Works by Wu, Chen-Han Wilfred

Results: 7

Increased risk of upper tract urothelial carcinoma in patients with kidney stones: a large-scale analysis of the UK biobank.

Published in:

Urolithiasis, 2025, v. 53, n. 1, p. 1, doi. 10.1007/s00240-025-01758-5

By:

Ziadeh, Hachem;
Calaway, Adam;
Gupta, Sanjay;
Bodner, Donald;
Brown, Jason R.;
Schumacher, Fredrick R.;
Wu, Chen-Han Wilfred

Publication type:

Article

Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.

Published in:

Nephrology Dialysis Transplantation, 2022, v. 37, n. 10, p. 1833, doi. 10.1093/ndt/gfab253

By:

Zheng, Bixia;
Seltzsam, Steve;
Wang, Chunyan;
Schierbaum, Luca;
Schneider, Sophia;
Wu, Chen-Han Wilfred;
Dai, Rufeng;
Connaughton, Dervla M;
Nakayama, Makiko;
Mann, Nina;
Stajic, Natasa;
Mane, Shrikant;
Bauer, Stuart B;
Tasic, Velibor;
Nam, Hyun Joo;
Shril, Shirlee;
Hildebrandt, Friedhelm

Publication type:

Article

Beyond the kidney: extra-renal manifestations of monogenic nephrolithiasis and their significance.

Published in:

Pediatric Nephrology, 2024, v. 39, n. 5, p. 1429, doi. 10.1007/s00467-023-06242-z

By:

Wu, Chen-Han Wilfred;
Badreddine, Jad;
Su, Ethan;
Tay, Kimberly;
Lin, Hsin-Ti Cindy;
Rhodes, Stephen;
Schumacher, Fredrick;
Bodner, Donald

Publication type:

Article

Recessive CHRM5 variant as a potential cause of neurogenic bladder.

Published in:

American Journal of Medical Genetics. Part A, 2023, v. 191, n. 8, p. 2083, doi. 10.1002/ajmg.a.63241

By:

Schneider, Sophia;
Schierbaum, Luca;
Burger, Wessel A. C.;
Seltzsam, Steve;
Wang, Chunyan;
Zheng, Bixia;
Wu, Chen‐Han Wilfred;
Nakayama, Makiko;
Connaughton, Dervla M.;
Mann, Nina;
Shalaby, Mohamed A.;
Kari, Jameela A.;
ElDesoky, Sherif;
Tasic, Velibor;
Eid, Loai A.;
Shril, Shirlee;
Thal, David M.;
Hildebrandt, Friedhelm

Publication type:

Article

Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models.

Published in:

American Journal of Medical Genetics. Part A, 2022, v. 188, n. 5, p. 1355, doi. 10.1002/ajmg.a.62644

By:

Wang, Chunyan;
Seltzsam, Steve;
Zheng, Bixia;
Wu, Chen‐Han Wilfred;
Nicolas‐Frank, Camille;
Yousef, Kirollos;
Au, Kit Sing;
Mann, Nina;
Pantel, Dalia;
Schneider, Sophia;
Schierbaum, Luca;
Kitzler, Thomas M.;
Connaughton, Dervla M.;
Mao, Youying;
Dai, Rufeng;
Nakayama, Makiko;
Kari, Jameela A.;
El Desoky, Sherif;
Shalaby, Mohammed;
Eid, Loai A.

Publication type:

Article

Population genetics analysis of SLC3A1 and SLC7A9 revealed the etiology of cystine stone may be more than what our current genetic knowledge can explain.

Published in:

Urolithiasis, 2023, v. 51, n. 1, p. 1, doi. 10.1007/s00240-023-01473-z

By:

Wu, Chen-Han Wilfred;
Badreddine, Jad;
Chang, Joshua;
Huang, Yu-Ren Mike;
Kim, Fernando J.;
Wild, Trevor;
Tsai, Anne Chun-Hui;
Meeks, Naomi;
Donalisio Da Silva, Rodrigo;
Molina, Wilson R.;
Schumacher, Fredrick R.

Publication type:

Article

Perspectives from cystinosis: access to healthcare may be a confounding factor for variant classification.

Published in:

Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1402667

By:

Wu, Chen-Han Wilfred;
Tomaszewski, Alicja;
Stark, Louisa;
Scaglia, Fernando;
Elenberg, Ewa;
Schumaker, Fredrick R.

Publication type:

Article