[HTML][HTML] Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary …

…, C Pavuluri, V Malik, BD Hobbs, M Moll, W Kim… - Nature …, 2023 - nature.com
Lung-function impairment underlies chronic obstructive pulmonary disease (COPD) and
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, …

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 …

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 …

Improving disease prediction by incorporating family disease history in risk prediction models with large-scale genetic data

J Gim, W Kim, SH Kwak, H Choi, C Park, KS Park… - Genetics, 2017 - academic.oup.com
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 …

[HTML][HTML] Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants

X Zhao, D Qiao, C Yang, S Kasela, W Kim, Y Ma… - Nature …, 2020 - nature.com
Chronic obstructive pulmonary disease (COPD), diagnosed by reduced lung function, is a
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

S Kim, YH Cho, I Lee, W Kim, S Won, JL Ku… - Environment …, 2018 - Elsevier
Prenatal exposure to persistent organic pollutants (POPs) has been linked to numerous
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 …

[PDF][PDF] Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program

X Hu, D Qiao, W Kim, M Moll, PP Balte… - The American Journal of …, 2022 - cell.com
While polygenic risk scores (PRSs) enable early identification of genetic risk for chronic
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

S Won, W Kim, S Lee, Y Lee, J Sung, T Park - BMC bioinformatics, 2015 - Springer
Background Many disease phenotypes are outcomes of the complicated interplay between
multiple genes, and multiple phenotypes are affected by a single or multiple genotypes. …