The DOI matches its Crossref record; 98 of the 98 references it cites were found in a registry or an index.
The Tuberous Sclerosis Complex
Abstract
The tuberous sclerosis complex (TSC), a multisystem, autosomal dominant disorder affecting children and adults, results from mutations in one of two genes, TSC1 (encoding hamartin) or TSC2 (encoding tuberin). In this article, the current knowledge of the pathogenesis of the disease and its management are discussed.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Tuberous sclerosis complex (TSC) is a genetic neurodevelopmental disorder characterized by focal brain malformations called cortical tubers, which are associated with severe, intractable epilepsy1.”
From mTORC1 drives cell-autonomous astrocyte reactivity in tuberous sclerosis (2026) · cites this paper as [1]
In the citing paper
“TSC leads to hamartomas in several organs and a constellation of neurological and psychiatric conditions, including severe, early-onset epilepsy1.”
From mTORC1 drives cell-autonomous astrocyte reactivity in tuberous sclerosis (2026) · cites this paper as [1]
Citations
Cites
1 retracted
Dan, H. C., Sun, M., Yang, L., Feldman, R. I., Sui, X.-M., Ou, C. C., Nellist, M. D., Yeung, R. S. W., Halley, D. J. J., Nicosia, S. V., et al. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m205838200 · Cited by 370
RetractedMutation and cancer: statistical study of retinoblastoma
Knudson, A. G. (1971) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.68.4.820 · Cited by 7,612
TSC2 Mediates Cellular Energy Response to Control Cell Growth and Survival
Inoki, K., Zhu, T., & Guan, K.-L. (2003) · Cell · doi:10.1016/s0092-8674(03)00929-2 · Cited by 3,914
Rheb GTPase is a direct target of TSC2 GAP activity and regulates mTOR signaling
Inoki, K., Li, Y., Xu, T., & Guan, K.-L. (2003) · Genes & Development · doi:10.1101/gad.1110003 · Cited by 1,911
Identification of the Tuberous Sclerosis Gene TSC1 on Chromosome 9q34
Slegtenhorst, M. V., Hoogt, R. D., Hermans, C., Nellist, M., Janssen, B., Verhoef, S., Lindhout, D., Ouweland, A. V. D., Halley, D., Young, J., et al. (1997) · Science · doi:10.1126/science.277.5327.805 · Cited by 1,648
Self-citationIdentification and characterization of the tuberous sclerosis gene on chromosome 16
(1993) · Cell · doi:10.1016/0092-8674(93)90618-z · Cited by 1,645
Manning, B. D., Tee, A. R., Logsdon, M. N., Blenis, J., & Cantley, L. C. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00568-3 · Cited by 1,555
Phosphorylation and Functional Inactivation of TSC2 by Erk
Ma, L., Chen, Z., Erdjument-Bromage, H., Tempst, P., & Pandolfi, P. P. (2005) · Cell · doi:10.1016/j.cell.2005.02.031 · Cited by 1,268
Fingar, D. C., & Blenis, J. (2004) · Oncogene · doi:10.1038/sj.onc.1207542 · Cited by 1,264
The LKB1 tumor suppressor negatively regulates mTOR signaling
Shaw, R. J., Bardeesy, N. M., Manning, B. D., Lopez, L. V., Kosmatka, M., DePinho, R. A., & Cantley, L. C. (2004) · Cancer Cell · doi:10.1016/j.ccr.2004.06.007 · Cited by 1,107
Research works printed but not linked: 7
- Bourneville DM, 1880, Arch Neurol (Paris), 1, 81
- Bjornsson J, 1996, Am J Pathol, 149, 1201
- Henske EP, 1996, Am J Hum Genet, 59, 400
- Plank TL, 1998, Cancer Res, 58, 4766
- Plank TL, 1999, Mod Pathol, 12, 539
- Wienecke R, 1996, Oncogene, 13, 913
- Liu MY, 2002, Cancer Res, 62, 6475
Cited by
Sorted by citations
Items 301–400 of 1,001
Epilepsy in TSC : Certain etiology does not mean certain prognosis
Vignoli, A., Briola, F. L., Turner, K., Scornavacca, G. F., Chiesa, V., Zambrelli, E., Piazzini, A., Savini, M. N., Alfano, R. M., & Canevini, M. P. (2013) · Epilepsia · doi:10.1111/epi.12430 · Cited by 77
Brain lesions in tuberous sclerosis complex. Review.
