Systematic review of genome-wide association studies of abdominal aortic aneurysm
Abdominal aortic aneurysm (AAA) is an important cause of death worldwide and has an estimated heritability between 70 and 77%. Genome-wide association studies (GWAS) are an established way to discover genetic risk variants. The aim of this study was to systematically review the findings and quality...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Singh, Tejas P. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2021 |
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| Schlagwörter: |
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| Umfang: |
10 |
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| Übergeordnetes Werk: |
Enthalten in: No title available - 327(2021), Seite 39-48 |
|---|---|
| Übergeordnetes Werk: |
volume:327 ; year:2021 ; pages:39-48 ; extent:10 |
| Links: |
|---|
| DOI / URN: |
10.1016/j.atherosclerosis.2021.05.001 |
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| 520 | |a Abdominal aortic aneurysm (AAA) is an important cause of death worldwide and has an estimated heritability between 70 and 77%. Genome-wide association studies (GWAS) are an established way to discover genetic risk variants. The aim of this study was to systematically review the findings and quality of previous AAA GWAS. | ||
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10.1016/j.atherosclerosis.2021.05.001 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001417.pica (DE-627)ELV05433067X (ELSEVIER)S0021-9150(21)00225-2 DE-627 ger DE-627 rakwb eng Singh, Tejas P. verfasserin aut Systematic review of genome-wide association studies of abdominal aortic aneurysm 2021 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abdominal aortic aneurysm (AAA) is an important cause of death worldwide and has an estimated heritability between 70 and 77%. Genome-wide association studies (GWAS) are an established way to discover genetic risk variants. The aim of this study was to systematically review the findings and quality of previous AAA GWAS. Genetic association study Elsevier Association study Elsevier Genetics Elsevier Genome-wide Elsevier Bioinformatics Elsevier Vascular biology Elsevier Field, Matt A. oth Bown, Matthew J. oth Jones, Gregory T. oth Golledge, Jonathan oth Enthalten in No title available 327(2021), Seite 39-48 (DE-627)ELV012595616 (DE-600)1-9150 nnns volume:327 year:2021 pages:39-48 extent:10 https://doi.org/10.1016/j.atherosclerosis.2021.05.001 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_20 GBV_ILN_40 GBV_ILN_105 AR 327 2021 39-48 10 |
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10.1016/j.atherosclerosis.2021.05.001 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001417.pica (DE-627)ELV05433067X (ELSEVIER)S0021-9150(21)00225-2 DE-627 ger DE-627 rakwb eng Singh, Tejas P. verfasserin aut Systematic review of genome-wide association studies of abdominal aortic aneurysm 2021 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abdominal aortic aneurysm (AAA) is an important cause of death worldwide and has an estimated heritability between 70 and 77%. Genome-wide association studies (GWAS) are an established way to discover genetic risk variants. The aim of this study was to systematically review the findings and quality of previous AAA GWAS. Genetic association study Elsevier Association study Elsevier Genetics Elsevier Genome-wide Elsevier Bioinformatics Elsevier Vascular biology Elsevier Field, Matt A. oth Bown, Matthew J. oth Jones, Gregory T. oth Golledge, Jonathan oth Enthalten in No title available 327(2021), Seite 39-48 (DE-627)ELV012595616 (DE-600)1-9150 nnns volume:327 year:2021 pages:39-48 extent:10 https://doi.org/10.1016/j.atherosclerosis.2021.05.001 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_20 GBV_ILN_40 GBV_ILN_105 AR 327 2021 39-48 10 |
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10.1016/j.atherosclerosis.2021.05.001 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001417.pica (DE-627)ELV05433067X (ELSEVIER)S0021-9150(21)00225-2 DE-627 ger DE-627 rakwb eng Singh, Tejas P. verfasserin aut Systematic review of genome-wide association studies of abdominal aortic aneurysm 2021 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abdominal aortic aneurysm (AAA) is an important cause of death worldwide and has an estimated heritability between 70 and 77%. Genome-wide association studies (GWAS) are an established way to discover genetic risk variants. The aim of this study was to systematically review the findings and quality of previous AAA GWAS. Genetic association study Elsevier Association study Elsevier Genetics Elsevier Genome-wide Elsevier Bioinformatics Elsevier Vascular biology Elsevier Field, Matt A. oth Bown, Matthew J. oth Jones, Gregory T. oth Golledge, Jonathan oth Enthalten in No title available 327(2021), Seite 39-48 (DE-627)ELV012595616 (DE-600)1-9150 nnns volume:327 year:2021 pages:39-48 extent:10 https://doi.org/10.1016/j.atherosclerosis.2021.05.001 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_20 GBV_ILN_40 GBV_ILN_105 AR 327 2021 39-48 10 |
