Published in IEEE Trans Image Process on March 30, 2017
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
IFI16 DNA sensor is required for death of lymphoid CD4 T cells abortively infected with HIV. Science (2013) 2.68
Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer. Am J Hum Genet (2008) 2.53
Exploratory undersampling for class-imbalance learning. IEEE Trans Syst Man Cybern B Cybern (2008) 2.29
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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
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Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X. PLoS Genet (2009) 1.81
The nuclear hormone receptor Coup-TFII is required for the initiation and early maintenance of Prox1 expression in lymphatic endothelial cells. Genes Dev (2010) 1.73
Analysis of DNA methylation status of the promoter of human telomerase reverse transcriptase in gastric carcinogenesis. Arch Med Res (2010) 1.49
Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein. Nat Genet (2008) 1.45
Caenorhabditis elegans transthyretin-like protein TTR-52 mediates recognition of apoptotic cells by the CED-1 phagocyte receptor. Nat Cell Biol (2010) 1.24
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
Ghrelin is a novel target of Pax4 in endocrine progenitors of the pancreas and duodenum. Dev Dyn (2008) 1.13
Blindly using Wald's test can miss rare disease-causal variants in case-control association studies. Ann Hum Genet (2012) 1.11
Maternal serum vitamin B12, folate and homocysteine and the risk of neural tube defects in the offspring in a high-risk area of China. Public Health Nutr (2008) 1.08
Tissue-specific distribution of aberrant DNA methylation associated with maternal low-folate status in human neural tube defects. J Nutr Biochem (2011) 1.08
Collaborative design and implementation of a multisite community coalition evaluation. Health Promot Pract (2006) 1.07
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
Regulation of the chemokine receptor CXCR4 and metastasis by hypoxia-inducible factor in non small cell lung cancer cell lines. Cancer Biol Ther (2006) 1.04
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Eating disorder predisposition is associated with ESRRA and HDAC4 mutations. J Clin Invest (2013) 0.97
Community coalitions to control chronic disease: Allies against asthma as a model and case study. Health Promot Pract (2006) 0.96
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
Transformation of benign Barrett's epithelium by repeated acid and bile exposure over 65 weeks: a novel in vitro model. Int J Cancer (2010) 0.94
Involvement of DNA mismatch repair in folate deficiency-induced apoptosis small star, filled. J Nutr Biochem (2002) 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
Six2 activity is required for the formation of the mammalian pyloric sphincter. Dev Biol (2009) 0.92
Isolation and sequencing of a novel tropomyosin isoform preferentially associated with colon cancer. Gastroenterology (2002) 0.91
Regulation of murine cardiac contractility by activation of α(1A)-adrenergic receptor-operated Ca(2+) entry. Cardiovasc Res (2011) 0.91
Depletion of thymosin β4 promotes the proliferation, migration, and activation of human hepatic stellate cells. Cell Physiol Biochem (2014) 0.90
S-adenosylmethionine inhibits the growth of cancer cells by reversing the hypomethylation status of c-myc and H-ras in human gastric cancer and colon cancer. Int J Biol Sci (2010) 0.89
Effect of eradication of Helicobacter pylori on the histology and cellular phenotype of gastric intestinal metaplasia. Clin Gastroenterol Hepatol (2008) 0.89
Repeated exposure to acid and bile selectively induces colonic phenotype expression in a heterogeneous Barrett's epithelial cell line. Lab Invest (2008) 0.88
The restoration after repetitive transcranial magnetic stimulation treatment on cognitive ability of vascular dementia rats and its impacts on synaptic plasticity in hippocampal CA1 area. J Mol Neurosci (2009) 0.86
Genetic variant I148M in PNPLA3 is associated with the ultrasonography-determined steatosis degree in a Chinese population. BMC Med Genet (2012) 0.86
Association of genomic instability, and the methylation status of imprinted genes and mismatch-repair genes, with neural tube defects. Eur J Hum Genet (2012) 0.86
Brg1-dependent epigenetic control of vascular smooth muscle cell proliferation by hydrogen sulfide. Biochim Biophys Acta (2013) 0.86
Self-reported weight status rather than BMI may be closely related to psychopathological symptoms among Mainland Chinese adolescents. J Trop Pediatr (2009) 0.85
Family factors associated with suicide attempts among Chinese adolescent students: a national cross-sectional survey. J Adolesc Health (2010) 0.85
A comparison of approaches to control for confounding factors by regression models. Hum Hered (2011) 0.83
Association between MTR A2756G and MTRR A66G polymorphisms and maternal risk for neural tube defects: a meta-analysis. Gene (2012) 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
Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4. Genet Epidemiol (2007) 0.82
Clinical report on external irradiation combined with californium-252 neutron intraluminal brachytherapy for cervical carcinoma treatment. Tumori (2008) 0.82