Grajkowska, W., Kotulska, K., Jurkiewicz, E., & Matyja, E. (2010) · PubMed · Cited by 77
Therapeutic role of mammalian target of rapamycin (mTOR) inhibition in preventing epileptogenesis
McDaniel, S. S., & Wong, M. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.02.037 · Cited by 78
Culotta, L., & Penzes, P. (2020) · Molecular Autism · doi:10.1186/s13229-020-00339-0 · Cited by 83
Ral GTPases: crucial mediators of exocytosis and tumourigenesis
Shirakawa, R., & Horiuchi, H. (2015) · Journal of Biochemistry · doi:10.1093/jb/mvv029 · Cited by 76
Vagus nerve stimulation for intractable epilepsy in tuberous sclerosis complex
Major, P., & Thiele, E. A. (2008) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2008.04.001 · Cited by 75
Comprehensive Imaging Manifestations of Tuberous Sclerosis
Manoukian, S. B., & Kowal, D. J. (2015) · American Journal of Roentgenology · doi:10.2214/ajr.13.12235 · Cited by 74
Renal angiomyolipoma without visible fat: Can we make the diagnosis using CT and MRI?
Lim, R. S., Flood, T. A., McInnes, M. D. F., Lavallée, L. T., & Schieda, N. (2017) · European Radiology · doi:10.1007/s00330-017-4988-4 · Cited by 74
Hassanian, S. M., Dinarvand, P., Smith, S. A., & Rezaie, A. R. (2015) · Journal of Thrombosis and Haemostasis · doi:10.1111/jth.12899 · Cited by 72
Impaired Language Pathways in Tuberous Sclerosis Complex Patients with Autism Spectrum Disorders
Angeles, W. W. L.-D. L., Şahin, M., Scherrer, B., Peters, J. M., Suarez, R. O., Vogel‐Farley, V. K., Jeste, S., Gregas, M., Prabhu, S. P., Nelson, C. A., et al. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs135 · Cited by 74
Lee, N. Y., Woodrum, C., Nobil, A. M., Rauktys, A., Messina, M. P., & Dabora, S. L. (2009) · BMC Pharmacology · doi:10.1186/1471-2210-9-8 · Cited by 72
Sunitinib resistance in renal cell carcinoma
Morais, C. (2014) · Journal of Kidney Cancer and VHL · doi:10.15586/jkcvhl.2014.7 · Cited by 70
Bergmann, C. (2011) · European Journal of Pediatrics · doi:10.1007/s00431-011-1553-z · Cited by 73
A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes
Scollon, S., Anglin, A. K., Thomas, M. H., Turner, J. T., & Schneider, K. W. (2017) · Journal of Genetic Counseling · doi:10.1007/s10897-017-0077-8 · Cited by 72
Long-term outcomes of epilepsy surgery in tuberous sclerosis complex
Liang, S., Zhang, J., Yang, Z., Zhang, S., Cui, Z., Cui, J., Zhang, J., Liu, N., & Ding, P. (2017) · Journal of Neurology · doi:10.1007/s00415-017-8507-y · Cited by 73
Liu, H.-J., Lizotte, P. H., Du, H., Speranza, M. C., Lam, H. C., Vaughan, S. W., Alesi, N., Wong, K., Freeman, G. J., Sharpe, A. H., et al. (2018) · JCI Insight · doi:10.1172/jci.insight.98674 · Cited by 73
Self-citationRenal manifestation of tuberous sclerosis complex
Bissler, J. J., & Kingswood, J. C. (2018) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.31654 · Cited by 73
Vascular involvement in tuberous sclerosis
Salerno, A. E., Marsenić, O., Meyers, K. E. C., Kaplan, B. S., & Hellinger, J. C. (2010) · Pediatric Nephrology · doi:10.1007/s00467-010-1466-5 · Cited by 70
Prospects for mTOR-mediated functional repair after central nervous system trauma
Berry, M., Ahmed, Z., Morgan-Warren, P. J., Fulton, D. J., & Logan, A. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.10.002 · Cited by 67
Ehninger, D. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.05.015 · Cited by 68
