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Journal of Biomedical Science|February 13, 2024
Germline mutations of homologous recombination genes and clinical outcomes in pancreatic cancer: a multicenter study in TaiwanSiao Muk Cheng, Yung-Yeh Su, Nai-Jung Chiang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 21, 2026
A New CA19-9 Cutoff Value Identifies Lewis Antigen Status and Refines Prognostic Stratification in PDACChia-Ming Yeh, Chih-Chuan Yu, An-Fu Lee, et al.
The Journal of Investigative Dermatology|January 13, 2024
Profibrotic Subsets of SPP1<sup>+</sup> Macrophages and POSTN<sup>+</sup> Fibroblasts Contribute to Fibrotic Scarring in Acne KeloidalisYi-Kai Hong, Daw-Yang Hwang, Chao-Chun Yang, et al.
Oncogene|May 29, 2025
Macrophage activation determines muscle wasting in pancreatic cancerChia-Jung Chang, Po-Hsien Huang, Szu-Ying Chen, et al.
Plos One|January 20, 2018
A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral refluxAmelie T van der Ven, Birgit Kobbe, Stefan Kohl, et al.
Human Genetics|June 1, 2015
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tractDaw-Yang Hwang, Stefan Kohl, Xueping Fan, et al.
Kidney International|October 25, 2013
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL associationPawaree Saisawat, Stefan Kohl, Alina C Hilger, et al.
American Journal of Human Genetics|August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter DevelopmentAsaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
American Journal of Human Genetics|October 8, 2013
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary DyskinesiaChristina Austin-Tse, Jan Halbritter, Maimoona A Zariwala, et al.
American Journal of Human Genetics|July 30, 2013
ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6Maimoona A Zariwala, Heon Yung Gee, Małgorzata Kurkowiak, et al.
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