PubRank

Afig Berdeli

Author PubWeight™ 58.40‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J Clin Invest 2011 2.21
2 Insulin-like growth factor attenuates apoptosis and mucosal damage in hypoxia/reoxygenation-induced intestinal injury. Biol Neonate 2004 1.59
3 Alterations of blood pressure in type 1 diabetic children and adolescents. Pediatr Nephrol 2006 1.56
4 Familial Mediterranean fever gene mutation frequencies and genotype-phenotype correlations in the Aegean region of Turkey. Rheumatol Int 2010 1.51
5 Positive association of macrophage migration inhibitory factor gene-173G/C polymorphism with biliary atresia. J Pediatr Gastroenterol Nutr 2006 1.13
6 G protein beta3 subunit gene polymorphism in Turkish hypertensives. Anadolu Kardiyol Derg 2008 0.98
7 TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome. Nephrol Dial Transplant 2011 0.96
8 Polymorphisms of the ICAM-1 gene are associated with biliary atresia. Dig Dis Sci 2008 0.92
9 The G894T polymorphism on endothelial nitric oxide synthase gene is associated with premature coronary artery disease in a Turkish population. Thromb Res 2005 0.92
10 Gingival crevicular fluid transforming growth factor-beta1 in several forms of periodontal disease. Arch Oral Biol 2006 0.91
11 Interleukin-10 (-1082G/A) gene polymorphism in patients with type 2 diabetes with and without nephropathy. Genet Test Mol Biomarkers 2011 0.89
12 Gene polymorphisms of matrix metalloproteinase-2, -9 and -12 in periodontal health and severe chronic periodontitis. Arch Oral Biol 2007 0.89
13 Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome. Turk J Haematol 2015 0.88
14 No association of interleukin-6 gene polymorphism (-174 G/C) with premature coronary artery disease in a Turkish cohort. Coron Artery Dis 2007 0.85
15 Gingival crevicular fluid EMAP-II, MIP-1alpha and MIP-1beta levels of patients with periodontal disease. J Clin Periodontol 2005 0.84
16 Macrophage migration inhibitory factor expression and MIF gene -173 G/C polymorphism in nonalcoholic fatty liver disease. Eur J Gastroenterol Hepatol 2010 0.84
17 Association between the ACE I/D gene polymorphism and physical performance in a homogeneous non-elite cohort. Can J Appl Physiol 2005 0.84
18 Toll-like receptor 2 and 4 gene polymorphisms in generalized aggressive periodontitis. J Periodontol 2007 0.84
19 4G/5G polymorphism of PAI-1 gene and Alu-repeat I/D polymorphism of TPA gene in Turkish patients with polycystic ovary syndrome. J Assist Reprod Genet 2007 0.83
20 Association of interleukin-6 -174 G>C promoter polymorphism with increased risk of type 2 diabetes mellitus patients with diabetic nephropathy in Turkey. Genet Test Mol Biomarkers 2013 0.83
21 ACE gene insertion/deletion polymorphism in childhood idiopathic nephrotic syndrome. Pediatr Nephrol 2005 0.83
22 Allelic frequency of the MCP-1 promoter -2518 polymorphism in the Turkish population and in Turkish patients with juvenile rheumatoid arthritis. Clin Rheumatol 2006 0.82
23 Arg753Gln polymorphism of the human toll-like receptor-2 gene in children with recurrent febrile infections. Biochem Genet 2007 0.82
24 Arg753Gln TLR-2 polymorphism in familial mediterranean fever: linking the environment to the phenotype in a monogenic inflammatory disease. J Rheumatol 2006 0.82
25 A case of hypomagnesemia with secondary hypocalcemia caused by Trpm6 gene mutation. Indian J Pediatr 2008 0.81
26 The Fc gammaRIIa polymorphism in Turkish children with asthma bronchial and allergic rhinitis. Clin Biochem 2007 0.81
27 Is ACE gene polymorphism a risk factor for renal scarring with low-grade reflux? Pediatr Nephrol 2004 0.81
28 Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency. Ital J Pediatr 2012 0.81
29 Effect of MMP-1 promoter polymorphisms on GCF MMP-1 levels and outcome of periodontal therapy in patients with severe chronic periodontitis. J Clin Periodontol 2008 0.81
