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Donohoe, G., Holland, J., Mothersill, D., McCarthy-Jones, S., Cosgrove, D., Harold, D., Richards, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, Gill, M., Corvin, A. and Morris, D. W. 2018. Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation. Psychological Medicine 48 (10) , pp. 1608-1615. 10.1017/S0033291717002987
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Bakhsh, Ameen D, Ladas, Ioannis, Hamshere, Marian L, Bullock, Martyn, Kirov, George, Zhang, Lei, Taylor, Peter N, Gregory, John W., Scott-Coombes, David, Völzke, Henry, Teumer, Alexander, Mantripragada, Kiran, Williams, E Dillwyn, Clifton-Bligh, Roderick J, Williams, Nigel M and Ludgate, Marian E 2018. An InDel in Phospholipase-C-B-1 is linked with euthyroid multinodular goiter. Thyroid 28 (7) , pp. 891-901. 10.1089/thy.2017.0312
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Bakhsh, Ameen D., Ladas, Ioannis, Hamshere, Marian L., Bullock, Martyn, Kirov, George, Zhang, Lei, Taylor, Peter N., Gregory, John W., Scott-Coombes, David, Völzke, Henry, Teumer, Alexander, Mantripragada, Kiran, Williams, E. Dillwyn, Clifton-Bligh, Roderick J., Williams, Nigel M. and Ludgate, Marian E. 2018. An indel in phospholipase-C-B-1 is linked with euthyroid multinodular goiter. Thyroid 28 (7) , p. 891. 10.1089/thy.2017.0312

Cosgrove, Donna, Mothersill, David O., Whitton, Laura, Harold, Denise, Kelly, Sinead, Holleran, Laurena, Holland, Jessica, Anney, Richard, Richards, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, Gill, Michael, Corvin, Aiden, Morris, Derek W. and Donohoe, Gary 2018. Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 (3) , pp. 369-376. 10.1002/ajmg.b.32620
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Pardinas, Antonio, Holmans, Peter, Pocklington, Andrew, Escott-Price, Valentina, Ripke, S, Carrera, Noa, Legge, Sophie, Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, J, McCarroll, S, Baune, B, Breen, G, Byrne, E, Dannlowski, U, Eley, T, Hayward, C, Martin, N, McIntosh, M, Plomin, R, Porteous, D, Wray, N, Caballero, A, Geschwind, D, Huckins, L, Ruderfer, D, Santiago, E, Sklar, P, Stahl, E, Won, H, Agerbo, E, Als, T, Andreassen, O, Bækvad-Hansen, M, Mortensen, P, Pedersen, CB, Børglum, A, Bybjerg-Grauholm, J, Djurovic, S, Durmishi, N, Giørtz Pedersenu, M, Golimbet, V, Grove, J, Hougaard, M, Mattheisen, M, Molden, E, Mors, O, Nordentoft, M, Pejovic-Milovancevic, M, Sigurdsson, E, Silagadze, T, Søholm Hansen, C, Stefansson, K, Stefansson, H, Steinberg, S, Tosato, S, Werge, T, Consortium, GERAD1, Collier, D, Rujescu, D, Kirov, George, Owen, Michael J and Walters, James 2018. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics 50 , pp. 381-389. 10.1038/s41588-018-0059-2
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Mihaljevic, Marina, Zeljic, Katarina, Soldatovic, Ivan, Andric, Sanja, Mirjanic, Tijana, Richards, Alexander, Mantripragada, Kiran, Pekmezovic, Tatjana, Novakovic, Ivana and Maric, Nadja P. 2017. The emerging role of the FKBP5 gene polymorphisms in vulnerability-stress model of schizophrenia: further evidence from a Serbian population. European Archives of Psychiatry and Clinical Neuroscience 267 (6) , pp. 527-539. 10.1007/s00406-016-0720-7
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Cosgrove, D, Harold, D, Mothersill, O, Anney, Richard, Hill, Martin, Bray, Nicholas, Blokland, G, Petryshen, T, Donnelly, Peter, Bates, Lesley, Barroso, Ines, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin N A, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas W, Spencer, Chris C A, Band, Gavin, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Giannoulatou, Eleni, Hopkins, Lucinda, Pirinen, Matti, Pearson, Richard, Strange, Amy, Su, Zhan, Vukcevic, Damjan, Langford, Cordelia, Hunt, Sarah E, Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J, Dronov, Serge, Gillman, Matthew, Gray, Emma, Hammond, Naomi, Jayakumar, Alagurevathi, McCann, Owen T, Liddle, Jennifer, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Waller, Matthew, Weston, PaulWeston, Widaa, SaraWidaa, Whittaker, Pamela, Richards, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, Gill, M, Corvin, A, Morris, D W and Donohoe, G 2017. MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls. Translational Psychiatry 7 (1) , e1012. 10.1038/tp.2016.286
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Legge, Sophie E., Hamshere, Marian L., Ripke, S., Pardinas, Antonio, Goldstein, J. I., Rees, Elliott, Richards, Alexander, Leonenko, Ganna M., Jorskog, L. F., Goldstein, Jacqueline I., Jarskog, L Fredrik, Hilliard, Chris, Alfirevic, Ana, Duncan, Laramie, Fourches, Denie, Huang, Hailiang, Lek, Monkol, Neale, Benjamin M, Ripke, Stephan, Shianna, Kevin, Szatkiewicz, Jin P, Tropsha, Alexander, van den Oord, Edwin JCG, Cascorbi, Ingolf, Dettling, Michael, Gazit, Ephraim, Goff, Donald C, Holden, Arthur L, Kelly, Deanna L, Malhotra, Anil K, Nielsen, Jimmi, Pirmohamed, Munir, Rujescu, Dan, Werge, Thomas, Levy, Deborah L, Josiassen, Richard C, Kennedy, James L, Lieberman, Jeffrey A, Daly, Mark J, Sullivan, Patrick F, Chambert, K. D., Collier, D. A., Genovese, G., Giegling, I., Holmans, Peter Alan, Jonasdottir, A., Kirov, George, McCarroll, S. A., MacCabe, J. H., Mantripragada, Kiran Kumar, Moran, J. L., Neale, B. M., Stefansson, H., Rujescu, D., Daly, M. J., Sullivan, P. F., Owen, Michael John, O'Donovan, Michael Conlon and Walters, James Tynan Rhys 2017. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular Psychiatry 22 , pp. 1502-1508. 10.1038/mp.2016.97
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Cosgrove, Donna, Mothersill, Omar, Kendall, Kimberley, Konte, Bettina, Harold, Denise, Giegling, Ina, Hartmann, Annette, Richards, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, Gill, Michael, Rujescu, Dan, Walters, James, Corvin, Aiden, Morris, Derek W and Donohoe, Gary 2017. Cognitive characterization of schizophrenia risk variants involved in synaptic transmission: evidence of CACNA1C's role in working memory. Neuropsychopharmacology 42 , pp. 2612-2622. 10.1038/npp.2017.123
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Whitton, Laura, Cosgrove, Donna, Clarkson, Christopher, Harold, Denise, Kendall, Kimberley, Richards, Alexander, Mantripragada, Kiran, Owen, Michael John, O'Donovan, Michael Conlon, Walters, James, Hartmann, Annette, Konte, Betina, Rujescu, Dan, Gill, Michael, Corvin, Aiden, Rea, Stephen, Donohoe, Gary and Morris, Derek W. 2016. Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 (8) , pp. 1170-1179. 10.1002/ajmg.b.32503
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Pardinas, Antonio, Holmans, Peter, Pocklington, Andrew, Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Stephen A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Consortium, ,the GERADI, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael, O'Donovan, Michael and Walters, James 2016. Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection. bioRxiv 10.1101/068593
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Fry, Andrew Evan, Rees, Elliott, Thompson, Rose, Mantripragada, Kiran, Blake, Penny, Jones, Glyn, Morgan, Sian, Jose, Sian, Mugalaasi, Hood, Archer, Hayley, McCann, Emma, Clarke, Angus John, 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 Alan, Owen, Michael John, Kirov, George, Pilz, Daniela T. and Kerr, Michael Patrick 2016. Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy. BMC Medical Genetics 17 , 34. 10.1186/s12881-016-0294-2
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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 Melville and Wood, Nicholas W 2016. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. The Lancet Neurology 15 (6) , pp. 585-596. 10.1016/S1474-4422(16)00071-5
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Lancaster, Thomas, Ihssen, Niklaas, Brindley, Lisa, Tansey, Katherine E., Mantripragada, Kiran Kumar, O'Donovan, Michael Conlon, Owen, Michael John and Linden, David Edmund Johannes 2016. Associations between polygenic risk for schizophrenia and brain function during probabilistic learning in healthy individuals. Human Brain Mapping 37 (2) , pp. 491-500. 10.1002/hbm.23044
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Lancaster, Thomas, Brindley, Lisa, Tansey, Katherine, Sims, Rebecca, Mantripragada, Kiran Kumar, Owen, Michael John, Williams, Julie and Linden, David Edmund Johannes 2015. Alzheimer's disease risk variant in CLU is associated with neural inefficiency in healthy individuals. Alzheimer's & Dementia 11 (10) , pp. 1144-1152. 10.1016/j.jalz.2014.10.012

Saville, Christopher W.N., Lancaster, Thomas M., Davies, Timothy J., Toumaian, Maida, Pappa, Eleni, Fish, Simon, Feige, Bernd, Bender, Stephan, Mantripragada, Kiran Kumar, Linden, David Edmund Johannes and Klein, Christoph 2015. Elevated P3b latency variability in carriers of ZNF804A risk allele for psychosis. NeuroImage 116 , pp. 207-13. 10.1016/j.neuroimage.2015.04.024

Lancaster, Thomas, Heerey, E. A., Mantripragada, Kiran Kumar and Linden, David Edmund Johannes 2015. Replication study implicates COMT val158met polymorphism as a modulator of probabilistic reward learning. Genes Brain and Behaviour 14 (6) , pp. 486-492. 10.1111/gbb.12228

Oertel-Knöchel, Viola, Lancaster, Thomas, Knöchel, Christian, Stäblein, Michael, Storchak, Helena, Reinke, Britta, Jurcoane, Alina, Kniep, Jonathan, Prvulovic, David, Mantripragada, Kiran Kumar, Tansey, Katherine E., O'Donovan, Michael Conlon, Owen, Michael John and Linden, David Edmund Johannes 2015. Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: Evidence from two independent cohorts. NeuroImage: Clinical 7 , pp. 764-770. 10.1016/j.nicl.2015.03.005
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Lancaster, Thomas, Heerey, E. A., Mantripragada, Kiran Kumar and Linden, David Edmund Johannes 2014. CACNA1C risk variant affects reward responsiveness in healthy individuals. Translational Psychiatry 4 (10) , e461. 10.1038/tp.2014.100
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Saville, C. W. N., Lancaster, Thomas, Stefanou, M. E., Salunkhe, G., Lourmpa, I., Nadkarni, A., Boehm, S. G., Bender, S., Smyrnis, N., Ettinger, U., Feige, B., Biscaldi, M., Mantripragada, Kiran Kumar, Linden, David Edmund Johannes and Klein, C. 2014. COMT Val158Met genotype is associated with fluctuations in working memory performance: converging evidence from behavioural and single-trial P3b measures. NeuroImage 100 , pp. 489-497. 10.1016/j.neuroimage.2014.06.006

Williams, Nigel Melville, Zaharieva, Irina, Martin, Andrew Kenneth, Langley, Kate, Mantripragada, Kiran Kumar, Fossdal, Ragnheidur, Stefansson, Hreinn, Stefansson, Kari, Magnusson, Pall, Gudmundsson, Olafur O., Gustafsson, Omar, Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2010. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. The Lancet 376 (9750) , pp. 1401-1408. 10.1016/S0140-6736(10)61109-9

Mantripragada, Kiran Kumar, Carroll, Liam S. and Williams, Nigel Melville 2010. Experimental approaches for identifying schizophrenia risk genes. Current Topics in Behavioral Neuroscience 4 , pp. 587-610. 10.1007/7854_2010_58

