what the future holds

scientific article published on May 2010

Correction: Population Genomics of Cardiometabolic Traits: Design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium.

artículo científico publicado en 2013

Corrigendum to “APOA5 variants predispose hyperlipidemic patients to atherogenic dyslipidemia and subclinical atherosclerosis” [Atherosclerosis 240/1 (2015) 98–104]

artículo científico publicado en 2016

DNA POLYMORPHISMS AND THE APOLIPOPROTEIN B GENE

artículo científico publicado en 1986

DNA Polymorphism Studies. Approaches to Elucidating Multifactorial Ischaemic Heart Disease: the Apo B Gene as an Example

article

DNA polymorphisms of the apoprotein B gene are associated with altered plasma lipoprotein concentrations but not with perceived risk of cardiovascular disease: European Atherosclerosis Research Study

artículo científico publicado en 1995

Demonstration of the presence of the "deleted" MIR122 gene in HepG2 cells

artículo científico publicado en 2015

Determination of the functionality of common APOA5 polymorphisms

artículo científico publicado en 2005

Dietary intake and gene variation influence the response of plasma lipids to dietary intervention

artículo científico publicado en 1992

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and randomised trials

artículo científico publicado en 2011

Effect of the PPARG2 Pro12Ala Polymorphism on Associations of Physical Activity and Sedentary Time with Markers of Insulin Sensitivity in Those with an Elevated Risk of Type 2 Diabetes

artículo científico publicado en 2015

Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor binding

artículo científico publicado en 2008

Enhanced bridging function and augmented monocyte adhesion by lipoprotein lipase N9: insights into increased risk of coronary artery disease in N9 carriers

artículo científico publicado en 2003

Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

artículo científico publicado en 2015

European Lipoprotein Club: Report of the 24th ELC Annual Conference, Tutzing, 10-13 September 2001.

artículo científico publicado en 2002

European Lipoprotein Club: report of the 21st Annual Conference, Tutzing, September 28-October 1, 1998.

artículo científico publicado en 1999

European Lipoprotein Club: report of the 26th ELC Annual Conference, Tutzing, 8-11 September 2003.

artículo científico publicado en 2004

European lipoprotein club: report of the 25th ELC annual conference. Tutzing, 9-12 September 2002.

artículo científico publicado en 2003

Evidence for a complex relationship between apoA-V and apoC-III in patients with severe hypertriglyceridemia

artículo científico publicado en 2006

Evidence of admixture from haplotyping in an epidemiological study of UK Caucasian males: implications for association analyses.

artículo científico publicado en 2004

Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases

scientific article published on 01 January 1990

Family history is a coronary heart disease risk factor in the Second Northwick Park Heart Study

artículo científico publicado en 2003

Four genetic loci influencing electrocardiographic indices of left ventricular hypertrophy

artículo científico publicado en 2011

Frequency and allelic association of common variants in the lipoprotein lipase gene in different ethnic groups: the Wandsworth Heart and Stroke Study

artículo científico publicado en 2000

From zebrafish heart jogging genes to mouse and human orthologs: using Gene Ontology to investigate mammalian heart development

artículo científico publicado en 2013

Functional analysis of two PLA2G2A variants associated with secretory phospholipase A2-IIA levels

artículo científico publicado en 2012

Gene Ontology Consortium: going forward

artículo científico publicado en 2015

Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChip

artículo científico publicado en 2013

Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip

artículo científico publicado en 2009

Gene-environment interaction and its impact on coronary heart disease risk

artículo científico publicado en 2006

Gene-targeted analysis of copy number variants identifies 3 novel associations with coronary heart disease traits.

artículo científico publicado en 2012

Gene:environment interaction in lipid metabolism and effect on coronary heart disease risk

artículo científico publicado en 2002

Genetic Susceptibility for Coronary Heart Disease and Type 2 Diabetes Complications

scientific article published on 23 February 2012

Genetic analysis of NR0B1 in congenital adrenal hypoplasia patients: identification of a rare regulatory variant resulting in congenital adrenal hypoplasia and hypogonadal hypogonadism without testicular carcinoma in situ.

artículo científico publicado en 2012

Genetic determination of plasma lipids and insulin in the Czech population

artículo científico publicado en 2001

Genetic evidence that the putative receptor binding domain of apolipoprotein B (residues 3130 to 3630) is not the only region of the protein involved in interaction with the low density lipoprotein receptor

artículo científico publicado en 1991

Genetic testing for cardiovascular disease susceptibility: a useful clinical management tool or possible misinformation?

