Items where Division is "Faculty of Medicine > Human Development and Health" and Year is 2013

Ahmad, G., Cheong, Y.C., Metwally, M.E. and Watson, A.J.S. (2013) The use of adhesion prevention agents in obstetrics and gynaecology. London, GB, Royal College of Obstetricians and Gynaecologists, 6pp. (Scientific Impact Paper, 39).

Al-Taan, Omer, Stephenson, James A., Spencer, Laura, Pollard, Cristina, West, Annette L., Calder, P.C., Metcalfe, Matthew and Dennison, Ashley R. (2013) Changes in plasma and erythrocyte omega-6 and omega-3 fatty acids in response to intravenous supply of omega-3 fatty acids in patients with hepatic colorectal metastases. Lipids in Health and Disease, 12, (64) (doi:10.1186/1476-511X-12-64). (PMID:23648075).

Ardern-Jones, M.R. (2013) Atypical erythema multiforme is a prognostic indicator of severe hepatic dysfunction in Dress (Drug Reaction with Eosinophilia and Systemic Symptoms). British Journal of Dermatology, 168, (2), 234-235. (doi:10.1111/bjd.12191). (PMID:23034060).

Balbus, J.M., Barouki, R., Birnbaum, L.S., Etzel, R.A., Gluckman, Peter D., Grandjean, P., Hancock, C., Hanson, Mark A., Heindel, J.J., Hoffman, K., Jensen, G.K., Keeling, A., Neira, M., Rabadan-Diehl, C., Ralston, J. and Tang, K.-C. (2013) Early-life prevention of non-communicable diseases. The Lancet, 381, (9860), 3-4.

Banka, Siddharth, Howard, Emma, Bunstone, Sancha, Chandler, Kate E., Kerr, Bronwyn, Lachlan, Katherine, McKee, Shane, Mehta, Sarju G., Tavares, Ana Lisa Taylor, Tolmie, John and Donnai, Dian (2013) MLL2 mosaic mutations and intragenic deletion-duplications in patients with Kabuki syndrome. Clinical Genetics, 83, (5), 467-471. (doi:10.1111/j.1399-0004.2012.01955.x).

Barber, J. C. K., Rodrigues, R., Maloney, V. K., Taborda, F., Rodrigues, M. do C. and Bateman, M. S. (2013) Another family with a euchromatic duplication variant of 9q13-q21.1 Derived from segmentally duplicated pericentromeric euchromatin. Cytogenetic and Genome Research (doi:10.1159/000350870). (PMID:23651944).

Barber, J.C.K., Brasch-Andersen, C., Maloney, V.K., Huang, S., Bateman, M.S., Graakjaer, J., Heinl, U.D. and Fagerberg, C. (2013) A novel pseudo-dicentric variant of 16p11.2-q11.2 contains Euchromatin from 16p11.2-p11.1 and resembles pathogenic duplications of proximal 16q. Cytogenetic and Genome Research, 139, (1), 59-64. (doi:10.1159/000342542).

Barber, John C.K., Hall, Victoria, Maloney, Viv K., Huang, Shuwen, Roberts, Angharad M., Brady, Angela F., Foulds, Nicki, Bewes, Beverley, Volleth, Marianne, Liehr, Thomas, Mehnert, Karl, Bateman, Mark and White, Helen (2013) 16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2. European Journal of Human Genetics, 21, (2), 182-189. (doi:10.1038/ejhg.2012.144). (PMID:22828807).

Barber, John C.K., Rosenfeld, Jill A., Foulds, Nicola, Laird, Sophie, Bateman, Mark S., Thomas, N. Simon, Baker, Samantha, Maloney, Viv K., Anilkumar, Arayamparambil, Smith, Wendy E., Banks, Valerie, Ellingwood, Sara, Kharbutli, Yara, Mehta, Lakshmi, Eddleman, Keith A., Marble, Michael, Zambrano, Regina, Crolla, John A. and Lamb, Allen N. (2013) 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients. American Journal of Medical Genetics Part A, 161, (3), 487-500. (doi:10.1002/ajmg.a.35767).

Barisic, Ingeborg, Odak, Ljubica, Loane, Maria, Garne, Ester, Wellesley, Diana, Calzolari, Elisa, Dolk, Helen, Addor, Marie-Claude, Arriola, Larraitz, Bergman, Jorieke, Bianca, Sebastiano, Boyd, Patricia A., Draper, Elizabeth S., Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Latos-Bielenska, Anna, McDonnell, Bob, Pierini, Anna, Rankin, Judith, Rissmann, Anke, Queisser-Luft, Annette, Verellen-Dumoulin, Christine, Stone, David and Tenconi, Romano (2013) Fraser syndrome: epidemiological study in a European population. American Journal of Medical Genetics Part A, 161, (5), 1012-1018. (doi:10.1002/ajmg.a.35839). (PMID:23532946).

Bench, Anthony J., White, Helen E., Foroni, Letizia, Godfrey, Anna L., Gerrard, Gareth, Akiki, Susanna, Awan, Abida, Carter, Ian, Goday-Fernandez, Andrea, Langabeer, Stephen E., Clench, Tim, Clark, Jordan, Evans, Paul A., Grimwade, David, Schuh, Anna, McMullin, Mary F., Green, Anthony R., Harrison, Claire N. and Cross, Nicholas C.P. (2013) Molecular diagnosis of the myeloproliferative neoplasms: UK guidelines for the detection ofJAK2V617F and other relevant mutations. British Journal of Haematology, 160, (1), 25-34. (doi:10.1111/bjh.12075).

Berland, Siren, Appelbäck, Mia, Bruland, Ove, Beygo, Jasmin, Buiting, Karin, Mackay, Deborah J.G., Karen Temple, I. and Houge, Gunnar (2013) Evidence for anticipation in Beckwith–Wiedemann syndrome. European Journal of Human Genetics (doi:10.1038/ejhg.2013.71). (PMID:23572028).

Blakely, Emma L., Yarham, John W., Alston, Charlotte L., Craig, Kate, Poulton, Joanna, Brierley, Charlotte, Park, Soo-Mi, Dean, Andrew, Xuereb, John H., Anderson, Kirstie N., Compston, Alistair, Allen, Chris, Sharif, Saba, Enevoldson, Peter, Wilson, Martin, Hammans, Simon R., Turnbull, Douglass M., McFarland, Robert and Taylor, Robert W. (2013) Pathogenic mitochondrial tRNA point mutations: nine novel mutations affirm their importance as a cause of mitochondrial disease. Human Mutation (doi:10.1002/humu.22358). (PMID:23696415).

Boonen, Susanne E., Mackay, Deborah J. G., Hahnemann, Johanne M. D., Docherty, Louise E., Grønskov, Karen, Lehmann, Anna, Larsen, Lise G., Haemers, Andreas P., Kockaerts, Yves, Dooms, Lutgarde, Vũ, Dũng Chí, Ngoc, C. T. Bich, Nguyen, Phuong Bich, Kordonouri, Olga, Sundberg, Frida, Dayanikli, Pinar, Puthi, Vijith, Acerini, Carlo, Massoud, Ahmed F., Tümer, Zeynep and Temple, I. Karen (2013) Transient Neonatal Diabetes, ZFP57, and Hypomethylation of Multiple Imprinted Loci: A detailed follow-up. Diabetes Care, 36, (3), 505-512. (doi:10.2337/dc12-0700). (PMID:23150280).

Bor, Jacob, Herbst, Abraham J., Newell, Marie-Louise and Barnighausen, Till (2013) Increases in adult life expectancy in rural South Africa: valuing the scale-up of HIV treatment. Science, 339, (6122), 961-965. (doi:10.1126/science.1230413). (PMID:23430655).

Borel, P., Lietz, G., Goncalves, A., Szabo de Edelenyi, F., Lecompte , S., Curtis, P., Goumidi , L., Caslake, M.J., Miles, Elizabeth A., Packard, C., Calder, P.C., Mathers, J.C ., Minihane, A.M., Tourniaire, F., Kesse-Guyot , E., Galan, P., Hercberg, S., Breidenassel , C., González Gross, M., Moussa, M., Meirhaeghe, A. and Reboul, E. (2013) CD36 and SR-BI are involved in cellular uptake of provitamin A carotenoids by Caco-2 and HEK Cells, and some of their genetic variants are associated with plasma concentrations of these micronutrients in humans. Journal of Nutrition, 143, (4), 448-456. (doi:10.3945/​jn.112.172734 ). (PMID:23427331).

Boyle, B., McConkey, R., Garne, E., Loane, M., Addor, M.C., Bakker, M.K., Boyd, P.A., Gatt, M., Greenlees, R., Haeusler, M., Klungsøyr, K., Latos-Bielenska, A., Lelong, N., McDonnell, R., Métneki, J., Mullaney, C., Nelen, V., O'Mahony, M., Pierini, A., Rankin, J., Rissmann, A., Tucker, D., Wellesley, D. and Dolk, H. (2013) Trends in the prevalence, risk and pregnancy outcome of multiple births with congenital anomaly: a registry-based study in 14 European countries 1984-2007. BJOG An International Journal of Obstetrics & Gynaecology, 120, (6), 707-716. (doi:10.1111/1471-0528.12146).

Boyraz, Mehmet, Ulucan, Korkut, Taşkın, Necati, Akçay, Teoman, Flanagan, Sarah E. and Mackay, Deborah J.G. (2013) Transient neonatal diabetes mellitus in a Turkish patient with three novel homozygous variants in the ZFP57 gene. Journal of Clinical Research in Pediatric Endocrinology, 5, (2), 125-128. (doi:10.4274/Jcrpe.928). (PMID:23748067).

