| Alterations of the PPP2R1B Gene in Human Lung and Colon Cancer SS Wang, ED Esplin, JL Li, L Huang, A Gazdar, J Minna, GA Evans Science 282 (5387), 284-287, 1998 | 508 | 1998 |
| The human body at cellular resolution: the NIH Human Biomolecular Atlas Program H Consortium Nature, 2019 | 473* | 2019 |
| The human tumor atlas network: charting tumor transitions across space and time at single-cell resolution O Rozenblatt-Rosen, A Regev, P Oberdoerffer, T Nawy, A Hupalowska, ... Cell 181 (2), 236-249, 2020 | 464 | 2020 |
| Prevalence of germline variants in prostate cancer and implications for current genetic testing guidelines P Nicolosi, E Ledet, S Yang, S Michalski, B Freschi, E O’Leary, ED Esplin, ... JAMA oncology 5 (4), 523-528, 2019 | 373 | 2019 |
| Underdiagnosis of Hereditary Breast Cancer: Are Genetic Testing Guidelines a Tool or an Obstacle? ed d esplin J Clin Oncol, 2019 | 371 | 2019 |
| Comparison of universal genetic testing vs guideline-directed targeted testing for patients with hereditary cancer syndrome NJ Samadder, D Riegert-Johnson, L Boardman, D Rhodes, M Wick, ... JAMA oncology 7 (2), 230-237, 2021 | 264 | 2021 |
| Single-cell analyses define a continuum of cell state and composition changes in the malignant transformation of polyps to colorectal cancer WR Becker, SA Nevins, DC Chen, R Chiu, AM Horning, TK Guha, ... Nature genetics 54 (7), 985-995, 2022 | 172 | 2022 |
| Organization of the human intestine at single-cell resolution JW Hickey, WR Becker, SA Nevins, A Horning, AE Perez, C Zhu, B Zhu, ... Nature 619 (7970), 572-584, 2023 | 148 | 2023 |
| Perinatal features of the RASopathies: Noonan syndrome, cardiofaciocutaneous syndrome and Costello syndrome A Myers, JA Bernstein, ML Brennan, C Curry, ED Esplin, J Fisher, ... American journal of medical genetics Part A 164 (11), 2814-2821, 2014 | 125 | 2014 |
| Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy R Truty, N Patil, R Sankar, J Sullivan, J Millichap, G Carvill, A Entezam, ... Epilepsia open 4 (3), 397-408, 2019 | 124 | 2019 |
| Personalized sequencing and the future of medicine: discovery, diagnosis and defeat of disease ED Esplin, L Oei, MP Snyder Pharmacogenomics 15 (14), 1771-1790, 2014 | 109 | 2014 |
| Yield and utility of germline testing following tumor sequencing in patients with cancer SE Lincoln, RL Nussbaum, AW Kurian, SM Nielsen, K Das, S Michalski, ... JAMA Network Open 3 (10), e2019452-e2019452, 2020 | 108 | 2020 |
| Underdiagnosis of hereditary breast and ovarian cancer in Medicare patients: genetic testing criteria miss the mark S Yang, JE Axilbund, E O’Leary, ST Michalski, R Evans, SE Lincoln, ... Annals of surgical oncology 25, 2925-2931, 2018 | 92 | 2018 |
| Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG) MM Li, E Chao, ED Esplin, DT Miller, KL Nathanson, SE Plon, ... Genetics in medicine 22 (7), 1142-1148, 2020 | 84 | 2020 |
| Addressing underrepresentation in genomics research through community engagement AA Lemke, ED Esplin, AJ Goldenberg, C Gonzaga-Jauregui, ... The American Journal of Human Genetics 109 (9), 1563-1571, 2022 | 77 | 2022 |
| Germline genetic testing after cancer diagnosis AW Kurian, P Abrahamse, A Furgal, KC Ward, AS Hamilton, R Hodan, ... Jama 330 (1), 43-51, 2023 | 75 | 2023 |
| Expanded gene panel use for women with breast cancer: identification and intervention beyond breast cancer risk E O’leary, D Iacoboni, J Holle, ST Michalski, ED Esplin, S Yang, K Ouyang Annals of surgical oncology 24, 3060-3066, 2017 | 75 | 2017 |
| Returning integrated genomic risk and clinical recommendations: The eMERGE study JE Linder, A Allworth, HT Bland, PJ Caraballo, RL Chisholm, EW Clayton, ... Genetics in Medicine 25 (4), 100006, 2023 | 71 | 2023 |
| Germline cancer susceptibility gene testing in unselected patients with colorectal adenocarcinoma: a multicenter prospective study PLS Uson Jr, D Riegert-Johnson, L Boardman, J Kisiel, L Mountjoy, ... Clinical Gastroenterology and Hepatology 20 (3), e508-e528, 2022 | 71 | 2022 |
| Prevalence of pathogenic germline cancer risk variants in high-risk urothelial carcinoma AH Nassar, S Abou Alaiwi, SH AlDubayan, N Moore, KW Mouw, ... Genetics in Medicine 22 (4), 709-718, 2020 | 65 | 2020 |
