HRS Bibliography
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C
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals. Human Molecular Genetics. 2015;24(12):3582-3594. doi:10.1093/hmg/ddv097.
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals. Human Molecular Genetics. 2015;24(12):3582-3594. doi:10.1093/hmg/ddv097.
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals. Human Molecular Genetics. 2015;24(12):3582-3594. doi:10.1093/hmg/ddv097.
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals. Human Molecular Genetics. 2015;24(12):3582-3594. doi:10.1093/hmg/ddv097.
D
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium. PLoS Genetics. 2017;13(4):e1006719. doi:10.1371/journal.pgen.1006719.
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium. PLoS Genetics. 2017;13(4):e1006719. doi:10.1371/journal.pgen.1006719.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. The American Journal of Human Genetics. 2021;108(4):564-582. doi:10.1016/j.ajhg.2021.02.011.
E
Exome Array Analysis of 9721 Ischemic Stroke Cases from the SiGN Consortium. Genes . 2022;14(1):61. doi:10.3390/genes14010061.
Exome Array Analysis of 9721 Ischemic Stroke Cases from the SiGN Consortium. Genes . 2022;14(1):61. doi:10.3390/genes14010061.
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Biological Psychiatry. 2019;85(11):946-955. doi:10.1016/j.biopsych.2018.11.024.
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Biological Psychiatry. 2019;85(11):946-955. doi:10.1016/j.biopsych.2018.11.024.
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Biological Psychiatry. 2019;85(11):946-955. doi:10.1016/j.biopsych.2018.11.024.
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Biological Psychiatry. 2019;85(11):946-955. doi:10.1016/j.biopsych.2018.11.024.
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Biological Psychiatry. 2019;85(11):946-955. doi:10.1016/j.biopsych.2018.11.024.