Megan Y Dennis
Cited by
Cited by
The complete sequence of a human genome
S Nurk, S Koren, A Rhie, M Rautiainen, AV Bzikadze, A Mikheenko, ...
Science 376 (6588), 44-53, 2022
Psychedelics promote structural and functional neural plasticity
C Ly, AC Greb, LP Cameron, JM Wong, EV Barragan, PC Wilson, ...
Cell reports 23 (11), 3170-3182, 2018
Resolving the complexity of the human genome using single-molecule sequencing
MJP Chaisson, J Huddleston, MY Dennis, PH Sudmant, M Malig, ...
Nature 517 (7536), 608-611, 2015
Telomere-to-telomere assembly of a complete human X chromosome
KH Miga, S Koren, A Rhie, MR Vollger, A Gershman, A Bzikadze, ...
Nature 585 (7823), 79-84, 2020
Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication
MY Dennis, X Nuttle, PH Sudmant, F Antonacci, TA Graves, M Nefedov, ...
Cell, 2012
Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder
S Girirajan, MY Dennis, C Baker, M Malig, BP Coe, CD Campbell, K Mark, ...
The American Journal of Human Genetics 92 (2), 221-237, 2013
Reconstructing complex regions of genomes using long-read sequencing technology
J Huddleston, S Ranade, M Malig, F Antonacci, M Chaisson, L Hon, ...
Genome research 24 (4), 688-696, 2014
Complete genomic and epigenetic maps of human centromeres
N Altemose, GA Logsdon, AV Bzikadze, P Sidhwani, SA Langley, ...
Science 376 (6588), eabl4178, 2022
Balancing selection maintains a form of ERAP2 that undergoes nonsense-mediated decay and affects antigen presentation
AM Andrés, MY Dennis, WW Kretzschmar, JL Cannons, SQ Lee-Lin, ...
PLoS genetics 6 (10), e1001157, 2010
A complete reference genome improves analysis of human genetic variation
S Aganezov, SM Yan, DC Soto, M Kirsche, S Zarate, P Avdeyev, ...
Science 376 (6588), eabl3533, 2022
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia
D Harold, S Paracchini, T Scerri, M Dennis, N Cope, G Hill, V Moskvina, ...
Molecular psychiatry 11 (12), 1085-1091, 2006
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
P Feliciano, X Zhou, I Astrovskaya, TN Turner, T Wang, L Brueggeman, ...
NPJ genomic medicine 4 (1), 19, 2019
Human adaptation and evolution by segmental duplication
MY Dennis, EE Eichler
Current opinion in genetics & development 41, 44-52, 2016
Detection of structural variants and indels within exome data
E Karakoc, C Alkan, BJ O'roak, MY Dennis, L Vives, K Mark, MJ Rieder, ...
Nature methods 9 (2), 176-178, 2012
The evolution and population diversity of human-specific segmental duplications
MY Dennis, L Harshman, BJ Nelson, O Penn, S Cantsilieris, J Huddleston, ...
Nature ecology & evolution 1 (3), 0069, 2017
A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene
MY Dennis, S Paracchini, TS Scerri, L Prokunina-Olsson, JC Knight, ...
PLoS genetics 5 (3), e1000436, 2009
Palindromic GOLGA8 core duplicons promote chromosome 15q13. 3 microdeletion and evolutionary instability
F Antonacci, MY Dennis, J Huddleston, PH Sudmant, KM Steinberg, ...
Nature genetics 46 (12), 1293-1302, 2014
Epigenetics of autism-related impairment: copy number variation and maternal infection
V Mazina, J Gerdts, S Trinh, K Ankenman, T Ward, MY Dennis, S Girirajan, ...
Journal of Developmental & Behavioral Pediatrics 36 (2), 61-67, 2015
Human local adaptation of the TRPM8 cold receptor along a latitudinal cline
FM Key, MA Abdul-Aziz, R Mundry, BM Peter, A Sekar, M D’Amato, ...
PLoS genetics 14 (5), e1007298, 2018
Selection on a Variant Associated with Improved Viral Clearance Drives Local, Adaptive Pseudogenization of Interferon Lambda 4 (IFNL4)
FM Key, B Peter, MY Dennis, E Huerta-Sanchez, W Tang, ...
PLoS Genet 10 (10), e1004681, 2014
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