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A Common Variant in the SETD7 Gene Predicts Serum Lycopene Concentrations

artículo científico publicado en 2016

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

artículo científico publicado en 2021

An innovative and efficient route to the synthesis of metal-based glycoconjugates: proof-of-concept and potential applications

scientific article published on 26 June 2018

Analysis of the bereavement effect after the death of a spouse in the Amish: a population-based retrospective cohort study

artículo científico publicado en 2014

Association between bilirubin and cardiovascular disease risk factors: using Mendelian randomization to assess causal inference

artículo científico publicado en 2012

Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish

artículo científico publicado en 2008

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

artículo científico publicado en 2013

Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease

artículo científico publicado en 2010

Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium

artículo científico publicado en 2011

Does having children extend life span? A genealogical study of parity and longevity in the Amish

scientific article published on 01 February 2006

Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish

artículo científico publicado en 2010

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

artículo científico publicado en 2008

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

Genetic variation at 16q24.2 is associated with small vessel stroke

artículo científico publicado en 2016

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

artículo científico publicado en 2016

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

artículo científico publicado en 2013

Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels

artículo científico publicado en 2009

Genotype-based changes in serum uric acid affect blood pressure

artículo científico publicado en 2011

Homozygosity by descent mapping of blood pressure in the Old Order Amish: evidence for sex specific genetic architecture

artículo científico publicado en 2007

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

artículo científico publicado en 2007

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

artículo científico publicado en 2015

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

artículo científico publicado en 2015

Living the good life? Mortality and hospital utilization patterns in the Old Order Amish

artículo científico publicado en 2012

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

artículo científico publicado en 2012

Meta-analysis of genome-wide association data identifies two loci influencing age at menarche

artículo científico publicado en 2009

NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium

artículo científico publicado en 2009

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

artículo científico publicado en 2014

Pathogenic ischemic stroke phenotypes in the NINDS-stroke genetics network

artículo científico publicado en 2014

Prevalence, control, and treatment of diabetes, hypertension, and high cholesterol in the Amish

artículo científico publicado en 2020

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

artículo científico publicado en 2019

Sex-specific effects of serum sulfate level and SLC13A1 nonsense variants on DHEA homeostasis.

artículo científico publicado en 2017

Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes

artículo científico publicado en 2013

The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations

artículo científico publicado en 2016

The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

artículo científico publicado en 2008

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

artículo científico publicado en 2010

Unprecedented morphology control of gas phase cocrystal growth using multi zone heating and tailor made additives

artículo científico publicado en 2020

Vitamin and supplement use among old order amish: sex-specific prevalence and associations with use

artículo científico publicado en 2014

White matter hyperintensity quantification in large-scale clinical acute ischemic stroke cohorts - The MRI-GENIE study.

artículo científico publicado en 2019