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Associations of psychotic symptom dimensions with clinical and developmental variables in twin and general clinical samples.
Cardno AG, Allardyce J, Bakker SC, Toulopoulou T, Kravariti E, Picchioni MM, Kane F, Rijsdijk FV, Mahmood T, Nasser El Din S, du Toit D, Jones LA, Quattrone D, Walters JTR, Legge SE, Holmans PA, Murray RM, Vassos E. Cardno AG, et al. Br J Psychiatry. 2024 Oct 30:1-8. doi: 10.1192/bjp.2024.129. Online ahead of print. Br J Psychiatry. 2024. PMID: 39474930
A Recessively Inherited Risk Locus on Chromosome 13q22-31 Conferring Susceptibility to Schizophrenia.
Mahmood T, El-Asrag ME, Poulter JA, Cardno AG, Tomlinson A, Ahmed S, Al-Amri A, Nazari J, Neill J, Chamali RS, Kiwan N, Ghuloum S, Alhaj HA, Randerson Moor J, Khan S, Al-Amin H, Johnson CA, Woodruff P, Wilkinson ID, Ali M, Clapcote SJ, Inglehearn CF. Mahmood T, et al. Schizophr Bull. 2021 Apr 29;47(3):796-802. doi: 10.1093/schbul/sbaa161. Schizophr Bull. 2021. PMID: 33159203 Free PMC article.
LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss.
Al-Amri AH, Al Saegh A, Al-Mamari W, El-Asrag ME, Al-Kindi MN, Al Khabouri M, Al Wardy N, Al Lamki K, Gabr A, Idris A, Inglehearn CF, Clapcote SJ, Ali M. Al-Amri AH, et al. Eur J Med Genet. 2019 Dec;62(12):103592. doi: 10.1016/j.ejmg.2018.11.026. Epub 2018 Nov 23. Eur J Med Genet. 2019. PMID: 30476627