Zohreh Talebizadeh

Author PubWeight™ 11.65^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.	Pediatrics	2004	1.81
2	Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?	J Autism Dev Disord	2004	1.14
3	Autism Genetic Database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites.	BMC Med Genet	2009	1.11
4	snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctions.	Gene	2007	1.07
5	Genetic studies of complex human diseases: characterizing SNP-disease associations using Bayesian networks.	BMC Syst Biol	2012	1.00
6	Plasma peptide YY and ghrelin levels in infants and children with Prader-Willi syndrome.	J Pediatr Endocrinol Metab	2004	0.98
7	Body composition and fatness patterns in Prader-Willi syndrome: comparison with simple obesity.	Obesity (Silver Spring)	2006	0.96
8	Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD.	Genomics	2005	0.93
9	X-chromosome inactivation patterns in females with Prader-Willi syndrome.	Am J Med Genet A	2007	0.91
10	DFNA2/KCNQ4 and its manifestations.	Adv Otorhinolaryngol	2002	0.90
11	FEPI-MB: identifying SNPs-disease association using a Markov Blanket-based approach.	BMC Bioinformatics	2011	0.85