Martin Farrall

Q: What Schools Are Affiliated With Martin Farrall

Martin Farrall is affiliated with the following schools: University of Oxford, Newcastle University, Stanford University, Royal Postgraduate Medical School, University of Cambridge

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Martin Farrall

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Machine Learning

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#3528

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Artificial Intelligence

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#3842

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Computer Science

Martin Farrall's Degrees

PhD Computer Science University of Oxford
Bachelors Computer Science University of Oxford

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Martin Farrall's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) (9208)
Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
Hundreds of variants clustered in genomic loci and biological pathways affect human height (2010) (1961)
Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk (2011) (1928)
Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
A large-scale, consortium-based genomewide association study of asthma. (2010) (1779)
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) (1567)
Large-scale association analysis identifies new risk loci for coronary artery disease (2012) (1507)
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma (2007) (1493)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007) (1421)
A genome-wide search for human type 1 diabetes susceptibility genes (1994) (1342)
Genetic variants associated with Lp(a) lipoprotein level and coronary disease. (2009) (1242)
New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
Genome-wide association study identifies eight loci associated with blood pressure (2009) (1225)
A genome-wide association study of global gene expression (2007) (1021)
Genome-wide association analysis identifies 20 loci that influence adult height (2008) (816)
Loss-of-function mutations in APOC3, triglycerides, and coronary disease. (2014) (799)
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries (2018) (735)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (659)
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease (2011) (638)
Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia. (2016) (630)
Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations (2009) (617)
Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. (2009) (614)
Meta-analysis and imputation refines the association of 15q25 with smoking quantity (2010) (605)
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (600)
Mendelian randomization of blood lipids for coronary heart disease (2014) (580)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data (2014) (547)
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples (2016) (529)
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. (2008) (527)
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma (2011) (526)
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 (2007) (498)
Association analyses based on false discovery rate implicate new loci for coronary artery disease (2017) (476)
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (465)
Localization of cystic fibrosis locus to human chromosome 7cen–q22 (1985) (464)
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. (2008) (450)
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies (2012) (446)
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (428)
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (428)
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction (2014) (426)
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure (2011) (424)
Bayesian refinement of association signals for 14 loci in 3 common diseases (2012) (416)
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke (2012) (392)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits (2013) (365)
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) (348)
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (2016) (347)
Aryl hydrocarbon receptor nuclear translocator-like (BMAL1) is associated with susceptibility to hypertension and type 2 diabetes (2007) (347)
Multiancestry association study identifies new asthma risk loci that colocalize with immune cell enhancer marks (2017) (337)
SLC2A9 Is a High-Capacity Urate Transporter in Humans (2008) (334)
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands (1987) (331)
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults (2007) (319)
Genetic Heritability of Ischemic Stroke and the Contribution of Previously Reported Candidate Gene and Genomewide Associations (2012) (314)
Localization of the malignant hyperthermia susceptibility locus to human chromosome 19ql2–13.2 (1990) (313)
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. (2016) (309)
Linkage of the angiotensinogen gene to essential hypertension. (1994) (305)
Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease: A Genome-Wide Analysis of Common Variants (2014) (303)
