BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

418 related articles for article (PubMed ID: 28527622)

  • 21. Candidate predisposing germline copy number variants in early onset colorectal cancer patients.
    Brea-Fernandez AJ; Fernandez-Rozadilla C; Alvarez-Barona M; Azuara D; Ginesta MM; Clofent J; de Castro L; Gonzalez D; Andreu M; Bessa X; Llor X; Xicola R; Jover R; Castells A; Castellvi-Bel S; Capella G; Carracedo A; Ruiz-Ponte C
    Clin Transl Oncol; 2017 May; 19(5):625-632. PubMed ID: 27888432
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A Genome-Wide Association Study to Identify Potential Germline Copy Number Variants for Sporadic Breast Cancer Susceptibility.
    Sapkota Y; Narasimhan A; Kumaran M; Sehrawat BS; Damaraju S
    Cytogenet Genome Res; 2016; 149(3):156-164. PubMed ID: 27668787
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Novel association strategy with copy number variation for identifying new risk Loci of human diseases.
    Chen X; Li X; Wang P; Liu Y; Zhang Z; Zhao G; Xu H; Zhu J; Qin X; Chen S; Hu L; Kong X
    PLoS One; 2010 Aug; 5(8):e12185. PubMed ID: 20808825
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
    Marshall CR; Howrigan DP; Merico D; Thiruvahindrapuram B; Wu W; Greer DS; Antaki D; Shetty A; Holmans PA; Pinto D; Gujral M; Brandler WM; Malhotra D; Wang Z; Fajarado KVF; Maile MS; Ripke S; Agartz I; Albus M; Alexander M; Amin F; Atkins J; Bacanu SA; Belliveau RA; Bergen SE; Bertalan M; Bevilacqua E; Bigdeli TB; Black DW; Bruggeman R; Buccola NG; Buckner RL; Bulik-Sullivan B; Byerley W; Cahn W; Cai G; Cairns MJ; Campion D; Cantor RM; Carr VJ; Carrera N; Catts SV; Chambert KD; Cheng W; Cloninger CR; Cohen D; Cormican P; Craddock N; Crespo-Facorro B; Crowley JJ; Curtis D; Davidson M; Davis KL; Degenhardt F; Del Favero J; DeLisi LE; Dikeos D; Dinan T; Djurovic S; Donohoe G; Drapeau E; Duan J; Dudbridge F; Eichhammer P; Eriksson J; Escott-Price V; Essioux L; Fanous AH; Farh KH; Farrell MS; Frank J; Franke L; Freedman R; Freimer NB; Friedman JI; Forstner AJ; Fromer M; Genovese G; Georgieva L; Gershon ES; Giegling I; Giusti-Rodríguez P; Godard S; Goldstein JI; Gratten J; de Haan L; Hamshere ML; Hansen M; Hansen T; Haroutunian V; Hartmann AM; Henskens FA; Herms S; Hirschhorn JN; Hoffmann P; Hofman A; Huang H; Ikeda M; Joa I; Kähler AK; Kahn RS; Kalaydjieva L; Karjalainen J; Kavanagh D; Keller MC; Kelly BJ; Kennedy JL; Kim Y; Knowles JA; Konte B; Laurent C; Lee P; Lee SH; Legge SE; Lerer B; Levy DL; Liang KY; Lieberman J; Lönnqvist J; Loughland CM; Magnusson PKE; Maher BS; Maier W; Mallet J; Mattheisen M; Mattingsdal M; McCarley RW; McDonald C; McIntosh AM; Meier S; Meijer CJ; Melle I; Mesholam-Gately RI; Metspalu A; Michie PT; Milani L; Milanova V; Mokrab Y; Morris DW; Müller-Myhsok B; Murphy KC; Murray RM; Myin-Germeys I; Nenadic I; Nertney DA; Nestadt G; Nicodemus KK; Nisenbaum L; Nordin A; O'Callaghan E; O'Dushlaine C; Oh SY; Olincy A; Olsen L; O'Neill FA; Van Os J; Pantelis C; Papadimitriou GN; Parkhomenko E; Pato MT; Paunio T; ; Perkins DO; Pers TH; Pietiläinen O; Pimm J; Pocklington AJ; Powell J; Price A; Pulver AE; Purcell SM; Quested D; Rasmussen HB; Reichenberg A; Reimers MA; Richards AL; Roffman JL; Roussos P; Ruderfer DM; Salomaa V; Sanders AR; Savitz A; Schall U; Schulze TG; Schwab SG; Scolnick EM; Scott RJ; Seidman LJ; Shi J; Silverman JM; Smoller JW; Söderman E; Spencer CCA; Stahl EA; Strengman E; Strohmaier J; Stroup TS; Suvisaari J; Svrakic DM; Szatkiewicz JP; Thirumalai S; Tooney PA; Veijola J; Visscher PM; Waddington J; Walsh D; Webb BT; Weiser M; Wildenauer DB; Williams NM; Williams S; Witt SH; Wolen AR; Wormley BK; Wray NR; Wu JQ; Zai CC; Adolfsson R; Andreassen OA; Blackwood DHR; Bramon E; Buxbaum JD; Cichon S; Collier DA; Corvin A; Daly MJ; Darvasi A; Domenici E; Esko T; Gejman PV; Gill M; Gurling H; Hultman CM; Iwata N; Jablensky AV; Jönsson EG; Kendler KS; Kirov G; Knight J; Levinson DF; Li QS; McCarroll SA; McQuillin A; Moran JL; Mowry BJ; Nöthen MM; Ophoff RA; Owen MJ; Palotie A; Pato CN; Petryshen TL; Posthuma D; Rietschel M; Riley BP; Rujescu D; Sklar P; St Clair D; Walters JTR; Werge T; Sullivan PF; O'Donovan MC; Scherer SW; Neale BM; Sebat J;
    Nat Genet; 2017 Jan; 49(1):27-35. PubMed ID: 27869829
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Expression patterns of candidate susceptibility genes HNF1β and CtBP2 in prostate cancer: association with tumor progression.
    Debiais-Delpech C; Godet J; Pedretti N; Bernard FX; Irani J; Cathelineau X; Cussenot O; Fromont G
    Urol Oncol; 2014 May; 32(4):426-32. PubMed ID: 24332637
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genome-wide Association Study (GWAS) of Germline Copy Number Variations (CNVs) Reveal Genetic Risks of Prostate Cancer in Chinese population.
    Wu Y; Chen H; Jiang G; Mo Z; Ye D; Wang M; Qi J; Lin X; Zheng SL; Zhang N; Na R; Ding Q; Xu J; Sun Y
    J Cancer; 2018; 9(5):923-928. PubMed ID: 29581771
    [No Abstract]   [Full Text] [Related]  