mTOR Signaling in Autophagy Regulation in the Kidney
Inoki, K. (2013) · Seminars in Nephrology · doi:10.1016/j.semnephrol.2013.11.002 · Cited by 71
Everolimus alters white matter diffusion in tuberous sclerosis complex
Tillema, J., Leach, J. L., Krueger, D. A., & Franz, D. N. (2012) · Neurology · doi:10.1212/wnl.0b013e318247ca8d · Cited by 69
Alfaiz, A. A., Micale, L., Mandriani, B., Augello, B., Pellico, M. T., Chrast, J., Xénarios, I., Zelante, L., Merla, G., & Reymond, A. (2014) · Human Mutation · doi:10.1002/humu.22529 · Cited by 69
Magers, M. J., Udager, A. M., & Mehra, R. (2015) · Archives of Pathology & Laboratory Medicine · doi:10.5858/arpa.2015-0196-ra · Cited by 69
Sun, S., Chen, S., Liu, F., Wu, H., McHugh, J. B., Bergin, I. L., Gupta, A., Adams, D. M., & Guan, J. (2015) · Cancer Cell · doi:10.1016/j.ccell.2015.10.004 · Cited by 69
Ophthalmic manifestations of tuberous sclerosis: a review
Hodgson, N. M., Kinori, M., Goldbaum, M. H., & Robbins, S. L. (2016) · Clinical and Experimental Ophthalmology · doi:10.1111/ceo.12806 · Cited by 69
Current Approaches and Future Directions for the Treatment of mTORopathies
Karalis, V., & Bateup, H. S. (2021) · Developmental Neuroscience · doi:10.1159/000515672 · Cited by 67
Yu, J. J., & Henske, E. P. (2010) · Lymphatic Research and Biology · doi:10.1089/lrb.2009.0020 · Cited by 68
Self-citationSpecific Killing of Rb Mutant Cancer Cells by Inactivating TSC2
Li, B., Gordon, G. M., Du, C. H., Xu, J., & Du, W. (2010) · Cancer Cell · doi:10.1016/j.ccr.2010.03.019 · Cited by 68
Characterization of the Intrinsic and TSC2-GAP–Regulated GTPase Activity of Rheb by Real-Time NMR
Marshall, C. B., Ho, J., Buerger, C., Plevin, M. J., Li, G., Li, Z., Ikura, M., & Stambolic, V. (2009) · Science Signaling · doi:10.1126/scisignal.2000029 · Cited by 70
Pema, M., Drusian, L., Chiaravalli, M., Castelli, M., Yao, Q., Ricciardi, S., Somlo, S., Qian, F., Biffo, S., & Boletta, A. (2016) · Nature Communications · doi:10.1038/ncomms10786 · Cited by 70
Smooth Muscle–like Cells in Pulmonary Lymphangioleiomyomatosis
Krymskaya, V. P. (2007) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200705-061vs · Cited by 69
Matthew, E. M., Hart, L. S., Astrinidis, A., Navaraj, A., Dolloff, N. G., Dicker, D. T., Henske, E. P., & El-Deiry, W. S. (2009) · Cell Cycle · doi:10.4161/cc.8.24.10800 · Cited by 67
Self-citationMartín‐Pérez, R., Palacios, C., Yerbes, R., Cano-González, A., Iglesias‐Serret, D., Gil, J., Reginato, M. J., & López‐Rivas, A. (2014) · Cancer Research · doi:10.1158/0008-5472.can-13-1747 · Cited by 68
Tuberous sclerosis complex: the past and the future
Waele, L. D., Lagae, L. G., & Mekahli, D. (2014) · Pediatric Nephrology · doi:10.1007/s00467-014-3027-9 · Cited by 67
Li, C., Lee, P., Sun, Y., Gu, X., Zhang, E. Y., Guo, Y., Wu, C., Auricchio, N., Priolo, C., Li, J., et al. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20131080 · Cited by 67
Self-citationTuberous sclerosis complex: Recent advances in manifestations and therapy
Wataya‐Kaneda, M., Uemura, M., Fujita, K., Hirata, H., Osuga, K., Kagitani‐Shimono, K., & Nonomura, N. (2017) · International Journal of Urology · doi:10.1111/iju.13390 · Cited by 69
Emerging Treatments in the Management of Tuberous Sclerosis Complex
Kohrman, M. H. (2012) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2012.02.015 · Cited by 66
