Cohort Studies
"Cohort Studies" 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.
Studies in which subsets of a defined population are identified. These groups may or may not be exposed to factors hypothesized to influence the probability of the occurrence of a particular disease or other outcome. Cohorts are defined populations which, as a whole, are followed in an attempt to determine distinguishing subgroup characteristics.
Descriptor ID |
D015331
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MeSH Number(s) |
E05.318.760.500.750 N05.715.360.775.175.250 N06.850.520.450.500.750
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Concept/Terms |
Cohort Studies- Cohort Studies
- Cohort Study
- Studies, Cohort
- Study, Cohort
- Concurrent Studies
- Studies, Concurrent
- Concurrent Study
- Study, Concurrent
Closed Cohort Studies- Closed Cohort Studies
- Cohort Studies, Closed
- Closed Cohort Study
- Cohort Study, Closed
- Study, Closed Cohort
- Studies, Closed Cohort
Historical Cohort Studies- Historical Cohort Studies
- Cohort Study, Historical
- Historical Cohort Study
- Study, Historical Cohort
- Studies, Historical Cohort
- Cohort Studies, Historical
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Below are MeSH descriptors whose meaning is more general than "Cohort Studies".
Below are MeSH descriptors whose meaning is more specific than "Cohort Studies".
This graph shows the total number of publications written about "Cohort Studies" by people in this website by year, and whether "Cohort Studies" 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 |
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1989 | 0 | 1 | 1 | 1990 | 0 | 3 | 3 | 1991 | 0 | 4 | 4 | 1992 | 0 | 3 | 3 | 1993 | 0 | 3 | 3 | 1994 | 0 | 1 | 1 | 1995 | 0 | 4 | 4 | 1996 | 0 | 8 | 8 | 1997 | 0 | 13 | 13 | 1998 | 0 | 7 | 7 | 1999 | 0 | 10 | 10 | 2000 | 0 | 15 | 15 | 2001 | 0 | 15 | 15 | 2002 | 0 | 14 | 14 | 2003 | 0 | 23 | 23 | 2004 | 0 | 25 | 25 | 2005 | 0 | 25 | 25 | 2006 | 0 | 27 | 27 | 2007 | 0 | 44 | 44 | 2008 | 0 | 59 | 59 | 2009 | 0 | 67 | 67 | 2010 | 0 | 48 | 48 | 2011 | 0 | 60 | 60 | 2012 | 0 | 69 | 69 | 2013 | 0 | 83 | 83 | 2014 | 0 | 70 | 70 | 2015 | 0 | 77 | 77 | 2016 | 0 | 96 | 96 | 2017 | 0 | 86 | 86 | 2018 | 0 | 109 | 109 | 2019 | 0 | 103 | 103 | 2020 | 1 | 53 | 54 | 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Cohort Studies" by people in Profiles.
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Bailey LC, Razzaghi H, Burrows EK, Bunnell HT, Camacho PEF, Christakis DA, Eckrich D, Kitzmiller M, Lin SM, Magnusen BC, Newland J, Pajor NM, Ranade D, Rao S, Sofela O, Zahner J, Bruno C, Forrest CB. Assessment of 135?794 Pediatric Patients Tested for Severe Acute Respiratory Syndrome Coronavirus 2 Across the United States. JAMA Pediatr. 2021 02 01; 175(2):176-184.
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Chai JF, Kao SL, Wang C, Lim VJ, Khor IW, Dou J, Podgornaia AI, Chothani S, Cheng CY, Sabanayagam C, Wong TY, van Dam RM, Liu J, Reilly DF, Paterson AD, Sim X. Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of Glycemia. J Clin Endocrinol Metab. 2020 12 01; 105(12).
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Dang H, Polineni D, Pace RG, Stonebraker JR, Corvol H, Cutting GR, Drumm ML, Strug LJ, O'Neal WK, Knowles MR. Mining GWAS and eQTL data for CF lung disease modifiers by gene expression imputation. PLoS One. 2020; 15(11):e0239189.
