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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1984 1
1985 2
1986 3
1987 1
1988 2
1994 1
2001 1
2006 1
2008 2
2009 1
2010 1
2011 2
2012 1
2015 1
2017 1
2018 2
2019 1
2020 1
2021 1
2022 2
2023 2
2024 0

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27 results

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Page 1
Multiple endocrine neoplasia type 2.
Forster-Gibson CJ, Mulligan LM. Forster-Gibson CJ, et al. Eur J Cancer. 1994;30A(13):1969-74. doi: 10.1016/0959-8049(94)00388-l. Eur J Cancer. 1994. PMID: 7734209 Review. No abstract available.
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data.
Hartley T, Soubry É, Acker M, Osmond M, Couse M, Gillespie MK, Ito Y, Marshall AE, Lemire G, Huang L, Chisholm C, Eaton AJ, Price EM, Dowling JJ, Ramani AK, Mendoza-Londono R, Costain G, Axford MM, Szuto A, McNiven V, Damseh N, Jobling R, de Kock L, Mojarad BA, Young T, Shao Z, Hayeems RZ, Graham ID, Tarnopolsky M, Brady L, Armour CM, Geraghty M, Richer J, Sawyer S, Lines M, Mercimek-Andrews S, Carter MT, Graham G, Kannu P, Lazier J, Li C, Aul RB, Balci TB, Dlamini N, Badalato L, Guerin A, Walia J, Chitayat D, Cohn R, Faghfoury H, Forster-Gibson C, Gonorazky H, Grunebaum E, Inbar-Feigenberg M, Karp N, Morel C, Rusnak A, Sondheimer N, Warman-Chardon J, Bhola PT, Bourque DK, Chacon IJ, Chad L, Chakraborty P, Chong K, Doja A, Goh ES, Saleh M; Care4Rare Canada; Potter BK, Marshall CR, Dyment DA, Kernohan K, Boycott KM. Hartley T, et al. Among authors: forster gibson c. Clin Genet. 2023 Mar;103(3):288-300. doi: 10.1111/cge.14262. Epub 2022 Nov 29. Clin Genet. 2023. PMID: 36353900
Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository.
Mighton C, Smith AC, Mayers J, Tomaszewski R, Taylor S, Hume S, Agatep R, Spriggs E, Feilotter HE, Semenuk L, Wong H, Lazo de la Vega L, Marshall CR, Axford MM, Silver T, Charames GS, Di Gioacchino V, Watkins N, Foulkes WD, Clavier M, Hamel N, Chong G, Lamont RE, Parboosingh J, Karsan A, Bosdet I, Young SS, Tucker T, Akbari MR, Speevak MD, Vaags AK, Lebo MS, Lerner-Ellis J; Canadian Open Genetics Repository Working Group. Mighton C, et al. J Med Genet. 2022 Jun;59(6):571-578. doi: 10.1136/jmedgenet-2021-107738. Epub 2021 Apr 19. J Med Genet. 2022. PMID: 33875564 Free PMC article.
Behaviour changes in an adult with Down syndrome.
Forster-Gibson CJ. Forster-Gibson CJ. Can Fam Physician. 2019 Apr;65(Suppl 1):S25-S26. Can Fam Physician. 2019. PMID: 31023775 Free PMC article. No abstract available.
Autism severity is associated with child and maternal MAOA genotypes.
Cohen IL, Liu X, Lewis ME, Chudley A, Forster-Gibson C, Gonzalez M, Jenkins EC, Brown WT, Holden JJ. Cohen IL, et al. Among authors: forster gibson c. Clin Genet. 2011 Apr;79(4):355-62. doi: 10.1111/j.1399-0004.2010.01471.x. Clin Genet. 2011. PMID: 20573161
Face-brain asymmetry in autism spectrum disorders.
Hammond P, Forster-Gibson C, Chudley AE, Allanson JE, Hutton TJ, Farrell SA, McKenzie J, Holden JJ, Lewis ME. Hammond P, et al. Among authors: forster gibson c. Mol Psychiatry. 2008 Jun;13(6):614-23. doi: 10.1038/mp.2008.18. Epub 2008 Mar 4. Mol Psychiatry. 2008. PMID: 18317467
27 results