Skip navigation
Home
Browse
Communities
& Collections
Browse Items by:
Issue Date
Author
Title
Advisor
Help
Sign on to:
My DSpace
Receive email
updates
Edit Profile
Adelaide Research & Scholarship
Adelaide Research & Scholarship
Search
Search:
All collections
University Library
Library Publications
Aurora harvest
Aurora harvest 2
Aurora harvest 3
Aurora harvest 4
Aurora harvest 5
Aurora harvest 6
Aurora harvest 7
Aurora harvest 8
Aurora submissions
Aurora submissions (restricted access)
Library publications
News / The University of Adelaide Libraries [1993-2001]
NEWSLINE
University of Adelaide Library News [1979-1993]
Untitled
for
Current filters:
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Start a new search
Add filters:
Use filters to refine the search results.
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Results 31-40 of 53 (Search time: 0.003 seconds).
previous
1
2
3
4
5
6
next
Item hits:
Preview
Issue Date
Title
Author(s)
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.
2010
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
Freathy, R.
;
Mook-Kanamori, D.
;
Sovio, U.
;
Prokopenko, I.
;
Timpson, N.
;
Berry, D.
;
Warrington, N.
;
Widen, E.
;
Jan Hottenga, J.
;
Kaakinen, M.
;
Lange, L.
;
Bradfield, J.
;
Kerkhof, M.
;
Marsh, J.
;
Mägi, R.
;
Chen, C.-M.
;
Lyon, H.
;
Kirin, M.
;
Adair, L.
;
Aulchenko, Y.
;
et al.
2010
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Allen, H.
;
Estrada, K.
;
Lettre, G.
;
Berndt, S.
;
Weedon, M.
;
Rivadeneira, F.
;
Willer, C.
;
Jackson, A.
;
Vedantam, S.
;
Raychaudhuri, S.
;
Ferreira, T.
;
Wood, A.
;
Weyant, R.
;
Segre, A.
;
Speliotes, E.
;
Wheeler, E.
;
Soranzo, N.
;
Park, J.-H.
;
Yang, J.
;
Gudbjartsson, D.
;
et al.
2011
A genome-wide significant linkage for severe depression on chromosome 3: the depression network study
Breen, G.
;
Webb, B.
;
Butler, A.
;
van den Oord, E.
;
Tozzi, F.
;
Craddock, N.
;
Gill, M.
;
Korszun, A.
;
Maier, W.
;
Middleton, L.
;
Mors, O.
;
Owen, M.
;
Cohen-Woods, S.
;
Perry, J.
;
Galwey, N.
;
Upmanyu, R.
;
Craig, I.
;
Lewis, C.
;
Ng, M.
;
Brewster, S.
;
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
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma
Khan, K.
;
Rudkin, A.
;
Parry, D.
;
Burdon, K.
;
McKibbin, M.
;
Logan, C.
;
Abdelhamed, Z.
;
Muecke, J.
;
Fernandez-Fuentes, N.
;
Laurie, K.
;
Shires, M.
;
Fogarty, R.
;
Carr, I.
;
Poulter, J.
;
Morgan, J.
;
Mohamed, M.
;
Jafri, H.
;
Raashid, Y.
;
Meng, N.
;
Piseth, H.
;
et al.
2007
Genome wide association study identifies novel breat cancer susceptibility loci
Easton, D.
;
Pooley, K.
;
Pharoah, P.
;
Thompson, D.
;
Ballinger, D.
;
Struewing, J.
;
Morrison, J.
;
Field, H.
;
Luben, R.
;
Wareham, N.
;
Ahmed, S.
;
Healey, C.
;
Bowman, R.
;
Luccarini, C.
;
Conroy, D.
;
Shah, M.
;
Munday, H.
;
Jordan, C.
;
Perkins, B.
;
West, J.
;
et al.
2007
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
Cavalleri, G.
;
Weale, M.
;
Shianna, K.
;
Singh, R.
;
Lynch, J.
;
Grinton, B.
;
Szoeke, C.
;
Murphy, K.
;
Kinirons, P.
;
O'Rourke, D.
;
Ge, D.
;
Depondt, C.
;
Claeys, K.
;
Pandolfo, M.
;
Gumbs, C.
;
Walley, N.
;
McNamara, J.
;
Mulley, J.
;
Linney, K.
;
Sheffield, L.
;
et al.
2011
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1
Burdon, K.
;
MacGregor, S.
;
Hewitt, A.
;
Sharma, S.
;
Chidlow, G.
;
Mills, R.
;
Danoy, P.
;
Casson, R.
;
Viswanathan, A.
;
Liu, J.
;
Landers, J.
;
Henders, A.
;
Wood, J.
;
Souzeau, E.
;
Crawford, A.
;
Leo, P.
;
Wang, J.
;
Rochtchina, E.
;
Nyholt, D.
;
Martin, N.
;
et al.
Discover
Author
3
Babic, M.
3
Burdon, K.
3
Esko, T.
3
Friend, K.
3
Gudbjartsson, D.
3
Guo, H.
3
Mulley, J.
3
Ripke, S.
3
Stefansson, H.
3
Warrington, N.
.
next >
Subject
36
Female
34
Polymorphism, Single Nucleotide
31
Male
23
Genome-Wide Association Study
20
Adult
19
Middle Aged
17
Case-Control Studies
16
Aged
15
Genotype
11
Risk Factors
.
next >
Date issued
5
2020 - 2021
43
2010 - 2019
5
2002 - 2009