Brian A. Clark, Ph.D., M.D., FACOG, FACMG

Book Chapters
Carp H, and Clark BA. Genetic and Metabolic Disease. In: Anesthetic and Obstetric Management of High-Risk Pregnancy. S. Datta (ed.), Mosby Year Book, Inc, 1991.

Clark BA, and Schwartz S. Molecular Cytogenetics. In: Diseases of the Fetus and Newborn, 2nd edition. Reed, Claireaus, Bain (ed.), Chapman and Hall, 1995.

Carp H, and Clark BA. Genetic and Metabolic Disease. In: Anesthetic and Obstetric Management of High-Risk Pregnancy, 2nd edition. S. Datta (ed.), Mosby Year Book, Inc, 1996.

Dickerman L, Park V, and Clark BA. Genetic Aspects of Perinatal Disease and Prenatal Diagnosis. In: Neonatal-Perinatal Medicine: Diseases of the Fetus and Infant, 6th edition. A. Fanaroff and R. Martin (eds.), Mosby Year Book, Inc, 1997.

Abstracts
Schafer IA, Stein J, Hyland JC, Byers P, and Clark BA. A new splice mutation producing a partial deficiency of type I collagen and a mild osteogenesis imperfecta (oi) phenotype, submitted.

Publications
Warden CR, Pillers DM, Rice MJ, Wildes J, Livingston JS, Clark BA, Gilhooly JT, and Magenis RE. Interstitial Duplication of the Short Arm of Chromosome 1 in a Newborn with Congenital Heart Disease and Multiple Malformations. American Journal of Human Genetics, In Press

Schafer, IA, Robin, N, Clark BA, Izumo S, Schwarz S. The Distal 5q Deletion Syndrome: Phenotypic Correlations. American Journal of Medical Genetics, In Press

Clark BA, Hereditary Hemochromatosis: Molecular Genetic Testing Issues for the Clinician. Cleveland Clinic Journal of Medicine, In Press

Clark BA, Burke C, and Church J. Cancer Genetics for the Clinician: Genetic Testing for Hereditary Colon Cancer, submitted.

Zervos A, Hunt K, Tong H-Q, Avallone J, Morales J, Friedman N, Cohen B, Clark B, Guo S-Q, Gazda H, Beggs A, and Traboulsi E. Clinical, Genetic and Histopathologic Findings in Two Siblings with Muscle-Eye-Brain Disease, in press.

Gupta PC, Peralta D, Crowe C, Clark B, and Traboulsi E. A Patient with Bilateral Microphthalmos with Cyst, Facial Clefts, and Limb Anomalies: Waardenburg Syndrome, Cerebro-Oculo-Nasal syndrome, or Craniotelencephalic Dysplasia, submitted.

Church JM, McGannon E, Burke C, and Clark BA. Teenagers with Familial Adenomatous Polyposis: what is their risk for Colorectal Cancer?, submitted.

Church JM, McGannon E, Burke C, and Clark BA. Familial Adenomatous Polyposis: When do rectosigmoid adenomas appear?, submitted.

Van Dalen R., Church J., McGannon E., Fay S., Burke C. Clark B., Patterns of surgery in patients belonging to Amsterdam positive families, submitted.

Church J., Burke C., McGannon E., Pastean O., Clark, B. Predicting polyposis severity by proctoscopy: how reliable is it? Dis Colon Rectum 2002 Sep; 44(9): 1249-1254.

Professional Activities, Invited Talks and Special Symposia
Cancer Genetics for the Clinician. Highlights of the 2002 ASCO Meeting. Columbus Community Clinical Oncology Program, Columbus, Ohio, June 5, 2002

Genetic Testing for VHL. Update on VHL, Cleveland Clinic Foundation and the VHL Family Alliance, Cleveland, Ohio, October 11-13, 2002.

Preimplantation Testing for Genetic Disorders, Cleveland Clinic Foundation and the VHL Family Alliance, Cleveland, Ohio, October 11-13, 2002.

Cancer Genetics for the Clinician: Update on the Management of Hereditary Female Malignancies, General Surgery RPAC educational day, South Point Hospital, Cleveland, Ohio, March 26, 2002.