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Results 1-10 of 11 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2019
Association of chromosome 9p21 with subsequent coronary heart disease events A GENIUS-CHD study of individual participant data
Patel, R.S.
;
Schmidt, A.F.
;
Tragante, V.
;
McCubrey, R.O.
;
Holmes, M.
;
Howe, L.J.
;
Direk, K.
;
Akerblom, A.
;
Leander, K.
;
Virani, S.S.
;
Kaminski, K.A.
;
Muehlschlegel, J.D.
;
Dube, M.-P.
;
Allayee, H.
;
Almgren, P.
;
Alver, M.
;
Baranova, E.
;
Behlouli, H.
;
Boeckx, B.
;
Braund, P.S.
;
et al.
2021
Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer
Singhal, D.
;
Hahn, C.N.
;
Feurstein, S.
;
Wee, L.Y.A.
;
Moma, L.
;
Kutyna, M.M.
;
Chhetri, R.
;
Eshraghi, L.
;
Schreiber, A.W.
;
Feng, J.
;
Wang, P.P.-S.
;
Babic, M.
;
Parker, W.T.
;
Gao, S.
;
Moore, S.
;
Das, S.
;
Thomas, D.
;
Pattnaik, S.
;
Brown, A.L.
;
D'Andrea, R.J.
;
et al.
2020
Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities
Armstrong, N.J.
;
Mather, K.A.
;
Sargurupremraj, M.
;
Knol, M.J.
;
Malik, R.
;
Satizabal, C.L.
;
Yanek, L.R.
;
Wen, W.
;
Gudnason, V.G.
;
Dueker, N.D.
;
Elliott, L.T.
;
Hofer, E.
;
Hofer, E.
;
Bis, J.
;
Jahanshad, N.
;
Li, S.
;
Logue, M.A.
;
Logue, M.A.
;
Luciano, M.
;
Scholz, M.
;
et al.
2014
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma
Gharahkhani, P.
;
Burdon, K.
;
Fogarty, R.
;
Sharma, S.
;
Hewitt, A.
;
Martin, S.
;
Law, M.
;
Cremin, K.
;
Bailey, J.
;
Loomis, S.
;
Pasquale, L.
;
Haines, J.
;
Hauser, M.
;
Viswanathan, A.
;
McGuffin, P.
;
Topouzis, F.
;
Foster, P.
;
Graham, S.
;
Casson, R.
;
Chehade, M.
;
et al.
2018
A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetes
Van Zuydam, N.R.
;
Ahlqvist, E.
;
Sandholm, N.
;
Deshmukh, H.
;
William Rayner, N.
;
Abdalla, M.
;
Ladenvall, C.
;
Ziemek, D.
;
Fauman, E.
;
Robertson, N.R.
;
McKeigue, P.M.
;
Valo, E.
;
Forsblom, C.
;
Harjutsalo, V.
;
Perna, A.
;
Rurali, E.
;
Loredana Marcovecchio, M.
;
Igo, R.P.
;
Salem, R.M.
;
Perico, N.
;
et al.
2016
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies
Lewinsohn, M.
;
Brown, A.L.
;
Weinel, L.M.
;
Phung, C.
;
Rafidi, G.
;
Lee, M.K.
;
Schreiber, A.W.
;
Feng, J.
;
Babic, M.
;
Chong, C.E.
;
Lee, Y.
;
Yong, A.
;
Suthers, G.K.
;
Poplawski, N.
;
Altree, M.
;
Phillips, K.
;
Jaensch, L.
;
Fine, M.
;
D'Andrea, R.J.
;
Lewis, I.D.
;
et al.
2021
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
Win, A.K.
;
Dowty, J.G.
;
Reece, J.C.
;
Lee, G.
;
Templeton, A.S.
;
Plazzer, J.P.
;
Buchanan, D.D.
;
Akagi, K.
;
Aksoy, S.
;
Alonso, A.
;
Alvarez, K.
;
Amor, D.J.
;
Ankathil, R.
;
Aretz, S.
;
Arnold, J.L.
;
Aronson, M.
;
Austin, R.
;
Backman, A.S.
;
Bajwa-ten Broeke, S.W.
;
Barca-Tierno, V.
;
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
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.
Discover
Author
2
Aoude, L.
2
Babic, M.
2
Bonazzi, V.
2
Brown, A.L.
2
D'Andrea, R.J.
2
Dutton-Regester, K.
2
Feng, J.
2
Gartside, M.
2
Harland, M.
2
Law, M.
.
next >
Subject
11
Humans
10
Male
9
Aged
7
Adult
7
Aged, 80 and over
4
Risk Factors
3
Case-Control Studies
3
Genotype
3
Germ-Line Mutation
3
Pedigree
.
next >
Date issued
2
2021
1
2020
1
2019
1
2018
2
2016
2
2014
2
2011