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 *

225 related articles for article (PubMed ID: 18533027)

  • 21. Allele Frequency Changes Provide Evidence for Selection and Identification of Candidate Loci for Survival in Red Clover (
    Ergon Å; Skøt L; Sæther VE; Rognli OA
    Front Plant Sci; 2019; 10():718. PubMed ID: 31244867
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Common genetic variants regulating ADD3 gene expression alter biliary atresia risk.
    Cheng G; Tang CS; Wong EH; Cheng WW; So MT; Miao X; Zhang R; Cui L; Liu X; Ngan ES; Lui VC; Chung PH; Chan IH; Liu J; Zhong W; Xia H; Yu J; Qiu X; Wu XZ; Wang B; Dong X; Tou J; Huang L; Yi B; Ren H; Chan EK; Ye K; O'Reilly PF; Wong KK; Sham PC; Cherny SS; Tam PK; Garcia-Barceló MM
    J Hepatol; 2013 Dec; 59(6):1285-91. PubMed ID: 23872602
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Extreme evolutionary disparities seen in positive selection across seven complex diseases.
    Corona E; Dudley JT; Butte AJ
    PLoS One; 2010 Aug; 5(8):e12236. PubMed ID: 20808933
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic variants associated with complex human diseases show wide variation across multiple populations.
    Adeyemo A; Rotimi C
    Public Health Genomics; 2010; 13(2):72-9. PubMed ID: 19439916
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study.
    Noth I; Zhang Y; Ma SF; Flores C; Barber M; Huang Y; Broderick SM; Wade MS; Hysi P; Scuirba J; Richards TJ; Juan-Guardela BM; Vij R; Han MK; Martinez FJ; Kossen K; Seiwert SD; Christie JD; Nicolae D; Kaminski N; Garcia JGN
    Lancet Respir Med; 2013 Jun; 1(4):309-317. PubMed ID: 24429156
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
    Rivas MA; Avila BE; Koskela J; Huang H; Stevens C; Pirinen M; Haritunians T; Neale BM; Kurki M; Ganna A; Graham D; Glaser B; Peter I; Atzmon G; Barzilai N; Levine AP; Schiff E; Pontikos N; Weisburd B; Lek M; Karczewski KJ; Bloom J; Minikel EV; Petersen BS; Beaugerie L; Seksik P; Cosnes J; Schreiber S; Bokemeyer B; Bethge J; ; ; ; Heap G; Ahmad T; Plagnol V; Segal AW; Targan S; Turner D; Saavalainen P; Farkkila M; Kontula K; Palotie A; Brant SR; Duerr RH; Silverberg MS; Rioux JD; Weersma RK; Franke A; Jostins L; Anderson CA; Barrett JC; MacArthur DG; Jalas C; Sokol H; Xavier RJ; Pulver A; Cho JH; McGovern DPB; Daly MJ
    PLoS Genet; 2018 May; 14(5):e1007329. PubMed ID: 29795570
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Crohn's disease risk alleles on the NOD2 locus have been maintained by natural selection on standing variation.
    Nakagome S; Mano S; Kozlowski L; Bujnicki JM; Shibata H; Fukumaki Y; Kidd JR; Kidd KK; Kawamura S; Oota H
    Mol Biol Evol; 2012 Jun; 29(6):1569-85. PubMed ID: 22319155
    [TBL] [Abstract][Full Text] [Related]  

  • 28. FstSNP-HapMap3: a database of SNPs with high population differentiation for HapMap3.
    Duan S; Zhang W; Cox NJ; Dolan ME
    Bioinformation; 2008; 3(3):139-41. PubMed ID: 19238253
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fine-mapping of 98 obesity loci in Mexican children.
    Liu HY; Alyass A; Abadi A; Peralta-Romero J; Suarez F; Gomez-Zamudio J; Audirac A; Parra EJ; Cruz M; Meyre D
    Int J Obes (Lond); 2019 Jan; 43(1):23-32. PubMed ID: 29769702
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Regional replication of association with refractive error on 15q14 and 15q25 in the Age-Related Eye Disease Study cohort.
    Simpson CL; Wojciechowski R; Yee SS; Soni P; Bailey-Wilson JE; Stambolian D
    Mol Vis; 2013; 19():2173-86. PubMed ID: 24227913
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population.
    Chan M; Ji SM; Liaw CS; Yap YS; Law HY; Yoon CS; Wong CY; Yong WS; Wong NS; Ng R; Ong KW; Madhukumar P; Oey CL; Tan PH; Li HH; Ang P; Ho GH; Lee AS
    Breast Cancer Res Treat; 2012 Nov; 136(1):209-20. PubMed ID: 22965832
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic Basis of Common Human Disease: Insight into the Role of Missense SNPs from Genome-Wide Association Studies.
    Pal LR; Moult J
    J Mol Biol; 2015 Jul; 427(13):2271-89. PubMed ID: 25937569
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genome-wide association analysis and replication of coronary artery disease in South Korea suggests a causal variant common to diverse populations.
    Cho EY; Jang Y; Shin ES; Jang HY; Yoo YK; Kim S; Jang JH; Lee JY; Yun MH; Park MY; Chae JS; Lim JW; Shin DJ; Park S; Lee JH; Han BG; Rae KH; Cardon LR; Morris AP; Lee JE; Clarke GM
    Heart Asia; 2010; 2(1):104-8. PubMed ID: 27325954
    [TBL] [Abstract][Full Text] [Related]  

