Nikkola received a BA in Mathematics and a BMus in Vocal Performance from Rice University and an MA in Musicology from the University of Chicago before discovering her true career path in genetic counseling. She pivoted with a MS in Genetic Counseling from Brandeis University, and then went on to complete a PhD in Health Professions Education at Simmons University, where her dissertation was a qualitative study focused on the training experiences of genetic counseling students who identify with a racial or ethnic minority group. Prior to joining the faculty at Boston University, Nikkola worked as a clinical and research genetic counselor at Brigham and Women’s Hospital and Boston Children’s Hospital. For the last 4 years, she has specialized in pulmonary genetics, providing genetic counseling to adult and pediatric patients with lung disease and spearheading gene discovery initiatives. Nikkola‘s research interests are centered on the education of genetic counseling students, the creation of equitable and inclusive training environments for students with identities that are currently underrepresented in the profession, and the ways in which being bicultural impacts genetic counselors’ interactions with patients.
Diversity, Equity, Inclusion and Accessibility
The faculty of the BU Genetic Counseling Program recognize and celebrate differences in ethnicity, race, gender identity, disability status, religion, sexuality, immigration status and socioeconomic backgrounds in our learning community. As we provide care and train learners at Boston Medical Center, an institution serving historically marginalized patients and clients, we work to integrate issues related to diversity, inclusion, justice and equity throughout all aspects of our curriculum. We are devoted to developing faculty’s and students’ roles as advocates for our colleagues and patients, and uplifting the voices of those who have been disempowered by the medical system.
As an educator, my goal is to create more equitable and inclusive genetic counseling training spaces. This commitment was fueled by my dissertation, which focused on the training experiences of genetic counseling students who identify with a racial or ethnic minority group. Within the BU genetic counseling program, I’m working with the other faculty to implement the recommendations from my prior research. One aspect of this work is to establish a mentorship program between students and practicing genetic counselors; when students have an identity that has been structurally marginalized, the goal is to find a mentor who shares this identity. On a profession-wide level, I lead workshops for genetic counselors about how to provide culturally-responsive supervision. Looking forward, I am launching a new longitudinal research project with my colleagues looking at how identity, particularly identities that have been structurally marginalized, impact the experience of genetic counseling training. I anticipate that this research will inform efforts to create equitable and inclusive spaces within genetic counseling programs and the ways that we train supervisors who interact with students.
Publications listed below are automatically derived from MEDLINE/PubMed and other
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Ramsey K, Carmichael N, Gutierrez-Kapheim M, Dell-Suguitan MD, Bao AK, Hoell C. Exploring the impact of microaggressions on the genetic counseling student-supervisor relationship: A qualitative study. J Genet Couns. 2024 Feb; 33(1):41-53. PMID: 38356454; DOI: 10.1002/jgc4.1876;
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Ramsey K, Carmichael N, Gutierrez-Kapheim M, Dell-Suguitan MD, Lopez Santibanez Jacome L, Bao AK, Hoell C. Exploring the occurrence of microaggressions in the genetic counseling student-supervisor relationship: A mixed-methods study. J Genet Couns. 2024 Feb; 33(1):28-40. PMID: 38217277; DOI: 10.1002/jgc4.1854;
