 Age of Onset
"Age of Onset" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The age, developmental stage, or period of life at which a disease or the initial symptoms or manifestations of a disease appear in an individual.
| Descriptor ID |
D017668
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| MeSH Number(s) |
N05.715.350.075.100 N06.850.490.250.100
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Age of Onset".
Below are MeSH descriptors whose meaning is more specific than "Age of Onset".
This graph shows the total number of publications written about "Age of Onset" by people in this website by year, and whether "Age of Onset" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 4 | 4 | | 1997 | 0 | 2 | 2 | | 1998 | 0 | 3 | 3 | | 1999 | 0 | 4 | 4 | | 2000 | 0 | 4 | 4 | | 2001 | 0 | 4 | 4 | | 2002 | 0 | 6 | 6 | | 2003 | 0 | 9 | 9 | | 2004 | 0 | 8 | 8 | | 2005 | 1 | 11 | 12 | | 2006 | 1 | 11 | 12 | | 2007 | 0 | 14 | 14 | | 2008 | 0 | 18 | 18 | | 2009 | 1 | 15 | 16 | | 2010 | 1 | 10 | 11 | | 2011 | 0 | 12 | 12 | | 2012 | 1 | 21 | 22 | | 2013 | 0 | 14 | 14 | | 2014 | 0 | 17 | 17 | | 2015 | 0 | 20 | 20 | | 2016 | 0 | 12 | 12 | | 2017 | 1 | 10 | 11 | | 2018 | 2 | 28 | 30 | | 2019 | 3 | 14 | 17 | | 2020 | 0 | 32 | 32 | | 2021 | 1 | 12 | 13 | | 2022 | 1 | 7 | 8 | | 2023 | 0 | 5 | 5 | | 2024 | 1 | 8 | 9 | | 2025 | 0 | 20 | 20 | | 2026 | 0 | 2 | 2 |
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Below are the most recent publications written about "Age of Onset" by people in Profiles.
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Vollenbrock CE, Roshandel D, Lee KE, Klein BE, Mul D, van der Klauw MM, Tack CJ, Rewers M, Snell-Bergeon JK, Costacou T, Miller RG, Caramori ML, Mauer M, Aanstoot HJ, Wolffenbuttel BHR, Paterson AD. Association of genetic variation with age at diagnosis in type 1 diabetes. BMJ Open Diabetes Res Care. 2026 Jan 16; 14(1).
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Lopriore P, Ünlütürk Z, Klopstock T, Karaa A, Rouzier C, Domínguez-González C, Lamperti C, Mancuso M, Cecchi G, Montano V, Siciliano G, Nicoletta V, Maioli M, Primiano G, Servidei S, La Morgia C, Carelli V, Valentino ML, Caporali L, Arena IG, Musumeci O, Lopergolo D, Malandrini A, Gallus GN, Filosto M, Bello L, Pegoraro E, Comi GP, Magri F, Ronchi D, Di Fonzo A, Percetti M, Azzimonti M, Büchner B, Prokisch H, Bermejo-Guerrero L, Procaccio V, Gaignard P, Echaniz-Laguna A, Schiff M, Rötig A, Toutain A, Paquis-Flucklinger V, Morel G, Robin S, Nadaj-Pakleza A, Chanson JB, Chaussenot A, Ait-El-Mkadem Saadi S, Trimouille A, Tranchant C, Salort-Campana E, Bieth E, Sacconi S, Duval F, Restrepo Vera JL, Molnar MJ, Vissing J, Haas R, Larson A, Enns GM, Parikh S, Goldstein A, Hirano M. Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study. Neurology. 2026 Feb 10; 106(3):e214401.
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Abbott M, Angione K, Stringfellow M, Malik K, Saenz M, Miele A, Syverson K, Maniar B, Borello J, Chaby L, Demarest S. Evaluation of epilepsy in 8p-related disorders. Epilepsy Res. 2026 Feb; 220:107720.
