| Year |
Citation |
Score |
| 2024 |
Lin YP, Shi Y, Zhang R, Xue X, Rao S, Yin L, Lui KFH, Pan DJ, Maurer U, Choy KW, Paracchini S, McBride C, So HC. A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children. Npj Science of Learning. 9: 26. PMID 38538593 DOI: 10.1038/s41539-024-00229-7 |
0.405 |
|
| 2023 |
Chung CY, Pan DJ, Paracchini S, Jiang W, So HC, McBride C, Maurer U, Zheng M, Choy KW. Dyslexia-related loci are significantly associated with language and literacy in Chinese-English bilingual Hong Kong Chinese twins. Human Genetics. 142: 1519-1529. PMID 37668838 DOI: 10.1007/s00439-023-02594-6 |
0.358 |
|
| 2023 |
Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B, Pourcain BS, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, et al. Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics. PMID 36823321 DOI: 10.1038/s41588-023-01336-8 |
0.58 |
|
| 2023 |
Abbondanza F, Dale PS, Wang CA, Hayiou-Thomas ME, Toseeb U, Koomar TS, Wigg KG, Feng Y, Price KM, Kerr EN, Guger SL, Lovett MW, Strug LJ, van Bergen E, Dolan CV, ... ... Paracchini S, et al. Language and reading impairments are associated with increased prevalence of non-right-handedness. Child Development. PMID 36780127 DOI: 10.1111/cdev.13914 |
0.513 |
|
| 2022 |
Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B, Pourcain BS, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, et al. Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics. PMID 36266505 DOI: 10.1038/s41588-022-01192-y |
0.651 |
|
| 2022 |
Eising E, Mirza-Schreiber N, de Zeeuw EL, Wang CA, Truong DT, Allegrini AG, Shapland CY, Zhu G, Wigg KG, Gerritse ML, Molz B, Alagöz G, Gialluisi A, Abbondanza F, Rimfeld K, ... ... Paracchini S, et al. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America. 119: e2202764119. PMID 35998220 DOI: 10.1073/pnas.2202764119 |
0.66 |
|
| 2021 |
Martinelli A, Rice M, Talcott JB, Diaz R, Smith S, Raza MH, Snowling MJ, Hulme C, Stein J, Hayiou-Thomas ME, Hawi Z, Kent L, Pitt SJ, Newbury DF, Paracchini S. A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures. Human Molecular Genetics. PMID 33864365 DOI: 10.1093/hmg/ddab111 |
0.359 |
|
| 2020 |
Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, Pourcain BS, Honbolygó F, Tóth D, Csépe V, Huguet G, Chaix Y, Iannuzzi S, ... ... Paracchini S, et al. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular Psychiatry. PMID 33057169 DOI: 10.1038/s41380-020-00898-x |
0.635 |
|
| 2020 |
Packheiser J, Schmitz J, Berretz G, Carey DP, Paracchini S, Papadatou-Pastou M, Ocklenburg S. Four meta-analyses across 164 studies on atypical footedness prevalence and its relation to handedness. Scientific Reports. 10: 14501. PMID 32879356 DOI: 10.1038/S41598-020-71478-W |
0.322 |
|
| 2020 |
Papadatou-Pastou M, Ntolka E, Schmitz J, Martin M, Munafò MR, Ocklenburg S, Paracchini S. Human handedness: A meta-analysis. Psychological Bulletin. PMID 32237881 DOI: 10.1037/Bul0000229 |
0.3 |
|
| 2019 |
Hitchcock TJ, Paracchini S, Gardner A. Genomic Imprinting As a Window into Human Language Evolution. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 41: e1800212. PMID 31132171 DOI: 10.1002/Bies.201800212 |
