Morteza Hashemzadeh Chaleshtori

Author PubWeight™ 8.34^‹?›

Top papers

Rank	Title	Journal	Year	PubWeight™‹?›
1	A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment.	Am J Hum Genet	2012	0.97
2	Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus.	Mol Vis	2011	0.95
3	Association between virulence factors of helicobacter pylori and gastric mucosal interleukin-18 mRNA expression in dyspeptic patients.	Microb Pathog	2013	0.91
4	Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Pendred syndrome.	Hum Genet	2010	0.83
5	Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss.	Int J Pediatr Otorhinolaryngol	2012	0.80
6	A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients.	J Genet	2009	0.80
7	Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.	Genet Test Mol Biomarkers	2011	0.79
8	Study of VSX1 mutations in patients with keratoconus in southwest Iran using PCR-single-strand conformation polymorphism/heteroduplex analysis and sequencing method.	Acta Cytol	2013	0.78
9	Diversity and relationship between Iranian ethnic groups: human dopamine transporter gene (DAT1) VNTR genotyping.	Am J Hum Biol	2007	0.78
10	A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame.	Am J Med Genet A	2011	0.77
11	A Simple, Rapid, and Efficient Method for Isolating Mesenchymal Stem Cells From the Entire Umbilical Cord.	Cell Transplant	2015	0.76
12	Variation of DAT1 VNTR alleles and genotypes among old ethnic groups in Mesopotamia to the Oxus region.	Hum Biol	2008	0.75