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10.1016/j.atherosclerosis.2021.05.001 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001417.pica (DE-627)ELV05433067X (ELSEVIER)S0021-9150(21)00225-2 DE-627 ger DE-627 rakwb eng Singh, Tejas P. verfasserin aut Systematic review of genome-wide association studies of abdominal aortic aneurysm 2021 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abdominal aortic aneurysm (AAA) is an important cause of death worldwide and has an estimated heritability between 70 and 77%. Genome-wide association studies (GWAS) are an established way to discover genetic risk variants. The aim of this study was to systematically review the findings and quality of previous AAA GWAS. Genetic association study Elsevier Association study Elsevier Genetics Elsevier Genome-wide Elsevier Bioinformatics Elsevier Vascular biology Elsevier Field, Matt A. oth Bown, Matthew J. oth Jones, Gregory T. oth Golledge, Jonathan oth Enthalten in No title available 327(2021), Seite 39-48 (DE-627)ELV012595616 (DE-600)1-9150 nnns volume:327 year:2021 pages:39-48 extent:10 https://doi.org/10.1016/j.atherosclerosis.2021.05.001 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_20 GBV_ILN_40 GBV_ILN_105 AR 327 2021 39-48 10 |
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Abdominal aortic aneurysm (AAA) is an important cause of death worldwide and has an estimated heritability between 70 and 77%. Genome-wide association studies (GWAS) are an established way to discover genetic risk variants. The aim of this study was to systematically review the findings and quality of previous AAA GWAS. |
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Abdominal aortic aneurysm (AAA) is an important cause of death worldwide and has an estimated heritability between 70 and 77%. Genome-wide association studies (GWAS) are an established way to discover genetic risk variants. The aim of this study was to systematically review the findings and quality of previous AAA GWAS. |
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Abdominal aortic aneurysm (AAA) is an important cause of death worldwide and has an estimated heritability between 70 and 77%. Genome-wide association studies (GWAS) are an established way to discover genetic risk variants. The aim of this study was to systematically review the findings and quality of previous AAA GWAS. |
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Systematic review of genome-wide association studies of abdominal aortic aneurysm |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV05433067X</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230624210455.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">210910s2021 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.atherosclerosis.2021.05.001</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">/cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001417.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV05433067X</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0021-9150(21)00225-2</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Singh, Tejas P.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Systematic review of genome-wide association studies of abdominal aortic aneurysm</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2021</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">10</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abdominal aortic aneurysm (AAA) is an important cause of death worldwide and has an estimated heritability between 70 and 77%. Genome-wide association studies (GWAS) are an established way to discover genetic risk variants. The aim of this study was to systematically review the findings and quality of previous AAA GWAS.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Genetic association study</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Association study</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Genetics</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Genome-wide</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Bioinformatics</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Vascular biology</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Field, Matt A.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bown, Matthew J.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Jones, Gregory T.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Golledge, Jonathan</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">No title available</subfield><subfield code="g">327(2021), Seite 39-48</subfield><subfield code="w">(DE-627)ELV012595616</subfield><subfield code="w">(DE-600)1-9150</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:327</subfield><subfield code="g">year:2021</subfield><subfield code="g">pages:39-48</subfield><subfield code="g">extent:10</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.atherosclerosis.2021.05.001</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_105</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">327</subfield><subfield code="j">2021</subfield><subfield code="h">39-48</subfield><subfield code="g">10</subfield></datafield></record></collection>
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