Wendy K. Kohlmann,
MS
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Languages Spoken: English
Specialties
Board Certification and Academic Information
| Academic Departments | Population Health Sciences
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Adjunct Assistant Professor Huntsman Cancer Institute - Midlevel |
| Academic Divisions | Cancer Population Science HCI Providers |
| Board Certification | American Board of Genetic Counseling |
Academic Locations
Huntsman Cancer Institute
801-587-5556
Board Certification and Academic Information
| Academic Departments | Population Health Sciences
-
Adjunct Assistant Professor Huntsman Cancer Institute - Midlevel |
| Academic Divisions | Cancer Population Science HCI Providers |
| Board Certification | American Board of Genetic Counseling |
Education History
| Graduate Training | University of Cincinatti Genetic Counseling M.S. |
| Undergraduate | University of Wisconsin B.S. |
Selected Publications - Journal Articles
Journal Article
- Daly MB, Pilarski R, Axilbund JE, Berry M, Buys SS, Crawford B, Farmer M, Friedman S, Garber JE, Khan S, Klein C, Kohlmann W, Kurian A, Litton JK, Madlensky L, Marcom PK, Merajver SD, Offit K, Pal T, Rana H, Reiser G, Robson ME, Shannon KM, Swisher E, Voian NC, Weitzel JN, Whelan A, Wick MJ, Wiesner GL, Dwyer M, Kumar R, Darlow S (2016 Feb). Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015. J Natl Compr Canc Netw, 14(2), 153-62.
- Young EL, Feng BJ, Stark AW, Damiola F, Durand G, Forey N, Francy TC, Gammon A, Kohlmann WK, Kaphingst KA, McKay-Chopin S, Nguyen-Dumont T, Oliver J, Paquette AM, Pertesi M, Robinot N, Rosenthal JS, Vallee M, Voegele C, Hopper JL, Southey MC, Andrulis IL, John EM, Hashibe M, Gertz J, Le Calvez-Kelm F, Lesueur F, Goldgar DE, Tavtigian SV (2016 Jan 19). Multigene testing of moderate-risk genes: be mindful of the missense.LID - jmedgenet-2015-103398 [pii]LID - 10.1136/jmedgenet-2015-103398 [doi]. (Epub ahead of print) J Med Genet.
- Wu YP, Aspinwall LG, Michaelis TC, Stump T, Kohlmann WG, Leachman SA (2016 Jan). Discussion of photoprotection, screening, and risk behaviors with children and grandchildren after melanoma genetic testing. J Community Genet, 7(1), 21-31.
- Chang Y, Near AM, Butler KM, Hoeffken A, Edwards SL, Stroup AM, Kohlmann W, Gammon A, Buys SS, Schwartz MD, Peshkin BN, Kinney AY, Mandelblatt JS, Chang Y, Near AM, Butler KM, Hoeffken A, Edwards SL, Stroup AM, Kohlmann W, Gammon A, Buys SS, Schwartz MD, Peshkin BN, Kinney AY, Mandelblatt JS (2016 Jan). ReCAP: Economic Evaluation Alongside a Clinical Trial of Telephone Versus In-Person Genetic Counseling for BRCA1/2 Mutations in Geographically Underserved Areas. J Oncol Pract, 12(1), 59.
- Aspinwall LG, Stump TK, Taber JM, Kohlmann W, Leaf SL, Leachman SA (2015 Oct). Impact of melanoma genetic test reporting on perceived control over melanoma prevention. J Behav Med, 38(5), 754-65.
- Taber JM, Aspinwall LG, Stump TK, Kohlmann W, Champine M, Leachman SA (2015 Oct). Genetic test reporting enhances understanding of risk information and acceptance of prevention recommendations compared to family history-based counseling alone. J Behav Med, 38(5), 740-53.
- Steffen LE, Boucher KM, Damron BH, Pappas LM, Walters ST, Flores KG, Boonyasiriwat W, Vernon SW, Stroup AM, Schwartz MD, Edwards SL, Kohlmann WK, Lowery JT, Wiggins CL, Hill DA, Higginbotham JC, Burt R, Simmons RG, Kinney AY (2015 Sep). Efficacy of a Telehealth Intervention on Colonoscopy Uptake When Cost Is a Barrier: The Family CARE Cluster Randomized Controlled Trial. Cancer Epidemiol Biomarkers Prev, 24(9), 1311-8.
- Birmingham WC, Hung M, Boonyasiriwat W, Kohlmann W, Walters ST, Burt RW, Stroup AM, Edwards SL, Schwartz MD, Lowery JT, Hill DA, Wiggins CL, Higginbotham JC, Tang P, Hon SD, Franklin JD, Vernon S, Kinney AY (2015 Jul 20). Effectiveness of the extended parallel process model in promoting colorectal cancer screening.LID - 10.1002/pon.3899 [doi]. (Epub ahead of print) Psychooncology.
