John J. Mulvihill

Contact Information:
John J. Mulvihill


Mulvihill, John J. (HSC)

Department of:

College Of Medicine/Peds - Genetics -Children's Medical Research Institute Kimberly V. Talley Chair

Center of:

OK Center for Neurosciences -Member


Dartmouth Medical School, University of Washington   MD   1969
Dartmouth Medical School,Hanover, NH   BMS   1967
College of the Holy Cross, Worcester, MA   BS   1965

Professional Interest/Expertise/Specializations:
Birth defects; neurofibromalosis; cleft palate & craniofacial team; research; genetics


OU Children's Physicians - Department of Pediatrics

Research Projects:

Oklahoma Native American Research Center for Health NARCH VI,Indian Health Service/NIH
Heartland Genetics and Newborn Screening Collaborative,Health Resources and Services Administration
Neurofibromatosis 1 in Old Age: International Interdisciplinary Analysis of the Issues,Department of Defense

Selected Publications:

Cancer chemotherapeutic agents as human teratogens.
2012    Selig BP, Furr JR, Huey RW, Moran C, Alluri VN, Medders GR, Mumm CD, Hallford HG, Mulvihill JJ.
Birth Defects Res A Clin Mol Teratol 94:626-650, 2012. PMID: 22851372
Congenital anomalies in the children of cancer survivors: a report from the childhood cancer survivor study.
2012    Signorello LB, Mulvihill JJ, Green DM, Munro HM, Stovall M, Weathers RE, Mertens AC, Whitton JA, Robison LL, Boice JD Jr.
J Clin Oncol 30:239-245, 2012. PMID: 22162566
Reversed clinical phenotype due to a microduplication of Sotos syndrome region detected by array CGH: microcephaly, developmental delay and delayed bone age.
2012    . Zhang H, Lu X, Beasley J, Mulvihill JJ, Liu R, Li S, Lee JY
Am J Med Genet A 155A:1374-1378, 2012. PMID: 21567906
Preconception exposure to mutagens: medical and other exposures to radiation and chemicals.
2012    Mulvihill JJ.
J Community Genet 3:205-211,2012. PMID:22752838
Genetic disease in the children of Danish survivors of childhood and adolescent cancer.
2012    Winther JF, Olsen JH, Wu H, Shyr Y, Mulvihill JJ, Stovall M, Nielsen A, Schmiegelow M, Boice JD Fr.
J Clin Oncol 30:27-33, 2012. PMID: 22124106
A clinical evaluation tool for SNP arrays, especially for autosomal recessive conditions in offspring of consanguinity.
2012    Wierenga, K, Jiang, Z, Yang, A, Mulvihill, JJ, Tsinoremas, N.
Genet Med 14:xxx-xxx, 2012. PMID: 2288xxxx
RBPJ mutations identified in two families affected by Adams-Oliver syndrome.
2012    Hassed SJ, Wiley GB, Wang S, Lee JY, Li S, Xu W, Zhao ZJ, Mulvihill JJ, Robertson J, Warner J, Gaffney PM.
Am J Hum Genet 91:391-395. PMID: 22883147
Harnessing genomics to identify environmental determinants of heritable disease.
   Yauk CL, Lucas Argueso J, Auerbach SS, Awadalla P, Davis SR, Demarini DM, Douglas GR, Dubrova YE,
Mutat Res.
How to talk to patients about genetic testing.
   Mulvihill JJ