0.415 |
|
| 2019 |
Gostic M, Martinelli A, Tucker C, Yang Z, Gasparoli F, Ewart JY, Dholakia K, Sillar KT, Tello JA, Paracchini S. The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration. The Journal of Comparative Neurology. PMID 30950042 DOI: 10.1002/Cne.24696 |
0.381 |
|
| 2019 |
Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, ... ... Paracchini S, et al. Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Translational Psychiatry. 9: 77. PMID 30741946 DOI: 10.1038/S41398-019-0402-0 |
0.677 |
|
| 2019 |
Paracchini S, Diaz R, Gostic M, Kronenberg N, Martinelli A, Sillar K, Tello J, Gather M. SA14THE KIAA0319 DYSLEXIA SUSCEPTIBILITY GENE PRESENTS A HIGHLY SPECIFIC EXPRESSION PATTERN DURING ZEBRAFISH DEVELOPMENT AND PLAYS A ROLE IN CYTOSKELETON DYNAMICS European Neuropsychopharmacology. 29: S1195. DOI: 10.1016/J.Euroneuro.2018.08.236 |
0.328 |
|
| 2019 |
Martinelli A, Diaz R, Feliciotti I, Pitt S, Paracchini S. SA13FUNCTIONAL CHARACTERIZATION OF ATP2C2, A RISK FACTOR FOR LANGUAGE DISORDERS European Neuropsychopharmacology. 29: S1194-S1195. DOI: 10.1016/J.Euroneuro.2018.08.235 |
0.316 |
|
| 2018 |
Guidi LG, Velayos-Baeza A, Martinez-Garay I, Monaco AP, Paracchini S, Bishop DVM, Molnár Z. The Neuronal Migration Hypothesis of Dyslexia: A Critical Evaluation Thirty Years On. The European Journal of Neuroscience. PMID 30218584 DOI: 10.1111/Ejn.14149 |
0.729 |
|
| 2017 |
Scerri TS, Macpherson E, Martinelli A, Wa WC, Monaco AP, Stein J, Zheng M, Suk-Han Ho C, McBride C, Snowling M, Hulme C, Hayiou-Thomas ME, Waye MMY, Talcott JB, Paracchini S. The DCDC2 deletion is not a risk factor for dyslexia. Translational Psychiatry. 7: e1182. PMID 28742079 DOI: 10.1038/Tp.2017.151 |
0.561 |
|
| 2016 |
Paracchini S, Diaz R, Stein J. Advances in Dyslexia Genetics-New Insights Into the Role of Brain Asymmetries. Advances in Genetics. 96: 53-97. PMID 27968731 DOI: 10.1016/Bs.Adgen.2016.08.003 |
0.408 |
|
| 2016 |
Pettigrew KA, Frinton E, Nudel R, Chan MT, Thompson P, Hayiou-Thomas ME, Talcott JB, Stein J, Monaco AP, Hulme C, Snowling MJ, Newbury DF, Paracchini S. Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes. Journal of Neurodevelopmental Disorders. 8: 24. PMID 27307794 DOI: 10.1186/S11689-016-9157-6 |
0.6 |
|
| 2016 |
Shore R, Covill L, Pettigrew KA, Brandler WM, Diaz R, Xu Y, Tello JA, Talcott JB, Newbury DF, Stein J, Monaco AP, Paracchini S. The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts. Human Molecular Genetics. PMID 26908617 DOI: 10.1093/Hmg/Ddw047 |
0.588 |
|
| 2015 |
Pettigrew KA, Reeves E, Leavett R, Hayiou-Thomas ME, Sharma A, Simpson NH, Martinelli A, Thompson P, Hulme C, Snowling MJ, Newbury DF, Paracchini S. Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment. Plos One. 10: e0134997. PMID 26262844 DOI: 10.1371/Journal.Pone.0134997 |
0.441 |
|
| 2015 |
Pettigrew KA, Fajutrao Valles SF, Moll K, Northstone K, Ring S, Pennell C, Wang C, Leavett R, Hayiou-Thomas ME, Thompson P, Simpson NH, Fisher SE, Whitehouse AJ, Snowling MJ, ... ... Paracchini S, et al. Lack of replication for the myosin-18B association with mathematical ability in independent cohorts. Genes, Brain, and Behavior. 14: 369-76. PMID 25778778 DOI: 10.1111/Gbb.12213 |
