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 *

148 related articles for article (PubMed ID: 37895311)

  • 1. Multi-Trait Exome-Wide Association Study of Back Pain-Related Phenotypes.
    Zorkoltseva IV; Elgaeva EE; Belonogova NM; Kirichenko AV; Svishcheva GR; Freidin MB; Williams FMK; Suri P; Tsepilov YA; Axenovich TI
    Genes (Basel); 2023 Oct; 14(10):. PubMed ID: 37895311
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Noncoding rare variants in PANX3 are associated with chronic back pain.
    Belonogova NM; Kirichenko AV; Freidin MB; Williams FMK; Suri P; Aulchenko YS; Axenovich TI; Tsepilov YA
    Pain; 2023 Apr; 164(4):864-869. PubMed ID: 36448979
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare variant analyses in large-scale cohorts identified SLC13A1 associated with chronic pain.
    Ao X; Parisien M; Zidan M; Grant AV; Martinsen AE; Winsvold BS; Diatchenko L
    Pain; 2023 Aug; 164(8):1841-1851. PubMed ID: 36943258
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
    Bjornsdottir G; Stefansdottir L; Thorleifsson G; Sulem P; Norland K; Ferkingstad E; Oddsson A; Zink F; Lund SH; Nawaz MS; Bragi Walters G; Skuladottir AT; Gudjonsson SA; Einarsson G; Halldorsson GH; Bjarnadottir V; Sveinbjornsson G; Helgadottir A; Styrkarsdottir U; Gudmundsson LJ; Pedersen OB; Hansen TF; Werge T; Banasik K; Troelsen A; Skou ST; Thørner LW; Erikstrup C; Nielsen KR; Mikkelsen S; ; ; Jonsdottir I; Bjornsson A; Olafsson IH; Ulfarsson E; Blondal J; Vikingsson A; Brunak S; Ostrowski SR; Ullum H; Thorsteinsdottir U; Stefansson H; Gudbjartsson DF; Thorgeirsson TE; Stefansson K
    Nat Commun; 2022 Feb; 13(1):634. PubMed ID: 35110524
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs.
    Li N; Rowley SM; Thompson ER; McInerny S; Devereux L; Amarasinghe KC; Zethoven M; Lupat R; Goode D; Li J; Trainer AH; Gorringe KL; James PA; Campbell IG
    Breast Cancer Res; 2018 Jan; 20(1):3. PubMed ID: 29316957
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses.
    Demirkan A; Henneman P; Verhoeven A; Dharuri H; Amin N; van Klinken JB; Karssen LC; de Vries B; Meissner A; Göraler S; van den Maagdenberg AM; Deelder AM; C 't Hoen PA; van Duijn CM; van Dijk KW
    PLoS Genet; 2015 Jan; 11(1):e1004835. PubMed ID: 25569235
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat Distribution.
    Koprulu M; Zhao Y; Wheeler E; Dong L; Rocha N; Li C; Griffin JD; Patel S; Van de Streek M; Glastonbury CA; Stewart ID; Day FR; Luan J; Bowker N; Wittemans LBL; Kerrison ND; Cai L; Lucarelli DME; Barroso I; McCarthy MI; Scott RA; Saudek V; Small KS; Wareham NJ; Semple RK; Perry JRB; O'Rahilly S; Lotta LA; Langenberg C; Savage DB
    J Clin Endocrinol Metab; 2022 Mar; 107(4):1065-1077. PubMed ID: 34875679
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Exome sequencing and analysis of 454,787 UK Biobank participants.
    Backman JD; Li AH; Marcketta A; Sun D; Mbatchou J; Kessler MD; Benner C; Liu D; Locke AE; Balasubramanian S; Yadav A; Banerjee N; Gillies CE; Damask A; Liu S; Bai X; Hawes A; Maxwell E; Gurski L; Watanabe K; Kosmicki JA; Rajagopal V; Mighty J; ; ; Jones M; Mitnaul L; Stahl E; Coppola G; Jorgenson E; Habegger L; Salerno WJ; Shuldiner AR; Lotta LA; Overton JD; Cantor MN; Reid JG; Yancopoulos G; Kang HM; Marchini J; Baras A; Abecasis GR; Ferreira MAR
    Nature; 2021 Nov; 599(7886):628-634. PubMed ID: 34662886
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Rare variant contribution to human disease in 281,104 UK Biobank exomes.
