Ann Haskins Olney, MD

Ann Haskins OlneyAnn Haskins Olney, MD
Genetic Medicine Department
Munroe-Meyer Institute
985440 Nebraska Medical Center
Omaha, NE 68198-5440

Phone: (402) 559-3602
E-mail: mailto:aolney@unmc.edu

Professional Summary:

Clinical Geneticist, Associate Professor of Pediatrics and Munroe-Meyer Institute for Genetics and Rehabilitation

Education:

MD University of Nebraska Medical Center, Omaha, NE, 1981
BS University of Nebraska, Lincoln, NE 1976

Courses Taught:

Cytogenetics 911
Electives in Clinical Genetics for fourth year medical students and Pediatrics residents
Education of Genetic Fellows
First year medical student Core 2 curriculum in Genetics

Research Interests and Projects:

  • Associate Director of Clinical Genetics Fellowship
  • Dysmorphology
  • Molecular Etiology of Multiple Congenital Anomaly Syndromes
  • Overgrowth Syndromes
  • Syndrome Delineation

Selected Publications:

Articles Published:

  • Solomon BD, Lacbawan F, Mercier S, Clegg NJ, Delgado MR, Rosenbaum K, Dubourg C, David V, Olney AH, Wehner LE, Hehr U, Bale S, Paulussen A, Smeets HJ, Hardisty E, Tylki-Szymanska A, Pronicka E, Clemens M, McPherson E, Hennekam RC, Hahn J, Stashinko E, Levey E, Wieczorek D, Roeder E, Schell-Apacik CC, Both CW, Thomas RL, Kenwrick S, Keaton A, Balog JZ, Hadley D, Zhou N, Long R, Velez JI, Pineda-Alvarez DE, Odent S, Roessler E, Muenke M, (2009) Mutations in ZIC2 in Human Holoprosencephaly: Description of a Novel ZIC2-Specific Phenotype and Comprehensive Analysis of 157 Individuals. Journal of Medical Genetics. 149A(10):2248-53.
  • Dave BJ,Olney AH, Zaleski DH, Pickering DL, Becker TA, Chipman HE, Sanger WG. (2009) Inherited 14q duplication and 21q deletion: rare adjacent-2 segregation in multiple family members. American Journal of Medical Genetics, 149A(10):2248-53.
  • Pickering DL, Eudy JD, Olney AH, Dave BJ, Golden D, Stevens J, Sanger WG (2008) Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations. Genetics in Medicine. 10(4):262-6
  • Asher NG, Olney AH, Schaefer GB (2008) Case report: two patients with oculocerebrocutaneous syndrome and terminal digital amputations. Seminars in Pediatric Neurology 15(4): 221-3.
  • Olney AH (2007) Macrocephaly Syndromes. Seminars in Pediatric Neurology. 14(3): 128-35.
  • Vasjar J, Zhang W, Dobyns WB, Biggar D, Holden KR, Hawkins C, Ray P, Olney AH, Burson CM, Srivastava AK, Schachter H. (2006) Carriers and Patients with Muscle-Eye-Brain Disease Can Be Rapidly Diagnosed by Enzymatic Analysis of Fibroblasts and Lymphoblasts. Neuromuscular Disorders,16(2):132-6.
  • Sanger TM, Olney AH, Zaleski D, Pickering D, Nelson M, Sanger WG, Dave BJ, (2005) Cryptic Duplication and Deletion of 9q34.3–>qter in a Family with a t(9;22)(q34.3;p11.2). American Journal of Medical Genetics, 138(1):51-5.

Abstracts Published:

  • Pickering DL, Dave BJ,Eudy JD, Olney AH, Lutz R, Platt K, Sanger WG, (2009) Clinical Genetics and Dysmorphology, (2618F) Presented a the 9th Annual Meeting of The American Society of Human Genetics October 23, 2009, Honolulu, Hawaii. http://www.ashg.org/cgi-bin/2009/ashg09s.
  • Baehr KM, Baum RJ, Smith CV, Berg TG, Tomich PG, Olney AH, Conover EA, Meza JL, Mack-Shipman LR (2008) Maternal and fetal outcomes in pregnancies complicated by diabetes and followed in the high-risk obstetrics-endocrinology clinic (HROBEC) at the University of Nebraska Medical Center. 90th Annual Meeting of the Endocrine Society.
  • Olney AH, Sanger WG, Burson CM, Nelson M, Pierson D (2006) CHARGE Syndrome Due to de novo CHD7 Gene Mutation. Proceedings of the Greenwood Genetic Center, 25, 153-154.
  • Olney AH, Schaefer GB, Burson C (2005) Macrocephaly - Cutis Marmorata Telangiectatica Congenita Following Assisted Reproductive Technology. Proceedings of the Greenwood Genetic Center, 24, 145-146.

Presentations:

  • The Kenneth B. Schwartz Center Rounds, Omaha, Nebraska. “The Difficulty of Maintaining the Big Picture during times of Crisis: Multiple Congenital Anomalies at Birth,” August 29, 2006.
  • American College of Medical Genetics Annual Meeting, Dallas, Texas, “Antley-Bixler Syndrome with Congenital Adrenal Hyperplasia due to Abnormal Steroidogenesis”, March, 2005.
  • American College of Medical Genetics Annual Meeting, Dallas, Texas, Invited Session Moderator, March 2005.
  • David W. Smith Workshop on Malformations and Morphogenesis, Iowa City, Iowa. “CHARGE Syndrome Due to de novo CHD7 Gene Deletion,” August, 2005.

Professional Affiliations:

  • American Society of Human Genetics
  • Great Plains Clinical Genetics Society
  • Nebraska Chapter of the American Academy of Pediatrics
  • American College of Medical Genetics