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next-era DNA sequencing identifies novel gene variations and pathways involved in inevitable language impairment | 920-173 real Questions and VCE exercise Test

  • 1.

    Norbury, C. F. et al. The acquire an sequel on of nonverbal capability on incidence and scientific presentation of language disorder: facts from a inhabitants analyze. J child Psychol Psychiatry 57, 1247–1257, doi: 10.1111/jcpp.12573 (2016).

  • 2.

    Tomblin, J. B., statistics, N. L. & Zhang, X. A paraphernalia for the prognosis of inevitable language impairment in kindergarten babies. J Speech Hear Res 39, 1284–1294 (1996).

  • 3.

    Bishop, D. V., North, T. & Donlan, C. Genetic basis of selected language impairment: facts from a twin witness at. Dev Med child Neurol 37, fifty six–seventy one (1995).

  • four.

    Newbury, D. F., Fisher, S. E. & Monaco, A. P. recent advances within the genetics of language impairment. Genome Med 2, 6, doi: 10.1186/gm127 (2010).

  • 5.

    Evans, P. D., Mueller, okay. L., Gamazon, E. R., Cox, N. J. & Tomblin, J. B. A genome-extensive sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13. Genes repartee Behav 14, 387–397, doi: 10.1111/gbb.12223 (2015).

  • 6.

    Bartlett, C. W. et al. an incredible susceptibility locus for particular language impairment is located on 13q21. Am J Hum Genet seventy one, forty five–55 (2002).

  • 7.

    SLIC. A genomewide scan identifies two novel loci concerned in particular Language Impairment. Am J Hum Genet 70, 384–398 (2002).

  • eight.

    Smith, S. D., Kimberling, W. J., Pennington, B. F. & Lubs, H. A. specific analyzing incapacity: identification of an inherited form through linkage evaluation. Science 219, 1345–1347 (1983).

  • 9.

    Cardon, L. R. et al. Quantitative trait locus for reading disability on chromosome 6. Science 266, 276–279 (1994).

  • 10.

    Fagerheim, T. et al. a new gene (DYX3) for dyslexia is located on chromosome 2. J Med Genet 36, 664–669 (1999).

  • 11.

    Nopola-Hemmi, J. et al. A paramount gene for developmental dyslexia on chromosome three. J Med Genet 38, 658–664 (2001).

  • 12.

    Fisher, S. E. et al. unbiased genome-large scans establish a chromosome 18 quantitative-trait locus influencing dyslexia. Nat Genet 30, 86–91 (2002).

  • 13.

    Hsiung, G. Y., Kaplan, B. J., Petryshen, T. L., Lu, S. & box, L. L. A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) site on chromosome 11p15.5. Am J Med Genet B Neuropsychiatr Genet 125B, 112–119, doi: 10.1002/ajmg.b.20082 (2004).

  • 14.

    Rabin, M. et al. Suggestive linkage of developmental dyslexia to chromosome 1p34-p36. Lancet 342, 178 (1993).

  • 15.

    de Kovel, C. G. et al. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in a long Dutch family unit. J Med Genet forty one, 652–657, doi: 10.1136/jmg.2003.012294 (2004).

  • 16.

    Newbury, D. F., Monaco, A. P. & Paracchini, S. reading and language problems: the significance of each quantity and fine. Genes (Basel) 5, 285–309, doi: 10.3390/genes5020285 (2014).

  • 17.

    Newbury, D. F. et al. CMIP and ATP2C2 modulate phonological brief-time era reminiscence in language impairment. Am J Hum Genet eighty five, 264–272, doi: 10.1016/j.ajhg.2009.07.004 (2009).

  • 18.

    Taipale, M. et al. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci u.s.100, 11553–11558 (2003).

  • 19.

    Francks, C. et al. A seventy seven-kilobase location of chromosome 6p22.2 is linked to dyslexia in families from the UK and from the united states. Am J Hum Genet seventy five, 1046–1058, doi: 10.1086/426404 (2004).

  • 20.

    Paracchini, S. et al. The chromosome 6p22 haplotype linked to dyslexia reduces the expression of KIAA0319, a novel gene worried in neuronal migration. Hum Mol Genet 15, 1659–1666, doi: 10.1093/hmg/ddl089 (2006).

  • 21.

    Meng, H. et al. DCDC2 is linked to studying disability and modulates neuronal edifice in the mind. Proc Natl Acad Sci u . s . 102, 17053–17058, doi: 10.1073/pnas.0508591102 (2005).

  • 22.

    Anthoni, H. et al. A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Hum Mol Genet sixteen, 667–677, doi: 10.1093/hmg/ddm009 (2007).

