| Year |
Citation |
Score |
| 2023 |
Yin X, Li J, Bose D, Okamoto J, Kwon A, Jackson AU, Silva LF, Oravilahti A, Stringham HM, Ripatti S, Daly M, Palotie A, Scott LJ, Burant CF, Fauman EB, ... ... Morrison J, et al. Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health. Medrxiv : the Preprint Server For Health Sciences. PMID 37425837 DOI: 10.1101/2023.06.26.23291721 |
0.426 |
|
| 2023 |
Okamoto J, Wang L, Yin X, Luca F, Pique-Regi R, Helms A, Im HK, Morrison J, Wen X. Probabilistic integration of transcriptome-wide association studies and colocalization analysis identifies key molecular pathways of complex traits. American Journal of Human Genetics. 110: 44-57. PMID 36608684 DOI: 10.1016/j.ajhg.2022.12.002 |
0.506 |
|
| 2022 |
Yin X, Bose D, Kwon A, Hanks SC, Jackson AU, Stringham HM, Welch R, Oravilahti A, Fernandes Silva L, Locke AE, Fuchsberger C, Service SK, Erdos MR, Bonnycastle LL, Kuusisto J, ... ... Morrison J, et al. Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk. American Journal of Human Genetics. PMID 36055244 DOI: 10.1016/j.ajhg.2022.08.007 |
0.496 |
|
| 2022 |
Yin X, Chan LS, Bose D, Jackson AU, VandeHaar P, Locke AE, Fuchsberger C, Stringham HM, Welch R, Yu K, Fernandes Silva L, Service SK, Zhang D, Hector EC, Young E, ... ... Morrison J, et al. Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nature Communications. 13: 1644. PMID 35347128 DOI: 10.1038/s41467-022-29143-5 |
0.507 |
|
| 2020 |
Zhang Z, Luo K, Zou Z, Qiu M, Tian J, Sieh L, Shi H, Zou Y, Wang G, Morrison J, Zhu AC, Qiao M, Li Z, Stephens M, He X, et al. Genetic analyses support the contribution of mRNA N-methyladenosine (mA) modification to human disease heritability. Nature Genetics. PMID 32601472 DOI: 10.1038/S41588-020-0644-Z |
0.577 |
|
| 2020 |
Morrison J, Knoblauch N, Marcus JH, Stephens M, He X. Publisher Correction: Mendelian randomization accounting for correlated and uncorrelated pleiotropic effects using genome-wide summary statistics. Nature Genetics. PMID 32472065 DOI: 10.1038/S41588-020-0655-9 |
0.504 |
|
| 2020 |
Morrison J, Knoblauch N, Marcus JH, Stephens M, He X. Mendelian randomization accounting for correlated and uncorrelated pleiotropic effects using genome-wide summary statistics. Nature Genetics. PMID 32451458 DOI: 10.1038/S41588-020-0631-4 |
0.567 |
|
| 2018 |
Morrison J, Simon N. Rank Conditional Coverage and Confidence Intervals in High-Dimensional Problems. Journal of Computational and Graphical Statistics : a Joint Publication of American Statistical Association, Institute of Mathematical Statistics, Interface Foundation of North America. 27: 648-656. PMID 30740009 DOI: 10.1080/10618600.2017.1411270 |
0.531 |
|
| 2018 |
Liu Y, Liang Y, Cicek AE, Li Z, Li J, Muhle RA, Krenzer M, Mei Y, Wang Y, Knoblauch N, Morrison J, Zhao S, Jiang Y, Geller E, Ionita-Laza I, et al. A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies. American Journal of Human Genetics. PMID 29754769 DOI: 10.1016/J.Ajhg.2018.03.023 |
0.348 |
|
| 2016 |
Morrison J, Simon N, Witten D. Simultaneous detection and estimation of trait associations with genomic phenotypes. Biostatistics (Oxford, England). PMID 27496912 DOI: 10.1093/Biostatistics/Kxw033 |
0.579 |
|
| 2013 |
Hayes MG, Urbanek M, Hivert MF, Armstrong LL, Morrison J, Guo C, Lowe LP, Scheftner DA, Pluzhnikov A, Levine DM, McHugh CP, Ackerman CM, Bouchard L, Brisson D, Layden BT, et al. Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies. Diabetes. 62: 3282-91. PMID 23903356 DOI: 10.2337/Db12-1692 |
0.382 |
|
| 2013 |
Urbanek M, Hayes MG, Armstrong LL, Morrison J, Lowe LP, Badon SE, Scheftner D, Pluzhnikov A, Levine D, Laurie CC, McHugh C, Ackerman CM, Mirel DB, Doheny KF, Guo C, et al. The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study. Human Molecular Genetics. 22: 3583-96. PMID 23575227 DOI: 10.1093/Hmg/Ddt168 |
0.328 |
|
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