PubRank

Zoran Gucev

Author PubWeight™ 15.12‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA. Nat Genet 2012 1.74
2 Copy-number disorders are a common cause of congenital kidney malformations. Am J Hum Genet 2012 1.63
3 Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum. Am J Med Genet A 2014 1.20
4 Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3. J Clin Endocrinol Metab 2014 1.05
5 Atypical presentation of distal renal tubular acidosis in two siblings. Pediatr Nephrol 2008 1.04
6 The impact of CFNS-causing EFNB1 mutations on ephrin-B1 function. BMC Med Genet 2010 0.93
7 Long-acting pegylated human GH in children with GH deficiency: a single-dose, dose-escalation trial investigating safety, tolerability, pharmacokinetics and pharmacodynamics. Eur J Endocrinol 2011 0.93
8 Clinical and functional characterization of URAT1 variants. PLoS One 2011 0.92
9 Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction. Nephrol Dial Transplant 2009 0.90
10 Clinical and laboratory features of Macedonian children with OCRL mutations. Pediatr Nephrol 2011 0.78
11 Game-based peripheral biofeedback for stress assessment in children. Pediatr Int 2009 0.78
12 Obesity in childhood and adolescence, genetic factors. Prilozi 2013 0.78
13 Aseptic necrosis of both tali in a child with steroid-dependent nephrotic syndrome. Nephrol Dial Transplant 2006 0.78
14 Nephrotic syndrome occurring during tiopronin treatment for cystinuria. Eur J Pediatr 2010 0.77
15 Chronic kidney disease - pediatric risk factors. Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2016 0.77
16 Autoimmune thyroiditis and diabetes mellitus type 1 after long-term gonadotropin-releasing hormone agonist treatment for central precocious puberty: evolution or coincidence? J Pediatr Endocrinol Metab 2010 0.77
17 QEEG characteristics and spectrum weighted frequency for children diagnosed as autistic spectrum disorder. Nonlinear Biomed Phys 2010 0.76
18 Weight, height and puberty in a cohort of Macedonian girls. Med Arh 2009 0.76
19 Nephrolithiasis and Nephrocalcinosis in Children - Metabolic and Genetic Factors. Pediatr Endocrinol Rev 2015 0.75
20 Compound Galactosylceramidase Gene (GALC) Heterozygosity in a Boy with Infantile Krabbe Disease (KD). Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2015 0.75
21 Steroid Resistant Nephrotic Syndrome-Genetic Consideration. Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2015 0.75
22 Failure to thrive and nephrolithiasis in a boy with congenital cyanotic heart anomaly. Pediatr Nephrol 2011 0.75
23 4th Rare Disease South Eastern Europe (See) Meeting Skopje, Macedonia (November 14th, 2015). Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2015 0.75
24 Some Psychological Aspects of T1DM in Children and Adolescents. Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2015 0.75
25 Tricho-rhino-phalangeal syndrome in a 13-year-old girl with chronic renal failure and severe growth retardation. Ren Fail 2014 0.75
26 LHX4 Gene Alterations: Patient Report and Review of the Literature. Pediatr Endocrinol Rev 2016 0.75
27 Autoimmune thyroiditis in a child with steroid-dependent nephrotic syndrome. Eur J Pediatr 2008 0.75
28 Where are we now in the investigation of rare diseases in the Republic of Macedonia? Prilozi 2014 0.75
29 Recurrent urinary tract infections in an infant with antenatal Bartter syndrome. World J Pediatr 2010 0.75
30 New insights into septo-optic dysplasia. Prilozi 2014 0.75
31 Kidney diseases in children - early diagnosis and prevention. Pril (Makedon Akad Nauk Umet Odd Med Nauki) 2016 0.75