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Devika Ganesamoorthy

Devika Ganesamoorthy,University of Melbourne,Genetics & Genealogy,Medicine,Molecular Biology

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Devika Ganesamoorthy

University of Melbourne

Publications: 4 | Citations: 32

Fields: Genetics & Genealogy, Medicine, Molecular Biology

Collaborated with 69 co-authors from 2008 to 2010 | Cited by 278 authors

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Publications (4)

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Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes (Citations: 11)

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Journal: Journal of Medical Genetics - J MED GENET , vol. 47, no. 5, pp. 299-311, 2010

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio (Citations: 6)

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Journal: Human Molecular Genetics - HUM MOL GENET , vol. 19, no. 8, pp. 1618-1632, 2010

A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33

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Journal: PLOS One , vol. 5, no. 8, 2010

Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice (Citations: 15)

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Journal: Journal of Medical Genetics - J MED GENET , vol. 46, no. 2, pp. 123-131, 2008

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A comparison of genomic copy number calls by Partek Genomics Suite, Genotyping Console and Birdsuite algorithms to quantitative PCR (Citations: 1)

Journal: Biodata Mining , vol. 4, no. 1, pp. 1-11, 2011

Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation (Citations: 1)

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Journal: BMC Medical Genomics - BMC MED GENOMICS , vol. 4, no. 1, pp. 1-10, 2011

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Co-authors (69)

Journals (3)

Keywords (25)

Devika Ganesamoorthy,University of Melbourne,Genetics & Genealogy,Medicine,Molecular Biology

Publications (4)

BibTeX | RIS | RefWorks Download

Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes (Citations: 11)

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio (Citations: 6)

A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33

Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice (Citations: 15)

Citations (32 times by 31 publications)

Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnostics

Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency

LIS1 Duplication: Expanding the Phenotype

A comparison of genomic copy number calls by Partek Genomics Suite, Genotyping Console and Birdsuite algorithms to quantitative PCR (Citations: 1)

Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation (Citations: 1)


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Devika Ganesamoorthy,University of Melbourne,Genetics & Genealogy,Medicine,Molecular Biology

Publications (4) BibTeX | RIS | RefWorks Download

Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes (Citations: 11)

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio (Citations: 6)

Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice (Citations: 15)

A comparison of genomic copy number calls by Partek Genomics Suite, Genotyping Console and Birdsuite algorithms to quantitative PCR (Citations: 1)

Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation (Citations: 1)

Publications (4)

BibTeX | RIS | RefWorks Download