  • 23.

    Hannula-Jouppi, ok. et al. The axon assistance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genet 1, e50 (2005).

  • 24.

    Graham, S. A. & Fisher, S. E. understanding Language from a Genomic viewpoint. Annu Rev Genet 49, 131–160, doi: 10.1146/annurev-genet-120213-092236 (2015).

  • 25.

    Blair, D. R. et al. A nondegenerate code of deleterious editions in Mendelian loci contributes to complicated sickness risk. telephone one hundred fifty five, 70–eighty, doi: 10.1016/ (2013).

  • 26.

    Franic, S. et al. Intelligence: shared genetic foundation between Mendelian issues and a polygenic trait. Eur J Hum Genet 23, 1378–1383, doi: 10.1038/ejhg.2015.3 (2015).

  • 27.

    Fisher, S. E. & Scharff, C. FOXP2 as a molecular window into speech and language. traits Genet 25, 166–177 (2009).

  • 28.

    Lai, C. S., Fisher, S. E., Hurst, J. A., Vargha-Khadem, F. & Monaco, A. P. A forkhead-domain gene is mutated in a austere speech and language sickness. Nature 413, 519–523 (2001).

  • 29.

    Viscount St. Albans, C. & Rappold, G. A. The discrete and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive issues. Hum Genet 131, 1687–1698, doi: 10.1007/s00439-012-1193-z (2012).

  • 30.

    Sollis, E. et al. Identification and useful characterization of de novo FOXP1 variants offers novel insights into the etiology of neurodevelopmental ailment. Hum Mol Genet 25, 546–557, doi: 10.1093/hmg/ddv495 (2016).

  • 31.

    Vernes, S. C. et al. A practical genetic link between discrete developmental language issues. N Engl J Med 359, 2337–2345 (2008).

  • 32.

    Graham, S. A. & Fisher, S. E. Decoding the genetics of speech and language. Curr Opin Neurobiol 23, 43–51, doi: 10.1016/j.conb.2012.eleven.006 (2013).

  • 33.

    Roll, P. et al. Molecular networks implicated in speech-linked disorders: FOXP2 regulates the SRPX2/uPAR complex. Hum Mol Genet 19, 4848–4860, doi: 10.1093/hmg/ddq415 (2010).

  • 34.

    Roll, P. et al. SRPX2 mutations in issues of language cortex and cognition. Hum Mol Genet 15, 1195–1207, doi: 10.1093/hmg/ddl035 (2006).

  • 35.

    Carvill, G. L. et al. GRIN2A mutations trigger epilepsy-aphasia spectrum disorders. Nat Genet forty five, 1073–1076, doi: 10.1038/ng.2727 (2013).

  • 36.

    Lesca, G. et al. GRIN2A mutations in obtained epileptic aphasia and connected childhood focal epilepsies and encephalopathies with speech and language dysfunction. Nat Genet forty five, 1061–1066, doi: 10.1038/ng.2726 (2013).

  • 37.

    Lemke, J. R. et al. Mutations in GRIN2A trigger idiopathic focal epilepsy with rolandic spikes. Nat Genet 45, 1067–1072, doi: 10.1038/ng.2728 (2013).

  • 38.

    O’Roak, B. J. et al. Exome sequencing in sporadic autism spectrum disorders identifies extreme de novo mutations. Nat Genet 43, 585–589, doi: 10.1038/ng.835 (2011).

  • 39.

    Dimassi, S. et al. Interstitial 12p13.1 deletion involving GRIN2B in three patients with highbrow disability. Am J Med Genet A 161A, 2564–2569, doi: 10.1002/ajmg.a.36079 (2013).

  • 40.

    Ocklenburg, S. et al. edition within the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization. Behav brain Res 225, 284–289, doi: 10.1016/j.bbr.2011.07.042 (2011).

  • forty one.

    Pagnamenta, A. T. et al. Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel possibility loci for autism and dyslexia. Biol Psychiatry 68, 320–328, doi: 10.1016/j.biopsych.2010.02.002 (2010).

  • forty two.

    Filges, I. et al. reduced expression by SETBP1 haploinsufficiency reasons developmental and eloquent language delay indicating a phenotype diverse from Schinzel-Giedion syndrome. J Med Genet forty eight, 117–122, doi: 10.1136/jmg.2010.084582 (2011).

  • forty three.

    Ercan-Sencicek, A. G. et al. A balanced t(10;15) translocation in a virile affected person with developmental language disorder. Eur J Med Genet 55, 128–131, doi: 10.1016/j.ejmg.2011.12.005 (2012).

  • forty four.