- Ribi S, Baumhoer D, Lee K, Edison, Teo AS, Madan B, Zhang K, Kohlmann WK, Yao F, Lee WH, Hoi Q, Cai S, Woo XY, Tan P, Jundt G, Smida J, Nathrath M, Sung WK, Schiffman JD, Virshup DM, Hillmer AM (2015 Apr 10). TP53 intron 1 hotspot rearrangements are specific to sporadic osteosarcoma and can cause Li-Fraumeni syndrome. Oncotarget, 6(10), 7727-40.
- Everett JN, Raymond VM, Dandapani M, Marvin M, Kohlmann W, Chittenden A, Koeppe E, Gustafson SL, Else T, Fullen DR, Johnson TM, Syngal S, Gruber SB, Stoffel EM (2014 Dec). Screening for germline mismatch repair mutations following diagnosis of sebaceous neoplasm. JAMA Dermatol, 150(12), 1315-21.
- Kinney AY, Butler KM, Schwartz MD, Mandelblatt JS, Boucher KM, Pappas LM, Gammon A, Kohlmann W, Edwards SL, Stroup AM, Buys SS, Flores KG, Campo RA (2014 Dec). Expanding access to BRCA1/2 genetic counseling with telephone delivery: a cluster randomized trial.LID - 10.1093/jnci/dju328 [doi]LID - dju328 [pii]. J Natl Cancer Inst, 106(12).
- Aspinwall LG, Taber JM, Kohlmann W, Leaf SL, Leachman SA (2014 Nov). Unaffected family members report improvements in daily routine sun protection 2 years following melanoma genetic testing. Genet Med, 16(11), 846-53.
- Daly MB, Pilarski R, Axilbund JE, Buys SS, Crawford B, Friedman S, Garber JE, Horton C, Kaklamani V, Klein C, Kohlmann W, Kurian A, Litton J, Madlensky L, Marcom PK, Merajver SD, Offit K, Pal T, Pasche B, Reiser G, Shannon KM, Swisher E, Voian NC, Weitzel JN, Whelan A, Wiesner GL, Dwyer MA, Kumar R (2014 Sep). Genetic/familial high-risk assessment: breast and ovarian, version 1.2014. J Natl Compr Canc Netw, 12(9), 1326-38.
- Venkatramani R, Spector LG, Georgieff M, Tomlinson G, Krailo M, Malogolowkin M, Kohlmann W, Curtin K, Fonstad RK, Schiffman JD (2014 Sep). Congenital abnormalities and hepatoblastoma: a report from the Children's Oncology Group (COG) and the Utah Population Database (UPDB). Am J Med Genet A, 164A(9), 2250-5.
- Jasperson KW, Kohlmann W, Gammon A, Slack H, Buchmann L, Hunt J, Kirchhoff AC, Baskin H, Shaaban A, Schiffman JD (2014 Jun). Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families. Fam Cancer, 13(2), 257-65.
- Aspinwall LG, Taber JM, Kohlmann W, Leaf SL, Leachman SA (2014 Jun). Perceived risk following melanoma genetic testing: a 2-year prospective study distinguishing subjective estimates from recall. J Genet Couns, 23(3), 421-37.
- Lu KH, Wood ME, Daniels M, Burke C, Ford J, Kauff ND, Kohlmann W, Lindor NM, Mulvey TM, Robinson L, Rubinstein WS, Stoffel EM, Snyder C, Syngal S, Merrill JK, Wollins DS, Hughes KS (2014 Mar 10). American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers. J Clin Oncol, 32(8), 833-40.
- Kinney AY, Boonyasiriwat W, Walters ST, Pappas LM, Stroup AM, Schwartz MD, Edwards SL, Rogers A, Kohlmann WK, Boucher KM, Vernon SW, Simmons RG, Lowery JT, Flores K, Wiggins CL, Hill DA, Burt RW, Williams MS, Higginbotham JC (2014 Mar 1). Telehealth personalized cancer risk communication to motivate colonoscopy in relatives of patients with colorectal cancer: the family CARE Randomized controlled trial. J Clin Oncol, 32(7), 654-62.
- Anderson AE, Flores KG, Boonyasiriwat W, Gammon A, Kohlmann W, Birmingham WC, Schwartz MD, Samadder J, Boucher K, Kinney AY (2014). Interest and informational preferences regarding genomic testing for modest increases in colorectal cancer risk. Public Health Genomics, 17(1), 48-60.
