BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 25578402)

  • 1. Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays.
    Veerappa AM; Lingaiah K; Vishweswaraiah S; Murthy MN; Suresh RV; Manjegowda DS; Ramachandra NB
    Genet Res (Camb); 2014 Dec; 96():e17. PubMed ID: 25578402
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.
    Haraksingh RR; Abyzov A; Gerstein M; Urban AE; Snyder M
    PLoS One; 2011; 6(11):e27859. PubMed ID: 22140474
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.
    Veerappa AM; Suresh RV; Vishweswaraiah S; Lingaiah K; Murthy M; Manjegowda DS; Padakannaya P; Ramachandra NB
    Genet Res (Camb); 2015 Sep; 97():e18. PubMed ID: 26390810
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans.
    Haraksingh RR; Abyzov A; Urban AE
    BMC Genomics; 2017 Apr; 18(1):321. PubMed ID: 28438122
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
    D'Amours G; Langlois M; Mathonnet G; Fetni R; Nizard S; Srour M; Tihy F; Phillips MS; Michaud JL; Lemyre E
    BMC Med Genomics; 2014 Dec; 7():70. PubMed ID: 25539807
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
    Sokolowski M; Wasserman J; Wasserman D
    PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.
    Komura D; Shen F; Ishikawa S; Fitch KR; Chen W; Zhang J; Liu G; Ihara S; Nakamura H; Hurles ME; Lee C; Scherer SW; Jones KW; Shapero MH; Huang J; Aburatani H
    Genome Res; 2006 Dec; 16(12):1575-84. PubMed ID: 17122084
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation of copy number variation detection for a SNP array platform.
    Zhang X; Du R; Li S; Zhang F; Jin L; Wang H
    BMC Bioinformatics; 2014 Feb; 15():50. PubMed ID: 24555668
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Origins and functional impact of copy number variation in the human genome.
    Conrad DF; Pinto D; Redon R; Feuk L; Gokcumen O; Zhang Y; Aerts J; Andrews TD; Barnes C; Campbell P; Fitzgerald T; Hu M; Ihm CH; Kristiansson K; Macarthur DG; Macdonald JR; Onyiah I; Pang AW; Robson S; Stirrups K; Valsesia A; Walter K; Wei J; ; Tyler-Smith C; Carter NP; Lee C; Scherer SW; Hurles ME
    Nature; 2010 Apr; 464(7289):704-12. PubMed ID: 19812545
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Exploiting sequence similarity to validate the sensitivity of SNP arrays in detecting fine-scaled copy number variations.
    Wong G; Leckie C; Gorringe KL; Haviv I; Campbell IG; Kowalczyk A
    Bioinformatics; 2010 Apr; 26(8):1007-14. PubMed ID: 20189937
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inter- and intra-breed genome-wide copy number diversity in a large cohort of European equine breeds.
    Solé M; Ablondi M; Binzer-Panchal A; Velie BD; Hollfelder N; Buys N; Ducro BJ; François L; Janssens S; Schurink A; Viklund Å; Eriksson S; Isaksson A; Kultima H; Mikko S; Lindgren G
    BMC Genomics; 2019 Oct; 20(1):759. PubMed ID: 31640551
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort.
    Valsesia A; Stevenson BJ; Waterworth D; Mooser V; Vollenweider P; Waeber G; Jongeneel CV; Beckmann JS; Kutalik Z; Bergmann S
    BMC Genomics; 2012 Jun; 13():241. PubMed ID: 22702538
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
    Liu J; Zhou Y; Liu S; Song X; Yang XZ; Fan Y; Chen W; Akdemir ZC; Yan Z; Zuo Y; Du R; Liu Z; Yuan B; Zhao S; Liu G; Chen Y; Zhao Y; Lin M; Zhu Q; Niu Y; Liu P; Ikegawa S; Song YQ; Posey JE; Qiu G; ; Zhang F; Wu Z; Lupski JR; Wu N
    Hum Genet; 2018 Jul; 137(6-7):553-567. PubMed ID: 30019117
    [TBL] [Abstract][Full Text] [Related]  

  • 18. CNVmap: A Method and Software To Detect and Map Copy Number Variants from Segregation Data.
    Falque M; Jebreen K; Paux E; Knaak C; Mezmouk S; Martin OC
    Genetics; 2020 Mar; 214(3):561-576. PubMed ID: 31882400
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression.
    Veerappa AM; Murthy MN; Vishweswaraiah S; Lingaiah K; Suresh RV; Nachappa SA; Prashali N; Yadav SN; Srikanta MA; Manjegowda DS; Seshachalam KB; Ramachandra NB
    PLoS One; 2014; 9(2):e90391. PubMed ID: 24587348
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Copy number variations and stroke.
    Colaianni V; Mazzei R; Cavallaro S
    Neurol Sci; 2016 Dec; 37(12):1895-1904. PubMed ID: 27393281
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.