[HTML][HTML] Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary …
Lung-function impairment underlies chronic obstructive pulmonary disease (COPD) and
predicts mortality. In the largest multi-ancestry genome-wide association meta-analysis of lung …
predicts mortality. In the largest multi-ancestry genome-wide association meta-analysis of lung …
[HTML][HTML] Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
…, K Schwander, SM Tajuddin, T Sofer, W Kim… - PLoS …, 2017 - journals.plos.org
Hypertension is a leading cause of global disease, mortality, and disability. While individuals
of African descent suffer a disproportionate burden of hypertension and its complications, …
of African descent suffer a disproportionate burden of hypertension and its complications, …
A genome-wide association study implicates NR2F2 in lymphangioleiomyomatosis pathogenesis
W Kim, K Giannikou, JR Dreier, S Lee… - European …, 2019 - Eur Respiratory Soc
Introduction Lymphangioleiomyomatosis (LAM) occurs either associated with tuberous
sclerosis complex (TSC) or as sporadic disease (S-LAM). Risk factors for development of S-LAM …
sclerosis complex (TSC) or as sporadic disease (S-LAM). Risk factors for development of S-LAM …
Rare genetic variants explain missing heritability in smoking
…, RC Kaplan, SLR Kardia, S Kelly, W Kim… - Nature human …, 2022 - nature.com
Common genetic variants explain less variation in complex phenotypes than inferred from
family-based studies, and there is a debate on the source of this ‘missing heritability’. We …
family-based studies, and there is a debate on the source of this ‘missing heritability’. We …
Improving disease prediction by incorporating family disease history in risk prediction models with large-scale genetic data
Despite the many successes of genome-wide association studies (GWAS), the known
susceptibility variants identified by GWAS have modest effect sizes, leading to notable skepticism …
susceptibility variants identified by GWAS have modest effect sizes, leading to notable skepticism …
[HTML][HTML] Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants
Chronic obstructive pulmonary disease (COPD), diagnosed by reduced lung function, is a
leading cause of morbidity and mortality. We performed whole genome sequence (WGS) …
leading cause of morbidity and mortality. We performed whole genome sequence (WGS) …
Prenatal exposure to persistent organic pollutants and methylation of LINE-1 and imprinted genes in placenta: A CHECK cohort study
Prenatal exposure to persistent organic pollutants (POPs) has been linked to numerous
adverse birth outcomes among newborn infants in many epidemiological studies. Although …
adverse birth outcomes among newborn infants in many epidemiological studies. Although …
[HTML][HTML] Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
…, P Desai, JS Floyd, Y Gao, K Kammers, W Kim… - Nature …, 2022 - nature.com
Genome-wide association studies have identified thousands of single nucleotide variants
and small indels that contribute to variation in hematologic traits. While structural variants are …
and small indels that contribute to variation in hematologic traits. While structural variants are …
[PDF][PDF] Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program
While polygenic risk scores (PRSs) enable early identification of genetic risk for chronic
obstructive pulmonary disease (COPD), predictive performance is limited when the discovery …
obstructive pulmonary disease (COPD), predictive performance is limited when the discovery …
[HTML][HTML] Family-based association analysis: a fast and efficient method of multivariate association analysis with multiple variants
Background Many disease phenotypes are outcomes of the complicated interplay between
multiple genes, and multiple phenotypes are affected by a single or multiple genotypes. …
multiple genes, and multiple phenotypes are affected by a single or multiple genotypes. …