Works matching AU Farrall, Martin
Results: 65
Mapping of mutation causing Friedreich's ataxia to human chromosome 9.
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- Nature, 1988, v. 334, n. 6179, p. 248, doi. 10.1038/334248a0
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- Article
A Quantitative Trait Locus for SBP Maps Near KCNB1 and PTGIS in a Population Isolate.
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- American Journal of Hypertension, 2009, v. 22, n. 6, p. 663, doi. 10.1038/ajh.2009.46
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- Article
Absence of linkage of the epithelial sodium channel to hypertension in black Caribbeans<sup>*</sup>.
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- American Journal of Hypertension, 1998, v. 11, n. 8, p. 942, doi. 10.1016/S0895-7061(98)00092-2
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- Article
Marked variation in heritability estimates of left ventricular mass depending on modality of measurement.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-49961-w
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- Article
Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene.
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- 2006
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- journal article
Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.
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- 2005
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- journal article
Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies.
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- Human Mutation, 2009, v. 30, n. 10, p. 1378, doi. 10.1002/humu.21079
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- Article
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
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- Nature, 2015, v. 518, n. 7537, p. 102, doi. 10.1038/nature13917
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- Article
Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease.
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- Bioinformatics, 2020, v. 36, n. 2, p. 552, doi. 10.1093/bioinformatics/btz590
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- Article
Genetic susceptibility to coronary artery disease: from promise to progress.
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- Nature Reviews Genetics, 2006, v. 7, n. 3, p. 163, doi. 10.1038/nrg1805
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- Article
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
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- Human Molecular Genetics, 2013, v. 22, n. 8, p. 1663
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- Article
Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.
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- Human Molecular Genetics, 2011, v. 20, n. R2, p. R198, doi. 10.1093/hmg/ddr384
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- Article
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.
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- Human Molecular Genetics, 2008, v. 17, n. 6, p. 806, doi. 10.1093/hmg/ddm352
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- Article
Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.
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- Human Molecular Genetics, 2006, v. 15, n. 8, p. 1365, doi. 10.1093/hmg/ddl058
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- Article
Interpreting gene-association studies.
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- Human Molecular Genetics, 2005, v. 14, n. 17, p. 2489, doi. 10.1093/hmg/ddi253
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- Article
Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.
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- Human Molecular Genetics, 2005, v. 14, n. 13, p. 1805, doi. 10.1093/hmg/ddi187
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- Article
Gearing up for genome-wide gene-association studies.
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- Human Molecular Genetics, 2005, v. 14, n. 2, p. r157, doi. 10.1093/hmg/ddi273
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- Article
Gearing up for genome-wide gene-association studies.
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- Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R157, doi. 10.1093/hmg/ddi273
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- Article
Quantitative genetic variation: a post-modern view.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R1
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- Article
Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides.
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- Human Molecular Genetics, 2002, v. 11, n. 23, p. 2969, doi. 10.1093/hmg/11.23.2969
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- Article
G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes.
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- Diabetes, 2008, v. 57, n. 10, p. 2843, doi. 10.2337/db08-0073
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- Article
Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations.
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- Diabetes, 2006, v. 55, n. 11, p. 3166, doi. 10.2337/db06-0271
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- Article
Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.
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- 2005
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- journal article
Association Between Common Polymorphisms of the Proopiomelanocortin Gene and Body Fat Distribution.
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- Diabetes, 2005, v. 54, n. 8, p. 2492, doi. 10.2337/diabetes.54.8.2492
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- Article
Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndrome.
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- 2004
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- journal article
Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes.
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- Genetic Epidemiology, 2022, v. 46, n. 1, p. 51, doi. 10.1002/gepi.22434
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- Article
Affected sibpair linkage tests for multiple linked susceptibility genes.
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- Genetic Epidemiology, 1997, v. 14, n. 2, p. 103, doi. 10.1002/(SICI)1098-2272(1997)14:2<103::AID-GEPI1>3.0.CO;2-8
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- Article
Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2.
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- Annals of Human Genetics, 2014, v. 78, n. 6, p. 434, doi. 10.1111/ahg.12077
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- Article
Quantitative Variation in Plasma Angiotensin-I Converting Enzyme Activity Shows Allelic Heterogeneity in the ABO Blood Group Locus.
