| Year |
Citation |
Score |
| 2023 |
Schönauer R, Sierks D, Boerrigter M, Jawaid T, Caroff L, Audrezet MP, Friedrich A, Shaw M, Degenhardt J, Forberger M, de Fallois J, Bläker H, Bergmann C, Gödiker J, Schindler P, ... ... Besse W, et al. Sex, genotype, and liver volume progression as risk of hospitalization determinants in autosomal dominant polycystic liver disease. Gastroenterology. PMID 38101549 DOI: 10.1053/j.gastro.2023.12.007 |
0.676 |
|
| 2023 |
Hanna C, Iliuta IA, Besse W, Mekahli D, Chebib FT. Cystic Kidney Diseases in Children and Adults: Differences and Gaps in Clinical Management. Seminars in Nephrology. 151434. PMID 37996359 DOI: 10.1016/j.semnephrol.2023.151434 |
0.463 |
|
| 2023 |
Roy SG, Li Z, Guo Z, Long K, Rehrl S, Tian X, Dong K, Besse W. DNAJB11 -Kidney Disease Develops from Reduced Polycystin-1 Dosage but not Unfolded Protein Response in Mice. Journal of the American Society of Nephrology : Jasn. PMID 37332102 DOI: 10.1681/ASN.0000000000000164 |
0.473 |
|
| 2023 |
Boulogne F, Claus LR, Wiersma H, Oelen R, Schukking F, de Klein N, Li S, Westra HJ, van der Zwaag B, van Reekum F, Sierks D, Schönauer R, Li Z, Bijlsma EK, Bos WJW, ... ... Besse W, et al. KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease. European Journal of Human Genetics : Ejhg. PMID 36807342 DOI: 10.1038/s41431-023-01296-x |
0.568 |
|
| 2022 |
Jafari Khamirani H, Palicharla VR, Dastgheib SA, Dianatpour M, Imanieh MH, Tabei SS, Besse W, Mukhopadhyay S, Liem KF. A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease. Frontiers in Genetics. 13: 1021037. PMID 36276950 DOI: 10.3389/fgene.2022.1021037 |
0.451 |
|
| 2022 |
Mirza H, Besse W, Somlo S, Weinreb J, Kenney B, Jain D. An Update on Ductal Plate Malformations and Fibropolycystic Diseases of the Liver. Human Pathology. PMID 35777701 DOI: 10.1016/j.humpath.2022.06.022 |
0.665 |
|
| 2020 |
Besse W. Genetic Analysis in Kidney Disease: Advancing Clinical Diagnosis and Research Discovery. Kidney360. 1: 720-723. PMID 34327334 DOI: 10.34067/kid.0003632020 |
0.363 |
|
| 2020 |
Besse W, Roosendaal C, Tuccillo L, Roy SG, Gallagher AR, Somlo S. Adult Inactivation of the Recessive Polycystic Kidney Disease Gene Causes Polycystic Liver Disease. Kidney360. 1: 1068-1076. PMID 33554127 DOI: 10.34067/Kid.0002522020 |
0.714 |
|
| 2020 |
Wilson EM, Choi J, Torres VE, Somlo S, Besse W. Large Deletions in and Explain 2 Cases of Polycystic Kidney and Liver Disease. Kidney International Reports. 5: 727-731. PMID 32405593 DOI: 10.1016/J.Ekir.2020.01.009 |
0.696 |
|
| 2020 |
Gulati A, Sevillano AM, Praga M, Gutierrez E, Alba I, Dahl NK, Besse W, Choi J, Somlo S. Collagen IV Gene Mutations in Adults With Bilateral Renal Cysts and CKD. Kidney International Reports. 5: 103-108. PMID 31922066 DOI: 10.1016/J.Ekir.2019.09.004 |
0.619 |
|
| 2020 |
Besse W. Genetic Analysis in Kidney Disease: Advancing Clinical Diagnosis and Research Discovery Kidney. 1: 720-723. DOI: 10.34067/Kid.0003632020 |
0.536 |
|
| 2019 |
Besse W, Chang AR, Luo JZ, Triffo WJ, Moore BS, Gulati A, Hartzel DN, Mane S, Torres VE, Somlo S, Mirshahi T. Mutation Carriers Develop Kidney and Liver Cysts. Journal of the American Society of Nephrology : Jasn. PMID 31395617 DOI: 10.1681/Asn.2019030298 |
0.729 |
|
| 2018 |
Cornec-Le Gall E, Olson RJ, Besse W, Heyer CM, Gainullin VG, Smith JM, Audrézet MP, Hopp K, Porath B, Shi B, Baheti S, Senum SR, Arroyo J, Madsen CD, Férec C, et al. Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease. American Journal of Human Genetics. PMID 29706351 DOI: 10.1016/J.Ajhg.2018.03.013 |
0.677 |
|
| 2017 |
Besse W, Choi J, Ahram D, Mane S, Sanna-Cherchi S, Torres V, Somlo S. A non-coding variant in GANAB explains isolated polycystic liver disease (PCLD) in a large family. Human Mutation. PMID 29243290 DOI: 10.1002/Humu.23383 |
0.661 |
|
| 2017 |
Besse W, Dong K, Choi J, Punia S, Fedeles SV, Choi M, Gallagher AR, Huang EB, Gulati A, Knight J, Mane S, Tahvanainen E, Tahvanainen P, Sanna-Cherchi S, Lifton RP, et al. Isolated polycystic liver disease genes define effectors of polycystin-1 function. The Journal of Clinical Investigation. 127: 3558. PMID 28862642 DOI: 10.1172/Jci96729 |
0.68 |
|
| 2017 |
Besse W, Dong K, Choi J, Punia S, Fedeles SV, Choi M, Gallagher AR, Huang EB, Gulati A, Knight J, Mane S, Tahvanainen E, Tahvanainen P, Sanna-Cherchi S, Lifton RP, et al. Isolated polycystic liver disease genes define effectors of polycystin-1 function. The Journal of Clinical Investigation. PMID 28375157 DOI: 10.1172/Jci90129 |
0.735 |
|
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