BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 30948450)

  • 21. Copy number variations in Friesian horses and genetic risk factors for insect bite hypersensitivity.
    Schurink A; da Silva VH; Velie BD; Dibbits BW; Crooijmans RPMA; Franҫois L; Janssens S; Stinckens A; Blott S; Buys N; Lindgren G; Ducro BJ
    BMC Genet; 2018 Jul; 19(1):49. PubMed ID: 30060732
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A targeted genetic association study of epithelial ovarian cancer susceptibility.
    Earp M; Winham SJ; Larson N; Permuth JB; Sicotte H; Chien J; Anton-Culver H; Bandera EV; Berchuck A; Cook LS; Cramer D; Doherty JA; Goodman MT; Levine DA; Monteiro AN; Ness RB; Pearce CL; Rossing MA; Tworoger SS; Wentzensen N; Bisogna M; Brinton L; Brooks-Wilson A; Carney ME; Cunningham JM; Edwards RP; Fogarty ZC; Iversen ES; Kraft P; Larson MC; Le ND; Lin HY; Lissowska J; Modugno F; Moysich KB; Olson SH; Pike MC; Poole EM; Rider DN; Terry KL; Thompson PJ; van den Berg D; Vierkant RA; Vitonis AF; Wilkens LR; Wu AH; Yang HP; Ziogas A; Phelan CM; Schildkraut JM; Chen YA; Sellers TA; Fridley BL; Goode EL
    Oncotarget; 2016 Feb; 7(7):7381-9. PubMed ID: 26848776
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The distribution and impact of common copy-number variation in the genome of the domesticated apple, Malus x domestica Borkh.
    Boocock J; Chagné D; Merriman TR; Black MA
    BMC Genomics; 2015 Oct; 16():848. PubMed ID: 26493398
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Multisite analysis of high-grade serous epithelial ovarian cancers identifies genomic regions of focal and recurrent copy number alteration in 3q26.2 and 8q24.3.
    Ballabio S; Craparotta I; Paracchini L; Mannarino L; Corso S; Pezzotta MG; Vescio M; Fruscio R; Romualdi C; Dainese E; Ceppi L; Calura E; Pileggi S; Siravegna G; Pattini L; Martini P; Delle Marchette M; Mangioni C; Ardizzoia A; Pellegrino A; Landoni F; D'Incalci M; Beltrame L; Marchini S
    Int J Cancer; 2019 Nov; 145(10):2670-2681. PubMed ID: 30892690
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Common Genetic Variation and Susceptibility to Ovarian Cancer: Current Insights and Future Directions.
    Kar SP; Berchuck A; Gayther SA; Goode EL; Moysich KB; Pearce CL; Ramus SJ; Schildkraut JM; Sellers TA; Pharoah PDP
    Cancer Epidemiol Biomarkers Prev; 2018 Apr; 27(4):395-404. PubMed ID: 28615364
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Epithelial ovarian cancer risk: A review of the current genetic landscape.
    Flaum N; Crosbie EJ; Edmondson RJ; Smith MJ; Evans DG
    Clin Genet; 2020 Jan; 97(1):54-63. PubMed ID: 31099061
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.
    da Silva JM; Giachetto PF; da Silva LO; Cintra LC; Paiva SR; Yamagishi ME; Caetano AR
    BMC Genomics; 2016 Jun; 17():454. PubMed ID: 27297173
    [TBL] [Abstract][Full Text] [Related]  