  • 27. Copy number variation in Fayoumi and Leghorn chickens analyzed using array comparative genomic hybridization.
    Abernathy J; Li X; Jia X; Chou W; Lamont SJ; Crooijmans R; Zhou H
    Anim Genet; 2014 Jun; 45(3):400-11. PubMed ID: 24628374
    [TBL] [Abstract][Full Text] [Related]  

  • 28. ABCC4 copy number variation is associated with susceptibility to esophageal squamous cell carcinoma.
    Sun Y; Shi N; Lu H; Zhang J; Ma Y; Qiao Y; Mao Y; Jia K; Han L; Liu F; Li H; Lin Z; Li X; Zhao X
    Carcinogenesis; 2014 Sep; 35(9):1941-50. PubMed ID: 24510239
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genome-wide copy number analysis in a family with p.G533C RET mutation and medullary thyroid carcinoma identified regions potentially associated with a higher predisposition to lymph node metastasis.
    Araujo AN; Moraes L; França MI; Hakonarson H; Li J; Pellegrino R; Maciel RM; Cerutti JM
    J Clin Endocrinol Metab; 2014 Jun; 99(6):E1104-12. PubMed ID: 24601688
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic predisposition in degenerative lumbar scoliosis due to the copy number variation.
    Shin JH; Ha KY; Jung SH; Chung YJ
    Spine (Phila Pa 1976); 2011 Oct; 36(21):1782-93. PubMed ID: 21587107
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Integrated Genome-Wide Analysis of Gene Expression and DNA Copy Number Variations Highlights Stem Cell-Related Pathways in Small Cell Esophageal Carcinoma.
    Liu D; Xu X; Wen J; Xie L; Zhang J; Shen Y; Jiang G; Chen J; Fan M
    Stem Cells Int; 2018; 2018():3481783. PubMed ID: 30228821
    [No Abstract]   [Full Text] [Related]  

