Weimin Bi

Author PubWeight™ 6.52^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing.	Eur J Hum Genet	2013	1.30
2	Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10,362 consecutive cases.	Eur J Hum Genet	2014	1.07
3	Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27.	Eur J Hum Genet	2014	0.91
4	Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays.	Prenat Diagn	2012	0.90
5	CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree.	Eur J Hum Genet	2014	0.89
6	Neurodevelopmental and neurobehavioral characteristics in males and females with CDKL5 duplications.	Eur J Hum Genet	2014	0.83
7	6q22.1 microdeletion and susceptibility to pediatric epilepsy.	Eur J Hum Genet	2014	0.77
8	Comparison of three whole genome amplification methods for detection of genomic aberrations in single cells.	Prenat Diagn	2016	0.75
9	Variable levels of tissue mosaicism can confound the interpretation of chromosomal microarray results from peripheral blood.	Eur J Med Genet	2014	0.75