Jennifer Ivanovich, MS, CGC
Assistant Professor of Medical and Molecular Genetics
Certified Genetic Counselor
Jen joined the Department of Medical and Molecular Genetics in 2017. Her primary role is to assist with the expansion of the clinical cancer genetic and precision genomic services offered throughout the IU Health system. Jen also participates in teaching graduate students in the Genetic Counseling training program as well as the genetic residents.
Prior to joining Indiana University, Jen worked as a genetic counselor at Washington University in St. Louis for over twenty years. She founded the Young Women’s Breast Cancer Program and was a member of the research team responsible for the discovery of the DICER1 gene as the basis for the pleuropulmonary blastoma cancer syndrome. She is a graduate of the University of Cincinnati Genetic Counseling Program and is certified by the American Board of Genetic Counseling.
Jen’s professional interests include cancer genetics and genomics, precision medicine, as well as the care of young adults with cancer. Jen’s personal interests are focused on issues of social justice and poverty.
Seo J, Ivanovich J, Goodman MS, Biesecker B, Kaphingst K. 2017. Information topics of greatest interest for return of genome sequencing results among women diagnosed with breast cancer at a young age. Journal of Genetic Counseling. June;26(3)511-521. PMID: 27542972.
Elrick A, Ashida S, Ivanovich J, Lyons S, Biesecker B, Goodman M, Kaphingst K. 2017. Psychosocial and Clinical Factors Associated with Family Communication of Cancer Genetic Test Results Among Women Diagnosed with Breast Cancer at a Young Age. Journal of Genetic Counseling. Feb;26(1) 173-181. PMID: 2742278
Kaphingst KA, Ivanovich J, Elrick A, Dresser R, Matsen C, Goodman MS. How, who, and when: preferences for delivery of genome sequencing results among women diagnosed with breast cancer at a young age. Molecular Genetics Genomic Medicine. 2016 Oct 24:4(6)684-695. PMID: 27896289.
Link D, Schuettpelz G, Shen D, Wang J, Walter J, Kulkarni S, Payton J, Ivanovich J, Goodfellow P, Le Beau M, Koboldt D, Dooling D, Fulton R, Bender R, Fulton L, Delehaunty K, Fronick C, Appelbaum E, Schmidt H, Abbott R, O’Laughlin M, Chen K, McLellan M, Varghese N, Nagarajan R, Heath S, Graubert T, Ding L, Ley T, Zambetti G, Wilson R, Mardis E. 2011. The identification of a novel TP53 germline mutation through whole genome sequencing of a patient with therapy-related AML. JAMA Apr;305(15)1568-1576. PMID: 21505135
Hill DA, Ivanovich J, Priest JR, Gurnett CA, Dehner LP, Desruisseau D, Jarzembowski JA, Wikenheiser-Brokamp KA, Suarez BK, Whelan AJ, Williams G, Bracamontes D, Messinger Y, Goodfellow PJ. Germline DICER1 Mutations in Familial Pleuropulmonary Blastoma. Science 325(5943):965, 2009. PMID: 19556464.
Du HY, Pumbo E, Ivanovich J, An P, Maziarz R, Reiss U, Chirnomas D, Shimamura A, Vlachos A, Lipton J, Goyal RK, Goldman F, Wilson DB, Mason PJ, and Bessler M . TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements. Blood. 113(2)309-316, 2009. PMID: 18931339.
Ley TJ, Mardis ER, Ding L, Fulton B, McLellan MD, Chen K, Dooling D, Dunford-Shore BH McGrath S, Hickenbotham M, Cook L, Abbott A, Larson DE, Koboldt DC, Pohl C, Smith S Hawkins A, Abbott S, Locke D, Hillier DW, Miner T, Fulton L, Magrini L, Wylie T, Glasscock J, Conyers J, Sander N, Shi X, Osborne JR, Minx P, Gordon D, Chinwalla A, Zhao Y, Ries RE, Payton JE, Westervelt P, Tomasson MH, Watson M, Baty J, Ivanovich J, Heath S, Shannon WD, Nagarajan R, Walter MJ, Link DC, Graubert TA, DiPersio JF, Wilson RK. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature. 456:66-72, 2008. PMID: 18931339.
Wells S, Chi D, Toshima K, Dehner L, Coffin C, Dowton SB, Ivanovich J, DeBenedetti M, Moley J, Donis-Keller H. Predictive DNA testing and prophylactic thyroidectomy in patients at risk for Multiple Endocrine Neoplasia Type 2A. Annals of Surgery;240:237-250, 1994. PMID: 7916559.