Citations

Get in touch

+44 (0)1506 424270

Send us a message

Nucleon Chemistry/Kits

  1. G6PD gene variants and its association with malaria in a Sri Lankan population, Rajika L Dewasurendra, Kirk A Rockett, S Fernando, Richard Carter, Dominic P Kwiatkowski, Nadira D Karunaweera, in collaboration with the MalariaGEN Consortium Malaria Journal 2015, 14:93 (22 February 2015)
  2. A novel mutation in TTC8 is associated with progressive retinal atrophy in the golden retriever, Louise M Downs, Berit Wallin-Håkansson, Tomas Bergström, Cathryn S Mellersh Canine Genetics and Epidemiology 2014, 1:4 (16 April 2014)
  3. Inactive alleles of cytochrome P450 2C19 may be positively selected in human evolution, Ramatoulie E Janha, Archibald Worwui, Kenneth J Linton, Seif O Shaheen, Fatoumatta Sisay-Joof, Robert T Walton BMC Evolutionary Biology 2014, 14:71 (1 April 2014)
  4. Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study, Shona M Kerr, Archie Campbell, Lee Murphy, Caroline Hayward, Cathy Jackson, Louise V Wain, Martin D Tobin, Anna Dominiczak, Andrew Morris, Blair H Smith, David J Porteous BMC Medical Genetics 2013, 14:38 (22 March 2013)
  5. Genetic polymorphisms associated with anti-malarial antibody levels in a low and unstable malaria transmission area in southern Sri Lanka, Rajika L Dewasurendra, Prapat Suriyaphol, Sumadhya D Fernando, Richard Carter, Kirk Rockett, Patrick Corran, Dominic Kwiatkowski, Nadira D Karunaweera, in collaboration with the 7 MalariaGEN Consortium Malaria Journal 2012, 11:281 (20 August 2012)
  6. Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation, Oliver P Forman, Luisa De Risio, Jennifer Stewart, Cathryn S Mellersh, Elsa Beltran BMC Genetics 2012, 13:55 (10 July 2012)
  7. Association of sub-microscopic malaria parasite carriage with transmission intensity in north-eastern Tanzania, Alphaxard Manjurano, Lucy Okell, Tedson Lukindo, Hugh Reyburn, Raimos Olomi, Cally Roper, Taane G Clark, Sarah Joseph, Eleanor M Riley, Chris Drakeley Malaria Journal 2011, 10:370 (16 December 2011)
  8. Investigation of an outbreak of mycobacteriosis in pigs, Angelika Agdestein, Tone B Johansen, Vladimir Polaček, Bjørn Lium, Gudmund Holstad, Dejan Vidanović, Sanja Aleksić-Kovačević, Anne Jørgensen, Jonas Žultauskas, Sigrun F Nilsen, Berit Djønne BMC Veterinary Research 2011, 7:63 (21 October 2011)
  9. Generation Scotland: Donor DNA Databank; A control DNA resource, Shona M Kerr, David CM Liewald, Archie Campbell, Kerrie Taylor, Sarah H Wild, David Newby, Marc Turner, David J Porteous BMC Medical Genetics 2010, 11:166 (23 November 2010)
  10. FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies, Amparo Tolosa, Julio Sanjuán, Adam M Dagnall, María D Moltó, Neus Herrero, Rosa de Frutos BMC Medical Genetics 2010, 11:114 (22 July 2010)
  11. Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry, Inês Sousa, Taane G Clark, Richard Holt, Alistair T Pagnamenta, Erik J Mulder, Ruud B Minderaa, Anthony J Bailey, Agatino Battaglia, Sabine M Klauck, Fritz Poustka, Anthony P Monaco, International Molecular Genetic Study of Autism Consortium (IMGSAC) Molecular Autism 2010, 1:7 (25 March 2010)
  12. Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data, Ozren Polašek, Caroline Hayward, Celine Bellenguez, Veronique Vitart, Ivana Kolčić, Ruth McQuillan, Vanja Saftić, Ulf Gyllensten, James F Wilson, Igor Rudan, Alan F Wright, Harry Campbell, Anne-Louise Leutenegger BMC Genomics 2010, 11:139 (25 February 2010)
  13. Genetic determinants of hair and eye colours in the Scottish and Danish populations, Jonas Mengel-From, Terence H Wong, Niels Morling, Jonathan L Rees, Ian J Jackson BMC Genetics 2009, 10:88 (30 December 2009)
  14. Glucose-6-phosphate dehydrogenase (G6PD) mutations and haemoglobinuria syndrome in the Vietnamese population, Nguyen Hue, Jean Charlieu, Tran Chau, Nick Day, Jeremy J Farrar, Tran Hien, Sarah J Dunstan Malaria Journal 2009, 8:152 (10 July 2009)
  15. The TNF alpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency, Alice M Wood, Matthew J Simmonds, Darren L Bayley, Paul R Newby, Stephen C Gough, Robert A Stockley Respiratory Research 2008, 9:52 (11 July 2008)
  16. Screening of the transcriptional regulatory regions of vascular endothelial growth factor receptor 2 (VEGFR2) in amyotrophic lateral sclerosis, Alice Brockington, Beatrijs Wokke, Hannah Nixon, Judith Hartley, Pamela J Shaw BMC Medical Genetics 2007, 8:23 (24 April 2007)
  17. Association of candidate gene polymorphisms and TGF-beta/IL-10 levels with malaria in three regions of Cameroon: a case–control study, Tobias O Apinjoh, Judith K Anchang-Kimbi, Clarisse Njua-Yafi, André N Ngwai, Regina N Mugri, Taane G Clark, Kirk A Rockett, Dominic P Kwiatkowski, Eric A Achidi, in collaboration with The MalariaGEN Consortium Malaria Journal 2014, 13:236 (16 June 2014)
  18. A genome-wide association study demonstrates significant genetic variation for fracture risk in Thoroughbred racehorses, Sarah C Blott, June E Swinburne, Charlene Sibbons, Laura Y Fox-Clipsham, Maud Helwegen, Lynn Hillyer, Tim DH Parkin, J Newton, Mark Vaudin BMC Genomics 2014, 15:147 (21 February 2014)
  19. Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease, Fujinami, Kaoru, et al., Ophthalmology (2014).