Lyle J. Palmer | Academic Influence

Lyle J. Palmer's AcademicInfluence.com Rankings

Lyle J. Palmer

Computer Science

#9159

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#9624

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Machine Learning

#3944

World Rank

#3992

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Artificial Intelligence

#4274

World Rank

#4334

Historical Rank

Database

#6144

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#6371

Historical Rank

computer-science Degrees

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Computer Science

Lyle J. Palmer's Degrees

PhD Computer Science University of California, Berkeley
Masters Computer Science Stanford University

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Lyle J. Palmer's Published Works

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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

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
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)
Replicating genotype–phenotype associations (2007) (1367)
Population stratification and spurious allelic association (2003) (1242)
New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction (2009) (790)
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance (2012) (756)
Genomewide scans of complex human diseases: true linkage is hard to find. (2001) (600)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
Genome-wide association study identifies five loci associated with lung function (2010) (560)
Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids. (2006) (544)
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies (2010) (477)
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure (2011) (424)
Decline in lung function in the Busselton Health Study: the effects of asthma and cigarette smoking. (2005) (407)
FTO genotype is associated with phenotypic variability of body mass index (2012) (407)
Genome-wide association and large scale follow-up identifies 16 new loci influencing lung function (2011) (401)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
A genome-wide association meta-analysis identifies new childhood obesity loci (2012) (375)
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits (2013) (365)
Neighborhood greenspace and health in a large urban center (2015) (344)
META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES THREE NEW RISK LOCI FOR ATOPIC DERMATITIS (2011) (325)
Corticosteroid pharmacogenetics: association of sequence variants in CRHR1 with improved lung function in asthmatics treated with inhaled corticosteroids. (2004) (310)
Genetic epidemiology and public health: hope, hype, and future prospects (2005) (286)
A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample (2011) (281)
Transforming growth factor-beta1 promoter polymorphism C-509T is associated with asthma. (2004) (257)
Ascaris lumbricoides infection is associated with increased risk of childhood asthma and atopy in rural China. (2002) (251)
Shaking the tree: mapping complex disease genes with linkage disequilibrium (2005) (251)
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight (2010) (250)
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L (2014) (247)
Diminished lipoxin biosynthesis in severe asthma. (2005) (244)
Single-nucleotide polymorphisms in the Toll-like receptor 9 gene (TLR9): frequencies, pairwise linkage disequilibrium, and haplotypes in three U.S. ethnic groups and exploratory case-control disease association studies. (2003) (235)
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. (2018) (221)
A whole-genome scan for obstructive sleep apnea and obesity. (2003) (221)
Single nucleotide polymorphisms in innate immunity genes: abundant variation and potential role in complex human disease (2002) (218)
The relationship between infant airway function, childhood airway responsiveness, and asthma. (2004) (210)
The transforming growth factor-β1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD) (2004) (210)
Airway responsiveness in early infancy predicts asthma, lung function, and respiratory symptoms by school age. (2001) (208)
Genetic evidence of assortative mating in humans (2017) (199)
Body mass index and asthma in adults in families of subjects with asthma in Anqing, China. (2001) (192)
Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease. (2002) (190)
A Bayesian Data Augmentation Approach for Learning Deep Models (2017) (189)
Association between Common Variation at the FTO Locus and Changes in Body Mass Index from Infancy to Late Childhood: The Complex Nature of Genetic Association through Growth and Development (2011) (187)
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. (2012) (187)
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. (2013) (176)
Sex differences in the association of regional fat distribution with the severity of obstructive sleep apnea. (2010) (169)
