These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


169 related items for PubMed ID: 23487342

  • 1. Combined genome-wide linkage and association analyses of fasting glucose level in healthy twins and families of Korea.
    Suh YJ, Kim S, Kim SH, Park J, Lim HA, Park HJ, Choi H, Ng D, Lee MK, Nam M.
    J Korean Med Sci; 2013 Mar; 28(3):415-23. PubMed ID: 23487342
    [Abstract] [Full Text] [Related]

  • 2. Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families.
    Ryu S, Won HH, Oh S, Kim JW, Park T, Cho EY, Cho Y, Park DY, Lee YS, Kwon JS, Hong KS.
    Psychiatry Res; 2013 Dec 30; 210(3):756-60. PubMed ID: 24035701
    [Abstract] [Full Text] [Related]

  • 3. Heritability and genome-wide association analyses of fasting plasma glucose in Chinese adult twins.
    Wang W, Zhang C, Liu H, Xu C, Duan H, Tian X, Zhang D.
    BMC Genomics; 2020 Jul 18; 21(1):491. PubMed ID: 32682390
    [Abstract] [Full Text] [Related]

  • 4. Quantitative genetic analysis of the retinal vascular caliber: the Australian Twins Eye Study.
    Sun C, Zhu G, Wong TY, Hewitt AW, Ruddle JB, Hodgson L, Montgomery GW, Young TL, Hammond CJ, Craig JE, Martin NG, He M, Mackey DA.
    Hypertension; 2009 Oct 18; 54(4):788-95. PubMed ID: 19687348
    [Abstract] [Full Text] [Related]

  • 5. Genome-wide linkage and positional association analyses identify associations of novel AFF3 and NTM genes with triglycerides: the GenSalt study.
    Li C, Bazzano LA, Rao DC, Hixson JE, He J, Gu D, Gu CC, Shimmin LC, Jaquish CE, Schwander K, Liu DP, Huang J, Lu F, Cao J, Chong S, Lu X, Kelly TN.
    J Genet Genomics; 2015 Mar 20; 42(3):107-17. PubMed ID: 25819087
    [Abstract] [Full Text] [Related]

  • 6. Genome-wide linkage and regional association study of blood pressure response to the cold pressor test in Han Chinese: the genetic epidemiology network of salt sensitivity study.
    Yang X, Gu D, He J, Hixson JE, Rao DC, Lu F, Mu J, Jaquish CE, Chen J, Huang J, Shimmin LC, Rice TK, Chen J, Wu X, Liu D, Kelly TN.
    Circ Cardiovasc Genet; 2014 Aug 20; 7(4):521-8. PubMed ID: 25028485
    [Abstract] [Full Text] [Related]

  • 7. Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysis.
    Ichihara S, Yamamoto K, Asano H, Nakatochi M, Sukegawa M, Ichihara G, Izawa H, Hirashiki A, Takatsu F, Umeda H, Iwase M, Inagaki H, Hirayama H, Sone T, Nishigaki K, Minatoguchi S, Cho MC, Jang Y, Kim HS, Park JE, Tada-Oikawa S, Kitajima H, Matsubara T, Sunagawa K, Shimokawa H, Kimura A, Lee JY, Murohara T, Inoue I, Yokota M.
    Circ Cardiovasc Genet; 2013 Dec 20; 6(6):569-78. PubMed ID: 24122612
    [Abstract] [Full Text] [Related]

  • 8. Insulin clearance: confirmation as a highly heritable trait, and genome-wide linkage analysis.
    Guo X, Cui J, Jones MR, Haritunians T, Xiang AH, Chen YD, Taylor KD, Buchanan TA, Davis RC, Hsueh WA, Raffel LJ, Rotter JI, Goodarzi MO.
    Diabetologia; 2012 Aug 20; 55(8):2183-92. PubMed ID: 22584727
    [Abstract] [Full Text] [Related]

  • 9. Genomewide linkage scan of hand osteoarthritis in female twin pairs showing replication of quantitative trait loci on chromosomes 2 and 19.
    Livshits G, Kato BS, Zhai G, Hart DJ, Hunter D, MacGregor AJ, Williams FM, Spector TD.
    Ann Rheum Dis; 2007 May 20; 66(5):623-7. PubMed ID: 17127684
    [Abstract] [Full Text] [Related]