artículo científico publicado en 2004

Genetic variants associated with Von Willebrand factor levels in healthy men and women identified using the HumanCVD BeadChip

artículo científico publicado en 2011

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genetic variation in alcohol dehydrogenase 1C and the beneficial effect of alcohol intake on coronary heart disease risk in the Second Northwick Park Heart Study

artículo científico publicado en 2005

Genetic variation in complement factor H and risk of coronary heart disease: eight new studies and a meta-analysis of around 48,000 individuals

artículo científico publicado en 2010

Genetic variation in the ADIPOR2 gene is associated with liver fat content and its surrogate markers in three independent cohorts

artículo científico publicado en 2009

Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile

artículo científico publicado en 2011

Genetics and molecular biology

artículo científico publicado en 2000

HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials

artículo científico publicado en 2014

Haplotype analyses of the APOA5 gene in patients with familial combined hyperlipidemia

article

Haplotype and genotype effects of the F7 gene on circulating factor VII, coagulation activation markers and incident coronary heart disease in UK men.

artículo científico publicado en 2010

Heritability of C-reactive protein and association with apolipoprotein E genotypes in Japanese Americans

artículo científico publicado en 2004

Heritability of multivariate factors of the metabolic syndrome in nondiabetic Japanese americans

artículo científico publicado en 2004

How to identify gene-environment interactions in a multifactorial disease: CHD as an example

artículo científico publicado en 2004

Human gene for physical performance

artículo científico publicado en 1998

Human paraoxonase gene cluster polymorphisms as predictors of coronary heart disease risk in the prospective Northwick Park Heart Study II.

artículo científico publicado en 2003

IRS1 gene variants, dysglycaemic metabolic changes and type-2 diabetes risk.

artículo científico publicado en 2011

Identification of genetic variation in the human hormone-sensitive lipase gene and 5' sequences: homology of 5' sequences with mouse promoter and identification of potential regulatory elements

artículo científico publicado en 1998

Identification of seven loci affecting mean telomere length and their association with disease

artículo científico publicado en 2013

Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease risk

artículo científico publicado en 2012

Improvements to cardiovascular gene ontology

artículo científico publicado en 2008

In search of genetic precision

artículo científico publicado en 2003

Inflammatory biomarkers and the prediction of coronary events among people at intermediate risk: the EPIC-Norfolk prospective population study

artículo científico publicado en 2009

Inflammatory biomarkers, physical activity, waist circumference, and risk of future coronary heart disease in healthy men and women

artículo científico publicado en 2009

Influence of common genetic variation on blood lipid levels, cardiovascular risk, and coronary events in two British prospective cohort studies

artículo científico publicado en 2012

Influence of the APOC3 -2854T>G polymorphism on plasma lipid levels: effect of age and gender

artículo científico publicado en 2002

Insulin stimulates hepatic low density lipoprotein receptor-related protein 1 (LRP1) to increase postprandial lipoprotein clearance

artículo científico publicado en 2008

Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk

artículo científico publicado en 2009

Integration of genetics into a systems model of electrocardiographic traits using HumanCVD BeadChip

artículo científico publicado en 2012

Interaction between insulin (VNTR) and hepatic lipase (LIPC-514C>T) variants on the response to an oral glucose tolerance test in the EARSII group of young healthy men.

artículo científico publicado en 2005

Investigation into the role of the hormone sensitive lipase -60C>G promoter variant in morbid obesity

artículo científico publicado en 2005

Lack of association between the insertion/deletion polymorphism of the angiotensin-converting enzyme gene and idiopathic dilated cardiomyopathy

article

Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci.

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

artículo científico publicado en 2012

Lipoprotein association studies: taking stock and moving forward

artículo científico publicado en 2011

Lipoprotein candidate genes for multivariate factors of the insulin resistance syndrome: a sib-pair linkage analysis in women twins

artículo científico publicado en 2001

Lipoprotein lipase activity in patients with combined hyperlipidaemia

artículo científico publicado en 1994

Lipoprotein lipase gene variants and the effect of environmental factors on cardiovascular disease risk

artículo científico publicado en 2004

Lipoprotein-associated phospholipase A2 A379V variant is associated with body composition changes in response to exercise training

