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For: Deriziotis P, Fisher SE. Speech and Language: Translating the Genome. Trends in Genetics 2017;33:642-56. [DOI: 10.1016/j.tig.2017.07.002] [Cited by in Crossref: 42] [Cited by in F6Publishing: 45] [Article Influence: 7.0] [Reference Citation Analysis]
Number Citing Articles
1 Hruby GG, Mitra A. A naturalized view of literacy education: what the neuro- and life sciences may offer language and literacy research. International Encyclopedia of Education(Fourth Edition) 2023. [DOI: 10.1016/b978-0-12-818630-5.07076-7] [Reference Citation Analysis]
2 Tielbeek JJ, Uffelmann E, Williams BS, Colodro-Conde L, Gagnon É, Mallard TT, Levitt BE, Jansen PR, Johansson A, Sallis HM, Pistis G, Saunders GRB, Allegrini AG, Rimfeld K, Konte B, Klein M, Hartmann AM, Salvatore JE, Nolte IM, Demontis D, Malmberg ALK, Burt SA, Savage JE, Sugden K, Poulton R, Harris KM, Vrieze S, McGue M, Iacono WG, Mota NR, Mill J, Viana JF, Mitchell BL, Morosoli JJ, Andlauer TFM, Ouellet-Morin I, Tremblay RE, Côté SM, Gouin JP, Brendgen MR, Dionne G, Vitaro F, Lupton MK, Martin NG, Castelao E, Räikkönen K, Eriksson JG, Lahti J, Hartman CA, Oldehinkel AJ, Snieder H, Liu H, Preisig M, Whipp A, Vuoksimaa E, Lu Y, Jern P, Rujescu D, Giegling I, Palviainen T, Kaprio J, Harden KP, Munafò MR, Morneau-Vaillancourt G, Plomin R, Viding E, Boutwell BB, Aliev F, Dick DM, Popma A, Faraone SV, Børglum AD, Medland SE, Franke B, Boivin M, Pingault JB, Glennon JC, Barnes JC, Fisher SE, Moffitt TE, Caspi A, Polderman TJC, Posthuma D; COGA Consortium, Spit for Science Working Group. Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis. Mol Psychiatry 2022;27:4453-63. [PMID: 36284158 DOI: 10.1038/s41380-022-01793-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 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, van Donkelaar M, Liao Z, Jansen PR, Andlauer TFM, Bates TC, Bernard M, Blokland K, Bonte M, Børglum AD, Bourgeron T, Brandeis D, Ceroni F, Csépe V, Dale PS, de Jong PF, DeFries JC, Démonet JF, Demontis D, Feng Y, Gordon SD, Guger SL, Hayiou-Thomas ME, Hernández-Cabrera JA, Hottenga JJ, Hulme C, Kere J, Kerr EN, Koomar T, Landerl K, Leonard GT, Lovett MW, Lyytinen H, Martin NG, Martinelli A, Maurer U, Michaelson JJ, Moll K, Monaco AP, Morgan AT, Nöthen MM, Pausova Z, Pennell CE, Pennington BF, Price KM, Rajagopal VM, Ramus F, Richer L, Simpson NH, Smith SD, Snowling MJ, Stein J, Strug LJ, Talcott JB, Tiemeier H, van der Schroeff MP, Verhoef E, Watkins KE, Wilkinson M, Wright MJ, Barr CL, Boomsma DI, Carreiras M, Franken MJ, Gruen JR, Luciano M, Müller-Myhsok B, Newbury DF, Olson RK, Paracchini S, Paus T, Plomin R, Reilly S, Schulte-Körne G, Tomblin JB, van Bergen E, Whitehouse AJO, Willcutt EG, St Pourcain B, Francks C, Fisher SE. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proc Natl Acad Sci U S A 2022;119:e2202764119. [PMID: 35998220 DOI: 10.1073/pnas.2202764119] [Cited by in F6Publishing: 5] [Reference Citation Analysis]
4 Anijs M, Devanna P, Vernes SC. ARHGEF39, a Gene Implicated in Developmental Language Disorder, Activates RHOA and Is Involved in Cell De-Adhesion and Neural Progenitor Cell Proliferation. Front Mol Neurosci 2022;15:941494. [DOI: 10.3389/fnmol.2022.941494] [Reference Citation Analysis]