Mapping of mutation causing Friedreich's ataxia to human chromosome 9 (1988) (295)
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. (2014) (292)
Genetic influences on F cells and other hematologic variables: a twin heritability study. (2000) (290)
Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1 (1993) (290)
Inactivating mutations in NPC1L1 and protection from coronary heart disease. (2014) (289)
Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near UMOD Associated with Hypertension (2010) (285)
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. (2012) (282)
PREDISPOSING LOCUS FOR ALZHEIMER'S DISEASE ON CHROMOSOME 21 (1989) (267)
Genetic loci influencing kidney function and chronic kidney disease (2010) (266)
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals (2018) (249)
Genetic susceptibility to coronary artery disease: from promise to progress (2006) (232)
Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease (2011) (228)
Measured haplotype analysis of the angiotensin-I converting enzyme gene. (1998) (221)
Genetically determined height and coronary artery disease. (2015) (220)
HLA has strongest association with IgA nephropathy in genome-wide analysis. (2010) (216)
Genome-wide mapping of human loci for essential hypertension (2003) (214)
Linkage of the angiotensinogen gene locus to human essential hypertension in African Caribbeans. (1995) (205)
Identification of multiple quantitative trait loci linked to prion disease incubation period in mice (2001) (204)
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (2017) (204)
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations (2009) (201)
Genetic evidence of assortative mating in humans (2017) (199)
Familial combined hyperlipidaemia linked to the apolipoprotein AI–CIII–AIV gene cluster on chromosome 11q23q–q24 (1991) (191)
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
Meta-Analysis of Gene Level Tests for Rare Variant Association (2013) (183)
Mapping of a major genetic modifier of embryonic lethality in TGFβ1 knockout mice (1997) (181)
Blood pressure loci identified with a gene-centric array. (2011) (177)
Integrating case-control and TDT studies. (2005) (172)
Panning for gold: genome-wide scanning for linkage in type 1 diabetes. (1996) (172)
Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels. (2016) (164)
Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour (2011) (162)
Variants in the fetal genome near FLT1 are associated with risk of preeclampsia (2017) (159)
Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. (2012) (158)
Patterns of polymorphism and linkage disequilibrium for cystic fibrosis. (1987) (157)
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke (2012) (156)
Two-locus maximum lod score analysis of a multifactorial trait: joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes. (1995) (154)
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. (2014) (150)
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. (1986) (148)
Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction (2014) (147)
Loci influencing blood pressure identified using a cardiovascular gene-centric array. (2013) (145)
Localization of the malignant hyperthermia susceptibility locus to human chromosome 19q12-13.2. (1990) (144)
Ischemic Stroke Is Associated with the ABO Locus: The EuroCLOT Study (2013) (142)
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease (2017) (135)
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. (2011) (133)
Integrating Case‐control and TDT Studies (2005) (128)
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney (2017) (121)
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 (2013) (119)
Linkage of an X-chromosome cleft palate gene (1987) (119)
The Genetical Analysis of Quantitative Traits (1996) (117)
Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study. (2005) (112)
Familial recurrence-pattern analysis of cleft lip with or without cleft palate. (1992) (111)
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. (2014) (110)
Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait loci. (1995) (109)
Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides. (2002) (107)
Targeting 160 Candidate Genes for Blood Pressure Regulation with a Genome-Wide Genotyping Array (2009) (106)
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis (2015) (106)
The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12. (1992) (103)
Genome-Wide Mapping of Susceptibility to Coronary Artery Disease Identifies a Novel Replicated Locus on Chromosome 17 (2006) (102)
Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1. (2001) (101)
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. (2018) (100)
Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis (2015) (100)
Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia. (2011) (99)
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity (2021) (99)
Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia (2013) (98)
FIRST-TRIMESTER PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS WITH LINKED DNA PROBES (1986) (98)
