214 related articles for article (PubMed ID: 21739582)
1. Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.
Osbun N; Li J; O'Driscoll MC; Strominger Z; Wakahiro M; Rider E; Bukshpun P; Boland E; Spurrell CH; Schackwitz W; Pennacchio LA; Dobyns WB; Black GC; Sherr EH
Am J Med Genet A; 2011 Aug; 155A(8):1865-76. PubMed ID: 21739582
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome.
Filges I; Röthlisberger B; Boesch N; Weber P; Wenzel F; Huber AR; Heinimann K; Miny P
Am J Med Genet A; 2010 Apr; 152A(4):987-93. PubMed ID: 20358614
[TBL] [Abstract][Full Text] [Related]
3. Anterior and posterior commissures in agenesis of the corpus callosum: Alternative pathways for attention processes?
Siffredi V; Wood AG; Leventer RJ; Vaessen M; McIlroy A; Anderson V; Vuilleumier P; Spencer-Smith MM
Cortex; 2019 Dec; 121():454-467. PubMed ID: 31731212
[TBL] [Abstract][Full Text] [Related]
4. Intra- and inter-hemispheric structural connectome in agenesis of the corpus callosum.
Shi M; Freitas LGA; Spencer-Smith MM; Kebets V; Anderson V; McIlroy A; Wood AG; Leventer RJ; Van De Ville D; Siffredi V
Neuroimage Clin; 2021; 31():102709. PubMed ID: 34130191
[TBL] [Abstract][Full Text] [Related]
5. Human brain imaging studies of DISC1 in schizophrenia, bipolar disorder and depression: a systematic review.
Duff BJ; Macritchie KAN; Moorhead TWJ; Lawrie SM; Blackwood DHR
Schizophr Res; 2013 Jun; 147(1):1-13. PubMed ID: 23602339
[TBL] [Abstract][Full Text] [Related]
6. Inhibitory control in children with agenesis of the corpus callosum compared with typically developing children.
Soon E; Siffredi V; Anderson PJ; Anderson VA; McIlroy A; Leventer RJ; Wood AG; Spencer-Smith MM
J Int Neuropsychol Soc; 2024 Jan; 30(1):18-26. PubMed ID: 37057871
[TBL] [Abstract][Full Text] [Related]
7. The role of primary cilia in corpus callosum formation is mediated by production of the Gli3 repressor.
Laclef C; Anselme I; Besse L; Catala M; Palmyre A; Baas D; Paschaki M; Pedraza M; Métin C; Durand B; Schneider-Maunoury S
Hum Mol Genet; 2015 Sep; 24(17):4997-5014. PubMed ID: 26071364
[TBL] [Abstract][Full Text] [Related]
8. A neonate with the Pelger-Huët anomaly, cleft lip and palate, and agenesis of the corpus callosum, with a chromosomal microdeletion involving 1q41 to 1q42.12.
Christensen RD; Yaish HM
J Perinatol; 2012 Mar; 32(3):238-40. PubMed ID: 22370897
[TBL] [Abstract][Full Text] [Related]
9. Chromosomal location and genomic structure of the human translin-associated factor X gene (TRAX; TSNAX) revealed by intergenic splicing to DISC1, a gene disrupted by a translocation segregating with schizophrenia.
Millar JK; Christie S; Semple CA; Porteous DJ
Genomics; 2000 Jul; 67(1):69-77. PubMed ID: 10945471
[TBL] [Abstract][Full Text] [Related]
10. A 6.9 Mb 1qter deletion/4.4 Mb 18pter duplication in a boy with extreme microcephaly with simplified gyral pattern, vermis hypoplasia and corpus callosum agenesis.
Andrieux J; Cuvellier JC; Duban-Bedu B; Joriot-Chekaf S; Dieux-Coeslier A; Manouvrier-Hanu S; Delobel B; Vallee L
Eur J Med Genet; 2008; 51(1):87-91. PubMed ID: 18053786
[TBL] [Abstract][Full Text] [Related]
11. Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum.
