Whelan, Christopher W.
Broad Institute · Harvard University · Stanley Center for Psychiatric Research
4 papers on CoChatORCID 0000-0001-8446-8468
Most cited papers
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A structural variation reference for medical and population genetics
Collins, R. L., Brand, H., Karczewski, K. J., Zhao, X., Alföldi, J., Francioli, L. C., Khera, A. V., Lowther, C., Gauthier, L. D., Wang, H., et al. (2020) · Nature
Genomic variations and chromosomal abnormalitiesGenomics and Rare Diseases
Cited by 1,037
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Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome Sequencing
Viswanathan, S. R., Ha, G., Hoff, A. M., Wala, J. A., Carrot-Zhang, J., Whelan, C. W., Haradhvala, N. J., Freeman, S. S., Reed, S. C., Rhoades, J., et al. (2018) · Cell
Prostate Cancer Treatment and ResearchChromatin Remodeling and Cancer
Cited by 365
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Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in mice
Yilmaz, M., Yalcin, E., Presumey, J., Aw, E., Ma, M., Whelan, C. W., Stevens, B., McCarroll, S. A., & Carroll, M. C. (2021) · Nature Neuroscience
Complement system in diseasesSchizophrenia research and treatment
Cited by 321
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Complement genes contribute sex-biased vulnerability in diverse disorders
Schizophrenia Working Group of the Psychiatric Genomics Consortium, Kamitaki, N., Sekar, A., Handsaker, R. E., de Rivera, H., Tooley, K., Morris, D. L., Taylor, K. E., Whelan, C. W., Tombleson, P., et al. (2020) · Nature
Systemic Lupus Erythematosus ResearchComplement system in diseases
Cited by 238
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