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 *

248 related articles for article (PubMed ID: 30957210)

  • 1. The Contribution of Low-Frequency and Rare Coding Variation to Susceptibility to Type 2 Diabetes.
    Flannick J
    Curr Diab Rep; 2019 Apr; 19(5):25. PubMed ID: 30957210
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic risk score combining six genetic variants associated with the cellular NRF2 expression levels correlates with Type 2 diabetes in the human population.
    Shin JH; Lee KM; Shin J; Kang KD; Nho CW; Cho YS
    Genes Genomics; 2019 May; 41(5):537-545. PubMed ID: 30767168
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diverse type 2 diabetes genetic risk factors functionally converge in a phenotype-focused gene network.
    Sandor C; Beer NL; Webber C
    PLoS Comput Biol; 2017 Oct; 13(10):e1005816. PubMed ID: 29059180
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic architecture of type 2 diabetes.
    Hara K; Shojima N; Hosoe J; Kadowaki T
    Biochem Biophys Res Commun; 2014 Sep; 452(2):213-20. PubMed ID: 25111817
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Progress in defining the genetic contribution to type 2 diabetes susceptibility.
    Morris AP
    Curr Opin Genet Dev; 2018 Jun; 50():41-51. PubMed ID: 29477131
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Shared genetic etiology underlying Alzheimer's disease and type 2 diabetes.
    Hao K; Di Narzo AF; Ho L; Luo W; Li S; Chen R; Li T; Dubner L; Pasinetti GM
    Mol Aspects Med; 2015; 43-44():66-76. PubMed ID: 26116273
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rare variants and autoimmune disease.
    Massey J; Eyre S
    Brief Funct Genomics; 2014 Sep; 13(5):392-7. PubMed ID: 24817515
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic markers of type 2 diabetes: Progress in genome-wide association studies and clinical application for risk prediction.
    Wang X; Strizich G; Hu Y; Wang T; Kaplan RC; Qi Q
    J Diabetes; 2016 Jan; 8(1):24-35. PubMed ID: 26119161
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A pathway analysis of genome-wide association study highlights novel type 2 diabetes risk pathways.
    Liu Y; Zhao J; Jiang T; Yu M; Jiang G; Hu Y
    Sci Rep; 2017 Oct; 7(1):12546. PubMed ID: 28970525
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Assessment of whole-genome regression for type II diabetes.
    Vazquez AI; Klimentidis YC; Dhurandhar EJ; Veturi YC; Paérez-Rodríguez P
    PLoS One; 2015; 10(4):e0123818. PubMed ID: 25885636
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recent advances in understanding the genetic architecture of type 2 diabetes.
    Mohlke KL; Boehnke M
    Hum Mol Genet; 2015 Oct; 24(R1):R85-92. PubMed ID: 26160912
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The genetic architecture of type 2 diabetes.
    Fuchsberger C; Flannick J; Teslovich TM; Mahajan A; Agarwala V; Gaulton KJ; Ma C; Fontanillas P; Moutsianas L; McCarthy DJ; Rivas MA; Perry JRB; Sim X; Blackwell TW; Robertson NR; Rayner NW; Cingolani P; Locke AE; Tajes JF; Highland HM; Dupuis J; Chines PS; Lindgren CM; Hartl C; Jackson AU; Chen H; Huyghe JR; van de Bunt M; Pearson RD; Kumar A; Müller-Nurasyid M; Grarup N; Stringham HM; Gamazon ER; Lee J; Chen Y; Scott RA; Below JE; Chen P; Huang J; Go MJ; Stitzel ML; Pasko D; Parker SCJ; Varga TV; Green T; Beer NL; Day-Williams AG; Ferreira T; Fingerlin T; Horikoshi M; Hu C; Huh I; Ikram MK; Kim BJ; Kim Y; Kim YJ; Kwon MS; Lee J; Lee S; Lin KH; Maxwell TJ; Nagai Y; Wang X; Welch RP; Yoon J; Zhang W; Barzilai N; Voight BF; Han BG; Jenkinson CP; Kuulasmaa T; Kuusisto J; Manning A; Ng MCY; Palmer ND; Balkau B; Stančáková A; Abboud HE; Boeing H; Giedraitis V; Prabhakaran D; Gottesman O; Scott J; Carey J; Kwan P; Grant G; Smith JD; Neale BM; Purcell S; Butterworth AS; Howson JMM; Lee HM; Lu Y; Kwak SH; Zhao W; Danesh J; Lam VKL; Park KS; Saleheen D; So WY; Tam CHT; Afzal U; Aguilar D; Arya R; Aung T; Chan E; Navarro C; Cheng CY; Palli D; Correa A; Curran JE; Rybin D; Farook VS; Fowler SP; Freedman BI; Griswold M; Hale DE; Hicks PJ; Khor CC; Kumar S; Lehne B; Thuillier D; Lim WY; Liu J; van der Schouw YT; Loh M; Musani SK; Puppala S; Scott WR; Yengo L; Tan ST; Taylor HA; Thameem F; Wilson G; Wong TY; Njølstad PR; Levy JC; Mangino M; Bonnycastle