Found: 144
Select item for more details and to access through your institution.
Cost-Effectiveness of Screening Algorithms for Familial Hypercholesterolaemia in Primary Care.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 3, p. 330, doi. 10.3390/jpm12030330
- By:
- Publication type:
- Article
Rapid detection of polymorphisms in exons 10, 11 and 12 of the low density lipoprotein receptor gene (LDLR) and their use in a clinical genetic diagnostic setting.
- Published in:
- Clinical Genetics, 1999, v. 55, n. 3, p. 212, doi. 10.1034/j.1399-0004.1999.550311.x
- By:
- Publication type:
- Article
Associations of genotypes at the apolipoprotein AI-CIII-AIV, apolipoprotein B and lipoprotein lipase gene loci with coronary atherosclerosis and high density lipoprotein subclasses.
- Published in:
- Clinical Genetics, 1994, v. 46, n. 4, p. 273, doi. 10.1111/j.1399-0004.1994.tb04159.x
- By:
- Publication type:
- Article
Identification of genetic variation that determines levels of plasma triglycerides and hypercoagulability.
- Published in:
- Clinical Genetics, 1994, v. 46, n. 1, p. 19, doi. 10.1111/j.1399-0004.1994.tb04198.x
- By:
- Publication type:
- Article
IL-6 polymorphisms: a useful genetic tool for inflammation research?
- Published in:
- Journal of Clinical Investigation, 2013, v. 123, n. 4, p. 1413, doi. 10.1172/JCI67221
- By:
- Publication type:
- Article
Higher Responsiveness to Rosuvastatin in Polygenic versus Monogenic Hypercholesterolemia: A Propensity Score Analysis.
- Published in:
- Life (2075-1729), 2020, v. 10, n. 5, p. 73, doi. 10.3390/life10050073
- By:
- Publication type:
- Article
Gender-modulated impact of apolipoprotein A5 gene ( APOA5) −1131T>C and c.56C>G polymorphisms on lipids, dyslipidemia and metabolic syndrome in Turkish adults.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2008, v. 46, n. 6, p. 778, doi. 10.1515/CCLM.2008.161
- By:
- Publication type:
- Article
Development of sensitive and specific age- and gender-specific low-density lipoprotein cholesterol cutoffs for diagnosis of first-degree relatives with familial hypercholesterolaemia in cascade testing.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2008, v. 46, n. 6, p. 791, doi. 10.1515/CCLM.2008.135
- By:
- Publication type:
- Article
Genotypes, obesity and type 2 diabetes – can genetic information motivate weight loss? A review.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2007, v. 45, n. 3, p. 301, doi. 10.1515/CCLM.2007.070
- By:
- Publication type:
- Article
Public Awareness of Genetic Influence on Chronic Disease Risk: Are Genetic and Lifestyle Causal Beliefs Compatible?
- Published in:
- Public Health Genomics, 2011, v. 14, n. 4/5, p. 290, doi. 10.1159/000294280
- By:
- Publication type:
- Article
Association of TLL1 Gene Polymorphism (rs1503298, T > C) with Coronary Heart Disease in PREDICT, UDACS and ED Cohorts.
- Published in:
- Journal of the College of Physicians & Surgeons Pakistan, 2014, v. 24, n. 9, p. 615
- By:
- Publication type:
- Article
Influence of cytokine gene polymorphisms on proinflammatory/anti-inflammatory cytokine imbalance in premature coronary artery disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Psychological and Behavioural Impact of Genetic Testing Smokers for Lung Cancer Risk: A Phase II Exploratory Trial.
- Published in:
- Journal of Health Psychology, 2008, v. 13, n. 4, p. 481, doi. 10.1177/1359105308088519
- By:
- Publication type:
- Article
Human apolipoprotein E isoforms differentially affect bone mass and turnover in vivo.
- Published in:
- Journal of Bone & Mineral Research, 2013, v. 28, n. 2, p. 236, doi. 10.1002/jbmr.1757
- By:
- Publication type:
- Article
Angiotensin-converting enzyme genotype and late respiratory complications of mustard gas exposure.
