| ردیف |
عنوان |
کد رهگیری |
نمایه |
تاریخ انتشار |
دوره (Volum) |
شماره |
ضریب تاثیر |
کد طرح های مرتبط |
| 1 | بررسی ملکولی جهش های حذفی ژن آلفا گلوبین در بیماران با کم خونی هیپوکرومی میکروسیتی در کرمانشاه | 1903 | index copernicus | | | | | |
| 2 | Gene and environment interaction in ... | 2405 | ISI | | | | 0.51 | |
| 3 | paraoxonase arg 192 allele is an independent risk factor for three-vessel stenosis of coronary artery disease | 3034 | ISI | | | | 1.875 | |
| 4 | molecular analysis of exons 6 and 7 of phenylalanine hydroxylase gene mutations in phenylketonuria patients in | 3817 | pubmed | | | | | |
| 5 | the spectrum of beta-thalassemia mutations in kermanshah province in west iran and its association with hematological paramenters | 4580 | ISI | | | 37 | 0.894 | |
| 6 | mutation analysis of pah gene in patients with pku in western iran and its association with polymorphisms: identification of four novel mutations | 4630 | ISI | | | 10 | 2.333 | |
| 7 | the proportion of tetrahydrobiopterin deficiency and pah gene deficiency variants among cases with hyperphenyalaninemia in western iran | 4947 | pubmed | | | 19 | | |
| 8 | mutation analysis of exons 10 and 17a of cftr gene in patients with cystic fibrosis in kermanshah province western iran | 4949 | pubmed | | | 15 | | |
| 9 | خطر بالای تولد نوزادان فنیل کتونوریایی در روستای مستعلی، استان کرمانشاه | 5140 | ایندکس شده3 | | | 18 | | |
| 10 | فراوانی شایعترین جهش مدیترانه ای در بیماران فنیل کتونوری استان کرمانشاه | 5321 | scopus | | | 19 | | |
| 11 | The Spectrum of a-Thalassemia Mutations in Kermanshah Province ,West Iran | 7548 | ISI | 1394/09/10 | 10.3109/03630269.2015.1070732 | 6 | 0.787 | 95374 |
| 12 | Molecular analysis of exon 13 of cystic fibrosis patients in Middle East:
High frequency of K710X mutation | 9684 | ISI | 1395/11/11 | http://dx.doi.org/10.1016/j.mgene.2016.12.002 | | 0.0 | 95525 |
| 13 | Cytogenetic Abnormalities and Y Chromosome Microdeletions in Azoospermic and Oligospermic Infertile Males from West of Iran | 10669 | علمی پژوهشی | 1396/03/11 | | 2 | | 97822 |
| 14 | TTY2 genes deletions as genetic risk factor of male infertility | 10670 | ISI | 1395/11/13 | | 2 | 0.92 | |
| 15 | IVS-II-648/649 (–T) (HBB: c.316−202del) Triggers a Novel β-Thalassemia Phenotype
Phenotype | 11107 | ISI | 1396/02/15 | | 1 | 0.598 | |
| 16 | Aberrant methylation of APAF-1 gene in acute myeloid leukemia patients | 11108 | pubmed | 1396/04/10 | | 3 | | |
| 17 | توزیع ژوتیپ ویروس هپاتیت ب در استان کرمانشاه | 11114 | علمی پژوهشی | 1394/11/12 | | 2 | | |
| 18 | Spectrum of Phenylalanine Hydroxylase Gene Mutations in Hamadan and Lorestan Provinces of Iran and Their Associations with Variable Number of Tandem Repeat Alleles | 12184 | ISI | 1397/02/11 | | 3 | | 95260 |
| 19 | The molecular analysis of mutations in exons 4, 11 and 21 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in cystic fibrosis patients in Kermanshah, Iran. Journal of Kermanshah University of Medical Sciences | 13057 | علمی پژوهشی | 1395/12/17 | | | | |
| 20 | Association between activity and genotypes of paraoxonase1 L55M
(rs854560) increases the disease activity of rheumatoid arthritis
through oxidative stress | 13662 | ISI | 1397/11/12 | | 1 | 1.889 | 97001 |
| 21 | The Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran. | 13801 | ISI | 1397/10/11 | | 1 | 0.598 | 97066 |
| 22 | The Spectrum of α-Thalassemia Mutations in the Lak Population of Iran | 13985 | ISI | 1397/12/10 | | 2 | 0.598 | 97066 |
| 23 | Characterization of the IVS-II-821 (A>C) (HBB: c.316-30A>C) Mutation in a β-Thalassemia Phenotype in Iran | 14103 | ISI | 1398/04/10 | | 1 | 0.598 | 97066 |
| 24 | The status of PAH gene-VNTR alleles and mini-haplotypes associations with PAH gene mutations in Iranian Kurdish PKU patients | 14584 | pubmed | 1398/06/04 | | 88 | | 95260 |
| 25 | Detection of SPG20 gene promoter methylated DNA, as a novel epigenetic biomarker, in plasma for colorectal cancer diagnosis using the MethyLight method. | 14907 | ISI | 1395/10/27 | | 13 | 1.871 | |
| 26 | α-Thalassemia Mutations in Ilam Province, West Iran | 14943 | ISI | 1399/06/11 | | | 0.526 | 980659 |
| 27 | Genetic linkage analysis of DFNB1 (GJB6) and DFNB4 (SLC26A4)
