The effects of spectral dimensionality reduction on hyperspectral pixel classification: A case study

por Mantripragada, Kiran, Dao, Phuong D., He, Yuhong, Qureshi, Faisal Z.
Publicado 2022

Array-CGH and multipoint FISH to decode complex chromosomal rearrangements

por Darai-Ramqvist, Eva, de Ståhl, Teresita Diaz, Sandlund, Agneta, Mantripragada, Kiran, Klein, George, Dumanski, Jan, Imreh, Stefan, Kost-Alimova, Maria
Publicado 2006

Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus

por Hansson, Caisa M, Buckley, Patrick G, Grigelioniene, Giedre, Piotrowski, Arkadiusz, Hellström, Anders R, Mantripragada, Kiran, Jarbo, Caroline, Mathiesen, Tiit, Dumanski, Jan P
Publicado 2007

Associations between polygenic risk for schizophrenia and brain function during probabilistic learning in healthy individuals

por Lancaster, Thomas M., Ihssen, Niklas, Brindley, Lisa M., Tansey, Katherine E., Mantripragada, Kiran, O'Donovan, Michael C., Owen, Michael J., Linden, David E.J.
Publicado 2015

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

por Williams, Nigel M, Zaharieva, Irina, Martin, Andrew, Langley, Kate, Mantripragada, Kiran, Fossdal, Ragnheidur, Stefansson, Hreinn, Stefansson, Kari, Magnusson, Pall, Gudmundsson, Olafur O, Gustafsson, Omar, Holmans, Peter, Owen, Michael J, O'Donovan, Michael, Thapar, Anita
Publicado 2010

Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: Evidence from two independent cohorts

por Oertel-Knöchel, Viola, Lancaster, Thomas M., Knöchel, Christian, Stäblein, Michael, Storchak, Helena, Reinke, Britta, Jurcoane, Alina, Kniep, Jonathan, Prvulovic, David, Mantripragada, Kiran, Tansey, Katherine E., O’Donovan, Michael C., Owen, Michael J., Linden, David E.J.
Publicado 2015

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

por Fry, Andrew E., Rees, Elliott, Thompson, Rose, Mantripragada, Kiran, Blake, Penny, Jones, Glyn, Morgan, Sian, Jose, Sian, Mugalaasi, Hood, Archer, Hayley, McCann, Emma, Clarke, Angus, Taylor, Clare, Davies, Sally, Gibbon, Frances, Te Water Naude, Johann, Hartley, Louise, Thomas, Gareth, White, Catharine, Natarajan, Jaya, Thomas, Rhys H., Drew, Cheney, Chung, Seo-Kyung, Rees, Mark I., Holmans, Peter, Owen, Michael J., Kirov, George, Pilz, Daniela T., Kerr, Michael P.
Publicado 2016

Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

por Mok, Kin Y, Sheerin, Una, Simón-Sánchez, Javier, Salaka, Afnan, Chester, Lucy, Escott-Price, Valentina, Mantripragada, Kiran, Doherty, Karen M, Noyce, Alastair J, Mencacci, Niccolo E, Lubbe, Steven J, Williams-Gray, Caroline H, Barker, Roger A, van Dijk, Karin D, Berendse, Henk W, Heutink, Peter, Corvol, Jean-Christophe, Cormier, Florence, Lesage, Suzanne, Brice, Alexis, Brockmann, Kathrin, Schulte, Claudia, Gasser, Thomas, Foltynie, Thomas, Limousin, Patricia, Morrison, Karen E, Clarke, Carl E, Sawcer, Stephen, Warner, Tom T, Lees, Andrew J, Morris, Huw R, Nalls, Mike A, Singleton, Andrew B, Hardy, John, Abramov, Andrey Y, Plagnol, Vincent, Williams, Nigel M, Wood, Nicholas W
Publicado 2016