Pejman Mohammadi - Publications

Affiliations: 
Integrative Structural and Computational Biology Scripps Research Institute 

20 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Munro D, Ehsan N, Esmaeili-Fard SM, Gusev A, Palmer AA, Mohammadi P. Multimodal analysis of RNA sequencing data powers discovery of complex trait genetics. Biorxiv : the Preprint Server For Biology. PMID 38798366 DOI: 10.1101/2024.05.14.594051  0.669
2024 Lu Z, Wang X, Carr M, Kim A, Gazal S, Mohammadi P, Wu L, Gusev A, Pirruccello J, Kachuri L, Mancuso N. Improved multi-ancestry fine-mapping identifies -regulatory variants underlying molecular traits and disease risk. Medrxiv : the Preprint Server For Health Sciences. PMID 38699369 DOI: 10.1101/2024.04.15.24305836  0.316
2024 de Jong TV, Pan Y, Rastas P, Munro D, Tutaj M, Akil H, Benner C, Chen D, Chitre AS, Chow W, Colonna V, Dalgard CL, Demos WM, Doris PA, Garrison E, ... ... Mohammadi P, et al. A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats. Cell Genomics. 100527. PMID 38537634 DOI: 10.1016/j.xgen.2024.100527  0.749
2024 Ehsan N, Kotis BM, Castel SE, Song EJ, Mancuso N, Mohammadi P. Haplotype-aware modeling of cis-regulatory effects highlights the gaps remaining in eQTL data. Nature Communications. 15: 522. PMID 38225224 DOI: 10.1038/s41467-024-44710-8  0.408
2023 Clifford R, Munro D, Dochtermann D, Devineni P, Pyarajan S, Telese F, Palmer AA, Mohammadi P, Friedman R. Genome-Wide Association Study of Chronic Dizziness in the Elderly Identifies Loci Implicating MLLT10, BPTF, LINC01224, and ROS1. Journal of the Association For Research in Otolaryngology : Jaro. PMID 38036714 DOI: 10.1007/s10162-023-00917-y  0.676
2023 Zhou JL, de Guglielmo G, Ho AJ, Kallupi M, Pokhrel N, Li HR, Chitre AS, Munro D, Mohammadi P, Carrette LLG, George O, Palmer AA, McVicker G, Telese F. Author Correction: Single-nucleus genomics in outbred rats with divergent cocaine addiction-like behaviors reveals changes in amygdala GABAergic inhibition. Nature Neuroscience. PMID 37845545 DOI: 10.1038/s41593-023-01489-z  0.703
2023 Zhou JL, de Guglielmo G, Ho AJ, Kallupi M, Pokhrel N, Li HR, Chitre AS, Munro D, Mohammadi P, Carrette LLG, George O, Palmer AA, McVicker G, Telese F. Single-nucleus genomics in outbred rats with divergent cocaine addiction-like behaviors reveals changes in amygdala GABAergic inhibition. Nature Neuroscience. PMID 37798411 DOI: 10.1038/s41593-023-01452-y  0.709
2023 de Jong TV, Pan Y, Rastas P, Munro D, Tutaj M, Akil H, Benner C, Chitre AS, Chow W, Colonna V, Dalgard CL, Demos WM, Doris PA, Garrison E, Geurts A, ... ... Mohammadi P, et al. A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats. Biorxiv : the Preprint Server For Biology. PMID 37214860 DOI: 10.1101/2023.04.13.536694  0.749
2023 Chitre AS, Polesskaya O, Munro D, Cheng R, Mohammadi P, Holl K, Gao J, Bimschleger H, Martinez AG, George A, Gileta AF, Horvath A, Hughson A, Ishiwari K, King CP, et al. Exponential increase in QTL detection with increased sample size. Genetics. PMID 36974931 DOI: 10.1093/genetics/iyad054  0.676
2023 Fowler S, Wang T, Munro D, Kumar A, Chitre AS, Hollingsworth TJ, Garcia Martinez A, St Pierre CL, Bimschleger H, Gao J, Cheng R, Mohammadi P, Chen H, Palmer AA, Polesskaya O, et al. Genome-wide association study finds multiple loci associated with intraocular pressure in HS rats. Frontiers in Genetics. 13: 1029058. PMID 36793389 DOI: 10.3389/fgene.2022.1029058  0.753