5 Nayak S, Gustavson DE, Wang Y, Below JE, Gordon RL, Magne CL. Test of Prosody via Syllable Emphasis (“TOPsy”): Psychometric Validation of a Brief Scalable Test of Lexical Stress Perception. Front Neurosci 2022;16:765945. [DOI: 10.3389/fnins.2022.765945] [Reference Citation Analysis]
6 Scott KE, Mann RS, Schormans AL, Schmid S, Allman BL. Hyperexcitable and Immature-Like Neuronal Activity in the Auditory Cortex of Adult Rats Lacking the Language-Linked CNTNAP2 Gene. Cereb Cortex 2022:bhab517. [PMID: 35106542 DOI: 10.1093/cercor/bhab517] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
7 Grigorenko EL. The Role of Genetic Factors in Reading and its Development Across Languages and Writing Systems. Scientific Studies of Reading. [DOI: 10.1080/10888438.2022.2033244] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Koomar T, Casten LG, Thomas TR, Koh J, Hofamman D, Thenuwara S, Momany A, O’brien M, Murray J, Tomblin JB, Michaelson JJ. Whole Genome Sequencing Illuminates the Developmental Signatures of Human Language Ability.. [DOI: 10.1101/2021.11.22.21266703] [Reference Citation Analysis]
9 Eising E, Mirza-schreiber N, de Zeeuw EL, Wang CA, Truong DT, Allegrini AG, Shapland CY, Zhu G, Wigg KG, Gerritse M, Molz B, Alagöz G, Gialluisi A, Abbondanza F, Rimfeld K, van Donkelaar M, Liao Z, Jansen PR, Andlauer TFM, Bates TC, Bernard M, Blokland K, Børglum AD, Bourgeron T, Brandeis D, Ceroni F, Dale PS, Landerl K, Lyytinen H, de Jong PF, Defries JC, Demontis D, Feng Y, Gordon SD, Guger SL, Hayiou-thomas ME, Hernández-cabrera JA, Hottenga J, Hulme C, Kerr EN, Koomar T, Lovett MW, Martin NG, Martinelli A, Maurer U, Michaelson JJ, Moll K, Monaco AP, Morgan AT, Nöthen MM, Pausova Z, Pennell CE, Pennington BF, Price KM, Rajagopal VM, Ramus F, Richer L, Simpson NH, Smith S, Snowling MJ, Stein J, Strug LJ, Talcott JB, Tiemeier H, van de Schroeff MM, Verhoef E, Watkins KE, Wilkinson M, Wright MJ, Barr CL, Boomsma DI, Carreiras M, Franken MJ, Gruen JR, Luciano M, Müller-myhsok B, Newbury DF, Olson RK, Paracchini S, Paus T, Plomin R, Schulte-körne G, Reilly S, Tomblin JB, van Bergen E, Whitehouse AJ, Willcutt EG, Pourcain BS, Francks C, Fisher SE. Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.. [DOI: 10.1101/2021.11.04.466897] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
10 Cirnaru MD, Song S, Tshilenge KT, Corwin C, Mleczko J, Galicia Aguirre C, Benlhabib H, Bendl J, Apontes P, Fullard J, Creus-Muncunill J, Reyahi A, Nik AM, Carlsson P, Roussos P, Mooney SD, Ellerby LM, Ehrlich ME. Unbiased identification of novel transcription factors in striatal compartmentation and striosome maturation. Elife 2021;10:e65979. [PMID: 34609283 DOI: 10.7554/eLife.65979] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
11 Tilot AK, Khramtsova EA, Liang D, Grasby KL, Jahanshad N, Painter J, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Liu S, Brotman SM, Thompson PM, Medland SE, Macciardi F, Stranger BE, Davis LK, Fisher SE, Stein JL. The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. Cereb Cortex 2021;31:1873-87. [PMID: 33290510 DOI: 10.1093/cercor/bhaa327] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
12 Du J, Palaniyappan L, Liu Z, Cheng W, Gong W, Zhu M, Wang J, Zhang J, Feng J. The genetic determinants of language network dysconnectivity in drug-naïve early stage schizophrenia. NPJ Schizophr 2021;7:18. [PMID: 33658499 DOI: 10.1038/s41537-021-00141-8] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
