 Lisen Hanna Axell
| Title | Instructor |
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| Institution | University of Colorado Denver - Anschutz Medical Campus |
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| Department | SOM-MED |
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| Phone | 303/724-0610 |
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 Bibliographic
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Hodan R, Gupta S, Weiss JM, Axell L, Burke CA, Chen LM, Chung DC, Clayback KM, Felder S, Foda Z, Giardiello FM, Grady W, Gustafson S, Hagemann A, Hall MJ, Hampel H, Idos G, Joseph N, Kassem N, Katona B, Kelly K, Kieber-Emmons A, Kupfer S, Lang K, Llor X, Markowitz AJ, Prats MM, Niell-Swiller M, Outlaw D, Pirzadeh-Miller S, Samadder NJ, Shibata D, Stanich PP, Swanson BJ, Szymaniak BM, Welborn J, Wiesner GL, Yurgelun MB, Dwyer M, Darlow S, Diwan Z. Genetic/Familial High-Risk Assessment: Colorectal, Endometrial, and Gastric, Version 3.2024, NCCN Clinical Practice Guidelines In Oncology. J Natl Compr Canc Netw. 2024 12; 22(10):695-711. PMID: 39689429.
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La Greca A, Dawes D, Albuja-Cruz M, Raeburn C, Axell L, Ku L, Klein C, Marshall C, Fishbein L. MEN2 phenotype in a family with germline heterozygous rare RET K666N variant. Endocrinol Diabetes Metab Case Rep. 2024 Jul 01; 2024(3). PMID: 39231479.
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Lowery JT, Axell L, Ku L, Todd EB, Kao D, Rafaels N, Taylor MRG, Kudron E, Wicks S, Jirikowic J, Shalowitz E, Crooks KR. Returning actionable genetic results to participants in the biobank at the Colorado Center for Personalized Medicine and UCHealth. Genet Med Open. 2024; 2:101852. PMID: 39669600.
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Wiley LK, Shortt JA, Roberts ER, Lowery J, Kudron E, Lin M, Mayer D, Wilson M, Brunetti TM, Chavan S, Phang TL, Pozdeyev N, Lesny J, Wicks SJ, Moore ET, Morgenstern JL, Roff AN, Shalowitz EL, Stewart A, Williams C, Edelmann MN, Hull M, Patton JT, Axell L, Ku L, Lee YM, Jirikowic J, Tanaka A, Todd E, White S, Peterson B, Hearst E, Zane R, Greene CS, Mathias R, Coors M, Taylor M, Ghosh D, Kahn MG, Brooks IM, Aquilante CL, Kao D, Rafaels N, Crooks KR, Hess S, Barnes KC, Gignoux CR. Building a vertically integrated genomic learning health system: The biobank at the Colorado Center for Personalized Medicine. Am J Hum Genet. 2024 01 04; 111(1):11-23. PMID: 38181729.
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Weiss JM, Gupta S, Burke CA, Axell L, Chen LM, Chung DC, Clayback KM, Dallas S, Felder S, Gbolahan O, Giardiello FM, Grady W, Hall MJ, Hampel H, Hodan R, Idos G, Kanth P, Katona B, Lamps L, Llor X, Lynch PM, Markowitz AJ, Pirzadeh-Miller S, Samadder NJ, Shibata D, Swanson BJ, Szymaniak BM, Wiesner GL, Wolf A, Yurgelun MB, Zakhour M, Darlow SD, Dwyer MA, Campbell M. NCCN Guidelines? Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 1.2021. J Natl Compr Canc Netw. 2021 10 15; 19(10):1122-1132. PMID: 34666312.
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Rosenblum A, Springer M, Eppolito A, Axell L, Mohler L. Homozygous Germline APC p.I1307K Variants: A Case Series. Case Rep Oncol. 2021 Sep-Dec; 14(3):1295-1303. PMID: 34720931.
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Wolfe Schneider K, Anguiano A, Axell L, Barth C, Crow K, Gilstrap M, Hamlington BA, Lesh S, Mullineaux L, Rahm AK, Strait E, Freivogel M. Collaboration of colorado cancer genetic counselors to integrate next generation sequencing panels into clinical practice. J Genet Couns. 2014 Aug; 23(4):640-6. PMID: 24781714.
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Lowery JT, Axell L, Vu K, Rycroft R. A novel approach to increase awareness about hereditary colon cancer using a state cancer registry. Genet Med. 2010 Nov; 12(11):721-5. PMID: 20808227.
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Lowery JT, Byers T, Axell L, Ku L, Jacobellis J. The impact of direct-to-consumer marketing of cancer genetic testing on women according to their genetic risk. Genet Med. 2008 Dec; 10(12):888-94. PMID: 19092441.
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Chen R, Axell L, Klein C. Attenuated familial adenomatosis polyposis. J Clin Oncol. 2007 Feb 20; 25(6):724-5. PMID: 17308276.
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Mouchawar J, Hensley-Alford S, Laurion S, Ellis J, Kulchak-Rahm A, Finucane ML, Meenan R, Axell L, Pollack R, Ritzwoller D. Impact of direct-to-consumer advertising for hereditary breast cancer testing on genetic services at a managed care organization: a naturally-occurring experiment. Genet Med. 2005 Mar; 7(3):191-7. PMID: 15775755.
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Mullineaux LG, Castellano TM, Shaw J, Axell L, Wood ME, Diab S, Klein C, Sitarik M, Deffenbaugh AM, Graw SL. Identification of germline 185delAG BRCA1 mutations in non-Jewish Americans of Spanish ancestry from the San Luis Valley, Colorado. Cancer. 2003 Aug 01; 98(3):597-602. PMID: 12879478.
This graph shows the total number of publications by year, by first, middle/unknown, or last author.
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| Year | Publications |
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| 2003 | 1 | | 2005 | 1 | | 2007 | 1 | | 2008 | 1 | | 2010 | 1 | | 2014 | 1 | | 2021 | 2 | | 2024 | 4 |
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