Pregnancy and neonatal outcomes of COVID-19: The PAN-COVID study

por Mullins, E., Perry, A., Banerjee, J., Townson, J., Grozeva, D., Milton, R., Kirby, N., Playle, R., Bourne, T., Lees, C.
Publicado 2022

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

por Green, E K, Grozeva, D, Jones, I, Jones, L, Kirov, G, Caesar, S, Gordon-Smith, K, Fraser, C, Forty, L, Russell, E, Hamshere, M L, Moskvina, V, Nikolov, I, Farmer, A, McGuffin, P, Holmans, P A, Owen, M J, O'Donovan, M C, Craddock, N
Publicado 2010

Copy number variation in bipolar disorder

por Green, E K, Rees, E, Walters, J T R, Smith, K-G, Forty, L, Grozeva, D, Moran, J L, Sklar, P, Ripke, S, Chambert, K D, Genovese, G, McCarroll, S A, Jones, I, Jones, L, Owen, M J, O'Donovan, M C, Craddock, N, Kirov, G
Publicado 2016

Polygenic dissection of the bipolar phenotype

por Hamshere, M. L., O’Donovan, M. C., Jones, I. R., Jones, L., Kirov, G., Green, E. K., Moskvina, V., Grozeva, D., Bass, N., McQuillin, A., Gurling, H., St Clair, D., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Sklar, P., Purcell, S., Holmans, P. A., Owen, M. J., Craddock, N.
Publicado 2011

Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept

por Hamshere, M. L., Green, E. K., Jones, I. R., Jones, L., Moskvina, V., Kirov, G., Grozeva, D., Nikolov, I., Vukcevic, D., Caesar, S., Gordon-Smith, K., Fraser, C., Russell, E., Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Holmans, P. A., Owen, M. J., O’Donovan, M. C., Craddock, N.
Publicado 2009

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

por Kirov, G, Pocklington, A J, Holmans, P, Ivanov, D, Ikeda, M, Ruderfer, D, Moran, J, Chambert, K, Toncheva, D, Georgieva, L, Grozeva, D, Fjodorova, M, Wollerton, R, Rees, E, Nikolov, I, van de Lagemaat, L N, Bayés, À, Fernandez, E, Olason, P I, Böttcher, Y, Komiyama, N H, Collins, M O, Choudhary, J, Stefansson, K, Stefansson, H, Grant, S G N, Purcell, S, Sklar, P, O'Donovan, M C, Owen, M J
Publicado 2012

Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

por Riazuddin, S, Hussain, M, Razzaq, A, Iqbal, Z, Shahzad, M, Polla, D L, Song, Y, van Beusekom, E, Khan, A A, Tomas-Roca, L, Rashid, M, Zahoor, M Y, Wissink-Lindhout, W M, Basra, M A R, Ansar, M, Agha, Z, van Heeswijk, K, Rasheed, F, Van de Vorst, M, Veltman, J A, Gilissen, C, Akram, J, Kleefstra, T, Assir, M Z, Grozeva, D, Carss, K, Raymond, F L, O'Connor, T D, Riazuddin, S A, Khan, S N, Ahmed, Z M, de Brouwer, A P M, van Bokhoven, H, Riazuddin, S
Publicado 2016