article

Lp-PLA2 activity and PLA2G7 A379V genotype in patients with diabetes mellitus

artículo científico publicado en 2006

Marginal role for 53 common genetic variants in cardiovascular disease prediction

artículo científico publicado en 2016

Mendelian randomization of blood lipids for coronary heart disease

artículo científico publicado en 2014

Meta analysis of candidate gene variants outside the LPA locus with Lp(a) plasma levels in 14,500 participants of six White European cohorts

artículo científico publicado en 2011

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

artículo científico publicado en 2010

Mutational synergism between p-fluorophenylalanine and UV in Coprinus lagopus

artículo científico publicado en 1977

No APOEepsilon4 effect on coronary heart disease risk in a cohort with low smoking prevalence: the Whitehall II study

artículo científico publicado en 2004

Nonfasting apolipoprotein B and triglyceride levels as a useful predictor of coronary heart disease risk in middle-aged UK men.

artículo científico publicado en 2002

Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA2)-V isoenzyme in coronary heart disease: modified Mendelian randomization analysis using PLA2G5 expression levels

artículo científico publicado en 2014

Oxidation-specific biomarkers, lipoprotein(a), and risk of fatal and nonfatal coronary events

artículo científico publicado en 2010

PLA2G10 Gene Variants, sPLA2 Activity, and Coronary Heart Disease Risk

artículo científico publicado en 2015

PLA2G7 genotype, lipoprotein-associated phospholipase A2 activity, and coronary heart disease risk in 10 494 cases and 15 624 controls of European Ancestry

artículo científico publicado en 2010

Peroxisome proliferator-activated receptor alpha gene variants influence progression of coronary atherosclerosis and risk of coronary artery disease

artículo científico publicado en 2002

Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysis

artículo científico publicado en 2016

Polymorphism in the promoter region of the apolipoprotein AI gene associated with differences in apolipoprotein AI levels: the European Atherosclerosis Research Study

artículo científico publicado en 1994

Polymorphisms in CYP-7A1, not APOE, influence the change in plasma lipids in response to population dietary change in an 8 year follow-up; results from the Czech MONICA study

artículo científico publicado en 2003

Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium

artículo científico publicado en 2013

Progression of atherosclerosis is associated with variation in the alpha1-antitrypsin gene

artículo científico publicado en 2003

RFLP studies in different ethnic groups

artículo científico publicado en 1989

RFLPs for the human apolipoprotein B gene: HincII and PvuII.

artículo científico publicado en 1986

Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemia

artículo científico publicado en 1991

Rapid testing for three mutations causing familial defective apolipoprotein B100 in 562 patients with familial hypercholesterolaemia

artículo científico publicado en 1996

Rare APOA5 mutations--clinical consequences, metabolic and functional effects: an ENID review

artículo científico publicado en 2007

Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries

artículo científico publicado en 2014

Relationship of IgG and IgM autoantibodies and immune complexes to oxidized LDL with markers of oxidation and inflammation and cardiovascular events: results from the EPIC-Norfolk Study

artículo científico publicado en 2011

Reply: limits of Mendelian randomization analyses in selection of secretory phospholipase A2-IIA as a valid therapeutic target for prevention of cardiovascular disease

artículo científico publicado en 2013

Response to micronized fenofibrate treatment is associated with the peroxisome-proliferator-activated receptors alpha G/C intron7 polymorphism in subjects with type 2 diabetes

artículo científico publicado en 2004

SERPINA1 11478G->A variant, serum 1-antitrypsin, exacerbation frequency and FEV1 decline in COPD

artículo científico publicado en 2011

Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study

scientific article published on 31 July 2013

Separating the mechanism-based and off-target actions of cholesteryl ester transfer protein inhibitors with CETP gene polymorphisms

artículo científico publicado en 2009

Sixty-five common genetic variants and prediction of type 2 diabetes

artículo científico publicado en 2014

Strong association of the APOA5-1131T>C gene variant and early-onset acute myocardial infarction

artículo científico publicado en 2010

Structure and function of the apoA-IV T347S and Q360H common variants

artículo científico publicado en 2010

Substitution of asparagine for aspartic acid at residue 9 (D9N) of lipoprotein lipase markedly augments risk of ischaemic heart disease in male smokers.

