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For: 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: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 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 J, Brendgen MR, Dionne G, Vitaro F, Lupton MK, Martin NG, Porjesz B, Hesselbrock V, Foroud T, Agrawal A, Edenberg HJ, Liu Y, Plawecki MH, Kuperman S, Kramer JR, Meyers JM, Kamarajan C, Pandey A, Bierut L, Rice J, Bucholz KK, Schuckit MA, Tischfield J, Hart R, Almasy L, Goate A, Slesinger P, Scott D, 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 J, 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. [DOI: 10.1038/s41380-022-01793-3] [Reference Citation Analysis]
2 Singh R. Connecting human voice profiling to genomics: A predictive algorithm for linking speech phenotypes to genetic microdeletion syndromes.. [DOI: 10.1101/2022.05.23.493126] [Reference Citation Analysis]
3 Meyer GP, da Silva BS, Bandeira CE, Tavares MEA, Cupertino RB, Oliveira EP, Müller D, Kappel DB, Teche SP, Vitola ES, Rohde LA, Rovaris DL, Grevet EH, Bau CHD. Dissecting the cross-trait effects of the FOXP2 GWAS hit on clinical and brain phenotypes in adults with ADHD. Eur Arch Psychiatry Clin Neurosci. [DOI: 10.1007/s00406-022-01388-7] [Reference Citation Analysis]
4 Wong MM, Kampen RA, Braden RO, Alagöz G, Hildebrand MS, Barnett C, Barnett M, Brusco A, Carli D, de Vries BB, Dingemans AJ, Elmslie F, Ferrero GB, Jansen NA, van de Laar IM, Moroni A, Mowat D, Murray L, Novara F, Peron A, Scheffer IE, Sirchia F, Turner SJ, Vignoli A, Vino A, Weber S, Chung WK, Gerard M, López-gonzález V, Palmer E, Morgan AT, van Bon BW, Fisher SE. SETBP1 variants outside the degron disrupt DNA-binding and transcription independent of protein abundance to cause a heterogeneous neurodevelopmental disorder.. [DOI: 10.1101/2022.03.04.22271462] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Haddad-Eid E, Gur N, Eid S, Pilowsky-Peleg T, Straussberg R. The phenotype of homozygous EMC10 variant: A new syndrome with intellectual disability and language impairment. Eur J Paediatr Neurol 2022;37:56-61. [PMID: 35124540 DOI: 10.1016/j.ejpn.2022.01.012] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Zug R. Developmental disorders caused by haploinsufficiency of transcriptional regulators: a perspective based on cell fate determination. Biol Open 2022;11:bio058896. [PMID: 35089335 DOI: 10.1242/bio.058896] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
7 Palaniyappan L, Du J, Zhang J, Feng J. Reply to: "Historical pursuits of the language pathway hypothesis of schizophrenia". NPJ Schizophr 2021;7:54. [PMID: 34753936 DOI: 10.1038/s41537-021-00183-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Palaniyappan L. Dissecting the neurobiology of linguistic disorganisation and impoverishment in schizophrenia. Semin Cell Dev Biol 2021:S1084-9521(21)00235-4. [PMID: 34507903 DOI: 10.1016/j.semcdb.2021.08.015] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
9 Carrion-Castillo A, Estruch SB, Maassen B, Franke B, Francks C, Fisher SE. Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family. Hum Genet 2021;140:1183-200. [PMID: 34076780 DOI: 10.1007/s00439-021-02289-w] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 Palazzo O, Rass M, Brembs B. Identification of FoxP circuits involved in locomotion and object fixation in Drosophila. Open Biol 2020;10:200295. [PMID: 33321059 DOI: 10.1098/rsob.200295] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
11 Palazzo O, Raß M, Brembs B. Identification of FoxP circuits involved in locomotion and object fixation in Drosophila.. [DOI: 10.1101/2020.07.15.204677] [Reference Citation Analysis]