Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (14) 14
humans (13) 13
male (10) 10
female (9) 9
genetics (9) 9
middle aged (7) 7
polymorphism, single nucleotide (7) 7
adult (6) 6
cardiac & cardiovascular systems (6) 6
gene expression (6) 6
blood pressure (5) 5
cohort studies (5) 5
coronary artery disease (5) 5
gene (5) 5
genetic aspects (5) 5
heritability (5) 5
risk factors (5) 5
young adult (5) 5
adolescent (4) 4
aged (4) 4
association (4) 4
blood-pressure (4) 4
cardiovascular disease (4) 4
cholesterol (4) 4
coronary artery disease - genetics (4) 4
european continental ancestry group - genetics (4) 4
hypertension - genetics (4) 4
medicine (4) 4
mortality (4) 4
peripheral vascular disease (4) 4
analysis (3) 3
blood pressure - genetics (3) 3
cardiovascular diseases (3) 3
coronary heart disease (3) 3
genes (3) 3
genome-wide association (3) 3
genomes (3) 3
genotype (3) 3
haplotypes (3) 3
hypertension (3) 3
loci (3) 3
macrophages - metabolism (3) 3
phenotype (3) 3
phylogeny (3) 3
replication (3) 3
research article (3) 3
risk (3) 3
science (3) 3
single-nucleotide polymorphism (3) 3
studies (3) 3
y chromosome (3) 3
aggression (2) 2
architecture (2) 2
article (2) 2
association analysis (2) 2
atherosclerosis (2) 2
biology (2) 2
biomedical research (2) 2
cardiovascular (2) 2
casings or constructional details of electric apparatus (2) 2
chromosomes, human, y - genetics (2) 2
clinical research (2) 2
common variants (2) 2
consortia (2) 2
coronary artery (2) 2
coronary vessels (2) 2
disease (2) 2
electric techniques not otherwise provided for (2) 2
electricity (2) 2
expression (2) 2
gene frequency (2) 2
genetic association studies (2) 2
genetics & heredity (2) 2
genomics (2) 2
health risks (2) 2
heart attacks (2) 2
heart diseases (2) 2
hematology (2) 2
internal medicine (2) 2
linkage (2) 2
linkage disequilibrium (2) 2
lipoprotein (2) 2
low density lipoprotein (2) 2
manufacture of assemblages of electrical components (2) 2
medical genetics (2) 2
men (2) 2
minor histocompatibility antigens (2) 2
monocytes - metabolism (2) 2
multidisciplinary sciences (2) 2
myocardial-infarction (2) 2
odds ratio (2) 2
physiological aspects (2) 2
polymorphism (2) 2
polymorphisms (2) 2
printed circuits (2) 2
protein-serine-threonine kinases - genetics (2) 2
sex steroids (2) 2
single nucleotide polymorphism (2) 2
single nucleotide polymorphisms (2) 2
testosterone (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Young Investigator Spotlight: Radoslaw Debiec, MD
by Debiec, R and Taylor, J
CIRCULATION, ISSN 0009-7322, 11/2010, Volume 122, Issue 20, pp. F119 - F120
CARDIAC & CARDIOVASCULAR SYSTEMS | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome
by Charchar, Fadi J, PhD and Bloomer, Lisa DS, MSc and Barnes, Timothy A, PhD and Cowley, Mark J, PhD and Nelson, Christopher P, PhD and Wang, Yanzhong, PhD and Denniff, Matthew, BSc and Debiec, Radoslaw, MD and Christofidou, Paraskevi, MSc and Nankervis, Scott, PhD and Dominiczak, Anna F, MD and Bani-Mustafa, Ahmed, PhD and Balmforth, Anthony J, MD and Hall, Alistair S, MD and Erdmann, Jeanette, PhD and Cambien, Francois, PhD and Deloukas, Panos, PhD and Hengstenberg, Christian, MD and Packard, Chris, MD and Schunkert, Heribert, MD and Ouwehand, Willem H, MD and Ford, Ian, PhD and Goodall, Alison H, PhD and Jobling, Mark A, PhD and Samani, Nilesh J, MD and Tomaszewski, Maciej, Dr
Lancet, The, ISSN 0140-6736, 2012, Volume 379, Issue 9819, pp. 915 - 922
Summary Background A sexual dimorphism exists in the incidence and prevalence of coronary artery disease—men are more commonly affected than are age-matched... 