13 Kalnak N, Löwgren K, Hansson K. Past-tense inflection of non-verbs: a potential clinical marker of developmental language disorder in Swedish children. Logoped Phoniatr Vocol 2020;:1-8. [PMID: 32894034 DOI: 10.1080/14015439.2020.1810311] [Reference Citation Analysis]
14 Walters CE Jr, Nitin R, Margulis K, Boorom O, Gustavson DE, Bush CT, Davis LK, Below JE, Cox NJ, Camarata SM, Gordon RL. Automated Phenotyping Tool for Identifying Developmental Language Disorder Cases in Health Systems Data (APT-DLD): A New Research Algorithm for Deployment in Large-Scale Electronic Health Record Systems. J Speech Lang Hear Res 2020;63:3019-35. [PMID: 32791019 DOI: 10.1044/2020_JSLHR-19-00397] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
15 den Hoed J, Fisher SE. Genetic pathways involved in human speech disorders. Curr Opin Genet Dev 2020;65:103-11. [PMID: 32622339 DOI: 10.1016/j.gde.2020.05.012] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 4.0] [Reference Citation Analysis]
16 Gianluca G, Stefania A. Theoretical and genetic correlations between language and movement. JAHC 2020. [DOI: 10.36017/jahc2006-002] [Reference Citation Analysis]
17 Cirnaru M, Song S, Tshilenge K, Corwin C, Mleczko J, Aguirre CG, Benlhabib H, Bendl J, Apontes P, Fullard JF, Muncunill JC, Reyah A, Nik AM, Carlsson P, Roussos P, Mooney SD, Ellerby LM, Ehrlich ME. Transcriptional and epigenetic characterization of early striosomes identifies Foxf2 and Olig2 as factors required for development of striatal compartmentation and neuronal phenotypic differentiation.. [DOI: 10.1101/2020.05.19.105171] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
18 Doust C, Gordon SD, Garden N, Fisher SE, Martin NG, Bates TC, Luciano M. The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults. Twin Res Hum Genet 2020;23:23-32. [PMID: 32248883 DOI: 10.1017/thg.2020.7] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
19 Ladányi E, Persici V, Fiveash A, Tillmann B, Gordon RL. Is atypical rhythm a risk factor for developmental speech and language disorders? Wiley Interdiscip Rev Cogn Sci 2020;11:e1528. [PMID: 32244259 DOI: 10.1002/wcs.1528] [Cited by in Crossref: 29] [Cited by in F6Publishing: 32] [Article Influence: 9.7] [Reference Citation Analysis]
20 Kosubek-Langer J, Scharff C. Dynamic FoxP2 levels in male zebra finches are linked to morphology of adult-born Area X medium spiny neurons. Sci Rep 2020;10:4787. [PMID: 32179863 DOI: 10.1038/s41598-020-61740-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
21 Kong X, Tzourio-mazoyer N, Joliot M, Fedorenko E, Liu J, Fisher SE, Francks C. Gene Expression Correlates of the Cortical Network Underlying Sentence Processing. Neurobiology of Language 2020;1:77-103. [DOI: 10.1162/nol_a_00004] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
22 Hitchcock TJ, Paracchini S, Gardner A. Genomic Imprinting As a Window into Human Language Evolution. Bioessays 2019;41:e1800212. [PMID: 31132171 DOI: 10.1002/bies.201800212] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
23 Kong Y, Zhou W, Sun Z. Nuclear receptor corepressors in intellectual disability and autism. Mol Psychiatry 2020;25:2220-36. [PMID: 32034290 DOI: 10.1038/s41380-020-0667-y] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
24 Koomar T, Michaelson JJ. Genetic Intersections of Language and Neuropsychiatric Conditions. Curr Psychiatry Rep 2020;22:4. [PMID: 31953567 DOI: 10.1007/s11920-019-1123-z] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
