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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 1
2013 1
2014 2
2015 3
2016 3
2017 2
2020 1
2021 1
2022 1
2023 2
2024 0

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16 results

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Page 1
Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study.
Walters NL, Lindsey-Mills ZT, Brangan A, Savage SK, Schmidlen TJ, Morgan KM, Tricou EP, Betts MM, Jones LK, Sturm AC, Campbell-Salome G. Walters NL, et al. Among authors: schmidlen tj. PEC Innov. 2023 Feb 4;2:100134. doi: 10.1016/j.pecinn.2023.100134. eCollection 2023 Dec. PEC Innov. 2023. PMID: 37214500 Free PMC article.
Optimizing communication strategies and designing a comprehensive program to facilitate cascade testing for familial hypercholesterolemia.
Campbell-Salome G, Jones LK, Walters NL, Morgan KM, Brangan A, Ladd IG, McGowan MP, Wilemon K, Schmidlen TJ, Simmons E, Schwartz MLB, McMinn MN, Tricou E, Rahm AK, Ahmed CD, Sturm AC. Campbell-Salome G, et al. Among authors: schmidlen tj. BMC Health Serv Res. 2023 Apr 5;23(1):340. doi: 10.1186/s12913-023-09304-y. BMC Health Serv Res. 2023. PMID: 37020233 Free PMC article.
Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial Hypercholesterolemia.
Campbell-Salome G, Jones LK, Masnick MF, Walton NA, Ahmed CD, Buchanan AH, Brangan A, Esplin ED, Kann DG, Ladd IG, Kelly MA, Kindt I, Kirchner HL, McGowan MP, McMinn MN, Morales A, Myers KD, Oetjens MT, Rahm AK, Schmidlen TJ, Sheldon A, Simmons E, Snir M, Strande NT, Walters NL, Wilemon K, Williams MS, Gidding SS, Sturm AC. Campbell-Salome G, et al. Among authors: schmidlen tj. Circ Genom Precis Med. 2021 Feb;14(1):e003120. doi: 10.1161/CIRCGEN.120.003120. Epub 2021 Jan 22. Circ Genom Precis Med. 2021. PMID: 33480803 Free PMC article.
Positive impact of genetic counseling assistants on genetic counseling efficiency, patient volume, and cost in a cancer genetics clinic.
Hallquist MLG, Tricou EP, Hallquist MN, Savatt JM, Rocha H, Evans AE, Deckard N, Hu Y, Kirchner HL, Pervola J, Rahm AK, Rashkin M, Schmidlen TJ, Schwartz MLB, Williams JL, Williams MS, Buchanan AH. Hallquist MLG, et al. Among authors: schmidlen tj. Genet Med. 2020 Aug;22(8):1348-1354. doi: 10.1038/s41436-020-0797-2. Epub 2020 Apr 30. Genet Med. 2020. PMID: 32350418 Free article.
Precision Military Medicine: Conducting a multi-site clinical utility study of genomic and lifestyle risk factors in the United States Air Force.
Delaney SK, Brenner R, Schmidlen TJ, Dempsey MP, London KE, Gordon ES, Bellafante M, Nasuti A, Scheinfeldt LB, Rajula KD, Jose L, Jarvis JP, Gerry NP, Christman MF. Delaney SK, et al. Among authors: schmidlen tj. NPJ Genom Med. 2017 Jan 19;2:2. doi: 10.1038/s41525-016-0004-1. eCollection 2017. NPJ Genom Med. 2017. PMID: 29263822 Free PMC article.
Challenges in Translating GWAS Results to Clinical Care.
Scheinfeldt LB, Schmidlen TJ, Gerry NP, Christman MF. Scheinfeldt LB, et al. Among authors: schmidlen tj. Int J Mol Sci. 2016 Aug 4;17(8):1267. doi: 10.3390/ijms17081267. Int J Mol Sci. 2016. PMID: 27527156 Free PMC article.
An expanded pharmacogenomics warfarin dosing table with utility in generalised dosing guidance.
Shahabi P, Scheinfeldt LB, Lynch DE, Schmidlen TJ, Perreault S, Keller MA, Kasper R, Wawak L, Jarvis JP, Gerry NP, Gordon ES, Christman MF, Dubé MP, Gharani N. Shahabi P, et al. Among authors: schmidlen tj. Thromb Haemost. 2016 Aug 1;116(2):337-48. doi: 10.1160/TH15-12-0955. Epub 2016 Apr 28. Thromb Haemost. 2016. PMID: 27121899 Free PMC article.
Using the Coriell Personalized Medicine Collaborative Data to conduct a genome-wide association study of sleep duration.
Scheinfeldt LB, Gharani N, Kasper RS, Schmidlen TJ, Gordon ES, Jarvis JP, Delaney S, Kronenthal CJ, Gerry NP, Christman MF. Scheinfeldt LB, et al. Among authors: schmidlen tj. Am J Med Genet B Neuropsychiatr Genet. 2015 Dec;168(8):697-705. doi: 10.1002/ajmg.b.32362. Epub 2015 Sep 3. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 26333835 Free PMC article.
16 results