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IEEE/ACM Transactions on Computational Biology and Bioinformatics|August 17, 2011
Exploiting the functional and taxonomic structure of genomic data by probabilistic topic modelingXin Chen, Xiaohua Hu, Tze Y Lim, et al.Journal of Applied Clinical Medical Physics|December 25, 2015
Evaluation of the MIM Symphony treatment planning system for low-dose-rate- prostate brachytherapySandeep K Dhanesar, Tze Y Lim, Weiliang Du, et al.Pediatric Nephrology (Berlin, Germany)|September 5, 2023
Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two familiesDalia Pantel, Nils D Mertens, Ronen Schneider, et al.Journal of the American Society of Nephrology : JASN|December 11, 2021
GWAS in Mice Maps Susceptibility to HIV-Associated Nephropathy to the Ssbp2 LocusNicholas J Steers, Yask Gupta, Vivette D D'Agati, et al.JCI Insight|December 9, 2025
Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral refluxMiguel Verbitsky, Pavan Khosla, Daniel Bivona, et al.Pediatric Nephrology (Berlin, Germany)|January 14, 2026
APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tractLisanne M Vendrig, Juntao Ke, Michael W T Tanck, et al.Journal of the American Society of Nephrology : JASN|October 27, 2022
Genomic Disorders in CKD across the LifespanMiguel Verbitsky, Sarathbabu Krishnamurthy, Priya Krithivasan, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2023
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomaliesJeremiah Martino, Qingxue Liu, Katarina Vukojevic, et al.European Urology Open Science|October 3, 2022
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary TractChen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, et al.JAMA Network Open|March 11, 2026
Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective VariantElena Martinelli, Juntao Ke, Atlas Khan, et al.Pageof 3