PubRank

Kathryn L Lunetta

Author PubWeight™ 170.81‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet 2008 20.66
2 Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet 2011 10.07
3 The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. Nat Genet 2007 9.80
4 Demonstrating stratification in a European American population. Nat Genet 2005 9.49
5 Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts. Circ Cardiovasc Genet 2009 8.42
6 Identifying SNPs predictive of phenotype using random forests. Genet Epidemiol 2005 5.43
7 Protective variant for hippocampal atrophy identified by whole exome sequencing. Ann Neurol 2015 5.10
8 The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports. BMC Med Genet 2007 5.02
9 Common variants in KCNN3 are associated with lone atrial fibrillation. Nat Genet 2010 3.97
10 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat Genet 2009 3.80
11 Genome-wide association study of PR interval. Nat Genet 2010 3.73
12 Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat Genet 2012 3.71
13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat Genet 2010 3.37
14 Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes. Arch Neurol 2010 2.91
15 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. Nat Genet 2009 2.58
16 Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. JAMA 2013 2.58
17 Genome-wide association with bone mass and geometry in the Framingham Heart Study. BMC Med Genet 2007 2.32
18 Testing for population subdivision and association in four case-control studies. Am J Hum Genet 2002 2.26
19 Relations of inflammatory biomarkers and common genetic variants with arterial stiffness and wave reflection. Hypertension 2008 2.14
20 Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat Genet 2012 2.12
21 Novel late-onset Alzheimer disease loci variants associate with brain gene expression. Neurology 2012 2.08
22 Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. Eur Heart J 2009 2.06
23 Comprehensive search for Alzheimer disease susceptibility loci in the APOE region. Arch Neurol 2012 1.97
24 Independent susceptibility markers for atrial fibrillation on chromosome 4q25. Circulation 2010 1.90
25 Genome-wide association with select biomarker traits in the Framingham Heart Study. BMC Med Genet 2007 1.90
26 Performance of random forest when SNPs are in linkage disequilibrium. BMC Bioinformatics 2009 1.81
27 Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat Genet 2013 1.72
28 A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. J Gerontol A Biol Sci Med Sci 2010 1.65
29 Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes. Neurobiol Dis 2008 1.58
30 Lack of replication in polymorphisms reported to be associated with atrial fibrillation. Heart Rhythm 2010 1.58
31 A genome-wide association study of aging. Neurobiol Aging 2011 1.54
32 A genome-wide association study of early menopause and the combined impact of identified variants. Hum Mol Genet 2013 1.50
33 The search for longevity and healthy aging genes: insights from epidemiological studies and samples of long-lived individuals. J Gerontol A Biol Sci Med Sci 2012 1.49
34 CYP2D6 inhibition and breast cancer recurrence in a population-based study in Denmark. J Natl Cancer Inst 2011 1.47
35 Genetic determinants of serum testosterone concentrations in men. PLoS Genet 2011 1.45
36 A comprehensive genetic association study of Alzheimer disease in African Americans. Arch Neurol 2011 1.33
37 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. PLoS Genet 2011 1.30
38 A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation. PLoS Genet 2012 1.23
39 The relation of genetic and environmental factors to systemic inflammatory biomarker concentrations. Circ Cardiovasc Genet 2009 1.19
40 Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease. Arch Neurol 2008 1.16
41 APOE genotype and MRI markers of cerebrovascular disease: systematic review and meta-analysis. Neurology 2013 1.14
42 Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls. Genet Epidemiol 2009 1.11
43 Two-stage approach for identifying single-nucleotide polymorphisms associated with rheumatoid arthritis using random forests and Bayesian networks. BMC Proc 2007 1.11
44 Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation. Circulation 2014 1.11
45 A common connexin-40 gene promoter variant affects connexin-40 expression in human atria and is associated with atrial fibrillation. Circ Arrhythm Electrophysiol 2010 1.09
46 Polymorphisms in the PON gene cluster are associated with Alzheimer disease. Hum Mol Genet 2005 1.08
47 Breast cancer recurrence risk related to concurrent use of SSRI antidepressants and tamoxifen. Acta Oncol 2010 1.07
48 Concordance of metabolic enzyme genotypes assayed from paraffin-embedded, formalin-fixed breast tumors and normal lymphatic tissue. Clin Epidemiol 2010 1.06
49 Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project. Circ Cardiovasc Genet 2011 1.06
50 Frailty models: Applications to biomedical and genetic studies. Stat Med 2011 1.04
51 Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG). Am J Med Genet A 2009 1.03
52 Estrogen receptor alpha gene variation is associated with risk of myocardial infarction in more than seven thousand men from five cohorts. Circ Res 2006 1.01
53 Assessment of cortical and striatal involvement in 523 Huntington disease brains. Neurology 2012 1.00
54 Expectation maximization algorithm based haplotype relative risk (EM-HRR): test of linkage disequilibrium using incomplete case-parents trios. Hum Hered 2005 0.97
55 Large common deletions associate with mortality at old age. Hum Mol Genet 2011 0.96
56 Multiple loci influencing hippocampal degeneration identified by genome scan. Ann Neurol 2012 0.93
57 Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. Am J Epidemiol 2013 0.93
58 Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circ Cardiovasc Genet 2014 0.93
59 Clinical and genetic factors associated with lipoprotein-associated phospholipase A2 in the Framingham Heart Study. Atherosclerosis 2008 0.93
60 Education attenuates the effect of medial temporal lobe atrophy on cognitive function in Alzheimer's disease: the MIRAGE study. J Alzheimers Dis 2009 0.88
61 Reproductive aging-associated common genetic variants and the risk of breast cancer. Breast Cancer Res 2012 0.87
62 Sex- and age-interacting eQTLs in human complex diseases. Hum Mol Genet 2013 0.86
63 Association of TTR polymorphisms with hippocampal atrophy in Alzheimer disease families. Neurobiol Aging 2009 0.86
64 Rarity of the Alzheimer disease-protective APP A673T variant in the United States. JAMA Neurol 2015 0.84
65 Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine. Circ Cardiovasc Genet 2014 0.83
66 Informative-transmission disequilibrium test (i-TDT): combined linkage and association mapping that includes unaffected offspring as well as affected offspring. Genet Epidemiol 2007 0.83
67 Choice of population structure informative principal components for adjustment in a case-control study. BMC Genet 2011 0.83
68 A case-control analysis of oral contraceptive use and breast cancer subtypes in the African American Breast Cancer Epidemiology and Risk Consortium. Breast Cancer Res 2015 0.82
69 A comparison of gene region simulation methods. PLoS One 2012 0.81
70 Functional polymorphisms in UDP-glucuronosyl transferases and recurrence in tamoxifen-treated breast cancer survivors. Cancer Epidemiol Biomarkers Prev 2011 0.81
71 PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation. Ann Neurol 2014 0.81
72 Serum paraoxonase activity is associated with variants in the PON gene cluster and risk of Alzheimer disease. Neurobiol Aging 2010 0.79
73 Evaluation of methods accounting for population structure with pedigree data and continuous outcomes. Genet Epidemiol 2011 0.79
74 Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat Commun 2015 0.75
75 Phenotypically Enriched Genotypic Imputation in Genetic Association Tests. Hum Hered 2016 0.75
76 Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat Genet 2017 0.75