Brioli, Annamaria, Boyd, Kevin D., Kaiser, Martin F., Pawlyn, Charlotte, Wu, Ping, Gregory, Walter M., Owen, Roger, Ross, Fiona M., Jackson, Graham H., Cavo, Michele, Davies, Faith E. and Morgan, Gareth J. (2013) Response and biological subtype of myeloma are independent prognostic factors and combine to define outcome after high-dose therapy. British Journal of Haematology, 161, (2), 291-294. (doi:10.1111/bjh.12218).

Brookes, K and Cheong, Y. (2013) Tubal infertility. In, Management of Infertility for the MRCOG and Beyond: 3rd edition. London, GB, Royal College of Obstetricians and Gynaecologists. (In Press).

Calder, P.C. (2013) Dietary fats and inflammation. In, Garg, M.L. and Wood, L.G. (eds.) Nutrition and Physical Activity in Inflammatory Diseases. Wallingford, GB, CAB International, 23-45.

Calder, P.C. (2013) Editorial: fat chance to enhance B cell function. Journal of Leukocyte Biology, 93, (4), 457-459. (doi:10.1189/jlb.1212646 ). (PMID:23547174).

Calder, P.C. (2013) Inflammation: an introduction. In, Garg, M.L. and Wood, L.G. (eds.) Nutrition and Physical Activity in Inflammatory Diseases. Wallingford, GB, CAB International, 1-22.

Calder, P.C. (2013) Marine omega-3 polyunsaturated fatty acids and rheumatoid arthritis. In, Watson, R.R. and Preedy, V.R. (eds.) Bioactive Food as Dietary Interventions for Arthritis and Related Inflammatory Diseases. San Diego, US, Academic Press, 113-132.

Calder, P.C. (2013) Omega 3 polyunsaturated fatty acids. In, Brahmachari, Goutam (ed.) Chemistry and Pharmacology of Naturally Occurring Bioactive Compounds. Boca Raton, US, CRC Press, 197-209.

Calder, P.C. (2013) Omega-3 fatty acid deficiency and rheumatoid arthritis. In, McNamara, R.K. (ed.) The Omega-3 Fatty Acid Deficiency Syndrome. New York, US, Nova, 193-212.

Calder, P.C. (2013) Omega-3 polyunsaturated fatty acids and inflammatory processes: nutrition or pharmacology? British Journal of Clinical Pharmacology, 75, (3), 645-662. (doi:10.1111/j.1365-2125.2012.04374.x). (PMID:22765297).

Calder, Philip C. and Deckelbaum, Richard J. (2013) Intravenous fish oil in hospitalized adult patients: reviewing the reviews. Current Opinion in Clinical Nutrition and Metabolic Care, 16, (2), 119-123. (doi:10.1097/MCO.0b013e32835dbde9). (PMID:23324901).

Calder , Philip C. (2013) Editorial. Old study sheds new light on the fatty acids and cardiovascular health debate. BMJ, 346, p.f493. (doi:10.1136/bmj.f493). (PMID:23386269).

Calder , Philip C. (2013) Omega-3 fatty acids in health and disease: the science behind the headlines. NHD Magazine, 83, 18-19.

Calder , Philip C., Ahluwalia, N., Albers, R., Bosco, N., Bourdet-Sicard, R., Haller, D., Holgate, S., Jonsson, L., Latulippe, M., Marcos, A., Moreines, J., M’Rini, C., Muller, M., Pawelec, G., van Neerven, R., Watzl, B. and Zhao, J. (2013) A consideration of biomarkers to be used for evaluation of inflammation in human nutritional studies. British Journal of Nutrition, 109, supplement 1, S1-S34. (doi:10.1017/S0007114512005119). (PMID:23343744).

Calton, Elizabeth A., Temple, I. Karen, Mackay, Deborah J.G., Lever, Margaret, Ellard, Sian, Flanagan, Sarah E., Davies, Justin H., Hussain, Khalid and Gray, Juliet C. (2013) Hepatoblastoma in a child with a paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p causing focal congenital hyperinsulinism. European Journal of Medical Genetics, 56, (2), 114-117. (doi:10.1016/j.ejmg.2012.12.001). (PMID:23261959).

Chase, A., Bryant, C., Score, J., Haferlach, C., Grossmann, V., Schwaab, J., Hofmann, W.-K., Reiter, A. and Cross, N. C. P. (2013) Ruxolitinib as potential targeted therapy for patients with JAK2 rearrangements. Haematologica, 98, (3), 404-408. (doi:10.3324/haematol.2012.067959).

Chase, Andrew, Bryant, Catherine, Score, Joannah and Cross, Nicholas C. P. (2013) Ponatinib as targeted therapy for FGFR1 fusions associated with the 8p11 myeloproliferative syndrome. Haematologica, 98, (1), 103-106. (doi:10.3324/haematol.2012.066407). (PMID:22875613).

Cheong, Y. (2013) Alternative therapies for chronic pelvic pain. In, Chronic Pelvic Pain. Cambridge, GB, Cambridge University Press. (In Press).

Cheong, Ying, Boomsma, Carolien, Heijnen, Cobi and Macklon, Nick (2013) Uterine secretomics: a window on the maternal-embryo interface. Fertility and Sterility, 99, (4), 1093-1099. (doi:10.1016/j.fertnstert.2013.01.144). (PMID:23433513).

Christodoulou, K., Wiskin, A.E., Gibson, J., Tapper, W., Willis, C., Afzal, N.A., Upstill-Goddard, R., Holloway, J.W., Simpson, M.A., Beattie, R.M., Collins, A. and Ennis, S. (2013) Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes. Gut, 62, (7), 977-984. (doi:10.1136/gutjnl-2011-301833). (PMID:22543157).

Citterio, Cintia E., Machiavelli, Gloria A., Miras, Mirta B., Gruñeiro-Papendieck, Laura, Lachlan, Katherine, Sobrero, Gabriela, Chiesa, Ana, Walker, Joanna, Muñoz, Liliana, Testa, Graciela, Belforte, Fiorella S., Gonzalez-Sarmiento, Rogelio, Rivolta, Carina M. and Targovnik, Héctor M. (2013) New insights into thyroglobulin gene: molecular analysis of seven novel mutations associated with goiter and hypothyroidism. Molecular and Cellular Endocrinology, 365, (2), 277-291. (doi:10.1016/j.mce.2012.11.002). (PMID:23164529).

Coggon, David, Ntani, G., Vergas-Prada, S., Martinez, J.M., Serra, C., Benavides, F.G., Palmer, K.T. and members of CUPID Collaboration (2013) International variation in musculoskeletal sickness absence: findings from the CUPID study. Occupational and Environmental Medicine (doi:10.1136/oemed-2012-101316). (PMID:23695413).

Coggon, David, Ntani, Georgia and Palmer, K.T. et al. (2013) Disabling musculoskeletal pain in working populations: is it the job, the person or the culture? Pain, 154, (6), 856-863. (doi:10.1016/j.pain.2013.02.008). (PMID:23688828).

Coggon, David, Ntani, Georgia, Palmer, Keith T., Felli, Vanda E., Herari, Raul, Barrero, Lope H., Felknor, Sarah A., Gimeno, David, Cattrell, Anna, Vargas-Prada, Sergio, Bonzini, Matteo, Solidaki, Eleni, Merisalu, Eda, Habib, Rima R., Sadeghianm, Farideh, Kadir, M. Masood, Warnakulasuriya, Sudath S.P., Matsudaira, Ko, Nyantumbu, Busisiwe, Sim, Malcolm R., Harcombe, Helen, Cox, Ken, Marziale, Maria H., Sarquis, Leila M., Harari, Leila M., Freire, Rocio, Harari, Natalia, Monroy, Magda V., Qintana, Leonardo A., Rojas, Marianela, Salazar Vega, Eduardo J., Harris, Clare E, Serra, Consol, Martinez, Miguel, Delclos, George, Benavides, Fernando G., Carugno, Michele, Ferrario, Marco M., Pesatori, Angela C., Chatzi, Leda, Bitsios, Panos, Kogevinas, Manolis, Oha, Kristel, Sirk, Tuuli, Sadeghian, Ali, Peiris-John, Roshini, Sathiakumar, Nalini, Wickremasinghe, A. Rajitha, Yoshimura, Noriko, Kelsall, Helen L., Hoe, Victor C.W., Urquhart, Donna M., Derrett, Sarah, McBride, David, Herbison, Peter and Gray, Andrew (2013) Patterns of multi-site pain and associations with risk factors. Pain (doi:10.1016/j.pain.2013.05.039). (PMID:23727463). (In Press).

Collins, S.A., Lucas, J.S.A., Inskip, H.M., Godfrey, K.M., Roberts, G., Holloway, J.W. and the Southampton Women’s Survey Study Group, (2013) HHIP, HDAC4, NCR3, and RARB polymorphisms affect fetal, childhood, and adult lung function. European Respiratory Journal, 41, (3), 756-757. (doi:10.1183/09031936.00171712). (PMID:23456936).

Collins, Samuel A., Lucas, Jane S.A., Inskip, Hazel M., Godfrey, Keith M., Roberts, Graham C. and Holloway, John W. (2013) HHIP, HDAC4, NCR3 and RARB polymorphisms affect fetal, childhood and adult lung function. European Respiratory Journal, 41, (3), 756-757. (doi:10.1183/09031936.00171712). (PMID:23456936).

Collins, Samuel A., Pike, Katharine C., Inskip, Hazel M., Godfrey, Keith M., Roberts, Graham, Holloway, John W. and Lucas, Jane S.A. (2013) Validation of novel wheeze phenotypes using longitudinal airway function and atopic sensitization data in the first 6 years of life: evidence from the Southampton women's survey. Pediatric Pulmonology (doi:10.1002/ppul.22766).