Mantripragada, Kiran Kumar, de Stahl, Teresita Diaz, Patridge, Chris, Menzel, Uwe, Andersson, Robin, Chuzhanova, Nadia, Kluwe, Lan, Guha, Abhijit, Mautner, Victor, Dumanski, Jan P. and Upadhyaya, Meena 2009. Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array. Genes Chromosomes and Cancer 48 (10) , pp. 897-907. 10.1002/gcc.20695

Kirov, George, Grozeva, Detelina Valentinova, Norton, Nadine, Ivanov, Dobril, Mantripragada, Kiran Kumar, Holmans, Peter Alan, Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 2009. Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. Human Molecular Genetics 18 (8) , pp. 1497-1503. 10.1093/hmg/ddp043

Dwyer, Sarah Lynne, Carroll, Liam Stuart, Mantripragada, Kiran Kumar, Owen, Michael John, O'Donovan, Michael Conlon and Williams, Nigel Melville 2009. Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (3) , pp. 766-774. 10.1002/ajmg.b.31045

Mantripragada, Kiran Kumar, de Ståhl, Teresita Díaz, Patridge, Chris, Menzel, Uwe, Andersson, Robin, Chuzhanova, Nadia, Kluwe, Lan, Guha, Abhijit Ranjan, Mautner, Victor, Dumanski, Jan P. and Upadhyaya, Meena 2009. Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array. Genes, Chromosomes and Cancer 48 (10) , pp. 897-907. 10.1002/gcc.20695

Mantripragada, Kiran Kumar, Spurlock, Gillian, Kluwe, Lan, Chuzhanova, Nadia, Ferner, Rosalie E., Frayling, Ian Martin, Dumanski, Jan P., Guha, Abhijit Ranjan, Mautner, Victor and Upadhyaya, Meena 2008. High-resolution DNA copy number profiling of malignant peripheral nerve sheath tumors using targeted microarray-based comparative genomic hybridization. Clinical Cancer Research 14 (4) , pp. 1015-1024. 10.1158/1078-0432.CCR-07-1305

Upadhyaya, Meena, Kluwe, Lan, Spurlock, Gillian, Monem, Bisma Qamar, Majounie, Elisa, Mantripragada, Kiran Kumar, Ruggieri, Martino, Chuzhanova, Nadia, Evans, D. G., Ferner, R., Thomas, Nicholas Stuart Tudor, Guha, A. and Mautner, Victor 2008. Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs). Human Mutation 29 (1) , pp. 74-82. 10.1002/humu.20601

Mantripragada, Kiran Kumar, Caley, Matthew, Stephens, Philip, Jones, Christopher John, Kluwe, Lan, Guha, Abhijit Ranjan, Mautner, Victor and Upadhyaya, Meena 2008. Telomerase activity is a biomarker for high grade malignant peripheral nerve sheath tumors in neurofibromatosis type I individuals. Genes Chromosomes and Cancer 47 (3) , pp. 238-246. 10.1002/gcc.20525

Shen, Ming Hong, Mantripragada, Kiran Kumar, Dumanski, J. P., Frayling, Ian Martin and Upadhyaya, Meena 2007. Detection of copy number changes at the NF1 locus with improved high-resolution array CGH. Clinical Genetics 72 (3) , pp. 238-244. 10.1111/j.1399-0004.2007.00858.x

Hansson, C. M., Buckley, P. G., Grigelioniene, G., Piotrowski, A., Hellstrom, A. R., Mantripragada, Kiran Kumar, Jarbo, C., Mathiesen, T. and Dumanski, J. P. 2007. Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus. BMC Genomics 8 , p. 16.

