Shared and distinct transcriptomic cell types across neocortical areas B Tasic, Z Yao, LT Graybuck, KA Smith, TN Nguyen, D Bertagnolli, ... Nature 563 (7729), 72-78, 2018 | 1658 | 2018 |
Conserved cell types with divergent features in human versus mouse cortex RD Hodge, TE Bakken, JA Miller, KA Smith, ER Barkan, LT Graybuck, ... Nature 573 (7772), 61-68, 2019 | 1620 | 2019 |
Disruptive CHD8 mutations define a subtype of autism early in development R Bernier, C Golzio, B Xiong, HA Stessman, BP Coe, O Penn, ... Cell 158 (2), 263-276, 2014 | 851 | 2014 |
GUIDANCE: a web server for assessing alignment confidence scores O Penn, E Privman, H Ashkenazy, G Landan, D Graur, T Pupko Nucleic acids research 38 (suppl_2), W23-W28, 2010 | 673 | 2010 |
Integrated morphoelectric and transcriptomic classification of cortical GABAergic cells NW Gouwens, SA Sorensen, F Baftizadeh, A Budzillo, BR Lee, T Jarsky, ... Cell 183 (4), 935-953. e19, 2020 | 418 | 2020 |
An alignment confidence score capturing robustness to guide tree uncertainty O Penn, E Privman, G Landan, D Graur, T Pupko Molecular biology and evolution 27 (8), 1759-1767, 2010 | 385 | 2010 |
FastML: a web server for probabilistic reconstruction of ancestral sequences H Ashkenazy, O Penn, A Doron-Faigenboim, O Cohen, G Cannarozzi, ... Nucleic acids research 40 (W1), W580-W584, 2012 | 369 | 2012 |
Rodent phylogeny revised: analysis of six nuclear genes from all major rodent clades S Blanga-Kanfi, H Miranda, O Penn, T Pupko, RW DeBry, D Huchon BMC evolutionary biology 9, 1-12, 2009 | 321 | 2009 |
The discovery of integrated gene networks for autism and related disorders F Hormozdiari, O Penn, E Borenstein, EE Eichler Genome research 25 (1), 142-154, 2015 | 291 | 2015 |
Disruption of POGZ is associated with intellectual disability and autism spectrum disorders HAF Stessman, MH Willemsen, M Fenckova, O Penn, A Hoischen, ... The American Journal of Human Genetics 98 (3), 541-552, 2016 | 182 | 2016 |
Pepitope: epitope mapping from affinity-selected peptides I Mayrose, O Penn, E Erez, ND Rubinstein, T Shlomi, NT Freund, ... Bioinformatics 23 (23), 3244-3246, 2007 | 169 | 2007 |
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 | 163 | 2017 |
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility X Nuttle, G Giannuzzi, MH Duyzend, JG Schraiber, I Narvaiza, ... Nature 536 (7615), 205-209, 2016 | 130 | 2016 |
Improving the performance of positive selection inference by filtering unreliable alignment regions E Privman, O Penn, T Pupko Molecular biology and Evolution 29 (1), 1-5, 2012 | 129 | 2012 |
Changes in exon–intron structure during vertebrate evolution affect the splicing pattern of exons S Gelfman, D Burstein, O Penn, A Savchenko, M Amit, S Schwartz, ... Genome research 22 (1), 35-50, 2012 | 129 | 2012 |
Stepwise prediction of conformational discontinuous B‐cell epitopes using the Mapitope algorithm EM Bublil, NT Freund, I Mayrose, O Penn, A Roitburd‐Berman, ... Proteins: Structure, Function, and Bioinformatics 68 (1), 294-304, 2007 | 114 | 2007 |
Transcriptional fates of human-specific segmental duplications in brain ML Dougherty, JG Underwood, BJ Nelson, E Tseng, KM Munson, O Penn, ... Genome research 28 (10), 1566-1576, 2018 | 65 | 2018 |
Deep panning: steps towards probing the IgOme A Ryvkin, H Ashkenazy, L Smelyanski, G Kaplan, O Penn, ... Public Library of Science 7 (8), e41469, 2012 | 62 | 2012 |
The birth of a human-specific neural gene by incomplete duplication and gene fusion ML Dougherty, X Nuttle, O Penn, BJ Nelson, J Huddleston, C Baker, ... Genome biology 18, 1-16, 2017 | 54 | 2017 |
Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders J Chow, M Jensen, H Amini, F Hormozdiari, O Penn, S Shifman, ... Genome medicine 11, 1-14, 2019 | 45 | 2019 |