| ردیف |
عنوان |
کد رهگیری |
نمایه |
تاریخ انتشار |
دوره (Volum) |
شماره |
ضریب تاثیر |
کد طرح های مرتبط |
| 1 | association between cholesteryl ester transfer... | 2428 | ISI | | | | 0.879 | |
| 2 | thrombophilic mutations and susceptibility to preeclapmsia in western iran | 2582 | ISI | | | | 1.539 | |
| 3 | concomitant presence of endothelial nitric oxide 894t and angiotensin ll-converting enzyme d alleles are ... | 2616 | ISI | | | | 1.172 | |
| 4 | thymidylate synthase and methionine synthase polymorphisms are not associated with susceptibility to childhood acute ... | 2705 | ISI | | | | 1.875 | 87050 |
| 5 | lack of association between mthfr c677t and a1298c polymorphisms and risk of childhood acute lymphoblastic leukemia in the kurdish population from western iran | 2940 | ISI | | | | 0.879 | 88011 |
| 6 | apolipoprotein e genotypes lipid peroxidation and antioxidant status among mild and severe preeclamptic ... | 3373 | ISI | | | | 1.52 | |
| 7 | interaction of thymidylate synthase polymorphism with MTHFR variants modify the risk of childhood acute lymphoblastic leukemia | 3457 | Chemical Abstract | | | | | 88011 |
| 8 | strong interaction between t allele of endothelial nitric oxide synthase with b1 allele of cholesteryl ester transfer protein taqlb highly elevates the risk of coronary ... | 3458 | pubmed | | | | | 87004 |
| 9 | mthfr c677t and enos g894t variants in preeclamptic women: contribution to lipid peroxidation and oxidative stress | 3600 | ISI | | | | 2.076 | |
| 10 | mmp-9(-1562c:t) polymorphism as a biomarker of susceptibility to severe pre-eclampsia | 3724 | ISI | | | | 2.63 | 90035 |
| 11 | association of factor v leiden mutation with pediatric acute lymphoblastic leukemia in kermanshah province | 3823 | scopus | | | | | 90226 |
| 12 | preeclampsia and angiotensin converting enzyme (ace)i/d and angiotensin ii type-i receptor (atir) aii66c polymorphisms: association with ace i/d polymorphism | 3892 | ISI | | | 14 | 2.439 | 89021 |
| 13 | enos 4a/b polymorphism and its interactionwith enos g894t variants in type 2 diabetes mellitus: modifying the risk of diabetic nephropathy | 3893 | ISI | | | 34 | 1.642 | 91208, 91246 |
| 14 | butyrylcholinesterase (bche) activity is associated with the risk of preeclampsia: influence on lipid and lipoprotein metabolism and oxidative stress | 4479 | ISI | | | 2013 | 1.518 | 92188 |
| 15 | prothrombin g20210a mutation is not a risk factor for pediatric acute lymphoblastic leukemia in western iran | 4622 | ایندکس شده3 | | | 4 | | |
| 16 | endothelial nitric oxide synthase (enos)4a/b and g894t polymorphisms and susceptibility to preeclampsia | 4812 | pubmed | | | 14 | | 91232 |
| 17 | at2r-1332 g: a polymorphism and its interaction with at1r 1166 a:c ace i/d and mmp-9-1562 c:t polymorphisms:risk factors for susceptibility to preeclampsia | 4898 | ISI | | | 538 | 2.196 | 90252 |
| 18 | synergistic effects of angiotensinogen -217 g-a and t704c (m235t) variants on the risk of severe preeclampsia | 5425 | ISI | | | | 2.286 | 90267 |
| 19 | The MMP-2 -735 C Allele is a Risk Factor for Susceptibility to Breast Cancer | 5479 | ISI | | | | 1.5 | 92396 |
| 20 | association of matrix metalloproteinase-7a-181g variants with the risk of multiple sclerosis | 5827 | ISI | | | | 1.132 | 91401 |
| 21 | matrix metalloproteinase -7 a-181g and its interaction with matrix metalloproteinase-9 c-1562t polymorphism in preeclamptic patients: association with malondialdehyde level and severe preeclampsia | 5944 | ISI | | | | 1.279 | 92200 |
| 22 | the serotonin transporter (5-httlpr) but not serotonin receptor (5-ht2c cys23ser) variant is associated with bipolar i disorder in kurdish population from western iran | 6040 | ISI | | | | 2.055 | 91397 |
| 23 | cancer notification at a referral hospital of kermanshah western iran (2006-2009) | 6046 | ISI | | | | 1.5 | 91409 |
| 24 | matrix metalloproteinase-9-1562t allele and its combionation with mmp-2-735 c allele are risk factors for breast cancer | 6175 | ISI | | | | 1.5 | 93082, 93083 |
| 25 | The Association Between Matrix Metalloproteinase-7 A-181G Polymorphism and the Risk of Relapsing-Remitting Multiple Sclerosis in Iranian Kurdish Patients from Kermanshah | 6365 | علمی پژوهشی | 1393/12/01 | | 1 | 0.0 | 95591 |
| 26 | AT1R A1166C variants in patients with type 2 diabetes
mellitus and diabetic nephropathy | 6818 | pubmed | 1394/04/25 | DOI: 10.12860/jnp.2015.14 | 3 | | 94050 |
| 27 | MMP-7 A-181G Polymorphism in Breast Cancer Patients
from Western Iran | 7632 | ISI | 1394/09/11 | DOI: 10.1159/000442231 | 6 | 0.627 | 95692 |
