Mantripragada, Kiran
Cardiff University
3 papers on CoChatORCID 0000-0003-2070-8105
Most cited papers
- Verified
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
GERAD1 Consortium, Pardiñas, A. F., CRESTAR Consortium, Holmans, P., Pocklington, A. J., Escott-Price, V., Ripke, S., Carrera, N., Legge, S. E., Bishop, S., et al. (2018) · Nature Genetics
Schizophrenia research and treatmentGenetic Associations and Epidemiology
Cited by 1,552
- Verified
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
Williams, N. M., Zaharieva, I., Martin, A., Langley, K., Mantripragada, K., Fossdal, R., Stefansson, H., Stefansson, K., Magnusson, P., Gudmundsson, O. O., et al. (2010) · The Lancet
Genomic variations and chromosomal abnormalitiesAttention Deficit Hyperactivity Disorder
Cited by 572
- Verified
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
Kirov, G., Grozeva, D., Norton, N., Ivanov, D., Mantripragada, K. K., Holmans, P., International Schizophrenia Consortium, the Wellcome Trust Case Control Consortium, Craddock, N., Owen, M. J., et al. (2009) · Human Molecular Genetics
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 390
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