- Curtin K, Smith KR, Fraser A, Pimentel R, Kohlmann W, Schiffman JD (2013 Nov 15). Familial risk of childhood cancer and tumors in the Li-Fraumeni spectrum in the Utah Population Database: implications for genetic evaluation in pediatric practice. Int J Cancer, 133(10), 2444-53.
- Jasperson KW, Kanth P, Kirchhoff AC, Huismann D, Gammon A, Kohlmann W, Burt RW, Samadder NJ (2013 Nov). Serrated polyposis: colonic phenotype, extracolonic features, and familial risk in a large cohort. Dis Colon Rectum, 56(11), 1211-6.
- Aspinwall LG, Taber JM, Leaf SL, Kohlmann W, Leachman SA (2013 Oct). Melanoma genetic counseling and test reporting improve screening adherence among unaffected carriers 2 years later. Cancer Epidemiol Biomarkers Prev, 22(10), 1687-97.
- Aspinwall LG, Taber JM, Leaf SL, Kohlmann W, Leachman SA (2013 Feb). Genetic testing for hereditary melanoma and pancreatic cancer: a longitudinal study of psychological outcome. Psychooncology, 22(2), 276-89.
- Birmingham WC, Agarwal N, Kohlmann W, Aspinwall LG, Wang M, Bishoff J, Dechet C, Kinney AY (2013). Patient and provider attitudes toward genomic testing for prostate cancer susceptibility: a mixed method study. BMC Health Serv Res, 13, 279.
- Yurgelun MB, Mercado R, Rosenblatt M, Dandapani M, Kohlmann W, Conrad P, Blanco A, Shannon KM, Chung DC, Terdiman J, Gruber SB, Garber JE, Syngal S, Stoffel EM (2012 Dec). Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome. Gynecol Oncol, 127(3), 544-51.
- Rothwell E, Kohlmann W, Jasperson K, Gammon A, Wong B, Kinney A (2012 Mar). Patient outcomes associated with group and individual genetic counseling formats. Fam Cancer, 11(1), 97-106.
- Knapke S, Zelley K, Nichols KE, Kohlmann W, Schiffman JD (2012). Identification, management, and evaluation of children with cancer-predisposition syndromes. Am Soc Clin Oncol Educ Book, 576-84.
- Pengchit W, Walters ST, Simmons RG, Kohlmann W, Burt RW, Schwartz MD, Kinney AY (2011 Nov). Motivation-based intervention to promote colonoscopy screening: an integration of a fear management model and motivational interviewing. J Health Psychol, 16(8), 1187-97.
- Jones KB, Schiffman JD, Kohlmann W, Randall RL, Lessnick SL, Cannon-Albright LA (2011 May). Complex genotype sarcomas display familial inheritance independent of known cancer predisposition syndromes. Cancer Epidemiol Biomarkers Prev, 20(5), 751-7.
- Taber JM, Aspinwall LG, Kohlmann W, Dow R, Leachman SA (2010 Dec). Parental preferences for CDKN2A/p16 testing of minors. Genet Med, 12(12), 823-38.
- Stoffel EM, Mercado RC, Kohlmann W, Ford B, Grover S, Conrad P, Blanco A, Shannon KM, Powell M, Chung DC, Terdiman J, Gruber SB, Syngal S (2010 Aug). Prevalence and predictors of appropriate colorectal cancer surveillance in Lynch syndrome. Am J Gastroenterol, 105(8), 1851-60.
- Daly MB, Axilbund JE, Buys S, Crawford B, Farrell CD, Friedman S, Garber JE, Goorha S, Gruber SB, Hampel H, Kaklamani V, Kohlmann W, Kurian A, Litton J, Marcom PK, Nussbaum R, Offit K, Pal T, Pasche B, Pilarski R, Reiser G, Shannon KM, Smith JR, Swisher E, Weitzel JN (2010 May). Genetic/familial high-risk assessment: breast and ovarian. J Natl Compr Canc Netw, 8(5), 562-94.
- Aspinwall LG, Leaf SL, Kohlmann W, Dola ER, Leachman SA (2009 May). Patterns of photoprotection following CDKN2A/p16 genetic test reporting and counseling. J Am Acad Dermatol, 60(5), 745-57.
- McKinnon W, Banks KC, Skelly J, Kohlmann W, Bennett R, Shannon K, Larson-Haidle J, Ashakaga T, Weitzel JN, Wood M (2009). Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individuals. Fam Cancer, 8(4), 363-9.
- Aspinwall LG, Leaf SL, Dola ER, Kohlmann W, Leachman SA (2008 Jun). CDKN2A/p16 genetic test reporting improves early detection intentions and practices in high-risk melanoma families. Cancer Epidemiol Biomarkers Prev, 17(6), 1510-9.