Polymorphisms in toll-like receptor 4 are not associated with asthma or atopy-related phenotypes. (2002) (169)
UK Biobank: bank on it (2007) (162)
Whole genome scan for obstructive sleep apnea and obesity in African-American families. (2004) (161)
Case-control association studies for the genetics of complex respiratory diseases. (2000) (160)
Meta‐Analysis of Genome‐wide Linkage Studies in BMI and Obesity (2007) (159)
Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies (2010) (154)
Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (153)
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits (2017) (149)
Role of prostanoid DP receptor variants in susceptibility to asthma. (2004) (149)
Toward a roadmap in global biobanking for health (2012) (146)
Asthma and genes encoding components of the vitamin D pathway (2009) (146)
Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function. (2011) (144)
Relation between tumour necrosis factor polymorphism TNFα-308 and risk of asthma (2002) (133)
Perinatal and childhood origins of cardiovascular disease (2007) (130)
Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes. (2002) (130)
High prevalence of undiagnosed obstructive sleep apnoea in the general population and methods for screening for representative controls (2013) (128)
Association Between Osteopontin and Human Abdominal Aortic Aneurysm (2007) (127)
Inhalant allergen‐specific T‐cell reactivity is detectable in close to 100% of atopic and normal individuals: covert responses are unmasked by serum‐free medium (1995) (127)
Precision Radiology: Predicting longevity using feature engineering and deep learning methods in a radiomics framework (2017) (124)
Common variants at 12q15 and 12q24 are associated with infant head circumference (2012) (121)
JLIN: A java based linkage disequilibrium plotter (2006) (119)
Analyses of associations with asthma in four asthma population samples from Canada and Australia (2009) (117)
Genome-wide linkage analysis of bronchodilator responsiveness and post-bronchodilator spirometric phenotypes in chronic obstructive pulmonary disease. (2003) (117)
A polymorphism of the CC16 gene is associated with an increased risk of asthma. (1998) (117)
A genome-wide association study of body mass index across early life and childhood (2015) (115)
Excessive daytime sleepiness increases the risk of motor vehicle crash in obstructive sleep apnea. (2013) (115)
Common variants at 6q22 and 17q21 are associated with intracranial volume (2012) (110)
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. (2014) (110)
The Association of C-Reactive Protein and CRP Genotype with Coronary Heart Disease: Findings from Five Studies with 4,610 Cases amongst 18,637 Participants (2008) (110)
Postdisaster Emotional Distress, Depression and Event-Related Variables: Findings Across Child and Adolescent Developmental Stages (2002) (107)
Genetic variance components analysis for binary phenotypes using generalized linear mixed models (GLMMs) and Gibbs sampling (1999) (106)
Toll-like receptor 6 gene (TLR6): single-nucleotide polymorphism frequencies and preliminary association with the diagnosis of asthma (2004) (105)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
Separating the Mechanism-Based and Off-Target Actions of Cholesteryl Ester Transfer Protein Inhibitors With CETP Gene Polymorphisms (2010) (104)
Association of Genetic Loci With Glucose Levels in Childhood and Adolescence (2011) (103)
Obstructive Sleep Apnoea: From pathogenesis to treatment: Current controversies and future directions (2010) (103)
Infants with flow limitation at 4 weeks: outcome at 6 and 11 years. (2002) (100)
Pharmacogenetics of asthma. (2002) (100)
The transforming growth factor-beta1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD). (2004) (98)
Depressive Symptoms before and after Treatment of Obstructive Sleep Apnea in Men and Women. (2015) (98)
Linkage of chromosome 5q and 11q gene markers to asthma-associated quantitative traits in Australian children. (1998) (98)
Genomic approaches to understanding asthma. (2000) (93)
Familial aggregation and heritability of adult lung function: results from the Busselton Health Study. (2001) (91)
Detecting hip fractures with radiologist-level performance using deep neural networks (2017) (89)
Sequence variants in three loci influence monocyte counts and erythrocyte volume. (2009) (87)
Genome‐wide association study of body mass index in 23 000 individuals with and without asthma (2013) (81)
Relationship between obstructive sleep apnea and diurnal leptin rhythms. (2004) (80)
A comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/R2), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndrome (2013) (79)
Association between liver‐specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease (2013) (79)
Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
Reading Race: AI Recognises Patient's Racial Identity In Medical Images (2021) (77)
FcεR1-b Polymorphism and Total Serum IgE Levels in Endemically Parasitized Australian Aborigines (1997) (76)