25 Smith M. Evolution. Gene Environment Interactions 2020. [DOI: 10.1016/b978-0-12-819613-7.00003-7] [Reference Citation Analysis]
26 Fitch RH. Language impairments. Neurodevelopmental Disorders 2020. [DOI: 10.1016/b978-0-12-814409-1.00014-8] [Reference Citation Analysis]
27 Tager-flusberg H, Finch KH. Early development of speech and language. Neural Circuit and Cognitive Development 2020. [DOI: 10.1016/b978-0-12-814411-4.00019-6] [Reference Citation Analysis]
28 Rakhlin N, Landi N, Lee M, Magnuson JS, Naumova OY, Ovchinnikova IV, Grigorenko EL. Cohesion of Cortical Language Networks During Word Processing Is Predicted by a Common Polymorphism in the SETBP1 Gene. New Directions for Child and Adolescent Development 2020;2020:131-155. [DOI: 10.1002/cad.20331] [Reference Citation Analysis]
29 Sánchez-Valpuesta M, Suzuki Y, Shibata Y, Toji N, Ji Y, Afrin N, Asogwa CN, Kojima I, Mizuguchi D, Kojima S, Okanoya K, Okado H, Kobayashi K, Wada K. Corticobasal ganglia projecting neurons are required for juvenile vocal learning but not for adult vocal plasticity in songbirds. Proc Natl Acad Sci U S A 2019;116:22833-43. [PMID: 31636217 DOI: 10.1073/pnas.1913575116] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 2.3] [Reference Citation Analysis]
30 Uddén J, Hultén A, Bendtz K, Mineroff Z, Kucera KS, Vino A, Fedorenko E, Hagoort P, Fisher SE. Toward Robust Functional Neuroimaging Genetics of Cognition. J Neurosci 2019;39:8778-87. [PMID: 31570534 DOI: 10.1523/JNEUROSCI.0888-19.2019] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 3.3] [Reference Citation Analysis]
31 Schreiweis C, Irinopoulou T, Vieth B, Laddada L, Oury F, Burguière E, Enard W, Groszer M. Mice carrying a humanized Foxp2 knock-in allele show region-specific shifts of striatal Foxp2 expression levels. Cortex 2019;118:212-22. [DOI: 10.1016/j.cortex.2019.01.008] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
32 Snijders Blok L, Kleefstra T, Venselaar H, Maas S, Kroes HY, Lachmeijer AMA, van Gassen KLI, Firth HV, Tomkins S, Bodek S, Õunap K, Wojcik MH, Cunniff C, Bergstrom K, Powis Z, Tang S, Shinde DN, Au C, Iglesias AD, Izumi K, Leonard J, Abou Tayoun A, Baker SW, Tartaglia M, Niceta M, Dentici ML, Okamoto N, Miyake N, Matsumoto N, Vitobello A, Faivre L, Philippe C, Gilissen C, Wiel L, Pfundt R, Deriziotis P, Brunner HG, Fisher SE; DDD Study. De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder. Am J Hum Genet 2019;105:403-12. [PMID: 31303265 DOI: 10.1016/j.ajhg.2019.06.007] [Cited by in Crossref: 24] [Cited by in F6Publishing: 26] [Article Influence: 6.0] [Reference Citation Analysis]
33 Tilot AK, Khramtsova EA, Grasby K, Jahanshad N, Painter J, Colodro-conde L, Bralten J, Hibar DP, Lind PA, Liu S, Brotman SM, Thompson PM, Medland SE, Macciardi F, Stranger BE, Davis LK, Fisher SE, Stein JL. The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area.. [DOI: 10.1101/703793] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
34 Mountford HS, Villanueva P, Fernández MA, Barbieri ZD, Cazier J, Newbury DF. Candidate gene variant effects on language disorders in Robinson Crusoe Island. Annals of Human Biology 2019;46:109-19. [DOI: 10.1080/03014460.2019.1622776] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