Internal Medicine | HAPLOGROUP-I | MORTALITY | MEDICINE, GENERAL & INTERNAL | ASSOCIATION ANALYSIS | LEUKOCYTE RECRUITMENT | ATHEROSCLEROSIS | RISK | BLOOD-PRESSURE | Haplotypes | Humans | Middle Aged | Risk Factors | Transcriptome | Genotype | Male | Monocytes - metabolism | Case-Control Studies | Chromosomes, Human, Y - genetics | Macrophages - metabolism | Coronary Artery Disease - genetics | Sex Distribution | Female | Polymorphism, Single Nucleotide | Physiological aspects | Genetic aspects | Research | Coronary heart disease | Y chromosome | Heart | Biomedical research | Heart attacks | Angioplasty | Alcohol | Cardiovascular disease | Dimorphism | Macrophages | Immunity | Risk factors | Consortia | Employment | Atherosclerosis | Blood pressure | Sexual dimorphism | Y Chromosomes | Chromosomes | Heart diseases | Deoxyribonucleic acid--DNA | Age | Medical research | Coronary artery | Health risks | Socio-economic aspects | Triglycerides | Heredity | Functional analysis | Risk analysis | Gene expression | Coronary artery disease | Low density lipoprotein | Cholesterol | Molecular chains | Educational attainment | Studies | Disease prevention | Monocytes | Arteriosclerosis | Coronary vessels | Men | Diabetes | Cardiovascular diseases
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text 12 Is echocardiography alone sufficient for reliable cascade screening of first degree relatives of patients with bicuspid aortic valves?
by Debiec, Radoslaw and Coolman, Sue and Samani, Nilesh J and Bolger, Aidan
Heart, ISSN 1355-6037, 04/2017, Volume 103, Issue Suppl 3, p. A5
BackgroundBicuspid aortic valve (BAV) is the commonest valvular congenital heart defect, affecting around 1% of the population. BAV shows strong familial... 
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Genetic Insights Into Bicuspid Aortic Valve Disease
by Debiec, Radoslaw and Sall, Hanish and Samani, Nilesh J and Bolger, Aidan
Cardiology in Review, ISSN 1061-5377, 07/2017, Volume 25, Issue 4, pp. 158 - 164
Bicuspid aortic valve (BAV) is the most common valvular congenital heart defect in the general population. BAV is commonly associated with the presence of... 
bicuspid aortic valve | genetics | heritability | CARDIAC & CARDIOVASCULAR SYSTEMS | STENOSIS | SURGICAL PATHOLOGY | NATURAL-HISTORY | DILATION | LEFT-HEART SYNDROME | CORONARY ARTERIAL SYSTEM | FREQUENCY | INFECTIVE ENDOCARDITIS | MUTATIONS | COARCTATION | Aortic Valve - abnormalities | Humans | Genetic Heterogeneity | Heart Valve Diseases - genetics | Genetic Linkage
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Analysis of gene-gene interactions among common variants in candidate cardiovascular genes in coronary artery disease
by Musameh, Muntaser D and Wang, William Y. S and Nelson, Christopher P and Lluís-Ganella, Carla and Debiec, Radoslaw and Subirana, Isaac and Elosua, Roberto and Balmforth, Anthony J and Ball, Stephen G and Hall, Alistair S and Kathiresan, Sekar and Thompson, John R and Lucas, Gavin and Samani, Nilesh J and Tomaszewski, Maciej
PLoS ONE, ISSN 1932-6203, 02/2015, Volume 10, Issue 2, p. e0117684
Objective Only a small fraction of coronary artery disease (CAD) heritability has been explained by common variants identified to date. Interactions between... 