30 TGF-beta1 gene polymorphisms in periodontal diseases. Clin Biochem 2006 0.81
31 Fas, Fas Ligand, and vitamin D Receptor FokI gene polymorphisms in patients with type 1 diabetes mellitus in the Aegean region of Turkey. Genet Test Mol Biomarkers 2012 0.80
32 [The relationship between paraoxanase gene Leu-Met (55) and Gln-Arg (192) polymorphisms and coronary artery disease]. Turk Kardiyol Dern Ars 2009 0.80
33 The progesterone receptor PROGINS polymorphism is not related to oxidative stress factors in women with polycystic ovary syndrome. Cardiovasc Diabetol 2007 0.80
34 Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency. J Clin Immunol 2012 0.80
35 Renin-angiotensin system gene polymorphisms and premature coronary heart disease. J Renin Angiotensin Aldosterone Syst 2005 0.79
36 Mcp-1, eNOS, tPA and PAI-1 gene polymorphism and correlation of genotypes and phenotypes in hepatopulmonary syndrome. Dig Dis Sci 2007 0.79
37 Variability in the age at diagnosis of diabetes in two unrelated patients with a homozygous glucokinase gene mutation. J Pediatr Endocrinol Metab 2012 0.79
38 Tissue plasminogen activator and plasminogen activator inhibitor-1 gene polymorphisms in patients with chronic periodontitis. J Periodontol 2007 0.79
39 Matrix metalloproteinase-2, -9, and -12 gene polymorphisms in generalized aggressive periodontitis. J Periodontol 2007 0.79
40 Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin. Am J Kidney Dis 2004 0.79
41 Lack of association between macrophage migration inhibitory factor gene promoter (-173 G/C) polymorphism and childhood Henoch-Schönlein purpura in Turkish patients. Cytokine 2013 0.79
42 A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree. J Pediatr Endocrinol Metab 2013 0.79
43 Hypertension and ace gene insertion/deletion polymorphism in pediatric renal transplant patients. Pediatr Transplant 2005 0.78
44 Determination of the effects of alcohol dehydrogenase (ADH) 1B and ADH1C polymorphisms on alcohol dependence in Turkey. Sci Justice 2011 0.78
45 Renal scarring and osteopontin gene C/T polymorphism in children with primary vesicoureteral reflux. Indian Pediatr 2011 0.78
46 Gene polymorphisms of tissue plasminogen activator and plasminogen activator inhibitor-1 in Turkish patients with generalized aggressive periodontitis. J Clin Periodontol 2007 0.78
47 LY96, UPKIB mutations and TLR4, CD14, MBL polymorphisms in children with urinary tract infection. Indian J Pediatr 2011 0.78
48 Matrix metalloproteinase (MMP)-8 and tissue inhibitor of MMP-1 (TIMP-1) gene polymorphisms in generalized aggressive periodontitis: gingival crevicular fluid MMP-8 and TIMP-1 levels and outcome of periodontal therapy. J Periodontol 2013 0.78
49 FcgammaRIIIa-V/F 158 polymorphism in Turkish children with asthma bronchiale and allergic rhinitis. Pediatr Allergy Immunol 2008 0.77
50 Effects of genetic polymorphisms of the renin-angiotensin system in children with nephrotic syndrome. J Renin Angiotensin Aldosterone Syst 2005 0.77
51 Renin-angiotensin gene polymorphisms in relation to severe chronic periodontitis. J Clin Periodontol 2009 0.77
52 Val2Ala mutation in the Atp6v0a4 gene causes early-onset sensorineural hearing loss in children with recessive distal renal tubular acidosis: a case report. Ren Fail 2014 0.77
53 MMP-13 promoter polymorphisms in patients with chronic periodontitis: effects on GCF MMP-13 levels and outcome of periodontal therapy. J Clin Periodontol 2009 0.77
54 [Familial Mediterranean fever with pulmonary manifestations alone; early diagnosis with genetic analysis]. Tuberk Toraks 2012 0.77
55 The place of androgen receptor gene mutation analysis in the molecular diagnosis of prostate cancer and genotype-phenotype relationship. Turk J Med Sci 2014 0.77
56 Interleukin 8 gene 2767 A/G polymorphism is associated with increased risk of nephritis in children with Henoch-Schönlein purpura. Rheumatol Int 2011 0.76
