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7. Universities Australia 2017-2020 Indigenous Strategy: A Meta-Synthesis of the Issues and Challenges

Author

Anderson, Peter J., Yip, Sun Yee, and Diamond, Zane M.

Abstract

The University Australia (UA) 2017-2020 Indigenous Strategy has offered Australian universities a focus that would work to increase Indigenous participation in the higher education sector in Australia. Despite the high-level involvement and detailed monitoring by Universities Australia as the sector's peak body, Australia's universities have not made significant progress in achieving the targets in the strategic plan. Using a meta-synthesis methodological approach, we provide an overview of published reviews and research on increasing Indigenous participation in the higher education sector in Australia, with particular reference to the three initiative foci and targets in the UA 2017-2020 Indigenous Strategy. Findings revealed that Indigenous students' experiences at university, the shortage of Indigenous academics, and the embedment of Indigenous knowledge and perspectives are significant elements that affect the achievement of the UA targets. We conclude by discussing the implications and gaps in the existing UA strategies and offering recommendations to enable higher educator stakeholders to progress the Indigenous Strategy agenda.

Published
2023
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8. The Knowledge Translation of Early Cerebral Palsy (KiTE CP) Study: Implementing Screening Among a High-Risk Prospective Cohort of Australian Infants

Author

Kwong, Amanda K.L., Eeles, Abbey L., Anderson, Peter J., Badawi, Nadia, Boyd, Roslyn N., Cameron, Kate L., Cheong, Jeanie L.Y., Colditz, Paul, Koorts, Pieter, Crowle, Cathryn, Dale, Russell C., Doyle, Lex W., Fahey, Michael, George, Joanne, Hunt, Rod W., McNamara, Lynda, Morgan, Catherine, Novak, Iona, Olsen, Joy E., Reid, Nadia, Rieger, Ingrid, Whittingham, Koa, and Spittle, Alicia J.

Published
2024
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13. ADHD symptoms and diagnosis in adult preterms: systematic review, IPD meta-analysis, and register-linkage study

Author

Robinson, Rachel, Girchenko, Polina, Pulakka, Anna, Heinonen, Kati, Lähdepuro, Anna, Lahti-Pulkkinen, Marius, Hovi, Petteri, Tikanmäki, Marjaana, Bartmann, Peter, Lano, Aulikki, Doyle, Lex W., Anderson, Peter J., Cheong, Jeanie L. Y., Darlow, Brian A., Woodward, Lianne J., Horwood, L. John, Indredavik, Marit S., Evensen, Kari Anne I., Marlow, Neil, Johnson, Samantha, de Mendonca, Marina Goulart, Kajantie, Eero, Wolke, Dieter, and Räikkönen, Katri

Published
2023
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14. Health-Related Quality-of-Life Outcomes of Very Preterm or Very Low Birth Weight Adults: Evidence From an Individual Participant Data Meta-Analysis

Author

Bolbocean, Corneliu, van der Pal, Sylvia, van Buuren, Stef, Anderson, Peter J., Bartmann, Peter, Baumann, Nicole, Cheong, Jeanie L. Y., Darlow, Brian A., Doyle, Lex W., Evensen, Kari Anne I., Horwood, John, Indredavik, Marit S., Johnson, Samantha, Marlow, Neil, Mendonça, Marina, Ni, Yanyan, Wolke, Dieter, Woodward, Lianne, Verrips, Erik, and Petrou, Stavros

Published
2023
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15. Intimate Partner Violence during Infancy and Cognitive Outcomes in Middle Childhood: Results from an Australian Community-Based Mother and Child Cohort Study

Author

Savopoulos, Priscilla, Brown, Stephanie, Anderson, Peter J., Gartland, Deirdre, Bryant, Christina, and Giallo, Rebecca

Abstract

The cognitive functioning of children who experience intimate partner violence (IPV) has received less attention than their emotional-behavioral outcomes. Drawing upon data from 615 (48.4% female) 10-year-old Australian-born children and their mothers (9.6% of mothers born in non-English speaking countries) participating in a community-based longitudinal study between 2004 and 2016, this study examined the associations between IPV in infancy and cognition in middle childhood (at age 10). Results showed that IPV in the first 12 months of life was associated with lower general cognitive ability and poorer executive attention but not working memory skills. IPV in middle childhood (in the 10th year postpartum) was not associated with cognition. This study provides evidence for the long-term impact of early life exposure to IPV on children's cognition, and points to the importance of early intervention to optimize development.

