Published in Ann Hum Genet on March 14, 2013
Enhancing the power to detect low-frequency variants in genome-wide screens. Genetics (2014) 0.77
Statistical tests for detecting rare variants using variance-stabilising transformations. Ann Hum Genet (2012) 1.39
Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease. Nat Genet (2008) 10.87
Adult-onset pulmonary fibrosis caused by mutations in telomerase. Proc Natl Acad Sci U S A (2007) 5.95
Telomere shortening in familial and sporadic pulmonary fibrosis. Am J Respir Crit Care Med (2008) 5.82
Transmembrane 6 superfamily member 2 gene variant disentangles nonalcoholic steatohepatitis from cardiovascular disease. Hepatology (2015) 2.81
Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer. Am J Hum Genet (2008) 2.53
Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations. PLoS One (2010) 2.19
PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome. Am J Hum Genet (2010) 2.05
Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X. PLoS Genet (2009) 1.81
Genomic, genetic and functional dissection of bitter taste responses to artificial sweeteners. Hum Mol Genet (2011) 1.18
Adjusting for covariates in logistic regression models. Genet Epidemiol (2010) 1.17
Blindly using Wald's test can miss rare disease-causal variants in case-control association studies. Ann Hum Genet (2012) 1.11
Genetics and bitter taste responses to goitrin, a plant toxin found in vegetables. Chem Senses (2010) 1.06
Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population. PLoS One (2009) 1.05
Hereditary lung cancer syndrome targets never smokers with germline EGFR gene T790M mutations. J Thorac Oncol (2014) 1.04
Eating disorder predisposition is associated with ESRRA and HDAC4 mutations. J Clin Invest (2013) 0.97
Genetic variant in PNPLA3 is associated with nonalcoholic fatty liver disease in China. Hepatology (2012) 0.95
Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans. PLoS One (2011) 0.94
Association and familial segregation of CTG18.1 trinucleotide repeat expansion of TCF4 gene in Fuchs' endothelial corneal dystrophy. Invest Ophthalmol Vis Sci (2014) 0.94
Genetic variant I148M in PNPLA3 is associated with the ultrasonography-determined steatosis degree in a Chinese population. BMC Med Genet (2012) 0.86
Family factors associated with suicide attempts among Chinese adolescent students: a national cross-sectional survey. J Adolesc Health (2010) 0.85
Self-reported weight status rather than BMI may be closely related to psychopathological symptoms among Mainland Chinese adolescents. J Trop Pediatr (2009) 0.85
A comparison of approaches to control for confounding factors by regression models. Hum Hered (2011) 0.83
Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4. Genet Epidemiol (2007) 0.82
Numbers and cytotoxicities of CD3+CD56+ T lymphocytes in peripheral blood of patients with acute myeloid leukemia and acute lymphocytic leukemia. Cancer Biol Ther (2013) 0.82
Higher waist-to-height ratio and waist circumference are predictive of metabolic syndrome and elevated serum alanine aminotransferase in adolescents and young adults in mainland China. Public Health (2011) 0.82
De novo heterozygous FBN1 mutations in the extreme C-terminal region cause progeroid fibrillinopathy. Am J Med Genet A (2014) 0.81
Linkage analysis of alcohol dependence using both affected and discordant sib pairs. BMC Genet (2005) 0.81
Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data. Genet Epidemiol (2007) 0.80
[Diagnostic value of ischemia-modified albumin in patients with acute coronary syndrome]. Zhonghua Xin Xue Guan Bing Za Zhi (2007) 0.78
Enhancing the power to detect low-frequency variants in genome-wide screens. Genetics (2014) 0.77
Power of genetic association studies with fixed and random genotype frequencies. Ann Hum Genet (2010) 0.77
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes. Hum Genet (2008) 0.76
Low serum 25-hydroxyvitamin D level and risk of urinary tract infection in infants. Medicine (Baltimore) (2016) 0.76
Minimum Information about a Genotyping Experiment (MIGEN). Stand Genomic Sci (2011) 0.76
Homozygosity mapping identifies a bile acid biosynthetic defect in an adult with cirrhosis of unknown etiology. Hepatology (2012) 0.76
Corrigendum: Hypoxia fate mapping identifies cycling cardiomyocytes in the adult heart. Nature (2015) 0.75
A logistic mixture model for a family-based association study. BMC Proc (2007) 0.75
Testing the Effect of Internal Genes Derived from a Wild-Bird-Origin H9N2 Influenza A Virus on the Pathogenicity of an A/H7N9 Virus. Cell Rep (2015) 0.75
Deep Label Distribution Learning With Label Ambiguity. IEEE Trans Image Process (2017) 0.75
[Spatiotemporal characteristics of zooplankton community structure and diversity in the strong temperature increment seawaters near Guohua power plant in Xiangshan Bay]. Huan Jing Ke Xue (2013) 0.75