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A. Hasanoğlu · SciRah

Researcher profile · Semantic Scholar

A. Hasanoğlu

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A. Hasanoğlu — researcher profile on SciRah

h-index: 24
Works: 126
Citations: 1,674

Most-cited papers

An overview of L‐2‐hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype–phenotype study
M. Steenweg, C. Jakobs, A. Errami, S. V. van Dooren +47 more
2010Human Mutation120 citations Open access
Semantic Scholar
Serum leptin, oxidized low density lipoprotein and plasma asymmetric dimethylarginine levels and their relationship with dyslipidaemia in adolescent girls with polycystic ovary syndrome
F. Demirel, A. Bideci, P. