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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. Among authors: baribeau d. 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.
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.
Developmental cascades between insistence on sameness behaviour and anxiety symptoms in autism spectrum disorder.
Baribeau DA, Vigod SN, Pullenayegum E, Kerns CM, Vaillancourt T, Duku E, Smith IM, Volden J, Zwaigenbaum L, Bennett T, Elsabbagh M, Zaidman-Zait A, Richard AE, Szatmari P. Baribeau DA, et al. Eur Child Adolesc Psychiatry. 2023 Nov;32(11):2109-2118. doi: 10.1007/s00787-022-02049-9. Epub 2022 Jul 24. Eur Child Adolesc Psychiatry. 2023. PMID: 35871413
Novel treatments in autism spectrum disorder.
Baribeau D, Vorstman J, Anagnostou E. Baribeau D, et al. Curr Opin Psychiatry. 2022 Mar 1;35(2):101-110. doi: 10.1097/YCO.0000000000000775. Curr Opin Psychiatry. 2022. PMID: 35044968 Review.
31 results