Chorea-acanthocytosis: genetic linkage to chromosome 9q21. (1997) (95)
Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndrome. (2004) (93)
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (93)
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12 (2014) (90)
Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population. (1990) (90)
Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies (2009) (89)
Shared genetic basis for migraine and ischemic stroke (2015) (89)
Quantitative genetic variation: a post-modern view. (2004) (89)
Eight blood pressure loci identified by genome-wide association study of 34,433 people of European ancestry (2009) (88)
Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations (2006) (88)
Genetic Variation on Chromosome 6 Influences F Cell Levels in Healthy Individuals of African Descent and HbF Levels in Sickle Cell Patients (2009) (85)
Haplotype mapping of a major quantitative-trait locus for fetal hemoglobin production, on chromosome 6q23. (1998) (85)
The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans. (2007) (84)
High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity (2002) (84)
Linkage of the gene for cystinosis to markers on the short arm of chromosome 17 (1995) (83)
Genome‐wide association study of body mass index in 23 000 individuals with and without asthma (2013) (81)
Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study. (2013) (80)
Large Scale Association Analysis Identifies Three Susceptibility Loci for Coronary Artery Disease (2011) (80)
Genetic homogeneity at the Friedreich ataxia locus on chromosome 9. (1989) (79)
Secretory Phospholipase A2-IIA and Cardiovascular Disease (2013) (78)
Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. (2019) (77)
Isolation of a further anonymous informative DNA sequence from chromosome seven closely linked to cystic fibrosis. (1986) (76)
Association between angiotensin-converting enzyme gene polymorphisms and diabetic nephropathy: case-control, haplotype, and family-based study in three European populations. (2007) (74)
Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass. (2002) (74)
Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: a collaborative study. (1988) (73)
Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis. (2013) (72)
Complex segregation analysis provides evidence for a major gene acting on serum triglyceride levels in 55 British families with familial combined hyperlipidemia. (1994) (72)
Physical and psychosocial functioning of adult survivors of allogeneic bone marrow transplantation. (1989) (71)
Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study (2017) (70)
Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study. (2005) (69)
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women (2020) (67)
Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation: Meta-Analysis of Three Genome-Wide Association Studies (2009) (67)
Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma (2013) (66)
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease (2017) (64)
Angiotensinogen in human essential hypertension. (1996) (63)
Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene. (1988) (62)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (61)
Gearing up for genome-wide gene-association studies. (2005) (60)
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape (2016) (59)
Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension. (2006) (57)
Experience with new DNA markers for the diagnosis of cystic fibrosis. (1988) (56)
Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion. (2005) (53)
Ambulatory Blood Pressure Is Associated With Polymorphic Variation in P2X Receptor Genes (2008) (52)
G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes (2008) (52)
Polymorphisms in the WNK1 Gene Are Associated with Blood Pressure Variation and Urinary Potassium Excretion (2009) (52)
A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families (2005) (51)
Affected sibpair linkage tests for multiple linked susceptibility genes (1997) (50)
Novel childhood asthma genes interact with in utero and early-life tobacco smoke exposure☆ (2014) (49)
A candidate gene study of F cell levels in sibling pairs using a joint linkage and association analysis. (1999) (49)
Identification of the BCAR1-CFDP1-TMEM170A Locus as a Determinant of Carotid Intima-Media Thickness and Coronary Artery Disease Risk (2012) (49)
Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis (2012) (48)
Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes (2009) (46)
Recombinations between IRP and cystic fibrosis. (1988) (46)
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants (2021) (45)
Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease (2014) (45)
GENETIC DIFFERENCES BETWEEN CYSTIC FIBROSIS WITH AND WITHOUT MECONIUM ILEUS (1988) (45)
Fine-mapping of an ancestral recombination breakpoint in DCP1 (1999) (43)
Genotype at the −174G/C Polymorphism of the Interleukin-6 Gene Is Associated With Common Carotid Artery Intimal-Medial Thickness: Family Study and Meta-Analysis (2005) (42)
Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions (2017) (41)
The gene CYP3 encoding P450pcn1 (nifedipine oxidase) is tightly linked to the gene COL1A2 encoding collagen type 1 alpha on 7q21-q22.1. (1988) (40)
Cloning and sequencing of the mouse Gli2 gene: localization to the Dominant hemimelia critical region. (1997) (40)
Chromosome 2p Shows Significant Linkage to Antihypertensive Response in the British Genetics of Hypertension Study (2006) (40)
A Common LPA Null Allele Associates With Lower Lipoprotein(a) Levels and Coronary Artery Disease Risk (2014) (40)
Diagnostic Yield of Sequencing Familial Hypercholesterolemia Genes in Patients with Severe Hypercholesterolemia. (2016) (39)
Glutathione S-transferase variants and hypertension (2008) (39)
European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy. (2007) (38)
Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield (2018) (37)
An estimation of the number of susceptibility loci for isolated cleft palate. (1993) (37)
Polymorphic Variation in the 11β-Hydroxylase Gene Associates With Reduced 11-Hydroxylase Efficiency (2007) (37)
Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension. (2008) (37)
Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
Association Between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7697 Cases and 13 125 Controls (2013) (37)
Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locus. (1992) (35)
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. (2016) (34)
An extension of the Maximum Lod Score method to X‐linked loci (1995) (33)
LINKAGE OF COL1A2 COLLAGEN GENE TO CYSTIC FIBROSIS, AND ITS CLINICAL IMPLICATIONS (1985) (32)
Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q. (1993) (30)
Angiotensin I-converting enzyme polymorphisms, ACE level and blood pressure among Nigerians, Jamaicans and African-Americans (2004) (30)
Common Polymorphisms in the CYP11B1 and CYP11B2 Genes: Evidence for a Digenic Influence on Hypertension (2013) (29)
Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene. (2006) (29)
Association of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regions. (1991) (29)
Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes (2018) (29)
A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. (2019) (28)
Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension. (2006) (28)
Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension Study (2006) (28)
Phenotypic consequences of variation across the aldosterone synthase and 11‐beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study (2007) (28)
Quantitative Variation in Plasma Angiotensin‐I Converting Enzyme Activity Shows Allelic Heterogeneity in the ABO Blood Group Locus (2013) (26)
Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities. (1994) (26)
Mutational mechanisms for generating microsatellite allele-frequency distributions: an analysis of 4,558 markers. (1998) (26)
Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2 (2014) (25)
Epistasis Between Type 2 Diabetes Susceptibility Loci on Chromosomes 1q21‐25 and 10q23‐26 in Northern Europeans (2006) (25)
No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis (2016) (25)
Genetic Variation in VEGF Does Not Contribute Significantly to the Risk of Congenital Cardiovascular Malformation (2009) (25)
Homozygosity mapping: familiarity breeds debility (1993) (24)
Twenty-five loci form a continuous linkage map of markers for human chromosome 7. (1989) (23)
Absence of linkage of the epithelial sodium channel to hypertension in black Caribbeans. (1998) (23)
INDIRECT CYSTIC FIBROSIS CARRIER DETECTION (1987) (22)
The cystic fibrosis locus. (1987) (22)
Plasma cytokines and risk of coronary heart disease in the PROCARDIS study (2018) (22)
Differential Gene Expression in Macrophages From Human Atherosclerotic Plaques Shows Convergence on Pathways Implicated by Genome-Wide Association Study Risk Variants (2018) (21)
Reevaluation of the South Asian MYBPC3Δ25bp Intronic Deletion in Hypertrophic Cardiomyopathy (2020) (21)
Gene targeting for somatic cell manipulation: rapid analysis of reduced chromosome hybrids by Alu-PCR fingerprinting and chromosome painting. (1992) (21)
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. (2007) (20)
Finding Associations in Dense Genetic Maps: A Genetic Algorithm Approach (2005) (19)
Identifying systematic heterogeneity patterns in genetic association meta-analysis studies (2017) (19)
Ambulatory Blood Pressure Is Associated With Polymorphic Variation in P 2 X Receptor Genes (2008) (19)
Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits (2016) (18)
Cystic fibrosis carrier detection using a linked gene probe. (1986) (18)
Correction: Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (18)
Multiple QTL influence the serum Lp(a) concentration: a genome-wide linkage screen in the PROCARDIS study (2007) (18)
A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis. (1990) (17)
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (17)
Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension (2007) (17)