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O'Sullivan L, Zayhowski K, Hoffman E, Carmichael N. A qualitative study of LGBTQIA+ genetic counselors' experiences while applying to graduate school. J Genet Couns. 2023 Dec; 32(6):1200-1212.View Related Profiles. PMID: 37574455; DOI: 10.1002/jgc4.1760;
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Chu V, Zayhowski K, Collin CR, Carmichael N. A qualitative study exploring LGBTQ genetic counseling students' relationships with peers and faculty in graduate school. J Genet Couns. 2024 Apr; 33(2):329-340.View Related Profiles. PMID: 37222227; DOI: 10.1002/jgc4.1724;
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Rose JA, Planchart Ferretto MA, Maeda AH, Perez Garcia MF, Carmichael NE, Gulati S, Rice MB, Goldberg HJ, Putman RK, Hatabu H, Raby BA, Rosas IO, Hunninghake GM. Progressive Interstitial Lung Disease in Relatives of Patients with Pulmonary Fibrosis. Am J Respir Crit Care Med. 2023 Jan 15; 207(2):211-214. PMID: 36099425; PMCID: PMC9893330; DOI: 10.1164/rccm.202208-1470LE;
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Newton CA, Oldham JM, Applegate C, Carmichael N, Powell K, Dilling D, Schmidt SL, Scholand MB, Armanios M, Garcia CK, Kropski JA, Talbert J. The Role of Genetic Testing in Pulmonary Fibrosis: A Perspective From the Pulmonary Fibrosis Foundation Genetic Testing Work Group. Chest. 2022 Aug; 162(2):394-405. PMID: 35337808; PMCID: PMC9424324; DOI: 10.1016/j.chest.2022.03.023;
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Rolle L, Zayhowski K, Koeller D, Chiluiza D, Carmichael N. Transgender patients' perspectives on their cancer genetic counseling experiences. J Genet Couns. 2022 06; 31(3):781-791.View Related Profiles. PMID: 34964220; DOI: 10.1002/jgc4.1544;
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Carmichael N, Redlinger-Grosse K, Birnbaum S. Examining clinical training through a bicultural lens: Experiences of genetic counseling students who identify with a racial or ethnic minority group. J Genet Couns. 2022 04; 31(2):411-423. PMID: 34545644; PMCID: PMC9293098; DOI: 10.1002/jgc4.1506;
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Carmichael N, Redlinger-Grosse K, Birnbaum S. Supporting a sense of inclusion and belonging for genetic counseling students who identify as racial or ethnic minorities. J Genet Couns. 2021 06; 30(3):813-827. PMID: 33550646; DOI: 10.1002/jgc4.1381;
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Carmichael N, Martinez Manzano JM, Quesada-Arias LD, Poli SF, Baumgartner MA, Planchart Ferretto MA, DiGianni L, Gampala-Sagar S, Leone DA, Gulati S, El-Chemaly SY, Goldberg HJ, Putman R, Hatabu H, Rosas IO, Hunninghake GM, Raby BA. Psychological impact of genetic and clinical screening for pulmonary fibrosis on asymptomatic first-degree relatives of affected individuals. Thorax. 2021 06; 76(6):621-623. PMID: 33483364; PMCID: PMC8238310; DOI: 10.1136/thoraxjnl-2020-216244;
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Pini J, Kueper J, Hu YD, Kawasaki K, Yeung P, Tsimbal C, Yoon B, Carmichael N, Maas RL, Cotney J, Grinblat Y, Liao EC. ALX1-related frontonasal dysplasia results from defective neural crest cell development and migration. EMBO Mol Med. 2020 10 07; 12(10):e12013. PMID: 32914578; PMCID: PMC7539331; DOI: 10.15252/emmm.202012013;
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Dutta D, Briere LC, Kanca O, Marcogliese PC, Walker MA, High FA, Vanderver A, Krier J, Carmichael N, Callahan C, Taft RJ, Simons C, Helman G, Network UD, Wangler MF, Yamamoto S, Sweetser DA, Bellen HJ. De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment. Hum Mol Genet. 2020 06 03; 29(9):1568-1579. PMID: 32356556; PMCID: PMC7268787; DOI: 10.1093/hmg/ddaa081;