Darai-Ramqvist, Eva, de Stahl, Teresita Diaz, Sandlund, Agneta, Mantripragada, Kiran Kumar, Klein, George, Dumanski, Jan, Imreh, Stefan and Kost-Alimova, Maria 2006. Array-CGH and multipoint FISH to decode complex chromosomal rearrangements. BMC Genomics 7 , 330. 10.1186/1471-2164-7-330
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Upadhyaya, Meena, Spurlock, Gillian, Kluwe, Lan, Mantripragada, Kiran Kumar, Majounie, Elisa, Pandit, A., Evans, G., Guha, A., Dumanski, J., Ferner, R. and Mautner, V. 2006. Comparison of germline and somatic mutational spectra in NF1-associated peripheral nerve sheath tumours (MPNSTs). Journal of Medical Genetics 43 (S3) , S75-S75.

Shen, Ming Hong, Mantripragada, Kiran Kumar, Dumanski, J., Frayling, Ian and Upadhyaya, Meena 2006. DNA microarray for detection of copy number changes at the NF1 locus using array comparative genomic hybridisation (CGH) analysis [Abstract]. Journal of Medical Genetics 43 (Supp.) , S19.

Mantripragada, Kiran Kumar, Spurlock, Gillian, Kluwe, L., Pandita, A., Guha, A., Evans, G., Ferner, R. E., Mautner, V., Frayling, Ian Martin, Dumanski, J. P. and Upadhyaya, Meena 2006. Comprehensive DNA copy number profiling of malignant peripheral nerve sheath tumours (MPNSTs) using array based comparative genomic hybridisation (array-CGH) [Abstract]. Journal of Medical Genetics 43 (Supp.) , S19.

Piotrowski, Arkadiusz, Benetkiewicz, Magdalena, Menzel, Uwe, de Ståhl, Teresita Díaz, Mantripragada, Kiran Kumar, Grigelionis, Gintautas, Buckley, Patrick G., Jankowski, Michal, Hoffman, Jacek, Bala, Dariusz, Srutek, Ewa, Laskowski, Ryszard, Zegarski, Wojciech and Dumanski, Jan P. 2006. Microarray-based survey of CpG islands identifies concurrent hyper- and hypomethylation patterns in tissues derived from patients with breast cancer. Genes, Chromosomes and Cancer 45 (7) , pp. 656-657. 10.1002/gcc.20331

Mantripragada, Kiran Kumar, Thuresson, A. C., Piotrowski, A., Diaz de Stahl, T., Menzel, U., Grigelionis, G., Ferner, R. E., Griffiths, S., Bolund, L., Mautner, V., Nordling, M., Legius, E., Vetrie, D., Dahl, N., Messiaen, L., Upadhyaya, M., Bruder, C. E. and Dumanski, J. P. 2006. Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH. Journal of Medical Genetics 43 (1) , pp. 28-38. 10.1136/jmg.2005.033795

de Bustos, Cecilia, Díaz de Ståhl, Teresita, Piotrowski, Arkadiusz, Mantripragada, Kiran Kumar, Buckley, Patrick G., Darai, Eva, Hansson, Caisa M., Grigelionis, Gintautas, Menzel, Uwe and Dumanski, Jan P. 2006. Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH. Genomics 88 (2) , pp. 152-162. 10.1016/j.ygeno.2006.03.016

Buckley, P. G., Mantripragada, Kiran Kumar, Diaz de Stahl, T., Piotrowski, A., Hansson, C. M., Kiss, H., Vetrie, D., Ernberg, I. T., Nordenskjold, M., Bolund, L., Sainio, M., Rouleau, G. A., Niimura, M., Wallace, A. J., Evans, D. G., Grigelionis, G., Menzel, U. and Dumanski, J. P. 2005. Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2. Human Mutation 26 (6) , pp. 540-549. 10.1002/humu.20255

Diaz de Stahl, T., Hansson, C. M., de Bustos, C., Mantripragada, Kiran Kumar, Piotrowski, A., Benetkiewicz, M., Jarbo, C., Wiklund, L., Mathiesen, T., Nyberg, G., Collins, V. P., Evans, D. G., Ichimura, K. and Dumanski, J. P. 2005. High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas. Human Genetics 118 (1) , pp. 35-44. 10.1007/s00439-005-0002-3