Costello, Paula M., Hollis, Lisa J., Cripps, Roselle L., Bearpark, Natasha, Patel, Harnish P., Sayer, Avan Aihie, Cooper, Cyrus, Hanson, Mark A., Ozanne, Susan E. and Green, Lucy R. (2013) Lower maternal body condition during pregnancy affects skeletal muscle structure and glut-4 protein levels but not glucose tolerance in mature adult sheep. Reproductive Sciences (doi:10.1177/1933719113477494). (PMID:23420826).

Danoux, Charlène, Tare, Rahul S., Smith, James, Bradley, Mark, Hunt, John A., Oreffo, Richard O.C. and Habibovic, Pamela (2013) Development of materials for regenerative medicine: from clinical need to clinical application. In, de Boer, Jan and van Blitterswijk, Clemens (eds.) Materiomics: High Throughput Screening of Biomaterial Properties. Cambridge, GB, Cambridge University Press. (In Press).

Dhami, Sangeeta, Panesar, Sukhmeet S., Rader, Tamara, Muraro, Antonella, Roberts, Graham, Worm, Margitta and Sheikh, Aziz (2013) The acute and long-term management of anaphylaxis: protocol for a systematic review. Clinical and Translational Allergy, 3, 14. (doi:10.1186/2045-7022-3-14). (PMID:23575342).

Dixit, A., Chandler, K.E., Lever, M., Poole, R.L., Bullman, H., Mughal, M.Z., Steggall, M. and Suri, M. (2013) Pseudohypoparathyroidism type 1b due to paternal uniparental disomy of chromosome 20q. Journal of Clinical Endocrinology & Metabolism, 98, (1), E103-E108. (doi:10.1210/jc.2012-2639). (PMID:23144470).

Docherty, L.E., Kabwama, S., Lehmann, A., Hawke, E., Harrison, L., Flanagan, S.E., Ellard, S., Hattersley, A.T., Shield, J. P. H., Ennis, S., Mackay, D. J .G. and Temple, I.K. (2013) Clinical presentation of 6q24 transient neonatal diabetes mellitus (6q24 TNDM) and genotype-phenotype correlation in an international cohort of patients. Diabetologia, 56, (4), 758-762. (PMID:23385738).

Dreborg, Sten, Roberts, Graham, Lau, Susanne, Santos, Alexandra F., Halken, Susanne and Høst, Arne (2013) The history of pediatric allergy in Europe: from a working group to ESPACI and SP-EAACI. Pediatric Allergy and Immunology, 24, (1), 88-96. (doi:10.1111/pai.12029). (PMID:23331532).

Eigenmann, P.A., Atanaskovic-Markovic, M., Hourihane, J.O'B., Lack, G., Lau, S., Matricardi, P.M., Muraro, A., Namazova Baranova, L., Nieto, A., Papadopoulos, N.G., Réthy, L.A., Roberts, G., Rudzeviciene, O., Wahn, U., Wickman, M. and Høst, A. (2013) Testing children for allergies: why, how, who and when: an updated statement of the European Academy of Allergy and Clinical Immunology (EAACI) section on pediatrics and the EAACI-Clemens von Pirquet foundation. Pediatric Allergy and Immunology, 24, (2), 195-209. (doi:10.1111/pai.12066). (PMID:23506293).

Elahi, M. M., Cagampang, F. R., Ohri, Sunil K. and Hanson, Mark A. (2013) Long-term statin administration to dams on high-fat diet protects not only them but also their offspring from cardiovascular risk. Annals of Nutrition & Metabolism, 62, (3), 248-254. (doi:10.1159/000346037). (PMID:23594919).

Evans, Nick R., Davies, Evan M., Dare, Chris J. and Oreffo, Richard O.C. (2013) Tissue engineering strategies in spinal arthrodesis: the clinical imperative and challenges to clinical translation. Regenerative Medicine, 8, (1), 49-64. (doi:10.2217/rme.12.106). (PMID:23259805).

Flanagan, S.E., Mackay, D.J.G., Greeley, S.A.W., McDonald, T.J., Mericq, V., Hassing, J., Richmond, E.J., Martin, W.R., Acerini, C., Kaulfers, A.M., Flynn, D.P., Popovic, J., Sperling, M.A., Hussain, K., Ellard, S. and Hattersley, A.T. (2013) Research letter. Hypoglycaemia following diabetes remission in patients with 6q24 methylation defects: expanding the clinical phenotype. Diabetologia, 56, (1), 218-221. (doi:10.1007/s00125-012-2766-z). (PMID:23111732).

Forristal, Catherine E., Christensen , DavidR., Chinnery, Fay E., Petruzzelli, Raffaella, Parry, Kate L., Sanchez-Elsner, Tilman and Houghton, Franchesca D. (2013) Environmental oxygen tension regulates the energy metabolism and self-renewal of human embryonic stem cells. PLoS ONE, 8, (5), e62507. (doi:10.1371/journal.pone.0062507). (PMID:23671606).

Freimuth, Julia, Bangen, Jörg-Martin, Lambertz, Daniela, Hu, Wei, Nevzorova, Yulia Alexandrovna, Sonntag, Roland, Gassler, Nikolaus, Riethmacher, Dieter, Trautwein, Christian and Liedtke, Christian (2013) Loss of caspase-8 in hepatocytes accelerates the onset of liver regeneration in mice through premature NF-κB activation. Hepatology (doi:10.1002/hep.26538). (In Press).

Garcia-Closas, Montserrat, Couch, Fergus J., Lindstrom, Sara, Michailidou, Kyriaki, Schmidt, Marjanka K., Brook, Mark N., Orr, Nick, Rhie, Suhn Kyong, Riboli, Elio, Feigelson, Heather S., Le Marchand, Loic, Buring, Julie E., Eccles, Diana, Miron, Penelope, Fasching, Peter A., Brauch, Hiltrud, Chang-Claude, Jenny, Carpenter, Jane, Godwin, Andrew K., Nevanlinna, Heli, Giles, Graham G., Cox, Angela, Hopper, John L., Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Dicks, Ed, Howat, Will J., Schoof, Nils, Bojesen, Stig E., Lambrechts, Diether, Broeks, Annegien, Andrulis, Irene L., Guénel, Pascal, Burwinkel, Barbara, Sawyer, Elinor J., Hollestelle, Antoinette, Fletcher, Olivia, Winqvist, Robert, Brenner, Hermann, Mannermaa, Arto, Hamann, Ute, Meindl, Alfons, Lindblom, Annika, Zheng, Wei, Devillee, Peter, Goldberg, Mark S., Lubinski, Jan, Kristensen, Vessela, Swerdlow, Anthony, Anton-Culver, Hoda, Dörk, Thilo, Muir, Kenneth, Matsuo, Keitaro, Wu, Anna H., Radice, Paolo, Teo, Soo Hwang, Shu, Xiao-Ou, Blot, William, Kang, Daehee, Hartman, Mikael, Sangrajrang, Suleeporn, Shen, Chen-Yang, Southey, Melissa C., Park, Daniel J., Hammet, Fleur, Stone, Jennifer, Veer, Laura J. Van't, Rutgers, Emiel J., Lophatananon, Artitaya, Stewart-Brown, Sarah, Siriwanarangsan, Pornthep, Peto, Julian, Schrauder, Michael G., Ekici, Arif B., Beckmann, Matthias W., dos Santos Silva, Isabel, Johnson, Nichola, Warren, Helen, Tomlinson, Ian, Kerin, Michael J, Miller, Nicola, Marme, Federick, Schneeweiss, Andreas, Sohn, Christof, Truong, Therese, Laurent-Puig, Pierre, Kerbrat, Pierre, Nordestgaard, Børge G., Nielsen, Sune F., Flyger, Henrik, Milne, Roger L., Perez, Jose Ignacio Arias, Menéndez, Primitiva, Müller, Heiko, Arndt, Volker, Stegmaier, Christa, Lichtner, Peter, Lochmann, Magdalena, Justenhoven, Christina, Ko, Yon-Dschun, Muranen, Taru A., Aittomäki, Kristiina, Blomqvist, Carl, Greco, Dario, Heikkinen, Tuomas, Ito, Hidemi, Iwata, Hiroji, Yatabe, Yasushi, Antonenkova, Natalia N., Margolin, Sara, Kataja, Vesa, Kosma, Veli-Matti, Hartikainen, Jaana M., Balleine, Rosemary, Tseng, Chiu-Chen, Berg, David Van Den, Stram, Daniel O., Neven, Patrick, Dieudonné, Anne-Sophie, Leunen, Karin, Rudolph, Anja, Nickels, Stefan, Flesch-Janys, Dieter, Peterlongo, Paolo, Peissel, Bernard, Bernard, Loris, Olson, Janet E., Wang, Xianshu, Stevens, Kristen, Severi, Gianluca, Baglietto, Laura, McLean, Catriona, Coetzee, Gerhard A., Feng, Ye, Henderson, Brian E., Schumacher, Fredrick, Bogdanova, Natalia V., Labrèche, France, Dumont, Martine, Yip, Cheng Har, Taib, Nur Aishah Mohd, Cheng, Ching-Yu, Shrubsole, Martha, Long, Jirong, Pylkäs, Katri, Jukkola-Vuorinen, Arja, Kauppila, Saila, Knight, Julia A., Glendon, Gord, Mulligan, Anna Marie, Tollenaar, Robertus A. E. M., Seynaeve, Caroline M., Kriege, Mieke, Hooning, Maartje J., van den Ouweland, Ans M. W., van Deurzen, Carolien H. M., Lu, Wei, Gao, Yu-Tang, Cai, Hui, Balasubramanian, Sabapathy P., Cross, Simon S., Reed, Malcolm W. R., Signorello, Lisa, Cai, Qiuyin, Shah, Mitul, Miao, Hui, Chan, Ching Wan, Chia, Kee Seng, Jakubowska, Anna, Jaworska, Katarzyna, Durda, Katarzyna, Hsiung, Chia-Ni, Wu, Pei-Ei, Yu, Jyh-Cherng, Ashworth, Alan, Jones, Michael, Tessier, Daniel C., González-Neira, Anna, Pita, Guillermo, Alonso, M. Rosario, Vincent, Daniel, Bacot, Francois, Ambrosone, Christine B., Bandera, Elisa V., John, Esther M., Chen, Gary K., Hu, Jennifer J., Rodriguez-Gil, Jorge L., Bernstein, Leslie, Press, Michael F., Ziegler, Regina G., Millikan, Robert M., Deming-Halverson, Sandra L., Nyante, Sarah, Ingles, Sue A., Waisfisz, Quinten, Tsimiklis, Helen, Makalic, Enes, Schmidt, Daniel, Bui, Minh, Gibson, Lorna, Müller-Myhsok, Bertram, Schmutzler, Rita K., Hein, Rebecca, Dahmen, Norbert, Beckmann, Lars, Aaltonen, Kirsimari, Czene, Kamila, Irwanto, Astrid, Liu, Jianjun, Turnbull, Clare, Rahman, Nazneen, Meijers-Heijboer, Hanne, Uitterlinden, Andre G., Rivadeneira, Fernando, Olswold, Curtis, Slager, Susan, Pilarski, Robert, Ademuyiwa, Foluso, Konstantopoulou, Irene, Martin, Nicholas G., Montgomery, Grant W., Slamon, Dennis J., Rauh, Claudia, Lux, Michael P., Jud, Sebastian M., Bruning, Thomas, Weaver, JoEllen, Sharma, Priyanka, Pathak, Harsh, Tapper, Will, Gerty, Sue, Durcan, Lorraine, Trichopoulos, Dimitrios, Tumino, Rosario, Peeters, Petra H., Kaaks, Rudolf, Campa, Daniele, Canzian, Federico, Weiderpass, Elisabete, Johansson, Mattias, Khaw, Kay-Tee, Travis, Ruth, Clavel-Chapelon, Françoise, Kolonel, Laurence N., Chen, Constance, Beck, Andy, Hankinson, Susan E., Berg, Christine D., Hoover, Robert N., Lissowska, Jolanta, Figueroa, Jonine D., Chasman, Daniel I., Gaudet, Mia M., Diver, W. Ryan, Willett, Walter C., Hunter, David J., Simard, Jacques, Benitez, Javier, Dunning, Alison M., Sherman, Mark E., Chenevix-Trench, Georgia, Chanock, Stephen J., Hall, Per, Pharoah, Paul D. P., Vachon, Celine, Easton, Douglas F., Haiman, Christopher A. and Kraft, Peter (2013) Genome-wide association studies identify four ER negative–specific breast cancer risk loci. Nature Genetics, 45, (4), 392-398. (doi:10.1038/ng.2561). (PMID:23535733).

