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Flynn, Robert and Washer, Sam and Jeffries, Aaron R and Andrayas, Alexandria and Shireby, Gemma and Kumari, Meena and Schalkwyk, Leonard C and Mill, Jonathan and Hannon, Eilis (2022) Evaluation of nanopore sequencing for epigenetic epidemiology: a comparison with DNA methylation microarrays. Human Molecular Genetics, 31 (18). pp. 3181-3190. DOI https://doi.org/10.1093/hmg/ddac112

Ahluwalia, Tarunveer S and Prins, Bram P and Kumari, Meena and et al (2021) Genome-wide association study of circulating interleukin 6 levels identifies novel loci. Human Molecular Genetics, 30 (5). pp. 393-409. DOI https://doi.org/10.1093/hmg/ddab023

Wong, CCY and Smith, RG and Hannon, E and Ramaswami, G and Parikshak, NN and Assary, E and Troakes, C and Poschmann, J and Schalkwyk, LC and Sun, W and Prabhakar, S and Geschwind, DH and Mill, J (2019) Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue. Human Molecular Genetics, 28 (13). pp. 2201-2211. DOI https://doi.org/10.1093/hmg/ddz052

Athanasiou, Dimitra and Aguila, Monica and Opefi, Chikwado A and South, Kieron and Bellingham, James and Bevilacqua, Dalila and Munro, Peter M and Kanuga, Naheed and Mackenzie, Francesca E and Dubis, Adam M and Georgiadis, Anastasios and Graca, Anna B and Pearson, Rachael A and Ali, Robin R and Sakami, Sanae and Palczewski, Krzysztof and Sherman, Michael Y and Reeves, Philip J and Cheetham, Michael E (2017) Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration. Human Molecular Genetics, 26 (2). pp. 305-319. DOI https://doi.org/10.1093/hmg/ddw387

Viana, J and Hannon, E and Dempster, E and Pidsley, R and Macdonald, R and Knox, O and Spiers, H and Troakes, C and Al-Saraj, S and Turecki, G and Schalkwyk, LC and Mill, J (2017) Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions. Human Molecular Genetics, 26 (1). pp. 210-225. DOI https://doi.org/10.1093/hmg/ddw373

Rahmioglu, N and Macgregor, S and Drong, AW and Hedman, AK and Harris, HR and Randall, JC and Prokopenko, I and Nyholt, DR and Morris, AP and Montgomery, GW and Missmer, SA and Lindgren, CM and Zondervan, KT (2015) Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci. Human Molecular Genetics, 24 (4). pp. 1185-1199. DOI https://doi.org/10.1093/hmg/ddu516

Dempster, Emma L and Pidsley, Ruth and Schalkwyk, Leonard C and Owens, Sheena and Georgiades, Anna and Kane, Fergus and Kalidindi, Sridevi and Picchioni, Marco and Kravariti, Eugenia and Toulopoulou, Timothea and Murray, Robin M and Mill, Jonathan (2011) Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder. Human Molecular Genetics, 20 (24). pp. 4786-4796. DOI https://doi.org/10.1093/hmg/ddr416

Ito, Yoko and Koessler, Thibaud and Ibrahim, Ashraf EK and Rai, Sushma and Vowler, Sarah L and Abu-Amero, Sayeda and Silva, Ana-Luisa and Maia, Ana-Teresa and Huddleston, Joanna E and Uribe-Lewis, Santiago and Woodfine, Kathryn and Jagodic, Maja and Nativio, Raffaella and Dunning, Alison and Moore, Gudrun and Klenova, Elena and Bingham, Sheila and Pharoah, Paul DP and Brenton, James D and Beck, Stephan and Sandhu, Manjinder S and Murrell, Adele (2008) Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer. Human Molecular Genetics, 17 (17). pp. 2633-2643. DOI https://doi.org/10.1093/hmg/ddn163

Butcher, Lee M and Meaburn, Emma and Knight, Jo and Sham, Pak C and Schalkwyk, Leonard C and Craig, Ian W and Plomin, Robert (2005) SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children. Human Molecular Genetics, 14 (10). pp. 1315-1325. DOI https://doi.org/10.1093/hmg/ddi142

Breen, M and Deakln, L and Macdonald, B and Miller, S and Sibson, R and Tarttelln, E and Avner, P and Bourgade, F and Guenet, JL and Montagutelli, X and Polrier, C and Simon, D and Tailor, D and Bishop, M and Kelly, M and Rysavy, F and Rastan, S and Norris, D and Shepherd, D and Abbott, C and Pllz, A and Hodge, S and Jackson, I and Boyd, Y and Blair, H and Maslen, G and A.todd, J and W.reed, P and Stoye, J and Ashworth, A and Mccarthy, L and Cox, R and Schalkwyk, L and Lehrach, H and Klose, J and Gangadharan, U and Brown, S (1994) Towards high resolution maps of the mouse and human genomes - a facility for ordering markers to 0.1 cm resolution. Human Molecular Genetics, 3 (4). 621 - 627. DOI https://doi.org/10.1093/hmg/3.4.621

Breen, M and Deakin, L and Macdonald, B and Miller, S and Sibson, R and Tarttelin, E and Avner, P and Bourgade, F and Guenet, JL and Montagutelli, X and Poirier, C and Simon, D and Tailor, D and Bishop, M and Kelly, M and Rysavy, F and Rastan, S and Norris, D and Shepherd, D and Abbott, C and Pilz, A and Hodge, S and Jackson, I and Boyd, Y and Blair, H and Maslen, G and Todd, JA and Reed, PW and Stoye, J and Ashworth, A and McCarthy, L and Cox, R and Schalkwyk, LC and Lehrach, H and Klose, J and Gangadharan, U and Brown, S (1994) Towards high resolution maps of the mouse and human genomes?a facility for ordering markers to 0.1 cM resolution. Human Molecular Genetics, 3 (4). pp. 621-627. DOI https://doi.org/10.1093/hmg/3.4.621

A.Jones, Karen and M.Black, Donald and A.Brown, Melissa and L.Griffiths, Beatrice and M.Nicolai, Hans and A.Chambers, Julie and Bonjardim, Marisa and Xu, Chun-Fang and Boyd, Marie and MeFariane, Robert and Korn, Bernhard and Poustka, Annemarie and A.North, Michael and Schalkwyk, Leo and Lehrach, Hans and Solomon, Ellen (1994) The detailed characterisation of a 400 kb cosmid walk in the <i>BRCA1</i> region: identification and localisation of 10 genes including a dual-specificity phosphatase. Human Molecular Genetics, 3 (11). pp. 1927-1934. DOI https://doi.org/10.1093/hmg/3.11.1927

Karasawa, M and Zwacka, RM and Reuter, A and Fink, T and Hsieh, CL and Lichter, P and Francke, U and Welher, H (1993) The human homolog of the glomerulosclerosis gene Mpv17: structure and genomic organization. Human Molecular Genetics, 2 (11). pp. 1829-1834. DOI https://doi.org/10.1093/hmg/2.11.1829