  • 10. A genome-wide scan for the Sasang constitution in a Korean family suggests significant linkage at chromosomes 8q11.22-23 and 11q22.1-3.
    Won HH, Lee S, Jang E, Kim KK, Park YK, Kim YJ, Kim YS, Kim BY, Kim JY, Kim JW.
    J Altern Complement Med; 2009 Jul 20; 15(7):765-9. PubMed ID: 19552595
    [Abstract] [Full Text] [Related]

  • 11. Genome-wide linkage and association scans for pulse pressure in Chinese twins.
    Zhang D, Pang Z, Li S, Jiang W, Wang S, Thomassen M, Hjelmborg JV, Kruse TA, Ohm Kyvik K, Christensen K, Zhu G, Tan Q.
    Hypertens Res; 2012 Nov 20; 35(11):1051-7. PubMed ID: 22763476
    [Abstract] [Full Text] [Related]

  • 12. Bivariate genome-wide scan for metabolic phenotypes in non-diabetic Chinese individuals from the Stanford, Asia and Pacific Program of Hypertension and Insulin Resistance Family Study.
    Chiu YF, Chuang LM, Kao HY, Ho LT, Ting CT, Hung YJ, Chen YD, Donlon T, Curb JD, Quertermous T, Hsiung CA.
    Diabetologia; 2007 Aug 20; 50(8):1631-40. PubMed ID: 17579830
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families.
    Concannon P, Erlich HA, Julier C, Morahan G, Nerup J, Pociot F, Todd JA, Rich SS, Type 1 Diabetes Genetics Consortium.
    Diabetes; 2005 Oct 20; 54(10):2995-3001. PubMed ID: 16186404
    [Abstract] [Full Text] [Related]

  • 15. Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits.
    Kim YJ, Go MJ, Hu C, Hong CB, Kim YK, Lee JY, Hwang JY, Oh JH, Kim DJ, Kim NH, Kim S, Hong EJ, Kim JH, Min H, Kim Y, Zhang R, Jia W, Okada Y, Takahashi A, Kubo M, Tanaka T, Kamatani N, Matsuda K, MAGIC consortium, Park T, Oh B, Kimm K, Kang D, Shin C, Cho NH, Kim HL, Han BG, Lee JY, Cho YS.
    Nat Genet; 2011 Sep 11; 43(10):990-5. PubMed ID: 21909109
    [Abstract] [Full Text] [Related]

  • 16. A genome-screen of a large twin cohort reveals linkage for quantitative ultrasound of the calcaneus to 2q33-37 and 4q12-21.
    Wilson SG, Reed PW, Andrew T, Barber MJ, Lindersson M, Langdown M, Thompson D, Thompson E, Bailey M, Chiano M, Kleyn PW, Spector TD.
    J Bone Miner Res; 2004 Feb 11; 19(2):270-7. PubMed ID: 14969397
    [Abstract] [Full Text] [Related]

  • 17. Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian families.
    Ammar M, Bouchlaka-Souissi C, Helms CA, Zaraa I, Jordan CT, Anbunathan H, Bouhaha R, Kouidhi S, Doss N, Dhaoui R, Ben Osman A, Ben Ammar El Gaied A, Marrakchi R, Mokni M, Bowcock AM.
    Br J Dermatol; 2013 Mar 11; 168(3):583-7. PubMed ID: 23013406
    [Abstract] [Full Text] [Related]

  • 18. Genome-widely significant evidence of linkage of schizophrenia to chromosomes 2p24.3 and 6q27 in an SNP-Based analysis of Korean families.
    Hong KS, Won HH, Cho EY, Jeun HO, Cho SS, Lee YS, Park DY, Jang YL, Choi KS, Lee D, Kim MJ, Kim S, Han WS, Kim JW.
    Am J Med Genet B Neuropsychiatr Genet; 2009 Jul 05; 150B(5):647-52. PubMed ID: 18980222
    [Abstract] [Full Text] [Related]

  • 19. Fine-mapping chromosome 20 in 230 systemic lupus erythematosus sib pair and multiplex families: evidence for genetic epistasis with chromosome 16q12.
    Gaffney PM, Langefeld CD, Graham RR, Ortmann WA, Williams AH, Rodine PR, Moser KL, Behrens TW.
    Am J Hum Genet; 2006 May 05; 78(5):747-758. PubMed ID: 16642431
    [Abstract] [Full Text] [Related]

  • 20. Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study.
    John J, Kukshal P, Sharma A, Bhatia T, Nimgaonkar VL, Deshpande SN, Thelma BK.
    Schizophr Res; 2019 Apr 05; 206():75-81. PubMed ID: 30594456
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 9.