Excludes commercial-in-confidence projects.
Research since 2008 is shown below. To see earlier years visit Scopus
Open access indicates that an output is open access.
Arts, P, Garland, J, Byrne, AB, Hardy, TS, Babic, M, Feng, J, Wang, P, Ha, T, King-Smith, SL, Schreiber, AW, Crawford, A, Manton, N, Moore, L, Barnett, CP & Scott, HS 2020, 'Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: phenotypic expansion of the PBX1 -related syndrome', American Journal of Medical Genetics Part A, vol. 182, no. 5, pp. 1273-1277.
Open access 1 1 4
Brown, AL, Arts, P, Babic, M, Dobbins, J, Feng, J, Ha, T, Homan, CC, King-Smith, SL, Li, X-C, Brautigan, P, Butcher, C, D'Andrea, RJ, Hahn, CN & Scott, HS and 46 other authors 2020, 'RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML', Blood Advances, vol. 4, no. 6, pp. pp. 1131-1144.
Open access 9 8 2
Byrne, AB, Mizumoto, S, Arts, P, Yap, P, Feng, J, Schreiber, AW, Babic, M, King-Smith, SL, Barnett, CP, Moore, L, Sugahara, K, Mutlu-Albayrak, H, Nishimura, G, Liebelt, JE, Yamada, S, Savarirayan, R & Scott, HS 2020, 'Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis', Journal of Medical Genetics, article no. 106700, pp. 1-7.
Open access 6
Venugopal, P, Gagliardi, L, Forsyth, C, Feng, J, Phillips, K, Babic, M, Poplawski, NK, Rienhoff, HY, Schreiber, AW, Hahn, CN, Brown, AL & Scott, HS 2020, 'Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss', BMC Medical Genetics, vol. 21, no. 1, article no. 35, pp. 1-5.
Open access 1
Cheah, JJ, Brown, AL, Schreiber, AW, Feng, J, Babic, M, Moore, S, Young, C-C, Fine, M, Phillips, K, Guandalini, M, Wilson, P, Poplawski, N, Hahn, CN & Scott, HS 2019, 'A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia', Haematologica: The Hematology Journal, vol. 104, no. 7, pp. e318-e321.
Open access 4 3 1
De Sousa, SM, Wang, PP, Santoreneos, S, Shen, A, Yates, CJ, Babic, M, Eshraghi, L, Feng, J, Koszyca, B, Roberts-Thomson, S, Schreiber, AW, Torpy, DJ & Scott, HS 2019, 'The genomic landscape of sporadic prolactinomas', Endocrine Pathology, vol. 30, no. 4, pp. 318-328.
3 2 1
Beck, D, Thoms, J, Palu, C, Herold, T, Brown, A, Babic, M, Hahn, C, Perugini, M, Scott, H, Lewis, I, D'Andrea, R & Pimanda, J 2018, 'A four-gene LincRNA expression signature predicts risk in multiple cohorts of acute myeloid leukemia patients', Leukemia, vol. 32, no. 2, pp. 263-272.
Open access 15 15 2
Chong, C-E, Venugopal, P, Stokes, P, Lee, Y, Brautigan, P, Yeung, D, Babic, M, Engler, G, Lane, S, Klingler-Hoffmann, M, Matthews, J, D'Andrea, R, Brown, A, Hahn, C & Scott, H 2018, 'Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes', Leukemia, vol. 32, no. 1, pp. 194-202.
Open access 24 22 4
External engagement & recognition
|Cengiz Gökcek Obstetrics and Children's Hospital||TURKEY|
|Imago Biosciences||UNITED STATES|
|Jarrett St Specialist Centre||AUSTRALIA|
|Lady Cilento Children's Hospital||AUSTRALIA|
|Royal Adelaide Hospital||AUSTRALIA|
|Royal Melbourne Hospital||AUSTRALIA|
|Tokyo Metropolitan Children’s Medical Center||JAPAN|
|Tokyo Metropolitan Children's Medical Center||JAPAN|
|University of Adelaide||AUSTRALIA|
|University of Auckland||NEW ZEALAND|
|University of Melbourne||AUSTRALIA|
|University of Munich||GERMANY|
|University of New South Wales||AUSTRALIA|
|University of Queensland||AUSTRALIA|
|University of South Australia||AUSTRALIA|
|University of Sydney||AUSTRALIA|
|Women's and Children's Hospital||AUSTRALIA|