Assessing the population impact of low rates of vitamin D supplementation on type 1 diabetes using a new statistical method

Por Zipitis, Christos S, Mughal, Zulf M, Clayton, Peter E
Publicado no JRSM Open (2016)

Identifying biological pathways that underlie primordial short stature using network analysis

Por Hanson, Dan, Stevens, Adam, Murray, Philip G, Black, Graeme C M, Clayton, Peter E
Publicado em 2014

Maternal malaria status and metabolic profiles in pregnancy and in cord blood: relationships with birth size in Nigerian infants

Por Ayoola, Omolola O, Whatmore, Andrew, Balogun, Williams O, Jarrett, Olatokunbo O, Cruickshank, John K, Clayton, Peter E
Publicado em 2012

Can network biology unravel the aetiology of congenital hyperinsulinism?

Por Stevens, Adam, Cosgrove, Karen E, Padidela, Raja, Skae, Mars S, Clayton, Peter E, Banerjee, Indraneel, Dunne, Mark J
Publicado em 2013

Metabolites involved in Glycolysis and Amino Acid Metabolism are Altered in Short Children Born Small for Gestational Age

Por Murray, Philip G, Butcher, Imogen, Dunn, Warwick B, Stevens, Adam, Perchard, Reena, Hanson, Daniel, Whatmore, Andrew, Westwood, Melissa, Clayton, Peter E
Publicado no Pediatr Res (2016)

Adiponectin and Lipid Profiles Compared with Insulins in Relation to Early Growth of British South Asian and European Children: The Manchester Children's Growth and Vascular Health...

Por Bansal, Narinder, Anderson, Simon G., Vyas, Avni, Gemmell, Isla, Charlton-Menys, Valentine, Oldroyd, John, Pemberton, Philip, Durrington, Paul N., Clayton, Peter E., Cruickshank, J. Kennedy
Publicado em 2011

X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions

Por Burkitt Wright, Emma M.M., Perveen, Rahat, Clayton, Peter E., Hall, Catherine M., Costa, Teresa, Procter, Annie M., Giblin, Carol A., Donnai, Dian, Black, Graeme C.
Publicado em 2009

The effect of different patterns of growth hormone administration on the IGF axis and somatic and skeletal growth of the dwarf rat

Por Westwood, Melissa, Maqsood, Arfa R., Solomon, Mattea, Whatmore, Andrew J., Davis, Julian R. E., Baxter, Robert C., Gevers, Evelien F., Robinson, Iain C. A. F., Clayton, Peter E.
Publicado em 2009

Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism

Por Banerjee, Indraneel, Forsythe, Lynette, Skae, Mars, Avatapalle, Hima Bindu, Rigby, Lindsey, Bowden, Louise E., Craigie, Ross, Padidela, Raja, Ehtisham, Sarah, Patel, Leena, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado no Front Endocrinol (Lausanne) (2016)

Reduced Glycemic Variability in Diazoxide-Responsive Children with Congenital Hyperinsulinism Using Supplemental Omega-3-Polyunsaturated Fatty Acids; A Pilot Trial with MaxEPA(R)

Por Skae, Mars, Avatapalle, Hima Bindu, Banerjee, Indraneel, Rigby, Lindsey, Vail, Andy, Foster, Peter, Charalambous, Christiana, Bowden, Louise, Padidela, Raja, Patel, Leena, Ehtisham, Sarah, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado em 2014

Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism

Por Avatapalle, Hima Bindu, Banerjee, Indraneel, Shah, Sajni, Pryce, Megan, Nicholson, Jacqueline, Rigby, Lindsey, Caine, Louise, Didi, Mohammed, Skae, Mars, Ehtisham, Sarah, Patel, Leena, Padidela, Raja, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado em 2013

The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1

Por Hanson, Dan, Murray, Philip G., Sud, Amit, Temtamy, Samia A., Aglan, Mona, Superti-Furga, Andrea, Holder, Sue E., Urquhart, Jill, Hilton, Emma, Manson, Forbes D.C., Scambler, Peter, Black, Graeme C.M., Clayton, Peter E.
Publicado em 2009

Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth

Por Hanson, Dan, Murray, Philip G., O'Sullivan, James, Urquhart, Jill, Daly, Sarah, Bhaskar, Sanjeev S., Biesecker, Leslie G., Skae, Mars, Smith, Claire, Cole, Trevor, Kirk, Jeremy, Chandler, Kate, Kingston, Helen, Donnai, Dian, Clayton, Peter E., Black, Graeme C.M.
Publicado em 2011

CR-24 A 5-YEAR UPDATE REPORT OF A NATIONAL, VIRTUAL, INTERDISCIPLINARY ENDEAVOUR TO IMPROVE OUTCOMES FOR CHILDREN WITH HYPOTHALAMIC PITUITARY AXIS TUMOURS (HPATS) USING MULTI-SITE...

