Karen J. Woodward

Perth, WA, Australia

Last Updated: 09/26/2026

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Found 10 publications

Healthcare experiences of refugees and asylum-seekers resettled in non-metropolitan high-income settings: a systematic review and thematic synthesis of qualitative evidence.

Healthcare experiences of refugees and asylum-seekers resettled in non-metropolitan high-income settings: a systematic review and thematic synthesis of qualitative evidence.

Journal: International journal for equity in health

Published: January 19, 2026

Prediction of m6A and m5C at single-molecule resolution reveals a transcriptome-wide co-occurrence of RNA modifications.

Prediction of m6A and m5C at single-molecule resolution reveals a transcriptome-wide co-occurrence of RNA modifications.

Journal: Nature communications

Published: February 23, 2024

Further heterogeneity in Silver-Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement.

Further heterogeneity in Silver-Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement.

Journal: American journal of medical genetics. Part A

Published: March 04, 2021

Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay.

Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay.

Journal: Cold Spring Harbor molecular case studies

Published: November 06, 2020

Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy.

Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy.

Journal: NPJ genomic medicine

Published: June 25, 2019

Distinct patterns of complex rearrangements and a mutational signature of microhomeology are frequently observed in PLP1 copy number gain structural variants.

Distinct patterns of complex rearrangements and a mutational signature of microhomeology are frequently observed in PLP1 copy number gain structural variants.

Journal: Genome medicine

Published: April 29, 2019

Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy.

Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy.

Journal: NPJ genomic medicine

Published: September 10, 2018

Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance.

Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance.

Journal: Molecular genetics & genomic medicine

Published: December 11, 2017

A review of structural brain abnormalities in Pallister-Killian syndrome.

A review of structural brain abnormalities in Pallister-Killian syndrome.

Journal: Molecular genetics & genomic medicine

Published: July 09, 2017

Reinforcing the association between distal 1q CNVs and structural brain disorder: A case of a complex 1q43-q44 CNV and a review of the literature.

Reinforcing the association between distal 1q CNVs and structural brain disorder: A case of a complex 1q43-q44 CNV and a review of the literature.

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Published: October 28, 2015

Showing 1-10 of 10

Last Updated: 09/26/2026