TY - JOUR AU - Tomblin, J. B. AU - Records, N. L. AU - Buckwalter, P. AU - Zhang, X. AU - Smith, E. AU - O’Brien, M. PY - 1997 DA - 1997// TI - Prevalence of specific language impairment in kindergarten children JO - J Speech Lang Hear Res VL - 40 UR - https://doi.org/10.1044/jslhr.4006.1245 DO - 10.1044/jslhr.4006.1245 ID - Tomblin1997 ER - TY - JOUR AU - Pennington, B. F. AU - Bishop, D. V. PY - 2009 DA - 2009// TI - Relations among speech, language, and reading disorders JO - Annu Rev Psychol VL - 60 UR - https://doi.org/10.1146/annurev.psych.60.110707.163548 DO - 10.1146/annurev.psych.60.110707.163548 ID - Pennington2009 ER - TY - JOUR AU - Bishop, D. V. AU - Snowling, M. J. PY - 2004 DA - 2004// TI - Developmental dyslexia and specific language impairment: same or different? JO - Psychol Bull VL - 130 UR - https://doi.org/10.1037/0033-2909.130.6.858 DO - 10.1037/0033-2909.130.6.858 ID - Bishop2004 ER - TY - JOUR AU - Barry, J. G. AU - Yasin, I. AU - Bishop, D. V. PY - 2007 DA - 2007// TI - Heritable risk factors associated with language impairments JO - Genes Brain Behav VL - 6 UR - https://doi.org/10.1111/j.1601-183X.2006.00232.x DO - 10.1111/j.1601-183X.2006.00232.x ID - Barry2007 ER - TY - JOUR AU - Bishop, D. V. PY - 2002 DA - 2002// TI - The role of genes in the etiology of specific language impairment JO - J Commun Disord VL - 35 UR - https://doi.org/10.1016/S0021-9924(02)00087-4 DO - 10.1016/S0021-9924(02)00087-4 ID - Bishop2002 ER - TY - JOUR AU - Bishop, D. V. AU - Hayiou-Thomas, M. E. PY - 2008 DA - 2008// TI - Heritability of specific language impairment depends on diagnostic criteria JO - Genes Brain Behav VL - 7 UR - https://doi.org/10.1111/j.1601-183X.2007.00360.x DO - 10.1111/j.1601-183X.2007.00360.x ID - Bishop2008 ER - TY - JOUR AU - Newbury, D. F. AU - Monaco, A. P. PY - 2010 DA - 2010// TI - Genetic advances in the study of speech and language disorders JO - Neuron VL - 68 UR - https://doi.org/10.1016/j.neuron.2010.10.001 DO - 10.1016/j.neuron.2010.10.001 ID - Newbury2010 ER - TY - JOUR AU - Newbury, D. F. AU - Monaco, A. P. AU - Paracchini, S. PY - 2014 DA - 2014// TI - Reading and language disorders: the importance of both quantity and quality JO - Genes (Basel) VL - 5 ID - Newbury2014 ER - TY - JOUR AU - Newbury, D. F. AU - Winchester, L. AU - Addis, L. AU - Paracchini, S. AU - Buckingham, L. L. AU - Clark, A. PY - 2009 DA - 2009// TI - CMIP and ATP2C2 modulate phonological short-term memory in language impairment JO - Am J Hum Genet VL - 85 UR - https://doi.org/10.1016/j.ajhg.2009.07.004 DO - 10.1016/j.ajhg.2009.07.004 ID - Newbury2009 ER - TY - JOUR AU - Vernes, S. C. AU - Newbury, D. F. AU - Abrahams, B. S. AU - Winchester, L. AU - Nicod, J. AU - Groszer, M. PY - 2008 DA - 2008// TI - A functional genetic link between distinct developmental language disorders JO - N Engl J Med VL - 359 UR - https://doi.org/10.1056/NEJMoa0802828 DO - 10.1056/NEJMoa0802828 ID - Vernes2008 ER - TY - JOUR AU - Wiszniewski, W. AU - Hunter, J. V. AU - Hanchard, N. A. AU - Willer, J. R. AU - Shaw, C. AU - Tian, Q. PY - 2013 DA - 2013// TI - TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities JO - Am J Hum Genet VL - 93 UR - https://doi.org/10.1016/j.ajhg.2013.05.027 DO - 10.1016/j.ajhg.2013.05.027 ID - Wiszniewski2013 ER - TY - JOUR AU - McArthur, G. M. AU - Hogben, J. H. AU - Edwards, V. T. AU - Heath, S. M. AU - Mengler, E. D. PY - 2000 DA - 2000// TI - On the “specifics” of specific reading disability and specific language impairment JO - J Child Psychol Psychiatry VL - 41 UR - https://doi.org/10.1111/1469-7610.00674 DO - 10.1111/1469-7610.00674 ID - McArthur2000 ER - TY - JOUR AU - Snowling, M. AU - Bishop, D. V. AU - Stothard, S. E. PY - 2000 DA - 2000// TI - Is preschool language impairment a risk factor for dyslexia in adolescence? JO - J Child Psychol Psychiatry VL - 41 UR - https://doi.org/10.1111/1469-7610.00651 DO - 10.1111/1469-7610.00651 ID - Snowling2000 ER - TY - JOUR AU - Harlaar, N. AU - Hayiou-Thomas, M. E. AU - Dale, P. S. AU - Plomin, R. PY - 2008 DA - 2008// TI - Why do preschool language abilities correlate with later reading? A twin study JO - J Speech Lang Hear Res VL - 51 UR - https://doi.org/10.1044/1092-4388(2008/049) DO - 10.1044/1092-4388(2008/049) ID - Harlaar2008 ER - TY - JOUR AU - Logan, J. AU - Petrill, S. A. AU - Flax, J. AU - Justice, L. M. AU - Hou, L. AU - Bassett, A. S. PY - 2011 DA - 2011// TI - Genetic covariation underlying reading, language and related measures in a sample selected for specific language impairment JO - Behav Genet VL - 41 UR - https://doi.org/10.1007/s10519-010-9435-0 DO - 10.1007/s10519-010-9435-0 ID - Logan2011 ER - TY - JOUR AU - Rice, M. L. AU - Smith, S. D. AU - Gayan, J. PY - 2009 DA - 2009// TI - Convergent genetic linkage and associations to language, speech and reading measures in families of probands with specific language impairment JO - J Neurodev Disord VL - 1 UR - https://doi.org/10.1007/s11689-009-9031-x DO - 10.1007/s11689-009-9031-x ID - Rice2009 ER - TY - JOUR AU - Newbury, D. AU - Paracchini, S. AU - Scerri, T. AU - Winchester, L. AU - Addis, L. AU - Richardson, A. J. PY - 2011 DA - 2011// TI - Investigation of dyslexia and SLI risk variants in reading-and language-impaired subjects JO - Behav Genet VL - 41 UR - https://doi.org/10.1007/s10519-010-9424-3 DO - 10.1007/s10519-010-9424-3 ID - Newbury2011 ER - TY - JOUR AU - Eicher, J. D. AU - Gruen, J. R. PY - 2015 DA - 2015// TI - Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders JO - Autism Res VL - 8 UR - https://doi.org/10.1002/aur.1436 DO - 10.1002/aur.1436 ID - Eicher2015 ER - TY - JOUR AU - St Pourcain, B. AU - Cents, R. A. AU - Whitehouse, A. J. AU - Haworth, C. M. AU - Davis, O. S. AU - O’Reilly, P. F. PY - 2014 DA - 2014// TI - Common variation near ROBO2 is associated with expressive vocabulary in infancy JO - Nat Commun VL - 5 UR - https://doi.org/10.1038/ncomms5831 DO - 10.1038/ncomms5831 ID - St Pourcain2014 ER - TY - JOUR AU - Gialluisi, A. AU - Newbury, D. F. AU - Wilcutt, E. G. AU - Olson, R. K. AU - DeFries, J. C. AU - Brandler, W. M. PY - 2014 DA - 2014// TI - Genome-wide screening for DNA variants associated with reading and language traits JO - Genes Brain Behav VL - 13 UR - https://doi.org/10.1111/gbb.12158 DO - 10.1111/gbb.12158 ID - Gialluisi2014 ER - TY - JOUR AU - Nudel, R. AU - Simpson, N. H. AU - Baird, G. AU - O’Hare, A. AU - Conti-Ramsden, G. AU - Bolton, P. F. PY - 2014 DA - 2014// TI - Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment JO - Genes Brain Behav VL - 13 UR - https://doi.org/10.1111/gbb.12127 DO - 10.1111/gbb.12127 ID - Nudel2014 ER - TY - JOUR AU - Chamberlain, S. J. AU - Lalande, M. PY - 2010 DA - 2010// TI - Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13 JO - Neurobiol Dis VL - 39 UR - https://doi.org/10.1016/j.nbd.2010.03.011 DO - 10.1016/j.nbd.2010.03.011 ID - Chamberlain2010 ER - TY - JOUR AU - Pettigrew, K. A. AU - Reeves, E. AU - Leavett, R. AU - Hayiou-Thomas, M. E. AU - Sharma, A. AU - Simpson, N. H. PY - 2015 DA - 2015// TI - Copy number variation screen identifies a rare de novo deletion at chromosome 15q13.1-13.3 in a child with language impairment JO - PLoS One VL - 10 UR - https://doi.org/10.1371/journal.pone.0134997 DO - 10.1371/journal.pone.0134997 ID - Pettigrew2015 ER - TY - JOUR AU - Mott, R. AU - Yuan, W. AU - Kaisaki, P. AU - Gan, X. AU - Cleak, J. AU - Edwards, A. PY - 2014 DA - 2014// TI - The architecture of parent-of-origin effects in mice JO - Cell VL - 156 UR - https://doi.org/10.1016/j.cell.2013.11.043 DO - 10.1016/j.cell.2013.11.043 ID - Mott2014 ER - TY - BOOK AU - Semel, E. M. AU - Wiig, E. H. AU - Secord, W. PY - 1992 DA - 1992// TI - Clinical evaluation of language fundamentals—revised PB - Psychological Corporation CY - San Antonio ID - Semel1992 ER - TY - JOUR AU - Nash, H. M. AU - Hulme, C. AU - Gooch, D. AU - Snowling, M. J. PY - 2013 DA - 2013// TI - Preschool language profiles of children at family risk of dyslexia: continuities with specific language impairment JO - J Child Psychol Psychiatry VL - 54 UR - https://doi.org/10.1111/jcpp.12091 DO - 10.1111/jcpp.12091 ID - Nash2013 ER - TY - JOUR AU - Scerri, T. S. AU - Paracchini, S. AU - Morris, A. AU - MacPhie, I. L. AU - Talcott, J. AU - Stein, J. PY - 2010 DA - 2010// TI - Identification of candidate genes for dyslexia susceptibility on chromosome 18 JO - PLoS One VL - 5 UR - https://doi.org/10.1371/journal.pone.0013712 DO - 10.1371/journal.pone.0013712 ID - Scerri2010 ER - TY - JOUR AU - Francks, C. AU - Paracchini, S. AU - Smith, S. D. AU - Richardson, A. J. AU - Scerri, T. S. AU - Cardon, L. R. PY - 2004 DA - 2004// TI - A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States JO - Am J Hum Genet VL - 75 UR - https://doi.org/10.1086/426404 DO - 10.1086/426404 ID - Francks2004 ER - TY - JOUR AU - Alarcon, M. AU - Abrahams, B. S. AU - Stone, J. L. AU - Duvall, J. A. AU - Perederiy, J. V. AU - Bomar, J. M. PY - 2008 DA - 2008// TI - Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene JO - Am J Hum Genet VL - 82 UR - https://doi.org/10.1016/j.ajhg.2007.09.005 DO - 10.1016/j.ajhg.2007.09.005 