Rosilio, C., Lounnas, N., Nebout, M., Imbert, V., Hagenbeek, T. J., Spits, H., Asnafi, V., Pontier-Bres, R., Reverso, J., Michiels, J., et al. (2013) · Cancer Letters · doi:10.1016/j.canlet.2013.04.015 · Cited by 70
Jacob‐Hirsch, J., Eyal, E., Knisbacher, B. A., Roth, J. F., Cesarkas, K., Dor, C., Barhom, S. F., Kunik, V., Simon, A. J., Gal, M., et al. (2018) · Cell Research · doi:10.1038/cr.2018.8 · Cited by 72
Loss of the tuberous sclerosis complex protein tuberin causes Purkinje cell degeneration
Reith, R. M., Way, S., McKenna, J., Haines, K., & Gambello, M. J. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.02.014 · Cited by 65
Increased risk of solid renal tumors in lithium-treated patients
Zaidan, M., Stucker, F., Stengel, B., Vasiliu, V., Hummel, A., Landais, P., Boffa, J., Ronco, P. M., Grünfeld, J., & Servais, A. (2014) · Kidney International · doi:10.1038/ki.2014.2 · Cited by 67
Acral lesions in tuberous sclerosis complex: Insights into pathogenesis
Cs, A., Hong, C., Groves, L., Olsen, C. H., Moss, J., & Darling, T. N. (2010) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2009.08.042 · Cited by 65
Biology of human melanocyte development, Piebaldism, and Waardenburg syndrome
Saleem, M. D. (2018) · Pediatric Dermatology · doi:10.1111/pde.13713 · Cited by 65
Targeted treatment trials for tuberous sclerosis and autism: no longer a dream
Şahin, M. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.04.008 · Cited by 66
Moon, U. Y., Park, J. Y., Park, R., Cho, J. Y., Hughes, L. J., McKenna, J., Goetzl, L. M., Cho, S., Crino, P. B., Gambello, M. J., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.07.013 · Cited by 69
Self-citationThe Natural History and Treatment of Epilepsy in a Murine Model of Tuberous Sclerosis
Altay, E. E., Zeng, L., Xu, L., Gutmann, D. H., & Wong, M. (2007) · Epilepsia · doi:10.1111/j.1528-1167.2007.01110.x · Cited by 64
Pollizzi, K. N., Malinowska-Kołodziej, I., Stumm, M., Lane, H. A., & Kwiatkowski, D. J. (2009) · Molecular Cancer · doi:10.1186/1476-4598-8-38 · Cited by 64
Epilepsy in Tuberous Sclerosis: Phenotypes, Mechanisms, and Treatments
Sampson, J. R., & Saxena, A. (2015) · Seminars in Neurology · doi:10.1055/s-0035-1552616 · Cited by 65
Auvin, S., Bissler, J. J., Cottin, V., Fujimoto, A., Hofbauer, G. F. L., Jansen, A., Jóźwiak, S., Kerecuk, L., Kingswood, J. C., Moavero, R., et al. (2019) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-019-1072-y · Cited by 65
Update on Drug Management of Refractory Epilepsy in Tuberous Sclerosis Complex
Clement, E. A. V. D. P., Jansen, F. E., Braun, K. P. J., & Peters, J. M. (2020) · Pediatric Drugs · doi:10.1007/s40272-019-00376-0 · Cited by 63
Karbowniczek, M., Zitserman, D., Khabibullin, D., Hartman, T. R., Yu, J. J., Morrison, T. A., Nicolas, É., Squillace, R. M., Roegiers, F., & Henske, E. P. (2010) · Journal of Clinical Investigation · doi:10.1172/jci40221 · Cited by 59
Self-citationKocabaş, A., Ekici, F., Çetin, İ. İ., Emir, S., Demir, H. A., Arı, M. E., Değerli̇yurt, A., & Güven, A. (2012) · Pediatric Hematology and Oncology · doi:10.3109/08880018.2012.734896 · Cited by 63
Lee, P., Tsang, S. W., Moses, M. A., Trayes-Gibson, Z., Hsiao, L., Jensen, R. V., Squillace, R. M., & Kwiatkowski, D. J. (2009) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2009-0050oc · Cited by 61
Decanoic acid inhibits mTORC1 activity independent of glucose and insulin signaling
