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Risk modifiers in carriers of BRCA1 mutations.
Narod SA, Goldgar D, Cannon-Albright L, Weber B, Moslehi R, Ives E, Lenoir G, Lynch H. Narod SA, et al. Among authors: ives e. Int J Cancer. 1995 Dec 20;64(6):394-8. doi: 10.1002/ijc.2910640608. Int J Cancer. 1995. PMID: 8550241
Sorsby's fundus dystrophy.
Hamilton WK, Ewing CC, Ives EJ, Carruthers JD. Hamilton WK, et al. Among authors: ives ej. Ophthalmology. 1989 Dec;96(12):1755-62. doi: 10.1016/s0161-6420(89)32647-9. Ophthalmology. 1989. PMID: 2695876 Review.
Juvenile hereditary retinoschisis.
Ewing CC, Ives EJ. Ewing CC, et al. Among authors: ives ej. Trans Ophthalmol Soc U K (1962). 1970;89:29-39. Trans Ophthalmol Soc U K (1962). 1970. PMID: 5276662 No abstract available.
VAMP1 mutation causes dominant hereditary spastic ataxia in Newfoundland families.
Bourassa CV, Meijer IA, Merner ND, Grewal KK, Stefanelli MG, Hodgkinson K, Ives EJ, Pryse-Phillips W, Jog M, Boycott K, Grimes DA, Goobie S, Leckey R, Dion PA, Rouleau GA. Bourassa CV, et al. Am J Hum Genet. 2012 Sep 7;91(3):548-52. doi: 10.1016/j.ajhg.2012.07.018. Am J Hum Genet. 2012. PMID: 22958904 Free PMC article.
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.
Doucette L, Merner ND, Cooke S, Ives E, Galutira D, Walsh V, Walsh T, MacLaren L, Cater T, Fernandez B, Green JS, Wilcox ER, Shotland LI, Li XC, Lee M, King MC, Young TL. Doucette L, et al. Among authors: ives e. Eur J Hum Genet. 2009 May;17(5):554-64. doi: 10.1038/ejhg.2008.231. Epub 2008 Dec 24. Eur J Hum Genet. 2009. PMID: 19107147 Free PMC article.
Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations.
Goldberg YP, MacFarlane J, MacDonald ML, Thompson J, Dube MP, Mattice M, Fraser R, Young C, Hossain S, Pape T, Payne B, Radomski C, Donaldson G, Ives E, Cox J, Younghusband HB, Green R, Duff A, Boltshauser E, Grinspan GA, Dimon JH, Sibley BG, Andria G, Toscano E, Kerdraon J, Bowsher D, Pimstone SN, Samuels ME, Sherrington R, Hayden MR. Goldberg YP, et al. Among authors: ives e. Clin Genet. 2007 Apr;71(4):311-9. doi: 10.1111/j.1399-0004.2007.00790.x. Clin Genet. 2007. PMID: 17470132
89 results