BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 30642840)

  • 1. Targeted Resequencing of the Coding Sequence of 38 Genes Near Breast Cancer GWAS Loci in a Large Case-Control Study.
    Decker B; Allen J; Luccarini C; Pooley KA; Shah M; Bolla MK; Wang Q; Ahmed S; Baynes C; Conroy DM; Brown J; Luben R; Ostrander EA; Pharoah PDP; Dunning AM; Easton DF
    Cancer Epidemiol Biomarkers Prev; 2019 Apr; 28(4):822-825. PubMed ID: 30642840
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare coding variants and breast cancer risk: evaluation of susceptibility Loci identified in genome-wide association studies.
    Zhang Y; Long J; Lu W; Shu XO; Cai Q; Zheng Y; Li C; Li B; Gao YT; Zheng W
    Cancer Epidemiol Biomarkers Prev; 2014 Apr; 23(4):622-8. PubMed ID: 24470074
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Fine mapping of breast cancer genome-wide association studies loci in women of African ancestry identifies novel susceptibility markers.
    Zheng Y; Ogundiran TO; Falusi AG; Nathanson KL; John EM; Hennis AJ; Ambs S; Domchek SM; Rebbeck TR; Simon MS; Nemesure B; Wu SY; Leske MC; Odetunde A; Niu Q; Zhang J; Afolabi C; Gamazon ER; Cox NJ; Olopade CO; Olopade OI; Huo D
    Carcinogenesis; 2013 Jul; 34(7):1520-8. PubMed ID: 23475944
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of breast cancer associated variants that modulate transcription factor binding.
    Liu Y; Walavalkar NM; Dozmorov MG; Rich SS; Civelek M; Guertin MJ
    PLoS Genet; 2017 Sep; 13(9):e1006761. PubMed ID: 28957321
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare Coding Variants Associated with Breast Cancer.
    Han MR
    Adv Exp Med Biol; 2021; 1187():435-453. PubMed ID: 33983593
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population.
    Low SK; Chin YM; Ito H; Matsuo K; Tanikawa C; Matsuda K; Saito H; Sakurai-Yageta M; Nakaya N; Shimizu A; Nishizuka SS; Yamaji T; Sawada N; Iwasaki M; Tsugane S; Takezaki T; Suzuki S; Naito M; Wakai K; Kamatani Y; Momozawa Y; Murakami Y; Inazawa J; Nakamura Y; Kubo M; Katagiri T; Miki Y
    Sci Rep; 2019 Nov; 9(1):17332. PubMed ID: 31757997
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trans-ethnic follow-up of breast cancer GWAS hits using the preferential linkage disequilibrium approach.
    Zhu Q; Shepherd L; Lunetta KL; Yao S; Liu Q; Hu Q; Haddad SA; Sucheston-Campbell L; Bensen JT; Bandera EV; Rosenberg L; Liu S; Haiman CA; Olshan AF; Palmer JR; Ambrosone CB
    Oncotarget; 2016 Dec; 7(50):83160-83176. PubMed ID: 27825120
    [TBL] [Abstract][Full Text] [Related]  

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

  • 10. A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study.
    Kim HC; Lee JY; Sung H; Choi JY; Park SK; Lee KM; Kim YJ; Go MJ; Li L; Cho YS; Park M; Kim DJ; Oh JH; Kim JW; Jeon JP; Jeon SY; Min H; Kim HM; Park J; Yoo KY; Noh DY; Ahn SH; Lee MH; Kim SW; Lee JW; Park BW; Park WY; Kim EH; Kim MK; Han W; Lee SA; Matsuo K; Shen CY; Wu PE; Hsiung CN; Lee JY; Kim HL; Han BG; Kang D
    Breast Cancer Res; 2012 Mar; 14(2):R56. PubMed ID: 22452962
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Targeted exon sequencing fails to identify rare coding variants with large effect in rheumatoid arthritis.
    Bang SY; Na YJ; Kim K; Joo YB; Park Y; Lee J; Lee SY; Ansari AA; Jung J; Rhee H; Lee JY; Han BG; Ahn SM; Won S; Lee HS; Bae SC
    Arthritis Res Ther; 2014 Sep; 16(5):447. PubMed ID: 25267259
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Computational Analysis of Breast Cancer GWAS Loci Identifies the Putative Deleterious Effect of STXBP4 and ZNF404 Gene Variants.
    Masoodi TA; Banaganapalli B; Vaidyanathan V; Talluri VR; Shaik NA
    J Cell Biochem; 2017 Dec; 118(12):4296-4307. PubMed ID: 28422318
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mining the LIPG allelic spectrum reveals the contribution of rare and common regulatory variants to HDL cholesterol.
    Khetarpal SA; Edmondson AC; Raghavan A; Neeli H; Jin W; Badellino KO; Demissie S; Manning AK; DerOhannessian SL; Wolfe ML; Cupples LA; Li M; Kathiresan S; Rader DJ
    PLoS Genet; 2011 Dec; 7(12):e1002393. PubMed ID: 22174694
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Negligible impact of rare autoimmune-locus coding-region variants on missing heritability.
    Hunt KA; Mistry V; Bockett NA; Ahmad T; Ban M; Barker JN; Barrett JC; Blackburn H; Brand O; Burren O; Capon F; Compston A; Gough SC; Jostins L; Kong Y; Lee JC; Lek M; MacArthur DG; Mansfield JC; Mathew CG; Mein CA; Mirza M; Nutland S; Onengut-Gumuscu S; Papouli E; Parkes M; Rich SS; Sawcer S; Satsangi J; Simmonds MJ; Trembath RC; Walker NM; Wozniak E; Todd JA; Simpson MA; Plagnol V; van Heel DA
    Nature; 2013 Jun; 498(7453):232-5. PubMed ID: 23698362
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two-phase designs to follow-up genome-wide association signals with DNA resequencing studies.
    Schaid DJ; Jenkins GD; Ingle JN; Weinshilboum RM
    Genet Epidemiol; 2013 Apr; 37(3):229-38. PubMed ID: 23348637
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Replication of genome-wide discovered breast cancer risk loci in the Cypriot population.
    Loizidou MA; Hadjisavvas A; Ioannidis JP; Kyriacou K
    Breast Cancer Res Treat; 2011 Jul; 128(1):267-72. PubMed ID: 21210208
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Weighting sequence variants based on their annotation increases the power of genome-wide association studies in dairy cattle.
    Cai Z; Guldbrandtsen B; Lund MS; Sahana G
    Genet Sel Evol; 2019 May; 51(1):20. PubMed ID: 31077144
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Large-Scale, Exome-Wide Association Study of Han Chinese Women Identifies Three Novel Loci Predisposing to Breast Cancer.
    Zhang B; Chen MY; Shen YJ; Zhuo XB; Gao P; Zhou FS; Liang B; Zu J; Zhang Q; Suleman S; Xu YH; Xu MG; Xu JK; Liu CC; Giannareas N; Xia JH; Zhao Y; Huang ZL; Yang Z; Cheng HD; Li N; Hong YY; Li W; Zhang MJ; Yu KD; Li G; Sun MH; Chen ZD; Wei GH; Shao ZM
    Cancer Res; 2018 Jun; 78(11):3087-3097. PubMed ID: 29572226
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci.
    Hamdi Y; Ben Rekaya M; Jingxuan S; Nagara M; Messaoud O; Benammar Elgaaied A; Mrad R; Chouchane L; Boubaker MS; Abdelhak S; Boussen H; Romdhane L
    BMC Cancer; 2018 Dec; 18(1):1295. PubMed ID: 30594178
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.