| Sex, Genotype, and Liver Volume Progression as Risk of Hospitalization Determinants in Autosomal Dominant Polycystic Liver Disease R Schönauer, D Sierks, M Boerrigter, T Jawaid, L Caroff, MP Audrezet, ... Gastroenterology 166 (5), 902-914, 2024 | 1 | 2024 |
| Genetic Analysis of Severe Polycystic Liver Disease in Japan H Mizuno, W Besse, A Sekine, KT Long, S Kurihara, Y Oba, ... Kidney360, 10.34067, 2024 | | 2024 |
| Cystic Kidney Diseases in Children and Adults: Differences and Gaps in Clinical Management C Hanna, IA Iliuta, W Besse, D Mekahli, FT Chebib Seminars in Nephrology, 151434, 2023 | 1 | 2023 |
| Combined Consideration of Sex, Genotype, and Total Liver Volume Progression Determines the Risk of Hospitalization in an International Multicenter Cohort of Autosomal Dominant … D Sierks, RA Schönauer, MM Boerrigter, T Jawaid, MP Audrezet, L Caroff, ... Journal of the American Society of Nephrology 34 (11S), 934-935, 2023 | | 2023 |
| KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease F Boulogne, LR Claus, H Wiersma, R Oelen, F Schukking, N de Klein, S Li, ... European Journal of Human Genetics 31 (11), 1300-1308, 2023 | 5 | 2023 |
| Dnajb11-kidney disease develops from reduced polycystin-1 dosage but not unfolded protein response in mice SG Roy, Z Li, Z Guo, KT Long, S Rehrl, X Tian, K Dong, W Besse Journal of the American Society of Nephrology 34 (9), 1521-1534, 2023 | 5 | 2023 |
| An update on ductal plate malformations and fibropolycystic diseases of the liver H Mirza, W Besse, S Somlo, J Weinreb, B Kenney, D Jain Human Pathology 132, 102-113, 2023 | 6 | 2023 |
| A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease H Jafari Khamirani, VR Palicharla, SA Dastgheib, M Dianatpour, ... Frontiers in Genetics 13, 1021037, 2022 | 7 | 2022 |
| A practical guide to genetic testing for kidney disorders of unknown etiology AW Aron, NK Dahl, W Besse Kidney360 3 (9), 1640-1651, 2022 | 7 | 2022 |
| KidneyNetwork: Using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease F Boulogne, L Claus, H Wiersma, R Oelen, F Schukking, N de Klein, S Li, ... | | 2022 |
| Genetic Diseases Associated with Tubulointerstitial Nephritis MTF Wolf, W Besse, AJ Bleyer, NK Dahl Tubulointerstitial Nephritis, 139-160, 2022 | | 2022 |
| A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease V Palicharla, S Dastgheib, M Dianatpour, M Imanieh, S Tabei, W Besse, ... Frontiers in Genetics 13, 2022 | | 2022 |
| Adult inactivation of the recessive polycystic kidney disease gene causes polycystic liver disease W Besse, C Roosendaal, L Tuccillo, SG Roy, AR Gallagher, S Somlo Kidney360 1 (10), 1068-1076, 2020 | 8 | 2020 |
| Genetic analysis in kidney disease: Advancing clinical diagnosis and research discovery W Besse Kidney360 1 (8), 720-723, 2020 | 2 | 2020 |
| Large Deletions in GANAB and SEC63 explain 2 cases of polycystic kidney and liver disease EM Wilson, J Choi, VE Torres, S Somlo, W Besse Kidney International Reports 5 (5), 727-731, 2020 | 8 | 2020 |
| Kidney360 Publish Ahead of Print, published on September 2, 2020 as doi: 10.34067/KID. 0002522020 W Besse, S Somlo | | 2020 |
| Collagen IV gene mutations in adults with bilateral renal cysts and CKD A Gulati, AM Sevillano, M Praga, E Gutierrez, I Alba, NK Dahl, W Besse, ... Kidney International Reports 5 (1), 103-108, 2020 | 42 | 2020 |
| ALG9 mutation carriers develop kidney and liver cysts W Besse, AR Chang, JZ Luo, WJ Triffo, BS Moore, A Gulati, DN Hartzel, ... Journal of the American Society of Nephrology 30 (11), 2091-2102, 2019 | 131 | 2019 |
| Monoallelic mutations to DNAJB11 cause atypical autosomal-dominant polycystic kidney disease E Cornec-Le Gall, RJ Olson, W Besse, CM Heyer, VG Gainullin, JM Smith, ... The American Journal of Human Genetics 102 (5), 832-844, 2018 | 286 | 2018 |
| A noncoding variant in GANAB explains isolated polycystic liver disease (PCLD) in a large family W Besse, J Choi, D Ahram, S Mane, S Sanna‐Cherchi, V Torres, S Somlo Human mutation 39 (3), 378-382, 2018 | 31 | 2018 |