- Published in:
- BMC Pulmonary Medicine, 2008, v. 8, p. 1, doi. 10.1186/1471-2466-8-15
- By:
- Publication type:
- Article
The use of a highly informative CA repeat polymorphism within the abetalipoproteinaemia locus (4q22-24).
- Published in:
- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1181, doi. 10.1002/(SICI)1097-0223(199712)17:12<1181::AID-PD205>3.0.CO;2-A
- By:
- Publication type:
- Article
Comparison of coronary heart disease genetic assessment with conventional cardiovascular risk assessment in primary care: reflections on a feasibility study.
- Published in:
- Primary Health Care Research & Development, 2015, v. 16, n. 6, p. 607, doi. 10.1017/S1463423615000122
- By:
- Publication type:
- Article
Correction: Clinical Utility of a Coronary Heart Disease Risk Prediction Gene Score in UK Healthy Middle Aged Men and in the Pakistani Population.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0139651
- By:
- Publication type:
- Article
Clinical Utility of a Coronary Heart Disease Risk Prediction Gene Score in UK Healthy Middle Aged Men and in the Pakistani Population.
- Published in:
- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0130754
- By:
- Publication type:
- Article
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.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0124062
- By:
- Publication type:
- Article
Networks in Coronary Heart Disease Genetics As a Step towards Systems Epidemiology.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0125876
- By:
- Publication type:
- Article
Demonstration of the Presence of the “Deleted” MIR122 Gene in HepG2 Cells.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0122471
- By:
- Publication type:
- Article
Analysis of the Role of Interleukin 6 Receptor Haplotypes in the Regulation of Circulating Levels of Inflammatory Biomarkers and Risk of Coronary Heart Disease.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0119980
- By:
- Publication type:
- Article
Common Genetic Determinants of Lung Function, Subclinical Atherosclerosis and Risk of Coronary Artery Disease.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104082
- By:
- Publication type:
- Article
Association of <i>TERC</i> and <i>OBFC1</i> Haplotypes with Mean Leukocyte Telomere Length and Risk for Coronary Heart Disease.
- Published in:
- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0083122
- By:
- Publication type:
- Article
The Effect of Pro-Inflammatory Conditioning and/or High Glucose on Telomere Shortening of Aging Fibroblasts.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0073756
- By:
- Publication type:
- Article
Functional Analysis of Two PLA2G2A Variants Associated with Secretory Phospholipase A2-IIA Levels.
- Published in:
- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0041139
- By:
- Publication type:
- Article
Cholesteryl Ester Transfer Protein (CETP ) Polymorphisms Affect mRNA Splicing, HDL Levels, and Sex-Dependent Cardiovascular Risk.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0031930
- By:
- Publication type:
- Article
Does High C-reactive Protein Concentration Increase Atherosclerosis? The Whitehall II Study.
- Published in:
- PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0003013
- By:
- Publication type:
- Article
Association of ACE and NOS3 Gene Polymorphism with Blood Pressure in a Case Control Study of Coronary Artery Disease in Punjab, Pakistan.
- Published in:
- Pakistan Journal of Zoology, 2016, v. 48, n. 4, p. 1125
- By:
- Publication type:
- Article
Should Familial Hypercholesterolaemia Be Included in the UK Newborn Whole Genome Sequencing Programme?
- Published in:
- Current Atherosclerosis Reports, 2023, v. 25, n. 12, p. 1083, doi. 10.1007/s11883-023-01177-0
- By:
- Publication type:
- Article
CETP TaqIB polymorphism in Turkish adults: association with dyslipidemia and metabolic syndrome.
- Published in:
- 2008
- By:
- Publication type:
- journal article
CETP TaqIB polymorphism in Turkish adults: association with dyslipidemia and metabolic syndrome.
- Published in:
- Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi, 2008, v. 8, n. 5, p. 324
- By:
- Publication type:
- Article
Angiotensin-I Converting Enzyme Genotype-Dependent Benefit from Hormone Replacement Therapy in Isometric Muscle Strength and Bone Mineral Density.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 5, p. 2200, doi. 10.1210/jcem.86.5.7514
- By:
- Publication type:
- Article
Telomeres are shorter in myocardial infarction patients compared to healthy subjects: correlation with environmental risk factors.