  • 28. No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort.
    Bagshaw AT; Horwood LJ; Liu Y; Fergusson DM; Sullivan PF; Kennedy MA
    PLoS One; 2013; 8(1):e55208. PubMed ID: 23383111
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Copy number variations in the genome of the Qatari population.
    Fakhro KA; Yousri NA; Rodriguez-Flores JL; Robay A; Staudt MR; Agosto-Perez F; Salit J; Malek JA; Suhre K; Jayyousi A; Zirie M; Stadler D; Mezey JG; Crystal RG
    BMC Genomics; 2015 Oct; 16():834. PubMed ID: 26490036
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The association of copy number variation and percent mammographic density.
    Atkinson EJ; Eckel-Passow JE; Wang A; Greenberg AJ; Scott CG; Pankratz VS; Purrington KN; Sellers TA; Rider DN; Heit JA; de Andrade M; Cunningham JM; Couch FJ; Vachon CM
    BMC Res Notes; 2015 Jul; 8():297. PubMed ID: 26152678
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genome-Wide Detection of CNVs and Their Association with Meat Tenderness in Nelore Cattle.
    Silva VH; Regitano LC; Geistlinger L; Pértille F; Giachetto PF; Brassaloti RA; Morosini NS; Zimmer R; Coutinho LL
    PLoS One; 2016; 11(6):e0157711. PubMed ID: 27348523
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in Koreans.
    Moon S; Keam B; Hwang MY; Lee Y; Park S; Oh JH; Kim YJ; Lee HS; Kim NH; Kim YJ; Kim DH; Han BG; Kim BJ; Lee J
    BMC Musculoskelet Disord; 2015 Apr; 16():76. PubMed ID: 25880085
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genome-wide association study of copy number variations (CNVs) with opioid dependence.
    Li D; Zhao H; Kranzler HR; Li MD; Jensen KP; Zayats T; Farrer LA; Gelernter J
    Neuropsychopharmacology; 2015 Mar; 40(4):1016-26. PubMed ID: 25345593
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility.
    Earp M; Tyrer JP; Winham SJ; Lin HY; Chornokur G; Dennis J; Aben KKH; Anton-Culver H; Antonenkova N; Bandera EV; Bean YT; Beckmann MW; Bjorge L; Bogdanova N; Brinton LA; Brooks-Wilson A; Bruinsma F; Bunker CH; Butzow R; Campbell IG; Carty K; Chang-Claude J; Cook LS; Cramer DW; Cunningham JM; Cybulski C; Dansonka-Mieszkowska A; Despierre E; Doherty JA; Dörk T; du Bois A; Dürst M; Easton DF; Eccles DM; Edwards RP; Ekici AB; Fasching PA; Fridley BL; Gentry-Maharaj A; Giles GG; Glasspool R; Goodman MT; Gronwald J; Harter P; Hein A; Heitz F; Hildebrandt MAT; Hillemanns P; Hogdall CK; Høgdall E; Hosono S; Iversen ES; Jakubowska A; Jensen A; Ji BT; Jung AY; Karlan BY; Kellar M; Kiemeney LA; Kiong Lim B; Kjaer SK; Krakstad C; Kupryjanczyk J; Lambrechts D; Lambrechts S; Le ND; Lele S; Lester J; Levine DA; Li Z; Liang D; Lissowska J; Lu K; Lubinski J; Lundvall L; Massuger LFAG; Matsuo K; McGuire V; McLaughlin JR; McNeish I; Menon U; Milne RL; Modugno F; Moysich KB; Ness RB; Nevanlinna H; Odunsi K; Olson SH; Orlow I; Orsulic S; Paul J; Pejovic T; Pelttari LM; Permuth JB; Pike MC; Poole EM; Rosen B; Rossing MA; Rothstein JH; Runnebaum IB; Rzepecka IK; Schernhammer E; Schwaab I; Shu XO; Shvetsov YB; Siddiqui N; Sieh W; Song H; Southey MC; Spiewankiewicz B; Sucheston-Campbell L; Tangen IL; Teo SH; Terry KL; Thompson PJ; Thomsen L; Tworoger SS; van Altena AM; Vergote I; Vestrheim Thomsen LC; Vierkant RA; Walsh CS; Wang-Gohrke S; Wentzensen N; Whittemore AS; Wicklund KG; Wilkens LR; Woo YL; Wu AH; Wu X; Xiang YB; Yang H; Zheng W; Ziogas A; Lee AW; Pearce CL; Berchuck A; Schildkraut JM; Ramus SJ; Monteiro ANA; Narod SA; Sellers TA; Gayther SA; Kelemen LE; Chenevix-Trench G; Risch HA; Pharoah PDP; Goode EL; Phelan CM
    PLoS One; 2018; 13(7):e0197561. PubMed ID: 29979793
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries.
    Costain G; Lionel AC; Ogura L; Marshall CR; Scherer SW; Silversides CK; Bassett AS
    Int J Cardiol; 2016 Feb; 204():115-21. PubMed ID: 26655555
    [TBL] [Abstract][Full Text] [Related]  

  • 36. No association between general cognitive ability and rare copy number variation.
    McRae AF; Wright MJ; Hansell NK; Montgomery GW; Martin NG
    Behav Genet; 2013 May; 43(3):202-7. PubMed ID: 23417127
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Association of Copy Number Variation Signature and Survival in Patients With Serous Ovarian Cancer.
    Graf RP; Eskander R; Brueggeman L; Stupack DG
    JAMA Netw Open; 2021 Jun; 4(6):e2114162. PubMed ID: 34181012
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genome-wide identification of copy number variations in Holstein cattle from Baja California, Mexico, using high-density SNP genotyping arrays.
    Salomón-Torres R; González-Vizcarra VM; Medina-Basulto GE; Montaño-Gómez MF; Mahadevan P; Yaurima-Basaldúa VH; Villa-Angulo C; Villa-Angulo R
    Genet Mol Res; 2015 Oct; 14(4):11848-59. PubMed ID: 26436509
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
    Bergen SE; Ploner A; Howrigan D; ; O'Donovan MC; Smoller JW; Sullivan PF; Sebat J; Neale B; Kendler KS
    Am J Psychiatry; 2019 Jan; 176(1):29-35. PubMed ID: 30392412
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Large common deletions associate with mortality at old age.
    Kuningas M; Estrada K; Hsu YH; Nandakumar K; Uitterlinden AG; Lunetta KL; van Duijn CM; Karasik D; Hofman A; Murabito J; Rivadeneira F; Kiel DP; Tiemeier H
    Hum Mol Genet; 2011 Nov; 20(21):4290-6. PubMed ID: 21835882
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.