Katherine Benson
Predoctoral Trainee
Boston University Chobanian & Avedisian School of Medicine, Graduate Medical Sciences
Molecular and Translational Medicine

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Pluripotent Stem Cell Modeling of Airway Epithelial Differentiation
09/01/2015 - 05/31/2017 (PI)
NIH/National Heart, Lung, and Blood Institute
5F31HL129777-02



Title


Yr Title Project-Sub Proj Pubs
2016 Pluripotent Stem Cell Modeling of Airway Epithelial Differentiation 5F31HL129777-02 4
2015 Pluripotent Stem Cell Modeling of Airway Epithelial Differentiation 1F31HL129777-01 4

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

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  1. Elhassan EAE, Cormican S, Osman SM, Sarihan S, Teltsh O, Poynton FE, Griffin MD, Casserly L, McCann E, Bleyer AJ, Kmoch S, Živná M, Benson KA, Cavalleri GL, Conlon PJ. Characterization of Monogenic Kidney Disease in Older Patients With CKD. Kidney Int Rep. 2025 Jul; 10(7):2140-2152. PMID: 40677324; PMCID: PMC12266177; DOI: 10.1016/j.ekir.2025.04.017;
     
  2. Collins KE, Gilbert E, Mauduit V, Benson KA, Elhassan EAE, O'Seaghdha C, Hill C, McKnight AJ, Maxwell AP, van der Most PJ, de Borst MH, Guan W, Jacobson PA, Israni AK, Keating BJ, Lord GM, Markkinen S, Helanterä I, Hyvärinen K, Partanen J, Madden SF, Lanktree MB, Limou S, Cavalleri GL, Conlon PJ. Donor and Recipient Polygenic Risk Scores Influence Kidney Transplant Function. Transpl Int. 2025; 38:14171. PMID: 40104404; PMCID: PMC11913612; DOI: 10.3389/ti.2025.14171;
     
  3. Collins KE, Gilbert E, Mauduit V, Gaheer P, Elhassan EAE, Benson KA, Osman SM, Hill C, McKnight AJ, Maxwell AP, van der Most PJ, de Borst MH, Guan W, Jacobson PA, Israni AK, Keating BJ, Lord GM, Markkinen S, Helanterä I, Hyvärinen K, Partanen J, Madden SF, Storrar J, Sinha S, Kalra PA, Lanktree MB, Limou S, Cavalleri GL, Conlon PJ. Polygenic risk scores for eGFR are associated with age at kidney failure. J Nephrol. 2025 Apr; 38(3):969-978. PMID: 40029548; PMCID: PMC12165877; DOI: 10.1007/s40620-025-02207-7;
     
  4. Cipriani V, Vestito L, Magavern EF, Jacobsen JOB, Arno G, Behr ER, Benson KA, Bertoli M, Bockenhauer D, Bowl MR, Burley K, Chan LF, Chinnery P, Conlon PJ, Costa MA, Davidson AE, Dawson SJ, Elhassan EAE, Flanagan SE, Futema M, Gale DP, García-Ruiz S, Corcia CG, Griffin HR, Hambleton S, Hicks AR, Houlden H, Houlston RS, Howles SA, Kleta R, Lekkerkerker I, Lin S, Liskova P, Mitchison HH, Morsy H, Mumford AD, Newman WG, Neatu R, O'Toole EA, Ong ACM, Pagnamenta AT, Rahman S, Rajan N, Robinson PN, Ryten M, Sadeghi-Alavijeh O, Sayer JA, Shovlin CL, Taylor JC, Teltsh O, Tomlinson I, Tucci A, Turnbull C, van Eerde AM, Ware JS, Watts LM, Webster AR, Westbury SK, Zheng SL, Caulfield M, Smedley D. Rare disease gene association discovery in the 100,000 Genomes Project. Nature. 2025 Feb 26. PMID: 40011789
     
  5. Elhassan EAE, O'Donoghue D, Heneghan S, Teltsh O, Sarihan S, Osman SM, Clince M, Synnott D, Craig S, Hudson A, Doyle B, Lappin D, Sexton DJ, Casserly L, Holian J, Magee C, Denton M, Sweeney C, Awan A, McCann E, Cavalleri GL, Benson KA, Conlon PJ. Phenotypic outcomes of PKD1 compared with non-PKD1 genetically confirmed autosomal dominant polycystic kidney disease. J Nephrol. 2025 Jun; 38(5):1445-1456. PMID: 39881088
     
