 Finland
"Finland" 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.
No definition found.
| Descriptor ID |
D005387
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| MeSH Number(s) |
Z01.542.816.186
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Finland".
Below are MeSH descriptors whose meaning is more specific than "Finland".
This graph shows the total number of publications written about "Finland" by people in this website by year, and whether "Finland" 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 |
|---|
| 1998 | 0 | 3 | 3 | | 2001 | 0 | 2 | 2 | | 2002 | 0 | 2 | 2 | | 2003 | 0 | 2 | 2 | | 2015 | 0 | 1 | 1 | | 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Finland" by people in Profiles.
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Huusko JM, Karjalainen MK, Graham BE, Zhang G, Farrow EG, Miller NA, Jacobsson B, Eidem HR, Murray JC, Bedell B, Breheny P, Brown NW, B?dker FL, Litterman NK, Jiang PP, Russell L, Hinds DA, Hu Y, Rokas A, Teramo K, Christensen K, Williams SM, R?met M, Kingsmore SF, Ryckman KK, Hallman M, Muglia LJ. Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth. PLoS Genet. 2018 07; 14(7):e1007394.
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Siuko M, Valori M, Kivel? T, Set?l? K, Morin A, Kwan T, Pastinen T, Tienari P. Exome and regulatory element sequencing of neuromyelitis optica patients. J Neuroimmunol. 2015 Dec 15; 289:139-42.
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Nejentsev S, Laaksonen M, Tienari PJ, Fernandez O, Cordell H, Ruutiainen J, Wikstr?m J, Pastinen T, Kuokkanen S, Hillert J, Ilonen J. Intercellular adhesion molecule-1 K469E polymorphism: study of association with multiple sclerosis. Hum Immunol. 2003 Mar; 64(3):345-9.
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Alfthan G, Laurinen MS, Valsta LM, Pastinen T, Aro A. Folate intake, plasma folate and homocysteine status in a random Finnish population. Eur J Clin Nutr. 2003 Jan; 57(1):81-8.
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Reunanen K, Finnil? S, Laaksonen M, Sumelahti ML, Wikstr?m J, Pastinen T, Kuokkanen S, Saarela J, Uimari P, Ruutiainen J, Ilonen J, Peltonen L, Tienari PJ. Chromosome 19q13 and multiple sclerosis susceptibility in Finland: a linkage and two-stage association study. J Neuroimmunol. 2002 May; 126(1-2):134-42.
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Laaksonen M, Pastinen T, Sj?roos M, Kuokkanen S, Ruutiainen J, Sumelahti ML, Reijonen H, Salonen R, Wikstr?m J, Panelius M, Partanen J, Tienari PJ, Ilonen J. HLA class II associated risk and protection against multiple sclerosis-a Finnish family study. J Neuroimmunol. 2002 Jan; 122(1-2):140-5.
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Pastinen T, Perola M, Ignatius J, Sabatti C, Tainola P, Levander M, Syv?nen AC, Peltonen L. Dissecting a population genome for targeted screening of disease mutations. Hum Mol Genet. 2001 Dec 15; 10(26):2961-72.
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Raitio M, Lindroos K, Laukkanen M, Pastinen T, Sistonen P, Sajantila A, Syv?nen AC. Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarrays. Genome Res. 2001 Mar; 11(3):471-82.
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Pastinen T, Perola M, Niini P, Terwilliger J, Salomaa V, Vartiainen E, Peltonen L, Syv?nen A. Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population. Hum Mol Genet. 1998 Sep; 7(9):1453-62.
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Pastinen T, Liitsola K, Niini P, Salminen M, Syv?nen AC. Contribution of the CCR5 and MBL genes to susceptibility to HIV type 1 infection in the Finnish population. AIDS Res Hum Retroviruses. 1998 May 20; 14(8):695-8.
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