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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2014 | 1 |
2015 | 2 |
2021 | 1 |
2022 | 1 |
2024 | 0 |
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Page 1
Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease.
Alzheimers Dement. 2022 Feb;18(2):294-306. doi: 10.1002/alz.12396. Epub 2021 Jun 20.
Alzheimers Dement. 2022.
PMID: 34152079
Free PMC article.
In silico prediction of splice-altering single nucleotide variants in the human genome.
Jian X, Boerwinkle E, Liu X.
Jian X, et al.
Nucleic Acids Res. 2014 Dec 16;42(22):13534-44. doi: 10.1093/nar/gku1206.
Nucleic Acids Res. 2014.
PMID: 25416802
Free PMC article.
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Coronary heart disease and genetic variants with low phospholipase A2 activity.
Polfus LM, Gibbs RA, Boerwinkle E.
Polfus LM, et al.
N Engl J Med. 2015 Jan 15;372(3):295-6. doi: 10.1056/NEJMc1409673.
N Engl J Med. 2015.
PMID: 25587968
Free PMC article.
No abstract available.
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Lipoprotein associated phospholipase A2 activity, apolipoprotein C3 loss-of-function variants and cardiovascular disease: The Atherosclerosis Risk In Communities Study.
Pokharel Y, Sun W, Polfus LM, Folsom AR, Heiss G, Sharrett AR, Boerwinkle E, Ballantyne CM, Hoogeveen RC.
Pokharel Y, et al.
Atherosclerosis. 2015 Aug;241(2):641-8. doi: 10.1016/j.atherosclerosis.2015.06.033. Epub 2015 Jun 18.
Atherosclerosis. 2015.
PMID: 26117401
Free PMC article.
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