Changes in the prevalence of asthma in adults since 1966: the Busselton health study (2009) (74)
Association of Genetic Loci with Sleep Apnea in European Americans and African-Americans: The Candidate Gene Association Resource (CARe) (2012) (73)
Familial aggregation and heritability of asthma-associated quantitative traits in a population-based sample of nuclear families (2000) (71)
Single-nucleotide polymorphisms in the interleukin-10 gene: differences in frequencies, linkage disequilibrium patterns, and haplotypes in three United States ethnic groups. (2002) (71)
Combined analysis of three whole genome linkage scans for Ankylosing Spondylitis. (2007) (70)
Genomic approaches to understanding obstructive sleep apnea (2003) (68)
Case-Control Association Studies in Pharmacogenetics (2001) (67)
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI (2019) (67)
Biostatistical genetics and genetic epidemiology (2002) (63)
Variance components analysis for pedigree‐based censored survival data using generalized linear mixed models (GLMMs) and Gibbs sampling in BUGS (2000) (63)
Using single nucleotide polymorphisms as a means to understanding the pathophysiology of asthma (2001) (63)
Association of an allelic variant of interleukin-6 with subclinical carotid atherosclerosis in an Australian community population. (2003) (62)
Ascertainment adjustment: where does it take us? (2000) (62)
Common variants at 6q22 and 17q21 are associated with intracranial volume (2012) (61)
Association of a Body Mass Index Genetic Risk Score with Growth throughout Childhood and Adolescence (2013) (60)
Endothelial nitric oxide synthase variants in cystic fibrosis lung disease. (2003) (60)
Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function (2014) (59)
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape (2016) (59)
Fine mapping versus replication in whole-genome association studies. (2007) (58)
Association of a missense mutation in the NOS3 gene with exhaled nitric oxide levels. (2003) (58)
The elimination half-life of urinary cotinine in children of tobacco-smoking mothers. (1998) (58)
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
Genetic Variants Associated with Increased Risk of Malignant Pleural Mesothelioma: A Genome-Wide Association Study (2013) (56)
Complement factor H Y402H and C-reactive protein polymorphism and photodynamic therapy response in age-related macular degeneration. (2009) (56)
A genome-wide association meta-analysis of preschool internalizing problems. (2014) (56)
Physical Inactivity Is Associated with Moderate-Severe Obstructive Sleep Apnea. (2015) (54)
Polymorphisms in the angiotensinogen gene are associated with carotid intimal-medial thickening in females from a community-based population. (2001) (54)
The Canadian Partnership for Tomorrow Project: a pan-Canadian platform for research on chronic disease prevention (2018) (53)
Independent inheritance of serum immunoglobulin E concentrations and airway responsiveness. (2000) (53)
Multiethnic Meta‐Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea‐related Quantitative Trait Locus in Men (2017) (53)
A first trial of retrospective collaboration for positional cloning in complex inheritance: assay of the cytokine region on chromosome 5 by the consortium on asthma genetics (COAG). (2000) (53)
Asthma, rhinitis, and skin test reactivity to aeroallergens in families of asthmatic subjects in Anqing, China. (2001) (52)
β2 adrenoceptor Arg16Gly polymorphism, airway responsiveness, lung function and asthma in infants and children (2004) (52)
A survey of clinicians on the use of artificial intelligence in ophthalmology, dermatology, radiology and radiation oncology (2021) (50)
Genome-Wide Association Study to Identify Common Variants Associated with Brachial Circumference: A Meta-Analysis of 14 Cohorts (2012) (50)
Constitutive and cytokine-induced expression of the ETS transcription factor ESE-3 in the lung. (2002) (48)
Apolipoprotein E Gene Polymorphisms Are Associated With Carotid Plaque Formation but Not With Intima-Media Wall Thickening: Results From the Perth Carotid Ultrasound Disease Assessment Study (CUDAS) (2003) (47)
Cohort profile: The Western Australian Family Connections Genealogical Project. (2008) (46)
The genetics of obstructive sleep apnoea (2018) (46)
Post-Disaster Service Provision Following Proactive Identification of Children with Emotional Distress and Depression (1999) (45)
Collaborative pooled analysis of data on C-reactive protein gene variants and coronary disease: judging causality by Mendelian randomisation (2008) (45)
The C‐480T hepatic lipase polymorphism is associated with HDL‐C but not with risk of coronary heart disease (2006) (43)
Familial aggregation of malignant mesothelioma in former workers and residents of Wittenoom, Western Australia (2013) (43)
Development of aptitude at altitude. (2010) (42)