  • 34. No Evidence for Widespread Positive Selection Signatures in Common Risk Alleles Associated with Schizophrenia.
    Yao Y; Yang J; Xie Y; Liao H; Yang B; Xu Q; Rao S
    Schizophr Bull; 2020 Apr; 46(3):603-611. PubMed ID: 31150552
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Analysis of risk allele frequencies of single nucleotide polymorphisms related to open-angle glaucoma in different ethnic groups.
    Shin HT; Yoon BW; Seo JH
    BMC Med Genomics; 2021 Mar; 14(1):80. PubMed ID: 33726755
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Integrating common and rare genetic variation in diverse human populations.
    ; Altshuler DM; Gibbs RA; Peltonen L; Altshuler DM; Gibbs RA; Peltonen L; Dermitzakis E; Schaffner SF; Yu F; Peltonen L; Dermitzakis E; Bonnen PE; Altshuler DM; Gibbs RA; de Bakker PI; Deloukas P; Gabriel SB; Gwilliam R; Hunt S; Inouye M; Jia X; Palotie A; Parkin M; Whittaker P; Yu F; Chang K; Hawes A; Lewis LR; Ren Y; Wheeler D; Gibbs RA; Muzny DM; Barnes C; Darvishi K; Hurles M; Korn JM; Kristiansson K; Lee C; McCarrol SA; Nemesh J; Dermitzakis E; Keinan A; Montgomery SB; Pollack S; Price AL; Soranzo N; Bonnen PE; Gibbs RA; Gonzaga-Jauregui C; Keinan A; Price AL; Yu F; Anttila V; Brodeur W; Daly MJ; Leslie S; McVean G; Moutsianas L; Nguyen H; Schaffner SF; Zhang Q; Ghori MJ; McGinnis R; McLaren W; Pollack S; Price AL; Schaffner SF; Takeuchi F; Grossman SR; Shlyakhter I; Hostetter EB; Sabeti PC; Adebamowo CA; Foster MW; Gordon DR; Licinio J; Manca MC; Marshall PA; Matsuda I; Ngare D; Wang VO; Reddy D; Rotimi CN; Royal CD; Sharp RR; Zeng C; Brooks LD; McEwen JE
    Nature; 2010 Sep; 467(7311):52-8. PubMed ID: 20811451
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population.
    He M; Bian Z
    PLoS One; 2016; 11(7):e0159940. PubMed ID: 27459192
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Characterization of SNPs associated with prostate cancer in men of Ashkenazic descent from the set of GWAS identified SNPs: impact of cancer family history and cumulative SNP risk prediction.
    Agalliu I; Wang Z; Wang T; Dunn A; Parikh H; Myers T; Burk RD; Amundadottir L
    PLoS One; 2013; 8(4):e60083. PubMed ID: 23573233
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic variation and recent positive selection in worldwide human populations: evidence from nearly 1 million SNPs.
    López Herráez D; Bauchet M; Tang K; Theunert C; Pugach I; Li J; Nandineni MR; Gross A; Scholz M; Stoneking M
    PLoS One; 2009 Nov; 4(11):e7888. PubMed ID: 19924308
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Natural Selection and Functional Potentials of Human Noncoding Elements Revealed by Analysis of Next Generation Sequencing Data.
    Jha P; Lu D; Xu S
    PLoS One; 2015; 10(6):e0129023. PubMed ID: 26053627
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.