POLYMORPHISMS | ARRAY | MYOCARDIAL-INFARCTION | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | ARCHITECTURE | LOCI | NETWORKS | COMPLEX DISEASES | EPISTASIS | GENOME-WIDE ASSOCIATION | Epistasis, Genetic | Humans | Middle Aged | Coronary Artery Disease - genetics | Adult | Female | Male | United Kingdom | Polymorphism, Single Nucleotide | Cohort Studies | Genetic aspects | Single nucleotide polymorphisms | Analysis | Genes | Heart attack | Myocardial infarction | Biomedical research | Heart attacks | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Epidemiology | Consortia | Proteins | Ethics | Genetics | Secondary analysis | Heart diseases | Significance | Cardiovascular system | Statistical analysis | Coronary artery | Gene expression | Coronary artery disease | Patients | Studies | Hospitals | Gene frequency | Coronary vessels | Quality control | Replication | Infarction | Heritability | Cardiovascular diseases
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Urotensin-II system in genetic control of blood pressure and renal function
by Debiec, Radoslaw and Christofidou, Paraskevi and Denniff, Matthew and Bloomer, Lisa D and Bogdanski, Pawel and Wojnar, Lukasz and Musialik, Katarzyna and Charchar, Fadi J and Thompson, John R and Waterworth, Dawn and Song, Kijoung and Vollenweider, Peter and Waeber, Gerard and Zukowska-Szczechowska, Ewa and Samani, Nilesh J and Lambert, David and Tomaszewski, Maciej
PLoS ONE, ISSN 1932-6203, 12/2013, Volume 8, Issue 12, p. e83137
Urotensin-II controls ion/water homeostasis in fish and vascular tone in rodents. We hypothesised that common genetic variants in urotensin-II pathway genes... 
POLYMORPHISMS | RAT | IMMUNOREACTIVITY | MULTIDISCIPLINARY SCIENCES | VASOCONSTRICTOR | ESSENTIAL-HYPERTENSION | RECEPTOR GENE | LINKAGE | ASSOCIATION | EXPRESSION | PEPTIDE | Kidney - physiology | Blood Pressure - genetics | Humans | Middle Aged | Male | Peptide Hormones - genetics | Glomerular Filtration Rate - physiology | Young Adult | Adult | Female | Blood Pressure - physiology | Glomerular Filtration Rate - genetics | Hypertension - genetics | Peptide Hormones - physiology | Receptors, G-Protein-Coupled - physiology | Gene Expression | Genetic Association Studies | Primates - physiology | Urotensins - genetics | Urotensins - physiology | Hypertension - physiopathology | Primates - genetics | Animals | Adolescent | Aged | Polymorphism, Single Nucleotide | Receptors, G-Protein-Coupled - genetics | Cohort Studies | Evolution, Molecular | Hypertension | Analysis | Genes | Genetic aspects | Blood pressure | Single nucleotide polymorphisms | Phylogeny | Neurophysiology | Divergence | Renal function | Biological evolution | Homeostasis | Genomes | Single-nucleotide polymorphism | Ii system | Gene polymorphism | Blood | Urology | Rodents | Primates | Evolution | Kidneys | Filtration | Internal medicine | Genetic control | Mammals | Glomerular filtration rate | Medicine | Studies | Genetic variance | Vertebrates | Tagging | Replication | Mutation | Metabolic disorders | Polymorphism | Kidney transplantation
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Large-scale candidate gene analysis of HDL particle features
by Kaess, Bernhard M and Tomaszewski, Maciej and Braund, Peter S and Stark, Klaus and Rafelt, Suzanne and Fischer, Marcus and Hardwick, Robert and Nelson, Christopher P and Debiec, Radoslaw and Huber, Fritz and Kremer, Werner and Kalbitzer, Hans Robert and Rose, Lynda M and Chasman, Daniel I and Hopewell, Jemma and Clarke, Robert and Burton, Paul R and Tobin, Martin D and Hengstenberg, Christian and Samani, Nilesh J
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 1, p. e14529
Background: HDL cholesterol (HDL-C) is an established marker of cardiovascular risk with significant genetic determination. However, HDL particles are not... 
COMMON VARIANTS | LIPOPROTEIN | SMOOTH-MUSCLE | MAGNETIC-RESONANCE-SPECTROSCOPY | LIPID-LEVELS | FIBULIN-5 | BIOLOGY | BINDING-PROTEIN | MACULAR DEGENERATION | LOCI | CORONARY-ARTERY-DISEASE | Cardiovascular Diseases | Phenotype | Lipoproteins, HDL - genetics | Magnetic Resonance Spectroscopy | Humans | Family | Female | Genotype | Male | United Kingdom | Cholesterol, HDL - genetics | Genome-Wide Association Study - methods | Genes | Genomics | Physiological aspects | Nuclear magnetic resonance spectroscopy | Genetic aspects | Cardiovascular diseases | Lipase | Cholesterol | Antilipemic agents | Phospholipid transfer protein | Particle size | Nuclear magnetic resonance--NMR | Health risks | Association analysis | Particulates | Genomes | Single-nucleotide polymorphism | Metabolism | Low density lipoprotein | Cholesteryl ester transfer protein | Macular degeneration | Magnetic resonance spectroscopy | Womens health | Spectrum analysis | Phenotyping | Lead | NMR spectroscopy | Lipoproteins (high density) | Genotypes | Nuclear magnetic resonance | NMR
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Male-Specific Region of the Y Chromosome and Cardiovascular Risk: Phylogenetic Analysis and Gene Expression Studies
by Bloomer, Lisa D.S and Nelson, Christopher P and Eales, James and Denniff, Matthew and Christofidou, Paraskevi and Debiec, Radoslaw and Moore, Jasbir and Consortium, Cardiogenics and Zukowska-Szczechowska, Ewa and Goodall, Alison H and Thompson, John and Samani, Nilesh J and Charchar, Fadi J and Tomaszewski, Maciej and Cardiogenics Consortium
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 07/2013, Volume 33, Issue 7, pp. 1722 - 1727
OBJECTIVE—Haplogroup I of male-specific region of the human Y chromosome is associated with 50% increased risk of coronary artery disease. It is not clear to... 
