Experience
My research spans academic and industry settings, focusing on the clinical utility of emerging reproductive technologies and their ethical and social implications. I have supervised more than a dozen graduate student research projects. My current work as a research fellow at University of Minnesota focuses on clinical outcomes and service delivery in pharmacogenomics and genomic screening.
PUBLICATIONS
Peer-reviewed Research
Llorin, H., Tennen, R., Laskey, S., Detweiler, S. & Abul-Husn, N. (2024). Shortcomings of ethnicity-based carrier screening for conditions associated with Ashkenazi Jewish ancestry. Genetics in Medicine Open.
Tyrie, D., Oliva, A., Llorin, H., & Zayhowski, K. (2024). Transgender and gender diverse individuals' perspectives on discussions of fetal sex chromosomes in obstetrics care. Journal of Genetic Counseling.
Stevens, C., Llorin, H., Gabriel, C., Mandigo, C., Gochyyev, P., & Studwell, C. (2023). Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities. Journal of Genetic Counseling.
Adams, S., Llorin, H., Dobson, L. J., Studwell, C., Wilkins‐Haug, L., Guseh, S., & Gray, K. J. (2023). Postnatal genetic testing on cord blood for prenatally identified high‐probability cases. Prenatal Diagnosis.
Adams, S., Llorin, H., Maher, O., Dean, M., Dobson, L. J., Gbur, S., ... & Gray, K. J. (2023). Single gene non‐invasive prenatal screening (NIPS-SGD) for autosomal dominant conditions in a high‐risk cohort. Prenatal Diagnosis.
Llorin, H., Graf, M., Chun, N., & Ford, J. (2022). Somatic tumor mutations in moderate risk cancer genes: Targets for germline confirmatory testing. Cancer Genetics.
Articles, Editorials, and Commentaries
Llorin, H., Lundeen, T., Collins, E., Geist, C., Myers, K., Cohen, S., Zayhowski, K. (2024). Gender and Sex Inclusive Approaches for Discussing Predicted Fetal Sex: A Call for Reflection and Research. Journal of Midwifery & Women’s Health.
Llorin, H., & Zayhowski, K. (2023). The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism. Journal of Genetic Counseling.
Llorin, H., & Kirkpatrick, B. (2023) Busting Common Misconceptions about Direct-To-Consumer Genetic Testing. NSGC Perspectives.
Llorin, H., & Zayhowski, K. (2021) Degendering ‘The Gender Test’: Reframing Gender Conversations in Prenatal Genetics Clinics. NSGC Perspectives.
Llorin, H., & Wand, H. (2021) National Organization of Rare Disorders (NORD) Database: Juvenile Hemochromatosis.
PEER REVIEW
Trainee Board Member, Journal of Genetic Counseling, 2025 – Present
Reviewer, Prenatal Diagnostics, 2025 - Current
Reviewer, Clinical Pediatrics, 2024 – Present
Reviewer, Journal of Genetic Counseling, 2022 – Present
Reviewer, Journal of Community Genetics, 2023
Reviewer, Psychiatric Genetics, 2023
My research spans academic and industry settings, focusing on the clinical utility of emerging reproductive technologies and their ethical and social implications. I have supervised more than a dozen graduate student research projects. My current work as a research fellow at University of Minnesota focuses on clinical outcomes and service delivery in pharmacogenomics and genomic screening.
PUBLICATIONS
Peer-reviewed Research
Llorin, H., Tennen, R., Laskey, S., Detweiler, S. & Abul-Husn, N. (2024). Shortcomings of ethnicity-based carrier screening for conditions associated with Ashkenazi Jewish ancestry. Genetics in Medicine Open.
Tyrie, D., Oliva, A., Llorin, H., & Zayhowski, K. (2024). Transgender and gender diverse individuals' perspectives on discussions of fetal sex chromosomes in obstetrics care. Journal of Genetic Counseling.
Stevens, C., Llorin, H., Gabriel, C., Mandigo, C., Gochyyev, P., & Studwell, C. (2023). Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities. Journal of Genetic Counseling.
Adams, S., Llorin, H., Dobson, L. J., Studwell, C., Wilkins‐Haug, L., Guseh, S., & Gray, K. J. (2023). Postnatal genetic testing on cord blood for prenatally identified high‐probability cases. Prenatal Diagnosis.
Adams, S., Llorin, H., Maher, O., Dean, M., Dobson, L. J., Gbur, S., ... & Gray, K. J. (2023). Single gene non‐invasive prenatal screening (NIPS-SGD) for autosomal dominant conditions in a high‐risk cohort. Prenatal Diagnosis.
Llorin, H., Graf, M., Chun, N., & Ford, J. (2022). Somatic tumor mutations in moderate risk cancer genes: Targets for germline confirmatory testing. Cancer Genetics.
Articles, Editorials, and Commentaries
Llorin, H., Lundeen, T., Collins, E., Geist, C., Myers, K., Cohen, S., Zayhowski, K. (2024). Gender and Sex Inclusive Approaches for Discussing Predicted Fetal Sex: A Call for Reflection and Research. Journal of Midwifery & Women’s Health.
Llorin, H., & Zayhowski, K. (2023). The erasure of transgender and intersex identities through fetal sex prediction and genetic essentialism. Journal of Genetic Counseling.
Llorin, H., & Kirkpatrick, B. (2023) Busting Common Misconceptions about Direct-To-Consumer Genetic Testing. NSGC Perspectives.
Llorin, H., & Zayhowski, K. (2021) Degendering ‘The Gender Test’: Reframing Gender Conversations in Prenatal Genetics Clinics. NSGC Perspectives.
Llorin, H., & Wand, H. (2021) National Organization of Rare Disorders (NORD) Database: Juvenile Hemochromatosis.
PEER REVIEW
Trainee Board Member, Journal of Genetic Counseling, 2025 – Present
Reviewer, Prenatal Diagnostics, 2025 - Current
Reviewer, Clinical Pediatrics, 2024 – Present
Reviewer, Journal of Genetic Counseling, 2022 – Present
Reviewer, Journal of Community Genetics, 2023
Reviewer, Psychiatric Genetics, 2023