Rationale, design and methods for a community-based study of clustering and cumulative effects of chronic disease processes and their effects on ageing: the Busselton healthy ageing study (2013) (42)
A Comprehensive Evaluation of a Two-Channel Portable Monitor to "Rule in" Obstructive Sleep Apnea. (2015) (41)
Associations of cord blood fatty acids with lymphocyte proliferation, IL-13, and IFN-gamma. (2006) (41)
The immune anti-tumor effects of GM-CSF and B7-1 gene transfection are enhanced by surgical debulking of tumor (2001) (41)
Covariance components models for longitudinal family data. (2005) (40)
SimHap GUI: An intuitive graphical user interface for genetic association analysis (2008) (40)
A genome-wide association study for malignant mesothelioma risk. (2013) (40)
Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypes (2008) (40)
Genome-wide linkage analysis of bronchodilator responsiveness and post-bronchodilator spirometric phenotypes in chronic obstructive pulmonary disease (vol 12, pg 1199, 2003) (2003) (39)
Detection and importance of laxative use in adolescents with anorexia nervosa. (2000) (38)
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)
Neurophysiological evidence for cognitive and brain functional adaptation in adolescents living at high altitude (2011) (37)
Modelling BMI Trajectories in Children for Genetic Association Studies (2013) (37)
Haseman and Elston revisited: The effects of ascertainment and residual familial correlations on power to detect linkage (2000) (36)
International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents (2016) (36)
MICA, HLA-B haplotypic variation in five population groups of sub-Saharan African ancestry (2003) (36)
Producing radiologist-quality reports for interpretable artificial intelligence (2018) (36)
Cholesteryl ester transfer protein gene haplotypes, plasma high-density lipoprotein levels and the risk of coronary heart disease (2007) (36)
Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population (2008) (36)
Polymorphisms of the interleukin-6 gene promoter and abdominal aortic aneurysm. (2008) (35)
Gibbs sampling–based segregation analysis of asthma‐associated quantitative traits in a population‐based sample of nuclear families (2001) (35)
Cholesteryl ester transfer protein gene polymorphisms increase the risk of fatty liver in females independent of adiposity (2012) (35)
Smoking status and occupational exposure affects oxidative DNA injury in boilermakers exposed to metal fume and residual oil fly ash. (2004) (34)
Sensitization to silk and childhood asthma in rural China. (2001) (34)
Family-based association test method: age of onset traits and covariates. (2001) (34)
Association of an allele on chromosome 9 and abdominal aortic aneurysm. (2010) (33)
AI recognition of patient race in medical imaging: a modelling study (2022) (33)
Lack of association between a polymorphism in the interleukin‐13 gene and total serum immunoglobulin E level among nuclear families in Costa Rica (2002) (32)
The apolipoprotein AII rs5082 variant is associated with reduced risk of coronary artery disease in an Australian male population. (2008) (32)
The association of common genetic variants in the APOA5, LPL and GCK genes with longitudinal changes in metabolic and cardiovascular traits (2008) (31)
Chest pain in asbestos-exposed individuals with benign pleural and parenchymal disease. (2000) (31)
Apolipoprotein E genotype is associated with serum C-reactive protein but not abdominal aortic aneurysm. (2010) (31)
Association of PPARγ allelic variation, osteoprotegerin and abdominal aortic aneurysm (2010) (31)
Hospitalisation with Infection, Asthma and Allergy in Kawasaki Disease Patients and Their Families: Genealogical Analysis Using Linked Population Data (2011) (30)
Gene frequencies of human platelet antigens 1–5 in indigenous Australians in Western Australia (2002) (30)
Prenatal, perinatal, and heritable influences on cord blood immune responses. (2006) (30)
Continuous Positive Airway Pressure Treatment, Glycemia, and Diabetes Risk in Obstructive Sleep Apnea and Comorbid Cardiovascular Disease (2020) (29)
Replicating genotype – phenotype associations What constitutes replication of a genotype – phenotype association , and how best can it be achieved ? (2007) (29)
Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits (2012) (28)
Variants near CCNL1/LEKR1 and in ADCY5 and fetal growth characteristics in different trimesters. (2011) (28)
Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophrenia (2010) (27)
Automated 5-year mortality prediction using deep learning and radiomics features from chest computed tomography (2016) (27)
Effect of Obstructive Sleep Apnea Treatment on Renal Function in Patients with Cardiovascular Disease (2017) (27)
Genetic Influences on Trajectories of Systolic Blood Pressure Across Childhood and Adolescence (2013) (26)
Producing Radiologist-Quality Reports for Interpretable Deep Learning. (2019) (26)
Mutation screening of interferon-gamma (IFNgamma) as a candidate gene for asthma. (1997) (24)