Genetics | Association | Cardiovascular Risk | Gene | Mrna | Dna | C-REACTIVE PROTEIN | MORTALITY | MULTILOCUS GENOTYPE DATA | gene | association | mRNA | INFERENCE | BLOOD-PRESSURE | INDIVIDUALS | genetics | DNA | DISEASE | POPULATION-STRUCTURE | PERIPHERAL VASCULAR DISEASE | cardiovascular risk | HEMATOLOGY | ANTIGEN | Haplotypes | Cardiovascular Diseases - ethnology | Minor Histocompatibility Antigens | Humans | Male | Gene Expression Profiling | Phylogeny | Cardiovascular Diseases - genetics | Young Adult | Chromosomes, Human, Y | Arterial Pressure - genetics | Cardiovascular Diseases - blood | Adult | Nuclear Proteins - genetics | Odds Ratio | Cardiovascular Diseases - diagnosis | Cardiovascular Diseases - physiopathology | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Risk Assessment | Europe | Risk Factors | Gene Expression Regulation | Protein-Serine-Threonine Kinases - genetics | Linear Models | Biomarkers - blood | Macrophages - metabolism | Phenotype | Pseudogenes | Adolescent | Sex Factors | Polymorphism, Single Nucleotide
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Coronary artery disease predisposing haplogroup I of the Ychromosome, aggression and sex steroids - Genetic associationanalysis
by Bloomer, Lisa D.S and Nelson, Christopher P and Denniff, Matthew and Christofidou, Paraskevi and Debiec, Radoslaw and Thompson, John and Zukowska-Szczechowska, Ewa and Samani, Nilesh J and Charchar, Fadi J and Tomaszewski, Maciej
Atherosclerosis, ISSN 0021-9150, 03/2014, Volume 233, Issue 1, pp. 160 - 164
Objective: Amongst middle-aged men, haplogroup I is associated with ≈50% higher risk of coronary artery disease than other paternal lineages of Y chromosome.... 
Testosterone | Aggression | Y chromosome | Coronary artery disease | Sex steroids
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Systematic review of studies that have evaluated screening tests in relatives of patients affected by nonsyndromic thoracic aortic disease
by Mariscalco, Giovanni and Debiec, Radoslaw and Elefteriades, John A and Samani, Nilesh J and Murphy, Gavin J
Journal of the American Heart Association, ISSN 2047-9980, 08/2018, Volume 7, Issue 15, p. e009302
Background-Nonsyndromic thoracic aortic diseases (NS-TADs) are often silent entities until they present as life-threatening emergencies. Despite familial... 
Screening | Genetic testing | Mortality | Aortic disease | screening | CARDIAC & CARDIOVASCULAR SYSTEMS | MUTATIONS PREDISPOSE | INTERNATIONAL REGISTRY | FAMILY-HISTORY | COMPUTED-TOMOGRAPHY | TASK-FORCE | 2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM GUIDELINES | genetic testing | aortic disease | MARFAN-SYNDROME | mortality | PATENT DUCTUS-ARTERIOSUS | ANEURYSM REPAIR | VALVE DISEASE
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. Full Text Heritability of Early Repolarization: A Population-Based Study
by Reinhard, Wibke and Kaess, Bernhard M and Debiec, Radoslaw and Nelson, Christopher P and Stark, Klaus and Tobin, Martin D and Macfarlane, Peter W and Tomaszewski, Maciej and Samani, Nilesh J and Hengstenberg, Christian
Circulation: Cardiovascular Genetics, ISSN 1942-325X, 04/2011, Volume 4, Issue 2, pp. 134 - 138
BACKGROUND—Early repolarization (ER), defined by J-point elevation in 12-lead ECG, was recently associated with increased risk for idiopathic ventricular... 
