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Genetics Faculty

Anne Matthews
Department of Genetics
School of Medicine
Case Western Reserve University
Biomedical Research Building 630
2109 Adelbert Road
Cleveland, Ohio 44106-4955
Tel: (216) 368-1821
Fax: (216) 368-3432

About Anne Matthews

Anne L. Matthews, R.N., Ph.D., LGC, FACMG is Professor of Genetics & Genome Sciences and Director of Genetic Counseling Training Program. Dr. Matthews, who was director of the Graduate Program in Genetic Counseling at the University of Colorado Health Sciences Center, Denver, Colorado for 8 years, was specifically recruited to develop, direct and teach in the Program.

Dr. Matthews received her diploma in nursing from the Massachusetts General Hospital School of Nursing in 1968 and her baccalaureate degree in 1971 from McGill University. In 1973, she received a master's degree and completed her doctorate in genetics and nursing in 1984 from the University of Colorado Health Sciences Center (UCHSC).

Dr. Matthews has had extensive experience in genetic counseling, first as Coordinator of the Regional Genetic Counseling Clinic for Colorado and Wyoming and later as a nurse geneticist with Genetic Services and the Maternal-Fetal Surgery and Medicine Program at UCHSC. She was an Assistant Professor on the faculties of the Schools of Medicine and Nursing at UCHSC. In 1996, she joined the Department of Genetics and Genome Sciences in the School of Medicine at Case Western Reserve University.

Dr. Matthews is board certified by the American Board of Medical Genetics and a charter member of the American Board of Genetic Counseling. She is a past President of the Association of Genetic Counseling Program Directors. She is also an advisory board member for the Genetic Counseling Program at Stanford University. She is a member of the National Society of Genetic Counselors, and a founding fellow of the American College of Medical Genetics. She is a past editor of the Journal of Genetic Counseling and past president of the International Society of Nurses in Genetics. Her areas of clinical interest and research include curriculum development and graduate education in genetic counseling as well as issues arising from the numerous and complex ethical, social legal and educational issues faced by genetic counselors.


The practice of genetic counseling is continually changing as a consequence of the rapid developments in human genetics. New technologies and extensive research in mapping and sequencing the human genome, and their clinical applications continue to shape the philosophy of genetic counseling and genetic services.

Genetic counselors face numerous and complex ethical, social, legal and educational issues. It is within this arena that my clinical and research interests are focused.

Most often, the education and counseling accompanying genetic testing is provided by genetic counselors as they support patients in the decision-making process regarding testing and dealing with test outcomes.

Counselors also play a role in determining how new genetic information and technology will be used. It is essential that curriculum in graduate education in genetic counseling reflect changes in this knowledge and technology. Such issues as human variation and diversity and how knowledge of one's genetic make-up affects individuals' assessment of self-concept and health, genetic discrimination in regards to health insurance and employment, patient confidentiality and rights to privacy, genetic screening and policy development, potential threats to non-directive approaches to counseling are but a few areas in the counseling curriculum that need to be addressed.

Providing students with innovative avenues for addressing some of these issues, through classroom and clinical experiences, is my area of interest.

Another major area of interest for me is providing both health care professionals and students, who are not specialists in genetics, with basic and current knowledge of applied genetics, thereby significantly increasing the incorporation of genetic information into health care delivery.

Currently, I am involved in developing educational programs for medical students as well as practicing physicians and am co-investigator of a NIH National Cancer Institute funded grant to develop and disseminate an electronic curriculum in clinical cancer genetics for medical students.

Selected Publications

Matthews AL, Grimes SJ, Wiesner GL, Acheson LS (2004)
Clinical consult: iron overload--hereditary hemochromatosis
Prim Care.;31(3):767-70, xii-xi
See PubMed abstract

Bubb JA, Matthews AL. (2004)
What's new in prenatal screening and diagnosis?
Prim Care.;31(3):561-82, ix.
See PubMed abstract

Wiesner GL, Cassidy SB, Grimes SJ, Matthews AL, Acheson LS. (2004)
Clinical consult: developmental delay/fragile X syndrome.
Prim Care.;31(3):621-5, x.
See PubMed abstract

Grimes SJ, Acheson LS, Matthews AL, Wiesner GL. (2004)
Clinical consult: Marfan syndrome.
Prim Care.;31(3):739-42, xii.
See PubMed abstract

Falk MJ, Dugan RB, O'Riordan MA, Matthews AL, Robin NH. (2003)
Medical Geneticists' duty to warn at-risk relatives for genetic disease.
Am J Med Genet A.;120(3):374-80.
See PubMed abstract

Dugan RB, Wiesner GL, Juengst ET, Matthews AL, Robin NH. (2003)
Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experience.
Am J Med Genet C Semin Med Genet.;119(1):27-34.
See PubMed abstract

Matthews AL and Robin NH (2002)
Genetics, Malformations and Inherited Inborn Errors of Metabolism.
Chapter in Handbook of Neonatal Intensive Care.

Brunger JW, Matthews AL, Smith RH, Robin NH. (2001)
Genetic testing and genetic counseling for deafness: the future is here.
Laryngoscope.;111(4 Pt 1):715-8.
See PubMed abstract

Matthews, AL and Robin, NH. (2001)
Genetic Issues in Otolaryngology. Chapter in ENT Secrets.
Chapter in ENT Secrets.

Brunger JW, Murray GS, O'Riordan M, Matthews AL, Smith RJ, Robin NH. (2000)
Parental attitudes toward genetic testing for pediatric deafness.
Am J Hum Genet.;67(6):1621-5.
See PubMed abstract

Ormond KE, Haun JM, Cook L, Duquette D, Ludowese CJ, Matthews AL. (2000)
Genetic Counseling.
Chapter in Encyclopedia of Biotechnology: Ethical, Legal and Policy Issues.

Matthews A. (1999)
Chromosomal abnormalities: trisomy 18, trisomy 13, deletions, and microdeletions.
J Perinat Neonatal Nurs.;13(2):59-75; quiz 10
See PubMed abstract