000 01747 a2200565 4500
005 20250517092508.0
264 0 _c20180727
008 201807s 0 0 eng d
022 _a2041-1723
024 7 _a10.1038/ncomms11433
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMosley, Jonathan D
245 0 0 _aIdentifying genetically driven clinical phenotypes using linear mixed models.
_h[electronic resource]
260 _bNature communications
_c04 2016
300 _a11433 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aAged, 80 and over
650 0 4 _aDisease
_xgenetics
650 0 4 _aExome
650 0 4 _aFemale
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGenetic Variation
650 0 4 _aGenome-Wide Association Study
650 0 4 _aGenotype
650 0 4 _aHLA Antigens
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aModels, Genetic
650 0 4 _aPhenotype
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aWhite People
_xgenetics
700 1 _aWitte, John S
700 1 _aLarkin, Emma K
700 1 _aBastarache, Lisa
700 1 _aShaffer, Christian M
700 1 _aKarnes, Jason H
700 1 _aStein, C Michael
700 1 _aPhillips, Elizabeth
700 1 _aHebbring, Scott J
700 1 _aBrilliant, Murray H
700 1 _aMayer, John
700 1 _aYe, Zhan
700 1 _aRoden, Dan M
700 1 _aDenny, Joshua C
773 0 _tNature communications
_gvol. 7
_gp. 11433
856 4 0 _uhttps://doi.org/10.1038/ncomms11433
_zAvailable from publisher's website
999 _c25954261
_d25954261