Warren, E. C., Dooves, S., Lugarà, E., Damstra‐Oddy, J., Schaf, J., Heine, V. M., Walker, M. C., & Williams, R. S. B. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2008980117 · Cited by 66
Kingswood, J. C., Belousova, E., Benedik, M. P., Carter, T., Cottin, V., Curatolo, P., Dahlin, M. G., D’Amato, L., d’Augères, G. B., de Vries, P. J., et al. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00972 · Cited by 62
Diffusion Features of White Matter in Tuberous Sclerosis With Tractography
Krishnan, M. L., Commowick, O., Jeste, S., Weisenfeld, N., Hans, A., Gregas, M. C., Şahin, M., & Warfield, S. K. (2010) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2009.08.001 · Cited by 64
Domańska‐Pakieła, D., Kaczorowska, M., Jurkiewicz, E., Kotulska, K., Dunin-Wąsowicz, D., & Jóźwiak, S. (2014) · European Journal of Paediatric Neurology · doi:10.1016/j.ejpn.2013.12.006 · Cited by 62
Kim, S.-H., Speirs, C. K., Solnica‐Krezel, L., & Ess, K. C. (2010) · Disease Models & Mechanisms · doi:10.1242/dmm.005587 · Cited by 61
Intracellular signalling during female gametogenesis
Sobinoff, A. P., Sutherland, J. M., & McLaughlin, E. A. (2012) · Molecular Human Reproduction · doi:10.1093/molehr/gas065 · Cited by 65
Franz, D. N., & Capal, J. K. (2017) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-017-0596-2 · Cited by 62
Brain Organoids as Tools for Modeling Human Neurodevelopmental Disorders
Adams, J. W., Cugola, F. R., & Muotri, A. R. (2019) · Physiology · doi:10.1152/physiol.00005.2019 · Cited by 68
Genetic and morphologic determinants of pneumothorax in lymphangioleiomyomatosis
Steagall, W. K., Glasgow, C. G., Hathaway, O. M., Avila, N. A., Taveira‐DaSilva, A. M., Rabel, A., Stylianou, M. P., Lin, J., Chen, X., & Moss, J. (2007) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00176.2007 · Cited by 62
The Tuberous Sclerosis Complex
(2007) · New England Journal of Medicine · doi:10.1056/nejmc062928 · Cited by 41
Sun, P., Kohrman, M. H., Liu, J., Guo, A., Rogerio, J. W., & Krueger, D. A. (2012) · Current Medical Research and Opinion · doi:10.1185/03007995.2012.658907 · Cited by 61
Zhang, L., Bartley, C. M., Gong, X., Hsieh, L. S., Lin, T. V., Feliciano, D. M., & Bordey, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.09.009 · Cited by 62
Fishwick, K. J., Li, R. A., Halley, P. A., Deng, P., & Storey, K. G. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.12.001 · Cited by 65
Homberg, J. R., Kyzar, E. J., Scattoni, M. L., Norton, W., Pittman, J. T., Gaikwad, S., Nguyen, M., Poudel, M. K., Ullmann, J. F. P., Diamond, D. M., et al. (2016) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.04.015 · Cited by 67
mTOR in health and in sickness
Liko, D., & Hall, M. N. (2015) · Journal of Molecular Medicine · doi:10.1007/s00109-015-1326-7 · Cited by 60
Metformin: A metabolic disruptor and anti-diabetic drug to target human leukemia
Rosilio, C., Ben‐Sahra, I., Bost, F., & Peyron, J. (2014) · Cancer Letters · doi:10.1016/j.canlet.2014.01.006 · Cited by 63
Pacheco–Rodriguez, G., Kumaki, F., Steagall, W. K., Zhang, Y., Ikeda, Y., Lin, J., Billings, E. M., & Moss, J. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.182.3.1270 · Cited by 62
Current Management of Tuberous Sclerosis Complex
Krueger, D., & Franz, D. (2008) · Paediatric drugs · doi:10.2165/00148581-200810050-00004 · Cited by 68
Inflammatory mechanisms contribute to the neurological manifestations of tuberous sclerosis complex
