Continuous Subcutaneous Insulin Infusion in Children: A Pilot Study Validating a Protocol to Avoid Hypoglycemia at Initiation

por Manousaki, Despoina, Deladoëy, Johnny, Geoffroy, Louis, Olivier, Patricia
Publicado en Front Endocrinol (Lausanne) (2017)

A 15-year-old adolescent with a rare pituitary lesion

por Manousaki, Despoina, Deal, Cheri, De Bruycker, Jean Jacques, Ovetchkine, Philippe, Mercier, Claude, Alos, Nathalie
Publicado 2014

Genetically decreased vitamin D and risk of Alzheimer disease

por Mokry, Lauren E., Ross, Stephanie, Morris, John A., Manousaki, Despoina, Forgetta, Vincenzo, Richards, J. Brent
Publicado en Neurology (2016)

Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization study

por Manousaki, Despoina, Harroud, Adil, Mitchell, Ruth E., Ross, Stephanie, Forgetta, Vince, Timpson, Nicholas J., Smith, George Davey, Polychronakos, Constantin, Richards, J Brent
Publicado en PLoS Med (2021)

Correction: Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization study

por Manousaki, Despoina, Harroud, Adil, Mitchell, Ruth E., Ross, Stephanie, Forgetta, Vince, Timpson, Nicholas J., Smith, George Davey, Polychronakos, Constantin, Richards, J Brent
Publicado en PLoS Med (2021)

A Polygenic Risk Score to Predict Future Adult Short Stature Among Children

por Lu, Tianyuan, Forgetta, Vincenzo, Wu, Haoyu, Perry, John R B, Ong, Ken K, Greenwood, Celia M T, Timpson, Nicholas J, Manousaki, Despoina, Richards, J Brent
Publicado en J Clin Endocrinol Metab (2021)

Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent Loci

por Manousaki, Despoina, Mitchell, Ruth, Dudding, Tom, Haworth, Simon, Harroud, Adil, Forgetta, Vincenzo, Shah, Rupal L., Luan, Jian’an, Langenberg, Claudia, Timpson, Nicholas J., Richards, J. Brent
Publicado en Am J Hum Genet (2020)

Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study

por Manousaki, Despoina, Paternoster, Lavinia, Standl, Marie, Moffatt, Miriam F., Farrall, Martin, Bouzigon, Emmanuelle, Strachan, David P., Demenais, Florence, Lathrop, Mark, Cookson, William O. C. M., Richards, J. Brent
Publicado en PLoS Med (2017)

Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes

por Forgetta, Vincenzo, Manousaki, Despoina, Istomine, Roman, Ross, Stephanie, Tessier, Marie-Catherine, Marchand, Luc, Li, Min, Qu, Hui-Qi, Bradfield, Jonathan P., Grant, Struan F.A., Hakonarson, Hakon, Paterson, Andrew D., Piccirillo, Ciriaco, Polychronakos, Constantin, Richards, J. Brent
Publicado en Diabetes (2020)

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

por Manousaki, Despoina, Dudding, Tom, Haworth, Simon, Hsu, Yi-Hsiang, Liu, Ching-Ti, Medina-Gómez, Carolina, Voortman, Trudy, van der Velde, Nathalie, Melhus, Håkan, Robinson-Cohen, Cassianne, Cousminer, Diana L., Nethander, Maria, Vandenput, Liesbeth, Noordam, Raymond, Forgetta, Vincenzo, Greenwood, Celia M.T., Biggs, Mary L., Psaty, Bruce M., Rotter, Jerome I., Zemel, Babette S., Mitchell, Jonathan A., Taylor, Bruce, Lorentzon, Mattias, Karlsson, Magnus, Jaddoe, Vincent V.W., Tiemeier, Henning, Campos-Obando, Natalia, Franco, Oscar H., Utterlinden, Andre G., Broer, Linda, van Schoor, Natasja M., Ham, Annelies C., Ikram, M. Arfan, Karasik, David, de Mutsert, Renée, Rosendaal, Frits R., den Heijer, Martin, Wang, Thomas J., Lind, Lars, Orwoll, Eric S., Mook-Kanamori, Dennis O., Michaëlsson, Karl, Kestenbaum, Bryan, Ohlsson, Claes, Mellström, Dan, de Groot, Lisette C.P.G.M., Grant, Struan F.A., Kiel, Douglas P., Zillikens, M. Carola, Rivadeneira, Fernando, Sawcer, Stephen, Timpson, Nicholas J., Richards, J. Brent
Publicado en Am J Hum Genet (2017)

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

por Manousaki, Despoina, Dudding, Tom, Haworth, Simon, Hsu, Yi-Hsiang, Liu, Ching-Ti, Medina-Gómez, Carolina, Voortman, Trudy, van der Velde, Nathalie, Melhus, Håkan, Robinson-Cohen, Cassianne, Cousminer, Diana L., Nethander, Maria, Vandenput, Liesbeth, Noordam, Raymond, Forgetta, Vincenzo, Greenwood, Celia M.T., Biggs, Mary L., Psaty, Bruce M., Rotter, Jerome I., Zemel, Babette S., Mitchell, Jonathan A., Taylor, Bruce, Lorentzon, Mattias, Karlsson, Magnus, Jaddoe, Vincent V.W., Tiemeier, Henning, Campos-Obando, Natalia, Franco, Oscar H., Utterlinden, Andre G., Broer, Linda, van Schoor, Natasja M., Ham, Annelies C., Ikram, M. Arfan, Karasik, David, de Mutsert, Renée, Rosendaal, Frits R., den Heijer, Martin, Wang, Thomas J., Lind, Lars, Orwoll, Eric S., Mook-Kanamori, Dennis O., Michaëlsson, Karl, Kestenbaum, Bryan, Ohlsson, Claes, Mellström, Dan, de Groot, Lisette C.P.G.M., Grant, Struan F.A., Kiel, Douglas P., Zillikens, M. Carola, Rivadeneira, Fernando, Sawcer, Stephen, Timpson, Nicholas J., Richards, J. Brent
Publicado en Am J Hum Genet (2018)