Boland E; Clayton-Smith J; Woo VG; McKee S; Manson FD; Medne L; Zackai E; Swanson EA; Fitzpatrick D; Millen KJ; Sherr EH; Dobyns WB; Black GC
Am J Hum Genet; 2007 Aug; 81(2):292-303. PubMed ID: 17668379
[TBL] [Abstract][Full Text] [Related]
12. Morphometric variability of neuroimaging features in children with agenesis of the corpus callosum.
Neal JB; Filippi CG; Mayeux R
BMC Neurol; 2015 Jul; 15():116. PubMed ID: 26209096
[TBL] [Abstract][Full Text] [Related]
13. Structural connectivity analysis reveals abnormal brain connections in agenesis of the corpus callosum in children.
Meoded A; Katipally R; Bosemani T; Huisman TA; Poretti A
Eur Radiol; 2015 May; 25(5):1471-8. PubMed ID: 25477275
[TBL] [Abstract][Full Text] [Related]
14. Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene.
Caliebe A; Kroes HY; van der Smagt JJ; Martin-Subero JI; Tönnies H; van 't Slot R; Nievelstein RA; Muhle H; Stephani U; Alfke K; Stefanova I; Hellenbroich Y; Gillessen-Kaesbach G; Hochstenbach R; Siebert R; Poot M
Eur J Med Genet; 2010; 53(4):179-85. PubMed ID: 20382278
[TBL] [Abstract][Full Text] [Related]
15. Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomalies.
Alby C; Boutaud L; Bessières B; Serre V; Rio M; Cormier-Daire V; de Oliveira J; Ichkou A; Mouthon L; Gordon CT; Bonnière M; Mechler C; Nitschke P; Bole C; Lyonnet S; Bahi-Buisson N; Boddaert N; Colleaux L; Roth P; Ville Y; Vekemans M; Encha-Razavi F; Attié-Bitach T; Thomas S
Am J Med Genet A; 2018 May; 176(5):1091-1098. PubMed ID: 29681083
[TBL] [Abstract][Full Text] [Related]
16. Agenesis of the corpus callosum associated with DiGeorge-velocardiofacial syndrome: a case report and review of the literature.
Kraynack NC; Hostoffer RW; Robin NH
J Child Neurol; 1999 Nov; 14(11):754-6. PubMed ID: 10593557
[TBL] [Abstract][Full Text] [Related]
17. Depletion of Inositol Polyphosphate 4-Phosphatase II Suppresses Callosal Axon Formation in the Developing Mice.
Ji L; Kim NH; Huh SO; Rhee HJ
Mol Cells; 2016 Jun; 39(6):501-7. PubMed ID: 27109423
[TBL] [Abstract][Full Text] [Related]
18. A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome.
Hill AD; Chang BS; Hill RS; Garraway LA; Bodell A; Sellers WR; Walsh CA
Am J Med Genet A; 2007 Aug; 143A(15):1692-8. PubMed ID: 17603806
[TBL] [Abstract][Full Text] [Related]
19. A Neuropsychological Profile for Agenesis of the Corpus Callosum? Cognitive, Academic, Executive, Social, and Behavioral Functioning in School-Age Children.
Siffredi V; Anderson V; McIlroy A; Wood AG; Leventer RJ; Spencer-Smith MM
J Int Neuropsychol Soc; 2018 May; 24(5):445-455. PubMed ID: 29510770
[TBL] [Abstract][Full Text] [Related]
20. Neural correlates of working memory in children and adolescents with agenesis of the corpus callosum: An fMRI study.
Siffredi V; Spencer-Smith MM; Barrouillet P; Vaessen MJ; Leventer RJ; Anderson V; Vuilleumier P
Neuropsychologia; 2017 Nov; 106():71-82. PubMed ID: 28893526
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