Por Pang, Gloria Shir Wey, Michaelidou, Maria, Morillon, Paul, Chang, Yen-Ching, Blair, Joanne C., Pettorini, Benedetta, Mallucci, Conor, Pizer, Barry, Kamaly, Ian, Clayton, Peter E., Banerjee, Indraneel, Hargrave, Darren, Michalski, Antony, Dorward, Neil, Aquilina, Kristian, Ederies, Ash, Spoudeas, Helen
Publicado no Neuro Oncol (2016)

Association Studies of Common Variants in 10 Hypogonadotropic Hypogonadism Genes with Age at Menarche

Por Gajdos, Zofia K. Z., Butler, Johannah L., Henderson, Katherine DeLellis, He, Chunyan, Supelak, Pamela J., Egyud, Matthew, Price, Alkes, Reich, David, Clayton, Peter E., Le Marchand, Loic, Hunter, David J., Henderson, Brian E., Palmert, Mark R., Hirschhorn, Joel N.
Publicado em 2008

Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

Por Flanagan, Sarah E., Xie, Weijia, Caswell, Richard, Damhuis, Annet, Vianey-Saban, Christine, Akcay, Teoman, Darendeliler, Feyza, Bas, Firdevs, Guven, Ayla, Siklar, Zeynep, Ocal, Gonul, Berberoglu, Merih, Murphy, Nuala, O’Sullivan, Maureen, Green, Andrew, Clayton, Peter E., Banerjee, Indraneel, Clayton, Peter T., Hussain, Khalid, Weedon, Michael N., Ellard, Sian
Publicado em 2013

Rare variants in single-minded 1 (SIM1) are associated with severe obesity

Por Ramachandrappa, Shwetha, Raimondo, Anne, Cali, Anna M.G., Keogh, Julia M., Henning, Elana, Saeed, Sadia, Thompson, Amanda, Garg, Sumedha, Bochukova, Elena G., Brage, Soren, Trowse, Victoria, Wheeler, Eleanor, Sullivan, Adrienne E., Dattani, Mehul, Clayton, Peter E., Datta, Vippan, Bruning, John B., Wareham, Nick J., O’Rahilly, Stephen, Peet, Daniel J., Barroso, Ines, Whitelaw, Murray L., Farooqi, I. Sadaf
Publicado em 2013

Rare variants in single-minded 1 (SIM1) are associated with severe obesity

Por Ramachandrappa, Shwetha, Raimondo, Anne, Cali, Anna M.G., Keogh, Julia M., Henning, Elana, Saeed, Sadia, Thompson, Amanda, Garg, Sumedha, Bochukova, Elena G., Brage, Soren, Trowse, Victoria, Wheeler, Eleanor, Sullivan, Adrienne E., Dattani, Mehul, Clayton, Peter E., Datta, Vipan, Bruning, John B., Wareham, Nick J., O’Rahilly, Stephen, Peet, Daniel J., Barroso, Ines, Whitelaw, Murray L., Farooqi, I. Sadaf
Publicado em 2013

A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype

Por Alston, Charlotte L, Howard, Caoimhe, Oláhová, Monika, Hardy, Steven A, He, Langping, Murray, Philip G, O'Sullivan, Siobhan, Doherty, Gary, Shield, Julian P H, Hargreaves, Iain P, Monavari, Ardeshir A, Knerr, Ina, McCarthy, Peter, Morris, Andrew A M, Thorburn, David R, Prokisch, Holger, Clayton, Peter E, McFarland, Robert, Hughes, Joanne, Crushell, Ellen, Taylor, Robert W
Publicado no J Med Genet (2016)

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability

Por Kasher, Paul R., Schertz, Katherine E., Thomas, Megan, Jackson, Adam, Annunziata, Silvia, Ballesta-Martinez, María J., Campeau, Philippe M., Clayton, Peter E., Eaton, Jennifer L., Granata, Tiziana, Guillén-Navarro, Encarna, Hernando, Cristina, Laverriere, Caroline E., Liedén, Agne, Villa-Marcos, Olaya, McEntagart, Meriel, Nordgren, Ann, Pantaleoni, Chiara, Pebrel-Richard, Céline, Sarret, Catherine, Sciacca, Francesca L., Wright, Ronnie, Kerr, Bronwyn, Glasgow, Eric, Banka, Siddharth
Publicado no Am J Hum Genet (2016)