    Marseglia, G. et al. 372 kb microdeletion in 18q12.3 inflicting SETBP1 haploinsufficiency associated with gentle mental retardation and eloquent speech impairment. Eur J Med Genet fifty five, 216–221, doi: 10.1016/j.ejmg.2012.01.005 (2012).

  • 45.

    Thevenon, J. et al. 12p13.33 microdeletion together with ELKS/ERC1, a brand new locus associated with childhood apraxia of speech. Eur J Hum Genet 21, eighty two–88, doi: 10.1038/ejhg.2012.116 (2013).

  • forty six.

    Amarillo, I. E., Li, W. L., Li, X., Vilain, E. & Kantarci, S. De novo lone exon deletion of AUTS2 in a affected person with speech and language disorder: a review of disrupted AUTS2 and additional proof for its position in neurodevelopmental problems. Am J Med Genet A 164A, 958–965, doi: 10.1002/ajmg.a.36393 (2014).

  • 47.

    Coe, B. P. et al. Refining analyses of replica quantity model identifies inevitable genes associated with developmental lengthen. Nat Genet forty six, 1063–1071, doi: 10.1038/ng.3092 (2014).

  • 48.

    Villanueva, P. et al. Exome Sequencing in an Admixed remoted population indicates NFXL1 editions consult a possibility for particular Language Impairment. PLoS Genet eleven, e1004925, doi: 10.1371/journal.pgen.1004925 (2015).

  • 49.

    Kornilov, S. A. et al. Genome-broad association and Exome Sequencing witness at of Language disorder in an remoted population. Pediatrics 137, doi: 10.1542/peds.2015-2469 (2016).

  • 50.

    DePristo, M. A. et al. A framework for edition discovery and genotyping the usage of next-technology DNA sequencing records. Nat Genet 43, 491–498, doi: 10.1038/ng.806 (2011).

  • fifty one.

    Nudel, R. et al. Genome-extensive association analyses of child genotype outcomes and dad or mum-of-beginning consequences in inevitable language impairment. Genes repartee Behav 13, 418–429, doi: 10.1111/gbb.12127 (2014).

  • 52.

    MacArthur, D. G. et al. guidelines for investigating causality of sequence editions in human disease. Nature 508, 469–476, doi: 10.1038/nature13127 (2014).

  • 53.

    Carrion-Castillo, A., Franke, B. & Fisher, S. E. Molecular genetics of dyslexia: a top flush view. Dyslexia 19, 214–240, doi: 10.1002/dys.1464 (2013).

  • fifty four.

    Mulley, J. C. et al. role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome. Epilepsia 54, e122–126, doi: 10.1111/epi.12323 (2013).

  • fifty five.

    Singh, N. A. et al. a chore of SCN9A in human epilepsies, as a intuition for febrile seizures and as a possible modifier of Dravet syndrome. PLoS Genet 5, e1000649, doi: 10.1371/journal.pgen.1000649 (2009).

  • 56.

    Liu, S. et al. Kabuki syndrome: a chinese case collection and systematic overview of the spectrum of mutations. BMC Med Genet 16, 26, doi: 10.1186/s12881-015-0171-four (2015).

  • 57.

    Micale, L. et al. Molecular analysis, pathogenic mechanisms, and readthrough therapy on a expansive cohort of Kabuki syndrome sufferers. Hum Mutat 35, 841–850, doi: 10.1002/humu.22547 (2014).

  • 58.

    Cheon, C. ok. et al. Identification of KMT2D and KDM6A mutations via exome sequencing in Korean patients with Kabuki syndrome. J Hum Genet 59, 321–325, doi: 10.1038/jhg.2014.25 (2014).

  • fifty nine.

    Morgan, A. T. et al. Speech and language in a genotyped cohort of people with Kabuki syndrome. Am J Med Genet A 167, 1483–1492, doi: 10.1002/ajmg.a.37026 (2015).

  • 60.

    Simpson, N. H. et al. Genome-vast evaluation identifies a chore for common replica number variants in selected language impairment. Eur J Hum Genet 23, 1370–1377, doi: 10.1038/ejhg.2014.296 (2015).

  • sixty one.

    Gialluisi, A. et al. Genome-broad screening for DNA variations associated with studying and language qualities. Genes repartee Behav 13, 686–701, doi: 10.1111/gbb.12158 (2014).

  • 62.

    Barnby, G. et al. Candidate-gene screening and affiliation evaluation at the autism-susceptibility locus on chromosome 16p: evidence of affiliation at GRIN2A and ABAT. Am J Hum Genet 76, 950–966, doi: 10.1086/430454 (2005).