A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11 (2017) (16)
Secretory Phospholipase A2-IIA and Cardiovascular Disease A Mendelian Randomization Study (2017) (16)
Prenatal diagnosis of Friedreich ataxia. (1989) (15)
Erratum: Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2017) (14)
Genetic analysis of over one million people identifies 535 novel loci for blood pressure (2017) (14)
Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11. (1986) (14)
Genetic homogeneity of cystic fibrosis. (1986) (13)
Measured haplotype analysis of the aldosterone synthase gene and heart size (2003) (13)
Functional annotations of diabetes nephropathy susceptibility loci through analysis of genome-wide renal gene expression in rat models of diabetes mellitus (2009) (13)
LOD wars: the affected-sib-pair paradigm strikes back! (1997) (12)
Physical and genetic analysis of cosmids from the vicinity of the cystic fibrosis locus. (1987) (12)
Mapping genetic susceptibility to multiple sclerosis (1996) (12)
A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19. (1986) (12)
Measured haplotype analysis of the aldosterone synthase gene and heart size (2005) (12)
Two unusual cases of first trimester prenatal diagnosis of cystic fibrosis using DNA probes (1987) (12)
Polymorphisms in genes involved in folate metabolism as risk factors for oedematous severe childhood malnutrition: a hypothesis-generating study (2006) (12)
Prenatal diagnosis of cystic fibrosis using linked DNA probes (1988) (11)
Linkage analysis of 62 X‐chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X‐linked recessive inheritance of neural tube defects (1994) (11)
Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus. (1994) (11)
Genotype at the 174 G / C Polymorphism of the Interleukin-6 Gene Is Associated With Common Carotid Artery Intimal-Medial Thickness Family Study and Meta-Analysis (2005) (10)
Glutathione S-transferase polymorphisms may be associated with risk of oedematous severe childhood malnutrition (2006) (10)
Cystic fibrosis linkage exclusion data. (1986) (9)
Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome (2019) (9)
Exclusion of catalytic and regulatory subunits of cAMP-dependent protein kinase as candidate genes for the defect causing cystic fibrosis. (1987) (8)
Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits : (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x) (2018) (8)
Reports of the death of the epistasis model are greatly exaggerated. (2003) (8)
A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markers. (1987) (8)
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals (2017) (7)
Linkage between the cystic fibrosis locus and markers on chromosome 7q. (1986) (7)
A G / T substitution in intron-1 of UNC 13 B gene is associated with increased risk of nephropathy in patients with type 1 diabetes (2008) (7)
Analysis of 7 polymorphic markers at chromosome 11q22-23 in 35 ataxia telangiectasia families; further evidence of linkage (1990) (7)
The Book of Man: The Human Genome Project and the Quest to Discover Our Genetic Heritage (1998) (7)
Cardiovascular twist to the rapidly evolving apolipoprotein L1 story. (2014) (7)
Meta-Analysis of Gene Level Association Tests (2013) (6)
Erratum: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci (American Journal of Human Genetics (2012) 90 (410-425)) (2012) (6)
Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer’s disease (2018) (5)
Chromosome 1p shows significant linkage to steroid metabolism in hypertension in the British Genetics of Hypertension Study (2006) (5)
Absence of genetic linkage between polymorphisms of the insulin receptor gene and essential hypertension. (1995) (5)
Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers (2019) (5)
Abstract 17123: Association of Apolipoprotein(a) Isoforms With Coronary Heart Disease is Mediated Through Plasma Lipoprotein(a) Levels (2010) (5)
The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4. (1986) (5)
Heritability of haemodynamics in the ascending aorta (2020) (4)
Panning for gold: Genomewide scanning in type 1 diabetes (1997) (4)
Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family (2019) (4)
A quantitative trait locus for SBP maps near KCNB1 and PTGIS in a population isolate. (2009) (4)
Isolation of a polymorphic genomic clone from chromosome 7 (1987) (4)
Further data on linkage between cystic fibrosis and 7C22 (D7S16) (1987) (3)
Supplementary Material 7 (2014) (3)
Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR 1 as a Major Determinant of Coronary Artery Stenosis (2012) (3)
Supplementary Material 3 (2015) (3)
Supplementary Material 6 (2014) (3)
Monday, 27 August 2012 (2012) (3)
Urinary albumin excretion in hypertensive siblings in the British Genetics of Hypertension study (2007) (3)
Crossovers in two German cystic fibrosis families determine probe order for MET, 7C22 and XV-2c/CS.7 (1987) (3)
Supplementary Material 5 (2014) (3)
Chromosome 2p Shows Genome Wide Significant Linkage to Anti-Hypertensive Medication Response in the British Genetics of Hypertension (BRIGHT) Study.: LB57 (2005) (3)