0.605 |
|
| 2014 |
Gialluisi A, Newbury DF, Wilcutt EG, Olson RK, DeFries JC, Brandler WM, Pennington BF, Smith SD, Scerri TS, Simpson NH, Luciano M, Evans DM, Bates TC, Stein JF, ... ... Paracchini S, et al. Genome-wide screening for DNA variants associated with reading and language traits. Genes, Brain, and Behavior. 13: 686-701. PMID 25065397 DOI: 10.1111/Gbb.12158 |
0.697 |
|
| 2014 |
Newbury DF, Monaco AP, Paracchini S. Reading and language disorders: the importance of both quantity and quality. Genes. 5: 285-309. PMID 24705331 DOI: 10.3390/Genes5020285 |
0.559 |
|
| 2014 |
Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER, Ring SM, Davey Smith G, Francks C, Paracchini S, Monaco AP, Fisher SE, Newbury DF. Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Genes, Brain, and Behavior. 13: 418-29. PMID 24571439 DOI: 10.1111/Gbb.12127 |
0.681 |
|
| 2014 |
Brandler WM, Paracchini S. The genetic relationship between handedness and neurodevelopmental disorders. Trends in Molecular Medicine. 20: 83-90. PMID 24275328 DOI: 10.1016/J.Molmed.2013.10.008 |
0.375 |
|
| 2014 |
Simpson NH, Addis L, Brandler WM, Slonims V, Clark A, Watson J, Scerri TS, Hennessy ER, Bolton PF, Conti-Ramsden G, Fairfax BP, Knight JC, Stein J, Talcott JB, O'Hare A, ... ... Paracchini S, et al. Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Developmental Medicine and Child Neurology. 56: 346-53. PMID 24117048 DOI: 10.1111/Dmcn.12294 |
0.571 |
|
| 2014 |
Becker J, Czamara D, Scerri TS, Ramus F, Csépe V, Talcott JB, Stein J, Morris A, Ludwig KU, Hoffmann P, Honbolygó F, Tóth D, Fauchereau F, Bogliotti C, Iannuzzi S, ... ... Paracchini S, et al. Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. European Journal of Human Genetics : Ejhg. 22: 675-80. PMID 24022301 DOI: 10.1038/Ejhg.2013.199 |
0.593 |
|
| 2013 |
Brandler WM, Morris AP, Evans DM, Scerri TS, Kemp JP, Timpson NJ, St Pourcain B, Smith GD, Ring SM, Stein J, Monaco AP, Talcott JB, Fisher SE, Webber C, Paracchini S. Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. Plos Genetics. 9: e1003751. PMID 24068947 DOI: 10.1371/Journal.Pgen.1003751 |
0.681 |
|
| 2012 |
Scerri TS, Darki F, Newbury DF, Whitehouse AJ, Peyrard-Janvid M, Matsson H, Ang QW, Pennell CE, Ring S, Stein J, Morris AP, Monaco AP, Kere J, Talcott JB, Klingberg T, ... Paracchini S, et al. The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. Plos One. 7: e50321. PMID 23209710 DOI: 10.1371/Journal.Pone.0050321 |
0.595 |
|
| 2011 |
Paracchini S. Dissection of genetic associations with language-related traits in population-based cohorts. Journal of Neurodevelopmental Disorders. 3: 365-73. PMID 21894572 DOI: 10.1007/S11689-011-9091-6 |
0.499 |
|
| 2011 |
Scerri TS, Morris AP, Buckingham LL, Newbury DF, Miller LL, Monaco AP, Bishop DV, Paracchini S. DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biological Psychiatry. 70: 237-45. PMID 21457949 DOI: 10.1016/J.Biopsych.2011.02.005 |
0.628 |
|
| 2011 |
Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Richardson AJ, Walter J, Stein JF, Talcott JB, Monaco AP. Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behavior Genetics. 41: 90-104. PMID 21165691 DOI: 10.1007/S10519-010-9424-3 |
0.603 |
|
| 2011 |
Scerri TS, Brandler WM, Paracchini S, Morris AP, Ring SM, Richardson AJ, Talcott JB, Stein J, Monaco AP. PCSK6 is associated with handedness in individuals with dyslexia. Human Molecular Genetics. 20: 608-14. PMID 21051773 DOI: 10.1093/Hmg/Ddq475 |
0.573 |
|
| 2011 |
Paracchini S, Ang QW, Stanley FJ, Monaco AP, Pennell CE, Whitehouse AJ. Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population. Genes, Brain, and Behavior. 10: 158-65. PMID 20846247 DOI: 10.1111/J.1601-183X.2010.00651.X |
0.594 |
|
| 2010 |
Paracchini S, Monaco AP, Knight JC. An allele-specific gene expression assay to test the functional basis of genetic associations. Journal of Visualized Experiments : Jove. PMID 21085102 DOI: 10.3791/2279 |
0.547 |
|
| 2010 |
Scerri TS, Paracchini S, Morris A, MacPhie IL, Talcott J, Stein J, Smith SD, Pennington BF, Olson RK, DeFries JC, Monaco AP, Richardson AJ. Identification of candidate genes for dyslexia susceptibility on chromosome 18. Plos One. 5: e13712. PMID 21060895 DOI: 10.1371/Journal.Pone.0013712 |
0.616 |
|
| 2010 |
Pagnamenta AT, Bacchelli E, de Jonge MV, Mirza G, Scerri TS, Minopoli F, Chiocchetti A, Ludwig KU, Hoffmann P, Paracchini S, Lowy E, Harold DH, Chapman JA, Klauck SM, Poustka F, et al. Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biological Psychiatry. 68: 320-8. PMID 20346443 DOI: 10.1016/J.Biopsych.2010.02.002 |
0.554 |
|
| 2010 |
Scerri TS, Paracchini S, Morris A, MacPhie IL, Talcott J, Stein J, Smith SD, Pennington BF, Olson RK, DeFries JC, Monaco AP, Richardson AJ. Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18 Plos One. 5. DOI: 10.1371/Annotation/2294A38B-878D-42F0-9Faf-0822Db4A0248 |
0.455 |
|
| 2009 |
Newbury DF, Winchester L, Addis L, Paracchini S, Buckingham LL, Clark A, Cohen W, Cowie H, Dworzynski K, Everitt A, Goodyer IM, Hennessy E, Kindley AD, Miller LL, Nasir J, et al. CMIP and ATP2C2 modulate phonological short-term memory in language impairment. American Journal of Human Genetics. 85: 264-72. PMID 19646677 DOI: 10.1016/J.Ajhg.2009.07.004 |
0.644 |
|
| 2009 |
Dennis MY, Paracchini S, Scerri TS, Prokunina-Olsson L, Knight JC, Wade-Martins R, Coggill P, Beck S, Green ED, Monaco AP. A common variant associated with dyslexia reduces expression of the KIAA0319 gene. Plos Genetics. 5: e1000436. PMID 19325871 DOI: 10.1371/Journal.Pgen.1000436 |
0.613 |
|
| 2008 |
Paracchini S, Steer CD, Buckingham LL, Morris AP, Ring S, Scerri T, Stein J, Pembrey ME, Ragoussis J, Golding J, Monaco AP. Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. The American Journal of Psychiatry. 165: 1576-84. PMID 18829873 DOI: 10.1176/Appi.Ajp.2008.07121872 |
0.61 |
|
| 2008 |
Velayos-Baeza A, Toma C, Paracchini S, Monaco AP. The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms. Human Molecular Genetics. 17: 859-71. PMID 18063668 DOI: 10.1093/Hmg/Ddm358 |
0.732 |
|
| 2007 |
Velayos-Baeza A, Toma C, da Roza S, Paracchini S, Monaco AP. Alternative splicing in the dyslexia-associated gene KIAA0319. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 627-34. PMID 17846832 DOI: 10.1007/S00335-007-9051-3 |