ID - Alarcon2008 ER - TY - JOUR AU - Whitehouse, A. J. AU - Bishop, D. V. AU - Ang, Q. W. AU - Pennell, C. E. AU - Fisher, S. E. PY - 2011 DA - 2011// TI - CNTNAP2 variants affect early language development in the general population JO - Genes Brain Behav ID - Whitehouse2011 ER - TY - JOUR AU - Bishop, D. V. AU - North, T. AU - Donlan, C. PY - 1996 DA - 1996// TI - Nonword repetition as a behavioural marker for inherited language impairment: evidence from a twin study JO - J Child Psychol Psychiatry VL - 37 UR - https://doi.org/10.1111/j.1469-7610.1996.tb01420.x DO - 10.1111/j.1469-7610.1996.tb01420.x ID - Bishop1996 ER - TY - BOOK AU - Seeff-Gabriel, H. AU - Chiat, S. AU - Roy, P. PY - 2008 DA - 2008// TI - The early repetition battery PB - Pearson Assessment CY - London ID - Seeff-Gabriel2008 ER - TY - BOOK AU - Wiig, E. H. AU - Secord, W. AU - Semel, E. PY - 2006 DA - 2006// TI - Clinical evaluation of language fundamentals—Preschool. Second UK edition PB - Harcourt Assessment CY - London ID - Wiig2006 ER - TY - STD TI - Torgesen JK, Wagner RK, Rashotte CA. Test of word reading efficiency (TOWRE). Austin, TX: Pro-Ed; 1999. ID - ref34 ER - TY - BOOK AU - Wechsler, D. PY - 2002 DA - 2002// TI - Wechsler individual achievement test PB - The Psychological Corporation CY - San Antonio ID - Wechsler2002 ER - TY - STD TI - Hulme C, Nash HM, Gooch D, Leavett R, Snowling MJ. Predictors of individual differences in the foundation of early literacy young children. Psychol Sci. 2015. (In press) ID - ref36 ER - TY - JOUR AU - Marlow, A. J. AU - Fisher, S. E. AU - Richardson, A. J. AU - Francks, C. AU - Talcott, J. B. AU - Monaco, A. P. PY - 2001 DA - 2001// TI - Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK JO - Behav Genet VL - 31 UR - https://doi.org/10.1023/A:1010209629021 DO - 10.1023/A:1010209629021 ID - Marlow2001 ER - TY - JOUR AU - Abecasis, G. R. AU - Cherny, S. S. AU - Cookson, W. O. AU - Cardon, L. R. PY - 2002 DA - 2002// TI - Merlin—rapid analysis of dense genetic maps using sparse gene flow trees JO - Nat Genet VL - 30 UR - https://doi.org/10.1038/ng786 DO - 10.1038/ng786 ID - Abecasis2002 ER - TY - JOUR AU - Abecasis, G. R. AU - Cardon, L. R. AU - Cookson, W. O. PY - 2000 DA - 2000// TI - A general test of association for quantitative traits in nuclear families JO - Am J Hum Genet VL - 66 UR - https://doi.org/10.1086/302698 DO - 10.1086/302698 ID - Abecasis2000 ER - TY - JOUR AU - Nudel, R. AU - Simpson, N. H. AU - Baird, G. AU - O’Hare, A. AU - Conti-Ramsden, G. AU - Bolton, P. F. PY - 2014 DA - 2014// TI - Associations of HLA alleles with specific language impairment JO - J Neurodev Disord VL - 6 UR - https://doi.org/10.1186/1866-1955-6-1 DO - 10.1186/1866-1955-6-1 ID - Nudel2014 ER - TY - JOUR AU - Howey, R. AU - Mamasoula, C. AU - Topf, A. AU - Nudel, R. AU - Goodship, J. A. AU - Keavney, B. D. PY - 2015 DA - 2015// TI - Increased power for detection of parent-of-origin effects via the use of haplotype estimation JO - Am J Hum Genet VL - 97 UR - https://doi.org/10.1016/j.ajhg.2015.07.016 