Chen‐Han Wilfred Wu

Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT

Steve Seltzsam, Chunyan Wang, Bixia Zheng et al. · Genetics in Medicine · 2021 · 36 citations · Full text

Allelic Variant, Genetic Disorder, Exome Sequencing +7

COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans

Thomas M. Kitzler, Ronen Schneider, Stefan Kohl et al. · Human Genetics · 2019 · 24 citations · Full text

Genetic Disorder, Medicine, Genetics +9

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 et al. · Genetics in Medicine · 2020 · 22 citations · Full text

Urological Research, Urology, Phenotype Expansion +9

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 Yin Lim, Chunyan Wang et al. · European Urology Open Science · 2022 · 10 citations · Full text