Pennacchio, Len A.
Lawrence Berkeley National Laboratory · Joint Genome Institute · University of California, Berkeley
29 papers on CoChatORCID 0000-0002-8748-3732
Most cited papers
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Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease
Romeo, S., Kozlitina, J., Xing, C., Pertsemlidis, A., Cox, D., Pennacchio, L. A., Boerwinkle, E., Cohen, J. C., & Hobbs, H. H. (2008) · Nature Genetics
Liver Disease Diagnosis and TreatmentGenetic Associations and Epidemiology
Cited by 3,416
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ChIP-seq accurately predicts tissue-specific activity of enhancers
Visel, A., Blow, M. J., Li, Z., Zhang, T., Akiyama, J. A., Holt, A., Plajzer-Frick, I., Shoukry, M., Wright, C., Chen, F., et al. (2009) · Nature
Genomics and Chromatin DynamicsChromatin Remodeling and Cancer
Cited by 1,639
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A Common Allele on Chromosome 9 Associated with Coronary Heart Disease
McPherson, R., Pertsemlidis, A., Kavaslar, N., Stewart, A., Roberts, R., Cox, D. R., Hinds, D. A., Pennacchio, L. A., Tybjaerg-Hansen, A., Folsom, A. R., et al. (2007) · Science
Genetic Associations and EpidemiologyCardiovascular Health and Risk Factors
Cited by 1,587
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Metagenomic discovery of biomass-degrading genes and genomes from cow rumen
Hess, M., Sczyrba, A., Egan, R., Kim, T.-W., Chokhawala, H., Schroth, G., Luo, S., Clark, D. S., Chen, F., Zhang, T., et al. (2011) · Science
Biofuel production and bioconversionAnaerobic Digestion and Biogas Production
Cited by 1,319
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Guidelines for investigating causality of sequence variants in human disease
MacArthur, D. G., Manolio, T. A., Dimmock, D. P., Rehm, H. L., Shendure, J., Abecasis, G. R., Adams, D. R., Altman, R. B., Antonarakis, S. E., Ashley, E. A., et al. (2014) · Nature
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 1,224
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In vivo enhancer analysis of human conserved non-coding sequences
Pennacchio, L. A., Ahituv, N., Moses, A. M., Prabhakar, S., Nobrega, M. A., Shoukry, M., Minovitsky, S., Dubchak, I., Holt, A., Lewis, K. D., et al. (2006) · Nature
Genomics and Chromatin DynamicsDevelopmental Biology and Gene Regulation
Cited by 1,165
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VISTA Enhancer Browser—a database of tissue-specific human enhancers
Visel, A., Minovitsky, S., Dubchak, I., & Pennacchio, L. A. (2007) · Nucleic Acids Research
Genomics and Chromatin DynamicsDevelopmental Biology and Gene Regulation
Cited by 1,080
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An Apolipoprotein Influencing Triglycerides in Humans and Mice Revealed by Comparative Sequencing
Pennacchio, L. A., Olivier, M., Hubacek, J. A., Cohen, J. C., Cox, D. R., Fruchart, J.-C., Krauss, R. M., & Rubin, E. M. (2001) · Science
Lipid metabolism and disordersLipoproteins and Cardiovascular Health
Cited by 921
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Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants
Parker, S. C. J., Stitzel, M. L., Taylor, D. L., Orozco, J. M., Erdos, M. R., Akiyama, J. A., van Bueren, K. L., Chines, P. S., Narisu, N., Program, N. C. S., et al. (2013) · Proceedings of the National Academy of Sciences
Genomics and Chromatin DynamicsGenetic Associations and Epidemiology
Cited by 665
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Enhancer redundancy provides phenotypic robustness in mammalian development
Osterwalder, M., Barozzi, I., Tissières, V., Fukuda-Yuzawa, Y., Mannion, B. J., Afzal, S. Y., Lee, E. A., Zhu, Y., Plajzer-Frick, I., Pickle, C. S., et al. (2018) · Nature
Genomics and Chromatin DynamicsDevelopmental Biology and Gene Regulation
Cited by 642
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Genomic views of distant-acting enhancers
Visel, A., Rubin, E. M., & Pennacchio, L. A. (2009) · Nature
Genomics and Chromatin DynamicsGenetic Associations and Epidemiology
Cited by 610
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Most Rare Missense Alleles Are Deleterious in Humans: Implications for Complex Disease and Association Studies
Kryukov, G. V., Pennacchio, L. A., & Sunyaev, S. R. (2007) · The American Journal of Human Genetics
Evolution and Genetic DynamicsGenomics and Rare Diseases
Cited by 598
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Massively parallel functional dissection of mammalian enhancers in vivo
