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The future of genetic case-control studies.
Schork NJ, Fallin D, Thiel B, Xu X, Broeckel U, Jacob HJ, Cohen D. Schork NJ, et al. Among authors: broeckel u. Adv Genet. 2001;42:191-212. doi: 10.1016/s0065-2660(01)42023-2. Adv Genet. 2001. PMID: 11037322 Review.
The ENTPD1 promoter polymorphism -860 A > G (rs3814159) is associated with increased gene transcription, protein expression, CD39/NTPDase1 enzymatic activity, and thromboembolism risk.
Maloney JP, Branchford BR, Brodsky GL, Cosmic MS, Calabrese DW, Aquilante CL, Maloney KW, Gonzalez JR, Zhang W, Moreau KL, Wiggins KL, Smith NL, Broeckel U, Di Paola J. Maloney JP, et al. Among authors: broeckel u. FASEB J. 2017 Jul;31(7):2771-2784. doi: 10.1096/fj.201600344R. Epub 2017 Mar 16. FASEB J. 2017. PMID: 28302652 Free PMC article.
R., Zhang, W., Moreau, K. L., Wiggins, K. L., Smith, N. L., Broeckel, U., Di Paola, J. The ENTPD1 promoter polymorphism -860 A > G (rs3814159) is associated with increased gene transcription, protein expression, CD39/NTPDase1 enzymatic activity, and thromboemboli …
R., Zhang, W., Moreau, K. L., Wiggins, K. L., Smith, N. L., Broeckel, U., Di Paola, J. The ENTPD1 promoter polymorphism -860 A …
Toward the etiologies of congenital heart diseases.
Pelech AN, Broeckel U. Pelech AN, et al. Among authors: broeckel u. Clin Perinatol. 2005 Dec;32(4):825-44, vii. doi: 10.1016/j.clp.2005.09.005. Clin Perinatol. 2005. PMID: 16325664 Review.
Clonal haematopoiesis and risk of chronic liver disease.
Wong WJ, Emdin C, Bick AG, Zekavat SM, Niroula A, Pirruccello JP, Dichtel L, Griffin G, Uddin MM, Gibson CJ, Kovalcik V, Lin AE, McConkey ME, Vromman A, Sellar RS, Kim PG, Agrawal M, Weinstock J, Long MT, Yu B, Banerjee R, Nicholls RC, Dennis A, Kelly M, Loh PR, McCarroll S, Boerwinkle E, Vasan RS, Jaiswal S, Johnson AD, Chung RT, Corey K, Levy D, Ballantyne C; NHLBI TOPMed Hematology Working Group; Ebert BL, Natarajan P. Wong WJ, et al. Nature. 2023 Apr;616(7958):747-754. doi: 10.1038/s41586-023-05857-4. Epub 2023 Apr 12. Nature. 2023. PMID: 37046084 Free PMC article.
Loss-of-function thrombospondin-1 mutations in familial pulmonary hypertension.
Maloney JP, Stearman RS, Bull TM, Calabrese DW, Tripp-Addison ML, Wick MJ, Broeckel U, Robbins IM, Wheeler LA, Cogan JD, Loyd JE. Maloney JP, et al. Among authors: broeckel u. Am J Physiol Lung Cell Mol Physiol. 2012 Mar 15;302(6):L541-54. doi: 10.1152/ajplung.00282.2011. Epub 2011 Dec 23. Am J Physiol Lung Cell Mol Physiol. 2012. PMID: 22198906 Free PMC article.
168 results