DO - 10.1016/j.ajhg.2015.07.016 ID - Howey2015 ER - TY - JOUR AU - Zollner, S. AU - Pritchard, J. K. PY - 2007 DA - 2007// TI - Overcoming the winner’s curse: estimating penetrance parameters from case-control data JO - Am J Hum Genet VL - 80 UR - https://doi.org/10.1086/512821 DO - 10.1086/512821 ID - Zollner2007 ER - TY - JOUR AU - Lawson, H. A. AU - Cheverud, J. M. AU - Wolf, J. B. PY - 2013 DA - 2013// TI - Genomic imprinting and parent-of-origin effects on complex traits JO - Nat Rev Genet VL - 14 UR - https://doi.org/10.1038/nrg3543 DO - 10.1038/nrg3543 ID - Lawson2013 ER - TY - JOUR AU - Kotzot, D. PY - 2001 DA - 2001// TI - Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region JO - Clin Genet VL - 60 UR - https://doi.org/10.1034/j.1399-0004.2001.600309.x DO - 10.1034/j.1399-0004.2001.600309.x ID - Kotzot2001 ER - TY - JOUR AU - Sutton, V. R. AU - Shaffer, L. G. PY - 2000 DA - 2000// TI - Search for imprinted regions on chromosome 14: comparison of maternal and paternal UPD cases with cases of chromosome 14 deletion JO - Am J Med Genet VL - 93 UR - https://doi.org/3.0.CO;2-9 DO - 3.0.CO;2-9 ID - Sutton2000 ER - TY - JOUR AU - Kong, A. AU - Steinthorsdottir, V. AU - Masson, G. AU - Thorleifsson, G. AU - Sulem, P. AU - Besenbacher, S. PY - 2009 DA - 2009// TI - Parental origin of sequence variants associated with complex diseases JO - Nature VL - 462 UR - https://doi.org/10.1038/nature08625 DO - 10.1038/nature08625 ID - Kong2009 ER - TY - JOUR AU - Small, K. S. AU - Hedman, A. K. AU - Grundberg, E. AU - Nica, A. C. AU - Thorleifsson, G. AU - Kong, A. PY - 2011 DA - 2011// TI - Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes JO - Nat Genet VL - 43 UR - https://doi.org/10.1038/ng.833 DO - 10.1038/ng.833 ID - Small2011 ER - TY - JOUR AU - Hoggart, C. J. AU - Venturini, G. AU - Mangino, M. AU - Gomez, F. AU - Ascari, G. AU - Zhao, J. H. PY - 2014 DA - 2014// TI - Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index JO - PLoS Genet VL - 10 UR - https://doi.org/10.1371/journal.pgen.1004508 DO - 10.1371/journal.pgen.1004508 ID - Hoggart2014 ER - TY - JOUR AU - Perry, J. R. AU - Day, F. AU - Elks, C. E. AU - Sulem, P. AU - Thompson, D. J. AU - Ferreira, T. PY - 2014 DA - 2014// TI - Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche JO - Nature VL - 514 UR - https://doi.org/10.1038/nature13545 DO - 10.1038/nature13545 ID - Perry2014 ER - TY - JOUR AU - Savova, V. AU - Chun, S. AU - Sohail, M. AU - McCole, R. B. AU - Witwicki, R. AU - Gai, L. PY - 2016 DA - 2016// TI - Genes with monoallelic expression contribute disproportionately to genetic diversity in humans JO - Nat Genet VL - 48 UR - https://doi.org/10.1038/ng.3493 DO - 10.1038/ng.3493 ID - Savova2016 ER - TY - JOUR AU - Manolio, T. A. AU - Collins, F. S. AU - Cox, N. J. AU - Goldstein, D. B. AU - Hindorff, L. A. AU - Hunter, D. J. PY - 2009 DA - 2009// TI - Finding the missing heritability of complex diseases JO - Nature VL - 461 UR - https://doi.org/10.1038/nature08494 DO - 10.1038/nature08494 ID - Manolio2009 ER -