  6. Elhassan EAE, Collins KE, Heneghan S, Gilbert E, Yang H, Senum SR, Schauer RS, Elbarougy DE, Madden SF, Murray SL, Sadeghi-Alavijeh O, Carmichael J, Gale D, Osman SM, Kennedy C, Griffin MD, Casserly L, Moloney B, O'Hara P, Mallawaarachchi A, Ciurli F, Graziano C, Wolff CA, Schönauer R, LaManna G, Durand A, Limou S, Halbritter J, Capelli I, McCann E, Harris PC, Cavalleri GL, Benson KA, Conlon PJ. The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney disease. J Nephrol. 2025 Jun; 38(5):1457-1467. PMID: 39883360; PMCID: PMC12289752; DOI: 10.1007/s40620-025-02211-x;
     
  7. Collins KE, Gilbert E, Mauduit V, Benson KA, Elhassan EAE, O'Seaghdha C, Hill C, McKnight AJ, Maxwell AP, van der Most PJ, de Borst MH, Guan W, Jacobson PA, Israni AK, Keating BJ, Lord GM, Markkinen S, Helanterä I, Hyvärinen K, Partanen J, Madden SF, Limou S, Cavalleri GL, Conlon PJ. Donor genetic burden for cerebrovascular risk and kidney transplant outcome. J Nephrol. 2024 Jul; 37(6):1643-1652. PMID: 38809363; PMCID: PMC11473625; DOI: 10.1007/s40620-024-01973-0;
     
  8. Elhassan EAE, Kmochová T, Benson KA, Fennelly NK, Barešová V, Kidd K, Doyle B, Dorman A, Morrin MM, Kyne NC, Vyletal P, Hartmannová H, Hodanová K, Sovová J, Mušálková D, Vrbacká A, Pristoupilová A, Živný J, Svojšová K, Radina M, Stránecký V, Loginov D, Pompach P, Novák P, Vanícková Z, Hansíková H, Rajnochová-Bloudícková S, Viklický O, Hulková H, Cavalleri GL, Hnízda A, Bleyer AJ, Kmoch S, Conlon PJ, Živná M. A Novel Monoallelic ALG5 Variant Causing Late-Onset ADPKD and Tubulointerstitial Fibrosis. Kidney Int Rep. 2024 Jul; 9(7):2209-2226. PMID: 39081747; PMCID: PMC11284371; DOI: 10.1016/j.ekir.2024.04.031;
     
  9. Schmidt RJ, Steeves M, Bayrak-Toydemir P, Benson KA, Coe BP, Conlin LK, Ganapathi M, Garcia J, Gollob MH, Jobanputra V, Luo M, Ma D, Maston G, McGoldrick K, Palculict TB, Pesaran T, Pollin TI, Qian E, Rehm HL, Riggs ER, Schilit SLP, Sergouniotis PI, Tvrdik T, Watkins N, Zec L, Zhang W, Lebo MS. Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group. Genet Med. 2024 Mar; 26(3):101036. PMID: 38054408; PMCID: PMC10939896; DOI: 10.1016/j.gim.2023.101036;
     
  10. Elhassan EAE, Murray SL, Connaughton DM, Kennedy C, Cormican S, Cowhig C, Stapleton C, Little MA, Kidd K, Bleyer AJ, Živná M, Kmoch S, Fennelly NK, Doyle B, Dorman A, Griffin MD, Casserly L, Harris PC, Hildebrandt F, Cavalleri GL, Benson KA, Conlon PJ. The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene Project. J Nephrol. 2022 Jul; 35(6):1655-1665. PMID: 35099770
     
Showing 10 of 13 results. Show More

This graph shows the total number of publications by year, by first, middle/unknown, or last author.

Bar chart showing 13 publications over 7 distinct years, with a maximum of 6 publications in 2025

YearPublications
20161
20201
20211
20221
20231
20242
20256


2013-2015 Boston University School of Medicine: Levinsky Fellowship
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