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Results 1-6 of 6 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2015
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
Onengut-Gumuscu, S.
;
Chen, W.-M.
;
Burren, O.
;
Cooper, N.J.
;
Quinlan, A.R.
;
Mychaleckyj, J.C.
;
Farber, E.
;
Bonnie, J.K.
;
Szpak, M.
;
Schofield, E.
;
Achuthan, P.
;
Guo, H.
;
Fortune, M.D.
;
Stevens, H.
;
Walker, N.M.
;
Ward, L.D.
;
Kundaje, A.
;
Kellis, M.
;
Daly, M.J.
;
Barrett, J.C.
;
et al.
2012
Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22
Cicek, M.
;
Cunningham, J.
;
Fridley, B.
;
Serie, D.
;
Bamlet, W.
;
Diergaarde, B.
;
Haile, R.
;
Le Marchand, L.
;
Krontiris, T.
;
Younghusband, H.
;
Gallinger, S.
;
Newcomb, P.
;
Hopper, J.
;
Jenkins, M.
;
Casey, G.
;
Schumacher, F.
;
Chen, Z.
;
DeRycke, M.
;
Templeton, A.
;
Winship, I.
;
et al.
;
Lo, A.
2012
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
Spain, S.
;
Carvajal-Carmona, L.
;
Howarth, K.
;
Jones, A.
;
Su, Z.
;
Cazier, J.
;
Williams, J.
;
Aaltonen, L.
;
Pharoah, P.
;
Kerr, D.
;
Cheadle, J.
;
Li, L.
;
Casey, G.
;
Vodicka, P.
;
Sieber, O.
;
Lipton, L.
;
Gibbs, P.
;
Martin, N.
;
Montgomery, G.
;
Young, J.
;
et al.
2015
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk
Painter, J.
;
O'Mara, T.
;
Batra, J.
;
Cheng, T.
;
Lose, F.
;
Dennis, J.
;
Michailidou, K.
;
Tyrer, J.
;
Ahmed, S.
;
Ferguson, K.
;
Healey, C.
;
Kaufmann, S.
;
Hillman, K.
;
Walpole, C.
;
Moya, L.
;
Pollock, P.
;
Jones, A.
;
Howarth, K.
;
Martin, L.
;
Gorman, M.
;
et al.
2011
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
Hahn, C.
;
Chong, C.
;
Carmichael, C.
;
Wilkins, E.
;
Brautigan, P.
;
Li, X.
;
Babic, M.
;
Lin, M.
;
Carmagnac, A.
;
Lee, Y.
;
Kok, C.
;
Gagliardi, L.
;
Friend, K.
;
Ekert, P.
;
Butcher, C.
;
Brown, A.
;
Lewis, I.
;
To, L.
;
Timms, A.
;
Storek, J.
;
et al.
2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2
Henden, L.
;
Freytag, S.
;
Afawi, Z.
;
Baldassari, S.
;
Berkovic, S.
;
Bisulli, F.
;
Canafoglia, L.
;
Casari, G.
;
Crompton, D.
;
Depienne, C.
;
Gecz, J.
;
Guerrini, R.
;
Helbig, I.
;
Hirsch, E.
;
Keren, B.
;
Klein, K.
;
Labauge, P.
;
LeGuern, E.
;
Licchetta, L.
;
Mei, D.
;
et al.
Discover
Author
2
Casey, G.
2
Howarth, K.
2
Jones, A.
1
Aaltonen, L.
1
Achuthan, P.
1
Afawi, Z.
1
Ahmed, S.
1
Babic, M.
1
Baldassari, S.
1
Bamlet, W.
.
next >
Subject
5
Humans
4
Female
4
Genetic Predisposition to Disease
3
Genotype
3
Haplotypes
3
Male
2
Alleles
2
Case-Control Studies
2
Chromosomes, Human, Pair 12
2
Colorectal Neoplasms
.
next >
Date issued
1
2016
2
2015
2
2012
1
2011