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For: Barnett CP, van Bon BWM. Monogenic and chromosomal causes of isolated speech and language impairment. J Med Genet 2015;52:719-29. [DOI: 10.1136/jmedgenet-2015-103161] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
1 Sebastián-lázaro D, Brun-gasca C, Fornieles A. Comunicación en personas con el síndrome de deleción de 22q11: voz y habla. Revista de Logopedia, Foniatría y Audiología 2022. [DOI: 10.1016/j.rlfa.2021.12.001] [Reference Citation Analysis]
2 Freitag CM, Noterdaeme M, Snippe K, Schulz P, Kim Z, Teufel K. [Developmental Speech and Language Disorders According to ICD-11]. Z Kinder Jugendpsychiatr Psychother 2021. [PMID: 34269095 DOI: 10.1024/1422-4917/a000821] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Savatt JM, Myers SM. Genetic Testing in Neurodevelopmental Disorders. Front Pediatr 2021;9:526779. [PMID: 33681094 DOI: 10.3389/fped.2021.526779] [Cited by in Crossref: 38] [Cited by in F6Publishing: 40] [Article Influence: 19.0] [Reference Citation Analysis]
4 Alsubaie LM, Alsuwat HS, Almandil NB, Alsulaiman A, Abdulazeez S, Borgio JF. Risk Y-haplotypes and pathogenic variants of Arab-ancestry boys with autism by an exome-wide association study. Mol Biol Rep 2020;47:7623-32. [DOI: 10.1007/s11033-020-05832-6] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
5 Rieger M, Krumbiegel M, Reuter MS, Schützenberger A, Reis A, Zweier C. 7q31.2q31.31 deletion downstream of FOXP2 segregating in a family with speech and language disorder. Am J Med Genet A 2020;182:2737-41. [PMID: 32885567 DOI: 10.1002/ajmg.a.61838] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
6 Lazzaro G, Caciolo C, Menghini D, Cumbo F, Digilio MC, Capolino R, Zampino G, Tartaglia M, Vicari S, Alfieri P. Defining language disorders in children and adolescents with Noonan Syndrome. Mol Genet Genomic Med 2020;8:e1069. [PMID: 32059087 DOI: 10.1002/mgg3.1069] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
7 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]
8 Coton J, Labalme A, Till M, Bussy G, Krifi Papoz S, Lesca G, Heron D, Sanlaville D, Edery P, des Portes V, Rossi M. Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations. Clin Case Rep 2018;6:827-834. [DOI: 10.1002/ccr3.1450] [Reference Citation Analysis]
9 Soblet J, Dimov I, Graf von Kalckreuth C, Cano-Chervel J, Baijot S, Pelc K, Sottiaux M, Vilain C, Smits G, Deconinck N. BCL11A frameshift mutation associated with dyspraxia and hypotonia affecting the fine, gross, oral, and speech motor systems. Am J Med Genet A 2018;176:201-8. [PMID: 28960836 DOI: 10.1002/ajmg.a.38479] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 2.5] [Reference Citation Analysis]
10 Shriberg LD, Strand EA, Fourakis M, Jakielski KJ, Hall SD, Karlsson HB, Mabie HL, McSweeny JL, Tilkens CM, Wilson DL. A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker. J Speech Lang Hear Res 2017;60:S1096-117. [PMID: 28384779 DOI: 10.1044/2016_JSLHR-S-15-0296] [Cited by in Crossref: 39] [Cited by in F6Publishing: 42] [Article Influence: 6.5] [Reference Citation Analysis]
11 Meerschaut I, Rochefort D, Revençu N, Pètre J, Corsello C, Rouleau GA, Hamdan FF, Michaud JL, Morton J, Radley J, Ragge N, García-Miñaúr S, Lapunzina P, Bralo MP, Mori MÁ, Moortgat S, Benoit V, Mary S, Bockaert N, Oostra A, Vanakker O, Velinov M, de Ravel TJ, Mekahli D, Sebat J, Vaux KK, DiDonato N, Hanson-Kahn AK, Hudgins L, Dallapiccola B, Novelli A, Tarani L, Andrieux J, Parker MJ, Neas K, Ceulemans B, Schoonjans AS, Prchalova D, Havlovicova M, Hancarova M, Budisteanu M, Dheedene A, Menten B, Dion PA, Lederer D, Callewaert B. FOXP1-related intellectual disability syndrome: a recognisable entity. J Med Genet 2017;54:613-23. [PMID: 28735298 DOI: 10.1136/jmedgenet-2017-104579] [Cited by in Crossref: 35] [Cited by in F6Publishing: 35] [Article Influence: 5.8] [Reference Citation Analysis]
12 Reuter MS, Krumbiegel M, Schlüter G, Ekici AB, Reis A, Zweier C. Haploinsufficiency of NR4A2 is associated with a neurodevelopmental phenotype with prominent language impairment. Am J Med Genet A 2017;173:2231-4. [PMID: 28544326 DOI: 10.1002/ajmg.a.38288] [Cited by in Crossref: 21] [Cited by in F6Publishing: 21] [Article Influence: 3.5] [Reference Citation Analysis]
13 Acuna-Hidalgo R, Deriziotis P, Steehouwer M, Gilissen C, Graham SA, van Dam S, Hoover-Fong J, Telegrafi AB, Destree A, Smigiel R, Lambie LA, Kayserili H, Altunoglu U, Lapi E, Uzielli ML, Aracena M, Nur BG, Mihci E, Moreira LM, Borges Ferreira V, Horovitz DD, da Rocha KM, Jezela-Stanek A, Brooks AS, Reutter H, Cohen JS, Fatemi A, Smitka M, Grebe TA, Di Donato N, Deshpande C, Vandersteen A, Marques Lourenço C, Dufke A, Rossier E, Andre G, Baumer A, Spencer C, McGaughran J, Franke L, Veltman JA, De Vries BB, Schinzel A, Fisher SE, Hoischen A, van Bon BW. Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies. PLoS Genet 2017;13:e1006683. [PMID: 28346496 DOI: 10.1371/journal.pgen.1006683] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 4.0] [Reference Citation Analysis]
14 Zavadenko NN. [Speech disorders in children: early diagnosis and treatment]. Zh Nevrol Psikhiatr Im S S Korsakova 2016;116:119-25. [PMID: 28139638 DOI: 10.17116/jnevro2016116121119-125] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.2] [Reference Citation Analysis]