Patwardhan, R. P., Hiatt, J. B., Witten, D. M., Kim, M. J., Smith, R. P., May, D., Lee, C., Andrie, J. M., Lee, S.-I., Cooper, G. M., et al. (2012) · Nature Biotechnology
Genomics and Chromatin DynamicsCRISPR and Genetic Engineering
Cited by 536
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The amphioxus genome illuminates vertebrate origins and cephalochordate biology
Holland, L. Z., Albalat, R., Azumi, K., Benito-Gutiérrez, È., Blow, M. J., Bronner-Fraser, M., Brunet, F., Butts, T., Candiani, S., Dishaw, L. J., et al. (2008) · Genome Research
Developmental Biology and Gene RegulationChromosomal and Genetic Variations
Cited by 512
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Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL
Romeo, S., Pennacchio, L. A., Fu, Y., Boerwinkle, E., Tybjaerg-Hansen, A., Hobbs, H. H., & Cohen, J. C. (2007) · Nature Genetics
Lipid metabolism and disordersGenetic Associations and Epidemiology
Cited by 511
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Rapid and Pervasive Changes in Genome-wide Enhancer Usage during Mammalian Development
Nord, A. S., Blow, M. J., Attanasio, C., Akiyama, J. A., Holt, A., Hosseini, R., Phouanenavong, S., Plajzer-Frick, I., Shoukry, M., Afzal, V., et al. (2013) · Cell
Genomics and Chromatin DynamicsEpigenetics and DNA Methylation
Cited by 375
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Combinatorial Regulation of Endothelial Gene Expression by Ets and Forkhead Transcription Factors
De Val, S., Chi, N. C., Meadows, S. M., Minovitsky, S., Anderson, J. P., Harris, I. S., Ehlers, M. L., Agarwal, P., Visel, A., Xu, S.-M., et al. (2008) · Cell
Developmental Biology and Gene RegulationGenomics and Chromatin Dynamics
Cited by 343
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Single-nucleus analysis of accessible chromatin in developing mouse forebrain reveals cell-type-specific transcriptional regulation
Preissl, S., Fang, R., Huang, H., Zhao, Y., Raviram, R., Gorkin, D. U., Zhang, Y., Sos, B. C., Afzal, V., Dickel, D. E., et al. (2018) · Nature Neuroscience
Single-cell and spatial transcriptomicsGenomics and Chromatin Dynamics
Cited by 332
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Germline Chd8 haploinsufficiency alters brain development in mouse
Gompers, A. L., Su-Feher, L., Ellegood, J., Copping, N. A., Riyadh, M. A., Stradleigh, T. W., Pride, M. C., Schaffler, M. D., Wade, A. A., Catta-Preta, R., et al. (2017) · Nature Neuroscience
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 266
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A High-Resolution Enhancer Atlas of the Developing Telencephalon
Visel, A., Taher, L., Girgis, H., May, D., Golonzhka, O., Hoch, R. V., McKinsey, G. L., Pattabiraman, K., Silberberg, S. N., Blow, M. J., et al. (2013) · Cell
Genomics and Chromatin DynamicsDevelopmental Biology and Gene Regulation
Cited by 257
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Homotypic clusters of transcription factor binding sites are a key component of human promoters and enhancers
Gotea, V., Visel, A., Westlund, J. M., Nobrega, M. A., Pennacchio, L. A., & Ovcharenko, I. (2010) · Genome Research
Genomics and Chromatin DynamicsChromosomal and Genetic Variations
Cited by 248
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Ultraconserved Enhancers Are Required for Normal Development
Dickel, D. E., Ypsilanti, A. R., Pla, R., Zhu, Y., Barozzi, I., Mannion, B. J., Khin, Y. S., Fukuda-Yuzawa, Y., Plajzer-Frick, I., Pickle, C. S., et al. (2018) · Cell
Genomics and Chromatin DynamicsDevelopmental Biology and Gene Regulation
Cited by 190
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Dlx1&2-Dependent Expression of Zfhx1b (Sip1, Zeb2) Regulates the Fate Switch between Cortical and Striatal Interneurons
McKinsey, G. L., Lindtner, S., Trzcinski, B., Visel, A., Pennacchio, L. A., Huylebroeck, D., Higashi, Y., & Rubenstein, J. L. R. (2013) · Neuron
Neurogenesis and neuroplasticity mechanismsDevelopmental Biology and Gene Regulation
Cited by 153
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Occupancy by key transcription factors is a more accurate predictor of enhancer activity than histone modifications or chromatin accessibility
Dogan, N., Wu, W., Morrissey, C. S., Chen, K.-B., Stonestrom, A., Long, M., Keller, C. A., Cheng, Y., Jain, D., Visel, A., et al. (2015) · Epigenetics & Chromatin
Genomics and Chromatin DynamicsEpigenetics and DNA Methylation
Cited by 114
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