- Stoffel EM, Ford B, Mercado RC, Punglia D, Kohlmann W, Conrad P, Blanco A, Shannon KM, Powell M, Gruber SB, Terdiman J, Chung DC, Syngal S (2008 Mar). Sharing genetic test results in Lynch syndrome: communication with close and distant relatives. Clin Gastroenterol Hepatol, 6(3), 333-8.
- Levin B, Barthel JS, Burt RW, David DS, Ford JM, Giardiello FM, Gruber SB, Halverson AL, Hamilton S, Kohlmann W, Ludwig KA, Lynch PM, Marino C, Martin EW Jr, Mayer RJ, Pasche B, Pirruccello SJ, Rajput A, Rao MS, Shike M, Steinbach G, Terdiman JP, Weinberg D, Winawer SJ (2006 Apr). Colorectal Cancer Screening Clinical Practice Guidelines. J Natl Compr Canc Netw, 4(4), 384-420.
- Lu KH, Dinh M, Kohlmann W, Watson P, Green J, Syngal S, Bandipalliam P, Chen LM, Allen B, Conrad P, Terdiman J, Sun C, Daniels M, Burke T, Gershenson DM, Lynch H, Lynch P, Broaddus RR (2005 Mar). Gynecologic cancer as a "sentinel cancer" for women with hereditary nonpolyposis colorectal cancer syndrome. Obstet Gynecol, 105(3), 569-74.
- Peterson SK, Watts BG, Koehly LM, Vernon SW, Baile WF, Kohlmann WK, Gritz ER (2003 May 15). How families communicate about HNPCC genetic testing: findings from a qualitative study. Am J Med Genet C Semin Med Genet, 119C(1), 78-86.
Review
- Chu D, Kohlmann W, Adler DG (2010). Identification and screening of individuals at increased risk for pancreatic cancer with emphasis on known environmental and genetic factors and hereditary syndromes. [Review]. JOP, 11(3), 203-12.
- Leachman SA, Carucci J, Kohlmann W, Banks KC, Asgari MM, Bergman W, Bianchi-Scarra G, Brentnall T, Bressac-de Paillerets B, Bruno W, Curiel-Lewandrowski C, de Snoo FA, Debniak T, Demierre MF, Elder D, Goldstein AM, Grant-Kels J, Halpern AC, Ingvar C, Kefford RF, Lang J, MacKie RM, Mann GJ, Mueller K, Newton-Bishop J, Olsson H, Petersen GM, Puig S, Rigel D, Swetter SM, Tucker MA, Yakobson E, Zitelli JA, Tsao H (2009 Oct). Selection criteria for genetic assessment of patients with familial melanoma. [Review]. J Am Acad Dermatol, 61(4), 677.e1-14.
- Gammon A, Jasperson K, Kohlmann W, Burt RW (2009). Hamartomatous polyposis syndromes. [Review]. Best Pract Res Clin Gastroenterol, 23(2), 219-31.
- Gammon A, Kohlmann W, Burt R (2007). Can we identify the high-risk patients to be screened? A genetic approach. [Review]. Digestion, 76(1), 7-19.
- Jeter JM, Kohlmann W, Gruber SB (2006 Mar). Genetics of colorectal cancer. [Review]. Oncology (Williston Park), 20(3), 269-76; discussion 285-6, 288-9.
- Gruber SB, Kohlmann W (2003 Jan). The genetics of hereditary non-polyposis colorectal cancer. [Review]. J Natl Compr Canc Netw, 1(1), 137-44.
- Kohlmann W, Gruber SB (1993). Lynch SyndromeBTI. [Review]. GeneReviews.
Conference Proceedings
Case Report
- Harris K, Florell SR, Papenfuss J, Kohlmann W, Jahromi M, Schiffman JD, Quackenbush J, Cassidy P, Leachman S (2012 Mar). Melanoma mimic: a case of multiple pagetoid Spitz nevi. Arch Dermatol, 148(3), 370-4.
- Chao MM, Levine JE, Ruiz RE, Kohlmann WK, Bower MA, Petty EM, Mody RJ (2007 Dec). Malignant triton tumor in a patient with Li-Fraumeni syndrome and a novel TP53 mutation. Pediatr Blood Cancer, 49(7), 1000-4.
- Su LK, Kohlmann W, Ward PA, Lynch PM (2002 Jul). Different familial adenomatous polyposis phenotypes resulting from deletions of the entire APC exon 15. Hum Genet, 111(1), 88-95.
- Su LK, Abdalla EK, Law CH, Kohlmann W, Rashid A, Vauthey JN (2001 Jul 15). Biallelic inactivation of the APC gene is associated with hepatocellular carcinoma in familial adenomatous polyposis coli. Cancer, 92(2), 332-9.