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Mental and Physical Activities Delay Cognitive Decline in Older Persons with Dementia

The American journal of geriatric psychiatry, 2014, Vol.22 (1), p.63-74

2014

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Th2 cell regulatory and effector molecules single nucleotide polymorphisms and periodontitis

Journal of leukocyte biology, 2020-11, Vol.108 (5), p.1641-1654

2020

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Pedigree analysis of lumbar developmental spinal stenosis: Determination of potential inheritance patterns

Journal of orthopaedic research, 2021-08, Vol.39 (8), p.1763-1776

2021

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Genetic Polymorphisms in Estrogen Metabolic Pathway Associated with Risks of Alzheimer's Disease: Evidence from a Southern Chinese Population

Journal of the American Geriatrics Society (JAGS), 2017-02, Vol.65 (2), p.332-339

2017

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A Functional Variation in CD55 Increases the Severity of 2009 Pandemic H1N1 Influenza A Virus Infection

The Journal of infectious diseases, 2012-08, Vol.206 (4), p.495-503

2012

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Polymorphisms of CR1 , CLU and PICALM confer susceptibility of Alzheimer's disease in a southern Chinese population

Neurobiology of aging, 2012, Vol.33 (1), p.210.e1-210.e7

2012

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Identification of Copy Number Variants in a Southern Chinese Cohort of Patients with Congenital Scoliosis

Genes, 2021-08, Vol.12 (8), p.1213

2021

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Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

Proceedings of the National Academy of Sciences - PNAS, 2009-02, Vol.106 (8), p.2694-2699

2009

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Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2

Human molecular genetics, 2010-07, Vol.19 (14), p.2917-2925

2010

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SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese

Journal of human genetics, 2012-04, Vol.57 (4), p.244-246

2012

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Can leisure activities slow dementia progression in nursing home residents? A cluster-randomized controlled trial

International psychogeriatrics, 2014-04, Vol.26 (4), p.637-643

2014

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Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

PLoS genetics, 2012-05, Vol.8 (5), p.e1002687

2012

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Novel complex disease allele mutations in cleidocranial dysplasia patients

Journal of oral pathology & medicine, 2014-11, Vol.43 (10), p.798-800

2014

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Association of the Taq I allele in vitamin D receptor with degenerative disc disease and disc bulge in a chinese population

Spine (Philadelphia, Pa. 1976), 2006-05, Vol.31 (10), p.1143-1148

2006

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The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degeneration

Spine (Philadelphia, Pa. 1976), 2005-12, Vol.30 (24), p.2735-2742

2005

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Genetics of Lumbar Disk Degeneration: Technology, Study Designs, and Risk Factors

The Orthopedic clinics of North America, 2011-10, Vol.42 (4), p.479-486

2011

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Identification of TMPRSS2 as a Susceptibility Gene for Severe 2009 Pandemic A(H1N1) Influenza and A(H7N9) Influenza

The Journal of infectious diseases, 2015-10, Vol.212 (8), p.1214-1221

2015

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Abnormal diffusion tensor in nonsymptomatic familial amyotrophic lateral sclerosis with a causative superoxide dismutase 1 mutation

Journal of magnetic resonance imaging, 2008-01, Vol.27 (1), p.8-13

2008

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Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant

The Journal of clinical investigation, 2013-11, Vol.123 (11), p.4909-4917

2013

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A novel intronic polymorphism of ABCA1 gene reveals risk for sporadic Alzheimer's disease in Chinese

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-12, Vol.144B (8), p.1007-1013

2007

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A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups

Journal of medical genetics, 2014-06, Vol.51 (6), p.401-406

2014

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Functional variants regulating LGALS1 (Galectin 1) expression affect human susceptibility to influenza A(H7N9)

Scientific reports, 2015-02, Vol.5 (1), p.8517-8517, Article 8517

2015

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A multiethnic meta-analysis defined the association of rs12946942 with severe adolescent idiopathic scoliosis

Journal of human genetics, 2019-05, Vol.64 (5), p.493-498

2019

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Association of the Asporin D14 Allele with Lumbar-Disc Degeneration in Asians

American journal of human genetics, 2008-03, Vol.82 (3), p.744-747

2008

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Mental and Physical Activities Delay Cognitive Decline in Older Persons with Dementia

Th2 cell regulatory and effector molecules single nucleotide polymorphisms and periodontitis

Pedigree analysis of lumbar developmental spinal stenosis: Determination of potential inheritance patterns

Genetic Polymorphisms in Estrogen Metabolic Pathway Associated with Risks of Alzheimer's Disease: Evidence from a Southern Chinese Population

A Functional Variation in CD55 Increases the Severity of 2009 Pandemic H1N1 Influenza A Virus Infection

Polymorphisms of CR1 , CLU and PICALM confer susceptibility of Alzheimer's disease in a southern Chinese population

Identification of Copy Number Variants in a Southern Chinese Cohort of Patients with Congenital Scoliosis

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2

SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese

Can leisure activities slow dementia progression in nursing home residents? A cluster-randomized controlled trial

Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

Novel complex disease allele mutations in cleidocranial dysplasia patients

Association of the Taq I allele in vitamin D receptor with degenerative disc disease and disc bulge in a chinese population

The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degeneration

Genetics of Lumbar Disk Degeneration: Technology, Study Designs, and Risk Factors

Identification of TMPRSS2 as a Susceptibility Gene for Severe 2009 Pandemic A(H1N1) Influenza and A(H7N9) Influenza

Abnormal diffusion tensor in nonsymptomatic familial amyotrophic lateral sclerosis with a causative superoxide dismutase 1 mutation

Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant

A novel intronic polymorphism of ABCA1 gene reveals risk for sporadic Alzheimer's disease in Chinese

A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups

Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis

Functional variants regulating LGALS1 (Galectin 1) expression affect human susceptibility to influenza A(H7N9)

A multiethnic meta-analysis defined the association of rs12946942 with severe adolescent idiopathic scoliosis

Association of the Asporin D14 Allele with Lumbar-Disc Degeneration in Asians

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