Start a new search
Add filters:

Use filters to refine the search results.

Results 381-390 of 390 (Search time: 0.012 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
1996Gene localisation for Wilson-Turner syndrome (WTS:MIM 309585)Gedeon, A.; Turner, G.; Mulley, J.
2020A paleogenomic reconstruction of the deep population history of the AndesNakatsuka, N.; Lazaridis, I.; Barbieri, C.; Skoglund, P.; Rohland, N.; Mallick, S.; Posth, C.; Harkins-Kinkaid, K.; Ferry, M.; Harney, É.; Michel, M.; Stewardson, K.; Novak-Forst, J.; Capriles, J.M.; Durruty, M.A.; Álvarez, K.A.; Beresford-Jones, D.; Burger, R.; Cadwallader, L.; Fujita, R.; et al.
2019A genome-wide association study of mitochondrial DNA copy number in two population-based cohortsGuyatt, A.; Brennan, R.; Burrows, K.; Guthrie, P.; Ascione, R.; Ring, S.; Gaunt, T.; Pyle, A.; Cordell, H.; Lawlor, D.; Chinnery, P.; Hudson, G.; Rodriguez, S.
1996How many X-linked genes for non-specific mental retardation (MRX) are there?Gedeon, A.; Donnelly, A.; Mulley, J.; Kerr, B.; Turner, G.
1999Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardationGecz, J.; Barnett, S.; Liu, J.; Hollway, G.; Donnelly, A.; Eyre, H.; Eshkevari, H.; Baltazar, R.; Grunn, A.; Nagaraja, R.; Gilliam, C.; Peltonen, L.; Sutherland, G.; Baron, M.; Mulley, J.
2016A method to exploit the structure of genetic ancestry space to enhance case-control studiesBodea, C.; Neale, B.; Ripke, S.; Barclay, M.; Peyrin-Biroulet, L.; Chamaillard, M.; Colombel, J.; Cottone, M.; Croft, A.; D'Incà, R.; Halfvarson, J.; Hanigan, K.; Henderson, P.; Hugot, J.; Karban, A.; Kennedy, N.; Khan, M.; Lémann, M.; Levine, A.; Massey, D.; et al.
2011Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1Bown, M.; Jones, G.; Harrison, S.; Wright, B.; Bumpstead, S.; Baas, A.; Gretarsdottir, S.; Badger, S.; Bradley, D.; Burnand, K.; Child, A.; Clough, R.; Cockerill, G.; Hafez, H.; Scott, D.; Futers, S.; Johnson, A.; Sohrabi, S.; Smith, A.; Thompson, M.; et al.
2018A genomic Neolithic time transect of hunter-farmer admixture in central PolandFernandes, D.; Strapagiel, D.; Borówka, P.; Marciniak, B.; Żądzińska, E.; Sirak, K.; Siska, V.; Grygiel, R.; Carlsson, J.; Manica, A.; Lorkiewicz, W.; Pinhasi, R.
2020Constraint and conservation of the paired-type homeodomains predicts the clinical outcome of missense variants of uncertain significanceThai, M.; Gardner, A.; Redpath, L.; Mattiske, T.; Dearsley, O.; Shaw, M.; Vulto-van Silfhout, A.T.; Pfundt, R.; Dixon, J.; McGaughran, J.; Pérez-Jurado, L.A.; Gécz, J.; Shoubridge, C.
1998A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy.Donnelly, A.; Haan, E.; Manson, J.; Mulley, J.