| Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants L Pizzo, M Jensen, A Polyak, JA Rosenfeld, K Mannik, A Krishnan, ... Genetics in Medicine 21 (4), 816-825, 2019 | 183 | 2019 |
| Novel metrics to measure coverage in whole exome sequencing datasets reveal local and global non-uniformity Q Wang, CS Shashikant, M Jensen, NS Altman, S Girirajan Scientific Reports 7 (1), 885, 2017 | 76 | 2017 |
| Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11. 2 deletion in Drosophila melanogaster J Iyer, MD Singh, M Jensen, P Patel, L Pizzo, E Huber, H Koerselman, ... Nature communications 9 (1), 2548, 2018 | 74 | 2018 |
| Single-cell multi-cohort dissection of the schizophrenia transcriptome WB Ruzicka, S Mohammadi, JF Fullard, J Davila-Velderrain, S Subburaju, ... Science 384 (6698), eadg5136, 2024 | 49 | 2024 |
| 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 | 47 | 2019 |
| A machine-learning approach for accurate detection of copy number variants from exome sequencing VK Pounraja, G Jayakar, M Jensen, N Kelkar, S Girirajan Genome research 29 (7), 1134-1143, 2019 | 45 | 2019 |
| An interaction-based model for neuropsychiatric features of copy-number variants M Jensen, S Girirajan PLOS Genetics 15 (1), e1007879, 2019 | 44 | 2019 |
| Mapping a shared genetic basis for neurodevelopmental disorders M Jensen, S Girirajan Genome Medicine 9 (1), 1-3, 2017 | 43 | 2017 |
| NCBP2modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models MD Singh, M Jensen, M Lasser, E Huber, T Yusuff, L Pizzo, B Lifschutz, ... PLOS Genetics 16 (2), e1008590, 2020 | 37 | 2020 |
| Single-cell genomics and regulatory networks for 388 human brains PS Emani, JJ Liu, D Clarke, M Jensen, J Warrell, C Gupta, R Meng, ... Science 384 (6698), eadi5199, 2024 | 36 | 2024 |
| Transcriptome Analyses of Heart and Liver Reveal Novel Pathways for Regulating Songbird Migration WJ Horton, M Jensen, A Sebastian, CA Praul, I Albert, PA Bartell Scientific reports 9 (1), 6058, 2019 | 26 | 2019 |
| A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11. 2 deletion syndrome M Jensen, RF Kooy, TJ Simon, E Reyniers, S Girirajan, F Tassone European journal of medical genetics 61 (4), 209-212, 2018 | 21 | 2018 |
| The chromatin remodeler ISWI acts during Drosophila development to regulate adult sleep NN Gong, LC Dilley, CE Williams, EH Moscato, M Szuperak, Q Wang, ... Science Advances 7 (8), eabe2597, 2021 | 19 | 2021 |
| Gene discoveries in autism are biased towards comorbidity with intellectual disability M Jensen, C Smolen, S Girirajan Journal of medical genetics 57 (9), 647-652, 2020 | 19 | 2020 |
| Functional assessment of the “two-hit” model for neurodevelopmental defects in Drosophila and X. laevis L Pizzo, M Lasser, T Yusuff, M Jensen, P Ingraham, E Huber, MD Singh, ... PLoS genetics 17 (4), e1009112, 2021 | 16 | 2021 |
| Artificial gravity partially protects space-induced neurological deficits in Drosophila melanogaster SD Mhatre, J Iyer, J Petereit, RM Dolling-Boreham, A Tyryshkina, AM Paul, ... Cell Reports 40 (10), 111279, 2022 | 15 | 2022 |
| Drosophila models of pathogenic copy-number variant genes show global and non-neuronal defects during development T Yusuff, M Jensen, S Yennawar, L Pizzo, S Karthikeyan, DJ Gould, ... PLoS Genetics 16 (6), e1008792, 2020 | 13 | 2020 |
| Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variants C Smolen, M Jensen, L Dyer, L Pizzo, A Tyryshkina, D Banerjee, L Rohan, ... The American Journal of Human Genetics 110 (12), 2015-2028, 2023 | 8 | 2023 |
| Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12. 1 deletion M Jensen, A Tyryshkina, L Pizzo, C Smolen, M Das, E Huber, A Krishnan, ... Genome Medicine 13, 1-21, 2021 | 7 | 2021 |
| Complex genetic variation in nearly complete human genomes GA Logsdon, P Ebert, PA Audano, M Loftus, D Porubsky, J Ebler, F Yilmaz, ... bioRxiv, 2024 | 5 | 2024 |
