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| Blood-brain barrier permeability assessed by perfusion CT predicts symptomatic hemorrhagic transformation and malignant edema in acute ischemic stroke J Hom, JW Dankbaar, BP Soares, T Schneider, SC Cheng, J Bredno, ... American journal of neuroradiology 32 (1), 41-48, 2011 | 207 | 2011 |
| Reperfusion is a more accurate predictor of follow-up infarct volume than recanalization: a proof of concept using CT in acute ischemic stroke patients BP Soares, E Tong, J Hom, SC Cheng, J Bredno, L Boussel, WS Smith, ... Stroke 41 (1), e34-e40, 2010 | 202 | 2010 |
| Clinical text summarization: adapting large language models can outperform human experts D Van Veen, C Van Uden, L Blankemeier, JB Delbrouck, A Aali, ... Research square, rs. 3. rs-3483777, 2023 | 116 | 2023 |
| IRF2BPL is associated with neurological phenotypes PC Marcogliese, V Shashi, RC Spillmann, N Stong, JA Rosenfeld, ... The American Journal of Human Genetics 103 (2), 245-260, 2018 | 108 | 2018 |
| Multiparametric MRI and CT models of infarct core and favorable penumbral imaging patterns in acute ischemic stroke CS Kidwell, M Wintermark, DA De Silva, TJ Schaewe, R Jahan, ... Stroke 44 (1), 73-79, 2013 | 108 | 2013 |
| Chatbot vs medical student performance on free-response clinical reasoning examinations E Strong, A DiGiammarino, Y Weng, A Kumar, P Hosamani, J Hom, ... JAMA internal medicine 183 (9), 1028-1030, 2023 | 104 | 2023 |
| Appyters: Turning Jupyter Notebooks into data-driven web apps DJB Clarke, M Jeon, DJ Stein, N Moiseyev, E Kropiwnicki, C Dai, Z Xie, ... Patterns 2 (3), 2021 | 99 | 2021 |
| A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative V Shashi, K Schoch, R Spillmann, H Cope, QKG Tan, N Walley, L Pena, ... Genetics in Medicine 21 (1), 161-172, 2019 | 90 | 2019 |
| Biallelic mutations in ATP5F1D, which encodes a subunit of ATP synthase, cause a metabolic disorder M Oláhová, WH Yoon, K Thompson, S Jangam, L Fernandez, ... The American Journal of Human Genetics 102 (3), 494-504, 2018 | 85 | 2018 |
| Lysosomal storage and albinism due to effects of a de novo CLCN7 variant on lysosomal acidification ER Nicoli, MR Weston, M Hackbarth, A Becerril, A Larson, WM Zein, ... The American Journal of Human Genetics 104 (6), 1127-1138, 2019 | 81 | 2019 |
| Expanding the spectrum of BAF-related disorders: de novo variants in SMARCC2 cause a syndrome with intellectual disability and developmental delay K Machol, J Rousseau, S Ehresmann, T Garcia, TTM Nguyen, ... The American Journal of Human Genetics 104 (1), 164-178, 2019 | 81 | 2019 |
| Dynamic perfusion CT assessment of the blood-brain barrier permeability: first pass versus delayed acquisition JW Dankbaar, J Hom, T Schneider, SC Cheng, BC Lau, I Van Der Schaaf, ... American Journal of Neuroradiology 29 (9), 1671-1676, 2008 | 78 | 2008 |
| Large language model influence on diagnostic reasoning: a randomized clinical trial E Goh, R Gallo, J Hom, E Strong, Y Weng, H Kerman, JA Cool, Z Kanjee, ... JAMA Network Open 7 (10), e2440969-e2440969, 2024 | 66 | 2024 |
| The COVID-19 drug and gene set library MV Kuleshov, DJ Stein, DJB Clarke, E Kropiwnicki, KM Jagodnik, A Bartal, ... Patterns 1 (6), 2020 | 64 | 2020 |
| Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate–binding region MK Kelly, M Park, I Mihalek, A Rochtus, M Gramm, E Pérez‐Palma, ... Epilepsia 60 (3), 406-418, 2019 | 63 | 2019 |
| Characterizing electronic health record usage patterns of inpatient medicine residents using event log data JK Wang, D Ouyang, J Hom, J Chi, JH Chen PLoS One 14 (2), e0205379, 2019 | 62 | 2019 |
| De novo EIF2AK1 and EIF2AK2 variants are associated with developmental delay, leukoencephalopathy, and neurologic decompensation D Mao, CM Reuter, MRZ Ruzhnikov, AE Beck, EG Farrow, LT Emrick, ... The American Journal of Human Genetics 106 (4), 570-583, 2020 | 58 | 2020 |
| Partial loss of USP9X function leads to a male neurodevelopmental and behavioral disorder converging on transforming growth factor β signaling BV Johnson, R Kumar, S Oishi, S Alexander, M Kasherman, MS Vega, ... Biological psychiatry 87 (2), 100-112, 2020 | 58 | 2020 |
| De novo variants in WDR37 are associated with epilepsy, colobomas, dysmorphism, developmental delay, intellectual disability, and cerebellar hypoplasia O Kanca, JC Andrews, PT Lee, C Patel, SR Braddock, AM Slavotinek, ... The American Journal of Human Genetics 105 (2), 413-424, 2019 | 56 | 2019 |
