"Pakistan" 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 country located in southern Asia, bordering the Arabian Sea, between India on the east and Iran and Afghanistan on the west and China in the north. The capital is Islamabad.
Descriptor ID |
D010154
|
MeSH Number(s) |
Z01.252.245.723
|
Concept/Terms |
Pakistan- Pakistan
- Islamic Republic of Pakistan
|
Below are MeSH descriptors whose meaning is more general than "Pakistan".
Below are MeSH descriptors whose meaning is more specific than "Pakistan".
This graph shows the total number of publications written about "Pakistan" by people in this website by year, and whether "Pakistan" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2010 | 0 | 1 | 1 |
2012 | 0 | 2 | 2 |
2013 | 0 | 1 | 1 |
2014 | 0 | 2 | 2 |
2015 | 0 | 1 | 1 |
2019 | 0 | 1 | 1 |
2021 | 0 | 3 | 3 |
2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Pakistan" by people in Profiles.
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A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani family. Clin Exp Dermatol. 2023 03 22; 48(4):434-437.
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A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family. Genes (Basel). 2021 09 24; 12(10).
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A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family. Genes (Basel). 2021 08 21; 12(8).
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A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome. Clin Genet. 2021 10; 100(4):486-488.
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UV-sensitive syndrome: Whole exome sequencing identified a nonsense mutation in the gene UVSSA in two consanguineous pedigrees from Pakistan. J Dermatol Sci. 2019 Sep; 95(3):113-118.
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A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family. Hum Genet. 2016 Feb; 135(2):157-70.
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Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy. Nat Genet. 2014 Dec; 46(12):1283-1292.
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A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family. Hum Mol Genet. 2014 Nov 15; 23(22):5940-9.
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Autosomal recessive isolated familial acanthosis nigricans in a Pakistani family due to a homozygous mutation in the insulin receptor gene. Br J Dermatol. 2013 Aug; 169(2):476-8.
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Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet. 2012 Sep; 44(9):981-90.