Published
2022
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17. Interrogating the G rainyhead-like 2 (Grhl2) genomic locus identifies an enhancer element that regulates palatogenesis in mouse

Author

de Vries, Michael, Carpinelli, Marina, Rutland, Emilie, Hatzipantelis, Aaron, Partridge, Darren, Auden, Alana, Anderson, Peter J, De Groef, Bert, Wu, Han, Osterwalder, Marco, Visel, Axel, Jane, Stephen M, and Dworkin, Sebastian

Subjects
Biological Sciences, Biomedical and Clinical Sciences, Genetics, Rare Diseases, Biotechnology, Pediatric Research Initiative, Pediatric, Prevention, Dental/Oral and Craniofacial Disease, Human Genome, Congenital Structural Anomalies, 1.1 Normal biological development and functioning, Underpinning research, Alleles, Animals, Enhancer Elements, Genetic, Female, Gene Deletion, Gene Expression, Gene Expression Regulation, Developmental, Genes, Reporter, Genetic Loci, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Neural Tube, Neural Tube Defects, Neurulation, Palate, Transcription Factors, Medical and Health Sciences, Developmental Biology, Biological sciences, Biomedical and clinical sciences, Health sciences
Abstract

The highly-conserved Grainyhead-like (Grhl) transcription factors are critical regulators of embryogenesis that regulate cellular survival, proliferation, migration and epithelial integrity, especially during the formation of the craniofacial skeleton. Family member Grhl2 is expressed throughout epithelial tissues during development, and loss of Grhl2 function leads to significant defects in neurulation, abdominal wall closure, formation of the face and fusion of the maxilla/palate. Whereas numerous downstream target genes of Grhl2 have been identified, very little is known about how this crucial developmental transcription factor itself is regulated. Here, using in silico and in utero expression analyses and functional deletion in mice, we have identified a novel 2.4 ​kb enhancer element (mm1286) that drives reporter gene expression in a pattern that strongly recapitulates endogenous Grhl2 in the craniofacial primordia, modulates Grhl2 expression in these tissues, and augments Grhl2-mediated closure of the secondary palate. Deletion of this genomic element, in the context of inactivation of one allele of Grhl2 (through generation of double heterozygous Grhl2+/-;mm1286+/- mice), results in a significant predisposition to palatal clefting at birth. Moreover, we found that a highly conserved 325 bp region of mm1286 is both necessary and sufficient for mediating the craniofacial-specific enhancer activity of this region, and that an extremely well-conserved 12-bp sequence within this element (CTGTCAAACAGGT) substantially determines full enhancer function. Together, these data provide valuable new insights into the upstream genomic regulatory landscape responsible for transcriptional control of Grhl2 during palatal closure.

Published
2020

18. Interrogating the Grainyhead-like 2 (Grhl2) genomic locus identifies an enhancer element that regulates palatogenesis in mouse.

Author

de Vries, Michael, Carpinelli, Marina, Rutland, Emilie, Hatzipantelis, Aaron, Partridge, Darren, Auden, Alana, Anderson, Peter J, De Groef, Bert, Wu, Han, Osterwalder, Marco, Visel, Axel, Jane, Stephen M, and Dworkin, Sebastian

Subjects
Palate, Animals, Mice, Inbred C57BL, Mice, Knockout, Mice, Neural Tube Defects, Transcription Factors, Gene Expression, Gene Expression Regulation, Developmental, Gene Deletion, Alleles, Genes, Reporter, Female, Male, Neural Tube, Neurulation, Enhancer Elements, Genetic, Genetic Loci, Biological Sciences, Medical and Health Sciences, Developmental Biology
Abstract

The highly-conserved Grainyhead-like (Grhl) transcription factors are critical regulators of embryogenesis that regulate cellular survival, proliferation, migration and epithelial integrity, especially during the formation of the craniofacial skeleton. Family member Grhl2 is expressed throughout epithelial tissues during development, and loss of Grhl2 function leads to significant defects in neurulation, abdominal wall closure, formation of the face and fusion of the maxilla/palate. Whereas numerous downstream target genes of Grhl2 have been identified, very little is known about how this crucial developmental transcription factor itself is regulated. Here, using in silico and in utero expression analyses and functional deletion in mice, we have identified a novel 2.4 ​kb enhancer element (mm1286) that drives reporter gene expression in a pattern that strongly recapitulates endogenous Grhl2 in the craniofacial primordia, modulates Grhl2 expression in these tissues, and augments Grhl2-mediated closure of the secondary palate. Deletion of this genomic element, in the context of inactivation of one allele of Grhl2 (through generation of double heterozygous Grhl2+/-;mm1286+/- mice), results in a significant predisposition to palatal clefting at birth. Moreover, we found that a highly conserved 325 bp region of mm1286 is both necessary and sufficient for mediating the craniofacial-specific enhancer activity of this region, and that an extremely well-conserved 12-bp sequence within this element (CTGTCAAACAGGT) substantially determines full enhancer function. Together, these data provide valuable new insights into the upstream genomic regulatory landscape responsible for transcriptional control of Grhl2 during palatal closure.

