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| The tuberous sclerosis complex PB Crino, KL Nathanson, EP Henske New England Journal of Medicine 355 (13), 1345-1356, 2006 | 2035 | 2006 |
| Identification of the Tuberous Sclerosis Gene TSC1 on Chromosome 9q34 M Slegtenhorst, R Hoogt, C Hermans, M Nellist, B Janssen, S Verhoef, ... Science 277 (5327), 805-808, 1997 | 1895 | 1997 |
| Tuberous sclerosis complex diagnostic criteria update: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference H Northrup, DA Krueger, S Roberds, K Smith, J Sampson, B Korf, ... Pediatric neurology 49 (4), 243-254, 2013 | 1579 | 2013 |
| HEF1-dependent Aurora A activation induces disassembly of the primary cilium EN Pugacheva, SA Jablonski, TR Hartman, EP Henske, EA Golemis Cell 129 (7), 1351-1363, 2007 | 955 | 2007 |
| Tuberous sclerosis complex surveillance and management: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference DA Krueger, H Northrup, S Roberds, K Smith, J Sampson, B Korf, ... Pediatric neurology 49 (4), 255-265, 2013 | 889 | 2013 |
| The cancer genome atlas comprehensive molecular characterization of renal cell carcinoma CJ Ricketts, AA De Cubas, H Fan, CC Smith, M Lang, E Reznik, R Bowlby, ... Cell reports 23 (1), 313-326. e5, 2018 | 815 | 2018 |
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| Mutations in the tuberous sclerosis complex gene TSC2 are a cause of sporadic pulmonary lymphangioleiomyomatosis T Carsillo, A Astrinidis, EP Henske Proceedings of the National Academy of Sciences 97 (11), 6085-6090, 2000 | 747 | 2000 |
| The mTORC1 pathway stimulates glutamine metabolism and cell proliferation by repressing SIRT4 A Csibi, SM Fendt, C Li, G Poulogiannis, AY Choo, DJ Chapski, SM Jeong, ... Cell 153 (4), 840-854, 2013 | 658 | 2013 |
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| Tuberous sclerosis complex EP Henske, S Jóźwiak, JC Kingswood, JR Sampson, EA Thiele Nature reviews Disease primers 2 (1), 1-18, 2016 | 571 | 2016 |
| A pan-cancer proteogenomic atlas of PI3K/AKT/mTOR pathway alterations Y Zhang, PKS Ng, M Kucherlapati, F Chen, Y Liu, YH Tsang, ... Cancer cell 31 (6), 820-832. e3, 2017 | 511 | 2017 |
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| Evidence that lymphangiomyomatosis is caused by TSC2 mutations: chromosome 16p13 loss of heterozygosity in angiomyolipomas and lymph nodes from women with lymphangiomyomatosis TA Smolarek, LL Wessner, FX McCormack, JC Mylet, AG Menon, ... The American Journal of Human Genetics 62 (4), 810-815, 1998 | 358 | 1998 |
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| Lymphangioleiomyomatosis—a wolf in sheep’s clothing EP Henske, FX McCormack The Journal of clinical investigation 122 (11), 3807-3816, 2012 | 337 | 2012 |
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| Apparent renal cell carcinomas in tuberous sclerosis are heterogeneous: the identification of malignant epithelioid angiomyolipoma M Pea, F Bonetti, G Martignoni, EP Henske, E Manfrin, C Colato, ... The American journal of surgical pathology 22 (2), 180-187, 1998 | 323 | 1998 |
| Hamartin, the Product of the Tuberous Sclerosis 1 (TSC1) Gene, Interacts with Tuberin and Appears to Be Localized to Cytoplasmic Vesicles TL Plank, RS Yeung, EP Henske Cancer research 58 (21), 4766-4770, 1998 | 316 | 1998 |
