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Megan Dennis

TitleASST PROF-HCOMP
InstitutionUniversity of California Davis
DepartmentBiochemistry and Molecular Medicine
AddressGBSF
CA 95616
Phone530-752-1357
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Ly C, Greb AC, Cameron LP, Wong JM, Barragan EV, Wilson PC, Burbach KF, Soltanzadeh Zarandi S, Sood A, Paddy MR, Duim WC, Dennis MY, McAllister AK, Ori-McKenney KM, Gray JA, Olson DE. Psychedelics Promote Structural and Functional Neural Plasticity. Cell Rep. 2018 Jun 12; 23(11):3170-3182. PMID: 29898390.
      View in: PubMed
    2. Dennis MY, Harshman L, Nelson BJ, Penn O, Cantsilieris S, Huddleston J, Antonacci F, Penewit K, Denman L, Raja A, Baker C, Mark K, Malig M, Janke N, Espinoza C, Stessman HAF, Nuttle X, Hoekzema K, Lindsay-Graves TA, Wilson RK, Eichler EE. The evolution and population diversity of human-specific segmental duplications. Nat Ecol Evol. 2017; 1(3):69. PMID: 28580430.
      View in: PubMed
    3. Dennis MY, Eichler EE. Human adaptation and evolution by segmental duplication. Curr Opin Genet Dev. 2016 Dec; 41:44-52. PMID: 27584858.
      View in: PubMed
    4. Mazina V, Gerdts J, Trinh S, Ankenman K, Ward T, Dennis MY, Girirajan S, Eichler EE, Bernier R. Epigenetics of autism-related impairment: copy number variation and maternal infection. J Dev Behav Pediatr. 2015 Feb-Mar; 36(2):61-7. PMID: 25629966; PMCID: PMC4318761.
    5. Chaisson MJ, Huddleston J, Dennis MY, Sudmant PH, Malig M, Hormozdiari F, Antonacci F, Surti U, Sandstrom R, Boitano M, Landolin JM, Stamatoyannopoulos JA, Hunkapiller MW, Korlach J, Eichler EE. Resolving the complexity of the human genome using single-molecule sequencing. Nature. 2015 Jan 29; 517(7536):608-11. PMID: 25383537; PMCID: PMC4317254.
    6. Antonacci F, Dennis MY, Huddleston J, Sudmant PH, Steinberg KM, Rosenfeld JA, Miroballo M, Graves TA, Vives L, Malig M, Denman L, Raja A, Stuart A, Tang J, Munson B, Shaffer LG, Amemiya CT, Wilson RK, Eichler EE. Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability. Nat Genet. 2014 Dec; 46(12):1293-302. PMID: 25326701; PMCID: PMC4244265.
    7. Huddleston J, Ranade S, Malig M, Antonacci F, Chaisson M, Hon L, Sudmant PH, Graves TA, Alkan C, Dennis MY, Wilson RK, Turner SW, Korlach J, Eichler EE. Reconstructing complex regions of genomes using long-read sequencing technology. Genome Res. 2014 Apr; 24(4):688-96. PMID: 24418700; PMCID: PMC3975067.
    8. Girirajan S, Dennis MY, Baker C, Malig M, Coe BP, Campbell CD, Mark K, Vu TH, Alkan C, Cheng Z, Biesecker LG, Bernier R, Eichler EE. Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder. Am J Hum Genet. 2013 Feb 07; 92(2):221-37. PMID: 23375656; PMCID: PMC3567267.
    9. Dennis MY, Nuttle X, Sudmant PH, Antonacci F, Graves TA, Nefedov M, Rosenfeld JA, Sajjadian S, Malig M, Kotkiewicz H, Curry CJ, Shafer S, Shaffer LG, de Jong PJ, Wilson RK, Eichler EE. Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication. Cell. 2012 May 11; 149(4):912-22. PMID: 22559943; PMCID: PMC3365555.
    10. Karakoc E, Alkan C, O'Roak BJ, Dennis MY, Vives L, Mark K, Rieder MJ, Nickerson DA, Eichler EE. Detection of structural variants and indels within exome data. Nat Methods. 2011 Dec 18; 9(2):176-8. PMID: 22179552; PMCID: PMC3269549.