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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 1
2005 4
2006 4
2007 2
2009 4
2010 1
2011 1
2012 2
2013 2
2014 4
2015 3
2016 2
2017 1
2018 1
2019 2
2020 7
2021 3
2024 0

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42 results

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Page 1
Clinical sequencing: is WGS the better WES?
Meienberg J, Bruggmann R, Oexle K, Matyas G. Meienberg J, et al. Among authors: matyas g. Hum Genet. 2016 Mar;135(3):359-62. doi: 10.1007/s00439-015-1631-9. Epub 2016 Jan 7. Hum Genet. 2016. PMID: 26742503 Free PMC article.
Potential of whole-genome sequencing-based pharmacogenetic profiling.
Caspar SM, Schneider T, Stoll P, Meienberg J, Matyas G. Caspar SM, et al. Among authors: matyas g. Pharmacogenomics. 2021 Feb;22(3):177-190. doi: 10.2217/pgs-2020-0155. Epub 2021 Feb 1. Pharmacogenomics. 2021. PMID: 33517770 Free article. Review.
Potential predictors of severe cardiovascular involvement in Marfan syndrome: the emphasized role of genotype-phenotype correlations in improving risk stratification-a literature review.
Stengl R, Ágg B, Pólos M, Mátyás G, Szabó G, Merkely B, Radovits T, Szabolcs Z, Benke K. Stengl R, et al. Among authors: matyas g. Orphanet J Rare Dis. 2021 May 31;16(1):245. doi: 10.1186/s13023-021-01882-6. Orphanet J Rare Dis. 2021. PMID: 34059089 Free PMC article. Review.
More Genes for Thoracic Aortic Aneurysms and Dissections.
Caspar SM, Dubacher N, Matyas G. Caspar SM, et al. Among authors: matyas g. J Am Coll Cardiol. 2019 Feb 5;73(4):528-529. doi: 10.1016/j.jacc.2018.09.094. J Am Coll Cardiol. 2019. PMID: 30704586 Free article. No abstract available.
Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database.
Collod-Béroud G, Le Bourdelles S, Ades L, Ala-Kokko L, Booms P, Boxer M, Child A, Comeglio P, De Paepe A, Hyland JC, Holman K, Kaitila I, Loeys B, Matyas G, Nuytinck L, Peltonen L, Rantamaki T, Robinson P, Steinmann B, Junien C, Béroud C, Boileau C. Collod-Béroud G, et al. Among authors: matyas g. Hum Mutat. 2003 Sep;22(3):199-208. doi: 10.1002/humu.10249. Hum Mutat. 2003. PMID: 12938084 Review.
A pilot clinical trial with losartan in Myhre syndrome.
Cappuccio G, Caiazza M, Roca A, Melis D, Iuliano A, Matyas G, Rubino M, Limongelli G, Brunetti-Pierri N. Cappuccio G, et al. Among authors: matyas g. Am J Med Genet A. 2021 Mar;185(3):702-709. doi: 10.1002/ajmg.a.62019. Epub 2020 Dec 24. Am J Med Genet A. 2021. PMID: 33369056 Free PMC article. Clinical Trial.
42 results