Gardner, D.S. and Poore, K.R. (2013) Do not turn to the hypothalamus for feedback on stress if you are growth restricted. Endocrinology (In Press).

Gavlak, Johanna C., Stocks, Janet, Laverty, Aidan, Fettes, Emma, Bucks, Romola, Sonnappa, Samatha, Cooper, Janine, Grocott, Michael P., Levett, Denny Z., Martin, Daniel S., Imray, Christopher H. and Kirkham, Fenella J. (2013) The Young Everest Study: preliminary report of changes in sleep and cerebral blood flow velocity during slow ascent to altitude in unacclimatised children. Archives of Disease in Childhood (doi:10.1136/archdischild-2012-302512 ). (PMID:23471157).

Gelsi-Boyer, Veronique, Cervera, Nathalie, Bertucci, Francois, Brecqueville, Mandy, Finetti, Pascal, Murati, Anne, Arnoulet, Christine, Mozziconacci, Marie-Joelle, Mills, Ken, Cross, Nicholas C P, Vey, Norbert and Birnbaum, Daniel (2013) Molecular similarity between myelodysplastic form of chronic myelomonocytic leukemia and refractory anemia with ring sideroblasts. Haematologica, 98, (4), 576-583. (doi:10.3324/haematol.2012.071506 ). (PMID:23065512).

Gibson, Jane, Tapper, William, Ennis, Sarah and Collins, Andrew (2013) Exome-based linkage disequilibrium maps of individual genes: functional clustering and relationship to disease. Human Genetics, 132, (2), 233-243. (doi:10.1007/s00439-012-1243-6).

Gilbert, Rodney D., Sukhtankar, Priya, Lachlan, Katherine and Fowler, Darren J. (2013) Bilineal inheritance of PKD1 abnormalities mimicking autosomal recessive polycystic disease. Pediatric Nephrology (doi:10.1007/s00467-013-2484-x). (PMID:23624871).

Gluckman, Peter D., Beedle, A.S., Hanson, Mark A. and Low, F.M. (2013) Human growth: evolutionary and life history perspectives. In, Recent Advances in Growth Research: Nutritional, Molecular and Endocrine Perspectives. Basel, CH, Karger, 89-102. ( Nestlé Nutrition Institute Workshop Series, 71).

Gothard, D., Dawson, J.I. and Oreffo, R.O.C. (2013) Assessing the potential of colony morphology for dissecting the CFU-F population from human bone marrow stromal cells. Cell and Tissue Research (doi:10.1007/s00441-013-1564-3). (PMID:23397425).

Hammed, T and Cheong, Y. (2013) Common and uncommon cases. In, Case Studies in Assisted Reproduction. Cambridge, GB, Cambridge University Press. (In Press).

Harlalka, Gaurav V., Baple, Emma L., Cross, Harold, Kuhnle, Simone, Cubillos-Rojas, Monica, Matentzoglu, Konstantin, Patton, Michael A., Wagner, Karin, Coblentz, Roselyn, Ford, Debra L., Mackay, Deborah J.G., Chioza, Barry A., Scheffner, Martin, Rosa, Jose Luis and Crosby, Andrew H. (2013) Mutation of HERC2 causes developmental delay with Angelman-like features. Journal of Medical Genetics, 50, (2), 65-73. (doi:10.1136/jmedgenet-2012-101367). (PMID:23243086).

Hogarth, P., Gregory, A., Kruer, M.C., Sanford, L., Wagoner, W., Natowicz, M.R., Egel, R.T., Subramony, S.H., Goldman, J.G., Berry-Kravis, E., Foulds, N.C., Hammans, S.R., Desguerre, I., Rodriguez, D., Wilson, C., Diedrich, A., Green, S., Tran, H., Reese, L., Woltjer, R.L. and Hayflick, S.J. (2013) New NBIA subtype: Genetic, clinical, pathologic, and radiographic features of MPAN. Neurology, 80, (3), 268-275. (doi:10.1212/WNL.0b013e31827e07be). (PMID:23269600).

Holt, R.I.G. (2013) A review of reviews: a virtual issue. Diabetes Obesity and Metabolism, 15, (1), 1-2. (doi:10.1111/dom.12044). (PMID:23241070).

Holt, R.I.G., Nicolucci, A., Kovacs Burn, K., Escalante, M., Forbes, A., Hermanns, N., Kalra, S., Massi-Benedetti, M., Mayorov, A., Menendez-Torre, E., Munro, N., Skovlund, S.E., Tarkun, I., Wens, J. and Peyrot, M. (2013) Diabetes Attitudes, Wishes and Needs: second study (DAWN): cross-national comparisons on barriers and resources for optimal care-healthcare professional perspective. Diabetic Medicine (doi:10.0000/dme.12242). (PMID:23710839).

Holt, Richard I.G., Jameson, Karen A., Cooper, Cyrus, Dennison, Elaine M. and Peveler, Robert C. (2013) The relationship between depression, anxiety and cardiovascular disease: Findings from the Hertfordshire Cohort Study. Journal of Affective Disorders (doi:10.1016/j.jad.2013.02.026). (PMID:23507368). (In Press).