Electrocardiography | Early repolarization | Genetics | Heritability | J-point elevation | MORTALITY | COMMON VARIANTS | CARDIAC & CARDIOVASCULAR SYSTEMS | VENTRICULAR-FIBRILLATION | CLINICAL CHARACTERISTICS | QT INTERVAL | BLOOD-PRESSURE | electrocardiography | early repolarization | heritability | ELECTROCARDIOGRAM | genetics | GENETICS & HEREDITY | SUDDEN CARDIAC DEATH | HEART-RATE | ST-SEGMENT ELEVATION | Humans | Middle Aged | Male | Risk | Phenotype | Adolescent | Ventricular Fibrillation - physiopathology | Adult | Female | Population | Odds Ratio | Population Surveillance - methods | Cohort Studies
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text Genetic Architecture of Ambulatory Blood Pressure in the General Population Insights From Cardiovascular Gene-Centric Array
by Tomaszewski, Maciej and Debiec, Radoslaw and Braund, Peter S and Nelson, Christopher P and Hardwick, Robert and Christofidou, Paraskevi and Denniff, Matthew and Codd, Veryan and Rafelt, Suzanne and van der Harst, Pim and Waterworth, Dawn and Song, Kijoung and Vollenweider, Peter and Waeber, Gerard and Zukowska-Szczechowska, Ewa and Burton, Paul R and Mooser, Vincent and Charchar, Fadi J and Thompson, John R and Tobin, Martin D and Samani, Nilesh J
Hypertension, ISSN 0194-911X, 12/2010, Volume 56, Issue 6, pp. 1069 - U146
Genetic determinants of blood pressure are poorly defined. We undertook a large-scale, gene-centric analysis to identify loci and pathways associated with... 
blood pressure | genetics | gene | single nucleotide polymorphism | association | UMCG Approved | heritability | PERIPHERAL VASCULAR DISEASE | Promoter Regions, Genetic | European Continental Ancestry Group - genetics | Prevalence | Genetic Association Studies | Oligonucleotide Array Sequence Analysis | Blood Pressure - genetics | Gene Frequency | Humans | Middle Aged | Genotype | Male | Chloride Channels - genetics | Genetic Loci | Young Adult | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Female | Polymorphism, Single Nucleotide | Hypertension - epidemiology | Hypertension - genetics | Blood Pressure Monitoring, Ambulatory | United Kingdom - epidemiology | Cohort Studies
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
13. Full Text Renal Mechanisms of Association between Fibroblast Growth Factor 1 and Blood Pressure
by Tomaszewski, Maciej and Eales, James and Denniff, Matthew and Myers, Stephen and Chew, Guat Siew and Nelson, Christopher P and Christofidou, Paraskevi and Desai, Aishwarya and Buesst, Cara and Wojnar, Lukasz and Musialik, Katarzyna and Jozwiak, Jacek and Debiec, Radoslaw and Dominiczak, Anna F and Navis, Gerjan and van Gilst, Wiek H and van der Harst, Pim and Samani, Nilesh J and Harrap, Stephen and Bogdanski, Pawel and Zukowska-Szczechowska, Ewa and Charchar, Fadi J
Journal of the American Society of Nephrology, ISSN 1046-6673, 12/2015, Volume 26, Issue 12, pp. 3151 - 3160
The fibroblast growth factor 1 (FGF1) gene is expressed primarily in the kidney and may contribute to hypertension. However, the biologic mechanisms underlying... 