2022 Munro D, Wang T, Chitre AS, Polesskaya O, Ehsan N, Gao J, Gusev A, Woods LCS, Saba LM, Chen H, Palmer AA, Mohammadi P. The regulatory landscape of multiple brain regions in outbred heterogeneous stock rats. Nucleic Acids Research. PMID 36263809 DOI: 10.1093/nar/gkac912  0.74
2022 Glinos DA, Garborcauskas G, Hoffman P, Ehsan N, Jiang L, Gokden A, Dai X, Aguet F, Brown KL, Garimella K, Bowers T, Costello M, Ardlie K, Jian R, Tucker NR, ... ... Mohammadi P, et al. Transcriptome variation in human tissues revealed by long-read sequencing. Nature. PMID 35922509 DOI: 10.1038/s41586-022-05035-y  0.304
2021 Pathak GA, Singh K, Miller-Fleming TW, Wendt FR, Ehsan N, Hou K, Johnson R, Lu Z, Gopalan S, Yengo L, Mohammadi P, Pasaniuc B, Polimanti R, Davis LK, Mancuso N. Integrative genomic analyses identify susceptibility genes underlying COVID-19 hospitalization. Nature Communications. 12: 4569. PMID 34315903 DOI: 10.1038/s41467-021-24824-z  0.345
2020 Chandra V, Bhattacharyya S, Schmiedel BJ, Madrigal A, Gonzalez-Colin C, Fotsing S, Crinklaw A, Seumois G, Mohammadi P, Kronenberg M, Peters B, Ay F, Vijayanand P. Promoter-interacting expression quantitative trait loci are enriched for functional genetic variants. Nature Genetics. PMID 33349701 DOI: 10.1038/s41588-020-00745-3  0.315
2020 Pathak GA, Singh K, Miller-Fleming TW, Wendt F, Ehsan N, Hou K, Johnson R, Lu Z, Gopalan S, Dimbou LY, Mohammadi P, Pasaniuc B, Polimanti R, Davis LK, Mancuso N. Integrative analyses identify susceptibility genes underlying COVID-19 hospitalization. Medrxiv : the Preprint Server For Health Sciences. PMID 33330876 DOI: 10.1101/2020.12.07.20245308  0.316
2020 Ferraro NM, Strober BJ, Einson J, Abell NS, Aguet F, Barbeira AN, Brandt M, Bucan M, Castel SE, Davis JR, Greenwald E, Hess GT, Hilliard AT, Kember RL, Kotis B, ... ... Mohammadi P, et al. Transcriptomic signatures across human tissues identify functional rare genetic variation. Science (New York, N.Y.). 369. PMID 32913073 DOI: 10.1126/Science.Aaz5900  0.4
2020 Oliva M, Muñoz-Aguirre M, Kim-Hellmuth S, Wucher V, Gewirtz ADH, Cotter DJ, Parsana P, Kasela S, Balliu B, Viñuela A, Castel SE, Mohammadi P, Aguet F, Zou Y, Khramtsova EA, et al. The impact of sex on gene expression across human tissues. Science (New York, N.Y.). 369. PMID 32913072 DOI: 10.1126/Science.Aba3066  0.305
2019 Mohammadi P, Castel SE, Cummings BB, Einson J, Sousa C, Hoffman P, Donkervoort S, Jiang Z, Mohassel P, Foley AR, Wheeler HE, Im HK, Bonnemann CG, MacArthur DG, Lappalainen T. Genetic regulatory variation in populations informs transcriptome analysis in rare disease. Science (New York, N.Y.). PMID 31601707 DOI: 10.1126/Science.Aay0256  0.302
2016 Castel SE, Mohammadi P, Chung WK, Shen Y, Lappalainen T. Rare variant phasing and haplotypic expression from RNA sequencing with phASER. Nature Communications. 7: 12817. PMID 27605262 DOI: 10.1038/ncomms12817  0.303
2015 Bartha I, Rausell A, McLaren PJ, Mohammadi P, Tardaguila M, Chaturvedi N, Fellay J, Telenti A. The Characteristics of Heterozygous Protein Truncating Variants in the Human Genome. Plos Computational Biology. 11: e1004647. PMID 26642228 DOI: 10.1371/Journal.Pcbi.1004647  0.385
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