  • 63.

    Turner, S. J., Morgan, A. T., Perez, E. R. & Scheffer, I. E. New genes for focal epilepsies with speech and language disorders. Curr Neurol Neurosci Rep 15, 35, doi: 10.1007/s11910-015-0554-0 (2015).

  • 64.

    Reinthaler, E. M. et al. analysis of ELP4, SRPX2, and interacting genes in benchmark and odd rolandic epilepsy. Epilepsia 55, e89–ninety three, doi: 10.1111/epi.12712 (2014).

  • sixty five.

    Salmi, M. et al. Tubacin prevents neuronal migration defects and epileptic endeavor led to by passage of rat Srpx2 silencing in utero. brain 136, 2457–2473, doi: 10.1093/brain/awt161 (2013).

  • 66.

    Sia, G. M., Clem, R. L. & Huganir, R. L. The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice. Science 342, 987–991, doi: 10.1126/science.1245079 (2013).

  • 67.

    Visser, A. M. et al. Febrile seizures and behavioural and cognitive consequences in preschool toddlers: the era R examine. Dev Med newborn Neurol fifty four, 1006–1011, doi: 10.1111/j.1469-8749.2012.04405.x (2012).

  • sixty eight.

    Liu, k. X. et al. Neuron-certain antioxidant OXR1 extends survival of a mouse model of amyotrophic lateral sclerosis. brain 138, 1167–1181, doi: 10.1093/brain/awv039 (2015).

  • sixty nine.

    Oliver, P. L. et al. Oxr1 is fundamental for protection in opposition t oxidative stress-induced neurodegeneration. PLoS Genet 7, e1002338, doi: 10.1371/journal.pgen.1002338 (2011).

  • 70.

    Girirajan, S. et al. Relative burden of big CNVs on a number Neurodevelopmental Phenotypes. PLoS Genet 7, e1002334, doi: 10.1371/journal.pgen.1002334 (2011).

  • 71.

    O’Roak, B. J. et al. Sporadic autism exomes prove a incredibly interconnected protein network of de novo mutations. Nature 485, 246–250, doi: 10.1038/nature10989 (2012).

  • 72.

    Sultana, R. et al. Identification of a novel gene on chromosome 7q11.2 interrupted via a translocation breakpoint in a pair of autistic twins. Genomics eighty, 129–134 (2002).

  • 73.

    Kalscheuer, V. M. et al. Mutations in autism susceptibility candidate 2 (AUTS2) in patients with intellectual retardation. Hum Genet 121, 501–509, doi: 10.1007/s00439-006-0284-0 (2007).

  • 74.

    Nagamani, S. C. et al. Detection of copy-quantity adaptation in AUTS2 gene through targeted exonic array CGH in sufferers with developmental prolong and autistic spectrum disorders. Eur J Hum Genet 21, 343–346, doi: 10.1038/ejhg.2012.157 (2013).

  • seventy five.

    Beunders, G. et al. Exonic deletions in AUTS2 trigger a syndromic variety of intellectual disability and indicate a essential role for the C terminus. Am J Hum Genet ninety two, 210–220, doi: 10.1016/j.ajhg.2012.12.011 (2013).

  • seventy six.

    Schneider, A. et al. Identification of disrupted AUTS2 and EPHA6 genes by using array portray in a patient carrying a de novo balanced translocation t(three;7) with intellectual disability and neurodevelopment sickness. Am J Med Genet A 167A, 3031–3037, doi: 10.1002/ajmg.a.37350 (2015).

  • seventy seven.

    Elia, J. et al. infrequent structural versions present in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Mol Psychiatry 15, 637–646, doi: 10.1038/mp.2009.57 (2010).

  • seventy eight.

    Mefford, H. C. et al. Genome-wide replica number model in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS Genet 6, e1000962, doi: 10.1371/journal.pgen.1000962 (2010).

  • 79.

    McCarthy, S. E. et al. De novo mutations in schizophrenia implicate chromatin home improvement and guide a genetic overlap with autism and intellectual incapacity. Mol Psychiatry 19, 652–658, doi: 10.1038/mp.2014.29 (2014).

  • 80.

    Talkowski, M. E. et al. Sequencing chromosomal abnormalities exhibits neurodevelopmental loci that consult possibility across diagnostic boundaries. cell 149, 525–537, doi: 10.1016/j.telephone.2012.03.028 (2012).

  • 81.

    Hori, ok. et al. Cytoskeletal law with the aid of AUTS2 in neuronal migration and neuritogenesis. mobilephone Rep 9, 2166–2179, doi: 10.1016/j.celrep.2014.11.045 (2014).

