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Results 11-20 of 22 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
2015
Single nucleotide variations in CLCN6 identified in patients with benign partial epilepsies in infancy and/or febrile seizures
Yamamoto, T.
;
Shimojima, K.
;
Sangu, N.
;
Komoike, Y.
;
Ishii, A.
;
Abe, S.
;
Yamashita, S.
;
Imai, K.
;
Kubota, T.
;
Fukasawa, T.
;
Okanishi, T.
;
Enoki, H.
;
Tanabe, T.
;
Saito, A.
;
Furukawa, T.
;
Shimizu, T.
;
Milligan, C.
;
Petrou, S.
;
Heron, S.
;
Dibbens, L.
;
et al.
;
Ishii, R.
2015
Association of the colorectal CpG island methylator phenotype with molecular features, risk factors, and family history
Weisenberger, D.
;
Levine, A.
;
Long, T.
;
Buchanan, D.
;
Walters, R.
;
Clendenning, M.
;
Rosty, C.
;
Joshi, A.
;
Stern, M.
;
Le Marchand, L.
;
Lindor, N.
;
Daftary, D.
;
Gallinger, S.
;
Selander, T.
;
Bapat, B.
;
Newcomb, P.
;
Campbell, P.
;
Casey, G.
;
Ahnen, D.
;
Baron, J.
;
et al.
2011
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
Yokoyama, S.
;
Woods, S.
;
Boyle, G.
;
Aoude, L.
;
MacGregor, S.
;
Zismann, V.
;
Gartside, M.
;
Cust, A.
;
Haq, R.
;
Harland, M.
;
Taylor, J.
;
Duffy, D.
;
Holohan, K.
;
Dutton-Regester, K.
;
Palmer, J.
;
Bonazzi, V.
;
Stark, M.
;
Symmons, J.
;
Law, M.
;
Schmidt, C.
;
et al.
2014
Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma
Aoude, L.
;
Pritchard, A.
;
Robles-Espinoza, C.
;
Wadt, K.
;
Harland, M.
;
Choi, J.
;
Gartside, M.
;
Quesada, V.
;
Johansson, P.
;
Palmer, J.
;
Ramsay, A.
;
Zhang, X.
;
Jones, K.
;
Symmons, J.
;
Holland, E.
;
Schmid, H.
;
Bonazzi, V.
;
Woods, S.
;
Dutton-Regester, K.
;
Stark, M.
;
et al.
2016
Multiplex families with epilepsy: success of clinical and molecular genetic characterization
Afawi, Z.
;
Oliver, K.L.
;
Kivity, S.
;
Mazarib, A.
;
Blatt, I.
;
Neufeld, M.Y.
;
Helbig, K.L.
;
Goldberg-Stern, H.
;
Misk, A.J.
;
Straussberg, R.
;
Walid, S.
;
Mahajnah, M.
;
Lerman-Sagie, T.
;
Ben-Zeev, B.
;
Kahana, E.
;
Masalha, R.
;
Kramer, U.
;
Ekstein, D.
;
Shorer, Z.
;
Wallace, R.H.
;
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.
2015
A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults
Perez-Andreu, V.
;
Roberts, K.
;
Xu, H.
;
Smith, C.
;
Zhang, H.
;
Yang, W.
;
Harvey, R.
;
Payne-Turner, D.
;
Devidas, M.
;
Cheng, I.
;
Carroll, W.
;
Heerema, N.
;
Carroll, A.
;
Raetz, E.
;
Gastier-Foster, J.
;
Marcucci, G.
;
Bloomfield, C.
;
Mrozek, K.
;
Kohlschmidt, J.
;
Stock, W.
;
et al.
2016
Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes
Machiela, M.
;
Lan, Q.
;
Slager, S.
;
Vermeulen, R.
;
Teras, L.
;
Camp, N.
;
Cerhan, J.
;
Spinelli, J.
;
Wang, S.
;
Nieters, A.
;
Vijai, J.
;
Yeager, M.
;
Wang, Z.
;
Ghesquières, H.
;
McKay, J.
;
Conde, L.
;
de Bakker, P.
;
Cox, D.
;
Burdett, L.
;
Monnereau, A.
;
et al.
2016
Integration of genetic and clinical risk factors improves prognostication in relapsed childhood B-cell precursor acute lymphoblastic leukemia
Irving, J.
;
Enshaei, A.
;
Parker, C.
;
Sutton, R.
;
Kuiper, R.
;
Erhorn, A.
;
Minto, L.
;
Venn, N.
;
Law, T.
;
Yu, J.
;
Schwab, C.
;
Davies, R.
;
Matheson, E.
;
Davies, A.
;
Sonneveld, E.
;
Den Boer, M.
;
Love, S.
;
Harrison, C.
;
Hoogerbrugge, P.
;
Revesz, T.
;
et al.
2013
Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
Permuth-Wey, J.
;
Lawrenson, K.
;
Shen, H.
;
Velkova, A.
;
Tyrer, J.
;
Chen, Z.
;
Lin, H.
;
Ann Chen, Y.
;
Tsai, Y.
;
Qu, X.
;
Ramus, S.
;
Karevan, R.
;
Lee, J.
;
Lee, N.
;
Larson, M.
;
Aben, K.
;
Anton-Culver, H.
;
Antonenkova, N.
;
Antoniou, A.
;
Armasu, S.
;
et al.
Discover
Author
4
Casey, G.
3
Gallinger, S.
2
Ahnen, D.
2
Aoude, L.
2
Babic, M.
2
Bapat, B.
2
Baron, J.
2
Bonazzi, V.
2
Buchanan, D.
2
Chen, Z.
.
next >
Subject
19
Humans
15
Female
13
Polymorphism, Single Nucleotide
12
Male
8
Middle Aged
7
Adult
7
Aged
7
Risk Factors
6
Genotype
5
Aged, 80 and over
.
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Date issued
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4
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3
2014
3
2013
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2012
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2011