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Davies RW, Fiksinski AM, Breetvelt EJ, Williams NM, Hooper SR, Monfeuga T, Bassett AS, Owen MJ, Gur RE, Morrow BE, McDonald-McGinn DM, Swillen A, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, van Amelsvoort T, Arango C, Armando M, Campbell LE, Cubells JF, Eliez S, Garcia-Minaur S, Gothelf D, Kates WR, Murphy KC, Murphy CM, Murphy DG, Philip N, Repetto GM, Shashi V, Simon TJ, Suñer DH, Vicari S, Scherer SW, Bearden CE, Vorstman JAS. Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Nat Med. 2020 12; 26(12):1912-1918.
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Turpin W, Bedrani L, Espin-Garcia O, Xu W, Silverberg MS, Smith MI, Garay JAR, Lee SH, Guttman DS, Griffiths A, Moayyedi P, Panaccione R, Huynh H, Steinhart HA, Aumais G, Dieleman LA, Turner D, Paterson AD, Croitoru K. Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn's disease subjects. BMC Med Genet. 2020 10 15; 21(1):204.
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Ebrahimi-Fakhari D, Teinert J, Behne R, Wimmer M, D'Amore A, Eberhardt K, Brechmann B, Ziegler M, Jensen DM, Nagabhyrava P, Geisel G, Carmody E, Shamshad U, Dies KA, Yuskaitis CJ, Salussolia CL, Ebrahimi-Fakhari D, Pearson TS, Saffari A, Ziegler A, Kölker S, Volkmann J, Wiesener A, Bearden DR, Lakhani S, Segal D, Udwadia-Hegde A, Martinuzzi A, Hirst J, Perlman S, Takiyama Y, Xiromerisiou G, Vill K, Walker WO, Shukla A, Dubey Gupta R, Dahl N, Aksoy A, Verhelst H, Delgado MR, Kremlikova Pourova R, Sadek AA, Elkhateeb NM, Blumkin L, Brea-Fernández AJ, Dacruz-Álvarez D, Smol T, Ghoumid J, Miguel D, Heine C, Schlump JU, Langen H, Baets J, Bulk S, Darvish H, Bakhtiari S, Kruer MC, Lim-Melia E, Aydinli N, Alanay Y, El-Rashidy O, Nampoothiri S, Patel C, Beetz C, Bauer P, Yoon G, Guillot M, Miller SP, Bourinaris T, Houlden H, Robelin L, Anheim M, Alamri AS, Mahmoud AAH, Inaloo S, Habibzadeh P, Faghihi MA, Jansen AC, Brock S, Roubertie A, Darras BT, Agrawal PB, Santorelli FM, Gleeson J, Zaki MS, Sheikh SI, Bennett JT, Sahin M. Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia. Brain. 2020 10 01; 143(10):2929-2944.
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Phillips NL, Widjaja E, Smith ML. Changes in caregiver depression, anxiety, and satisfaction with family relationships in families of children who did and did not undergo resective epilepsy surgery. Epilepsia. 2020 10; 61(10):2265-2276.
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Tarride JE, Doumouras AG, Hong D, Paterson JM, Tibebu S, Perez R, Ma J, Taylor VH, Xie F, Boudreau V, Pullenayegum E, Urbach DR, Anvari M. Association of Roux-en-Y Gastric Bypass With Postoperative Health Care Use and Expenditures in Canada. JAMA Surg. 2020 09 01; 155(9):e201985.
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Chao BK, Claessens NHP, Lim JM, Gorodetsky C, Au-Young SH, Guerguerian AM, Marini D, Blaser S, Shroff M, Saini AK, Seed M, Chau V, Miller SP. Decreased Brain Volumes and Infants With Congenital Heart Disease Undergoing Venoarterial Extracorporeal Membrane Oxygenation. Pediatr Crit Care Med. 2020 08; 21(8):738-745.
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Chen Z, Miao F, Braffett BH, Lachin JM, Zhang L, Wu X, Roshandel D, Carless M, Li XA, Tompkins JD, Kaddis JS, Riggs AD, Paterson AD, Natarajan R. DNA methylation mediates development of HbA1c-associated complications in type 1 diabetes. Nat Metab. 2020 08; 2(8):744-762.
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