- Published in:
- Journal of Molecular Medicine, 2010, v. 88, n. 8, p. 785, doi. 10.1007/s00109-010-0624-3
- By:
- Publication type:
- Article
The association of telomere length with paternal history of premature myocardial infarction in the European Atherosclerosis Research Study II.
- Published in:
- Journal of Molecular Medicine, 2008, v. 86, n. 7, p. 815, doi. 10.1007/s00109-008-0347-x
- By:
- Publication type:
- Article
Mutational analysis in UK patients with a clinical diagnosis of familial hypercholesterolaemia: relationship with plasma lipid traits, heart disease risk and utility in relative tracing.
- Published in:
- Journal of Molecular Medicine, 2006, v. 84, n. 3, p. 203, doi. 10.1007/s00109-005-0019-z
- By:
- Publication type:
- Article
Variation in the lipoprotein lipase gene influences exercise-induced left ventricular growth.
- Published in:
- Journal of Molecular Medicine, 2006, v. 84, n. 2, p. 126, doi. 10.1007/s00109-005-0002-8
- By:
- Publication type:
- Article
Hugh Markus (Editor) Report on stroke genetics: Oxford University Press (2003), ISBN 0-19-851586-3, hardcover, £79.50.
- Published in:
- 2004
- By:
- Publication type:
- Book Review
Assessing family history of heart disease in primary care consultations: a qualitative study.
- Published in:
- Family Practice, 2007, v. 24, n. 5, p. 435, doi. 10.1093/fampra/cmm037
- By:
- Publication type:
- Article
The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin.
- Published in:
- British Journal of Clinical Pharmacology, 2012, v. 73, n. 2, p. 303, doi. 10.1111/j.1365-2125.2011.04090.x
- By:
- Publication type:
- Article
Homozigot ailevi hiperkolesterolemi: klinisyenlerin tanıyı ve klinik yönetimi geliştirmelerine yönelik yeni anlayışlar ve rehberlik. Avrupa Ateroskleroz Derneği’nin Ailevi Hiperkolesterolemi Üzerine Uzlaşı Paneli yazılı görüşü
- Published in:
- Archives of the Turkish Society of Cardiology / Türk Kardiyoloji Derneği Arşivi, 2015, v. 43, p. 1
- By:
- Publication type:
- Article
Functional analysis of four LDLR 5′UTR and promoter variants in patients with familial hypercholesterolaemia.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 6, p. 790, doi. 10.1038/ejhg.2014.199
- By:
- Publication type:
- Article
Clinical utility gene card for: Hyperlipoproteinemia, TYPE II.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 7, p. 1, doi. 10.1038/ejhg.2013.271
- By:
- Publication type:
- Article
The frequency of an IL-18-associated haplotype in Africans.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 4, p. 465, doi. 10.1038/ejhg.2012.184
- By:
- Publication type:
- Article
Sequence variant on 9p21 is associated with the presence of abdominal aortic aneurysm disease but does not have an impact on aneurysmal expansion.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 3, p. 391, doi. 10.1038/ejhg.2008.196
- By:
- Publication type:
- Article
A functional mutation in the LDLR promoter (−139C>G) in a patient with familial hypercholesterolemia.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 11, p. 1186, doi. 10.1038/sj.ejhg.5201897
- By:
- Publication type:
- Article
Cascade testing in familial hypercholesterolaemia: how should family members be contacted?
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 4, p. 401, doi. 10.1038/sj.ejhg.5201360
- By:
- Publication type:
- Article
A molecular genetic service for diagnosing individuals with familial hypercholesterolaemia (FH) in the United Kingdom.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 4, p. 244, doi. 10.1038/sj.ejhg.5200633
- By:
- Publication type:
- Article
Cross-sectional analysis of baseline data to identify the major determinants of carotid intima–media thickness in a European population: the IMPROVE study.
- Published in:
- European Heart Journal, 2010, v. 31, n. 5, p. 614, doi. 10.1093/eurheartj/ehp496
- By:
- Publication type:
- Article