Wei F, Raaijmakers A, Melgarejo J, Cauwenberghs N, Thijs L, Zhang Z
    
    
    J Am Heart Assoc. 2020; 9(15):e014305.
  
  
    PMID: 32750311
    
          PMC: 7792278.
    
          DOI: 10.1161/JAHA.119.014305.
      
 
                                  
  
    Yang W, Melgarejo J, Thijs L, Zhang Z, Boggia J, Wei F
    
    
    JAMA. 2019; 322(5):409-420.
  
  
    PMID: 31386134
    
          PMC: 6822661.
    
          DOI: 10.1001/jama.2019.9811.
      
 
                                  
  
    Khalid M, Driessen T, Lee J, Tejwani L, Rasool A, Saqlain M
    
    
    Gene. 2018; 664:119-126.
  
  
    PMID: 29684488
    
          PMC: 5970093.
    
          DOI: 10.1016/j.gene.2018.04.061.
      
 
                                  
  
    Wang H, Gong C, Liu X, Rao S, Li T, He L
    
    
    J Bone Miner Metab. 2017; 36(4):488-497.
  
  
    PMID: 28884379
    
    
          DOI: 10.1007/s00774-017-0862-3.
      
 
                                  
  
    Yang Y, Chang T, Chen T, Lin W, Chang S, Lee Y
    
    
    Oncotarget. 2016; 7(50):82798-82803.
  
  
    PMID: 27779103
    
          PMC: 5347733.
    
          DOI: 10.18632/oncotarget.12636.
      
 
                              
              
                              
                                      
  Association of Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA4) Gene Polymorphisms with Autoimmune Thyroid Disease in Children and Adults: Case-Control Study.
  
    Ting W, Chien M, Lo F, Wang C, Huang C, Lin C
    
    
    PLoS One. 2016; 11(4):e0154394.
  
  
    PMID: 27111218
    
          PMC: 4844099.
    
          DOI: 10.1371/journal.pone.0154394.
      
 
                                          
                                                          
  Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population.
  
    Yang W, Petit T, Thijs L, Zhang Z, Jacobs L, Hara A
    
    
    BMC Genet. 2015; 16:116.
  
  
    PMID: 26428460
    
          PMC: 4591634.
    
          DOI: 10.1186/s12863-015-0272-2.
      
 
                                          
                                                          
  Does white matter structure or hippocampal volume mediate associations between cortisol and cognitive ageing?.
  
    Cox S, MacPherson S, Ferguson K, Royle N, Munoz Maniega S, Valdes Hernandez M
    
    
    Psychoneuroendocrinology. 2015; 62:129-37.
  
  
    PMID: 26298692
    
          PMC: 4642652.
    
          DOI: 10.1016/j.psyneuen.2015.08.005.
      
 
                                          
                                                          
  Association between AKT1 Gene Polymorphism rs2498794 and Smoking-Related Traits with reference to Cancer Susceptibility.
  
    Nishizawa D, Kasai S, Hasegawa J, Sato N, Tanioka F, Sugimura H
    
    
    Biomed Res Int. 2015; 2015:316829.
  
  
    PMID: 26137473
    
          PMC: 4475560.
    
          DOI: 10.1155/2015/316829.
      
 
                                          
                                                          
  Correlational structure of 'frontal' tests and intelligence tests indicates two components with asymmetrical neurostructural correlates in old age.
  
    Cox S, MacPherson S, Ferguson K, Nissan J, Royle N, MacLullich A
    
    
    Intelligence. 2014; 46:94-106.
  
  
    PMID: 25278641
    
          PMC: 4175012.
    
          DOI: 10.1016/j.intell.2014.05.006.
      
 
                                          
                                                          
  The -665 C>T polymorphism in the eNOS gene predicts cardiovascular mortality and morbidity in white Europeans.
  
    Olivi L, Gu Y, Salvi E, Liu Y, Thijs L, Velayutham D
    
    
    J Hum Hypertens. 2014; 29(3):167-72.
  
