Chen-HanWilfredWuMD

PubMed

• The evolving landscape of monogenic nephrolithiasis and therapeutic innovations.
  Yu-Ren Huang, Fredrick R Schumacher, Chen-Han Wilfred Wu, Donald Bodner, Michelle Baum, Friedhelm Hildebrandt> ;Nature Reviews. Urology. 2024 Apr 17
• Genomic Risk Factors for Urethral Stricture: A Systematic Review and Gene Network Analysis.
  Ilaha Isali, Thomas R Wong, Chen-Han Wilfred Wu, Kyle Scarberry, Shubham Gupta, Bradley A Erickson, Benjamin N Breyer> ;Urology. 2024 Feb 1
• Recurrent urinary tract infection genetic risk: a systematic review and gene network analysis.
  Ilaha Isali, Thomas R Wong, Ali Furkan Batur, Chen-Han Wilfred Wu, Fredrick R Schumacher, Rachel Pope, Adonis Hijaz, David Sheyn, Sheyn, D.> ;International Urogynecology Journal. 2024 Feb 1
• 3 citations
  Population genetics analysis of SLC3A1 and SLC7A9 revealed the etiology of cystine stone may be more than what our current genetic knowledge can explain.
  Chen-Han Wilfred Wu, Jad Badreddine, Joshua Chang, Yu-Ren Mike Huang, Fernando J Kim, Trevor Wild, Anne Chun-Hui Tsai, Naomi Meeks, Rodrigo Donalisio Da Silva, Wilson ...> ;Urolithiasis. 2023 Aug 10
• 1 citations
  Recessive CHRM5 variant as a potential cause of neurogenic bladder.
  Sophia Schneider, Luca Schierbaum, Wessel A C Burger, Steve Seltzsam, Chunyan Wang, Bixia Zheng, Chen-Han Wilfred Wu, Makiko Nakayama, Dervla M Connaughton, Nina Mann,...> ;American Journal of Medical Genetics. Part A. 2023 Aug 1
• OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis.
  Amar J Majmundar, Eugen Widmeier, John F Heneghan, Ankana Daga, Chen-Han Wilfred Wu, Florian Buerger, Hannah Hugo, Ihsan Ullah, Ali Amar, Isabel Ottlewski, Daniela A B...> ;Genetics in Medicine. 2023 Mar 1
• 1 citations
  Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.
  Verena Klämbt, Florian Buerger, Chunyan Wang, Thomas Naert, Karin Richter, Theresa Nauth, Anna-Carina Weiss, Tobias Sieckmann, Ethan Lai, Dervla M Connaughton, Steve S...> ;Journal of the American Society of Nephrology. 2023 Feb 1
• 3 citations
  A systematic review and in silico study of potential genetic markers implicated in cases of overactive bladder.
  Ilaha Isali, Phillip McClellan, Thomas R Wong, Clara Sun, Amber Catherine Stout, Fredrick R Schumacher, Sarah Markt, Chen-Han Wilfred Wu, Kathryn L Penney, Sherif El-N...> ;American Journal of Obstetrics and Gynecology. 2023 Jan 1
• 2 citations
  Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
  Chen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, Steve Seltzsam, Bixia Zheng, Luca Schierbaum, Sophia Schneider, Nina Mann, Dervla M Connaughton, Makiko Nakayama, Amelie ...> ;European Urology Open Science. 2022 Oct 1
• 1 citations
  Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models.
  Chunyan Wang, Steve Seltzsam, Bixia Zheng, Chen-Han Wilfred Wu, Camille Nicolas-Frank, Kirollos Yousef, Kit Sing Au, Nina Mann, Dalia Pantel, Sophia Schneider, Luca Sc...> ;American Journal of Medical Genetics. Part A. 2022 May 1
• 10 citations
  Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT
  Steve Seltzsam, Chunyan Wang, Bixia Zheng, Nina Mann, Dervla M. Connaughton, Chen-Han Wilfred Wu, Sophia Schneider, Luca Schierbaum, Franziska Kause, Caroline M. Kolve...> ;Genetics in Medicine. 2021 Nov 30
• 4 citations
  Whole exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.
  Bixia Zheng, Steve Seltzsam, Chunyan Wang, Luca Schierbaum, Sophia Schneider, Chen-Han Wilfred Wu, Rufeng Dai, Dervla M. Connaughton, Makiko Nakayama, Nina Mann, Natas...> ;Nephrology, Dialysis, Transplantation. 2021 Sep 2
• 17 citations
  Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations
  Dervla M. Connaughton, Rufeng Dai, Danielle J. Owen, Jonathan Marquez, Nina Mann, Adda L. Graham-Paquin, Makiko Nakayama, Etienne Coyaud, Estelle M.N. Laurent, Jonatha...> ;American Journal of Human Genetics. 2020 Oct 1
• 18 citations
  Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT).
  Chen-Han Wilfred Wu, Nina Mann, Makiko Nakayama, Dervla M. Connaughton, Rufeng Dai, Caroline M. Kolvenbach, Franziska Kause, Isabel Ottlewski, Chunyan Wang, Verena Klä...> ;Genetics in Medicine. 2020 Jun 1
• 12 citations
  CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations
  Nina Mann, Franziska Kause, Erik Henze, Anant Gharpure, Shirlee Shril, Dervla M. Connaughton, Makiko Nakayama, Verena Klämbt, Amar J. Majmundar, Chen Han W. Wu, Caroli...> ;American Journal of Human Genetics. 2019 Dec 5
• 11 citations
  COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans
  Thomas M. Kitzler, Ronen Schneider, Stefan Kohl, Caroline M. Kolvenbach, Dervla M. Connaughton, Rufeng Dai, Nina Mann, Makiko Nakayama, Amar J. Majmundar, Chen-Han W. ...> ;Human Genetics. 2019 Jun 22
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