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Frontiers in Genetics|August 8, 2024
Perspectives from cystinosis: access to healthcare may be a confounding factor for variant classificationChen-Han Wilfred Wu, Alicja Tomaszewski, Louisa Stark, et al.
European Journal of Human Genetics : EJHG|April 9, 2026
How variant discovery redefines genetic prevalence: the case of cystine stone diseaseChen-Han Wilfred Wu, Joshua Chang, Katreya Lovrenert, et al.
Basic and Clinical Andrology|June 11, 2026
Gene set enrichment analysis of curated monogenic loci highlights key pathways and multisystem involvement in male infertilityMatthew Yang, Katreya Lovrenert, Nannan Thirumavalavan, et al.
Molecular Genetics and Metabolism|June 24, 2023
Sengers syndrome and AGK-related disorders - Minireview of phenotypic variability and clinical outcomes in molecularly confirmed casesChen-Han Wilfred Wu, Martin Caha, Leslie Smoot, et al.
Urology|December 31, 2023
Genomic Risk Factors for Urethral Stricture: A Systematic Review and Gene Network AnalysisIlaha Isali, Thomas R Wong, Chen-Han Wilfred Wu, et al.
Pediatric Nephrology (Berlin, Germany)|December 6, 2023
Beyond the kidney: extra-renal manifestations of monogenic nephrolithiasis and their significanceChen-Han Wilfred Wu, Jad Badreddine, Ethan Su, et al.
International Urogynecology Journal|November 2, 2023
Recurrent urinary tract infection genetic risk: a systematic review and gene network analysisIlaha Isali, Thomas R Wong, Ali Furkan Batur, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 24, 2024
The role of double heterozygotes of SLC3A1 and SLC7A9 in the prevalence of cystine stonesChen-Han Wilfred Wu, Ishita Patel, Katreya Lovrenert, et al.
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