Horikoshi, Momoko, Yaghootkar, Hanieh, Mook-Kanamori, Dennis O., Sovio, Ulla, Taal, H Rob, Hennig, Branwen J., Bradfield, Jonathan P., St Pourcain, Beate, Evans, David M., Charoen, Pimphen, Kaakinen, Marika, Cousminer, Diana L., Lehtimäki, Terho, Kreiner-Møller, Eskil, Warrington, Nicole M., Bustamante, Mariona, Feenstra, Bjarke, Berry, Diane J., Thiering, Elisabeth, Pfab, Thiemo, Barton, Sheila J., Shields, Beverley M., Kerkhof, Marjan, van Leeuwen, Elisabeth M., Fulford, Anthony J., Kutalik, Zoltán, Zhao, Jing Hua, den Hoed, Marcel, Mahajan, Anubha, Lindi, Virpi, Goh, Liang-Kee, Hottenga, Jouke-Jan, Wu, Ying, Raitakari, Olli T., Harder, Marie N., Meirhaeghe, Aline, Ntalla, Ioanna, Salem, Rany M., Jameson, Karen A., Zhou, Kaixin, Monies, Dorota M., Lagou, Vasiliki, Kirin, Mirna, Heikkinen, Jani, Adair, Linda S., Alkuraya, Fowzan S., Al-Odaib, Ali, Amouyel, Philippe, Andersson, Ehm Astrid, Bennett, Amanda J., Blakemore, Alexandra I.F., Buxton, Jessica L., Dallongeville, Jean, Das, Shikta, de Geus, Eco J. C., Estivill, Xavier, Flexeder, Claudia, Froguel, Philippe, Geller, Frank, Godfrey, Keith M., Gottrand, Frédéric, Groves, Christopher J., Hansen, Torben, Hirschhorn, Joel N., Hofman, Albert, Hollegaard, Mads V., Hougaard, David M., Hyppönen, Elina, Inskip, Hazel M., Isaacs, Aaron, Jørgensen, Torben, Kanaka-Gantenbein, Christina, Kemp, John P., Kiess, Wieland, Kilpeläinen, Tuomas O., Klopp, Norman, Knight, Bridget A., Kuzawa, Christopher W., McMahon, George, Newnham, John P., Niinikoski, Harri, Oostra, Ben A., Pedersen, Louise, Postma, Dirkje S., Ring, Susan M., Rivadeneira, Fernando, Robertson, Neil R., Sebert, Sylvain, Simell, Olli, Slowinski, Torsten, Tiesler, Carla M.T., Tönjes, Anke, Vaag, Allan, Viikari, Jorma S., Vink, Jacqueline M., Vissing, Nadja Hawwa, Wareham, Nicholas J., Willemsen, Gonneke, Witte, Daniel R., Zhang, Haitao, Zhao, Jianhua, Wilson, James F., Stumvoll, Michael, Prentice, Andrew M., Meyer, Brian F., Pearson, Ewan R., Boreham, Colin A.G., Cooper, Cyrus, Gillman, Matthew W., Dedoussis, George V., Moreno, Luis A., Pedersen, Oluf, Saarinen, Maiju, Mohlke, Karen L., Boomsma, Dorret I., Saw, Seang-Mei, Lakka, Timo A., Körner, Antje, Loos, Ruth J.F., Ong, Ken K., Vollenweider, Peter, van Duijn, Cornelia M., Koppelman, Gerard H., Hattersley, Andrew T., Holloway, John W., Hocher, Berthold, Heinrich, Joachim, Power, Chris, Melbye, Mads, Guxens, Mònica, Pennell, Craig E., Bønnelykke, Klaus, Bisgaard, Hans, Eriksson, Johan G., Widén, Elisabeth, Hakonarson, Hakon, Uitterlinden, André G., Pouta, Anneli, Lawlor, Debbie A., Smith, George Davey, Frayling, Timothy M., McCarthy, Mark I., Grant, Struan F.A., Jaddoe, Vincent W.V., Jarvelin, Marjo-Riitta, Timpson, Nicholas J., Prokopenko, Inga and Freathy, Rachel M. (2013) New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Nature Genetics, 45, (1), 76-82. (doi:10.1038/ng.2477).

Itzykson, Raphaël, Kosmider, Olivier, Renneville, Aline, Gelsi-Boyer, Véronique, Meggendorfer, Manja, Morabito, Margot, Berthon, Céline, Adès, Lionel, Fenaux, Pierre, Beyne-Rauzy, Odile, Vey, Norbert, Braun, Thorsten, Haferlach, Torsten, Dreyfus, François, Cross, Nicholas C.P., Preudhomme, Claude, Bernard, Oliver A., Fontenay, Michaela, Vainchenker, William, Schnittger, Susanne, Birnbaum, Daniel, Droin, Nathalie and Solary, Eric (2013) Prognostic score including gene mutations in chronic myelomonocytic leukemia. Journal of Clinical Oncology (doi:10.1200/JCO.2012.47.3314). (PMID:23690417).

Jacobs, P. A., Maloney, V., Cooke, R., Crolla, J A, Ashworth, A. and Swerdlow, A. J. (2013) Male breast cancer, age and sex chromosome aneuploidy. British Journal of Cancer, 108, (4), 959-963. (doi:10.1038/bjc.2012.577). (PMID:23299533).

Johnson, Lauren, Shah, Imran, Loh, Andrew X., Vinall, Lynne E., Teixeira, Ana S., Rousseau, Karine, Holloway, John W., Hardy, Rebecca and Swallow, Dallas M. (2013) MUC5AC & inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort. Respirology (doi:10.1111/resp.12092). (PMID:23551418).

Jones, Emma, Sinclaire, Julia M.A., Holt, Richard I.G. and Barnard, Katharine (2013) Social networking and understanding alcohol-associated risk for people with type 1 diabetes: friend or foe? Diabetes Technology & Therapeutics, 15, (4) (doi:10.1089/dia.2012.0327).

Kaiser, M.F., Walker, B. A., Hockley, S. L., Begum, D. B., Wardell, C. P., Gonzalez, D., Ross, F. M., Davies, F. E. and Morgan, G. J. (2013) A TC classification based predictor for multiple myeloma using multiplexed real-time quantitative PCR. Leukemia (doi:10.1038/leu.2013.12). (In Press).

Karmaus, Wilfried, Ziyab, Ali H., Everson, Todd and Holloway, John W. (2013) Epigenetic mechanisms and models in the origins of asthma. Current Opinion in Allergy and Clinical Immunology, 13, (1), 63-69. (doi:10.1097/ACI.0b013e32835ad0e7). (PMID:23242116).

Khan, Ferdous, Smith, James O., Kanczler, Janos M., Tare, Rahul S., Oreffo, Richard O.C. and Bradley, Mark (2013) Discovery and evaluation of a functional ternary polymer blend for bone repair: translation from a microarry to a clinical model. Advanced Functional Materials, 1-13. (doi:10.1002/adfm.201202710).

Khandhadia, Samir, Hakobyan, Svetlana, Heng, Ling Z., Gibson, Jane, Adams, David H., Alexander, Graeme J., Gibson, Jonathan M., Martin, Keith R., Menon, Geeta, Nash, Kathryn, Sivaprasad, Sobha, Ennis, Sarah, Cree, Angela J., Morgan, B. Paul and Lotery, Andrew J. (2013) Age-related macular degeneration and modification of systemic complement factor H production through liver transplantation. Ophthalmology (doi:10.1016/j.ophtha.2013.01.004). (In Press).

Khoshnood, Babak, Loane, Maria, Garne, Ester, Addor, Marie-Claude, Arriola, Larraitz, Bakker, Marian, Barisic, Ingeborg, Bianca, Sebastiano, Boyd, Patricia, Calzolari, Elisa, Doray, Berenice, Draper, Elizabeth, Gatt, Miriam, Haeusler, Martin, Melve, Kari Klungsoyr, Latos-Bielenska, Anna, McDonnell, Bob, Mullaney, Carmel, Nelen, Vera, O'Mahony, Mary, Pierini, Anna, Queisser-Luft, Annette, Randrianaivo, Hanitra, Rankin, Judith, Rissmann, Anke, Salvador, Joaquin, Tucker, David, Verellen-Dumoulin, Christine, Wellesley, Diana, Zymak-Zakutnya, Natalya and Dolk, Helen (2013) Recent decrease in the prevalence of congenital heart defects in Europe. The Journal of Pediatrics, 162, (1), 108-113. (doi:10.1016/j.jpeds.2012.06.035). (PMID:22835879).

Kingham, Emma Jayne and Oreffo, Richard O.C. (2013) Embryonic and induced pluripotent stem cells: understanding, creating, and exploiting the nano-niche for regenerative medicine. ACS Nano (doi:10.1021/nn3037094). (PMID:23414366).

Kingham, Emma Jayne, White, Kate, Gadegaard, Nikolaj, Dalby, Matthew J. and Oreffo, Richard O.C. (2013) Nanotopographical cues augment mesenchymal differentiation of human embryonic stem cells. Small (doi:10.1002/smll.201202340). (PMID:23362187).

Krauss-Etschmann, S., Bush, A., Bellusci, S., Brusselle, G. G., Erik K Dahlen, S., Dehmel, S., Eickelberg, O., Gibson, G., Hylkema, M. N., Knaus, P., Konigshoff, M., Lloyd, C. M., Macciarini, P., Mailleux, A., Marsland, B. J., Postma, D. S., Roberts, G., Samakovlis, C., Stocks, J., Vandesompele, J., Wjst, M. and Holloway, J. (2013) Of flies, mice and men: a systematic approach to understanding the early life origins of chronic lung disease. Thorax, 68, (4), 380-384. (doi:10.1136/thoraxjnl-2012-201902).

L'Esperance, V., Cox, S.E., Simpson, D.M., Gill, C., Makani, J., Soka, D., Mgaya, J., Kirkham, Fenella J. and Clough, Geraldine F. (2013) Peripheral vascular response to inspiratory breath hold in paediatric homozygous sickle cell disease. Experimental Physiology, 98, (1 ), 49-56. (doi:10.1113/expphysiol.2011.064055). (In Press).

Lambert, K. and Holt, R.I.G. (2013) The use of insulin analogues in pregnancy. Diabetes, Obesity, and Metabolism (doi:10.1111/dom.12098). (PMID:23489521).

Lanham, S.A., Roberts, C., Habgood, A.K., Alexander, S, Burne, T.H.J., Eyles, D.W., Cooper , Cyrus, McGrath, J.J. and Oreffo, Richard O.C. (2013) Effect of Vitamin D deficiency during pregnancy on offspring bone structure, composition and quality in later life. Journal of Developmental Origins of Health and Disease, 4, (1), 49-55. (doi:10.1017/S2040174412000542).

Lench, Nicholas, Barrett, Angela, Fielding, Sarah, McKay, Fiona, Hill, Melissa, Jenkins, Lucy, White, Helen and Chitty, Lyn (2013) The clinical implementation of non-invasive prenatal diagnosis for single gene disorders: Challenges and progress made. Prenatal Diagnosis, 33, (6), 555-562. (doi:10.1002/pd.4124).

