 Genotype
"Genotype" 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 genetic constitution of the individual, comprising the ALLELES present at each GENETIC LOCUS.
| Descriptor ID |
D005838
|
| MeSH Number(s) |
G05.380
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Genotype".
Below are MeSH descriptors whose meaning is more specific than "Genotype".
This graph shows the total number of publications written about "Genotype" by people in this website by year, and whether "Genotype" 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 |
|---|
| 1995 | 0 | 3 | 3 | | 1996 | 1 | 7 | 8 | | 1997 | 1 | 6 | 7 | | 1998 | 0 | 7 | 7 | | 1999 | 0 | 8 | 8 | | 2000 | 1 | 13 | 14 | | 2001 | 1 | 28 | 29 | | 2002 | 1 | 21 | 22 | | 2003 | 0 | 28 | 28 | | 2004 | 2 | 41 | 43 | | 2005 | 1 | 40 | 41 | | 2006 | 1 | 53 | 54 | | 2007 | 2 | 57 | 59 | | 2008 | 4 | 63 | 67 | | 2009 | 1 | 70 | 71 | | 2010 | 3 | 56 | 59 | | 2011 | 4 | 68 | 72 | | 2012 | 7 | 59 | 66 | | 2013 | 2 | 68 | 70 | | 2014 | 7 | 95 | 102 | | 2015 | 5 | 78 | 83 | | 2016 | 6 | 66 | 72 | | 2017 | 4 | 65 | 69 | | 2018 | 7 | 55 | 62 | | 2019 | 8 | 51 | 59 | | 2020 | 6 | 43 | 49 | | 2021 | 7 | 34 | 41 | | 2022 | 1 | 23 | 24 | | 2023 | 0 | 23 | 23 | | 2024 | 5 | 27 | 32 | | 2025 | 0 | 28 | 28 |
To return to the timeline, click here.
Below are the most recent publications written about "Genotype" by people in Profiles.
-
Daines CL, Polineni D, Tullis E, Costa S, Linnemann RW, Mall MA, McKone EF, Quon BS, Ringshausen FC, Selvadurai H, Taylor-Cousar JL, Withers NJ, Sawicki GS, Lee T, Ahluwalia N, Morlando Geiger J, Jennings M, Tan YV, Waltz D, Ramsey B, Griese M. Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Adults and Adolescents with Cystic Fibrosis and at Least One F508del Allele: A Phase 3 Open-Label Extension Study. Am J Respir Crit Care Med. 2025 10; 211(10):1901-1914.
-
Befano B, Kalpathy-Cramer J, Egemen D, Inturrisi F, Jeronimo J, Rodríguez AC, Campos N, Cremer M, Ribeiro A, Ajenifuja KO, Goldstein A, Haider A, Yeates K, Madeleine M, Norris T, Figueroa J, Alfaro K, Raiol T, Adepiti C, Norman J, Chilinda GK, Mchome B, Donastorg Y, Dlamini X, Conzuelo G, Banjo AA, Chone P, Mremi A, Benitez A, Rosberger Z, Vantha T, Prieto-Egido I, Boyd-Morin J, Clark C, Kinder S, Wentzensen N, Desai K, Perkins R, de Sanjosé S, Schiffman M. Initial evaluation of a new cervical screening strategy combining human papillomavirus genotyping and automated visual evaluation: the Human Papillomavirus-Automated Visual Evaluation Consortium. J Natl Cancer Inst. 2025 Oct 01; 117(10):2124-2129.
-
Ramadan DJ, Kichula KM, Tao S, Porfilio T, Lande A, Fluge Ø, Mella O, Strand EB, Saugstad OD, Norman PJ, Lie BA, Viken MK. Killer cell immunoglobulin-like receptor (KIR) alleles suggested to be associated with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Brain Behav Immun. 2025 Nov; 130:106098.
-
Andersen SE, Duerkop BA. Charting a phage genome atlas. Cell Host Microbe. 2025 Aug 13; 33(8):1311-1312.
-
Haukoos J, Rothman RE, Galbraith JW, Hopkins E, Hsieh YH, Lyle C, Gravitz S, Kamis KF, White DAE, Lyons MS, Gardner EM, Al-Tayyib AA, Sabel AL, Linas BP, Morgan JR, Wyles DL, Rowan SE. Hepatitis C Screening in Emergency Departments: The DETECT Hep C Randomized Clinical Trial. JAMA. 2025 08 12; 334(6):497-507.
-
Harrall KK, Glueck DH, Lange LA, Litkowski EM, Vanderlinden LA, Konigsberg IR, Cree MG, Perng W, Dabelea D. GLP-1R Gene Polymorphisms and Metabolic Traits During Childhood and Adolescence: The EPOCH Study. J Clin Endocrinol Metab. 2025 Aug 07; 110(9):e3031-e3040.
-
Walsemann KM, Jackson HM, Boardman JD, Herd P. APOE genotype and cognitive decline: educational context as a moderator of genetic risk. J Gerontol B Psychol Sci Soc Sci. 2025 Jul 25; 80(8).
-
Logsdon GA, Ebert P, Audano PA, Loftus M, Porubsky D, Ebler J, Yilmaz F, Hallast P, Prodanov T, Yoo D, Paisie CA, Harvey WT, Zhao X, Martino GV, Henglin M, Munson KM, Rabbani K, Chin CS, Gu B, Ashraf H, Scholz S, Austine-Orimoloye O, Balachandran P, Bonder MJ, Cheng H, Chong Z, Crabtree J, Gerstein M, Guethlein LA, Hasenfeld P, Hickey G, Hoekzema K, Hunt SE, Jensen M, Jiang Y, Koren S, Kwon Y, Li C, Li H, Li J, Norman PJ, Oshima KK, Paten B, Phillippy AM, Pollock NR, Rausch T, Rautiainen M, Song Y, Söylev A, Sulovari A, Surapaneni L, Tsapalou V, Zhou W, Zhou Y, Zhu Q, Zody MC, Mills RE, Devine SE, Shi X, Talkowski ME, Chaisson MJP, Dilthey AT, Konkel MK, Korbel JO, Lee C, Beck CR, Eichler EE, Marschall T. Complex genetic variation in nearly complete human genomes. Nature. 2025 Aug; 644(8076):430-441.
-
Han WM, Solomon SS, Smeaton L, Avihingsanon A, Wagner Cardoso S, Li J, Parvangada A, Sulkowski M, Naggie S, Martin R, Mo H, Maiorova E, Wyles D. Reinfection and Resistance Associated Substitutions Following a Minimal Monitoring Approach for Hepatitis C Virus Treatment in MINMON Trial. Clin Infect Dis. 2025 Jul 18; 80(6):1293-1301.
-
Perotto M, Paldino A, Mazzarotto F, Barbati G, Stroeks SLVM, Verdonschot JAJ, Akhtar M, Elliott P, Ochoa JP, Garcia-Pavia P, de Frutos F, Sepp R, Hategan L, Prasad S, Yazdani M, Morris-Rosendahl D, Palinkas ED, Girolami F, Olivotto I, Parikh VN, Fatkin D, Lakdawala N, McKenna WJ, Stolfo D, Gigli M, Brun F, Collesi C, Giacca M, Zacchigna S, Severini GM, Lenarduzzi S, Spedicati B, Santin A, Girotto G, Gasparini P, Taylor MRG, Mestroni L, Merlo M, Sinagra G, Dal Ferro M. Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study. JACC Heart Fail. 2025 Sep; 13(9):102529.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|