Alipanahi, Babak
23andMe (United States)
9 papers on CoChatORCID 0000-0001-8216-7178
Most cited papers
- Verified
Predicting the sequence specificities of DNA- and RNA-binding proteins by deep learning
Alipanahi, B., Delong, A., Weirauch, M. T., & Frey, B. J. (2015) · Nature Biotechnology
Genomics and Chromatin DynamicsMachine Learning in Bioinformatics
Cited by 2,873
- Verified
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls, M. A., Blauwendraat, C., Vallerga, C. L., Heilbron, K., Bandres-Ciga, S., Chang, D., Tan, M., Kia, D. A., Noyce, A. J., Xue, A., et al. (2019) · The Lancet Neurology
Parkinson's Disease Mechanisms and TreatmentsGenetic Associations and Epidemiology
Cited by 2,454
- Verified
Widespread intron retention in mammals functionally tunes transcriptomes
Braunschweig, U., Barbosa-Morais, N. L., Pan, Q., Nachman, E. N., Alipanahi, B., Gonatopoulos-Pournatzis, T., Frey, B., Irimia, M., & Blencowe, B. J. (2014) · Genome Research
RNA Research and SplicingCancer-related molecular mechanisms research
Cited by 664
- Verified
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
Okbay, A., Wu, Y., Wang, N., Jayashankar, H., Bennett, M., Nehzati, S. M., Sidorenko, J., Kweon, H., Goldman, G., Gjorgjieva, T., et al. (2022) · Nature Genetics
Genetic Associations and EpidemiologyGenetic and phenotypic traits in livestock
Cited by 654
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Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways
Howard, D. M., Adams, M. J., Shirali, M., Clarke, T.-K., Marioni, R. E., Davies, G., Coleman, J. R. I., Alloza, C., Shen, X., Barbu, M. C., et al. (2018) · Nature Communications
Genetic Associations and EpidemiologyTreatment of Major Depression
Cited by 612
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Underspecification Presents Challenges for Credibility in Modern Machine Learning
D'Amour, A., Heller, K., Moldovan, D., Adlam, B., Alipanahi, B., Beutel, A., Chen, C., Deaton, J., Eisenstein, J., Hoffman, M. D., et al. (2020) · arXiv
Domain Adaptation and Few-Shot LearningAdversarial Robustness in Machine Learning
Cited by 398
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Genome-wide characteristics of de novo mutations in autism
Yuen, R. K., Merico, D., Cao, H., Pellecchia, G., Alipanahi, B., Thiruvahindrapuram, B., Tong, X., Sun, Y., Cao, D., Zhang, T., et al. (2016) · npj Genomic Medicine
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 216
- Verified
Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder
Uddin, M., Tammimies, K., Pellecchia, G., Alipanahi, B., Hu, P., Wang, Z., Pinto, D., Lau, L., Nalpathamkalam, T., Marshall, C. R., et al. (2014) · Nature Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 163
- Verified
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment
Shaffer, J. R., Li, J., Lee, M. K., Roosenboom, J., Orlova, E., Adhikari, K., Gallo, C., Poletti, G., Schuler-Faccini, L., Bortolini, M.-C., et al. (2017) · The American Journal of Human Genetics
Genetic Associations and EpidemiologyDermatoglyphics and Human Traits
Cited by 47
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