Hannah Llorin, MS, CGC, is a certified genetic counselor and researcher. She is currently the Director of Genetic Counseling at the Atria Health and Research Institute in Manhattan, NY. Her work focuses on the clinical integration of genomic medicine into primary care, with a focus on technical and clinical strategies that enable genetics to inform routine healthcare decision-making. As a GC-FIRST Research Fellow at University of Minnesota, Ms. Llorin studies the clinical and experiential outcomes of pharmacogenomics service delivery models.

Ms. Llorin previously served as a primary care genetic counselor with LMND Medical Group, where she oversaw the development of a telegenetics service and developed a structured genetics training program for internal and family medicine physicians. Earlier in her career at Brigham and Women’s Hospital in Boston, she specialized in reproductive genetics, counseling patients on prenatal screening and diagnostic testing for fetal anomalies, pregnancy loss, and single-gene disorders.

Ms. Llorin's scholarly work examines the ethical, social, and clinical dimensions of genetic testing in reproductive endocrinology, obstetrics, and primary care. Her work frequently explores the limitations of traditional genetics in diverse populations using implementation science frameworks and qualitative methods.

In addition to her clinical and research roles, Llorin is actively involved in professional service and education. She serves on the advisory board for Stanford University’s MS Program in Human Genetics and Genetic Counseling, has served as executive editor for the National Society of Genetic Counselors’ Perspectives in Genetic Counseling, and contributes to national initiatives focused on inclusive genetic counseling practices. She received her Master of Science and Bachelor of Science from Stanford University.

  • BS in Human Biology, Stanford University, Palo Alto, CA
  • MS in Human Genetics and Genetic Counseling, Stanford University School of Medicine, Palo Alto, CA,

Ms. Llorin’s research interests include the clinical implementation of genomic medicine in preventive and primary care settings, including direct to consumer genetic testing, population genomic screening, and pharmacogenomics. She is particularly interested in evaluating the clinical utility of genetic information in routine (primary) care. She also studies the ethical and social implications of preimplantation and prenatal genetic screening. Her work further explores inclusive genetic counseling practices, with a focus on improving genetics care for LGBTQIA+ individuals.

The selected publications collectively represent work focused on the clinical implementation of genetic testing. Each paper addresses a practical gap between emerging genomic technologies and real-world implementation, and position genetic counselors as a bridge between molecular diagnosis and precision prevention (in primary care) or treatment (in prenatal care).

 

Health actions following direct-to-consumer genetic testing for medically actionable conditions

Shortcomings of ethnicity-based carrier screening for conditions associated with Ashkenazi Jewish ancestry

Postnatal genetic testing on cord blood for prenatally identified high‐probability cases

Single gene non‐invasive prenatal screening (NIPS-SGD) for autosomal dominant conditions in a high‐risk cohort.

Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities

 

View Google Scholar Profile

 

In addition, Ms. Llorin regularly presents at conferences and industry events. Please see her CV for a complete list of presentations.

 

Implementation Science in Pharmacogenomics: A Dual Clinical and Research Perspective. NHGRI Trainee Meeting. (2026)

Non-Invasive Prenatal Screening for Single Gene Disorders. NSGC Member Webinar Series (2023)

Empowering and Inclusive Care for Sexual and Gender Minority Patients. Myriad Genetics Evolving Strategies in Hereditary Cancer Continuing Education Series (2022)

Gender Affirming Genetics Care: From Medicalization to Empowerment. Minnesota Genetic Counselors Association Spring Education Conference (2022)

Gender Inclusive Genetics. Emory Department of Genetics Grand Rounds (2022)
Awards/Honors :    Massachusetts General Hospital Institute of Health Professions Genetic Counseling Program Outstanding Capstone Committee Member Award (2024). This award honors a distinguished Capstone Committee member who demonstrates excellence in supporting the education, growth, and development of GC students.

ASHG Annual Meeting ‘Reviewer’s Choice Award’ Abstract (2021). The Reviewer’s Choice Award is awarded to the top submitted poster abstracts for their high scientific quality and innovation.

Stanford University Class of 2019 Award of Excellence (2019). Award of Excellence honors graduating seniors who have demonstrated a sincere commitment to the university.

Media Highlights

Perspectives: The Next Chapter
Wed, 03/11/2026
News
Perspectives Research Future
Wed, 03/11/2026
News