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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 27060904)

  • 1. Candidate gene resequencing to identify rare, pedigree-specific variants influencing healthy aging phenotypes in the long life family study.
    Druley TE; Wang L; Lin SJ; Lee JH; Zhang Q; Daw EW; Abel HJ; Chasnoff SE; Ramos EI; Levinson BT; Thyagarajan B; Newman AB; Christensen K; Mayeux R; Province MA
    BMC Geriatr; 2016 Apr; 16():80. PubMed ID: 27060904
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification and genomic analysis of pedigrees with exceptional longevity identifies candidate rare variants.
    Miller JB; Ward E; Staley LA; Stevens J; Teerlink CC; Tavana JP; Cloward M; Page M; Dayton L; ; Cannon-Albright LA; Kauwe JSK
    Neurobiol Dis; 2020 Sep; 143():104972. PubMed ID: 32574725
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic variation and human longevity.
    Soerensen M
    Dan Med J; 2012 May; 59(5):B4454. PubMed ID: 22549493
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Testing genetic association with rare and common variants in family data.
    Chen H; Malzahn D; Balliu B; Li C; Bailey JN
    Genet Epidemiol; 2014 Sep; 38 Suppl 1(0 1):S37-43. PubMed ID: 25112186
    [TBL] [Abstract][Full Text] [Related]  

  • 5. NIA Long Life Family Study: Objectives, Design, and Heritability of Cross-Sectional and Longitudinal Phenotypes.
    Wojczynski MK; Jiuan Lin S; Sebastiani P; Perls TT; Lee J; Kulminski A; Newman A; Zmuda JM; Christensen K; Province MA
    J Gerontol A Biol Sci Med Sci; 2022 Apr; 77(4):717-727. PubMed ID: 34739053
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Models to explore genetics of human aging.
    Karasik D; Newman A
    Adv Exp Med Biol; 2015; 847():141-61. PubMed ID: 25916590
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Discovery of novel non-synonymous SNP variants in 988 candidate genes from 6 centenarians by target capture and next-generation sequencing.
    Han J; Ryu S; Moskowitz DM; Rothenberg D; Leahy DJ; Atzmon G; Barzilai N; Suh Y
    Mech Ageing Dev; 2013 Oct; 134(10):478-85. PubMed ID: 23376243
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder.
    Cruceanu C; Ambalavanan A; Spiegelman D; Gauthier J; Lafrenière RG; Dion PA; Alda M; Turecki G; Rouleau GA
    Genome; 2013 Oct; 56(10):634-40. PubMed ID: 24237345
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetics of healthy aging and longevity.
    Brooks-Wilson AR
    Hum Genet; 2013 Dec; 132(12):1323-38. PubMed ID: 23925498
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High-throughput sequencing analysis of nuclear-encoded mitochondrial genes reveals a genetic signature of human longevity.
    Gonzalez B; Tare A; Ryu S; Johnson SC; Atzmon G; Barzilai N; Kaeberlein M; Suh Y
    Geroscience; 2023 Feb; 45(1):311-330. PubMed ID: 35948858
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare variant association test with multiple phenotypes.
    Lee S; Won S; Kim YJ; Kim Y; ; Kim BJ; Park T
    Genet Epidemiol; 2017 Apr; 41(3):198-209. PubMed ID: 28039885
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study.
    Lee JH; Cheng R; Honig LS; Feitosa M; Kammerer CM; Kang MS; Schupf N; Lin SJ; Sanders JL; Bae H; Druley T; Perls T; Christensen K; Province M; Mayeux R
    Front Genet; 2013; 4():310. PubMed ID: 24478790
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome and whole genome sequencing in aging and longevity.
    van den Akker EB; Deelen J; Slagboom PE; Beekman M
    Adv Exp Med Biol; 2015; 847():127-39. PubMed ID: 25916589
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families.
    Timms AE; Dorschner MO; Wechsler J; Choi KY; Kirkwood R; Girirajan S; Baker C; Eichler EE; Korvatska O; Roche KW; Horwitz MS; Tsuang DW
    JAMA Psychiatry; 2013 Jun; 70(6):582-90. PubMed ID: 23553203
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathies.
    Forleo C; D'Erchia AM; Sorrentino S; Manzari C; Chiara M; Iacoviello M; Guaricci AI; De Santis D; Musci RL; La Spada A; Marangelli V; Pesole G; Favale S
    PLoS One; 2017; 12(7):e0181842. PubMed ID: 28750076
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The role of large pedigrees in an era of high-throughput sequencing.
    Wijsman EM
    Hum Genet; 2012 Oct; 131(10):1555-63. PubMed ID: 22714655
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.
    Hu H; Roach JC; Coon H; Guthery SL; Voelkerding KV; Margraf RL; Durtschi JD; Tavtigian SV; Shankaracharya ; Wu W; Scheet P; Wang S; Xing J; Glusman G; Hubley R; Li H; Garg V; Moore B; Hood L; Galas DJ; Srivastava D; Reese MG; Jorde LB; Yandell M; Huff CD
    Nat Biotechnol; 2014 Jul; 32(7):663-9. PubMed ID: 24837662
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Monogenic and polygenic determinants of sarcoma risk: an international genetic study.
    Ballinger ML; Goode DL; Ray-Coquard I; James PA; Mitchell G; Niedermayr E; Puri A; Schiffman JD; Dite GS; Cipponi A; Maki RG; Brohl AS; Myklebost O; Stratford EW; Lorenz S; Ahn SM; Ahn JH; Kim JE; Shanley S; Beshay V; Randall RL; Judson I; Seddon B; Campbell IG; Young MA; Sarin R; Blay JY; O'Donoghue SI; Thomas DM;
    Lancet Oncol; 2016 Sep; 17(9):1261-71. PubMed ID: 27498913
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Family-Specific Variants and the Limits of Human Genetics.
    Shirts BH; Pritchard CC; Walsh T
    Trends Mol Med; 2016 Nov; 22(11):925-934. PubMed ID: 27742414
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A methodology for gene level omics-WAS integration identifies genes influencing traits associated with cardiovascular risks: the Long Life Family Study.
    Acharya S; Liao S; Jung WJ; Kang YS; Moghaddam VA; Feitosa MF; Wojczynski MK; Lin S; Anema JA; Schwander K; Connell JO; Province MA; Brent MR
    Hum Genet; 2024 Oct; 143(9-10):1241-1252. PubMed ID: 39276247
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.