Results 151 to 160 of about 35,658 (190)

Phenome-wide association studies of genetic variants in microRNAs

European Journal of Human Genetics, 2023
Mustafa, Rima, Ghanbari, Mohsen, Evangelou, Marina, Dehghan, Abbas   +3 more
openaire   +1 more source

Excess CMS morbidity and FEMA declarations: Phenome Wide Association Study of Generalized Linear Model interactions between CMS diagnostic code utilization and FEMA Incident types, 1999-2020. [PDF]

Inform Med Unlocked
Williams N.
europepmc   +1 more source

Phenome-wide association study of loci harboring de novo tandem repeat mutations in UK Biobank exomes. [PDF]

Nat Commun, 2022
Wendt FR, Pathak GA, Polimanti R.
europepmc   +1 more source

Exploring beyond diagnoses in electronic health records to improve discovery: a review of the phenome-wide association study. [PDF]

JAMIA Open
Wan NC, Grabowska ME, Kerchberger VE, Wei WQ.   +3 more
europepmc   +1 more source

PCSK9 inhibition and broad health outcomes: A Mendelian randomization phenome‑wide association study

Pharmacological Research
Kai Zhang, Qin Bian
doaj   +1 more source

Unraveling the influence of body mass index on complex diseases in East Asians: Insights from Mendelian randomization phenome-wide association study. [PDF]

Medicine (Baltimore)
Wu B, Li W, Xu S, Chen R, Ding Y, Xu R, Wu Z, Bao M, He B, Li S.   +9 more
europepmc   +1 more source

A Phenome-Wide association study (PheWAS) of genetic risk for C-reactive protein in children of European Ancestry: Results from the ABCD study. [PDF]

Brain Behav Immun
Norton SA, Gorelik AJ, Paul SE, Johnson EC, Baranger DA, Siudzinski JL, Li ZA, Bondy E, Modi H, Karcher NR, Hershey T, Hatoum AS, Agrawal A, Bogdan R.   +13 more
europepmc   +1 more source

A hypothesis-free approach to identifying potential effects of relative age in school year: an instrumental variable phenome-wide association study in the UK Biobank. [PDF]

Am J Epidemiol
de Lange MA, Davies NM, Millard LAC, Tilling K.   +3 more
europepmc   +1 more source

A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank. [PDF]

Nat Commun
Manigbas CA, Jadhav B, Garg P, Shadrina M, Lee W, Altman G, Martin-Trujillo A, Sharp AJ.   +7 more
europepmc   +1 more source

Whole-genome sequencing coupled to imputation discovers genetic signals for anthropometric traits [PDF]

, 2017
et al,, Locke, Adam
core   +1 more source