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Elena J. Tucker
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Australian geneticist
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Works
10
ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism
scientific article
Premature Ovarian Insufficiency: New Perspectives on Genetic Cause and Phenotypic Spectrum
scientific article
Identification of variants in pleiotropic genes causing "isolated" premature ovarian insufficiency: implications for medical practice
article
Recent advances in the genetics of mitochondrial encephalopathies
scientific article published on July 2010
Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression
scientific article
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss
scientific article published in 2021
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing
scientific article
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency
scientific article
Next-generation sequencing in molecular diagnosis:NUBPLmutations highlight the challenges of variant detection and interpretation
scientific article published on 22 December 2011
Rare variants in non-coding regulatory regions of the genome that affect gene expression in systemic lupus erythematosus
scientific article published on 28 October 2019
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Elena Jane Tucker is an Australian geneticist and medical genomics researcher and a 2016 Rising Talent in the L'Oréal-UNESCO For Women in Science Awards.

Instance of
Human
Occupation
Researcher
Geneticist
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