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- Annals of Human Genetics, 2013, v. 77, n. 6, p. 465, doi. 10.1111/ahg.12034
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- Article
Multiple QTL influence the serum Lp(a) concentration: a genome-wide linkage screen in the PROCARDIS study.
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- European Journal of Human Genetics, 2007, v. 15, n. 2, p. 221, doi. 10.1038/sj.ejhg.5201732
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- Article
Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations.
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- PLoS Genetics, 2009, v. 5, n. 6, p. 1, doi. 10.1371/journal.pgen.1000504
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- Article
Genome-Wide Mapping of Susceptibility to Coronary Artery Disease Identifies a Novel Replicated Locus on Chromosome 17.
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- PLoS Genetics, 2006, v. 2, n. 5, p. e72, doi. 10.1371/journal.pgen.0020072
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- Article
Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study.
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- 2017
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- Publication type:
- journal article
SLC2A9 Is a High-Capacity Urate Transporter in Humans.
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- PLoS Medicine, 2008, v. 5, n. 10, p. 1509, doi. 10.1371/journal.pmed.0050197
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- Article
European rational approach for the genetics of diabetic complications EURAGEDIC: patient populations and strategy.
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- Nephrology Dialysis Transplantation, 2008, v. 23, n. 1, p. 161
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- Article
The C-532T polymorphism of the angiotensinogen gene is associated with pulse pressure: A possible explanation for heterogeneity in genetic association studies of AGT and hypertension.
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- International Journal of Epidemiology, 2007, v. 36, n. 6, p. 1356, doi. 10.1093/ije/dym213
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- Article
Measured haplotype analysis of the angiotensin-I converting enzyme gene.
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- Human Molecular Genetics, 1998, v. 7, n. 11, p. 1745, doi. 10.1093/hmg/7.11.1745
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- Article
Autosomal dominant cerebellar ataxia with dementla: evidence for a fourth disease locus.
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- Human Molecular Genetics, 1994, v. 3, n. 1, p. 177
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- Article
Gene targeting for somatic cell manipulation: rapid analysis of reduced chromosome hybrids by Alu-PCR fingerprinting and chromosome painting.
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- Human Molecular Genetics, 1992, v. 1, n. 1, p. 53
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- Article
Fine-mapping of an ancestral recombination breakpoint in DCP1.
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- Nature Genetics, 1999, v. 23, n. 3, p. 270, doi. 10.1038/15449
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- Article
Identifying systematic heterogeneity patterns in genetic association meta-analysis studies.
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- PLoS Genetics, 2017, v. 13, n. 5, p. 1, doi. 10.1371/journal.pgen.1006755
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- Article
Quantitative Trait Genetic Linkage Analysis of Body Mass Index in Familial Coronary Artery Disease.
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- Human Heredity, 2008, v. 66, n. 1, p. 19, doi. 10.1159/000114162
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- Article
Finding Associations in Dense Genetic Maps: A Genetic Algorithm Approach.
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- Human Heredity, 2005, v. 60, n. 2, p. 97, doi. 10.1159/000088845
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- Article
Measured haplotype analysis of the aldosterone synthase gene and heart size.
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- 2005
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- Correction Notice
Angiotensin I-converting enzyme polymorphisms, ACE level and blood pressure among Nigerians, Jamaicans and African-Americans.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 460, doi. 10.1038/sj.ejhg.5201166
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- Article
Measured haplotype analysis of the aldosterone synthase gene and heart size.
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- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 395, doi. 10.1038/sj.ejhg.5200967
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- Article
High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 553, doi. 10.1038/sj.ejhg.5200847
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- Article
Meta-analysis of gene-level tests for rare variant association.
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- Nature Genetics, 2014, v. 46, n. 2, p. 200, doi. 10.1038/ng.2852
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- Article
Large-scale association analysis identifies new risk loci for coronary artery disease.
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- Nature Genetics, 2013, v. 45, n. 1, p. 25, doi. 10.1038/ng.2480
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- Article
Bayesian refinement of association signals for 14 loci in 3 common diseases.
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- Nature Genetics, 2012, v. 44, n. 12, p. 1294, doi. 10.1038/ng.2435
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- Article