Genetic Predisposition to Disease
"Genetic Predisposition to Disease" 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.
A latent susceptibility to disease at the genetic level, which may be activated under certain conditions.
| Descriptor ID |
D020022
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| MeSH Number(s) |
C23.550.291.687.500 G05.380.355
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| Concept/Terms |
Genetic Predisposition to Disease- Genetic Predisposition to Disease
- Genetic Susceptibility
- Genetic Susceptibilities
- Susceptibilities, Genetic
- Susceptibility, Genetic
- Genetic Predisposition
- Genetic Predispositions
- Predispositions, Genetic
- Predisposition, Genetic
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Below are MeSH descriptors whose meaning is more general than "Genetic Predisposition to Disease".
Below are MeSH descriptors whose meaning is more specific than "Genetic Predisposition to Disease".
This graph shows the total number of publications written about "Genetic Predisposition to Disease" by people in this website by year, and whether "Genetic Predisposition to Disease" 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 | 1 | 1 | 2 | | 1997 | 1 | 0 | 1 | | 1998 | 1 | 1 | 2 | | 1999 | 3 | 2 | 5 | | 2000 | 8 | 6 | 14 | | 2001 | 7 | 12 | 19 | | 2002 | 13 | 13 | 26 | | 2003 | 12 | 14 | 26 | | 2004 | 17 | 20 | 37 | | 2005 | 21 | 20 | 41 | | 2006 | 25 | 24 | 49 | | 2007 | 19 | 33 | 52 | | 2008 | 27 | 37 | 64 | | 2009 | 25 | 34 | 59 | | 2010 | 31 | 48 | 79 | | 2011 | 27 | 45 | 72 | | 2012 | 25 | 52 | 77 | | 2013 | 37 | 51 | 88 | | 2014 | 32 | 47 | 79 | | 2015 | 37 | 75 | 112 | | 2016 | 30 | 48 | 78 | | 2017 | 43 | 55 | 98 | | 2018 | 28 | 64 | 92 | | 2019 | 43 | 61 | 104 | | 2020 | 19 | 34 | 53 | | 2021 | 25 | 57 | 82 | | 2022 | 9 | 38 | 47 | | 2023 | 5 | 34 | 39 | | 2024 | 18 | 33 | 51 | | 2025 | 20 | 55 | 75 | | 2026 | 12 | 20 | 32 |
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Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
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Perrino MR, MacFarland SP, Maese L, Vagher J, Kamihara J, Rednam S, Lupo PJ, Brodeur GM, Schiffman J, Diller L, Desrosiers-Battu L, Plon SE, Nichols KE, Volchenboum SL, Malkin D, Villani A, Porter CC. Childhood cancer predisposition study: a prospective registry and biorepository protocol. BMJ Open. 2026 08 05; 16(8):e120576.
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Bright U, Beck S, Levey DF, Deak JD, Gaziano JM, Stein MB, Gelernter J. The genetics of fibromyalgia and its relationships to psychiatric and medical traits. Nat Commun. 2026 Jul 28; 17(1).
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Benthal JT, Avila JA, Smith JR, Southard-Smith EM. Combinatorial multiomic analysis from a pedigree of Sox10Dom Hirschsprung mice identifies multiple high confidence candidate modifiers of Enteric Nervous System development. PLoS Comput Biol. 2026 Jul; 22(7):e1014424.
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Melin J, Tamura R, O'Donnell H, Johnson SB. Child and mother study satisfaction in a longitudinal study of children at-risk for type 1 diabetes. BMC Pediatr. 2026 Jul 02; 26(1).
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Peljto AL, Furusawa H, Puthenvedu D, Lee JS, Steele MP, Brancato J, Cardwell J, Blumhagen RZ, de Andrade J, Bendstrup E, Blackwell TS, Bonella F, Borie R, Braybrooke R, Brown KK, Carbone RG, Christie JD, Costabel U, Crestani B, Davidsen JR, Dieude P, Donnelly SC, Egan J, Eickelberg O, Fernández Pérez ER, Fiddler CA, Foster EE, Gibson KF, Gudmundsson G, Guthridge JM, Henry MT, Hirani N, Jenkins RG, Kass DJ, Keane MP, Kokturk N, Kropski JA, Lederer D, Leone PM, Linderholm AL, Maher TM, Mathai SK, McCarthy C, McElroy AN, Mogulkoc N, Molina-Molina M, Molyneaux PL, Montesi SB, Nathan SD, Noth I, Olaniyi JA, Oldham JM, O'Reilly KMA, Palmisciano AJ, Pardo A, Parfrey H, Planas-Cerezales L, Poletti V, Porteous MK, Puppo F, Richeldi L, Rojas M, Salinas M, Schluger N, Selman M, Shea BS, Sterclova M, Solomon JJ, Tomassetti S, Vasakova MK, Zhang Y, Corte TJ, Dickinson JL, Glaspole I, Moodley YP, Prele CMA, Ryerson CJ, Wolters PJ, Jinno M, Miyata Y, Akagawa S, Narumoto O, Kita T, Shibayama T, Li T, Owan I, Wakamatsu K, Arai T, Hirose M, Kim DS, Ohta K, Ohta S, Park JS, Park MS, Yang IV, Fingerlin TE, Miyazaki Y, Okamoto T, Inoue Y, Song JW, Schwartz DA. Idiopathic pulmonary fibrosis risk loci in East Asian populations mirror those of European populations. Am J Respir Crit Care Med. 2026 07 01; 212(7):1522-1532.