  • 82.

    Senese, S. et al. a discrete insertion in STARD9′s motor domain regulates its steadiness. Mol Biol cell 26, 440–452, doi: 10.1091/mbc.E14-03-0829 (2015).

  • eighty three.

    Massinen, S. et al. expanded expression of the dyslexia candidate gene DCDC2 affects size and signaling of simple cilia in neurons. PLoS One 6, e20580, doi: 10.1371/journal.pone.0020580 (2011).

  • eighty four.

    Tammimies, okay. et al. Molecular networks of DYX1C1 gene parade connection to neuronal migration genes and cytoskeletal proteins. Biol Psychiatry seventy three, 583–590, doi: 10.1016/j.biopsych.2012.08.012 (2013).

  • 85.

    Tarkar, A. et al. DYX1C1 is required for axonemal dynein assembly and ciliary motility. Nat Genet forty five, 995–1003, doi: 10.1038/ng.2707 (2013).

  • 86.

    Brandler, W. M. & Paracchini, S. The genetic relationship between handedness and neurodevelopmental problems. traits Mol Med 20, eighty three–ninety, doi: 10.1016/j.molmed.2013.10.008 (2014).

  • 87.

    SLIC. extremely big linkage to the SLI1 locus in an extended pattern of people plagued by SLI. Am J Hum Genet seventy four, 1225–1238 (2004).

  • 88.

    Falcaro, M. et al. Genetic and phenotypic outcomes of phonological short-time era recollection and grammatical morphology in inevitable language impairment. Genes brain Behav 7, 393–402 (2008).

  • 89.

    Semel, E. M., Wiig, E. H. & Secord, W. scientific evaluation of Language Fundamentals - Revised(Psychological company, 1992).

  • ninety.

    Wechsler, D. Wechsler Intelligence Scale for babies - Third UK edition(Psychological commerce enterprise, 1992).

  • ninety one.

    Nudel, R. et al. Associations of HLA alleles with selected language impairment. J Neurodev Disord 6, 1, doi: 10.1186/1866-1955-6-1 (2014).

  • ninety two.

    Ceroni, F. et al. Homozygous microdeletion of exon 5 in ZNF277 in a woman with selected language impairment. Eur J Hum Genet 22, 1165–1171, doi: 10.1038/ejhg.2014.4 (2014).

  • ninety three.

    Ceroni, F. et al. Reply to Pembrey et al.: ‘ZNF277 microdeletions, selected language impairment and the meiotic mismatch methylation (three M) speculation’. Eur J Hum Genet 23, 1113–1115, doi: 10.1038/ejhg.2014.275 (2015).

  • 94.

    Gathercole, S. E., Willis, C. S., Baddeley, A. D. & Emslie, H. The toddlers’s test of Nonword Repetition: a examine of phonological working reminiscence. recollection 2, 103–127 (1994).

  • 95.

    McKenna, A. et al. The Genome analysis Toolkit: a MapReduce framework for examining subsequent-technology DNA sequencing information. Genome Res 20, 1297–1303, doi: 10.1101/ hundred ten (2010).

  • ninety six.

    Wang, k., Li, M. & Hakonarson, H. ANNOVAR: practical annotation of genetic editions from high-throughput sequencing records. Nucleic Acids Res 38, e164, doi: 10.1093/nar/gkq603 (2010).

  • 97.

    Durbin, R. M. et al. A map of human genome version from inhabitants-scale sequencing. Nature 467, 1061–1073, doi: 10.1038/nature09534 (2010).

  • 98.

    1000 Genomes venture, C. et al. An integrated map of genetic version from 1,092 human genomes. Nature 491, fifty six–65, doi: 10.1038/nature11632 (2012).

  • 99.

    Kanehisa, M., Goto, S., Sato, Y., Furumichi, M. & Tanabe, M. KEGG for integration and interpretation of colossal-scale molecular facts sets. Nucleic Acids Res forty, D109–114, doi: 10.1093/nar/gkr988 (2012).

  • 100.

    Matthews, L. et al. Reactome knowledgebase of human organic pathways and strategies. Nucleic Acids Res 37, D619–622, doi: 10.1093/nar/gkn863 (2009).

  • 101.

    Ashburner, M. et al. Gene ontology: appliance for the unification of biology. The Gene Ontology Consortium. Nat Genet 25, 25–29, doi: 10.1038/75556 (2000).

  • 102.

    Falcon, S. & Gentleman, R. the exercise of GOstats to examine gene lists for Go term association. Bioinformatics 23, 257–258, doi: 10.1093/bioinformatics/btl567 (2007).

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