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Hunninghake GM, Quesada-Arias LD, Carmichael NE, Martinez Manzano JM, Poli De Frías S, Baumgartner MA, DiGianni L, Gampala-Sagar SN, Leone DA, Gulati S, El-Chemaly S, Goldberg HJ, Putman RK, Hatabu H, Raby BA, Rosas IO. Interstitial Lung Disease in Relatives of Patients with Pulmonary Fibrosis. Am J Respir Crit Care Med. 2020 05 15; 201(10):1240-1248. PMID: 32011908; PMCID: PMC7233344; DOI: 10.1164/rccm.201908-1571OC;
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Carmichael N, Redlinger-Grosse K, Birnbaum S. Conscripted curriculum: The experiences of minority genetic counseling students. J Genet Couns. 2020 04; 29(2):303-314. PMID: 32198906; DOI: 10.1002/jgc4.1260;
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Haghighi A, Krier JB, Toth-Petroczy A, Cassa CA, Frank NY, Carmichael N, Fieg E, Bjonnes A, Mohanty A, Briere LC, Lincoln S, Lucia S, Gupta VA, Söylemez O, Sutti S, Kooshesh K, Qiu H, Fay CJ, Perroni V, Valerius J, Hanna M, Frank A, Ouahed J, Snapper SB, Pantazi A, Chopra SS, Leshchiner I, Stitziel NO, Feldweg A, Mannstadt M, Loscalzo J, Sweetser DA, Liao E, Stoler JM, Nowak CB, Sanchez-Lara PA, Klein OD, Perry H, Patsopoulos NA, Raychaudhuri S, Goessling W, Green RC, Seidman CE, MacRae CA, Sunyaev SR, Maas RL, Vuzman D. An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery. NPJ Genom Med. 2018; 3:21.View Related Profiles. PMID: 30131872; PMCID: PMC6089983; DOI: 10.1038/s41525-018-0060-9;
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Dutton E, Carmichael N, Michal U, Cripps PJ, Boswood A. Serum cardiac troponin I concentrations in dogs with generalised seizures. J Small Anim Pract. 2018 03; 59(3):167-173. PMID: 29023739; DOI: 10.1111/jsap.12771;
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Wojcik MH, Carmichael N, Bieber FR, Wiener DC, Madan R, Pober BR, Raby BA. A new diagnosis of Williams-Beuren syndrome in a 49-year-old man with severe bullous emphysema. Am J Med Genet A. 2017 Aug; 173(8):2235-2239.View Related Profiles. PMID: 28574231; PMCID: PMC5509496; DOI: 10.1002/ajmg.a.38289;
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Lee VS, Halabi CM, Hoffman EP, Carmichael N, Leshchiner I, Lian CG, Bierhals AJ, Vuzman D, Mecham RP, Frank NY, Stitziel NO. Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans. Proc Natl Acad Sci U S A. 2016 08 02; 113(31):8759-64.View Related Profiles. PMID: 27432961; PMCID: PMC4978273; DOI: 10.1073/pnas.1601442113;
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Bates N, Sharman M, Lam A, Kent A, Walker D, Smith V, Carmichael N. Reporting cases of Fanconi syndrome in dogs in the UK. Vet Rec. 2016 May 14; 178(20):510. PMID: 27179094; DOI: 10.1136/vr.i2677;
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Sharman M, Seth M, Lam A, Kent A, Smith V, Carmichael N. Acquired Fanconi-like syndrome cases associated with dried chicken and duck meat ingestion. Vet Rec. 2016 Feb 20; 178(8):196. PMID: 26893338; DOI: 10.1136/vr.i968;
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Carmichael N, Tsipis J, Windmueller G, Mandel L, Estrella E. "Is it going to hurt?": the impact of the diagnostic odyssey on children and their families. J Genet Couns. 2015 Apr; 24(2):325-35. PMID: 25277096; DOI: 10.1007/s10897-014-9773-9;
This graph shows the total number of publications by year, by first, middle/unknown,
or last author.
Year | Publications |
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2014 | 1 |
2016 | 3 |
2017 | 2 |
2018 | 1 |
2020 | 4 |
2021 | 4 |
2022 | 1 |
2023 | 3 |
2024 | 4 |