HRS Bibliography

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2017

Li M, Li Y, Weeks O, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology . 2017;28(3):981-994. doi:10.1681/ASN.2016020131.
Li M, Li Y, Weeks O, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology . 2017;28(3):981-994. doi:10.1681/ASN.2016020131.
Li M, Li Y, Weeks O, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology . 2017;28(3):981-994. doi:10.1681/ASN.2016020131.
Li M, Li Y, Weeks O, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology . 2017;28(3):981-994. doi:10.1681/ASN.2016020131.
Li M, Li Y, Weeks O, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology . 2017;28(3):981-994. doi:10.1681/ASN.2016020131.
Li M, Li Y, Weeks O, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology . 2017;28(3):981-994. doi:10.1681/ASN.2016020131.
Li M, Li Y, Weeks O, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology . 2017;28(3):981-994. doi:10.1681/ASN.2016020131.
Li M, Li Y, Weeks O, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology . 2017;28(3):981-994. doi:10.1681/ASN.2016020131.
Li M, Li Y, Weeks O, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology . 2017;28(3):981-994. doi:10.1681/ASN.2016020131.
Li M, Li Y, Weeks O, et al. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. Journal of the American Society of Nephrology . 2017;28(3):981-994. doi:10.1681/ASN.2016020131.

2016

Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Liu C, Kraja AT, Smith JA, Morrison AC, et al. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Nat Genet. 2016;48(10):1162-70. doi:10.1038/ng.3660.