Diaz de Stahl, T., Hartmann, C., de Bustos, C., Piotrowski, A., Benetkiewicz, M., Mantripragada, Kiran Kumar, Tykwinski, T., von Deimling, A. and Dumanski, J. P. 2005. Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme. Genes, Chromosomes and Cancer 44 (2) , pp. 161-169. 10.1002/gcc.20226

Ammerlaan, A. C., de Bustos, C., Ararou, A., Buckley, P. G., Mantripragada, Kiran Kumar, Verstegen, M. J., Hulsebos, T. J. and Dumanski, J. P. 2005. Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray. Genes, Chromosomes and Cancer 43 (4) , pp. 329-338. 10.1002/gcc.20207

Buckley, P. G., Mantripragada, Kiran Kumar, Piotrowski, A., Diaz de Stahl, T. and Dumanski, J. P. 2005. Copy-number polymorphisms: mining the tip of an iceberg. Trends in Genetics 21 (6) , pp. 315-317.

Benetkiewicz, M., Wang, Y., Schaner, M., Wang, P., Mantripragada, Kiran Kumar, Buckley, P. G., Kristensen, G., Borresen-Dale, A. L. and Dumanski, J. P. 2005. High-resolution gene copy number and expression profiling of human chromosome 22 in ovarian carcinomas. Genes, Chromosomes and Cancer 42 (3) , pp. 228-237. 10.1002/gcc.20128

Mantripragada, Kiran Kumar, Tapia-Páez, Isabel, Blennow, Elisabeth, Nilsson, Peter, Wedell, Anna and Dumanski, Jan 2004. DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets. International Journal of Molecular Medicine 13 (2) , pp. 273-279. 10.3892/ijmm.13.2.273

Mantripragada, Kiran Kumar, Buckley, Patrick G, Diaz de Ståhl, Teresita and Dumanski, Jan P 2004. Genomic microarrays in the spotlight. Trends in Genetics 20 (2) , pp. 87-94. 10.1016/j.tig.2003.12.008

Erickson, Robert P., Skinner, Steve, Jacquet, Helene, Campion, Dominique, Buckley, Patrick G., Mantripragada, Kiran Kumar and Dumanski, Jan P. 2003. Does chromosome 22 have anything to do with sex determination: Further studies on a 46,XX,22q11.2 del male. American Journal of Medical Genetics 123A (1) , pp. 64-67. 10.1002/ajmg.a.20489

Mantripragada, Kiran Kumar, Buckley, Patrick G., Jarbo, Caroline, Menzel, Uwe and Dumanski, Jan P. 2003. Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection. Journal of Molecular Medicine 81 (7) , pp. 443-451. 10.1007/s00109-003-0458-3

Mantripragada, Kiran Kumar, Buckley, PG, Benetkiewicz, M, De Bustos, C, Hirvela, C, Jarbo, C, Bruder, CE, Wensman, H, Mathiesen, T, Nyberg, G, Papi, L, Collins, VP, Ichimura, K, Evans, G and Dumanski, JP 2003. High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH. International Journal of Oncology 22 (3) , pp. 615-622.

Buckley, Patrick G., Mantripragada, Kiran Kumar, Benetkiewicz, Magdalena, Tapia-Páez, Isabel, Diaz de Ståhl, Teresita, Rosenquist, Magnus, Ali, Haider, Jarbo, Caroline, de Bustos, Cecilía, Hirvelä, Carina, Sinder Wilén, Birgitta, Fransson, Ingegerd, Thyr, Charlotte, Johnsson, Britt-Inger, Bruder, Carl E.G., Menzel, Uwe, Hergersberg, Martin, Mandahl, Nils, Blennow, Elisabeth, Wedell, Anna, Beare, David M., Collins, John E., Dunham, Ian, Albertson, Donna, Pinkel, Daniel, Bastian, Boris C., Faruqi, A. Fawad, Lasken, Roger S., Ichimura, Koichi, Collins, V. Peter and Dumanski, Jan P. 2002. A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications. Human Molecular Genetics 11 (25) , pp. 3221-3229. 10.1093/hmg/11.25.3221

This list was generated on Tue Feb 19 04:08:48 2019 GMT.