    Wang Q; Dhindsa RS; Carss K; Harper AR; Nag A; Tachmazidou I; Vitsios D; Deevi SVV; Mackay A; Muthas D; Hühn M; Monkley S; Olsson H; ; Wasilewski S; Smith KR; March R; Platt A; Haefliger C; Petrovski S
    Nature; 2021 Sep; 597(7877):527-532. PubMed ID: 34375979
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Efficient identification of trait-associated loss-of-function variants in the UK Biobank cohort by exome-sequencing based genotype imputation.
    Yu WY; Yan SS; Zhang SH; Ni JJ; Bin-Li ; Pei YF; Zhang L
    Genet Epidemiol; 2023 Mar; 47(2):121-134. PubMed ID: 36490288
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exome sequencing and characterization of 49,960 individuals in the UK Biobank.
    Van Hout CV; Tachmazidou I; Backman JD; Hoffman JD; Liu D; Pandey AK; Gonzaga-Jauregui C; Khalid S; Ye B; Banerjee N; Li AH; O'Dushlaine C; Marcketta A; Staples J; Schurmann C; Hawes A; Maxwell E; Barnard L; Lopez A; Penn J; Habegger L; Blumenfeld AL; Bai X; O'Keeffe S; Yadav A; Praveen K; Jones M; Salerno WJ; Chung WK; Surakka I; Willer CJ; Hveem K; Leader JB; Carey DJ; Ledbetter DH; ; Cardon L; Yancopoulos GD; Economides A; Coppola G; Shuldiner AR; Balasubramanian S; Cantor M; ; Nelson MR; Whittaker J; Reid JG; Marchini J; Overton JD; Scott RA; Abecasis GR; Yerges-Armstrong L; Baras A
    Nature; 2020 Oct; 586(7831):749-756. PubMed ID: 33087929
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of novel rare variants for anxiety: an exome-wide association study in the UK Biobank.
    Pan C; Cheng S; Liu L; Chen Y; Meng P; Yang X; Li C; Zhang J; Zhang Z; Zhang H; Cheng B; Wen Y; Jia Y; Zhang F
    Prog Neuropsychopharmacol Biol Psychiatry; 2024 Mar; 130():110928. PubMed ID: 38154517
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Scalable mixed model methods for set-based association studies on large-scale categorical data analysis and its application to exome-sequencing data in UK Biobank.
    Bi W; Zhou W; Zhang P; Sun Y; Yue W; Lee S
    Am J Hum Genet; 2023 May; 110(5):762-773. PubMed ID: 37019109
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results From a National Biobank.
    Choi SH; Jurgens SJ; Weng LC; Pirruccello JP; Roselli C; Chaffin M; Lee CJ; Hall AW; Khera AV; Lunetta KL; Lubitz SA; Ellinor PT
    Circ Res; 2020 Jan; 126(2):200-209. PubMed ID: 31691645
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Polygenic architecture of rare coding variation across 394,783 exomes.
    Weiner DJ; Nadig A; Jagadeesh KA; Dey KK; Neale BM; Robinson EB; Karczewski KJ; O'Connor LJ
    Nature; 2023 Feb; 614(7948):492-499. PubMed ID: 36755099
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-Exome Sequencing Analyses Support a Role of Vitamin D Metabolism in Ischemic Stroke.
    Xie Y; Acosta JN; Ye Y; Demarais ZS; Conlon CJ; Chen M; Zhao H; Falcone GJ
    Stroke; 2023 Mar; 54(3):800-809. PubMed ID: 36762557
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Insight into the genetic architecture of back pain and its risk factors from a study of 509,000 individuals.
    Freidin MB; Tsepilov YA; Palmer M; Karssen LC; Suri P; Aulchenko YS; Williams FMK;
    Pain; 2019 Jun; 160(6):1361-1373. PubMed ID: 30747904
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes.
    Melton PE; Johnson MP; Gokhale-Agashe D; Rea AJ; Ariff A; Cadby G; Peralta JM; McNab TJ; Allcock RJ; Abraham LJ; Blangero J; Brennecke SP; Moses EK
    J Hypertens; 2019 May; 37(5):997-1011. PubMed ID: 30633125
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular genetic studies of complex phenotypes.
    Marian AJ
    Transl Res; 2012 Feb; 159(2):64-79. PubMed ID: 22243791
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.