Lu, Yi, Vitart, Veronique, Burdon, Kathryn P., Khor, Chiea Chuen, Bykhovskaya, Yelena, Mirshahi, Alireza, Hewitt, Alex W., Koehn, Demelza, Hysi, Pirro G., Ramdas, Wishal D., Zeller, Tanja, Vithana, Eranga N., Cornes, Belinda K., Tay, Wan-Ting, Tai, E Shyong, Cheng, Ching-Yu, Liu, Jianjun, Foo, Jia-Nee, Saw, Seang Mei, Thorleifsson, Gudmar, Stefansson, Kari, Dimasi, David P., Mills, Richard A., Mountain, Jenny, Ang, Wei, Hoehn, René, Verhoeven, Virginie J.M., Grus, Franz, Wolfs, Roger, Castagne, Raphaële, Lackner, Karl J., Springelkamp, Henriët, Yang, Jian, Jonasson, Fridbert, Leung, Dexter Y.L., Chen, Li J, Tham, Clement C.Y., Rudan, Igor, Vatavuk, Zoran, Hayward, Caroline, Gibson, Jane, Cree, Angela J., MacLeod, Alex, Ennis, Sarah, Polasek, Ozren, Campbell, Harry, Wilson, James F., Viswanathan, Ananth C., Fleck, Brian, Li, Xiaohui, Siscovick, David, Taylor, Kent D, Rotter, Jerome I., Yazar, Seyhan, Ulmer, Megan, Li, Jun, Yaspan, Brian L., Ozel, Ayse B., Richards, Julia E., Moroi, Sayoko E., Haines, Jonathan L, Kang, Jae H., Pasquale, Louis R., Allingham, R. Rand, Ashley-Koch, Allison, Mitchell, Paul, Wang, Jie Jin, Wright, Alan F., Pennell, Craig, Spector, Timothy D., Young, Terri L., Klaver, Caroline C.W., Martin, Nicholas G., Montgomery, Grant W., Anderson, Michael G., Aung, Tin, Willoughby, Colin E., Wiggs, Janey L., Pang, Chi P., Thorsteinsdottir, Unnur, Lotery, Andrew J., Hammond, Christopher J., van Duijn, Cornelia M., Hauser, Michael A., Rabinowitz, Yaron S., Pfeiffer, Norbert, Mackey, David A., Craig, Jamie E., Macgregor, Stuart and Wong, Tien Y. (2013) Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nature Genetics, 45, (2), 155-163. (doi:10.1038/ng.2506). (PMID:23291589).

Mant, Alexandra, Williams, Sarah and O'Kelly, Ita (2013) Acid sensitive background potassium channels K2P3.1 and K2P9.1 undergo rapid dynamin-dependent endocytosis. Channels (In Press).

Mant, Alexandra, Williams, Sarah, Roncoroni, Laura, Lowry, Eleanor, Johnson, Daniel and O'Kelly, Ita (2013) N-glycosylation-dependent control of functional expression of background potassium channels K2P3.1 and K2P9.1. Journal of Biological Chemistry, 288, (5), 3251-3264. (doi:10.1074/jbc.M112.405167).

Mazomenos, E.B., Biswas, D., Acharyya, A., Chen, T., Maharatna, K., Rosengarten, J., Morgan, J. and Curzen, N. (2013) A low-complexity ECG feature extraction algorithm for mobile healthcare applications. IEEE Journal of Biomedical and Health Informatics, 17, (2), 459-469. (doi:10.1109/TITB.2012.2231312). (PMID:23362250).

McGrath, Sophie, Webb, Andrew and Walker-Bone, Karen (2013) Bleomycin-induced Raynaud's phenomenon after single-dose exposure: risk factors and treatment with intravenous iloprost infusion. Journal of Clinical Oncology, 31, (4), e51-e52. (doi:10.1200/JCO.2012.43.2872). (PMID:23270004).

Mehta, H.M., Glaubach, T., Long, A., Lu, H., Przychodzen, B., Makishima, H., McDevitt, M. A., Cross, N.C.P., Maciejewski, J. and Corey, S.J. (2013) Granulocyte colony stimulating factor mutant receptor T595I (T618I) confers ligand independence and enhanced signaling. Leukemia (doi:10.1038/leu.2013.164). (In Press).

Mercer, Catherine, Lachlan, Katherine, Karcanias, Alexandra, Affara, Nabeel, Huang, Shuwen, Jacobs, Patricia A. and Thomas, N. Simon (2013) Detailed clinical and molecular study of 20 females with Xq deletions with special reference to menstruation and fertility. European Journal of Medical Genetics, 56, (1), 1-6. (doi:10.1016/j.ejmg.2012.08.012).

Mommersteeg, P.M., Herr, R., Pouwer, F., Holt, R.I.G. and Loerbroks, A. (2013) The association between diabetes and an episode of depressive symptoms in the 2002 World Health Survey: an analysis of 231 797 individuals from 47 countries. Diabetic Medicine, 30, (6) (doi:10.1111/dme.12193). (PMID:23614792).

Moon, R. J., Harvey, N. C., Robinson, S. M., Ntani, G., Davies, J. H., Inskip, H. M., Godfrey, K. M., Dennison, E. M., Calder, P. C., Cooper, C. and SWS Study Group (2013) Maternal plasma polyunsaturated fatty acid status in late pregnancy is associated with offspring body composition in childhood. Journal of Clinical Endocrinology & Metabolism, 98, (1), 299-307. (doi:10.1210/jc.2012-2482). (PMID:23162098).

Murray, Anna, Schoemaker, Minouk J., Bennett, Claire E., Ennis, Sarah, Macpherson, James N., Jones, Michael, Morris, Danielle H., Orr, Nick, Ashworth, Alan, Jacobs, Patricia A. and Swerdlow, Anthony J. (2013) Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency. Genetics in Medicine (doi:10.1038/gim.2013.64). (In Press).

Neves, Nuno M., de Andrés, María C., Kingham, Emmajayne, Imagawa, Kei, Gonzalez, Antonio, Roach, Helmtrud I., Wilson, David I. and Oreffo, Richard O. C. (2013) Epigenetic regulation during fetal femur development: DNA methylation matters. PLoS ONE, 8, (1), e54957. (doi:10.1371/journal.pone.0054957).

Newell, Louise, Polak, Marta E., Perera, Jay, Owen, Charlotte, Boyd, Peter, Pickard, Christopher, Howarth, Peter, Healy, Eugene, Holloway, John W., Friedmann, Peter S. and Ardern-Jones, Michael R. (2013) Sensitization via healthy skin programmes: Th2 responses in individuals with atopic dermatitis. Journal of Investigative Dermatology, [29pp.]. (doi:10.1038/jid.2013.148). (PMID:23528819).

Newman, T.A., Bailey, J.L., Stocker, L., Macklon, N.S. and Cheong, Y. (2013) Expression of neuronal markers in the endometrium of women with and without endometriosis. Human Reproduction (In Press).

Nikkel, Sarah M, Dauber, Andrew, de Munnik, Sonja, Connolly, Meghan, Hood, Rebecca L, Caluseriu, Oana, Hurst, Jane, Kini, Usha, Nowaczyk, Malgorzata J, Afenjar, Alexandra, Albrecht, Beate, Allanson, Judith E, Balestri, Paolo, Ben-Omran, Tawfeg, Brancati, Francesco, Cordeiro, Isabel, da Cunha, Bruna Santos, Delaney, Louisa A, Destrée, Anne, Fitzpatrick, David, Forzano, Francesca, Ghali, Neeti, Gillies, Greta, Harwood, Katerina, Hendriks, Yvonne M, Héron, Delphine, Hoischen, Alexander, Honey, Engela Magdalena, Hoefsloot, Lies H, Ibrahim, Jennifer, Jacob, Claire M, Kant, Sarina G, Kim, Chong Ae, Kirk, Edwin P, Knoers, Nine V, Lacombe, Didier, Lee, Chung, Lo, Ivan F, Lucas, Luiza S, Mari, Francesca, Mericq, Veronica, Moilanen, Jukka S, Møller, Sanne Traasdahl, Moortgat, Stephanie, Pilz, Daniela T, Pope, Kate, Price, Susan, Renieri, Alessandra, Sá, Joaquim, Schoots, Jeroen, Silveira, Elizabeth L, Simon, Marleen E, Slavotinek, Anne, Temple, I Karen, van der Burgt, Ineke, de Vries, Bert B, Weisfeld-Adams, James D, Whiteford, Margo L, Wierczorek, Dagmar, Wit, Jan M, Yee, Connie Fung, Beaulieu, Chandree L, White, Sue M, Bulman, Dennis E, Bongers, Ernie, Brunner, Han, Feingold, Murray and Boycott, Kym M (2013) The phenotype of floating-harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP. Orphanet Journal of Rare Diseases, 8, (1), 63. (doi:10.1186/1750-1172-8-63).

Nwaru, Bright I., Panesar, Sukhmeet S., Hickstein, Lennart, Rader, Tamara, Werfel, Thomas, Muraro, Antonella, Hoffmann-Sommergruber, Karin, Roberts, Graham and Sheikh, Aziz (2013) The epidemiology of food allergy in Europe: protocol for a systematic review. Clinical and Translational Allergy, 3, 13. (doi:10.1186/2045-7022-3-13). (PMID:23547766).

O'Doherty, A.F., West, M., Jack, S. and Grocott, M.P.W. (2013) Preoperative aerobic exercise training in elective intra-cavity surgery: a systematic review. British Journal of Anaesthesia (doi:10.1093/bja/aes514 ). (PMID:23393151).