0.756 |
|
| 2007 |
Paracchini S, Scerri T, Monaco AP. The genetic lexicon of dyslexia. Annual Review of Genomics and Human Genetics. 8: 57-79. PMID 17444811 DOI: 10.1146/Annurev.Genom.8.080706.092312 |
0.589 |
|
| 2007 |
Zerjal T, Pandya A, Thangaraj K, Ling EY, Kearley J, Bertoneri S, Paracchini S, Singh L, Tyler-Smith C. Y-chromosomal insights into the genetic impact of the caste system in India. Human Genetics. 121: 137-44. PMID 17075717 DOI: 10.1007/S00439-006-0282-2 |
0.367 |
|
| 2006 |
Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O'Donovan MC, Williams J, Monaco AP. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Molecular Psychiatry. 11: 1085-91, 1061. PMID 17033633 DOI: 10.1038/Sj.Mp.4001904 |
0.621 |
|
| 2006 |
Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, Keating BJ, Taylor JM, Hacking DF, Scerri T, Francks C, Richardson AJ, Wade-Martins R, Stein JF, Knight JC, et al. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Human Molecular Genetics. 15: 1659-66. PMID 16600991 DOI: 10.1093/Hmg/Ddl089 |
0.595 |
|
| 2006 |
Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O'Donovan MC, Williams J, Monaco AP. Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia Molecular Psychiatry. 11: 1061. DOI: 10.1038/Sj.Mp.4001930 |
0.535 |
|
| 2004 |
Scerri TS, Fisher SE, Francks C, MacPhie IL, Paracchini S, Richardson AJ, Stein JF, Monaco AP. Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. Journal of Medical Genetics. 41: 853-7. PMID 15520411 DOI: 10.1136/Jmg.2004.018341 |
0.666 |
|
| 2004 |
Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. American Journal of Human Genetics. 75: 1046-58. PMID 15514892 DOI: 10.1086/426404 |
0.685 |
|
| 2004 |
Arredi B, Poloni ES, Paracchini S, Zerjal T, Fathallah DM, Makrelouf M, Pascali VL, Novelletto A, Tyler-Smith C. A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa. American Journal of Human Genetics. 75: 338-45. PMID 15202071 DOI: 10.1086/423147 |
0.372 |
|
| 2004 |
Fernandes S, Paracchini S, Meyer LH, Floridia G, Tyler-Smith C, Vogt PH. A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N. American Journal of Human Genetics. 74: 180-7. PMID 14639527 DOI: 10.1086/381132 |
0.438 |
|
| 2002 |
Paracchini S, Stuppia L, Gatta V, De Santo M, Palka G, Tyler-Smith C. Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. Journal of Endocrinological Investigation. 25: 993-5. PMID 12553561 DOI: 10.1007/Bf03344074 |
0.301 |
|
| 2002 |
Paracchini S, Arredi B, Chalk R, Tyler-Smith C. Hierarchical high-throughput SNP genotyping of the human Y chromosome using MALDI-TOF mass spectrometry. Nucleic Acids Research. 30: e27. PMID 11884646 DOI: 10.1093/Nar/30.6.E27 |
0.348 |
|
| 2000 |
Paracchini S, Stuppia L, Gatta V, Palka G, Moro E, Foresta C, Mengua L, Oliva R, Ballescà JL, Kremer JA, van Golde RJ, Tuerlings JH, Hargreave T, Ross A, Cooke H, et al. Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. Journal of Endocrinological Investigation. 23: 671-6. PMID 11097432 DOI: 10.1007/Bf03343792 |
0.335 |
|
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