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Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci.
Chen H, Fan S, Stone J, Thompson DJ, Douglas J, Li S, Scott C, Bolla MK, Wang Q, Dennis J, Michailidou K, Li C, Peters U, Hopper JL, Southey MC, Nguyen-Dumont T, Nguyen TL, Fasching PA, Behrens A, Cadby G, Murphy RA, Aronson K, Howell A, Astley S, Couch F, Olson J, Milne RL, Giles GG, Haiman CA, Maskarinec G, Winham S, John EM, Kurian A, Eliassen H, Andrulis I, Evans DG, Newman WG, Hall P, Czene K, Swerdlow A, Jones M, Pollan M, Fernandez-Navarro P, McConnell DS, Kristensen VN; NBCS Investigators; Rothstein JH, Wang P, Habel LA, Sieh W, Dunning AM, Pharoah PDP, Easton DF, Gierach GL, Tamimi RM, Vachon CM, Lindström S. Chen H, et al. Among authors: milne rl. Breast Cancer Res. 2022 Apr 12;24(1):27. doi: 10.1186/s13058-022-01524-0. Breast Cancer Res. 2022. PMID: 35414113 Free PMC article.
A twin study of genetic influences on epilepsy outcome.
Johnson MR, Milne RL, Torn-Broers Y, Hopper JL, Scheffer IE, Berkovic SF. Johnson MR, et al. Among authors: milne rl. Twin Res. 2003 Apr;6(2):140-6. doi: 10.1375/136905203321536263. Twin Res. 2003. PMID: 12724000
Is benign rolandic epilepsy genetically determined?
Vadlamudi L, Harvey AS, Connellan MM, Milne RL, Hopper JL, Scheffer IE, Berkovic SF. Vadlamudi L, et al. Among authors: milne rl. Ann Neurol. 2004 Jul;56(1):129-32. doi: 10.1002/ana.20153. Ann Neurol. 2004. PMID: 15236411
Two ATM variants and breast cancer risk.
Thompson D, Antoniou AC, Jenkins M, Marsh A, Chen X, Wayne T, Tesoriero A, Milne R, Spurdle A, Thorstenson Y, Southey M, Giles GG, Khanna KK, Sambrook J, Oefner P, Goldgar D, Hopper JL, Easton D, Chenevix-Trench G; KConFab Investigators. Thompson D, et al. Hum Mutat. 2005 Jun;25(6):594-5. doi: 10.1002/humu.9344. Hum Mutat. 2005. PMID: 15880680
570 results