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Steven J. Pastor - Publications

Affiliations: 
2013-2018 Biomedical Engineering Drexel University, Philadelphia, PA, United States 
 2018- Biomedical and Health Informatics Children’s Hospital of Philadelphia / University of Pennsylvania, Philadelphia, PA, United States 
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8 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
2022 Pastor S, Tran O, McGinn DE, Crowley TB, Zackai EH, McDonald-McGinn DM, Emanuel BS. A Novel Non-Allelic Homologous Recombination Event in a Parent with an 11;22 Reciprocal Translocation Leading to 22q11.2 Deletion Syndrome. Genes. 13. PMID 36140835 DOI: 10.3390/genes13091668  0.474
2020 Pastor S, Tran O, Jin A, Carrado D, Silva BA, Uppuluri L, Abid HZ, Young E, Crowley TB, Bailey AG, McGinn DE, McDonald-McGinn DM, Zackai EH, Xie M, Taylor D, et al. Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR). Scientific Reports. 10: 12235. PMID 32699385 DOI: 10.1038/S41598-020-69134-4  0.569
2019 Heft IE, Mostovoy Y, Levy-Sakin M, Ma W, Stevens AJ, Pastor S, McCaffrey J, Boffelli D, Martin DI, Xiao M, Kennedy MA, Kwok PY, Sikela JM. The Driver of Extreme Human-Specific Olduvai Repeat Expansion Remains Highly Active in the Human Genome. Genetics. PMID 31754017 DOI: 10.1534/Genetics.119.302782  0.611
2019 Król JE, Hall DC, Balashov S, Pastor S, Sibert J, McCaffrey J, Lang S, Ehrlich RL, Earl J, Mell JC, Xiao M, Ehrlich GD. Genome rearrangements induce biofilm formation in Escherichia coli C - an old model organism with a new application in biofilm research. Bmc Genomics. 20: 767. PMID 31640553 DOI: 10.1186/S12864-019-6165-4  0.44
2019 Demaerel W, Mostovoy Y, Yilmaz F, Vervoort L, Pastor S, Hestand MS, Swillen A, Vergaelen E, Geiger EA, Coughlin CR, Chow SK, McDonald-McGinn D, Morrow B, Kwok PY, Xiao M, et al. The 22q11 low copy repeats are characterized by unprecedented size and structural variability. Genome Research. 29: 1389-1401. PMID 31481461 DOI: 10.1101/Gr.248682.119  0.621
2019 Levy-Sakin M, Pastor S, Mostovoy Y, Li L, Leung AKY, McCaffrey J, Young E, Lam ET, Hastie AR, Wong KHY, Chung CYL, Ma W, Sibert J, Rajagopalan R, Jin N, et al. Genome maps across 26 human populations reveal population-specific patterns of structural variation. Nature Communications. 10: 1025. PMID 30833565 DOI: 10.1038/S41467-019-08992-7  0.586
2017 McCaffrey J, Young E, Lassahn K, Sibert J, Pastor S, Riethman H, Xiao M. High-throughput single-molecule telomere characterization. Genome Research. PMID 29025896 DOI: 10.1101/Gr.222422.117  0.569
2017 Young E, Pastor S, Rajagopalan R, McCaffrey J, Sibert J, Mak AC, Kwok PY, Riethman H, Xiao M. High-throughput single-molecule mapping links subtelomeric variants and long-range haplotypes with specific telomeres. Nucleic Acids Research. PMID 28180280 DOI: 10.1093/Nar/Gkx017  0.615
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