Oana Caluseriu

Oana Caluseriu

Assistant Professor

Medical Genetics
Medical Sciences Building
(780) 407-2993
caluseri@ualberta.ca


Education, training and current affiliation:

1996 –MD, University of Medicine and Pharmacy, Tirgu-Mures, Romania

2001 –Specialist in Medical Genetics, Catholic University, Rome, Italy

2001-2005- Fellow, University of Toronto

2005-2010- Resident in Medical Genetics, University of Calgary

2010-2012- Fellow, CIHR Program in Genetics, Child Development and Health, Alberta Children’s Hospital Research Institute, Calgary, AB

2011- Fellow of the Royal College of Physicians and Surgeons of Canada, Medical Genetics

2012- Fellow of the Canadian College of Medical Genetics

2012- Clinical geneticist, and Assistant Professor, Department of Medical Genetics, University of Alberta, Edmonton, AB

Interests and grant support: I am a clinician scientist with interest in phenotypic and molecular characterization of rare disorders in particular conditions involving craniofacial and limb anomalies. Prospective students will have exposure to clinical and molecular research including the use of next generation sequencing technology. I am a site representative for the Canadian Pediatric Genetics Sequencing Consortium “Enhanced Care for Rare Genetic Diseases in Canada”. Current grant support as a PI and Co-PI is provided by The Rare Disease Foundation, Women and Children Health Research Institute, and Dart Neuroscience.

Selected recent presentations and publications:

  1. Caluseriu O, Bamforth JS. To the Bone: Natural History of Four Cases with Fibrodysplasia Ossificans Progressiva. 34th Annual David W. Smith Workshop, August 9-14, 2013, Mont Tremblant, QC, Canada (platform presentation)
  2. Caluseriu, O, Beaulieu C, Boycott KM. FORGE supports evidence based health care in the practice of medical genetics. Evidence Live 2013 Conference, March 25-26, 2013, Oxford, UK (poster)
  3. Caluseriu O, Reardon W. 2012. Malformation Syndromes. In: Rennie JM, editor. Textbook of Neonatology, Fifth Edition. London, UK: Elsevier Limited. p791-817.
  4. Nikkel SM, Dauber A, de Munnik S, Connolly M, Hood RL, Caluseriu O, Hurst J, Kini U, Nowaczyk MJ, Afenjar A, Albrecht B, Allanson JE, Balestri P, Ben-Omran T, Brancati F, Cordeiro I, da Cunha BS, Delaney LA, Destrée A, Fitzpatrick D, Forzano F, Ghali N, Gillies G, Harwood K, Hendriks YM, Héron D, Hoischen A, Honey EM, Hoefsloot LH, Ibrahim J, Jacob CM, Kant SG, Kim CA, Kirk EP, Knoers NV, Lacombe D, Lee C, Lo IF, Lucas LS, Mari F, Mericq V, Moilanen JS, Møller ST, Moortgat S, Pilz DT, Pope K, Price S, Renieri A, Sá J, Schoots J, Silveira EL, Simon ME, Slavotinek A, Temple IK, van der Burgt I, de Vries BB, Weisfeld-Adams JD, Whiteford ML, Wierczorek D, Wit JM, Yee CF, Beaulieu CL, White SM, Bulman DE, Bongers E, Brunner H, Feingold M, Boycott KM. The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP. Orphanet J Rare Dis 2013; 8(1):63.(doi:10.1186/1750-1172-8-63).
  5. Rivière JP, Mirzaa GM, O’Roak BJ , Beddaoui M, Alcantara D, Conway RL,     St-Onge J, Schwartzentruber JA, Gripp KW, Nikkel SM, Worthylake T, Sullivan CT, Ward TR, Butler HE, Kramer NA, Albrecht B, Armour CM, Armstrong L, Caluseriu O, Cytrynbaum C, Drolet BA, Innes AM, Lauzon JL, Lin AE, Mancini GMS, Meschino WS, Reggin JD, Saggar AK, Lerman-Sagie T, Uyanik G, Weksberg R, Birgit Zirn, Beaulieu CL, FORGE Canada Consortium, Majewski J, Bulman DE,  O’Driscoll M, Shendure J, Graham JMJr, Kym M. Boycott, William B., Dobyns. De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes. Nat Genet 2012;44(8):934-40
  6. Bernier FP, Caluseriu O, Ng S, Schwartzentruber J, Buckingham KJ, Innes AM, Jabs EW, Innis JW, Schuette JL, Gorski JL, Byers PH, Andelfinger G, Siu V, Lauzon J, Fernandez BA, McMillin M, Scott RH, Racher H, FORGE Canada Consortium, Majewski J, Nickerson DA, Shendure J, Bamshad MJ, Parboosingh JS. Haploinsufficiency of SF3B4, a Component of the pre-mRNA Spliceosomal Complex, Causes Nager Syndrome, Am J Hum Genet (2012), doi:10.1016/j.ajhg.2012.04.004
Research Associate

Rika Maruyama


Graduate Student


Christelle Dzolang
Allison Lewis