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Results 11-20 of 49 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Geisheker, M.
;
Heymann, G.
;
Wang, T.
;
Coe, B.
;
Turner, T.
;
Stessman, H.
;
Hoekzema, K.
;
Kvarnung, M.
;
Shaw, M.
;
Friend, K.
;
Liebelt, J.
;
Barnett, C.
;
Thompson, E.
;
Haan, E.
;
Guo, H.
;
Anderlid, B.
;
Nordgren, A.
;
Lindstrand, A.
;
Vandeweyer, G.
;
Alberti, A.
;
et al.
1999
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
Gedeon, A.
;
Colley, A.
;
Jamieson, R.
;
Thompson, E.
;
Rogers, J.
;
Sillence, D.
;
Tiller, G.
;
Mulley, J.
;
Gecz, J.
2020
Genetic history from the Middle Neolithic to present on the Mediterranean island of Sardinia
Marcus, J.H.
;
Posth, C.
;
Ringbauer, H.
;
Lai, L.
;
Skeates, R.
;
Sidore, C.
;
Beckett, J.
;
Furtwängler, A.
;
Olivieri, A.
;
Chiang, C.W.K.
;
Al-Asadi, H.
;
Dey, K.
;
Joseph, T.A.
;
Liu, C.-C.
;
Der Sarkissian, C.
;
Radzevičiūtė, R.
;
Michel, M.
;
Gradoli, M.G.
;
Marongiu, P.
;
Rubino, S.
;
et al.
2020
Cohort profile: the Australian genetics of depression study
Byrne, E.M.
;
Kirk, K.M.
;
Medland, S.E.
;
McGrath, J.J.
;
Colodro-Conde, L.
;
Parker, R.
;
Cross, S.
;
Sullivan, L.
;
Statham, D.J.
;
Levinson, D.F.
;
Licinio, J.
;
Wray, N.R.
;
Hickie, I.B.
;
Martin, N.G.
2020
Can we blame fathers who are obese peri-conception, for increasing chronic disease risk in children?
McPherson, N.O.
1997
Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogenetics
Callen, D.
;
Yip, M.Y.
;
Eyre, H.
2018
ADCY9 genetic variants and cardiovascular outcomes with evacetrapib in patients with high-risk vascular disease: a nested case-control study
Nissen, S.
;
Pillai, S.
;
Nicholls, S.
;
Wolski, K.
;
Riesmeyer, J.
;
Weerakkody, G.
;
Foster, W.
;
McErlean, E.
;
Li, L.
;
Bhatnagar, P.
;
Ruotolo, G.
;
Lincoff, A.
2017
Mapping complex traits in a diversity outbred f1 mouse population identifies germline modifiers of metastasis in human prostate cancer
Winter, J.
;
Gildea, D.
;
Andreas, J.
;
Gatti, D.
;
Williams, K.
;
Lee, M.
;
Hu, Y.
;
Zhang, S.
;
Mullikin, J.
;
Wolfsberg, T.
;
McDonnell, S.
;
Fogarty, Z.
;
Larson, M.
;
French, A.
;
Schaid, D.
;
Thibodeau, S.
;
Churchill, G.
;
Crawford, N.
2015
HENMT1 and piRNA stability are required for adult male germ cell transposon repression and to define the spermatogenic program in the mouse
Lim, S.
;
Qu, Z.
;
Kortschak, R.
;
Lawrence, D.
;
Geoghegan, J.
;
Hempfling, A.
;
Bergmann, M.
;
Goodnow, C.
;
Ormandy, C.
;
Wong, L.
;
Mann, J.
;
Scott, H.
;
Jamsai, D.
;
Adelson, D.
;
O'Bryan, M.
;
Frye, M.
2015
Alzheimer's disease-related peptide PS2V plays ancient, conserved roles in suppression of the unfolded protein response under hypoxia and stimulation of γ-secretase activity
Moussavi Nik, S.
;
Newman, M.
;
Wilson, L.
;
Ebrahimie, E.
;
Wells, S.
;
Musgrave, I.
;
Verdile, G.
;
Martins, R.
;
Lardelli, M.
Discover
Author
16
Mulley, J.
9
Gedeon, A.
7
Callen, D.
7
et al.
7
Gecz, J.
6
Eyre, H.
6
Sutherland, G.
5
Colley, A.
5
Haan, E.
5
Richards, R.
.
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Subject
41
Female
17
Chromosome Mapping
17
Pedigree
12
Genetic Linkage
12
Intellectual Disability
12
Molecular Sequence Data
12
X Chromosome
9
Amino Acid Sequence
9
Animals
9
Genetic Markers
.
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Date issued
5
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2010 - 2019
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2000 - 2009
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1995 - 1999