Ockhuijsen, H.D., Boivin, J., van den Hoogen, A. and Macklon, N.S. (2013) Coping after recurrent miscarriage: uncertainty and bracing for the worst. Journal of Family Planning & Reproductive Health Care (doi:10.1136/jfprhc-2012-100346). (PMID:23329740).

Oscier, David G., Rose-Zerilli, Matthew J.J., Winkelmann, Nils, Gonzalez de Castro, David, Gomez, Belen, Forster, Jade, Parker, Helen, Parker, Anton, Gardiner, Anne, Collins, Andrew, Else, Monica, Cross, Nicholas C.P., Catovsky, Daniel and Strefford, Jonathan C. (2013) The clinical significance of NOTCH1 and SF3B1 mutations in the UK LRF CLL4 trial. Blood, 121, (3), 468-475. (doi:10.1182/blood-2012-05-429282). (PMID:23086750).

Panesar, Sukhmeet S., Nwaru, Bright, Hickstein, Lennart, Rader, Tamara, Hamadah, Hala, Ali, Dana Fawziah-Ibrahim, Patel, Bhavesh, Muraro, Antonella, Roberts, Graham, Worm, Margitta, Sheikh, Aziz and Wierzoch, Anna (2013) The epidemiology of anaphylaxis in Europe: protocol for a systematic review. Clinical and Translational Allergy, 3, (1), [9pp.]. (doi:10.1186/2045-7022-3-9). (PMID:23537345).

Perez, C., Pascual, M., Martin-Subero, J. I., Bellosillo, B., Segura, V., Delabesse, E., Alvarez, S., Larrayoz, M. J., Rifon, J., Cigudosa, J. C., Besses, C., Calasanz, M. J., Cross, N. C. P., Prosper, F. and Agirre, X. (2013) Aberrant DNA methylation profile of chronic and transformed classicphiladelphia-negative myeloproliferative neoplasms. Haematologica (doi:10.3324/haematol.2013.084160). (In Press).

Piazza, Rocco, Valletta, Simona, Winkelmann, Nils, Redaelli, Sara, Spinelli, Roberta, Pirola, Alessandra, Antolini, Laura, Mologni, Luca, Donadoni, Carla, Papaemmanuil, Elli, Schnittger, Susanne, Kim, Dong-Wook, Boultwood, Jacqueline, Rossi, Fabio, Gaipa, Giuseppe, De Martini, Greta P., di Celle, Paola Francia, Jang, Hyun Gyung, Fantin, Valeria, Bignell, Graham R., Magistroni, Vera, Haferlach, Torsten, Pogliani, Enrico Maria, Campbell, Peter J., Chase, Andrew J, Tapper, William J., Cross, Nicholas C. P. and Gambacorti-Passerini, Carlo (2013) Recurrent SETBP1 mutations in atypical chronic myeloid leukemia. Nature Genetics, 45, (1), 18-24. (doi:10.1038/ng.2495). (PMID:23222956).

Rafiq, Sajjad, Tapper, William, Collins, Andrew, Khan, Sofia, Politopoulos, Ionnis, Gerty, Sue, Blomqvist, Carl, Couch, Fergus J., Nevanlinna, Heli, Liu, Jianjun and Eccles, Diana (2013) Identification of inherited genetic variations influencing prognosis in early-onset breast cancer. Cancer Research, 73, (6), 1883-1891. (doi:10.1158/0008-5472.CAN-12-3377). (PMID:23319801).

Rawstron, Andy C., Child, J. Anthony, de Tute, Ruth, Davies, Faith E., Gregory, Walter M., Bell, Sue E., Szubert, Alexander J., Navarro-Coy, Nuria, Drayson, Mark T., Feyler, Sylvia, Ross, Fiona M., Cook, Gordon, Jackson, Graham H., Morgan, Gareth J. and Owen, Roger G. (2013) Minimal residual disease assessed by multiparameter flow cytometry in multiple myeloma: impact on outcome in the medical research council myeloma IX study. Journal of Clinical Oncology (doi:10.1200/JCO.2012.46.2119). (PMID:23733781).

Ross, D.M., O'Hely, M., Bartley, P.A., Dang, P., Score, J., Goyne, J.M., Sobrinho-Simoes, M., Cross, N.C.P., Melo, J.V., Speed, T.P., Hughes, T.P. and Morley, A.A. (2013) Letter to the editor. Distribution of genomic breakpoints in chronic myeloid leukemia: analysis of 308 patients. Leukemia (doi:10.1038/leu.2013.116). (In Press).

Schmidts, M., Arts, H.H., Bongers, E.M.H.F., Yap, Z., Oud, M.M., Antony, D., Duijkers, L., Emes, R.D., Stalker, J., Yntema, J.-B.L., Plagnol, V., Hoischen, A., Gilissen, C., Forsythe, E., Lausch, E., Veltman, J.A., Roeleveld, N., Superti-Furga, A., Kutkowska-Kazmierczak, A., Kamsteeg, E.-J., Elcioglu, N., van Maarle, M.C., Graul-Neumann, L.M., Devriendt, K., Smithson, S.F., Wellesley, D., Verbeek, N.E., Hennekam, R.C.M., Kayserili, H., Scambler, P.J., Beales, P.L., Knoers, N.V., Roepman, R. and Mitchison, H.M. (2013) Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement. Journal of Medical Genetics, 50, (5), 309-323. (doi:10.1136/jmedgenet-2012-101284).

Schwenke, M., Knofler, M., Velicky, P., Weimar, C.H., Kruse, M., Samalecos, A., Wolf, A., Macklon, N.S., Bamberger, A.M. and Gellersen, B. (2013) Control of human endometrial stromal cell motility by PDGF-BB, HB-EGF and trophoblast-secreted factors. PLoS ONE, 8, (1), e54336-[14pp]. (doi:10.1371/journal.pone.0054336). (PMID:23349855).

Scorletti , E. and Byrne, Christopher D. (2013) Omega-3 fatty acids, hepatic lipid metabolism and non-alcoholic fatty liver disease. Annual Review of Nutrition (In Press).

Shreeve, N., Cagampang, F., Sadek, K., Tolhurst, M., Houldey, A., Hill, C. M., Brook, N., Macklon , N. and Cheong, Y. (2013) Poor sleep in PCOS; is melatonin the culprit? Human Reproduction, 28, (5), 1348-1353. (doi:10.1093/humrep/det013 ). (PMID:23438443).

Sirker, A., Sohal, M., Oldroyd, K., Curzen, N., Stables, R., De Belder, A. and Hildick-Smith, D. (2013) The impact of coronary bifurcation stenting strategy on health-related functional status: a quality-of-life analysis from the BBC One (British Bifurcation Coronary; Old, New, and Evolving Strategies) study. JACC Cardiovascular Interventions, 6, 139-145. (doi:10.1016/j.jcin.2012.10.010).

Smyth, M., Andreoletti, G., Willis, C., Gibson, J., Holloway, J., Batra, A., Afzal, N., Beattie, R.M. and Ennis, S. (2013) Concurrent autoimmune disease in paediatric IBD: incidence, exomes and focus on asthma. Journal of Allergy and Clinical Immunology (Submitted).

Soto-Ramírez, Nelís, Arshad, Syed Hasan, Holloway, John W, Zhang, Hongmei, Schauberger, Eric, Ewart, Susan, Patil, Veeresh and Karmaus, Wilfried (2013) The interaction of genetic variants and DNA methylation of the interleukin-4 receptor gene increase the risk of asthma at age 18 years. Clinical Epigenetics, 5, (1), 1. (doi:10.1186/1868-7083-5-1). (PMID:23286427).

Spalluto, Cosma, Wilson, David I. and Hearn, Tom (2013) Evidence for centriolar satellite localization of CDK1 and cyclin B2. Cell Cycle, 12, (11) (PMID:23656781).

Stephenson, James A., Al-Taan, Omer, Arshad, Ali, West, Annette L., Calder, Philip C., Morgan, Bruno, Metcalfe, Matthew S. and Dennison, Ashely R. (2013) Unsaturated fatty acids differ between hepatic colorectal metastases and liver tissue without tumour in humans: results from a randomised controlled trial of intravenous eicosapentaenoic and docosahexaenoic acids. Prostaglandins Leukotrienes and Essential Fatty Acids, 88, (6), 405-410. (doi:10.1016/j.plefa.2013.04.002). (PMID:23647811).

Tanser, Frank, Barnighausen, Till, Grapsa, Erofili, Zaidi, Jaffer and Newell, Marie-Louise (2013) High coverage of ART associated with decline in risk of HIV acquisition in rural KwaZulu-Natal, South Africa. Science, 339, (6122), 966-971. (doi:10.1126/science.1228160). (PMID:23430656).

Targher, G., Valbusa , F., Bonapace, S., Bertolini, L., Zenari, L., Rodella, S., Zoppini, G., Mantovani, W., Barbieri, E. and Byrne, Christopher D. (2013) Non-alcoholic fatty liver disease is associated with an increased incidence of atrial fibrillation in patients with type 2 diabetes. PLoS ONE (In Press).

Targher , G. and Byrne, Christopher D. (2013) Diagnosis and management of non-alcoholic fatty liver disease and its hemostatic/thrombotic and vascular complications. Seminars in Thrombosis and Hemostasis (PMID:23397556). (In Press).

Targher , G. and Byrne, Christopher D. (2013) Nonalcoholic fatty liver disease: a novel cardiometabolic risk factor for type 2 diabetes and its complications. Journal of Clinical Endocrinology & Metabolism, 98, (2), 483-495. (doi:10.1210/jc.2012-3093 ). (PMID:23293330).