URINARY ALBUMIN EXCRETION | GENERAL-POPULATION | MESSENGER-RNA | VARIANTS | TRANSCRIPTOME | CHOLESTEROL | DISEASE | HYPERTENSION | EXPRESSION | GENOME | UROLOGY & NEPHROLOGY | Blood Pressure - genetics | Minor Histocompatibility Antigens | Humans | Middle Aged | Protein-Serine-Threonine Kinases - genetics | RNA, Messenger - analysis | Male | Fibroblast Growth Factor 1 - genetics | Receptor-Like Protein Tyrosine Phosphatases, Class 3 - genetics | Signal Transduction - genetics | Young Adult | Renin - genetics | WNK Lysine-Deficient Protein Kinase 1 | Solute Carrier Family 12, Member 3 - genetics | Adolescent | Adult | Female | Kidney - chemistry | Neprilysin - genetics | Aged | Polymorphism, Single Nucleotide | Hypertension - genetics | Intracellular Signaling Peptides and Proteins - genetics | blood pressure | kidney | gene transcription | Clinical Research | hypertension | gene expression | glomerulus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
14. Full Text Coronary artery disease predisposing haplogroup I of the Y chromosome, aggression and sex steroids – Genetic association analysis
by Bloomer, Lisa D.S and Nelson, Christopher P and Denniff, Matthew and Christofidou, Paraskevi and Debiec, Radoslaw and Thompson, John and Zukowska-Szczechowska, Ewa and Samani, Nilesh J and Charchar, Fadi J and Tomaszewski, Maciej
Atherosclerosis, ISSN 0021-9150, 2014, Volume 233, Issue 1, pp. 160 - 164
Abstract Objective Amongst middle-aged men, haplogroup I is associated with ≈50% higher risk of coronary artery disease than other paternal lineages of Y... 
Cardiovascular | Testosterone | Aggression | Sex steroids | Coronary artery disease | Y chromosome | CARDIAC & CARDIOVASCULAR SYSTEMS | MEN | ARCHITECTURE | RISK | PERIPHERAL VASCULAR DISEASE | Chromosomes, Human, Y - genetics | Chromosomes, Human, Y - physiology | Haplotypes | Young Adult | European Continental Ancestry Group - genetics | Gonadal Steroid Hormones - genetics | Humans | Coronary Artery Disease - genetics | Male | Phylogeny | Genetic research | Coronary heart disease | Analysis | Estrogen
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
15. Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages
by Paraskevi Christofidou and Christopher P Nelson and Majid Nikpay and Liming Qu and Mingyao Li and Christina Loley and Radoslaw Debiec and Peter S Braund and Matthew Denniff and Fadi J Charchar and Ares Rocanin Arjo and David-Alexandre Trégouët and Alison H Goodall and Francois Cambien and Willem H Ouwehand and Robert Roberts and Heribert Schunkert and Christian Hengstenberg and Muredach P Reilly and Jeanette Erdmann and Ruth McPherson and Inke R König and John R Thompson and Nilesh J Samani and Maciej Tomaszewski
American Journal of Human Genetics, ISSN 0002-9297, 08/2015, Volume 97, Issue 2, p. 228
  Runs of homozygosity (ROHs) are recognized signature of recessive inheritance. Contributions of ROHs to the genetic architecture of coronary artery disease... 
Genomics | Atherosclerosis | Cardiovascular disease | Genetics | Gene expression | Ribonucleic acid--RNA | Risk factors
Journal Article
Details down arrow
16. Full Text Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages
by Christofidou, Paraskevi and Nelson, Christopher P and Nikpay, Majid and Qu, Liming and Li, Mingyao and Loley, Christina and Debiec, Radoslaw and Braund, Peter S and Denniff, Matthew and Charchar, Fadi J and Arjo, Ares Rocanin and Trégouët, David-Alexandre and Goodall, Alison H and Cambien, Francois and Ouwehand, Willem H and Roberts, Robert and Schunkert, Heribert and Hengstenberg, Christian and Reilly, Muredach P and Erdmann, Jeanette and McPherson, Ruth and König, Inke R and Thompson, John R and Samani, Nilesh J and Tomaszewski, Maciej
The American Journal of Human Genetics, ISSN 0002-9297, 08/2015, Volume 97, Issue 2, pp. 228 - 237
Runs of homozygosity (ROHs) are recognized signature of recessive inheritance. Contributions of ROHs to the genetic architecture of coronary artery disease and... 
LINKAGE DISEQUILIBRIUM | RISK-FACTORS | MYOCARDIAL-INFARCTION | GENETICS & HEREDITY | NO EVIDENCE | SCHIZOPHRENIA | DETECTABLE CLONAL MOSAICISM | CANCER | LOCUS | GENOME-WIDE ASSOCIATION | HUMAN-POPULATIONS | Homozygote | European Continental Ancestry Group - genetics | Macrophages - metabolism | Age Factors | Gene Expression Regulation - genetics | Genes, Recessive - genetics | Humans | Coronary Artery Disease - genetics | Monocytes - metabolism | RNA, Messenger - metabolism | Genetic aspects | Homozygosity | Gene expression | Health aspects | Coronary heart disease | Risk factors
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights