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Serum Uric Acid Levels and Risk of Metabolic Syndrome: A Dose-Response Meta-Analysis of Prospective Studies

The journal of clinical endocrinology and metabolism, 2015-11, Vol.100 (11), p.4198-4207

2015

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Serum branched-chain amino acids are associated with leukocyte telomere length and frailty based on residents from Guangxi longevity county

Scientific reports, 2020-06, Vol.10 (1), p.10252-10252, Article 10252

2020

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Prevalence of Glaucoma in a Rural Northern China Adult Population: A Population-Based Survey in Kailu County, Inner Mongolia

Ophthalmology (Rochester, Minn.), 2011-10, Vol.118 (10), p.1982-1988

2011

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The relationship between sleep duration and activities of daily living (ADL) disability in the Chinese oldest-old: A cross-sectional study

PeerJ (San Francisco, CA), 2023-02, Vol.11, p.e14856-e14856, Article e14856

2023

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Distance‐ and near‐visual impairment in rural Chinese adults in Kailu, Inner Mongolia

Acta ophthalmologica (Oxford, England), 2016-06, Vol.94 (4), p.407-413

2016

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Copolymer-1 immunization reduces damage in retinal ganglion cells under high intraocular pressure through altering the expression of retinal neurotrophins

Journal of ocular pharmacology and therapeutics, 2010-02, Vol.26 (1), p.11-20

2010

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Association between co-inhibitory molecule gene tagging single nucleotide polymorphisms and the risk of colorectal cancer in Chinese

Journal of cancer research and clinical oncology, 2015-09, Vol.141 (9), p.1533-1544

2015

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Identification and replication of novel genetic variants of ABO gene to reduce the incidence of diseases and promote longevity by modulating lipid homeostasis

Aging (Albany, NY.), 2021-11, Vol.13 (22), p.24655-24674

2021

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Exploration on the 24 hour intraocular pressure fluctuation in glaucoma patients

Chung-hua yen k'o tsa chih, 2017-02, Vol.53 (2), p.85

2017

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Gene–gene interaction between CETP and APOE polymorphisms confers higher risk for hypertriglyceridemia in oldest-old Chinese women

Experimental gerontology, 2014-07, Vol.55, p.129-133

2014

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Identification of new genetic variants of HLA-DQB1 associated with human longevity and lipid homeostasis-a cross-sectional study in a Chinese population

Aging (Albany, NY.), 2017-11, Vol.9 (11), p.2316-2333

2017

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Prevalence and causes of visual impairment in a rural North‐east China adult population: a population‐based survey in Bin County, Harbin

Acta ophthalmologica (Oxford, England), 2010-09, Vol.88 (6), p.669-674

2010

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Functional FCGR2B gene variants influence intravenous immunoglobulin response in patients with Kawasaki disease

Journal of allergy and clinical immunology, 2011-09, Vol.128 (3), p.677-680.e1

2011

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Identification of a novel mutation of the gene for gap junction protein α3 (GJA3) in a Chinese family with congenital cataract

Molecular biology reports, 2014-07, Vol.41 (7), p.4753-4758

2014

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A 556 kb deletion in the downstream region of the PAX6 gene causes familial aniridia and other eye anomalies in a Chinese family

Molecular vision, 2011-02, Vol.17, p.448-455

2011

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Intronic and promoter polymorphisms of hMLH1/hMSH2 and colorectal cancer risk in Heilongjiang Province of China

Journal of cancer research and clinical oncology, 2015-08, Vol.141 (8), p.1393-1404

2015

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Analysis of the Relationship Between ADIPOR1 Variants and the Susceptibility of Chronic Metabolic Diseases in a Northeast Han Chinese Population

Genetic testing and molecular biomarkers, 2016-02, Vol.20 (2), p.81-85

2016

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Identification and study of a FBN1 gene mutation in a Chinese family with ectopia lentis

Molecular vision, 2012-02, Vol.18, p.504-511

2012

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A novel optineurin genetic mutation associated with open-angle glaucoma in a Chinese family

Molecular vision, 2009-08, Vol.15, p.1649-1654

2009

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A novel splicing mutation of the FRMD7 gene in a Chinese family with X-linked congenital nystagmus

Molecular vision, 2012, Vol.18, p.87-91

2012

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Identification of a novel FBN1 gene mutation in a Chinese family with Marfan syndrome

Molecular vision, 2011-09, Vol.17, p.2421-2427

2011

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Coordinated gene expression of Th17- and Treg-associated molecules correlated with resolution of the monophasic experimental autoimmune uveitis

Molecular vision, 2011, Vol.17, p.1493-1507

2011

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Two novel PAX6 mutations identified in northeastern Chinese patients with aniridia

Molecular vision, 2007-08, Vol.13, p.1555-1561

2007

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Functional relevance for associations between osteoporosis and genetic variants

PloS one, 2017-04, Vol.12 (4), p.e0174808-e0174808

2017

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Attenuated replication and pathogenicity of SARS-CoV-2 B.1.1.529 Omicron

Nature (London), 2022-03, Vol.603 (7902), p.693-699

2022

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Serum Uric Acid Levels and Risk of Metabolic Syndrome: A Dose-Response Meta-Analysis of Prospective Studies

Serum branched-chain amino acids are associated with leukocyte telomere length and frailty based on residents from Guangxi longevity county

Prevalence of Glaucoma in a Rural Northern China Adult Population: A Population-Based Survey in Kailu County, Inner Mongolia

The relationship between sleep duration and activities of daily living (ADL) disability in the Chinese oldest-old: A cross-sectional study

Distance‐ and near‐visual impairment in rural Chinese adults in Kailu, Inner Mongolia

Copolymer-1 immunization reduces damage in retinal ganglion cells under high intraocular pressure through altering the expression of retinal neurotrophins

Association between co-inhibitory molecule gene tagging single nucleotide polymorphisms and the risk of colorectal cancer in Chinese

Identification and replication of novel genetic variants of ABO gene to reduce the incidence of diseases and promote longevity by modulating lipid homeostasis

Exploration on the 24 hour intraocular pressure fluctuation in glaucoma patients

Gene–gene interaction between CETP and APOE polymorphisms confers higher risk for hypertriglyceridemia in oldest-old Chinese women

Identification of new genetic variants of HLA-DQB1 associated with human longevity and lipid homeostasis-a cross-sectional study in a Chinese population

Prevalence and causes of visual impairment in a rural North‐east China adult population: a population‐based survey in Bin County, Harbin

Functional FCGR2B gene variants influence intravenous immunoglobulin response in patients with Kawasaki disease

Identification of a novel mutation of the gene for gap junction protein α3 (GJA3) in a Chinese family with congenital cataract

A 556 kb deletion in the downstream region of the PAX6 gene causes familial aniridia and other eye anomalies in a Chinese family

Intronic and promoter polymorphisms of hMLH1/hMSH2 and colorectal cancer risk in Heilongjiang Province of China

Analysis of the Relationship Between ADIPOR1 Variants and the Susceptibility of Chronic Metabolic Diseases in a Northeast Han Chinese Population

Identification and study of a FBN1 gene mutation in a Chinese family with ectopia lentis

A novel optineurin genetic mutation associated with open-angle glaucoma in a Chinese family

A novel splicing mutation of the FRMD7 gene in a Chinese family with X-linked congenital nystagmus

Identification of a novel FBN1 gene mutation in a Chinese family with Marfan syndrome

Coordinated gene expression of Th17- and Treg-associated molecules correlated with resolution of the monophasic experimental autoimmune uveitis

Two novel PAX6 mutations identified in northeastern Chinese patients with aniridia

Functional relevance for associations between osteoporosis and genetic variants

Attenuated replication and pathogenicity of SARS-CoV-2 B.1.1.529 Omicron

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