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Sökning: WFRF:(Morris Andrew D.) > (2006-2009) > A common variant of...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003966naa a2200661 4500
001oai:lup.lub.lu.se:4af0d455-41fa-47be-ba6f-6397106760a5
003SwePub
008160401s2007 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/6559632 URI
024a https://doi.org/10.1038/ng21212 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Weedon, Michael N.4 aut
2451 0a A common variant of HMGA2 is associated with adult and childhood height in the general population
264 c 2007-09-02
264 1b Springer Science and Business Media LLC,c 2007
520 a Human height is a classic, highly heritable quantitative trait. To begin to identify genetic variants influencing height, we examined genome-wide association data from 4,921 individuals. Common variants in the HMGA2 oncogene, exemplified by rs1042725, were associated with height (P= 4x10(-8)). HMGA2 is also a strong biological candidate for height, as rare, severe mutations in this gene alter body size in mice and humans, so we tested rs1042725 in additional samples. We confirmed the association in 19,064 adults from four further studies (P= 3x10(-11), overall P= 4x10(-16), including the genome-wide association data). We also observed the association in children (P=1x 10(-6), N= 6,827) and a tall/short case-control study (P= 4x10(-6), N=3,207). We estimate that rs1042725 explains similar to 0.3% of population variation in height (similar to 0.4 cm increased adult height per C allele). There are few examples of common genetic variants reproducibly associated with human quantitative traits; these results represent, to our knowledge, the first consistently replicated association with adult and childhood height.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Endokrinologi och diabetes0 (SwePub)302052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Endocrinology and Diabetes0 (SwePub)302052 hsv//eng
700a Lettre, Guillaume4 aut
700a Freathy, Rachel M.4 aut
700a Lindgren, Cecilia M.4 aut
700a Voight, Benjamin F.4 aut
700a Perry, John R. B.4 aut
700a Elliott, Katherine S.4 aut
700a Hackett, Rachel4 aut
700a Guiducci, Candace4 aut
700a Shields, Beverley4 aut
700a Zeggini, Eleftheria4 aut
700a Lango, Hana4 aut
700a Lyssenko, Valeriya4 aut
700a Timpson, Nicholas J.4 aut
700a Burtt, Noel P.4 aut
700a Rayner, Nigel W.4 aut
700a Saxena, Richa4 aut
700a Ardlie, Kristin4 aut
700a Tobias, Jonathan H.4 aut
700a Ness, Andrew R.4 aut
700a Ring, Susan M.4 aut
700a Palmer, Colin N. A.4 aut
700a Morris, Andrew D.4 aut
700a Peltonen, Leena4 aut
700a Salomaa, Veikko4 aut
700a Smith, George Davey4 aut
700a Groop, Leifu Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Genomics, Diabetes and Endocrinology,Lund University Research Groups4 aut0 (Swepub:lu)endo-lgr
700a Hattersley, Andrew T.4 aut
700a McCarthy, Mark I.4 aut
700a Hirschhorn, Joel N.4 aut
700a Frayling, Timothy M.4 aut
710a Genomik, diabetes och endokrinologib Forskargrupper vid Lunds universitet4 org
773t Nature Geneticsd : Springer Science and Business Media LLCg 39:10, s. 1245-1250q 39:10<1245-1250x 1546-1718x 1061-4036
856u http://dx.doi.org/10.1038/ng2121y FULLTEXT
856u https://www.pure.ed.ac.uk/ws/files/17154591/A_common_variant_of_HMGA2_is_associated_with_adult_and_childhood_height_in_the_general_population.pdf
8564 8u https://lup.lub.lu.se/record/655963
8564 8u https://doi.org/10.1038/ng2121

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