Fc epsilon R1-beta polymorphism and total serum IgE levels in endemically parasitized Australian aborigines. (1997) (24)
Angiotensinogen gene T235 variant: a marker for the development of persistent microalbuminuria in children and adolescents with type 1 diabetes mellitus. (2008) (23)
Common variants at 12q15 and 12q24 are associated with infant head circumference (2013) (22)
Parental Effects (2001) (22)
Loosening the cuff: important new advances in modeling antihypertensive treatment effects in genetic studies of hypertension. (2003) (22)
Determinants of airway responsiveness to histamine in children (2005) (22)
Genome‐wide linkage analysis using genetic variance components of alcohol dependency‐associated censored and continuous traits (1999) (22)
The relationship between ACE genotype and risk of severe hypoglycaemia in a large population-based cohort of children and adolescents with type 1 diabetes (2007) (22)
A genome-wide association scan for asthma in a general Australian population (2008) (22)
Environmental factors and asthma and allergy in schoolchildren from Western Australia. (1999) (21)
Cohort profile: the Western Australian Sleep Health Study (2012) (21)
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep (2019) (21)
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease (2008) (20)
Genetic Analysis Workshop 13: Analysis of Longitudinal Family Data for Complex Diseases and Related Risk Factors (2003) (20)
The longitudinal association of common susceptibility variants for type 2 diabetes and obesity with fasting glucose level and BMI (2010) (20)
DNA sequence variants in epithelium-specific ETS-2 and ETS-3 are not associated with asthma. (2002) (20)
Associations between anxious-depressed symptoms and cardiovascular risk factors in a longitudinal childhood study. (2012) (19)
Meta-analysis for linkage to asthma and atopy in the chromosome 5q31-33 candidate region. (2001) (17)
Prevalence of Factor V Leiden and Prothrombin 20210A Mutations in Indigenous Australians (2001) (16)
beta2 adrenoceptor Arg16Gly polymorphism, airway responsiveness, lung function and asthma in infants and children. (2004) (16)
Linkage Analysis of Alpha 1-Antitrypsin Deficiency: Lessons for Complex Diseases (2001) (15)
1-Hydroxypyrene as a Biomarker of Occupational Exposure to Polycyclic Aromatic Hydrocarbons (PAH) in Boilermakers (2002) (15)
Definition and diagnosis of cerebral palsy in genetic studies: a systematic review (2020) (15)
Functional Genomics of Lung Disease (2004) (15)
Stromelysin-1 (MMP-3) gene 5A/6A promoter polymorphism is associated with blood pressure in a community population. (2004) (15)
SimHap: A comprehensive modelling framework and a simulation-based approach to haplotypic analysis of population-based data (2006) (15)
15-Lipoxygenase gene variants are associated with carotid plaque but not carotid intima-media thickness (2008) (15)
Linkages and associations to intermediate phenotypes underlying asthma and allergic disease (2001) (14)
Physical Activity is Associated With Reduced Prevalence of Self-Reported Obstructive Sleep Apnea in a Large, General Population Cohort Study. (2020) (14)
Urinary metal and polycyclic aromatic hydrocarbon biomarkers in boilermakers exposed to metal fume and residual oil fly ash. (2005) (13)
Medical journals should embrace preprints to address the reproducibility crisis. (2018) (13)
The association of host and genetic melanoma risk factors with Breslow thickness in the Western Australian Melanoma Health Study (2014) (12)
Stromelysin-1 (MMP-3) gene 5A/6A promoter polymorphism is associated with blood pressure in a community population (2005) (12)
Pooling Data and Linkage Analysis in the Chromosome 5q Candidate Region for Asthma (2001) (11)
Matrix metalloproteinase-2 gene variants and abdominal aortic aneurysm. (2009) (11)
The Western Australian Melanoma Health Study: study design and participant characteristics. (2011) (11)
Functional haplotypes in the PTGDR gene fail to associate with asthma in two Australian populations (2011) (11)
Validation and algorithmic audit of a deep learning system for the detection of proximal femoral fractures in patients in the emergency department: a diagnostic accuracy study. (2022) (10)
The PHF11 gene is not associated with asthma or asthma phenotypes in two independent populations (2009) (10)
A Java based Linkage Disequilibrium plotter (2006) (10)
Make it HuGE: human genome epidemiology reviews, population health, and the IJE. (2006) (10)
Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level. (2019) (10)
Celestial3D: a novel method for 3D visualization of familial data (2008) (10)
Respiratory infections and lung function in an Australian Aboriginal community (2008) (10)
Fat mass and obesity-associated obesity-risk genotype is associated with lower foetal growth: an effect that is reversed in the offspring of smoking mothers (2011) (10)