LL; Schwarzmayr T; Fadista J; Surdulescu GL; Herder C; Groves CJ; Wieland T; Bork-Jensen J; Brandslund I; Christensen C; Koistinen HA; Doney ASF; Kinnunen L; Esko T; Farmer AJ; Hakaste L; Hodgkiss D; Kravic J; Lyssenko V; Hollensted M; Jørgensen ME; Jørgensen T; Ladenvall C; Justesen JM; Käräjämäki A; Kriebel J; Rathmann W; Lannfelt L; Lauritzen T; Narisu N; Linneberg A; Melander O; Milani L; Neville M; Orho-Melander M; Qi L; Qi Q; Roden M; Rolandsson O; Swift A; Rosengren AH; Stirrups K; Wood AR; Mihailov E; Blancher C; Carneiro MO; Maguire J; Poplin R; Shakir K; Fennell T; DePristo M; de Angelis MH; Deloukas P; Gjesing AP; Jun G; Nilsson P; Murphy J; Onofrio R; Thorand B; Hansen T; Meisinger C; Hu FB; Isomaa B; Karpe F; Liang L; Peters A; Huth C; O'Rahilly SP; Palmer CNA; Pedersen O; Rauramaa R; Tuomilehto J; Salomaa V; Watanabe RM; Syvänen AC; Bergman RN; Bharadwaj D; Bottinger EP; Cho YS; Chandak GR; Chan JCN; Chia KS; Daly MJ; Ebrahim SB; Langenberg C; Elliott P; Jablonski KA; Lehman DM; Jia W; Ma RCW; Pollin TI; Sandhu M; Tandon N; Froguel P; Barroso I; Teo YY; Zeggini E; Loos RJF; Small KS; Ried JS; DeFronzo RA; Grallert H; Glaser B; Metspalu A; Wareham NJ; Walker M; Banks E; Gieger C; Ingelsson E; Im HK; Illig T; Franks PW; Buck G; Trakalo J; Buck D; Prokopenko I; Mägi R; Lind L; Farjoun Y; Owen KR; Gloyn AL; Strauch K; Tuomi T; Kooner JS; Lee JY; Park T; Donnelly P; Morris AD; Hattersley AT; Bowden DW; Collins FS; Atzmon G; Chambers JC; Spector TD; Laakso M; Strom TM; Bell GI; Blangero J; Duggirala R; Tai ES; McVean G; Hanis CL; Wilson JG; Seielstad M; Frayling TM; Meigs JB; Cox NJ; Sladek R; Lander ES; Gabriel S; Burtt NP; Mohlke KL; Meitinger T; Groop L; Abecasis G; Florez JC; Scott LJ; Morris AP; Kang HM; Boehnke M; Altshuler D; McCarthy MI
    Nature; 2016 Aug; 536(7614):41-47. PubMed ID: 27398621
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Advances in the Genetics of Youth-Onset Type 2 Diabetes.
    Todd JN; Srinivasan S; Pollin TI
    Curr Diab Rep; 2018 Jun; 18(8):57. PubMed ID: 29931398
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Increased identification of novel variants in type 2 diabetes, birth weight and their pleiotropic loci.
    Zeng CP; Chen YC; Lin X; Greenbaum J; Chen YP; Peng C; Wang XF; Zhou R; Deng WM; Shen J; Deng HW
    J Diabetes; 2017 Oct; 9(10):898-907. PubMed ID: 27896934
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Whole-exome sequencing in maya indigenous families: variant in PPP1R3A is associated with type 2 diabetes.
    Sánchez-Pozos K; Ortíz-López MG; Peña-Espinoza BI; de Los Ángeles Granados-Silvestre M; Jiménez-Jacinto V; Verleyen J; Tekola-Ayele F; Sanchez-Flores A; Menjivar M
    Mol Genet Genomics; 2018 Oct; 293(5):1205-1216. PubMed ID: 29948331
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The genetic regulatory signature of type 2 diabetes in human skeletal muscle.
    Scott LJ; Erdos MR; Huyghe JR; Welch RP; Beck AT; Wolford BN; Chines PS; Didion JP; Narisu N; Stringham HM; Taylor DL; Jackson AU; Vadlamudi S; Bonnycastle LL; Kinnunen L; Saramies J; Sundvall J; Albanus RD; Kiseleva A; Hensley J; Crawford GE; Jiang H; Wen X; Watanabe RM; Lakka TA; Mohlke KL; Laakso M; Tuomilehto J; Koistinen HA; Boehnke M; Collins FS; Parker SC
    Nat Commun; 2016 Jun; 7():11764. PubMed ID: 27353450
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.
    Wagner MJ
    Pharmacogenomics; 2013 Mar; 14(4):413-24. PubMed ID: 23438888
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Contribution of rare variants in monogenic diabetes-genes to early-onset type 2 diabetes.
    Pezzilli S; Tohidirad M; Biagini T; Scarale MG; Alberico F; Mercuri L; Mannino GC; Garofolo M; Filardi T; Tang Y; Giuffrida F; Mendonca C; Andreozzi F; Baroni MG; Buzzetti R; Cavallo MG; Cossu E; D'Angelo P; De Cosmo S; Lamacchia O; Leonetti F; Morano S; Morviducci L; Penno G; Pozzilli P; Pugliese G; Sesti G; Mazza T; Doria A; Trischitta V; Prudente S
    Diabetes Metab; 2022 Sep; 48(5):101353. PubMed ID: 35487478
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of rare coding variants in 200,000 exome-sequenced subjects reveals novel genetic risk factors for type 2 diabetes.
    Curtis D
    Diabetes Metab Res Rev; 2022 Jan; 38(1):e3482. PubMed ID: 34216101
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.