The MRC British Genetics of Hypertension Study - Genome-wide screen results (2002) (3)
The application of molecular genetics to the study of the basic defect causing cystic fibrosis. (1987) (2)
Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (2)
The canosinase gene (CNDP1) is not a protection factor of diabetic nephropathy in type 1 diabetics (2006) (2)
A new tool for checks of data precision within the MRC British genetics of hypertension study (2000) (2)
Molecular Approaches to identify the cystic fibrosis gene defect (1987) (2)
Association between Variants of the Human GSTM Gene Family and Hypertension: 8 (2006) (2)
Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney (2017) (2)
Genome-Wide Analysis Identifies Strong Association Between HLA and IgA Nephropathy (2010) (2)
Investigation of the epithelial sodium channel (hENaC) as a candidate gene for essential hypertension (EH) in African Caribbeans (1997) (2)
Linkage of the Col1A2 collagen gene to cystic fibrosis (1985) (2)
Genetic loci influencing C-reactive protein levels and coronary heart disease risk: results of genetic association and Mendelian randomisation study with meta-analysis in 80 614 people (2009) (2)
Quantitative Trait Genetic Linkage Analysis of Body Mass Index in Familial Coronary Artery Disease (2008) (2)
Marked variation in heritability estimates of left ventricular mass depending on modality of measurement (2019) (2)
Exclusion of the Friedreich ataxia gene from chromosome 19 (1987) (2)
Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential (2007) (2)
Data-driven modelling of mutational hotspots and in-silico predictors in hypertrophic cardiomyopathy (2019) (2)
Mapping Inherited Diseases by Linkage Analysis (1991) (1)
Genome-Wide Association Study of Over One Million Participants Identifies 49 Novel Loci Associated With Coronary Artery Disease (2019) (1)
Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18)) (2012) (1)
ENHANCED SUPPORT FOR LINKAGE TO CHROMOSOME 5Q13.1 AND HYPERTENSION IN THE BRITISH GENETICS OF HYPERTENSION (BRIGHT) STUDY.: 5.1 (2005) (1)
Title : Polymorphisms in the WNK 1 Gene Are Associated with Blood Pressure Variation and Urinary Potassium Excretion (2009) (1)
Supplementary Material 15 (2013) (1)
No Association of the Wnk1 Gene With Essential Hypertension in the Mrc Bright Study (2004) (1)
High glucose and low lactate: a metabolic signature of hypertension in human serum? (2008) (1)
Molecular genetics and the basic defect causing cystic fibrosis. (1986) (1)
Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide lipidome reveal genetic influence over circulating lipids (2019) (1)
Supplementary Material 4 (2015) (1)
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies | NOVA. The University of Newcastle's Digital Repository (2012) (1)
Measured haplotype analysis of the aldosterone synthase gene and cardiac hypertrophy (2002) (1)
2 Linkage of the angiotensinogen gene to human essential hypertension in African Caribbeans (1994) (1)
The Tyrosinase-positive Oculocutaneous Albinism Locus Maps to Chromosome I Sq I 1.2-q 12 (2006) (1)
Supplementary Material 9 (2013) (1)
No support for linkage of chromosome 17(q21-24) to Essential Hypertension in the MRC British Genetics of Hypertension (MRC BRIGHT) Study. (2001) (1)
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals (2018) (1)
Intergenic variants of HBSIL-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing HbF levels in adults. (2006) (1)
Data-driven modelling of mutational hotspots and in silico predictors in hypertrophic cardiomyopathy (2020) (1)
Loci influencing blood pressure identified using a cardiovascular gene-centric array (Correction to Ganesh et al. 22 (8): 1663) (2013) (1)
Analysis of the angiotensinogen gene in the MRC British genetics of Hypertension study. (2015) (1)
The C-532T polymorphism of the angiotensinogen (AGT) gene is associated with arterial stiffness: A possible explanation for heterogeneity in genetic association studies of AGT and hypertension (2007) (1)
Individuals with a genetic shift in haematological indices (2008) (1)
Evidence for a shared genetic determination of Ischemic Stroke And Coronary Artery Disease - a genome-wide analysis (2013) (0)
Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers (2019) (0)
Detecting Gene-gene Interactions in Complex Diseases using Lasso Penalized Regression (2010) (0)
Erratum (2012) (0)
Model selection methods applied to genetic association studies (2009) (0)
A rare variant of the leptin (LEP) gene has large effects on blood pressure (BP) and carotid intima-medial thickness (CIMT): Study of 1428 individuals in 248 families (2005) (0)
ALLHAT Revisited: How Have the Findings Held Up 5 Years Later? (2007) (0)
Does CRP Play a Causal Role in the Development of Coronary Heart Disease: Results of a Mendelian Randomisation Experiment Involving 128,935 People (2009) (0)
Discovery and validation of 107 blood pressure loci from UK Biobank offers novel biological insights into cardiovascular risk (2016) (0)
EURAGEDIC; European consortium for the genetics of diabetic nephropathy: strategy and first results. (2003) (0)