| 28 | Evaluation of beta-casein locus for detection of A1 and A2 alleles frequency
using allele specific PCR in native cattle of Kermanshah, Iran | 7751 | scopus | 1394/09/10 | | 2 | | 92187 |
| 29 | Evaluation of MMP-7 A-181G and MMP-2 C-735T polymorphisms in healthy population from western Iran | 8026 | ISI | 1394/11/15 | doi: 10.14715/cmb/2016.62.2.4 | 2 | 1.234 | 93504 |
| 30 | Functional Promoter Polymorphisms of MMP-2 C-735T and MMP-9 C-1562T and Their Synergism with MMP-7 A-181G in Multiple Sclerosis | 8783 | ISI | 1395/05/11 | 10.1080/08820139.2016.1180303 | 6 | 1.78 | 94318 |
| 31 | The T allele of MTHFR c.C677T and its synergism with G (Val 158) allele of COMT c.G472A polymorphism are associated with the risk of bipolar I disorder | 9200 | ISI | 1395/06/11 | 10.1089/gtmb.2016.0061 | 9 | 1.297 | 93488 |
| 32 | Angiotensin II type 1 receptor A1166C (rs5186) gene polymorphism increased risk and severity of psoriasis, contribution to oxidative stress, antioxidant statues, lipid peroxidation and correlation with vascular
adhesion protein 1, preliminary
report | 9601 | ISI | 1395/05/11 | | 8 | 3.029 | 95180 |
| 33 | Functional promoter polymorphism of matrix metalloproteinase (MMP)-3 5A/6A and its interaction with MMP-7 A-181G polymorphism in multiple sclerosis | 9632 | scopus | 1395/09/26 | - | 2 | | 93522 |
| 34 | Brain-Derived Neurotrophic Factor Val66Met Polymorphism and Its Synergism with L/S Polymorphism in the Promoter Region of Serotonin Transporter in Bipolar I Disorder Patients in Western Iran | 9830 | pubmed | 1395/10/11 | doi: 10.17795/ijpbs-5173 | 4 | | 94275 |
| 35 | ACE I/D and MMP-7 A-181G variants and risk of end stage
renal disease | 10442 | ISI | 1395/12/30 | PMID: 28447048 | 1 | | 96032 |
| 36 | MMP-8 C-799T and MMP-8 C+17G polymorphisms in mild and severe preeclampsia: Association between MMP-8 C-799T with susceptibility to severe preeclampsia | 10749 | ISI | 1396/12/10 | | 2 | 1.162 | 980970 |
| 37 | PPAR gamma Pro12Ala and C161T polymorphisms in patients with acne vulgaris: Contribution to lipid and lipoprotein profile | 11153 | ISI | 1396/12/10 | | 1 | 1.364 | |
| 38 | Matrix metalloproteinase-2 C-735T and its interaction with matrix metalloproteinase-7 A-181G polymorphism are associated with the risk of preeclampsia: influence on total antioxidant capacity and blood pressure | 11693 | ISI | 1397/01/12 | | 3 | 0.629 | 97603 |
| 39 | Association of the CYP17 MSP AI (T-34C) and CYP19 codon 39 (Trp/Arg) polymorphisms with susceptibility to acne vulgaris | 11702 | ISI | 1396/12/10 | | 2 | 1.589 | 96074 |
| 40 | The Association of PPAR gamma Pro12Ala and C161T Polymorphisms with Polycystic Ovary Syndrome and Their Influence on Lipid and Lipoprotein Profiles | 11914 | ISI | 1397/06/10 | | 2 | 0.471 | |
| 41 | The Prevalence of Hemoglobinopathies in Reference Laboratory of Kermanshah, Western Iran | 13293 | ISI | 1397/11/10 | | 2 | 1.053 | |
| 42 | NOTCH1, SF3B1, MDM2 and MYD88 mutations in patients with chronic lymphocytic leukemia | 13416 | ISI | 1398/01/12 | | 4 | 1.664 | |
| 43 | The effect of VDR gene polymorphisms and vitamin D level on blood pressure, risk of preeclampsia, gestational age, and body mass index | 13421 | ISI | 1398/01/12 | | | 2.959 | 96500 |
| 44 | MTHFR C677T Polymorphism Is Associated with the Risk of Breast
Cancer Among Kurdish Population from Western Iran | 13582 | ISI | 1397/12/10 | | 3 | | |
| 45 | Association between CYP19A | 14426 | ISI | 1398/03/11 | | 2 | | 96074 |
| 46 | The Insulin-like Growth Factor-1 (G>A) and 5,10-methylenetetrahydrofolate Reductase (C677T) Gene Variants and the Serum Levels of Insulin-like Growth Factor-1, Insulin, and Homeostasis Model Assessment in Patients with Acne Vulgaris | 14913 | pubmed | 1398/10/11 | | 1 | | 94280 |
| 47 | Gene variants and haplotypes of Vitamin D biosynthesis, transport, and function in preeclampsia | 16298 | ISI | 1399/11/10 | | 1 | 1.787 | |
| 48 | Variants of Genes Involved in Metabolism of Folate Among Patients with Breast
Cancer: Association of TYMS3R Allele with Susceptibility to Breast Cancer and
Metastasis | 16416 | pubmed | 1399/12/01 | | 1 | | 94275 |
| 49 | p53 p.Pro72Arg (rs1042522) and Mouse Double Minute 2 (MDM2) Single-Nucleotide Polymorphism (SNP) 309 Variants and Their Interaction in chronic Lymphocytic
Leukemia(CLL): A Survey in CLL Patients from
Western Iran | 16870 | pubmed | 1400/04/15 | | 15 | | 96032 |
| 50 | Oxidative stress parameters and keap 1 variants in T2DM:
Association with T2DM, diabetic neuropathy, diabetic
retinopathy, and obesity | 17506 | ISI | 1400/10/26 | https://doi.org/10.1002/jcla.24163 | 1 | 2.352 | 3006694 |