Tayton, Edward R, Smith, James O., Evans, Nicholas R, Dickinson, Alexander, Aarvold, Alexander, Kalra, Spandan, Purcell, Matthew, Howdle, Steven, Dunlop, D.G. and Oreffo, Richard O.C. (2013) Effects of Setting Bone Cement on Tissue-Engineered Bone Graft: a Potential Barrier to Clinical Translation? The Journal of Bone and Joint Surgery, 95, (8), 192-197. (doi:10.2106/JBJS.L.00164).

Travers, M. E., Mackay, D. J. G., Nitert, M. D., Morris, A. P., Lindgren, C. M., Berry, A., Johnson, P. R., Hanley, N., Groop, L. C., McCarthy, M. I. and Gloyn, A. L. (2013) Insights into the molecular mechanism for Type 2 diabetes susceptibility at the KCNQ1 locus From temporal changes in imprinting status in human islets. Diabetes, 62, (3), 987-992. (doi:10.2337/db12-0819).

Tsimbouri, P.M., Murawski, Kate, Hamilton, Graham, Herzyk, Pawel, Oreffo, Richard O.C., Gadegaard, Nikolaj and Dalby, Matthew J. (2013) A genomics approach in determining nanotopographical effects on MSC phenotype. Biomaterials, 34, (9), 2177-2184. (doi:10.1016/j.biomaterials.2012.12.019). (PMID:23312853).

Turnock, Amy, Calder, Philip C., West, Annette L., Izzard, Mark, Morton, Randall P. and Plank, Lindsay D. (2013) Perioperative immunonutrition in well-nourished patients undergoing surgery for head and neck cancer: evaluation of inflammatory and immunologic outcomes. Nutrients, 5, (4), 1186-1199. (doi:10.3390/nu5041186). (PMID:23571650).

Umranikar, Aarti, Saran, Mili, Brook, Nick, Singh, Neeta, Fowler, Darren and Cheong, Ying (2013) Role of anti-Müllerian hormone in diagnosing granulosa cell tumour: a case report. Clinical Ovarian and Other Gynecologic Cancer (doi:10.1016/j.cogc.2012.12.001). (In Press).

Urwin, Heidi, Zhang, Jian, Gao, Yixong, Wang, Chunrong, Li, Lixiang, Song, Pengkun, Man , Qingqing, Meng, Lipeng, Frøyland, Livar, Miles, Elizabeth A., Calder, Philip C. and Yaqoob, Parveen (2013) Immune factors and fatty acid composition in human milk from river/lake, coastal and inland regions of China. British Journal Of Nutrition, 109, (11), 1949-1961. (doi:10.1017/S0007114512004084). (PMID:23148871).

Veerbeek, Jan H.W., Smit, Janine G., Koster, Maria P.H., Post Uiterweer, Emiel D., van Rijn, Bas B., Koenen, Steven V. and Franx, Arie (2013) Maternal cardiovascular risk profile after placental abruption. Hypertension (doi:10.1161/hypertensionaha.111.00930). (PMID:23529170). (In Press).

Velloso, C.P., Aperghis, M., Godfrey, R., Blazevich, A J., Bartlett, C., Cowan, D., Holt, R.I.G., Bouloux, P., Harridgre, S.D.R. and Goldspink, G. (2013) The effects of two weeks of recombinant growth hormone administration on the response of IGF-I and N-terminal pro-peptide of collagen type III (P-III-NP) during a single bout of high resistance exercise in resistance trained young men. Growth Hormone and IGF Research, 23, (3), 76-80. (doi:10.1016/j.ghir.2013.01.002). (PMID:23433656).

Vorechovsky, I., Jones, A.V. and Cross, N.C.P. (2013) Why do we see JAK2 exon 12 mutations in myeloproliferative neoplasms? Leukemia (doi:10.1038/leu.2013.85). (PMID:23511126).

Walker, C.G., Jebb, S.A. and Calder, Philip C. (2013) Stearidonic acid as a supplemental source of ω-3 polyunsaturated fatty acids to enhance status for improved human health. Nutrition, 29, (2), 363-369. (doi:10.1016/j.nut.2012.06.003). (PMID:23102888).

Wang, J., Xu, Z., Liu, L., Gale, R. P., Cross, N. C. P., Jones, A. V., Qin, T., Ai, X., Xu, J., Zhang, T., Sun, X., Li, Q., Zhang, P., Zhang, Ye and Xiao, Z. (2013) JAK2V617F allele burden, JAK2 46/1 haplotype and clinical features of Chinese with myeloproliferative neoplasms. Leukemia (doi:10.1038/leu.2013.21). (In Press).

Ware, James S., John, Shibu, Roberts, Angharad M., Buchan, Rachel, Gong, Sungsam, Peters, Nicholas S., Robinson, David O., Lucassen, Anneke, Behr, Elijah R. and Cook, Stuart A. (2013) Next generation diagnostics in inherited arrhythmia syndromes. Journal of Cardiovascular Translational Research, 6, (1), 94-103. (doi:10.1007/s12265-012-9401-8). (PMID:22956155).

Weinhold, Niels, Johnson, David C., Chubb, Daniel, Chen, Bowang, Försti, Asta, Hosking, Fay J., Broderick, Peter, Ma, Yussanne P., Dobbins, Sara E., Hose, Dirk, Walker, Brian A., Davies, Faith E., Kaiser, Martin F., Li, Ni L., Gregory, Walter A., Jackson, Graham H., Witzens-Harig, Mathias, Neben, Kai, Hoffmann, Per, Nöthen, Markus M., Mühleisen, Thomas W., Eisele, Lewin, Ross, Fiona M, Jauch, Anna, Goldschmidt, Hartmut, Houlston, Richard S., Morgan, Gareth J. and Hemminki, Kari (2013) The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Nature Genetics, 45, (5), 522-525. (doi:10.1038/ng.2583). (PMID:23502783).

Weston-Bell, N., Gibson, J., John, M., Ennis, S., Pfeifer, S., Cezard, T., Ludwig, H., Collins, Andrew, Zojer, N. and Sahota, S. S. (2013) Exome sequencing in tracking clonal evolution in multiple myeloma following therapy. Leukemia, 27, (5), 1188-1191. (doi:10.1038/leu.2012.287). (PMID:23147253).

White, H. E., Hedges, J., Bendit, I., Branford, S., Colomer, D., Hochhaus, A., Hughes, T., Kamel-Reid, S., Kim, D.-W., Modur, V., Muller, M C., Pagnano, K.B., Pane, F., Radich, J., Cross, N.C.P. and Labourier, E. (2013) Establishment and validation of analytical reference panels for the standardization of quantitative BCR-ABL1 measurements on the international scale. Clinical Chemistry, 59, (6), 938-948. (doi:10.1373/clinchem.2012.196477).

White, M., Conroy, J., Bullman, H., Lever, M., Daly, E., Betts, D. R., Cody, D., Crolla, John A. and Lynch, S. A. (2013) Duplication of 17q11.2 and features of albright hereditary osteodystrophy secondary to methylation defects within the GNAS cluster: coincidence or causal? Case Reports in Genetics , 2013, 1-3. (doi:10.1155/2013/764152). (In Press).

Xu, J., Cao, J., Iguchi, N., Riethmacher, D. and Huang, L. (2013) Functional characterization of bitter-taste receptors expressed in mammalian testis. Molecular Human Reproduction, 19, (1), 17-28. (doi:10.1093/molehr/gas040). (PMID:22983952).

Yousefi, Mitra, Karmaus, Wilfried, Zhang, Hongmei, Roberts, Graham, Matthews, Sharon, Clayton, Bernie and Arshad, Syed Hasan (2013) Relationships between age of puberty onset and height at age 18 years in girls and boys. World Journal of Pediatrics, [9pp.]. (doi:10.1007/s12519-013-0399-z). (PMID:23335183).

Zaba, B., Calvert, C., Marston, M., Isingo, R., Nakiyingi-Miiro, J., Lutalo, T., Crampin, A., Robertson, L., Herbst, K., Newell, M.L., Todd, J., Byass, P., Boerma, T. and Ronsmans, C. (2013) Effect of HIV infection on pregnancy-related mortality in sub-Saharan Africa: secondary analyses of pooled communitybased data from the network for Analysing Longitudinal Population-based HIV/AIDS data on Africa (ALPHA). The Lancet, 381, (9879), 1763-1771. (doi:10.1016/S0140-6736(13)60803-X). (PMID:23683643).

Ziyab, A.H., Karmaus, W., Holloway, J.W., Zhang, H, Ewart, S. and Arshad, S.H. (2013) DNA methylation of the filaggrin gene adds to the risk of eczema associated with loss-of-function variants. Journal of the European Academy of Dermatology and Venereology, 27, (3), e420-e423. (doi:10.1111/jdv.12000). (PMID:23003573).

de Silva, Debra, Panesar, Sukhmeet S., Thusu, Sundeep, Rader, Tamara, Werfel, Thomas, Muraro, Antonella, Hoffmann-Sommergruber, Karin, Roberts, Graham and Sheikh, Aziz (2013) The acute and long-term management of food allergy: protocol for a rapid systematic review. Clinical and Translational Allergy, 3, (1), [12pp.]. (doi:10.1186/2045-7022-3-12). (PMID:23547741).

van Rijn, Bas B., Nijdam, Marie-Elise, Bruinse, Hein W., Roest, Mark, Uiterwaal, Cuno S., Grobbee, Diederick E., Bots, Michiel L. and Franx, Arie (2013) Cardiovascular disease risk factors in women with a history of early-onset preeclampsia. Obstetrics & Gynecology , 121, (5), 1040-1048. (doi:10.1097/AOG.0b013e31828ea3b5).