BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 22384383)

  • 21. Genome-wide copy number variant discovery in dogs using the CanineHD genotyping array.
    Molin AM; Berglund J; Webster MT; Lindblad-Toh K
    BMC Genomics; 2014 Mar; 15():210. PubMed ID: 24640994
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease.
    Hu X; Pickering E; Liu YC; Hall S; Fournier H; Katz E; Dechairo B; John S; Van Eerdewegh P; Soares H;
    PLoS One; 2011 Feb; 6(2):e16616. PubMed ID: 21390209
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
    Williams NM; Zaharieva I; Martin A; Langley K; Mantripragada K; Fossdal R; Stefansson H; Stefansson K; Magnusson P; Gudmundsson OO; Gustafsson O; Holmans P; Owen MJ; O'Donovan M; Thapar A
    Lancet; 2010 Oct; 376(9750):1401-8. PubMed ID: 20888040
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The 15q11.2 BP1-BP2 Microdeletion (
    Rafi SK; Butler MG
    Int J Mol Sci; 2020 May; 21(9):. PubMed ID: 32384786
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genome-wide copy-number variation study of psychosis in Alzheimer's disease.
    Zheng X; Demirci FY; Barmada MM; Richardson GA; Lopez OL; Sweet RA; Kamboh MI; Feingold E
    Transl Psychiatry; 2015 Jun; 5(6):e574. PubMed ID: 26035058
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Inference of Causative Genes for Alzheimer's Disease Due to Dosage Imbalance.
    Sekine M; Makino T
    Mol Biol Evol; 2017 Sep; 34(9):2396-2407. PubMed ID: 28666362
    [TBL] [Abstract][Full Text] [Related]  

  • 27. CNV Concordance in 1,097 MZ Twin Pairs.
    Abdellaoui A; Ehli EA; Hottenga JJ; Weber Z; Mbarek H; Willemsen G; van Beijsterveldt T; Brooks A; Hudziak JJ; Sullivan PF; de Geus EJ; Davies GE; Boomsma DI
    Twin Res Hum Genet; 2015 Feb; 18(1):1-12. PubMed ID: 25578775
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.
    Degenhardt F; Priebe L; Herms S; Mattheisen M; Mühleisen TW; Meier S; Moebus S; Strohmaier J; Groß M; Breuer R; Lange C; Hoffmann P; Meyer-Lindenberg A; Heinz A; Walter H; Lucae S; Wolf C; Müller-Myhsok B; Holsboer F; Maier W; Rietschel M; Nöthen MM; Cichon S
    Am J Med Genet B Neuropsychiatr Genet; 2012 Apr; 159B(3):263-73. PubMed ID: 22344817
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Ohnologs are overrepresented in pathogenic copy number mutations.
    McLysaght A; Makino T; Grayton HM; Tropeano M; Mitchell KJ; Vassos E; Collier DA
    Proc Natl Acad Sci U S A; 2014 Jan; 111(1):361-6. PubMed ID: 24368850
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Endometriosis is associated with rare copy number variants.
    Chettier R; Ward K; Albertsen HM
    PLoS One; 2014; 9(8):e103968. PubMed ID: 25083881
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.
    Swaminathan S; Huentelman MJ; Corneveaux JJ; Myers AJ; Faber KM; Foroud T; Mayeux R; Shen L; Kim S; Turk M; Hardy J; Reiman EM; Saykin AJ;
    PLoS One; 2012; 7(12):e50640. PubMed ID: 23227193
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families.
    AlAyadhi LY; Hashmi JA; Iqbal M; Albalawi AM; Samman MI; Elamin NE; Bashir S; Basit S
    Neuroscience; 2016 Dec; 339():561-570. PubMed ID: 27771533
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjects.
    de Jesús Ascencio-Montiel I; Pinto D; Parra EJ; Valladares-Salgado A; Cruz M; Scherer SW
    Sci Rep; 2017 Dec; 7(1):17105. PubMed ID: 29213072
    [TBL] [Abstract][Full Text] [Related]  

  • 35. CNV-RF Is a Random Forest-Based Copy Number Variation Detection Method Using Next-Generation Sequencing.
    Onsongo G; Baughn LB; Bower M; Henzler C; Schomaker M; Silverstein KA; Thyagarajan B
    J Mol Diagn; 2016 Nov; 18(6):872-881. PubMed ID: 27597741
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Copy number variation associates with mortality in long-lived individuals: a genome-wide assessment.
    Nygaard M; Debrabant B; Tan Q; Deelen J; Andersen-Ranberg K; de Craen AJ; Beekman M; Jeune B; Slagboom PE; Christensen K; Christiansen L
    Aging Cell; 2016 Feb; 15(1):49-55. PubMed ID: 26446717
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
    Blauw HM; Al-Chalabi A; Andersen PM; van Vught PW; Diekstra FP; van Es MA; Saris CG; Groen EJ; van Rheenen W; Koppers M; Van't Slot R; Strengman E; Estrada K; Rivadeneira F; Hofman A; Uitterlinden AG; Kiemeney LA; Vermeulen SH; Birve A; Waibel S; Meyer T; Cronin S; McLaughlin RL; Hardiman O; Sapp PC; Tobin MD; Wain LV; Tomik B; Slowik A; Lemmens R; Rujescu D; Schulte C; Gasser T; Brown RH; Landers JE; Robberecht W; Ludolph AC; Ophoff RA; Veldink JH; van den Berg LH
    Hum Mol Genet; 2010 Oct; 19(20):4091-9. PubMed ID: 20685689
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prioritization of Copy Number Variation Loci Associated with Autism from AutDB-An Integrative Multi-Study Genetic Database.
    Menashe I; Larsen EC; Banerjee-Basu S
    PLoS One; 2013; 8(6):e66707. PubMed ID: 23825557
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Copy Number Variation Identification on 3,800 Alzheimer's Disease Whole Genome Sequencing Data from the Alzheimer's Disease Sequencing Project.
    Lee WP; Tucci AA; Conery M; Leung YY; Kuzma AB; Valladares O; Chou YF; Lu W; Wang LS; Schellenberg GD; Tzeng JY
    Front Genet; 2021; 12():752390. PubMed ID: 34804120
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle.
    Rafter P; Gormley IC; Parnell AC; Kearney JF; Berry DP
    BMC Genomics; 2020 Mar; 21(1):205. PubMed ID: 32131735
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.