BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

223 related articles for article (PubMed ID: 36306736)

  • 1. Influences of rare copy-number variation on human complex traits.
    Hujoel MLA; Sherman MA; Barton AR; Mukamel RE; Sankaran VG; Terao C; Loh PR
    Cell; 2022 Oct; 185(22):4233-4248.e27. PubMed ID: 36306736
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Haplotype function score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits.
    Song W; Shi Y; Lin GN
    Elife; 2024 Apr; 12():. PubMed ID: 38639992
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The individual and global impact of copy-number variants on complex human traits.
    Auwerx C; Lepamets M; Sadler MC; Patxot M; Stojanov M; Baud D; Mägi R; ; Porcu E; Reymond A; Kutalik Z
    Am J Hum Genet; 2022 Apr; 109(4):647-668. PubMed ID: 35240056
    [TBL] [Abstract][Full Text] [Related]  

  • 5. BIOFILTER AS A FUNCTIONAL ANNOTATION PIPELINE FOR COMMON AND RARE COPY NUMBER BURDEN.
    Kim D; Lucas A; Glessner J; Verma SS; Bradford Y; Li R; Frase AT; Hakonarson H; Peissig P; Brilliant M; Ritchie MD
    Pac Symp Biocomput; 2016; 21():357-68. PubMed ID: 26776200
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity.
    Shrine N; Tobin MD; Schurmann C; Soler Artigas M; Hui J; Lehtimäki T; Raitakari OT; Pennell CE; Ang QW; Strachan DP; Homuth G; Gläser S; Felix SB; Evans DM; Henderson J; Granell R; Palmer LJ; Huffman J; Hayward C; Scotland G; Malarstig A; Musk B; James AL; ; Wain LV
    BMC Genet; 2016 Aug; 17(1):116. PubMed ID: 27514831
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Copy number polymorphisms and anticancer pharmacogenomics.
    Gamazon ER; Huang RS; Dolan ME; Cox NJ
    Genome Biol; 2011; 12(5):R46. PubMed ID: 21609475
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome-wide CNV analysis reveals variants associated with growth traits in Bos indicus.
    Zhou Y; Utsunomiya YT; Xu L; Hay el HA; Bickhart DM; Alexandre PA; Rosen BD; Schroeder SG; Carvalheiro R; de Rezende Neves HH; Sonstegard TS; Van Tassell CP; Ferraz JB; Fukumasu H; Garcia JF; Liu GE
    BMC Genomics; 2016 Jun; 17():419. PubMed ID: 27245577
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Haplotype phasing and inheritance of copy number variants in nuclear families.
    Palta P; Kaplinski L; Nagirnaja L; Veidenberg A; Möls M; Nelis M; Esko T; Metspalu A; Laan M; Remm M
    PLoS One; 2015; 10(4):e0122713. PubMed ID: 25853576
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.
    Gamazon ER; Nicolae DL; Cox NJ
    PLoS Genet; 2011 Feb; 7(2):e1001292. PubMed ID: 21304891
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.
    Uebe S; Ehrlicher M; Ekici AB; Behrens F; Böhm B; Homuth G; Schurmann C; Völker U; Jünger M; Nauck M; Völzke H; Traupe H; Krawczak M; Burkhardt H; Reis A; Hüffmeier U
    BMC Med Genet; 2017 Aug; 18(1):92. PubMed ID: 28835222
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Genome-wide association analyses of carcass traits using copy number variants and raw intensity values of single nucleotide polymorphisms in cattle.
    Rafter P; Gormley IC; Purfield D; Parnell AC; Naderi S; Berry DP
    BMC Genomics; 2021 Oct; 22(1):757. PubMed ID: 34688258
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tissue-Specific eQTL in Zebrafish.
    Dobrinski KP
    Methods Mol Biol; 2020; 2082():239-249. PubMed ID: 31849020
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. A comprehensive survey of copy number variation in 18 diverse pig populations and identification of candidate copy number variable genes associated with complex traits.
    Chen C; Qiao R; Wei R; Guo Y; Ai H; Ma J; Ren J; Huang L
    BMC Genomics; 2012 Dec; 13():733. PubMed ID: 23270433
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Genome wide CNV analysis reveals additional variants associated with milk production traits in Holsteins.
    Xu L; Cole JB; Bickhart DM; Hou Y; Song J; VanRaden PM; Sonstegard TS; Van Tassell CP; Liu GE
    BMC Genomics; 2014 Aug; 15(1):683. PubMed ID: 25128478
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.