Projects per year
Personal profile
Keywords
- Genetic epidemiology
- Molecular biology
- Molecular cell biology
- Molecular genetics
- Transcriptional profiling
- Developmental origins of health and disease
- Preeclampsia, genetics of
- Pre-term birth, genetics of
- Cardiovascular disease, genetics of
Fingerprint Fingerprint is based on mining the text of the person's scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.
- 27 Similar Profiles
Single Nucleotide Polymorphism
Medicine & Life Sciences
Pre-Eclampsia
Medicine & Life Sciences
Genome
Medicine & Life Sciences
Genes
Medicine & Life Sciences
Genome-Wide Association Study
Medicine & Life Sciences
Exome
Medicine & Life Sciences
Schizophrenia
Medicine & Life Sciences
Alleles
Medicine & Life Sciences
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Projects 2012 2020
MHRIF Round 21 - Eric Moses
Health Department of Western Australia
1/01/18 → 31/12/18
Project: Research
The Busselton Family Heart Study
Watts, G., Moses, E., Cadby, G., Van Bockxmeer, F., Hung, J. & Melton, P.
National Health & Medical Research Council NHMRC
1/01/16 → 31/12/20
Project: Research
N/3 Pedigree Based Whole Genome Sequencing of Affective & Psychotic Disorders
McCarthy, N., Moses, E., Melton, P. & Jablensky, A.
University of Texas at San Antonio
1/03/15 → 28/02/19
Project: Research
Mammographic density in families with high-risk of breast cancer
Moses, E., Saunders, C. & Stone, J.
1/01/17 → 31/12/17
Project: Research
Research Output 2006 2018
Clinical significance of circulating microRNAs as markers in detecting and predicting congenital heart defects in children
Song, Y., Higgins, H., Guo, J., Harrison, K., Schultz, E. N., Hales, B. J., Moses, E. K., Goldblatt, J., Pachter, N. & Zhang, G. 27 Feb 2018 In : Journal of Translational Medicine. 16, 1, 42Research output: Contribution to journal › Article
Open Access
Congenital Heart Defects
MicroRNAs
Atrial Heart Septal Defects
Defects
Cardiovascular Diseases
Genetic approaches in preeclampsia
Yong, H. E. J., Murthi, P., Brennecke, S. P. & Moses, E. K. 1 Jan 2018 Genetic Approaches in Preeclampsia. Murthi, P. & Vaillancourt, C. (eds.). Humana Press, Vol. 1710, p. 53-72 20 p. (Methods in Molecular Biology; vol. 1710)Research output: Chapter in Book/Report/Conference proceeding › Chapter
Pre-Eclampsia
Causality
Genes
Research Personnel
Genome
Identification of Pre-eclampsia susceptibility genes
Gokhale-Agashe, D. S. 2018 (Unpublished)Research output: Thesis › Doctoral Thesis
File
Pre-Eclampsia
Genes
Collagen Type IV
Genome
Pregnancy
Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study
Cadby, G., Melton, P. E., McCarthy, N. S., Almeida, M., Williams-Blangero, S., Curran, J. E., VandeBerg, J. L., Hui, J., Beilby, J., Musk, A. W., James, A. L., Hung, J., Blangero, J. & Moses, E. K. 2018 In : Human Genetics. 137, 1, p. 45–53 9 p.Research output: Contribution to journal › Article
Obesity
Health
Waist-Hip Ratio
Single Nucleotide Polymorphism
Triglycerides
Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity
Khan, F. F., Melton, P. E., McCarthy, N. S., Morar, B., Blangero, J., Moses, E. K. & Jablensky, A. Feb 2018 (Accepted/In press) In : Schizophrenia Research.Research output: Contribution to journal › Article
Genetic Heterogeneity
Schizophrenia
Genome
Psychotic Disorders
Base Pairing