Personal profile
Fingerprint
- 1 Similar Profiles
Collaborations and top research areas from the last five years
-
A precision medicine approach to interpret a GATA4 genetic variant in a paediatric patient with congenital heart disease
Forbes, C. A., Shaw, N. C., Chen, K. G., Hedges, M., Er, T. S., Hool, L., Ward, M., Poulton, C., Baynam, G., Lassmann, T. & Fear, V. S., Dec 2026, In: Human genomics. 20, 1, 29.Research output: Contribution to journal › Article › peer-review
Open Access -
Functional characterization of the MED12 p.Arg1138Trp variant in females: implications for neural development and disease mechanism
Shaw, N. C., Harrison, S., Chen, K., Forbes, C. A., Kuzminski, E., Hedges, M., Farley, K. O., Ward, M., Loughman, L., Poulton, C., Baynam, G., Lassmann, T. & Fear, V. S., Dec 2025, In: Molecular Medicine. 31, 1, 300.Research output: Contribution to journal › Article › peer-review
Open Access -
Interleukin-4 modulates type I interferon to augment antitumor immunity
Newnes, H. V., Armitage, J. D., Buzzai, A. C., de Jong, E., Audsley, K. M., Barnes, S. A., Srinivasan, S., Serralha, M., Fear, V. S., Guo, B. B., Jones, M. E., Forrest, A. R. R., Foley, B., Darcy, P. K., Beavis, P. A., Bosco, A. & Waithman, J., 16 May 2025, In: Science Advances. 11, 20, 14 p., eadt3618.Research output: Contribution to journal › Article › peer-review
4 Link opens in a new tab Citations (Scopus) -
Titin-related familial dilated cardiomyopathy: factors associated with disease onset
Australian Genomics Cardiac Flagship, 2025, In: European Heart Journal. 46, 48, p. 5240-5257 18 p.Research output: Contribution to journal › Article › peer-review
Open Access6 Link opens in a new tab Citations (Scopus) -
A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship
Australian Genomics Cardiovascular Disorders Flagship, Austin, R., Brown, J. S., Casauria, S., Madelli, E. O., Mattiske, T., Boughtwood, T., Metke, A., Davis, A., Horton, A. E., Winlaw, D., Das, D., Soka, M., Giannoulatou, E., Rath, E. M., Haan, E., Blue, G. M., Vohra, J., Atherton, J. J. & van Spaendonck-Zwarts, K. & 22 others, , Jan 2024, In: Genetics in Medicine Open. 2, 101842.Research output: Contribution to journal › Article › peer-review
Open Access6 Link opens in a new tab Citations (Scopus)
Datasets
-
Additional file 2 of Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling
Shaw, N. C. (Creator), Chen, K. (Creator), Farley, K. O. (Creator), Hedges, M. (Creator), Forbes, C. (Creator), Baynam, G. (Creator), Lassmann, T. (Creator) & Fear, V. S. (Creator), Figshare, 1 Oct 2024
DOI: 10.6084/m9.figshare.27140535.v1, https://springernature.figshare.com/articles/dataset/Additional_file_2_of_Identifying_SETBP1_haploinsufficiency_molecular_pathways_to_improve_patient_diagnosis_using_induced_pluripotent_stem_cells_and_neural_disease_modelling/27140535/1
Dataset
-
Additional file 2 of Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling
Shaw, N. C. (Creator), Chen, K. (Creator), Farley, K. O. (Creator), Hedges, M. (Creator), Forbes, C. (Creator), Baynam, G. (Creator), Lassmann, T. (Creator) & Fear, V. S. (Creator), Figshare, 1 Oct 2024
DOI: 10.6084/m9.figshare.27140535, https://springernature.figshare.com/articles/dataset/Additional_file_2_of_Identifying_SETBP1_haploinsufficiency_molecular_pathways_to_improve_patient_diagnosis_using_induced_pluripotent_stem_cells_and_neural_disease_modelling/27140535
Dataset
-
Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling
Shaw, N. C. (Contributor), Chen, K. (Contributor), Farley, K. O. (Contributor), Hedges, M. (Contributor), Forbes, C. (Contributor), Baynam, G. (Contributor), Lassmann, T. (Contributor) & Fear, V. S. (Contributor), Figshare, 1 Oct 2024
DOI: 10.6084/m9.figshare.c.7474071
Dataset
-
Additional file 5 of A precision medicine approach to interpret a GATA4 genetic variant in a paediatric patient with congenital heart disease
Forbes, C. A. (Creator), Shaw, N. C. (Creator), Chen, K. G. (Creator), Hedges, M. (Creator), Er, T. S. (Creator), Hool, L. (Creator), Ward, M. (Creator), Poulton, C. (Creator), Baynam, G. (Creator), Lassmann, T. (Creator) & Fear, V. S. (Creator), Figshare, 4 Feb 2026
DOI: 10.6084/m9.figshare.31246343
Dataset
-
Additional file 2 of Functional characterization of the MED12 p.Arg1138Trp variant in females: implications for neural development and disease mechanism
Shaw, N. C. (Creator), Harrison, S. (Creator), Chen, K. (Creator), Forbes, C. A. (Creator), Kuzminski, E. (Creator), Hedges, M. (Creator), Farley, K. O. (Creator), Ward, M. (Creator), Loughman, L. (Creator), Poulton, C. (Creator), Baynam, G. (Creator), Lassmann, T. (Creator) & Fear, V. S. (Creator), Figshare, 30 Sept 2025
DOI: 10.6084/m9.figshare.30240448
Dataset
-
AFGN_ FBN1 genetic variant interpretation in iPSC-derived cardiomyocytes
Fear, V. (Investigator 01) & Lassmann, T. (Investigator 02)
Australian Functional Genomics Network
1/01/25 → 30/04/26
Project: Research
-
SCRIPT, Single-cell CRISPR to Identify Pathogenesis and Treatment, in genetic diagnosis
Fear, V. (Investigator 01) & Lassmann, T. (Investigator 02)
1/11/24 → 31/10/27
Project: Research
-
Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis and treatment.
Fear, V. (Investigator 01), Lassmann, T. (Investigator 02) & Baynam, G. (Investigator 03)
1/02/22 → 31/01/23
Project: Research
-
Treatments for those who have none (C3676)
Lassmann, T. (Investigator 01) & Fear, V. (Investigator 02)
1/01/22 → 31/12/22
Project: Research
-
Functional genomics and neuronal disease modelling to facilitate rare disease diagnosis
Fear, V. (Investigator 01), Lassmann, T. (Investigator 02), Baynam, G. (Investigator 03) & Groza, T. (Investigator 04)
Department of Health (Western Australia)
1/10/21 → 30/09/23
Project: Research