Erratum: Genetic variants associated with increased risk of malignant pleural mesothelioma: A genome-wide association study (PLoS ONE (2015) 8:4 (e61253) DOI: 10.1371/journal.pone.0061253) (2015) (10)
Association of TGFβ1 and clinical factors with scar outcome following melanoma excision (2012) (10)
Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure (2021) (9)
Association of PARL rs3732581 genetic variant with insulin levels, metabolic syndrome and coronary artery disease (2008) (9)
Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (9)
The New Epidemiology: putting the pieces together in complex disease aetiology. (2004) (9)
The role of prostaglandin D receptor gene in asthma pathogenesis. (2005) (9)
Linkage of serum leptin levels in families with sleep apnea (2005) (8)
Familial aggregation and segregation analysis of eosinophil levels. (2000) (8)
The effect of missing data on linkage disequilibrium mapping and haplotype association analysis in the GAW14 simulated datasets (2005) (8)
Genome-wide linkage analysis of longitudinal phenotypes using σ2A random effects (SSARs) fitted by Gibbs sampling (2003) (8)
Genome‐Wide Linkage Analysis in a General Population Sample Using σ2A Random Effects (SSARs) Fitted by Gibbs Sampling (2001) (8)
Do regular check ups and preventive drug use reduce asthma severity in school children? (2004) (7)
An introduction to genetic epidemiology. (2011) (7)
A population-based study of polymorphisms in genes related to sex hormones and abdominal aortic aneurysm (2010) (7)
The transforming growth factor- b 1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD) (2004) (7)
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program (2019) (7)
A single-nucleotide polymorphism in the gene encoding osteoprotegerin is associated with diastolic blood pressure in older men. (2009) (7)
Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals (2019) (6)
Nuclear Factor Kappa B Activation in Human Cord Blood Mononuclear Cells (2004) (6)
Effectiveness of individual‐focused interventions to prevent chronic disease (2014) (6)
Artificial Intelligence in Medicine: Validation and Study Design (2019) (6)
Improved Evidence for Linkage on 6p and 5p with Retrospective Pooling of Data from Three Asthma Genome Screens (2001) (6)
A vision for chronic disease prevention and intervention research: Report from a workshop (2014) (5)
Airway responsiveness (AR) and lung function at 1 month of age predict airway responsiveness, lung function, asthma and atopy at 6 years of age. (1995) (5)
Approaches to Evaluate Gene-Environment Interactions Underlying the Developmental Origins of Health and Disease (2009) (5)
Lack of reproducibility of linkage results in serially measured blood pressure data (2003) (5)
The Relationship of Sleep Duration with Ethnicity and Chronic Disease in a Canadian General Population Cohort (2020) (5)
Wilderness area and wildfire disasters: Insights from a child and adolescent screening program. (2002) (5)
Docs are ROCs: A simple off-the-shelf approach for estimating average human performance in diagnostic studies (2020) (4)
Biobanks and biobank harmonisation (2011) (4)
Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity (2017) (4)
Validation of self-reported melanoma diagnosis history (2013) (4)
The Western Australian Twin Register: a population-based register of adult and child multiples. (2006) (4)
Parametric linkage analysis. (2002) (4)
Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea. (2022) (3)
Pharmacogenomics of Asthma Treatment (2003) (3)
Supplementary Material 6 (2014) (3)
Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure (2020) (3)
Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits (2019) (3)
Combining Multiple Phenotypic Traits Optimally for Detecting Linkage with Sib‐Pair Observations (2001) (3)
Supplementary Material 3 (2015) (3)
Response to Epstein et al. (2002) (3)
Supplementary Material 7 (2014) (3)
Supplementary Material 5 (2014) (3)
Polymorphisms in genes within the IGF-axis influence antenatal and postnatal growth (2012) (3)
Estimation of genetic and environmental factors for binary traits using family data by Y. Pawitan, M. Reilly, E. Nilsson, S. Cnattingius and P. Lichtenstein, Statistics in Medicine 2004; 23:449–465 (2005) (2)
Pulmonary function at 4 weeks correlates with pulmonary function at 6 and 12 years (2001) (2)
Genome-Wide Association Studies Identify CHRNA5/3 and HTR4 in the Development of Airﬂow Obstruction (2012) (2)
Major gene focusing: A novel technique for high efficiency linkage analysis and genomic screening for complex traits (1998) (2)
Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume (2013) (2)
Single Region Linkage Analyses of Asthma: Description of Data Sets (2001) (2)
Novel Associations of Genetic Polymorphisms in the Interleukin-1 receptor/Toll-like Receptor Signaling Pathways with Atopy and Atopic Asthma (2009) (2)
Segregation Analysis of Asthma and Respiratory Allergy in Population‐Based Samples of Families (2001) (2)