  • 32. Genome-wide association study of prostate cancer mortality.
    Penney KL; Pyne S; Schumacher FR; Sinnott JA; Mucci LA; Kraft PL; Ma J; Oh WK; Kurth T; Kantoff PW; Giovannucci EL; Stampfer MJ; Hunter DJ; Freedman ML
    Cancer Epidemiol Biomarkers Prev; 2010 Nov; 19(11):2869-76. PubMed ID: 20978177
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genome-wide copy-number variation analysis identifies common genetic variants at 20p13 associated with aggressiveness of prostate cancer.
    Jin G; Sun J; Liu W; Zhang Z; Chu LW; Kim ST; Sun J; Feng J; Duggan D; Carpten JD; Wiklund F; Grönberg H; Isaacs WB; Zheng SL; Xu J
    Carcinogenesis; 2011 Jul; 32(7):1057-62. PubMed ID: 21551127
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Understanding the impact of 1q21.1 copy number variant.
    Harvard C; Strong E; Mercier E; Colnaghi R; Alcantara D; Chow E; Martell S; Tyson C; Hrynchak M; McGillivray B; Hamilton S; Marles S; Mhanni A; Dawson AJ; Pavlidis P; Qiao Y; Holden JJ; Lewis SM; O'Driscoll M; Rajcan-Separovic E
    Orphanet J Rare Dis; 2011 Aug; 6():54. PubMed ID: 21824431
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genome-Wide Detection of Copy Number Variations in Unsolved Inherited Retinal Disease.
    Huang XF; Mao JY; Huang ZQ; Rao FQ; Cheng FF; Li FF; Wang QF; Jin ZB
    Invest Ophthalmol Vis Sci; 2017 Jan; 58(1):424-429. PubMed ID: 28118666
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Validation of copy number variants associated with prostate cancer risk and prognosis.
    Blackburn A; Wilson D; Gelfond J; Yao L; Hernandez J; Thompson IM; Leach RJ; Lehman DM
    Urol Oncol; 2014 Jan; 32(1):44.e15-44.e20. PubMed ID: 24054869
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic variations in UGT2B28, UGT2B17, UGT2B15 genes and the risk of prostate cancer: A case-control study.
    Habibi M; Mirfakhraie R; Khani M; Rakhshan A; Azargashb E; Pouresmaeili F
    Gene; 2017 Nov; 634():47-52. PubMed ID: 28882566
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A gender-specific association of CNV at 6p21.3 with NPC susceptibility.
    Tse KP; Su WH; Yang ML; Cheng HY; Tsang NM; Chang KP; Hao SP; Yao Shugart Y; Chang YS
    Hum Mol Genet; 2011 Jul; 20(14):2889-96. PubMed ID: 21536588
    [TBL] [Abstract][Full Text] [Related]  

  • 39. High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts.
    Murthy MN; Veerappa AM; Seshachalam KB; Ramachandra NB
    Neurol Res; 2016 Sep; 38(9):775-85. PubMed ID: 27399248
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Copy number variation analysis reveals additional variants contributing to endometriosis development.
    Mafra F; Mazzotti D; Pellegrino R; Bianco B; Barbosa CP; Hakonarson H; Christofolini D
    J Assist Reprod Genet; 2017 Jan; 34(1):117-124. PubMed ID: 27817035
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.