Kathryn L Lunetta


Ontology type: schema:Person     


Person Info

NAME

Kathryn L

SURNAME

Lunetta

Publications in SciGraph latest 50 shown

  • 2018-12 Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer’s disease in ALZHEIMER'S RESEARCH & THERAPY
  • 2018-12 A survey of microRNA single nucleotide polymorphisms identifies novel breast cancer susceptibility loci in a case-control, population-based study of African-American women in BREAST CANCER RESEARCH
  • 2018-12 GWAS of epigenetic aging rates in blood reveals a critical role for TERT in NATURE COMMUNICATIONS
  • 2018-09 Multi-ethnic genome-wide association study for atrial fibrillation in NATURE GENETICS
  • 2018-08-14 Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation in MOLECULAR PSYCHIATRY
  • 2018-06 Tau Phosphorylation is Impacted by Rare AKAP9 Mutations Associated with Alzheimer Disease in African Americans in JOURNAL OF NEUROIMMUNE PHARMACOLOGY
  • 2017-12 Evaluation of logistic regression models and effect of covariates for case–control study in RNA-Seq analysis in BMC BIOINFORMATICS
  • 2017-12 Methylome-wide Association Study of Atrial Fibrillation in Framingham Heart Study in SCIENTIFIC REPORTS
  • 2017-12 Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium in SCIENTIFIC REPORTS
  • 2017-12 A functionally significant SNP in TP53 and breast cancer risk in African-American women in NPJ BREAST CANCER
  • 2017-12 Cardiovascular risk factors among women with self-reported infertility in FERTILITY RESEARCH AND PRACTICE
  • 2017-09 Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease in NATURE GENETICS
  • 2017-06 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation in NATURE GENETICS
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk in NATURE GENETICS
  • 2016-12 Gene-gene Interaction Analyses for Atrial Fibrillation in SCIENTIFIC REPORTS
  • 2016-12 Genetic variation in the insulin, insulin-like growth factor, growth hormone, and leptin pathways in relation to breast cancer in African-American women: the AMBER consortium in NPJ BREAST CANCER
  • 2016-10 Imputing rare variants in families using a two-stage approach in BMC PROCEEDINGS
  • 2016-01 Gene-based analysis of the fibroblast growth factor receptor signaling pathway in relation to breast cancer in African American women: the AMBER consortium in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-01 A novel Alzheimer disease locus located near the gene encoding tau protein in MOLECULAR PSYCHIATRY
  • 2015-12 Corrigendum: Rare coding variants and X-linked loci associated with age at menarche in NATURE COMMUNICATIONS
  • 2015-12 A case–control analysis of oral contraceptive use and breast cancer subtypes in the African American Breast Cancer Epidemiology and Risk Consortium in BREAST CANCER RESEARCH
  • 2015-12 Rare coding variants and X-linked loci associated with age at menarche in NATURE COMMUNICATIONS
  • 2015-12 DNA methylation age of blood predicts all-cause mortality in later life in GENOME BIOLOGY
  • 2015-11 Hormone-related pathways and risk of breast cancer subtypes in African American women in BREAST CANCER RESEARCH AND TREATMENT
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2014-12 Genetic diversity is a predictor of mortality in humans in BMC GENETICS
  • 2014-10 Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche in NATURE
  • 2014-03 Correction for multiple testing in a gene region in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-12 Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease in NATURE GENETICS
  • 2013-08 Incremental value of rare genetic variants for the prediction of multifactorial diseases in GENOME MEDICINE
  • 2013-06 Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders in NATURE GENETICS
  • 2012-12 Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis in NATURE GENETICS
  • 2012-06 Meta-analysis identifies six new susceptibility loci for atrial fibrillation in NATURE GENETICS
  • 2012-04 Reproductive aging-associated common genetic variants and the risk of breast cancer in BREAST CANCER RESEARCH
  • 2012-03 Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways in NATURE GENETICS
  • 2012 Genetics of Human Longevity and Healthy Aging in THE EPIDEMIOLOGY OF AGING
  • 2011-12 Choice of population structure informative principal components for adjustment in a case-control study in BMC GENETICS
  • 2011-05 Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease in NATURE GENETICS
  • 2010-12 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies in NATURE GENETICS
  • 2010-03 Common variants in KCNN3 are associated with lone atrial fibrillation in NATURE GENETICS
  • 2010-02 Genome-wide association study of PR interval in NATURE GENETICS
  • 2009-12 Principal-component-based population structure adjustment in the North American Rheumatoid Arthritis Consortium data: impact of single-nucleotide polymorphism set and analysis method in BMC PROCEEDINGS
  • 2009-12 Performance of random forest when SNPs are in linkage disequilibrium in BMC BIOINFORMATICS
  • 2009-08 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry in NATURE GENETICS
  • 2009-06 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche in NATURE GENETICS
  • 2009-01 Common variants at 30 loci contribute to polygenic dyslipidemia in NATURE GENETICS
  • 2008-08 Tamoxifen's protection against breast cancer recurrence is not reduced by concurrent use of the SSRI citalopram in BRITISH JOURNAL OF CANCER
  • 2007-12 Two-stage approach for identifying single-nucleotide polymorphisms associated with rheumatoid arthritis using random forests and Bayesian networks in BMC PROCEEDINGS
  • 2007-09 Genome-wide association with bone mass and geometry in the Framingham Heart Study in BMC MEDICAL GENETICS
  • 2007-09 The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports in BMC MEDICAL GENETICS
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