BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 22430448)

  • 1. Role of copy number variants in structural birth defects.
    Southard AE; Edelmann LJ; Gelb BD
    Pediatrics; 2012 Apr; 129(4):755-63. PubMed ID: 22430448
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The impact of human copy number variation on a new era of genetic testing.
    Choy KW; Setlur SR; Lee C; Lau TK
    BJOG; 2010 Mar; 117(4):391-8. PubMed ID: 20105165
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.
    Bruno DL; Ganesamoorthy D; Schoumans J; Bankier A; Coman D; Delatycki M; Gardner RJ; Hunter M; James PA; Kannu P; McGillivray G; Pachter N; Peters H; Rieubland C; Savarirayan R; Scheffer IE; Sheffield L; Tan T; White SM; Yeung A; Bowman Z; Ngo C; Choy KW; Cacheux V; Wong L; Amor DJ; Slater HR
    J Med Genet; 2009 Feb; 46(2):123-31. PubMed ID: 19015223
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection and characterization of copy number variation in autism spectrum disorder.
    Marshall CR; Scherer SW
    Methods Mol Biol; 2012; 838():115-35. PubMed ID: 22228009
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.
    Hochstenbach R; Buizer-Voskamp JE; Vorstman JA; Ophoff RA
    Cytogenet Genome Res; 2011; 135(3-4):174-202. PubMed ID: 22056632
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies.
    Lee AS; Gutiérrez-Arcelus M; Perry GH; Vallender EJ; Johnson WE; Miller GM; Korbel JO; Lee C
    Hum Mol Genet; 2008 Apr; 17(8):1127-36. PubMed ID: 18180252
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Structural variants: changing the landscape of chromosomes and design of disease studies.
    Feuk L; Marshall CR; Wintle RF; Scherer SW
    Hum Mol Genet; 2006 Apr; 15 Spec No 1():R57-66. PubMed ID: 16651370
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomic changes detected by array CGH in human embryos with developmental defects.
    Rajcan-Separovic E; Qiao Y; Tyson C; Harvard C; Fawcett C; Kalousek D; Stephenson M; Philipp T
    Mol Hum Reprod; 2010 Feb; 16(2):125-34. PubMed ID: 19778950
    [TBL] [Abstract][Full Text] [Related]  

  • 10. What have studies of genomic disorders taught us about our genome?
    Simmons AD; Carvalho CM; Lupski JR
    Methods Mol Biol; 2012; 838():1-27. PubMed ID: 22228005
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.
    Cho SC; Yim SH; Yoo HK; Kim MY; Jung GY; Shin GW; Kim BN; Hwang JW; Kang JJ; Kim TM; Chung YJ
    Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome.
    Busse T; Graham JM; Feldman G; Perin J; Catherwood A; Knowlton R; Rappaport EF; Emanuel B; Driscoll DA; Saitta SC
    Hum Mutat; 2011 Jan; 32(1):91-7. PubMed ID: 21120947
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Implications of gene copy-number variation in health and diseases.
    Almal SH; Padh H
    J Hum Genet; 2012 Jan; 57(1):6-13. PubMed ID: 21956041
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
    Geng J; Picker J; Zheng Z; Zhang X; Wang J; Hisama F; Brown DW; Mullen MP; Harris D; Stoler J; Seman A; Miller DT; Fu Q; Roberts AE; Shen Y
    BMC Genomics; 2014 Dec; 15(1):1127. PubMed ID: 25516202
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosome copy number variants in fetuses with syndromic malformations.
    Wang H; Chau MHK; Cao Y; Kwok KY; Choy KW
    Birth Defects Res; 2017 Jun; 109(10):725-733. PubMed ID: 28568742
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comparative analysis of copy number variation in primate genomes.
    Kehrer-Sawatzki H; Cooper DN
    Cytogenet Genome Res; 2008; 123(1-4):288-96. PubMed ID: 19287167
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.
    Striano P; Coppola A; Paravidino R; Malacarne M; Gimelli S; Robbiano A; Traverso M; Pezzella M; Belcastro V; Bianchi A; Elia M; Falace A; Gazzerro E; Ferlazzo E; Freri E; Galasso R; Gobbi G; Molinatto C; Cavani S; Zuffardi O; Striano S; Ferrero GB; Silengo M; Cavaliere ML; Benelli M; Magi A; Piccione M; Dagna Bricarelli F; Coviello DA; Fichera M; Minetti C; Zara F
    Arch Neurol; 2012 Mar; 69(3):322-30. PubMed ID: 22083797
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Interpretation of array comparative genome hybridization data: a major challenge.
    Gijsbers AC; Schoumans J; Ruivenkamp CA
    Cytogenet Genome Res; 2011; 135(3-4):222-7. PubMed ID: 22086107
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Assessment of the role of copy-number variants in 150 patients with congenital heart defects.
    Derwińska K; Bartnik M; Wiśniowiecka-Kowalnik B; Jagła M; Rudziński A; Pietrzyk JJ; Kawalec W; Ziółkowska L; Kutkowska-Kaźmierczak A; Gambin T; Sykulski M; Shaw CA; Gambin A; Mazurczak T; Obersztyn E; Bocian E; Stankiewicz P
    Med Wieku Rozwoj; 2012; 16(3):175-82. PubMed ID: 23378395
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia.
    Poot M; van der Smagt JJ; Brilstra EH; Bourgeron T
    Cytogenet Genome Res; 2011; 135(3-4):228-40. PubMed ID: 22085975
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.