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Large-scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and hand.
Evangelou E, Chapman K, Meulenbelt I, Karassa FB, Loughlin J, Carr A, Doherty M, Doherty S, Gómez-Reino JJ, Gonzalez A, Halldorsson BV, Hauksson VB, Hofman A, Hart DJ, Ikegawa S, Ingvarsson T, Jiang Q, Jonsdottir I, Jonsson H, Kerkhof HJ, Kloppenburg M, Lane NE, Li J, Lories RJ, van Meurs JB, Näkki A, Nevitt MC, Rodriguez-Lopez J, Shi D, Slagboom PE, Stefansson K, Tsezou A, Wallis GA, Watson CM, Spector TD, Uitterlinden AG, Valdes AM, Ioannidis JP. Evangelou E, et al. Among authors: watson cm. Arthritis Rheum. 2009 Jun;60(6):1710-21. doi: 10.1002/art.24524. Arthritis Rheum. 2009. PMID: 19479880 Free PMC article.
A meta-analysis of European and Asian cohorts reveals a global role of a functional SNP in the 5' UTR of GDF5 with osteoarthritis susceptibility.
Chapman K, Takahashi A, Meulenbelt I, Watson C, Rodriguez-Lopez J, Egli R, Tsezou A, Malizos KN, Kloppenburg M, Shi D, Southam L, van der Breggen R, Donn R, Qin J, Doherty M, Slagboom PE, Wallis G, Kamatani N, Jiang Q, Gonzalez A, Loughlin J, Ikegawa S. Chapman K, et al. Hum Mol Genet. 2008 May 15;17(10):1497-504. doi: 10.1093/hmg/ddn038. Epub 2008 Feb 24. Hum Mol Genet. 2008. PMID: 18299287
Structure of ubiquitin-fold modifier 1-specific protease UfSP2.
Ha BH, Jeon YJ, Shin SC, Tatsumi K, Komatsu M, Tanaka K, Watson CM, Wallis G, Chung CH, Kim EE. Ha BH, et al. Among authors: watson cm. J Biol Chem. 2011 Mar 25;286(12):10248-57. doi: 10.1074/jbc.M110.172171. Epub 2011 Jan 12. J Biol Chem. 2011. PMID: 21228277 Free PMC article.
Desirability of Outcome Ranking and Response Adjusted for Antibiotic Risk (DOOR/RADAR) Post Hoc Analysis Supports Equipoise for Antibiotic Initiation Strategies in Intensive Care Unit-Acquired Pneumonia.
Guidry CA, Chollet-Hinton L, Baker J, O'Dell JC, Beyene RT, Watson CM, Sawyer RG, Simpson SQ, Atchison L, Derickson M, Cooper LC, Pennington GP 2nd, VandenBerg S, Halimeh BN. Guidry CA, et al. Among authors: watson cm. Surg Infect (Larchmt). 2024 Apr;25(3):221-224. doi: 10.1089/sur.2023.367. Epub 2024 Mar 7. Surg Infect (Larchmt). 2024. PMID: 38466941 Clinical Trial.
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability.
Smith CEL, Laugel-Haushalter V, Hany U, Best S, Taylor RL, Poulter JA, Wortmann SB, Feichtinger RG, Mayr JA, Al Bahlani S, Nikolopoulos G, Rigby A, Black GC, Watson CM, Mansour S, Inglehearn CF, Mighell AJ, Bloch-Zupan A; UK Inherited Retinal Disease Consortium, Genomics England Research Consortium. Smith CEL, et al. Among authors: watson cm. J Med Genet. 2024 Apr 8:jmg-2023-109728. doi: 10.1136/jmg-2023-109728. Online ahead of print. J Med Genet. 2024. PMID: 38458752 Free article.
Provider Perceptions of Antibiotic Initiation Strategies for Hospital-Acquired Pneumonia.
Swilling AC, O'Dell JC, Beyene RT, Watson CM, Sawyer RG, Chollet-Hinton L, Simpson SQ, Atchison L, Derickson M, Cooper LC, Pennington GP 2nd, VandenBerg S, Halimeh BN, Hughes D, Guidry CA. Swilling AC, et al. Among authors: watson cm. Surg Infect (Larchmt). 2024 Mar;25(2):109-115. doi: 10.1089/sur.2023.310. Epub 2024 Jan 22. Surg Infect (Larchmt). 2024. PMID: 38252553 Clinical Trial.
3D printed models are an accurate, cost-effective, and reproducible tool for quantifying terrestrial thermal environments.
Alujević K, Bakewell L, Clifton IT, Cox CL, Frishkoff LO, Gangloff EJ, Garcia-Costoya G, Gifford ME, Glenwinkel M, Gulati SAK, Head A, Miles M, Pettit C, Watson CM, Wuthrich KL, Logan ML. Alujević K, et al. Among authors: watson cm. J Therm Biol. 2024 Jan;119:103762. doi: 10.1016/j.jtherbio.2023.103762. Epub 2023 Dec 4. J Therm Biol. 2024. PMID: 38071898
Novel Ameloblastin Variants, Contrasting Amelogenesis Imperfecta Phenotypes.
Hany U, Watson CM, Liu L, Nikolopoulos G, Smith CEL, Poulter JA, Brown CJ, Patel A, Rodd HD, Balmer R, Harfoush A, Al-Jawad M, Inglehearn CF, Mighell AJ. Hany U, et al. Among authors: watson cm. J Dent Res. 2024 Jan;103(1):22-30. doi: 10.1177/00220345231203694. Epub 2023 Dec 6. J Dent Res. 2024. PMID: 38058155 Free PMC article.
Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta.
Hany U, Watson CM, Liu L, Smith CEL, Harfoush A, Poulter JA, Nikolopoulos G, Balmer R, Brown CJ, Patel A, Simmonds J, Charlton R, Acosta de Camargo MG, Rodd HD, Jafri H, Antanaviciute A, Moffat M, Al-Jawad M, Inglehearn CF, Mighell AJ. Hany U, et al. Among authors: watson cm. J Med Genet. 2024 Mar 21;61(4):347-355. doi: 10.1136/jmg-2023-109510. J Med Genet. 2024. PMID: 37979963 Free PMC article.
149 results