Lista de obras -

Adjusting for covariates on a slippery slope: linkage analysis of change over time

artículo científico publicado en 2003

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.

artículo científico publicado en 2012

Extent and distribution of linkage disequilibrium in the Old Order Amish

artículo científico publicado en 2010

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 Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer

artículo científico publicado en 2018

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

artículo científico publicado en 2018

Genome-wide association of body fat distribution in African ancestry populations suggests new loci

artículo científico publicado en 2013

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

artículo científico publicado en 2011

Germline deletion of in familial acute lymphoblastic leukemia

scientific article published on 01 April 2019

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

New loci associated with kidney function and chronic kidney disease

artículo científico publicado en 2010

Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants

scientific article published on 22 August 2019

Physical activity and the association of common FTO gene variants with body mass index and obesity

artículo científico publicado en 2008

Rare variant mutations identified in pediatric patients with dilated cardiomyopathy ⬇️

artículo científico publicado el 1 de enero de 2011

Serum 25-hydroxyvitamin d levels are not associated with subclinical vascular disease or C-reactive protein in the old order amish

artículo científico publicado en 2009

The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults

artículo científico publicado en 2008

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

Lista de obras de

Adjusting for covariates on a slippery slope: linkage analysis of change over time

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.

Extent and distribution of linkage disequilibrium in the Old Order Amish

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

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

Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

Genome-wide association of body fat distribution in African ancestry populations suggests new loci

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

Germline deletion of in familial acute lymphoblastic leukemia

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

New loci associated with kidney function and chronic kidney disease

Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants

Physical activity and the association of common FTO gene variants with body mass index and obesity

Rare variant mutations identified in pediatric patients with dilated cardiomyopathy ⬇️

Serum 25-hydroxyvitamin d levels are not associated with subclinical vascular disease or C-reactive protein in the old order amish

The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults

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