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Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.
Costain G, Walker S, Argiropoulos B, Baribeau DA, Bassett AS, Boot E, Devriendt K, Kellam B, Marshall CR, Prasad A, Serrano MA, Stavropoulos DJ, Twede H, Vermeesch JR, Vorstman JAS, Scherer SW. Costain G, et al. Among authors: baribeau da. J Neurodev Disord. 2019 Feb 7;11(1):3. doi: 10.1186/s11689-019-9263-3. J Neurodev Disord. 2019. PMID: 30732576 Free PMC article.
Developmental implications of genetic testing for physical indications.
Baribeau DA, Hoang N, Selvanayagam T, Stavropoulos DJ, Costain G, Scherer SW, Vorstman J. Baribeau DA, et al. Eur J Hum Genet. 2022 Nov;30(11):1297-1300. doi: 10.1038/s41431-022-01181-z. Epub 2022 Sep 6. Eur J Hum Genet. 2022. PMID: 36068265 Free PMC article.
Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions.
AlMail A, Jamjoom A, Pan A, Feng MY, Chau V, D'Gama AM, Howell K, Liang NSY, McTague A, Poduri A, Wiltrout K; IPCHiP Executive Committee; Bassett AS, Christodoulou J, Dupuis L, Gill P, Levy T, Siper P, Stark Z, Vorstman JAS, Diskin C, Jewitt N, Baribeau D, Costain G. AlMail A, et al. NPJ Genom Med. 2024 Apr 6;9(1):27. doi: 10.1038/s41525-024-00408-w. NPJ Genom Med. 2024. PMID: 38582909 Free PMC article.
Structural neuroimaging correlates of social deficits are similar in autism spectrum disorder and attention-deficit/hyperactivity disorder: analysis from the POND Network.
Baribeau DA, Dupuis A, Paton TA, Hammill C, Scherer SW, Schachar RJ, Arnold PD, Szatmari P, Nicolson R, Georgiades S, Crosbie J, Brian J, Iaboni A, Kushki A, Lerch JP, Anagnostou E. Baribeau DA, et al. Transl Psychiatry. 2019 Feb 4;9(1):72. doi: 10.1038/s41398-019-0382-0. Transl Psychiatry. 2019. PMID: 30718456 Free PMC article.
33 results