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International Journal of Epidemiology|January 9, 2022
Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney diseaseJie Zheng, Yuemiao Zhang, Humaira Rasheed, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Kidney International|December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Nature Communications|April 2, 2020
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosisJingyuan Xie, Lili Liu, Nikol Mladkova, et al.
Nature Genetics|October 10, 2018
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome mapsAnubha Mahajan, Daniel Taliun, Matthias Thurner, et al.
Kidney International|November 2, 2020
Meta-analysis uncovers genome-wide significant variants for rapid kidney function declineMathias Gorski, Bettina Jung, Yong Li, et al.
Nature Communications|September 13, 2019
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuriaAlexander Teumer, Yong Li, Sahar Ghasemi, et al.
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