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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2013 | 2 |
2014 | 3 |
2015 | 2 |
2020 | 1 |
2021 | 1 |
2022 | 1 |
2024 | 0 |
Search Results
7 results
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Page 1
Sexual knowledge and behaviour in 22q11.2 deletion syndrome, a complex care condition.
J Appl Res Intellect Disabil. 2022 Jul;35(4):966-975. doi: 10.1111/jar.12927. Epub 2021 Jul 21.
J Appl Res Intellect Disabil. 2022.
PMID: 34291536
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature.
Lowther C, Costain G, Stavropoulos DJ, Melvin R, Silversides CK, Andrade DM, So J, Faghfoury H, Lionel AC, Marshall CR, Scherer SW, Bassett AS.
Lowther C, et al.
Genet Med. 2015 Feb;17(2):149-57. doi: 10.1038/gim.2014.83. Epub 2014 Jul 31.
Genet Med. 2015.
PMID: 25077648
Free PMC article.
Review.
Item in Clipboard
Adult neuropsychiatric expression and familial segregation of 2q13 duplications.
Costain G, Lionel AC, Fu F, Stavropoulos DJ, Gazzellone MJ, Marshall CR, Scherer SW, Bassett AS.
Costain G, et al.
Am J Med Genet B Neuropsychiatr Genet. 2014 Jun;165B(4):337-44. doi: 10.1002/ajmg.b.32236. Epub 2014 May 8.
Am J Med Genet B Neuropsychiatr Genet. 2014.
PMID: 24807792
Free PMC article.
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Copy number variable microRNAs in schizophrenia and their neurodevelopmental gene targets.
Warnica W, Merico D, Costain G, Alfred SE, Wei J, Marshall CR, Scherer SW, Bassett AS.
Warnica W, et al.
Biol Psychiatry. 2015 Jan 15;77(2):158-66. doi: 10.1016/j.biopsych.2014.05.011. Epub 2014 May 29.
Biol Psychiatry. 2015.
PMID: 25034949
Free PMC article.
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Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.
Lionel AC, Vaags AK, Sato D, Gazzellone MJ, Mitchell EB, Chen HY, Costain G, Walker S, Egger G, Thiruvahindrapuram B, Merico D, Prasad A, Anagnostou E, Fombonne E, Zwaigenbaum L, Roberts W, Szatmari P, Fernandez BA, Georgieva L, Brzustowicz LM, Roetzer K, Kaschnitz W, Vincent JB, Windpassinger C, Marshall CR, Trifiletti RR, Kirmani S, Kirov G, Petek E, Hodge JC, Bassett AS, Scherer SW.
Lionel AC, et al.
Hum Mol Genet. 2013 May 15;22(10):2055-66. doi: 10.1093/hmg/ddt056. Epub 2013 Feb 7.
Hum Mol Genet. 2013.
PMID: 23393157
Clinical Trial.
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Personalized medical information card for adults with 22q11.2 deletion syndrome: An initiative to improve communication between patients and healthcare providers.
Loo JCY, Boot E, Corral M, Bassett AS.
Loo JCY, et al.
J Appl Res Intellect Disabil. 2020 Nov;33(6):1534-1540. doi: 10.1111/jar.12747. Epub 2020 May 14.
J Appl Res Intellect Disabil. 2020.
PMID: 32407568
Free PMC article.
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Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.
Costain G, Lionel AC, Merico D, Forsythe P, Russell K, Lowther C, Yuen T, Husted J, Stavropoulos DJ, Speevak M, Chow EW, Marshall CR, Scherer SW, Bassett AS.
Costain G, et al.
Hum Mol Genet. 2013 Nov 15;22(22):4485-501. doi: 10.1093/hmg/ddt297. Epub 2013 Jun 27.
Hum Mol Genet. 2013.
PMID: 23813976
Free PMC article.
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