Zhang, B., Zou, J., Rensing, N. R., Yang, M., & Wong, M. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.04.016 · Cited by 61
Neuropsychological attention deficits in tuberous sclerosis complex (TSC)
de Vries, P. J., GARDINER, J. S., & Bolton, P. (2009) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.32690 · Cited by 59
Rüegg, S. J., Baybis, M., Juul, H., Dichter, M. A., & Crino, P. B. (2007) · Epilepsy Research · doi:10.1016/j.eplepsyres.2007.09.009 · Cited by 59
Self-citationRyther, R. C. C., & Wong, M. (2012) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-012-0276-5 · Cited by 60
Sirolimus and Temsirolimus for Epithelioid Angiomyolipoma
Wolff, N. C., Kabbani, W., Bradley, T. P., Raj, G. V., Watumull, L. M., & Brugarolas, J. (2010) · Journal of Clinical Oncology · doi:10.1200/jco.2009.26.3061 · Cited by 59
Parkhitko, A. A., Priolo, C., Coloff, J. L., Yun, J., Wu, J. J., Mizumura, K., Xu, W., Malinowska, I. A., Yu, J. J., Kwiatkowski, D. J., et al. (2013) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-13-0258-t · Cited by 58
Self-citationFranz, D. N. (2013) · Biologics · doi:10.2147/btt.s25095 · Cited by 59
Molecular Pathways and Therapies in Autosomal-Dominant Polycystic Kidney Disease
Saigusa, T., & Bell, P. D. (2015) · Physiology · doi:10.1152/physiol.00032.2014 · Cited by 60
Long-term High Fat Ketogenic Diet Promotes Renal Tumor Growth in a Rat Model of Tuberous Sclerosis
Liśkiewicz, A., Liśkiewicz, D., Wojakowska, A., Polański, K., Lewin‐Kowalik, J., Kotulska, K., & Jędrzejowska–Szypułka, H. (2016) · Scientific Reports · doi:10.1038/srep21807 · Cited by 58
Jiang, M., Liu, L., He, X., Wang, H., Lin, W., Wang, H., Yoon, S. O., Wood, T. L., & Lu, Q. R. (2016) · Nature Communications · doi:10.1038/ncomms12185 · Cited by 59
Cutaneous manifestations of tuberous sclerosis complex and the paediatrician's role
Cardis, M. A., & DeKlotz, C. M. C. (2017) · Archives of Disease in Childhood · doi:10.1136/archdischild-2016-312001 · Cited by 59
Molecular Therapies for Tuberous Sclerosis and Neurofibromatosis
Franz, D. N., & Weiss, B. D. (2012) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-012-0269-4 · Cited by 58
Tuberous Sclerosis: Current Update
Wang, M. X., Segaran, N. L., Bhalla, S., Pickhardt, P. J., Lubner, M. G., Katabathina, V. S., & Ganeshan, D. (2021) · Radiographics · doi:10.1148/rg.2021210103 · Cited by 58
TFEB drives mTORC1 hyperactivation and kidney disease in Tuberous Sclerosis Complex
Alesi, N., Khabibullin, D., Rosenthal, D. M., Akl, E. W., Cory, P. M., Alchoueiry, M., Salem, S., Daou, M., Gibbons, W. F., Chen, J. A., et al. (2024) · Nature Communications · doi:10.1038/s41467-023-44229-4 · Cited by 61
Self-citationA Case of Solitary Subependymal Giant Cell Astrocytoma
Ichikawa, T., Wakisaka, A., Daido, S., Takao, S., Tamiya, T., Date, I., Koizumi, S., & Niida, Y. (2005) · Journal of Molecular Diagnostics · doi:10.1016/s1525-1578(10)60586-7 · Cited by 58
Mlczoch, E., Hanslik, A., Luckner, D., Kitzmüller, E., Prayer, D., & Michel‐Behnke, I. (2014) · Ultrasound in Obstetrics and Gynecology · doi:10.1002/uog.13434 · Cited by 58
Nervous system involvement in von Hippel–Lindau disease: pathology and mechanisms
Vortmeyer, A. O., Falke, E., Gläsker, S., Li, J., & Oldfield, E. H. (2013) · Acta Neuropathologica · doi:10.1007/s00401-013-1091-z · Cited by 57