Repression through a distal TCF-3 binding site restricts Xenopus myf-5 expression in gastrula mesoderm. Mech Dev (2002) 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
Soy-derived isoflavones inhibit HeLa cell growth by inducing apoptosis. Plant Foods Hum Nutr (2011) 0.81
Linkage analysis of alcohol dependence using both affected and discordant sib pairs. BMC Genet (2005) 0.81
Coordinated processing of 3' slipped (CAG)n/(CTG)n hairpins by DNA polymerases β and δ preferentially induces repeat expansions. J Biol Chem (2013) 0.81
De novo heterozygous FBN1 mutations in the extreme C-terminal region cause progeroid fibrillinopathy. Am J Med Genet A (2014) 0.81
Changes of the alternative splicing variants of human telomerase reverse transcriptase during gastric carcinogenesis. Pathobiology (2009) 0.80
Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data. Genet Epidemiol (2007) 0.80
Brain-derived neurotrophic factor is up-regulated in severe acute cauda equina syndrome dog model. Int J Clin Exp Med (2013) 0.80
T-box binding site mediates the dorsal activation of myf-5 in Xenopus gastrula embryos. Dev Dyn (2003) 0.79
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Deficiency of a novel mismatch repair activity in a bladder tumor cell line. Nucleic Acids Res (2002) 0.78
Antibody to tropomyosin isoform 5 and complement induce the lysis of colonocytes in ulcerative colitis. Am J Gastroenterol (2009) 0.78
Engaging health care providers in coalition activities. Health Promot Pract (2006) 0.78
[Diagnostic value of ischemia-modified albumin in patients with acute coronary syndrome]. Zhonghua Xin Xue Guan Bing Za Zhi (2007) 0.78
Association of the ADIPOQ T45G polymorphism with insulin resistance and blood glucose: a meta-analysis. Endocr J (2014) 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
Mechanism of folate deficiency-induced apoptosis in mouse embryonic stem cells: Cell cycle arrest/apoptosis in G1/G0 mediated by microRNA-302a and tumor suppressor gene Lats2. Int J Biochem Cell Biol (2012) 0.77
Current advances in tumor proteomics and candidate biomarkers for hepatic cancer. Expert Rev Proteomics (2009) 0.77
Meta-analysis of the association of ADIPOQ G276T polymorphism with insulin resistance and blood glucose. Endocrine (2014) 0.77
A comparison of the likelihood ratio test and the variance-stabilising transformation-based tests for detecting association of rare variants. Ann Hum Genet (2013) 0.77
Novel SiOC nanocomposites for high-yield preparation of ultra-large-scale SiC nanowires. Nanotechnology (2010) 0.77
Meta-analyses on the association of MTR A2756G and MTRR A66G polymorphisms with neural tube defect risks in Caucasian children. J Matern Fetal Neonatal Med (2013) 0.76
[Characterization of intertype specific epitopes on adenoviruses hexon]. Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi (2002) 0.76
Autoantibodies against human tropomyosin isoform 5 in ulcerative colitis destroys colonic epithelial cells through antibody and complement-mediated lysis. Cell Immunol (2007) 0.76
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes. Hum Genet (2008) 0.76
[Preliminary study on the alternative splicing pattern of human telomerase reverse transcriptase gene during gastric carcinogenesis]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2009) 0.76
Homozygosity mapping identifies a bile acid biosynthetic defect in an adult with cirrhosis of unknown etiology. Hepatology (2012) 0.76
Minimum Information about a Genotyping Experiment (MIGEN). Stand Genomic Sci (2011) 0.76
Combination of symptoms and oxygen desaturation index in predicting childhood obstructive sleep apnea. Int J Pediatr Otorhinolaryngol (2012) 0.76
Low serum 25-hydroxyvitamin D level and risk of urinary tract infection in infants. Medicine (Baltimore) (2016) 0.76
Mesalamine suppresses the expression of TC22, a novel tropomyosin isoform associated with colonic neoplasia. Mol Pharmacol (2009) 0.76
Corrigendum: Cell death by pyroptosis drives CD4 T-cell depletion in HIV-1 infection. Nature (2017) 0.75
The neuroprotection of repetitive transcranial magnetic stimulation pre-treatment in vascular dementia rats. J Mol Neurosci (2015) 0.75
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
[Changes of alternative splicing variants of human telomerase reverse transcriptase during gastric carcinogenesis]. Ai Zheng (2008) 0.75
A Chinese girl with novel PLCE1 mutations and proliferation of the mesangium responded to tacrolimus therapy. Nephrology (Carlton) (2014) 0.75
Piecewise Classifier Mappings: Learning Fine-Grained Learners for Novel Categories With Few Examples. IEEE Trans Image Process (2019) 0.75
[Differential expression of motility-related protein-1/CD9 gene in gastric cancers and premalignant lesions]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2004) 0.75
[A simple and universal method for molecular sexing of birds]. Shi Yan Sheng Wu Xue Bao (2003) 0.75
[Improvement of transcriptional activity of hTERT promoter by SV40 enhancer]. Zhonghua Bing Li Xue Za Zhi (2006) 0.75
ThiNet: Pruning CNN Filters for a Thinner Net. IEEE Trans Pattern Anal Mach Intell (2018) 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