Australian experience with total pancreatectomy with islet autotransplantation to treat chronic pancreatitis (2021) (1)
Pre-thrombectomy prognostic prediction of large-vessel ischemic stroke using machine learning: A systematic review and meta-analysis (2022) (1)
Single-Nucleotide Polymorphisms (2005) (1)
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (1)
Supplementary Material 4 (2015) (1)
Monoamine oxidase a gene polymorphisms common to blood pressure and depression scores in caucasian children (2014) (1)
The changing profile of obstructive sleep apnea: long term trends in characteristics of patients presenting for diagnostic polysomnography (2022) (1)
The pharmacogenetics of asthma and allergic disease (2002) (1)
University of Groningen Genome-wide association studies identify CHRNA 5 / 3 and HTR 4 in the development of airflow obstruction (2017) (1)
Meta-analysis in ankylosing spondylitis (AS) - Genomewide linkage map including 589 affected sibling pairs. (2005) (1)
The aggregation of early-onset melanoma in young Western Australian families. (2015) (1)
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program (2021) (1)
Supplementary Material 9 (2013) (1)
Mapping complex disease genes using linkage disequilibrium and genome-wide association scans (2011) (1)
Association between airway responsiveness (AR) at 1 month and AR and development of asthma (1995) (1)
Artificial intelligence and the future of radiographic scoring in rheumatoid arthritis: a viewpoint (2022) (1)
Human Genome Project (2005) (1)
Genome-wide association and large scale follow-up identifies 16 novel loci for lung function (2011) (1)
Subject Index Vol. 52, 2001 (2001) (1)
A Genome-Wide Association Scan For Malignant Mesothelioma (2011) (1)
Association between infant and childhood pulmonary function and B2 adrenoreceptor polymorphisms (2001) (1)
Supplementary Material 15 (2013) (1)
Genome-wide linkage and association mapping of disease genes with the GAW14 simulated datasets (2005) (1)
2 Familial clustering of mesothelioma in subjects exposed to crocidolite at Wittenoom (2006) (1)
A note on the calculation of empirical P values from Monte Carlo procedures - Response (2002) (0)
Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals (2019) (0)
The use of serum-free medium unmasks covert allergen-specific T-cell reactivity in close to 100% of atopic and normal individuals. (1995) (0)
Cohort Profile: The Ontario Health Study (OHS). (2022) (0)
Genetic Basis for Gestation Length (2011) (0)
5D-5 Antenatal growth trajectories are associated with postnatal growth trajectories and cardiovascular outcomes (2007) (0)
The Western Australian Melanoma Health Study: A resource for melanoma research (2010) (0)
The Western Australian Twin Register: A Population-Based Register of Adult and Child Multiples (2006) (0)
Variance Components for Exhaled Nitric Oxide in Twin Families (2007) (0)
P1-29 The definition of antenatal growth trajectories (2007) (0)
Relationship between obstructive sleep apnoea, other cardiovascular risk factors and cardiovascular disease (2019) (0)
Replication strategies for whole genome association (WGA) studies (2007) (0)
The clinical and genetic features of hereditary pancreatitis in South Australia (2022) (0)
Introduction: Linkage Analyses of Single Regions (2001) (0)
Living near trees could add years to your life (2015) (0)
Precision Radiology: Predicting longevity using feature engineering and deep learning methods in a radiomics framework (2017) (0)
Results : A novel SNP , downstream from the FAM 120 AOS gene on chromosome 9 , was detected in the meta-analysis of ALSPAC and Raine (2015) (0)
Cardiovascular Risk Factors and Age-Related Macular Degeneration: Large Case-Control Study Using a Comprehensive, Long-Term Administrative Database (2008) (0)
Age‐related differences in association of OSA with cancer incidence in a large sleep clinic cohort (2019) (0)
Cross-sectional association of traditional and novel polysomnography metrics with atherosclerosis in obstructive sleep apnoea (2019) (0)
Antenatal and postnatal growth trajectories predict systolic blood pressure in adolescence (2008) (0)
The Western Australian Family Connections Genealogical Database (2006) (0)
OBSTRUCTIVE SLEEP APNEA (OSA) IS A COMMON DISORDER WITH A PREVALENCE OF 2% TO 4% IN MIDDLE-AGED (2004) (0)
Analysis of SNP haplotypes (2007) (0)
The Genetic Understanding of Asbestos Related Diseases (GUARD) Project (2008) (0)
Population health aspects of genetic epidemiology: genomic profiling, personalised medicine and mendelian randomisation. (2011) (0)
Antenatal and postnatal growth trajectories predict hsCRP in adolescence (2008) (0)
Meta-analysis of genome-wide association studies on atopic dermatitis identifies three novel risk loci (2012) (0)
Predictors of asthma severity in children - results from a longitudinal cohort study beginning in early infancy (2002) (0)
Medication Usage In Patients Undergoing Polysomnography (2011) (0)