  
    PMID: 25102225
    
    
          DOI: 10.1038/jhh.2014.66.
      
 
                                          
                                                          
  Brain white matter integrity and cortisol in older men: the Lothian Birth Cohort 1936.
  
    Cox S, Bastin M, Ferguson K, Munoz Maniega S, MacPherson S, Deary I
    
    
    Neurobiol Aging. 2014; 36(1):257-64.
  
  
    PMID: 25066239
    
          PMC: 4274312.
    
          DOI: 10.1016/j.neurobiolaging.2014.06.022.
      
 
                                          
                                                          
  Polymorphisms of SP110 are associated with both pulmonary and extra-pulmonary tuberculosis among the Vietnamese.
  
    Fox G, Sy D, Nhung N, Yu B, Ellis M, Van Hung N
    
    
    PLoS One. 2014; 9(7):e99496.
  
  
    PMID: 25006821
    
          PMC: 4090157.
    
          DOI: 10.1371/journal.pone.0099496.
      
 
                                          
                                                          
  Alzheimer's disease susceptibility genes APOE and TOMM40, and brain white matter integrity in the Lothian Birth Cohort 1936.
  
    Lyall D, Harris S, Bastin M, Munoz Maniega S, Murray C, Lutz M
    
    
    Neurobiol Aging. 2014; 35(6):1513.e25-33.
  
  
    PMID: 24508314
    
          PMC: 3969262.
    
          DOI: 10.1016/j.neurobiolaging.2014.01.006.
      
 
                                          
                                                          
  Sustainable Reduction of Sleepiness through Salutogenic Self-Care Procedure in Lunch Breaks: A Pilot Study.
  
    Schnieder S, Stappert S, Takahashi M, Fricchione G, Esch T, Krajewski J
    
    
    Evid Based Complement Alternat Med. 2014; 2013:387356.
  
  
    PMID: 24381633
    
          PMC: 3870120.
    
          DOI: 10.1155/2013/387356.
      
 
                                          
                                                          
  Association between polymorphisms in osteopontin gene (SPP1) and first episode calcium oxalate urolithiasis.
  
    Safarinejad M, Shafiei N, Safarinejad S
    
    
    Urolithiasis. 2013; 41(4):303-13.
  
  
    PMID: 23784265
    
    
          DOI: 10.1007/s00240-013-0582-7.
      
 
                                          
                                                          
  Genome-wide association study identifies a potent locus associated with human opioid sensitivity.
  
    Nishizawa D, Fukuda K, Kasai S, Hasegawa J, Aoki Y, Nishi A
    
    
    Mol Psychiatry. 2012; 19(1):55-62.
  
  
    PMID: 23183491
    
          PMC: 3873034.
    
          DOI: 10.1038/mp.2012.164.
      
 
                                          
                                                          
  Association between variants in IDE-KIF11-HHEX and plasma amyloid β levels.
  
    Reitz C, Cheng R, Schupf N, Lee J, Mehta P, Rogaeva E
    
    
    Neurobiol Aging. 2010; 33(1):199.e13-7.
  
  
    PMID: 20724036
    
          PMC: 3117070.
    
          DOI: 10.1016/j.neurobiolaging.2010.07.005.
      
 
                                          
                                                          
  A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.
  
    Schrauwen I, Ealy M, Huentelman M, Thys M, Homer N, Vanderstraeten K
    
    
    Am J Hum Genet. 2009; 84(3):328-38.
  
  
    PMID: 19230858
    
          PMC: 2667982.
    
          DOI: 10.1016/j.ajhg.2009.01.023.
      
 
                                          
                                                          
  Examination of association of genes in the serotonin system to autism.
  
    Anderson B, Schnetz-Boutaud N, Bartlett J, Wotawa A, Wright H, Abramson R
    
    
    Neurogenetics. 2009; 10(3):209-16.
  
  
    PMID: 19184136
    
          PMC: 2753863.
    
          DOI: 10.1007/s10048-009-0171-7.