Published
2020

29. Psychiatric disorders in individuals born very preterm / very low-birth weight: An individual participant data (IPD) meta-analysis

Author

Anderson, Peter J, de Miranda, Debora Marques, Albuquerque, Maicon Rodrigues, Indredavik, Marit Sæbø, Evensen, Kari Anne I., Van Lieshout, Ryan, Saigal, Saroj, Taylor, H. Gerry, Raikkonen, Katri, Kajantie, Eero, Marlow, Neil, Johnson, Samantha, Woodward, Lianne J., Austin, Nicola, Nosarti, Chiara, Jaekel, Julia, Wolke, Dieter, Cheong, Jeanie LY, Burnett, Alice, Treyvaud, Karli, Lee, Katherine J, and Doyle, Lex W

Published
2021
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38. Harmonisation of assessments of attention, social, emotional, and behaviour problems using the Child Behavior Checklist and the Strengths and Difficulties Questionnaire

Author

Baumann, Nicole, Anderson, Peter J., Johnson, Samantha, Marlow, Neil, Wolke, Dieter, Jäkel, Julia, Baumann, Nicole, Anderson, Peter J., Johnson, Samantha, Marlow, Neil, Wolke, Dieter, and Jäkel, Julia

Abstract

Objectives: Retrospective harmonisation of data obtained through different instruments creates measurement error, even if the underlying concepts are assumed the same. We tested a novel method for item-level data harmonisation of two widely used instruments that measure emotional and behavioural problems: the Child Behavior Checklist (CBCL) and the Strengths and Difficulties Questionnaire (SDQ). Methods: Item content of the CBCL and SDQ was mapped onto four dimensions: emotional problems, peer relationship problems, hyperactivity/inattention and conduct problems. A diverse test sample was drawn from four prospective longitudinal birth cohort studies in Australia and Europe who used one or both instruments. The pooled sample included 5188 data points assessing children and adolescents aged 6–13 years (N = 257–704 participants per cohort). Measurement invariance was assessed using latent variable multi-group confirmatory factor analysis. Results: Fifteen items from the CBCL and SDQ were mapped onto four dimensions allowing for measurement invariance testing as part of a stepwise process. Partial strict invariance between CBCL and SDQ assessments was established for all four dimensions. Conclusions: The harmonised dimensions of emotional, peer relationship, hyperactivity/inattention and conduct problems are invariant across the CBCL and SDQ suggesting that these dimensions can be reliably compared with limited measurement error.

Published
2024

39. Fibrodysplasia Ossificans Progressiva: A Case Report with Pseudo-Ankylosis of the Temporomandibular Joint.

Author

Chaisrisawadisuk, Sarut, Oliver, Kelly J., Constantine, Sarah, Azzopardi, Jonathan, Anderson, Peter J., and Moore, Mark H.

Subjects
FIBRODYSPLASIA ossificans progressiva, TEMPOROMANDIBULAR joint, RARE diseases, ANKYLOSIS, TREATMENT effectiveness, METAPLASTIC ossification, QUALITY of life, DENTAL extraction
Abstract

Fibrodysplasia ossificans progressiva (FOP) is a rare condition characterized by progressive heterotopic ossifications and congenital hallux valgus deformities. The common underlying genetic cause is an ACVR1 mutation, resulting in altered bone morphogenetic protein (BMP) regulation. Trauma and/or minor procedures aggravate the abnormal bony formation in soft tissues. This report presents a 3-year-old child with this condition who presented pseudo-ankylosis of the temporomandibular joint (TMJ) after minor craniofacial trauma. Abnormal ossification in the medial pterygoid muscle was identified as the causative abnormality for the presentation with trismus. [ABSTRACT FROM AUTHOR]

Published
2024
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40. Indigenous Doctoral Literacy in the Humanities and Social Sciences

Author

Diamond, Zane M., Anderson, Peter J., Lo Bianco, Joseph, Series Editor, Wiley, Terrence G., Series Editor, Kramsch, Claire, Editorial Board Member, Lüdi, Georges, Editorial Board Member, Labrie, Normand, Editorial Board Member, Pakir, Anne, Editorial Board Member, Trim, John, Editorial Board Member, Valdes, Guadalupe, Editorial Board Member, Rennie, Jennifer, editor, and Harper, Helen, editor

Published
2019
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41. Preparing Pre-service Teachers to Teach Literacy in Remote Spaces

Author

Rennie, Jennifer, Anderson, Peter J., Lo Bianco, Joseph, Series Editor, Wiley, Terrence G., Series Editor, Kramsch, Claire, Editorial Board Member, Lüdi, Georges, Editorial Board Member, Labrie, Normand, Editorial Board Member, Pakir, Anne, Editorial Board Member, Trim, John, Editorial Board Member, Valdes, Guadalupe, Editorial Board Member, Rennie, Jennifer, editor, and Harper, Helen, editor

Published
2019
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47. High-Dose Docosahexaenoic Acid in Newborns Born at Less Than 29 Weeks’ Gestation and Behavior at Age 5 Years

Author

Gould, Jacqueline F., primary, Roberts, Rachel M., additional, Anderson, Peter J., additional, Makrides, Maria, additional, Sullivan, Thomas R., additional, Gibson, Robert A., additional, McPhee, Andrew J., additional, Doyle, Lex W., additional, Bednarz, Jana M., additional, Best, Karen P., additional, Opie, Gillian, additional, Travadi, Javeed, additional, Cheong, Jeanie L. Y., additional, Davis, Peter G., additional, Sharp, Mary, additional, Simmer, Karen, additional, Tan, Kenneth, additional, Morris, Scott, additional, Lui, Kei, additional, Bolisetty, Srinivas, additional, Liley, Helen, additional, Stack, Jacqueline, additional, and Collins, Carmel T., additional

Published
2024
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