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (0)
126 CHROMOSOME 9P21 LOCUS AND ANGIOGRAPHIC CORONARY ARTERY DISEASE BURDEN: A COLLABORATIVE META-ANALYSIS (2013) (0)
The MRC BRIGHT study: Demographic and biochemical characteristics of the sibling-pair resource (2004) (0)
Evidence from a family based study of gene association of lymphotoxin alpha with coronary artery disease (CAD) (2004) (0)
Independent Relevance of Cytokines for Risk of Coronary Heart Disease (2012) (0)
Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield (2018) (0)
Loci on Chromosomes 5p and 20q are Linked to Multiple Hypertension Phenotypes in the BRItish Genetics of HyperTension (BRIGHT) Study: LB13 (2005) (0)
Association between the-174G/C polymorphism of the interleukin-6 gene and carotid atherosclerosis: Family study and meta-analysis (2005) (0)
EURAGEDIC study: analyses of 144 candidate genes for diabetic nephropathy (2006) (0)
Genetic determinants of interventricular septal anatomy and the risk of ventricular septal defects and hypertrophic cardiomyopathy (2021) (0)
Association of the CYP11B1 and CYP11B2 gene polymorphisms with hypertension in the British Genetics of Hypertension case-control study (2007) (0)
Author's response to reviews Title: Discovery and Replication of SNP-SNP Interactions for Quantitative Lipid Traits in over 60,000 Individuals Authors: (2017) (0)
Genome-wide association study identifies common variation associated with congenital heart disease (2013) (0)
Oxidized phospholipids, Lp(a) and coronary heart disease risk (2012) (0)
Analysis of the transgenome of MET transfectant cell lines reveals that MET activation is accompanied by an interstitial insertion (1990) (0)
THE USE OF THE MLINK LINKAGE PROGRAM IN EXCLUSION MAPPING USING CYSTIC-FIBROSIS AND CHROMOSOME-4 AS A MODEL SYSTEM (1985) (0)
Abstract 534: A Common Null Allele of LPA is Associated With Lp(a) Levels and Coronary Artery Disease Risk (2014) (0)
Absent uvula in a large Egyptian family is caused by a mutation in FOXF 2 (2019) (0)
Genetic studies of diabetic nephropathy in three European populations (EURAGEDIC consortium): analyses of 14 candidate genes on chromosome 3q (2005) (0)
Independent relevance of renal function for coronary artery disease (2010) (0)
Screening Duchenne and Becker Muscular Dystrophy Patients for Deletions in 30 Exons of the Dystrophin Gene by Three-Multiplex PCR (2006) (0)
Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes (2021) (0)
Beyond Burden Testing - Association Analysis of Ultra-Rare Variants (2017) (0)
Cystic fibrosis (1989) (0)
Abstract 16339: Independent Relevance of Cytokines for Risk of Coronary Heart Disease (2012) (0)
on behalf of the International Stroke Genetics Consortium. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies (vol 11, pg 951, 2012) (2015) (0)
Adolescent vicissitudes and medical judgement: a case study. (1987) (0)
USE OF ENCODE DATA TO IDENTIFY PUTATIVE FUNCTIONAL VARIANTS IN CORONARY ARTERY DISEASE GWAS (2014) (0)
WNK1 - functional analyses of variants associated with blood pressure and essential hypertension (2008) (0)
VARIANTS AND HAPLOTYPES OF THE ANGIOTENSINOGEN GENE ARE ASSOCIATED WITH HYPERTENSION IN THE CAERPHILLY PROSPECTIVE STUDY: PE.14 (2005) (0)
63 PRENATAL DIAGNOSIS OF CYSTIC FIBEOSIS BY LINKED DNAPROBES (1986) (0)
Genetic Recombination Events Which Position the Friedreich Ataxia Locus Proximal to the D 9 S I 5 / D 9 S 5 Linkage Group on Chromosome 9 q (2006) (0)
Validation of Association of Hypertension at the CYP11B1/B2 Locus in Caucasians. (2010) (0)
Systematic analysis of 123 candidate genes reveals two novel genes for hypertension (2008) (0)
Quantifying Systematic Heterogeneity in Meta-Analysis [R package getmstatistic version 0.2.1] (2020) (0)
Variants of the human mu type glutathione-s-transferase (GSTM) gene family are associated with hypertension (2006) (0)
Abstract 17979: A Genome-Wide Association Study of Risk of Coronary Artery Disease in European and South Asian Populations (2010) (0)
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy. (2023) (0)
Annual Scientific Meeting of the British Hypertension Society, Cambridge, UK, 11–13 September 2000 (2000) (0)
GeneticLociAssociatedWithC-ReactiveProtein Levels and Risk of Coronary Heart Disease (2017) (0)
LPA null mutation genotyping and qPCR analysis refine kringle isoform analysis of Lp(a) levels (2014) (0)
Abstract 10667: Mendelian Randomization of Lp(a) Levels and Coronary Disease Risk (2011) (0)
EURAGEDIC study: identification of new candidate genes for diabetic nephropathy (2007) (0)
THE GENETIC-MAP OF THE REGION SURROUNDING THE CYSTIC-FIBROSIS GENE DEFECT (1986) (0)
Adolescent pregnancy and severe heart defect. A risky combination. (1988) (0)
Acknowledgement to the Reviewers (2009) (0)
Discovery of novel genes for serum urate and low-density lipoprotein cholesterol - Two biomarkers of cardiovascular disease (2007) (0)
Edinburgh Research Explorer Secretory Phospholipase A2-IIA and Cardiovascular Disease (2018) (0)