Successful treatment of angiofibromata of tuberous sclerosis complex with rapamycin
McNamara, E. K., Curtis, A. R., & Fleischer, A. B. (2010) · Journal of Dermatological Treatment · doi:10.3109/09546634.2010.489598 · Cited by 58
Hasbani, D. M., & Crino, P. B. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64076-5.00052-1 · Cited by 58
Self-citationBissler, J. J., Budde, K., Sauter, M., Franz, D. N., Zonnenberg, B. A., Frost, M., Белоусова, Е. Д., Berkowitz, N. C., Ridolfi, A., & Kingswood, J. C. (2018) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfy132 · Cited by 58
Li, H., Liu, P., Li, D., Wang, Z., Ding, Z., Zhou, M., Chen, X., Miao, M., Ding, J., Lin, W., et al. (2022) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-022-02513-z · Cited by 57
Neuhaus, A. A., Rabie, T., Sutherland, B. A., Papadakis, M., Hadley, G., Cai, R., & Buchan, A. M. (2014) · JAMA Neurology · doi:10.1001/jamaneurol.2013.6299 · Cited by 57
Shima, A., Nitta, N., Suzuki, F., Laharie, A., Nozaki, K., & Depaulis, A. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12835 · Cited by 57
Role of LKB1 in lung cancer development
Makowski, L., & Hayes, D. N. (2008) · British Journal of Cancer · doi:10.1038/sj.bjc.6604515 · Cited by 59
Tuberous sclerosis complex inactivation disrupts melanogenesis via mTORC1 activation
Cao, J., Tyburczy, M. E., Moss, J., Darling, T. N., Widlund, H. R., & Kwiatkowski, D. J. (2016) · Journal of Clinical Investigation · doi:10.1172/jci84262 · Cited by 57
Arulrajah, S., Ertan, G., Jordan, L. C., Tekes, A., Khaykin, E., Izbudak, I., & Huisman, T. A. G. M. (2009) · Neuroradiology · doi:10.1007/s00234-009-0563-2 · Cited by 57
Graham, R. M., & Cox, N. H. (2004) · Wiley eBooks · doi:10.1002/9780470750520.ch59 · Cited by 55
McMaster, M. L., Goldstein, A. M., & Parry, D. M. (2011) · Journal of Medical Genetics · doi:10.1136/jmg.2010.085092 · Cited by 56
Metadata
- Authors
- Crino, P. B., Nathanson, K. L., & Henske, E. P.
- Affiliations
- University of Pennsylvania Health System (US)
- University of Pennsylvania (US)
- Fox Chase Cancer Center (US)
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2006-09-28
- Volume
- 355
- Issue
- 13
- Pages
- 1345-1356
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2383259826
- Cited by
- 1,793
- References
- 98
- Citations by year
- 2026: 39 · 2025: 61 · 2024: 73 · 2023: 61 · 2022: 79 · 2021: 96 · 2020: 94 · 2019: 67 · 2018: 95 · 2017: 101 · 2016: 102 · 2015: 109 · 2014: 119 · 2013: 146 · 2012: 129
- FWCI
- 7.94
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL60746, R01HL060746)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK-51052)
- National Institute of Neurological Disorders and Stroke (NS045021, R01NS045021)
- Topics
- Health Sciences › Medicine › Genetics (clinical) › Tuberous Sclerosis Complex Research
- Health Sciences › Medicine › Dermatology › Genetic and rare skin diseases.
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Keywords
- tuberous sclerosis complex, TSC1, hamartin, TSC2, tuberin, autosomal dominant disorder, pathogenesis, disease management, multisystem disease
- MeSH terms
- Tuberous Sclerosis Complex 1 Protein, Tuberous Sclerosis Complex 2 Protein, Estrogens, Female, Humans, Genetic Linkage, Male, Mutation, Protein Kinases, Tuberous Sclerosis, Signal Transduction, Tumor Suppressor Proteins, TOR Serine-Threonine Kinases
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review