loci with autosomal recessive non-Syndromic hearing loss
Archives of Medical Laboratory Sciences
(ARNSHL) in Kermanshah, Iran | 15022 | ISC | 1396/03/11 | | 2 | | 90235 |
| 28 | CFTR Mutation Analysis in Western Iran: Identification of Two Novel Mutations | 15023 | pubmed | 1396/12/10 | | 19 | | |
| 29 | بررسی رابطه چند شکلی ژن HIWI2 با ناباروری ایدیوپاتیک مردان | 15028 | ISC | 1398/06/10 | | 3 | | |
| 30 | Relationship between microRNA-206 plasma levels with the severity of coronary artery confl icts in patients with coronary artery disease | 15029 | ISI | 1398/02/11 | | 120 | 0.859 | |
| 31 | بررسی واژگونی اینترون 22 و مارکر HindIII در اینترون 19 ژن فاکتور VIII انعقادی در بیماران هموفیل A | 15030 | علمی پژوهشی | 1396/02/12 | | 12 | | |
| 32 | The Spectrum of a-Thalassemia Mutations in Kurdistan Province, West Iran | 15449 | ISI | 1399/03/13 | | 3 | 0.526 | 980659 |
| 33 | Severe a-Thalassemia Due to Compound Heterozygosity for Hb Adana (a59 Gly>Asp) (HBA1: c.179G>A) and Codon 127 (A>T) (HBA2: c.382A>T) in an Iranian Family | 15450 | ISI | 1398/12/11 | | 2 | 0.526 | |
| 34 | Distribution of HBB Gene Mutations in the Kurdish Population of Ilam Province,
West Iran | 15927 | ISI | 1399/06/11 | | | 0.526 | 97066 |
| 35 | Cytogenetic analysis of 570 couples with recurrent pregnancy loss: Reporting 11 years of experience | 15968 | pubmed | 1399/06/11 | | 3 | | 990034 |
| 36 | Molecular Genetic Analysis of a-Thalassemia in Hamadan Province, West Iran | 16153 | ISI | 1399/06/11 | | 5 | 0.526 | 980659 |
| 37 | Spectrum of PAH gene mutations in 1547 phenylketonuria patients from Iran: a comprehensive systematic review | 16468 | ISI | 1399/11/12 | https://doi.org/10.1007/s11011-021-00698-4 | 5 | 2.726 | 990713 |
| 38 | CFTR gene mutation spectrum among 735 Iranian patients with cystic fibrosis: A comprehensive systematic review | 17350 | ISI | 1400/09/12 | https://doi.org/10.1002/ppul.25647 | 12 | 3.039 | 991003 |
| 39 | Spectrum of MEFV gene mutations in 4,256 familial Mediterranean fever patients from Iran: a comprehensive systematic review | 17511 | ISI | 1400/10/28 | https://doi.org/10.1186/s43042-022-00222-y | 5 | | 990822 |
| 40 | Problem of borderline hemoglobin A2 levels in an Iranian population with a high prevalence of α- and β-thalassemia carriers | 17723 | ISI | 1400/12/16 | | | | 980659 |
| 41 | The pathogenicity classification of PAH gene variants in the Iranian population | 17724 | ISI | 1401/03/15 | | | 2.877 | 991010 |
| 42 | ارتباط واریانتهای ژنتیکی مسیر ترارسانی نیتریک اکسید/cGMP
با استعداد ابتلا به پرفشاری خون در جمعیت استان کرمانشاه | 18953 | scopus | 1402/01/20 | | | | 97354 |
| 43 | The Potential of miR-21 in Stem Cell Differentiation and its Application in Tissue Engineering and Regenerative Medicine | 19216 | ISI | 1401/12/20 | https://doi.org/10.1007/s12015-023-10510-8 | 5 | 4.8 | |
| 44 | The influence of Nrf2 gene promoter
methylation on gene expression and oxidative
stress parameters in preeclampsia | 19817 | ISI | 1402/12/09 | | 64 | 2.7 | 990949 |
| 45 | Contribution of chromosomal aberrations to the pathogenesis of primary and secondary amenorrhea: A study from Western Iran | 20126 | ISI | 1403/05/01 | https://doi.org/10.5653/cerm.2024.06807 | 1 | 1.8 | 4010776 |
| 46 | Deciphering the Role of Calcium Signaling Pathway-Associated Single Nucleotide Variants in Susceptibility to Hypertension | 20732 | ISI | 1403/10/27 | | | 2.6 | 4010397 |
| 47 | نقش پلیمورفیسمهای miRNA در ناباروری مردان و زنان و شکست مکرر لانه گزینی | 20830 | ISI | 1404/01/13 | https://doi.org/10.1111/jog.16281 | 1341-8076, 1447-0756 | 1.6 | 4020547 |
| 48 | miR-184 in hepatocellular carcinoma: a promising therapeutic target | 21096 | ISI | 1404/04/25 | https://doi.org/10.1007/s13105-025-01104-8 | | 3.7 | 4020580 |
| 49 | A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy | 21617 | ISI | 1404/08/13 | https://doi.org/10.1186/s12920-025-02254-w | 1 | 2.0 | |
| 50 | A novel Bi-Allelic pathogenic MCOLN1 variant
underlying mucolipidosis type IV in an
Iranian family: clinical, genetic, and molecular
dynamics-based structural analysis | 21618 | ISI | 1404/10/01 | https://doi.org/10.1186/s12920-025-02271-9 | 1 | 2.0 | |
