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| Preview | Issue Date | Title | Author(s) |
| 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. |
| 2018 | Genome-wide gene-environment interaction in depression: a systematic evaluation of candidate genes: the childhood trauma working-group of PGC-MDD | Van der Auwera, S.; Peyrot, W.; Milaneschi, Y.; Hertel, J.; Baune, B.; Breen, G.; Byrne, E.; Dunn, E.; Fisher, H.; Homuth, G.; Levinson, D.; Lewis, C.; Mills, N.; Mullins, N.; Nauck, M.; Pistis, G.; Preisig, M.; Rietschel, M.; Ripke, S.; Sullivan, P.; et al. |
| 2019 | Genomic balance: two genomes establishing synchrony to modulate cellular fate and function | St John, J.C. |
| 1997 | Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3 | Mitchison, H.; Munroe, P.; O'Rawe, A.; Taschner, P.; De Vos, N.; Kremmidiotis, G.; Lensink, I.; Munk, A.; D'Arigo, K.; Anderson, J.; Lerner, T.; Moyzis, R.; Callen, D.; Breuning, M.; Doggett, N.; Gardiner, R.; Mole, S. |
| 1999 | Genomic structure and expression analysis of the spastic paraplegia gene, SPG7 | Settasatian, C.; Whitmore, S.; Crawford, J.; Bilton, R.; Cleton-Jansen, A.M.; Sutherland, G.; Callen, D. |
| 1999 | Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes | McDermott, M.; Aksentijevich, I.; Galon, J.; McDermott, E.; Ogunkolade, B.; Centola, M.; Mansfield, E.; Gadina, M.; Karenko, L.; Petterson, T.; McCarthy, J.; Frucht, D.; Aringer, M.; Torosyan, Y.; Teppo, A.M.; Wilson, M.; Karaarslan, H.; Wan, Y.; Todd, I.; Wood, G.; et al. |
| 2019 | GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in Cameroon | Tingang Wonkam, E.; Chimusa, E.; Noubiap, J.J.; Adadey, S.M.; F Fokouo, J.V.; Wonkam, A. |
| 2017 | Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsy | Ewans, L.J.; Field, M.; Zhu, Y.; Turner, G.; Leffler, M.; Dinger, M.E.; Cowley, M.J.; Buckley, M.F.; Scheffer, I.E.; Jackson, M.R.; Roscioli, T.; Shoubridge, C. |
| 2010 | Great expectations: using massively parallel sequencing to solve inherited disorders | Corbett, M.; Gecz, J. |
| 2018 | Guidelines for whole genome bisulphite sequencing of intact and FFPET DNA on the Illumina HiSeq X Ten | Nair, S.S.; Luu, P.-L.; Qu, W.; Maddugoda, M.; Huschtscha, L.; Reddel, R.; Chenevix-Trench, G.; Toso, M.; Kench, J.G.; Horvath, L.G.; Hayes, V.M.; Stricker, P.D.; Hughes, T.P.; White, D.L.; Rasko, J.E.; Wong, J.J.-L.; Clark, S.J. |
| 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. |
| 2012 | Hepatitis C virus entry: role of host and viral factors | Samreen, B.; Khaliq, S.; Ashfaq, U.; Khan, M.; Afzal, N.; Shahzad, M.; Riaz, S.; Jahan, S. |
| 2023 | Heritable defects in telomere and mitotic function selectively predispose to sarcomas | Ballinger, M.L.; Pattnaik, S.; Mundra, P.A.; Zaheed, M.; Rath, E.; Priestley, P.; Baber, J.; Ray-Coquard, I.; Isambert, N.; Causeret, S.; van der Graaf, W.T.A.; Puri, A.; Duffaud, F.; Le Cesne, A.; Seddon, B.; Chandrasekar, C.; Schiffman, J.D.; Brohl, A.S.; James, P.A.; Kurtz, J.-E.; et al. |
