Lakshmi, B.
Cold Spring Harbor Laboratory
5 papers on CoChatORCID 0000-0003-4702-5734
Most cited papers
- Verified
Strong association of de novo copy number mutations with autism
Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., Walsh, T., Yamrom, B., Yoon, S., Krasnitz, A., Kendall, J., et al. (2007) · Science
Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research
Cited by 2,795
- Verified
Large-scale copy number polymorphism in the human genome
Sebat, J., Lakshmi, B., Troge, J., Alexander, J., Young, J., Lundin, P., Månér, S., Massa, H., Walker, M., Chi, M., et al. (2004) · Science
Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms
Cited by 2,557
- Verified
Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
Walsh, T., McClellan, J. M., McCarthy, S. E., Addington, A. M., Pierce, S. B., Cooper, G. M., Nord, A. S., Kusenda, M., Malhotra, D., Bhandari, A., et al. (2008) · Science
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 1,800
- Verified
Rare de novo and transmitted copy-number variation in autistic spectrum disorders
Levy, D., Ronemus, M., Yamrom, B., Lee, Y.-H., Leotta, A., Kendall, J., Marks, S., Lakshmi, B., Pai, D., Ye, K., et al. (2011) · Neuron
Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research
Cited by 712
- Verified
Microduplications of 16p11.2 are associated with schizophrenia
Wellcome Trust Case Control Consortium, McCarthy, S. E., Makarov, V., Kirov, G., Addington, A. M., McClellan, J., Yoon, S., Perkins, D. O., Dickel, D. E., Kusenda, M., et al. (2009) · Nature Genetics
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 711
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