artículo científico publicado en 2000

Tagging SNP haplotype analysis of the secretory PLA2-V gene, PLA2G5 , shows strong association with LDL and oxLDL levels, suggesting functional distinction from sPLA2-IIA: results from the UDACS study

article

Tagging-SNP haplotype analysis of the secretory PLA2IIa gene PLA2G2A shows strong association with serum levels of sPLA2IIa: results from the UDACS study

artículo científico publicado en 2005

Telomere shortening over 6 years is associated with increased subclinical carotid vascular damage and worse cardiovascular prognosis in the general population.

artículo científico publicado en 2014

The 5A/6A polymorphism in the promoter of the stromelysin-1 (MMP-3) gene predicts progression of angiographically determined coronary artery disease in men in the LOCAT gemfibrozil study

article

The APOA4 T347S variant is associated with reduced plasma TAOS in subjects with diabetes mellitus and cardiovascular disease

artículo científico publicado en 2004

The amino terminus of apolipoprotein B is necessary but not sufficient for microsomal triglyceride transfer protein responsiveness

artículo científico publicado en 1996

The apolipoprotein A-V genotype and plasma apolipoprotein A-V and triglyceride levels: prospective risk of type 2 diabetes. Results from the Northwick Park Heart Study II.

artículo científico publicado en 2006

The association between free fatty acid concentrations and triglyceride-rich lipoproteins in the post-prandial state is altered by a common deletion polymorphism of the apo B signal peptide

artículo científico publicado en 1996

The association of telomere length with paternal history of premature myocardial infarction in the European Atherosclerosis Research Study II.

artículo científico publicado en 2008

The benefits of using genetic information to design prevention trials

artículo científico publicado en 2013

The effect of APOA5 and APOC3 variants on lipid parameters in European Whites, Indian Asians and Afro-Caribbeans with type 2 diabetes

article

The functional interaction on in vitro gene expression of APOA5 SNPs, defining haplotype APOA52, and their paradoxical association with plasma triglyceride but not plasma apoAV levels

artículo científico publicado en 2008

The genetic architecture of the familial hyperlipidaemia syndromes: rare mutations and common variants in multiple genes

artículo científico

The genetic determinants of plasma cholesterol and response to diet

artículo científico publicado en 1995

The impact of focused Gene Ontology curation of specific mammalian systems

artículo científico publicado en 2011

The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis

artículo científico publicado en 2012

The isolation of genomic recombinants for the human apolipoprotein B gene and the mapping of three common DNA polymorphisms of the gene ?a useful marker for human chromosome 2

article

The lipoprotein lipase gene serine 447 stop variant influences hypertension-induced left ventricular hypertrophy and risk of coronary heart disease

article

The relationship between plasma angiopoietin-like protein 4 levels, angiopoietin-like protein 4 genotype, and coronary heart disease risk

artículo científico publicado en 2010

The representation of heart development in the gene ontology

artículo científico

The significant increase in cardiovascular disease risk in APOEepsilon4 carriers is evident only in men who smoke: potential relationship between reduced antioxidant status and ApoE4.

artículo científico publicado en 2005

The use of a highly informative CA repeat polymorphism within the abetalipoproteinaemia locus (4q22–24)

artículo científico publicado en 1997

Three New Polymorphisms of the ApoAI-CIII-AIV Gene Cluster

article

Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies

artículo científico publicado en 2010

Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays

artículo científico publicado en 2012

Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study

artículo científico publicado en 2013

Utility of genetic and non-genetic risk factors in prediction of type 2 diabetes: Whitehall II prospective cohort study

artículo científico publicado en 2010

Utility of genetic determinants of lipids and cardiovascular events in assessing risk

artículo científico publicado en 2011

Variable effects of the APOC3-482C > T variant on insulin, glucose and triglyceride concentrations in different ethnic groups

artículo científico publicado en 2001

Variants in the APOC3 promoter insulin responsive element modulate insulin secretion and lipids in middle-aged men.

artículo científico publicado en 2003

Variants in the cholesterol ester transfer protein and lipoprotein lipase genes are predictors of plasma cholesterol response to dietary change

article

Variants of ADRA2A are associated with fasting glucose, blood pressure, body mass index and type 2 diabetes risk: meta-analysis of four prospective studies

artículo científico publicado en 2011

Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.

artículo científico publicado en 2004

Variation in the PPARα gene is associated with altered function in vitro and plasma lipid concentrations in Type II diabetic subjects

article

Variation in the human ApoB signal peptide modulates ApoB17 translocation

artículo científico publicado en 2001

Variation in the lipoprotein lipase gene influences exercise-induced left ventricular growth.

artículo científico publicado en 2006

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