[HTML][HTML] A saturated map of common genetic variants associated with human height
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40–
50% of phenotypic variation in human height, but identifying the specific variants and …
50% of phenotypic variation in human height, but identifying the specific variants and …
[HTML][HTML] A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko… - Nature, 2022 - econpapers.repec.org
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40–
50% of phenotypic variation in human height, but identifying the specific variants and …
50% of phenotypic variation in human height, but identifying the specific variants and …
A saturated map of common genetic variants associated with human height
Y Loïc, V Sailaja, M Eirini, S Julia, B Eric, S Saori… - Nature, 2022 - agris.fao.org
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40–
50% of phenotypic variation in human height, but identifying the specific variants and …
50% of phenotypic variation in human height, but identifying the specific variants and …
[HTML][HTML] A saturated map of common genetic variants associated with human height.
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell… - Nature, 2022 - swepub.kb.se
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sekundära innehåll (sidomenyn) SwePub Om SwePub In English Sökhistorik/mina poster …
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell… - NATURE, 2022 - arts.units.it
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40-
50% of phenotypic variation in human height, but identifying the specific variants and …
50% of phenotypic variation in human height, but identifying the specific variants and …
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli… - …, 2022 - repository.escholarship.umassmed …
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40-
50% of phenotypic variation in human height, but identifying the specific variants and …
50% of phenotypic variation in human height, but identifying the specific variants and …
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell… - 2022 - munin.uit.no
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40–
50% of phenotypic variation in human height, but identifying the specifc variants and …
50% of phenotypic variation in human height, but identifying the specifc variants and …
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell… - 2022 - figshare.utas.edu.au
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40-
50% of phenotypic variation in human height, but identifying the specific variants and …
50% of phenotypic variation in human height, but identifying the specific variants and …
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell… - paper.sciencenet.cn
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40–
50% of phenotypic variation in human height, but identifying the specific variants and …
50% of phenotypic variation in human height, but identifying the specific variants and …
[HTML][HTML] A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell… - 2022 - oda.oslomet.no
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40–
50% of phenotypic variation in human height, but identifying the specific variants and …
50% of phenotypic variation in human height, but identifying the specific variants and …