AGOG: Australian Genomics and Clinical Outcomes of Glioma - A World Class Resource for the Braing Tumour Community (2008) (0)
The Western Australian Melanoma Health Study. (2009) (0)
Genetic factors associated with scar outcome following melanoma excision (2011) (0)
Iconographies supplémentaires de l'article : Associations of cord blood fatty acids with lymphocyte proliferation, IL-13, and IFN-γ (2011) (0)
The impact of psychological trauma on language in school age children (2000) (0)
The Role of Common Copy Number Variation in Amyotrophic Lateral Sclerosis (ALS) (2010) (0)
Lipid metabolism gene polymorphisms and risk of fatty liver in adolecents: A population based cohort study (2010) (0)
Analyses of Genotype-Phenotype Associations in Asthma and Atopy in Four Population Samples (2012) (0)
Genome-wide meta-analysis of brachial circumference. (2011) (0)
The definition of postnatal growth trajectories (2007) (0)
P1-28 Postnatal growth trajectories can predict cardiovascular risk in adolescence (2007) (0)
VISUALIZATION OF SUB-SURFACE STRUCTURES IN SCAR TISSUE USING OPTICAL COHERENCE TOMOGRAPHY (2010) (0)
The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4610 cases amongst 18637 participants (2015) (0)
Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity (2016) (0)
METHODOLOGY Covariance components models for longitudinal family data (2005) (0)
INACTIVITY IS A RISK FACTOR FOR MODERATE-SEVERE OBSTRUCTIVE SLEEP APNOEA (OSA) (2012) (0)
Correction: Genetic Variants Associated with Increased Risk of Malignant Pleural Mesothelioma: A Genome-Wide Association Study (2015) (0)
PHENOTYPIC AND GENOTYPIC ANALYSIS OF HEREDITARY PANCREATITIS IN PATIENTS AND POTENTIAL CANDIDATES FOR TOTAL PANCREATECTOMY WITH ISLET AUTOTRANSPLANTATION (TP-IAT) (2020) (0)
Cohort Profile: The Western Australian Sleep Health Study, a Prospective Sleep Clinic Cohort Study (2021) (0)
IGF Gene-network Identifies Specific Interactions Underlying Extreme SBP in Developing Children (2015) (0)
Contents Vol. 52, 2001 (2001) (0)
Original Communication Lack of association of NAT2 (N-acetyl transferase 2) gene polymorphism with atopic asthma in Turkish subjects (2004) (0)
Association between hypoxemia in OSA and cancer incidence in a large sleep clinic cohort (2019) (0)
Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for Forced Vital Capacity. BMC Genetics (2016) (0)
The impact of psychological trauma on executive functioning in school-aged children (1999) (0)
Scar outcome post melanoma excision (2009) (0)
The Assocation of Environmental factors with Asthma and Allergy in a population based sample of school children (1999) (0)
Increased Doctor-Diagnosed Asthma in Busselton Adults: Is It Really Asthma?. (2009) (0)
International travel by Australians for overseas transplantation (2019) (0)
P1-27 The definition of postnatal growth trajectories (2007) (0)
Postnatal growth trajectories predict cardiovascular risk in adolescence (2008) (0)
Changing trends of obstructive sleep apnoea in Western Australia from 1988 to 2014 (2017) (0)
ASSOCIATION OF WOUND REPAIR AND PIGMENTATION GENES WITH SCAR OUTCOME FOLLOWING SUCCESSFUL PRIMARY CLOSURE OF SKIN TUMOR EXCISION (2012) (0)
Shared Genetic Architecture Between Sleep and Blood Pressure Traits in Humans (2019) (0)
214.4: The Genetic Epidemiology of Hereditary Pancreatitis in Australia and Its Effect on Patients of Total Pancreatectomy and Islet Auto Translation (TP-IAT) (2022) (0)
T cell reactivity to allergens in atopic and normal subjects: covert in-vitro responses unmasked by serum free medium (1995) (0)
Modification of the effect of Flg on allergic disease risk by maternal smoking and siblings (2012) (0)
The relationship of respiratory infections to lung function in an Australian Aboriginal Community (1997) (0)
Common functional polymorphisms in toll-like receptor 4 (TLR4) are not associated with asthma or atopy-related phenotypes. (2002) (0)
Effects in Genetic Studies of Hypertension Loosening the Cuff : Important New Advances in Modeling Antihypertensive Treatment (2003) (0)
The definition of antenatal growth trajectories (2007) (0)
The Western Australian Melanoma Health Study (WAMHS) (2008) (0)
Author's response to reviews Title: A comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/R2), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndrome. Authors: (2012) (0)
4C-6 Inflammation and altered liver function is present in 13 year old children with features of the metabolic syndrome (2007) (0)
Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity (2016) (0)
CPAP treatment, glycemia and diabetes risk in obstructive sleep apnea and comorbid cardiovascular disease (2019) (0)
SAT-075 AUSTRALIAN ENGAGEMENT IN INTERNATIONAL TRAVEL FOR ORGAN TRANSPLANTATION: A DESCRIPTIVE SURVEY (2019) (0)
Meta-Analysis Of Genome-Wide Association Studies Of Longitudinal Decline In Lung Function (2012) (0)
2C-2 Human genome epidemiology, biobanks, and DOHaD (2007) (0)

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