57 SPP1 gene polymorphisms associated with nephrolithiasis in Turkish pediatric patients. Urol J 2012 0.76
58 Effect of monocyte chemoattractant protein-1 (MCP-1) gene polymorphism in Turkish patients with premature coronary artery disease. Scand J Clin Lab Invest 2008 0.76
59 Association between mannose-binding lectin levels and gene polymorphisms in chronic periodontitis and response to treatment. Arch Oral Biol 2010 0.76
60 A rare cause of chronic renal failure in a girl with elevated serum uric acid level. Pediatr Nephrol 2009 0.76
61 Association of platelet-activating factor acetylhydrolase gene polymorphism with premature coronary artery disease in Turkish patients. Anadolu Kardiyol Derg 2006 0.76
62 Angiotensin-converting enzyme (ACE), angiotensinogen (AGT), and angiotensin II type 1 receptor (AT1R) gene polymorphisms in generalized aggressive periodontitis. Arch Oral Biol 2009 0.76
63 A novel p.S34N mutation of CAMP gene in patients with periodontal disease. Arch Oral Biol 2011 0.76
64 X-linked agammaglobulinemia presenting with secondary hemophagocytic syndrome: a case report. Case Rep Med 2013 0.75
65 Association of FAS -670A/G and FASL -843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients. Iran J Pediatr 2010 0.75
66 Complement-4 deficiency in a child with systemic lupus erythematosus presenting with standard treatment-resistant severe skin lesion. ISRN Rheumatol 2011 0.75
67 Escherichia coli brain abscess in a twin pair associated with TLR4 gene mutation. Pediatr Int 2013 0.75
68 NOD2/CARD15 gene mutations in patients with gouty arthritis. Bosn J Basic Med Sci 2016 0.75
69 X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis. Case Rep Med 2011 0.75
70 Common SPINK-1 mutations do not predispose to the development of non-alcoholic fatty liver disease. Ann Hepatol 2009 0.75
71 A molecular case report of autosomal dominant retinitis pigmentosa: RP1/RHO sequence variants in a Turkish family. OMICS 2012 0.75
72 Familial Mediterranean fever in children from the Aegean region of Turkey: gene mutation frequencies and phenotype-genotype correlation. Turk J Med Sci 2015 0.75
73 The influence of α-adducin gene polymorphism on response of blood pressure to exercise in patients with hypertension. Anadolu Kardiyol Derg 2010 0.75
74 Does NPHS1 polymorphism modulate P118l mutation in NPHS2? Saudi J Kidney Dis Transpl 2013 0.75
75 The predictive value of urinary UPIb mRNA levels in VUR and recurrent urinary tract infections. Clin Nephrol 2014 0.75
76 A puzzling case of phospho-soda-induced hypocalcemia in a patient with multiple endocrine neoplasia type 1-associated primary hyperparathyroidism. Intern Med 2012 0.75
77 Effects of bodybuilding and protein supplements in saliva, gingival crevicular fluid, and serum. J Oral Sci 2017 0.75
78 Fcγ receptor polymorphisms in patients with transient hypogammaglobulinemia of infancy presenting with mild and severe infections. Asian Pac J Allergy Immunol 2015 0.75
79 A newborn with pertussis accompanying nephrotic syndrome. Turk J Pediatr 2015 0.75
80 The relationship of the Fas 670 A/G gene polymorphism with cardiovascular risk factors in polycystic ovary syndrome (PCOS) patients. Gynecol Endocrinol 2010 0.75
81 Gene polymorphism of complement factor H in a Turkish patient with membranoproliferative glomerulonephritis type II. Iran J Kidney Dis 2012 0.75
82 Podocin mutations in a patient with congenital nephrotic syndrome and cardiac malformation. Pediatr Int 2008 0.75
83 Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation. Pediatr Int 2015 0.75
84 Association between RAS gene polymorphisms (ACE I/D, AGT M235T) and Henoch-Schönlein purpura in a Turkish population. Dis Markers 2013 0.75
85 Relationship between ace genotype and short duration aerobic performance development. Eur J Appl Physiol 2006 0.75