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Wu, Chen-Han Wilfred
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1

The evolving landscape of monogenic nephrolithiasis and the..:

Wu, Chen-Han Wilfred ; Huang, Yu-Ren ; Bodner, Donald...
Nature Reviews Urology.  , 2024
Link: https://doi.org/10.1038/..
 
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2

Polygenic and polyphenotypic dimensions of nephrolithiasis:..:

Huang, Yu-Ren ; Su, Ethan ; Bodner, Donald..
Molecular Genetics and Metabolism.  141 (2024)  4 - p. 108190 , 2024
Link: https://doi.org/10.1016/..
 
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3

Genomic Risk Factors for Urethral Stricture: A Systematic R..:

Isali, Ilaha ; Wong, Thomas R. ; Wu, Chen-Han Wilfred...
Urology.  184 (2024)  - p. 251-258 , 2024
Link: https://doi.org/10.1016/..
 
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4

Sengers syndrome and AGK-related disorders - Minireview of ..:

Wu, Chen-Han Wilfred ; Caha, Martin ; Smoot, Leslie...
Molecular Genetics and Metabolism.  139 (2023)  3 - p. 107626 , 2023
Link: https://doi.org/10.1016/..
 
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5

Beyond the kidney: extra-renal manifestations of monogenic ..:

Wu, Chen-Han Wilfred ; Badreddine, Jad ; Su, Ethan...
Pediatric Nephrology.  39 (2023)  5 - p. 1429-1434 , 2023
Link: https://doi.org/10.1007/..
 
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6

Recurrent urinary tract infection genetic risk: a systemati..:

Isali, Ilaha ; Wong, Thomas R. ; Batur, Ali Furkan...
International Urogynecology Journal.  35 (2023)  2 - p. 259-271 , 2023
Link: https://doi.org/10.1007/..
 
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7

OXGR1 is a candidate disease gene for human calcium oxalate..:

Majmundar, Amar J. ; Widmeier, Eugen ; Heneghan, John F....
Genetics in Medicine.  25 (2023)  3 - p. 100351 , 2023
Link: https://doi.org/10.1016/..
 
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8

Population genetics analysis of SLC3A1 and SLC7A9 revealed ..:

Wu, Chen-Han Wilfred ; Badreddine, Jad ; Chang, Joshua...
Urolithiasis.  51 (2023)  1 - p. , 2023
Link: https://doi.org/10.1007/..
 
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9

Copy Number Variation Analysis Facilitates Identification o..:

Wu, Chen-Han Wilfred ; Lim, Tze Y. ; Wang, Chunyan...
European Urology Open Science.  44 (2022)  - p. 106-112 , 2022
Link: https://doi.org/10.1016/..
 
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10

Reverse phenotyping facilitates disease allele calling in e..:

Seltzsam, Steve ; Wang, Chunyan ; Zheng, Bixia...
Genetics in Medicine.  24 (2022)  2 - p. 307-318 , 2022
Link: https://doi.org/10.1016/..
 
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11

Whole-exome sequencing identifiesFOXL2,FOXA2andFOXA3as cand..:

Zheng, Bixia ; Seltzsam, Steve ; Wang, Chunyan...
Nephrology Dialysis Transplantation.  37 (2021)  10 - p. 1833-1843 , 2021
Link: https://doi.org/10.1093/..
 
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12

Phenotype expansion of heterozygous FOXC1 pathogenic varian..:

Wu, Chen-Han Wilfred ; Mann, Nina ; Nakayama, Makiko...
Genetics in Medicine.  22 (2020)  10 - p. 1673-1681 , 2020
Link: https://doi.org/10.1038/..
 
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13

P262: Assessing urolithiasis polygenic risk score predictiv..:

Salem, Amr ; Bodner, Donald ; Schumacher, Fredrick.
Genetics in Medicine Open.  2 (2024)  - p. 101158 , 2024
Link: https://doi.org/10.1016/..
 
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14

P269: The genetic prevalence of molybdenum cofactor deficie..:

Patel, Ishita ; Su, Ethan ; Lovrenert, Katreya...
Genetics in Medicine Open.  2 (2024)  - p. 101165 , 2024
Link: https://doi.org/10.1016/..
 
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15

P009: Genetics prevalence of cystine stone: A 6 year longit..:

Chang, Joshua ; Badreddine, Jad ; Eam, Euhun...
Genetics in Medicine Open.  1 (2023)  1 - p. 100019 , 2023
Link: https://doi.org/10.1016/..
 
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