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Chiles JW, Rocco A, Srinivasasainagendra V, Rossiter HB, Casaburi R, Thalacker-Mercer A, Wells JM, Wan ES, Silverman EK, Cho MH, Hersh CP, Psaty BM, Gharib SA, Gao Y, O'Connor GT, Lange LA, Rich SS, Manichaikul AW, Barr RG, Ortega VE, Meyers DA, Smith AV, Tiwari HK, McDonald MN. Whole Genome Sequence Analysis of Weight Loss in 16?972 Participants With COPD Reveals Novel Risk Loci in DRAIC and RFX3. J Cachexia Sarcopenia Muscle. 2026 Jun; 17(3):e70293.
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Swetter SM, Johnson D, Albertini MR, Barker CA, Bateni S, Baumgartner J, Bhatia S, Bichakjian C, Boland G, Chandra S, Chen D, Chmielowski B, Choi J, DiMaio D, Dronca R, Fleming MD, Galan A, Guild S, Hu-Lieskovan S, Karakousis G, Kendra K, Kiuru M, Lange JR, Lanning R, Logan T, Materin M, Nelson K, Olson D, Olszanski AJ, Ott PA, Puzanov I, Rothermel L, Salama AK, Shannon A, Sharma R, Singh A, Stacey A, Tsai K, Wuthrick E, Xing Y, McMillian N, Espinosa S. Melanoma: Cutaneous, Version 2.2026, NCCN Clinical Practice Guidelines In Oncology. J Natl Compr Canc Netw. 2026 Jun; 24(6):272-277.
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Stroeks SLVM, Bart NK, Rossano J, Claggett B, Beelen NJ, Buchan RJ, Day S, Fornaro A, Halliday BP, Wheeler MT, Hammersley DJ, Helms A, Heymans ABM, Ho CY, Khan SS, Lin K, Lota A, Merlo M, Mestroni L, Olivotto I, Owens A, Seidman CE, Shore S, Sinnette C, Sinagra G, Stevenson LW, Stewart GC, Theotakis P, Venner MFGHM, Ware JS, Taylor MRG, Verdonschot JAJ, Wilsbacher L, Prasad S, Heymans SR, Parikh VN, Tayal U, Lakdawala NK. Sex and Age Specific Genetic Risk Across the Dilated and Arrhythmogenic Cardiomyopathy Spectrum: Insights From the SHaRe Registry. J Am Coll Cardiol. 2026 Jun 30; 87(25):3573-3588.
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Wang Y, Hennessy C, Dobrinskikh E, Humphries SM, Hatakka K, Ackert-Bicknell CL, Godfrey DA, Kelada SNP, Keele GR, Cardwell J, Peljto A, Clouthier DE, Yang IV, Schwartz DA. Genes, other than Muc5b, are associated with bleomycin-induced lung injury. Commun Biol. 2026 May 12; 9(1).
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Patel SG, Loomans-Kropp HA, Foda ZH, Katona BW, Birz S, Burke CA, Clawson J, Furner B, Hochheimer C, Magnan E, Ricciardiello L, Singh H, Volchenboum S, Watkins M, Yen T, Abbass M, Bartell NJ, Dudley B, Engelking L, Guillem J, Hollis R, Idos G, Jones BA, Kanth P, Kastrinos F, Li D, Lucas AL, Mankaney GN, Maratt JK, Marino D, Melson J, Nguyen LH, Reddy KM, Schrader KA, Silva-Smith R, Singh A, Stanich PP, Stoffel EM, Syngal S, Weiss JM, Yurgelun MB, Zakalik D, Gupta S, Bansal A, Kupfer SS. Lynch syndrome integrative epidemiology and genetics (LINEAGE): rationale for cohort design. Fam Cancer. 2026 May 06; 25(2).
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