Devika Ganesamoorthy

Author PubWeight™ 7.66^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes.	J Med Genet	2010	1.50
2	Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio.	Hum Mol Genet	2010	1.31
3	Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature.	Am J Med Genet B Neuropsychiatr Genet	2013	1.13
4	Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarrays.	Hum Mutat	2011	0.99
5	A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33.	PLoS One	2010	0.95
6	Phenotypic variability of distal 22q11.2 copy number abnormalities.	Am J Med Genet A	2011	0.93
7	Application of a new molecular technique for the genetic evaluation of products of conception.	Prenat Diagn	2012	0.80
8	High-resolution microarray in the assessment of fetal anomalies detected by ultrasound.	Aust N Z J Obstet Gynaecol	2014	0.75