| A structural variation reference for medical and population genetics RL Collins, H Brand, KJ Karczewski, X Zhao, J Alföldi, LC Francioli, ... Nature 581 (7809), 444-451, 2020 | 762* | 2020 |
| Spatial transcriptomics at subspot resolution with BayesSpace E Zhao, MR Stone, X Ren, J Guenthoer, KS Smythe, T Pulliam, ... Nature Biotechnology 39 (11), 1375-1384, 2021 | 339 | 2021 |
| The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies C Redin, H Brand, RL Collins, T Kammin, E Mitchell, JC Hodge, ... Nature Genetics 49 (1), 36-45, 2017 | 307 | 2017 |
| An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder DM Werling, H Brand, JY An, MR Stone, L Zhu, JT Glessner, RL Collins, ... Nature genetics 50 (5), 727-736, 2018 | 276 | 2018 |
| Mutations in DCHS1 cause mitral valve prolapse R Durst, K Sauls, DS Peal, K Toomer, M Leyne, M Salani, ME Talkowski, ... Nature 525 (7567), 109-113, 2015 | 199 | 2015 |
| Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome RL Collins, H Brand, CE Redin, C Hanscom, C Antolik, MR Stone, ... Genome Biology 18 (1), 36, 2017 | 197 | 2017 |
| Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders H Brand, V Pillalamarri, RL Collins, S Eggert, C O’Dushlaine, EB Braaten, ... The American Journal of Human Genetics 95 (4), 454-461, 2014 | 54 | 2014 |
| Paired-duplication signatures mark cryptic inversions and other complex structural variation H Brand, RL Collins, C Hanscom, JA Rosenfeld, V Pillalamarri, MR Stone, ... The American Journal of Human Genetics 97 (1), 170-176, 2015 | 53 | 2015 |
| Functional annotation of rare structural variation in the human brain L Han, X Zhao, ML Benton, T Perumal, RL Collins, GE Hoffman, ... Nature communications 11 (1), 2990, 2020 | 41 | 2020 |
| Identifying strengths and weaknesses of methods for computational network inference from single-cell RNA-seq data SG McCalla, A Fotuhi Siahpirani, J Li, S Pyne, M Stone, V Periyasamy, ... G3: Genes, Genomes, Genetics 13 (3), jkad004, 2023 | 18* | 2023 |
| CNView: a visualization and annotation tool for copy number variation from whole-genome sequencing RL Collins, MR Stone, H Brand, JT Glessner, ME Talkowski bioRxiv, 049536, 2016 | 14 | 2016 |
| Author Correction: A structural variation reference for medical and population genetics RL Collins, H Brand, KJ Karczewski, X Zhao, J Alföldi, LC Francioli, ... Nature 590 (7846), E55-E55, 2021 | 7 | 2021 |
| Switching circuits: Modulating NK cell response to TGF-β using novel receptors R Turk, L Guo, BJ Belmont, N Bogard, AT Chen, MD Williams, M Young, ... bioRxiv, 2023.12. 10.570687, 2023 | | 2023 |
| TRAFfic signals: High-throughput CAR discovery in NK cells reveals novel TRAF-binding endodomains that drive enhanced persistence and cytotoxicity MD Williams, AT Chen, MR Stone, L Guo, BJ Belmont, R Turk, N Bogard, ... bioRxiv, 2023.08. 02.551530, 2023 | | 2023 |