35 Peter B, Dougherty MJ, Reed EK, Edelman E, Hanson K. Perceived Gaps in Genetics Training Among Audiologists and Speech-Language Pathologists: Lessons From a National Survey. Am J Speech Lang Pathol 2019;28:408-23. [PMID: 31091132 DOI: 10.1044/2018_AJSLP-18-0069] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
36 Shriberg LD, Kwiatkowski J, Mabie HL. Estimates of the prevalence of motor speech disorders in children with idiopathic speech delay. Clin Linguist Phon 2019;33:679-706. [PMID: 30987467 DOI: 10.1080/02699206.2019.1595731] [Cited by in Crossref: 23] [Cited by in F6Publishing: 16] [Article Influence: 5.8] [Reference Citation Analysis]
37 A. Reid A. Neuroimaging Reveals Heterogeneous Neural Correlates of Reading Deficit in Individuals with Dyslexia Consistent with a Multiple Deficit Model. Neuroimaging - Structure, Function and Mind 2019. [DOI: 10.5772/intechopen.80677] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
38 Schreiweis C, Irinopoulou T, Vieth B, Laddada L, Oury F, Burguière E, Enard W, Groszer M. Mice carrying a humanizedFoxp2knock-in allele show region-specific shifts of striatal Foxp2 expression levels.. [DOI: 10.1101/514893] [Reference Citation Analysis]
39 Kong X, Tzourio-mazoyer N, Joliot M, Fedorenko E, Liu J, Fisher SE, Francks C. Gene Expression Correlates of the Cortical Network Underlying Sentence Processing.. [DOI: 10.1101/439984] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
40 Benítez-Burraco A, Moran S. Editorial: The Adaptive Value of Languages: Non-linguistic Causes of Language Diversity. Front Psychol 2018;9:1827. [PMID: 30323782 DOI: 10.3389/fpsyg.2018.01827] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
41 Scott KE, Schormans AL, Pacoli KY, De Oliveira C, Allman BL, Schmid S. Altered Auditory Processing, Filtering, and Reactivity in the Cntnap2 Knock-Out Rat Model for Neurodevelopmental Disorders. J Neurosci 2018;38:8588-604. [PMID: 30126973 DOI: 10.1523/JNEUROSCI.0759-18.2018] [Cited by in Crossref: 25] [Cited by in F6Publishing: 28] [Article Influence: 5.0] [Reference Citation Analysis]
42 Xu S, Liu P, Chen Y, Chen Y, Zhang W, Zhao H, Cao Y, Wang F, Jiang N, Lin S, Li B, Zhang Z, Wei Z, Fan Y, Jin Y, He L, Zhou R, Dekker JD, Tucker HO, Fisher SE, Yao Z, Liu Q, Xia X, Guo X. Foxp2 regulates anatomical features that may be relevant for vocal behaviors and bipedal locomotion. Proc Natl Acad Sci U S A 2018;115:8799-804. [PMID: 30104377 DOI: 10.1073/pnas.1721820115] [Cited by in Crossref: 28] [Cited by in F6Publishing: 29] [Article Influence: 5.6] [Reference Citation Analysis]
43 Franklin AM, Giacheti CM, Silva NCD, Campos LMG, Pinato L. Correlation between sleep profile and behavior in individuals with specific learning disorder. Codas 2018;30:e20170104. [PMID: 29972444 DOI: 10.1590/2317-1782/20182017104] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
44 Kalnak N, Stamouli S, Peyrard-Janvid M, Rabkina I, Becker M, Klingberg T, Kere J, Forssberg H, Tammimies K. Enrichment of rare copy number variation in children with developmental language disorder. Clin Genet 2018;94:313-20. [PMID: 29851021 DOI: 10.1111/cge.13389] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
45 Mei C, Fedorenko E, Amor DJ, Boys A, Hoeflin C, Carew P, Burgess T, Fisher SE, Morgan AT. Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion. Eur J Hum Genet 2018;26:676-86. [PMID: 29445122 DOI: 10.1038/s41431-018-0102-x] [Cited by in Crossref: 33] [Cited by in F6Publishing: 34] [Article Influence: 6.6] [Reference Citation Analysis]