• The University of Western Australia (M575), 35 Stirling Highway,

    6009 Perth


  • 13000 Citations
  • 45 h-Index
1994 …2023
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Fingerprint Dive into the research topics where Alistair Forrest is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 31 Similar Profiles
Genes Medicine & Life Sciences
Gene Expression Medicine & Life Sciences
Transcription Factors Medicine & Life Sciences
Transcriptome Medicine & Life Sciences
Gene Expression Profiling Medicine & Life Sciences
Genome Medicine & Life Sciences
Transcription Initiation Site Medicine & Life Sciences
Gene Regulatory Networks Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1994 2019

Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases

FANTOM Consortium, 15 Aug 2019, In : Molecular Neurobiology. 56, 8, p. 5392-5415 24 p.

Research output: Contribution to journalArticle

Open Access
Nervous System Heredodegenerative Disorders
Neurodegenerative Diseases
Long Noncoding RNA
Transcription Initiation Site

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

Olivé, M., Engvall, M., Ravenscroft, G., Cabrera-Serrano, M., Jiao, H., Bortolotti, C. A., Pignataro, M., Lambrughi, M., Jiang, H., Forrest, A. R. R., Benseny-Cases, N., Hofbauer, S., Obinger, C., Battistuzzi, G., Bellei, M., Borsari, M., Di Rocco, G., Viola, H. M., Hool, L. C., Cladera, J. & 24 othersLagerstedt-Robinson, K., Xiang, F., Wredenberg, A., Miralles, F., Baiges, J. J., Malfatti, E., Romero, N. B., Streichenberger, N., Vial, C., Claeys, K. G., Straathof, C. S. M., Goris, A., Freyer, C., Lammens, M., Bassez, G., Kere, J., Clemente, P., Sejersen, T., Udd, B., Vidal, N., Ferrer, I., Edström, L., Wedell, A. & Laing, N. G., 1 Dec 2019, In : Nature Communications. 10, 1, 1396.

Research output: Contribution to journalArticle

Open Access
Muscular Diseases
2 Citations (Scopus)
10 Downloads (Pure)

Bi-allelic mutations in MYL1 cause a severe congenital myopathy

Ravenscroft, G., Zaharieva, I. T., Bortolotti, C. A., Lambrughi, M., Pignataro, M., Borsari, M., Sewry, C. A., Phadke, R., Haliloglu, G., Ong, R., Goullée, H., Whyte, T., Consortium, U. K., Manzur, A., Talim, B., Kaya, U., Osborn, D. P. S., Forrest, A. R. R., Laing, N. G. & Muntoni, F., 15 Dec 2018, In : Human Molecular Genetics. 27, 24, p. 4263-4272 10 p.

Research output: Contribution to journalArticle

Open Access
Myotonia Congenita
Skeletal Muscle
Myosin Light Chains

Circulating MDSC modulate IPF progression by orchestrating immunosuppressive and pro-fibrotic networks

Fernandez, I. E., Greiffo, F. R., Roi, R., Behr, J., Forrest, A. & Eickelberg, O., 15 Sep 2018, In : European Respiratory Journal. 52, 1 p.

Research output: Contribution to journalAbstract/Meeting Abstract

Open Access
Immediate-Early Genes
Chemical activation
Gene Expression
Untranslated RNA


Transcription start site profiling of 15 anatomical regions of the Macaca mulatta central nervous system

Francescatto, M. (Creator), Lizio, M. (Creator), Philippens, I. (Creator), Bontrop, R. (Creator), Sakai, M. (Creator), Watanabe, S. (Creator), Itoh, M. (Creator), Hasegawa, A. (Creator), Lassmann, T. (Creator), Severin, J. (Creator), Harshbarger, J. (Creator), Abugessaisa, I. (Creator), Kasukawa, T. (Creator), Carninci, P. (Creator), Hayashizaki, Y. (Creator), Forrest, A. (Creator), Kawaji, H. (Creator), Rizzu, P. (Creator), Heutink, P. (Creator), Scientific Data, 31 Oct 2017


Projects 2015 2023