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Johnson R, Fletcher RA, Peters S, Ohanian M, Soka M, Smolnikov A, Abihider KE, Ackerman MJ, Ader F, Akhtar MM, Amin AS, Ashley EA, Atherton JJ, Austin R, Baas AF, Bagnall RD, Ross SB, Blouin JL, Brown EE, Bundgaard H, Cannie D, Chmielewski P, Correnti G, Crespo-Leiro MG, Dal Ferro M, Dellefave-Castillo LM, Dominguez F, Dooijes D, Dybro AM, Ed Demri Y, El Hachmi M, Escobar-Lopez L, Foye SJ, Franaszczyk M, Gigli M, Lopez EG, Goudal A, Graw S, Guipponi M, Haan E, Haas J, Hammersley DJ, Hansen FG, Hayward CS, Hey TM, Heymans S, Ho CY, Houweling AC, Ingles J, Ingrey A, Jabbour A, James PA, Jansweijer JA, Jongbloed JDH, Keogh AM, Larrañaga-Moreira JM, Lekanne Deprez RH, Macciocca I, Macdonald PS, Mansencal N, Mansour J, Martinez-Veira C, McDonough B, McGaughran J, Medo K, Merlo M, Michalak E, Monserrat L, Mountain H, Muller SA, Murphy AM, Murray B, Oates EC, Ormondroyd E, Pachter N, Paldino A, Palmyre A, Pereira NL, Picard KC, Poplawski N, Prasad S, Proukhnitzky J, Pruny JF, Reant P, Richard P, Ronan A, Sedaghat-Hamedani F, Semsarian C, Storm G, Stroeks S, Syrris P, Taylor MRG, Thomson K, Thompson T, van Tintelen JP, Vissing CR, Waddell-Smith KE, Wallis M, Zentner D, Arnott C, Marian AJ, Oh J, Fokstuen S, James CA, Barriales-Villa R, Meder B, Wahbi K, Giudicessi JR, Parikh VN, Ware JS, Piriou N, Rooryck C, Lakdawala NK, Mestroni L, Sinagra G, Elliott PM, Watkins H, McNally EM, Charron P, van Spaendonck-Zwarts KY, Garcia-Pavia P, Peña-Peña ML, Mogensen J, Christensen AH, Bilinska ZT, Rasmussen TB, Seidman JG, Seidman CE, Te Riele ASJM, Verdonschot JAJ, Pinto YM, Christiaans I, Fatkin D. Titin-related familial dilated cardiomyopathy: factors associated with disease onset. Eur Heart J. 2025 Dec 22; 46(48):5240-5257.
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Hickman J, Tsai A, Fullard M, Korsmo M, Forbes E, Aslam S, Baumgartner AJ, Feuerstein JS, Bayram E. Early-Onset Parkinson's Disease: Unique Features and Management Approaches. Curr Neurol Neurosci Rep. 2025 Dec 18; 26(1):3.
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Dong OX, Ren BO, Sturm P, Garg S, Pahys J, Glotzbecker MP. Children With Presumed Early-Onset Idiopathic Scoliosis and Treated in Cast May Have Delayed Ambulation. J Pediatr Orthop. 2026 Mar 01; 46(3):129-132.
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Yang JH, Race J, Sumowski P, Jacques K, Fardad S, Fair A, Hazlett A, Lin J, Yilmaz D, Aaen G, Abrams A, Benson L, Casper TC, Chitnis T, Gorman M, Lotze T, Krupp L, Mar S, Ness J, Rensel M, Rose J, Schreiner T, Tillema JM, Waldman A, Wheeler Y, Barcellos LF, Waubant E, Graves JS. Epigenetic age and telomere length correlations in pediatric-onset multiple sclerosis. Mult Scler. 2025 Dec; 31(14):1641-1650.
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Lemke JR, Eoli A, Krey I, Popp B, Strehlow V, Wittekind DA, Vuorinen AL, Aldhalaan HM, Baer S, de Saint Martin A, Hammer TB, Herman I, Hornemann F, Ingebrigtsen T, Lederer D, Lesca G, Marafie D, Mathot M, Rosenfeld JA, Møller RS, Schelhaas HJ, Stillman C, Orsini A, Patel AD, Piard J, Veggiotti P, Vlaskamp DRM, Weckhuysen S, Traynelis SF, Benke TA, Heyne HO, Syrbe S. GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy. Mol Psychiatry. 2026 Jan; 31(1):374-382.
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Jinnah HA, Velucci V, Belvisi D, Kilic-Berkmen G, Perlmutter JS, Wright LJ, Klein C, Feuerstein JS, Bellows S, Jankovic J, Comella C, Barbano RL, Wagle Shukla A, Reich SG, LeDoux MS, Espay AJ, Duque KR, Chang FCF, Fung VSC, Pirio-Richardson S, Terranova C, Moukheiber ES, Idrissi S, Vitucci B, Fox SH, Frank S, Stover N, Berman BD, Saunders-Pullman R, Ondo WG, Groth CL, Esposito M, Avanzino L, Bono F, Erro R, Mascia MM, Muroni A, Berardelli A, Defazio G. Segmental and Multifocal Isolated Dystonias: Similarities and Differences. Mov Disord Clin Pract. 2026 Mar; 13(3):748-756.
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Dai J, Chau T, Corrada MM, Manson SM, O'Connell J, Jiang L. Race and Ethnicity and Comorbidities Among Medicare Beneficiaries With Young-Onset Dementia. JAMA Netw Open. 2025 Aug 01; 8(8):e2528001.
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