PubRank

H Onay

Author PubWeight™ 6.99‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Vitiligo pathogenesis: autoimmune disease, genetic defect, excessive reactive oxygen species, calcium imbalance, or what else? Exp Dermatol 2008 1.39
2 Assessment of Toll-like receptor-4 gene polymorphism on pyelonephritis and renal scar. Int J Immunogenet 2012 0.85
3 Lack of association between catalase gene polymorphism (T/C exon 9) and susceptibility to vitiligo in a Turkish population. Genet Mol Res 2011 0.82
4 Low levels of mannose-binding lectin confers protection against tuberculosis in Turkish children. Eur J Clin Microbiol Infect Dis 2008 0.81
5 Duane anomaly, meningomyelocele, dextroposition of heart and localized vertebrocostal alterations with associated anomalies in a girl. Genet Couns 2007 0.80
6 Evidence that the wider social environment moderates the association between familial liability and psychosis spectrum outcome. Psychol Med 2012 0.79
7 Cleidocranial dysplasia with new additional findings. Genet Couns 2004 0.79
8 Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes. Genet Couns 2006 0.78
9 Trends in cytogenetic prenatal diagnosis in a reference hospital in Izmir/Turkey: a comparative study for four years. Genet Couns 2004 0.75
10 Genome-wide copy number variation analysis in idiopathic intellectual disability/multiple congenital anomalies. Genet Couns 2014 0.75
11 Unusual presentation of biliary atresia splenic malformation syndrome with autosomal dominant hypospadias. Genet Couns 2011 0.75
12 Ventricular septal defect in Crouzon Syndrome: case report. Genet Couns 2012 0.75
13 A rare chromosomal rearrangement [inv (2)(p11.q13)] in a 37-year-old normal male and 45,X/46,X,+ mar in his daughter. Genet Couns 2005 0.75
14 Two extra euchromatic bands in the qh region of chromosome 9. Genet Couns 2005 0.75
15 Analysis of the sphingomyelin phosphodiesterase 1 gene (SMPD1) in Turkish Niemann-Pick disease patients: mutation profile and description of a novel mutation. Gene 2013 0.75
16 A twin sibling with Prader-Willi syndrome caused by uniparental disomy conceived after in vitro fertilization. Genet Couns 2014 0.75
17 Detection of trisomy 21 in a fetus during the investigation for Tay-Sachs disease. Genet Couns 2004 0.75
18 Chromosomal rearrangements in children with idiopathic mental retardation using subtelomeric fluorescent in situ hybridization. Genet Couns 2006 0.75
19 Why is lip augmentation with autologous fat injection less effective in the vermilion border? Aesthetic Plast Surg 2001 0.75
20 A cardio-facio-cutaneous syndrome case with tight Achilles tendons. Genet Couns 2012 0.75