| 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 | 2222 | 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 | 1038 | 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 | 864 | 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 | 723 | 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 | 475 | 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 | 349 | 2013 |
| Complete genomic and epigenetic maps of human centromeres N Altemose, GA Logsdon, AV Bzikadze, P Sidhwani, SA Langley, ... Science 376 (6588), eabl4178, 2022 | 322 | 2022 |
| 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 | 291 | 2014 |
| 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 | 261 | 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 | 256 | 2010 |
| 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 | 213 | 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 | 211 | 2019 |
| Human adaptation and evolution by segmental duplication MY Dennis, EE Eichler Current opinion in genetics & development 41, 44-52, 2016 | 180 | 2016 |
| 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 | 156 | 2017 |
| 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 | 150 | 2012 |
| 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 | 142 | 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 | 134 | 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 | 131 | 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 | 122 | 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 | 111 | 2014 |
Evan EichlerProfessor of Genome Sciences, University of WashingtonVerified email at gs.washington.edu