COMMON OR RARE GENETIC VARIATION IN THE CHEMOKINE RECEPTORS CCR2, CCR5, AND CX3CR1 DOES NOT RELATE TO CORONARY HEART DISEASE OR MYOCARDIAL INFARCTION IN HUMANS (2016) (0)
FURTHER LINKAGE DISEQUILIBRIUM DATA FOR CYSTIC-FIBROSIS (1987) (0)
Physical andgenetic analysis ofcosmids fromthevicinity ofthecystic fibrosis locus (1987) (0)
Linkage ofautosomal dominant dystrophic epidermolysis bullosa inthree British families to themarker D3S2close totheCOL7A1locus (1992) (0)
Association between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7,697 Cases and 13,125 Controls Running title: Mamasoula: MTHFR C677T polymorphism and congenital heart disease (2017) (0)
Phenotypic effects of inositol 5-phosphatase variants in siblings of UK white Caucasians with type 2 diabetes and non-diabetic controls (2004) (0)
Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer’s disease (2018) (0)
Genetic variation at the CYP11B locus accounts for heritabilities of aldosterone excretion and 11-beta hydroxylase activity (2007) (0)
ASSOCIATION STUDY OF CORONARY ARTERY DISEASE (CAD) USING HUMANCVD 50K CHIP (2009) (0)
Progress towards identification of the gene defect in cystic fibrosis (1987) (0)
Muscular dystrophy and cystic fibrosis (1987) (0)
DNA markers for the cystic fibrosis locus. (1987) (0)
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals (2017) (0)
Genomewide linkage analysis for loci affecting electrocardiographic LV mass (2006) (0)
Genetic Variation at the CYP11B Locus Accounts for Heritabilities of Aldosterone Metabolite (THAldo) Excretion and 11Beta-Hydroxylase Activity: 56 (2006) (0)
A power comparison of multilocus mapping approaches in the presence of epistasis and heterogeneity (2005) (0)
Enhanced prediction of gene and missense rare-variant pathogenicity by joint analysis of gene burden and amino-acid residue position (2019) (0)
University of Dundee Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (0)
Disease Presenting as Autosomal Recessive Hypercholesterolemia Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage (2013) (0)
A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11 (2017) (0)
Multi-ancestry association study identifies new asthma risk loci that co-localize with 1 immune cell enhancer marks 2 (2017) (0)
Review Panning for gold: genome-wide scanning for linkage in type 1 (1996) (0)
Erratum: Ischemic stroke is associated with the ABO locus: The EuroCLOT study (2014) (0)
SPRE Statistics for Exploring Heterogeneity in Meta-Analysis [R package getspres version 0.1.1] (2020) (0)
Association between aldosterone production and variation in the gene encoding 11-beta hydroxylase (CYP11B1) (2007) (0)
Familial Atherosclerotic Disease and Hypertension Localised To Chromosome 7p in the British Genetics of Hypertension Study: LB19 (2006) (0)
Replicated association of regions at CYP11B1/B2 locus with hypertension in Caucasians (2010) (0)
Absence of linkage of the epithelial sodium channel to hypertension in African Caribbeans (1997) (0)
Further linkage disequilibrium data at the cystic fibrosis locus (1988) (0)
A major quantitative trait locus on chromosome 6q23 for HbF levels - An update (2007) (0)
Spot the Difference: Multi-Variant Statistics to Identify Systematic Patterns of Heterogeneity in GWAS Meta-Analysis (2015) (0)
Association of angiotensin I-converting enzyme polymorphisms with obesity in Nigerians, Jamaicans, and African Americans. (2003) (0)
GENETIC POLYMORPHISMS LINKED TO CORONARY ARTERY DISEASE ARE NOT ASSOCIATED WITH CAROTID ARTERY INTIMA-MEDIA THICKNESS, LEFT VENTRICULAR SIZE, OR INTERMEDIATE RISK PHENOTYPES (2009) (0)
University of Groningen Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci Tragante, (2014) (0)
Association ofTreacher Collins SyndromeandTranslocation 6p2l.31/16p 13.11:Exclusion oftheLocusfromThese Candidate Regions (1991) (0)
Electrocardiographic markers of cardiac hypertrophy show greater heritability than echocardiographic left ventricular mass: A family study (2002) (0)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
Interpreting gene-association studies. (2005) (0)
Autosomal DominantAtaxia: Genetic Evidence forLocus Heterogeneity froma CubanFounder-Effect Population (1990) (0)
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks (2017) (0)
Genetic Variants in Lp(a) Lipoprotein and Coronary Disease REPLY (2010) (0)
sickle cell anemia Genetics of fetal hemoglobin in Tanzanian and British patients with (2011) (0)
FurtherDataSupporting LinkagebetweenCystic Fibrosis andthemetOncogene andHaplotype Analysis withmetandpJ3.11 (1986) (0)
Association analyses based on false discovery rate implicate 243 susceptibility loci for coronary artery disease (2017) (0)
Abstract 11789: Genetic Determinants of Interventricular Septal Anatomy and Risk of Congenital Heart Disease (2021) (0)
Vitamin D levels and susceptibility to asthma, elevated IgE levels 3 and atopic dermatitis (2017) (0)
A novel quantitative trait locus controlling fetal haemoglobin on chromosome 2p15 (2008) (0)
PRENATAL-DIAGNOSIS OF CYSTIC-FIBROSIS BY LINKED DNA-PROBES (1986) (0)

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