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Professor Maureen J O'Sullivan

CONSULTANT PAEDIATRIC PATHOLOGIST/CLINIC (Paediatrics)

 Maureen.OSullivan@tcd.ie

 

Clinical Professor (Histopathology)


Languages

Language Skill Reading Skill Writing Skill Speaking
English Fluent Fluent Fluent
French Fluent Medium Medium
German Fluent Fluent Fluent
Irish Fluent Medium Medium
Spanish Medium Medium Basic

Memberships

Membership of Professional Institutions, Associations, Societies

Details Date From Date To
Fellow, The Royal College of Pathologists of Great Britain and Ireland.
Member, American Association for Cancer Research.
Member, Societe Internationale d'Oncologie Paediatrique [SIOP].
Member, SIOP Renal Tumor Study Group.
Member, US and Canadian Academy of Pathology.
Member, Connective Tissue Oncology Society.
Member, Paediatric Pathology Society
Member, National Institutes of Health [NIH] Pediatric and Wild-type GIST Clinic
Stenke E, Stallard L, Cooper S, Dominik A, Pilkington A, Sugrue S, O'Sullivan M, McDermott M, Quinn S, Broderick A, Bourke B, Hussey S., Mucosal atrophy predicts poorer outcomes in pediatric ulcerative colitis- a national inception cohort study., Journal of pediatric gastroenterology and nutrition, 2023, pe003746 , Journal Article, PUBLISHED  DOI
Sasaki, E. and Phelan, E. and O'Regan, M. and Kassim, A.H. and Miletin, J. and McMahon, C. and O'Sullivan, M.J. and Baptista, J. and Lynch, S.A., HK1 haemolytic anaemia in association with a neurological phenotype and co-existing CEP290 Meckelâ€"Gruber in a Romani family, Clinical Genetics, 101, (1), 2022, p142-143 , Notes: [cited By 0], Journal Article, PUBLISHED  DOI
Coyle, R. and O'Sullivan, M.J. and Zisterer, D.M., Targeting inhibitor of apoptosis proteins (IAPs) with IAP inhibitors sensitises malignant rhabdoid tumour cells to cisplatin, Cancer Treatment and Research Communications, 32, (100579), 2022, Notes: [cited By 0], Journal Article, PUBLISHED  DOI
Hannon Barroeta, P. and Magnano, S. and O'Sullivan, M.J. and Zisterer, D.M., Evaluation of targeting autophagy for the treatment of malignant rhabdoid tumours, Cancer Treatment and Research Communications, 32, (100584), 2022, Notes: [cited By 0], Journal Article, PUBLISHED  DOI
Marek-Yagel D, Stenke E, Pode-Shakked B, Dunne C, Crushell E, Bryce-Smith A, McDermott M, O'Sullivan MJ, Veber A, Krishnamurthy M, Wells JM, Anikster Y, Bourke B., Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathy., Human genetics, 2022, Journal Article, PUBLISHED  DOI
Shi Y, Yuan J, Rraklli V, Maxymovitz E, Cipullo M, Liu M, Li S, Westerlund I, Bedoya-Reina OC, Bullova P, Rorbach J, Juhlin CC, Stenman A, Larsson C, Kogner P, O'Sullivan MJ, Schlisio S, Holmberg J., Aberrant splicing in neuroblastoma generates RNA-fusion transcripts and provides vulnerability to spliceosome inhibitors., Nucleic acids research, 49, (5), 2021, p2509-2521 , Journal Article, PUBLISHED  DOI
McCarthy P, Harford J, O'Marcaigh A, Malone A, Evans P, Sills A, Storey L, Rooney S, Betts D, O'Sullivan MJ, McDermott M, Bond J, Trinquand A, Smith OP., Ongoing excellent outcomes with reduced toxicities following integration of molecular targeted therapies in pediatric anaplastic large cell lymphoma., Leukemia & lymphoma, 62, (8), 2021, p1995-1999 , Journal Article, PUBLISHED  DOI
Kenny C, O'Meara E, Ula" M, Hokamp K, O'Sullivan MJ., Global Chromatin Changes Resulting from Single-Gene Inactivation-The Role of SMARCB1 in Malignant Rhabdoid Tumor., Cancers, 13, (11), 2021, Journal Article, PUBLISHED  DOI
Sahoo SS, Pastor VB, Goodings C, Voss RK, Kozyra EJ, Szvetnik A, Noellke P, Dworzak M, Starý J, Locatelli F, Masetti R, Schmugge M, De Moerloose B, Catala A, Kállay K, Turkiewicz D, Hasle H, Buechner J, Jahnukainen K, Ussowicz M, Polychronopoulou S, Smith OP, Fabri O, Barzilai S, de Haas V, Baumann I, Schwarz-Furlan S, European Working Group of MDS in Children (EWOG-MDS), Niewisch MR, Sauer MG, Burkhardt B, Lang P, Bader P, Beier R, Müller I, Albert MH, Meisel R, Schulz A, Cario G, Panda PK, Wehrle J, Hirabayashi S, Derecka M, Durruthy-Durruthy R, Göhring G, Yoshimi-Noellke A, Ku M, Lebrecht D, Erlacher M, Flotho C, Strahm B, Niemeyer CM, Wlodarski MW., Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes., Nature medicine, 27, (10), 2021, p1806-1817 , Journal Article, PUBLISHED  DOI
Sahoo SS, Pastor VB, Goodings C, Voss RK, Kozyra EJ, Szvetnik A, Noellke P, Dworzak M, Starý J, Locatelli F, Masetti R, Schmugge M, De Moerloose B, Catala A, Kállay K, Turkiewicz D, Hasle H, Buechner J, Jahnukainen K, Ussowicz M, Polychronopoulou S, Smith OP, Fabri O, Barzilai S, de Haas V, Baumann I, Schwarz-Furlan S, European Working Group of MDS in Children (EWOG-MDS), Niewisch MR, Sauer MG, Burkhardt B, Lang P, Bader P, Beier R, Müller I, Albert MH, Meisel R, Schulz A, Cario G, Panda PK, Wehrle J, Hirabayashi S, Derecka M, Durruthy-Durruthy R, Göhring G, Yoshimi-Noellke A, Ku M, Lebrecht D, Erlacher M, Flotho C, Strahm B, Niemeyer CM, Wlodarski MW., Publisher Correction: Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes., Nature medicine, 27, (12), 2021, p2248 , Journal Article, PUBLISHED  DOI
  

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Awards and Honours

Award Date
University Entrance Scholarship, University College Cork.
First Place in Class, Third Medical Year.
British Paediatric Association Bursary, 1992
NUI Travelling Studentship in Pathology Prize, Dublin, September, 1997
ASCP/CAP American Society of Clinical Pathologists/College of American Pathologists, Resident prize, Fall Meeting, 1997. [Short-listed and I withdrew].
INAPS award for best presentation USCAP (US and Canadian Academy of Pathology) meeting, 1999.
BC Research Institute for Children's & Women's Health, Establishment Award, 2004-7.
SPP (Society for Pediatric Pathology) Young Investigator Award, February 2005.
Children's Cancer Fund Young Investigator Award, August, 2005.
Best presentation award, European Workshop for the Cytogenetics and Molecular Genetics of Solid Tumors, Nijmegen, The Netherlands, June 2010.
Best Presentation, International Cancer Conference, TCD, Cancer Genetics Section,September 2011.