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Year Number of Results
2015 2
2018 3
2020 3
2021 1
2022 0
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Page 1
Genetic Insights into Alzheimer's Disease.
Latimer CS, Lucot KL, Keene CD, Cholerton B, Montine TJ. Latimer CS, et al. Among authors: lucot kl. Annu Rev Pathol. 2021 Jan 24;16:351-376. doi: 10.1146/annurev-pathmechdis-012419-032551. Annu Rev Pathol. 2021. PMID: 33497263 Free PMC article. Review.
Canine NAPEPLD-associated models of human myelin disorders.
Minor KM, Letko A, Becker D, Drögemüller M, Mandigers PJJ, Bellekom SR, Leegwater PAJ, Stassen QEM, Putschbach K, Fischer A, Flegel T, Matiasek K, Ekenstedt KJ, Furrow E, Patterson EE, Platt SR, Kelly PA, Cassidy JP, Shelton GD, Lucot K, Bannasch DL, Martineau H, Muir CF, Priestnall SL, Henke D, Oevermann A, Jagannathan V, Mickelson JR, Drögemüller C. Minor KM, et al. Among authors: lucot k. Sci Rep. 2018 Apr 11;8(1):5818. doi: 10.1038/s41598-018-23938-7. Sci Rep. 2018. PMID: 29643404 Free PMC article.
Whole genome variant association across 100 dogs identifies a frame shift mutation in DISHEVELLED 2 which contributes to Robinow-like syndrome in Bulldogs and related screw tail dog breeds.
Mansour TA, Lucot K, Konopelski SE, Dickinson PJ, Sturges BK, Vernau KL, Choi S, Stern JA, Thomasy SM, Döring S, Verstraete FJM, Johnson EG, York D, Rebhun RB, Ho HH, Brown CT, Bannasch DL. Mansour TA, et al. Among authors: lucot k. PLoS Genet. 2018 Dec 6;14(12):e1007850. doi: 10.1371/journal.pgen.1007850. eCollection 2018 Dec. PLoS Genet. 2018. PMID: 30521570 Free PMC article.