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Preview | Issue Date | Title | Author(s) |
| 1998 | Gene localisation for an autosomal dominant familial periodic fever to 12p13. | Mulley, J.; Saar, K.; Hewitt, G.; Rueschendorf, F.; Phillips, H.; Colley, A.; Sillence, D.; Reis, A.; Wilson, M. |
| 1996 | Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470) | Gedeon, A.; Haan, E.; Mulley, J. |
| 1996 | Gene localisation for Wilson-Turner syndrome (WTS:MIM 309585) | Gedeon, A.; Turner, G.; Mulley, J. |
| 2017 | Gene Ontology-based analysis of zebrafish’ omics data using the web tool Comparative Gene Ontology | Ebrahimie, E.; Fruzangohar, M.; Moussavi Nik, S.H.; Newman, M. |
| 1997 | Gene structure and subcellular localisation of FMR2, a member of a new family of putative transcription activators | Gecz, J.; Bielby, S.; Sutherland, G.; Mulley, J. |
| 2020 | Gene-specific facial dysmorphism in Axenfeld-Rieger syndrome caused by FOXC1 and PITX2 variants | Souzeau, E.; Siggs, O.M.; Pasutto, F.; Knight, L.S.W.; Perez-Jurado, L.A.; McGregor, L.; Le Blanc, S.; Barnett, C.P.; Liebelt, J.; Craig, J.E. |
| 2023 | General Practitioners perspectives on infant telomere length screening after a pregnancy complication: a qualitative analysis. | Puglisi, C.J.; McDonough, J.; Bianco-Miotto, T.; A Grieger, J. |
| 2014 | Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies | Bras, J.; Guerreiro, R.; Darwent, L.; Parkkinen, L.; Ansorge, O.; Escott-Price, V.; Hernandez, D.G.; Nalls, M.A.; Clark, L.N.; Honig, L.S.; Marder, K.; Van Der Flier, W.M.; Lemstra, A.; Scheltens, P.; Rogaeva, E.; St George-Hyslop, P.; Londos, E.; Zetterberg, H.; Ortega-Cubero, S.; Pastor, P.; et al. |
| 2011 | Genetic ancestry and indigenous heritage in a Native American descendant community in Bermuda | Gaieski, J.; Owings, A.; Vilar, M.; Dulik, M.; Gaieski, D.; Gittelman, R.; Lindo, J.; Gau, L.; Schurr, T. |
| 2020 | Genetic and environmental determinants of variation in the plasma lipidome of older Australian twins | Wong, M.W.; Thalamuthu, A.; Braidy, N.; Mather, K.A.; Liu, Y.; Ciobanu, L.; Baune, B.T.; Armstrong, N.J.; Kwok, J.; Schofield, P.; Wright, M.J.; Ames, D.; Pickford, R.; Lee, T.; Poljak, A.; Sachdev, P.S. |
| 1997 | Genetic and physical mapping of the Aspergillus nidulans pyruvate decarboxylase encoding gene, pdcA, allowing the anchoring of a small floating contig in the ordered cosmid library | Lockington, R.; Kelly, J. |
| 2014 | Genetic bottlenecks in time and space: reconstructing invasions from contemporary and historical collections | Dormontt, E.; Gardner, M.; Breed, M.; Rodger, J.; Prentis, P.; Lowe, A.; Gilbert, T. |
| 2020 | Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression | Hagenaars, S.P.; Coleman, J.R.I.; Choi, S.W.; Gaspar, H.; Adams, M.J.; Howard, D.M.; Hodgson, K.; Traylor, M.; Air, T.M.; Andlauer, T.F.M.; Arolt, V.; Baune, B.T.; Binder, E.B.; Blackwood, D.H.R.; Boomsma, D.I.; Campbell, A.; Cearns, M.; Czamara, D.; Dannlowski, U.; Domschke, K.; et al. |
| 2016 | Genetic consequences of forest fragmentation by agricultural land in an arboreal marsupial | Lancaster, M.; Cooper, S.; Carthew, S. |
| 2015 | Genetic heritage of the balto-slavic speaking populations: a synthesis of autosomal, mitochondrial and Y-chromosomal data | Kushniarevich, A.; Utevska, O.; Chuhryaeva, M.; Agdzhoyan, A.; Dibirova, K.; Uktveryte, I.; Möls, M.; Mulahasanovic, L.; Pshenichnov, A.; Frolova, S.; Shanko, A.; Metspalu, E.; Reidla, M.; Tambets, K.; Tamm, E.; Koshel, S.; Zaporozhchenko, V.; Atramentova, L.; Kučinskas, V.; Davydenko, O.; et al.; Calafell, F. |
| 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. |
| 1996 | Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation | Gedeon, A.; Glass, I.; Connor, J.; Mulley, J. |
| 1997 | Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2 | Horwitz, M.; Benson, K.; Li, F.Q.; Wolff, J.; Leppert, M.; Hobson, L.; Mangelsdorf, M.; Yu, S.; Hewett, D.; Richards, R.; Raskind, W. |
| 2020 | Genome-wide analysis of diamondback moth, Plutella xylostella L., from Brassica crops and wild host plants reveals no genetic structure in Australia | Perry, K.; Keller, M.A.; Baxter, S. |
| 2019 | Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology | Han, X.; Qassim, A.; An, J.; Marshall, H.; Zhou, T.; Ong, J.-S.; Hassall, M.M.; Hysi, P.G.; Foster, P.J.; Khaw, P.T.; Mackey, D.A.; Gharahkhani, P.; Khawaja, A.P.; Hewitt, A.W.; Craig, J.E.; MacGregor, S. |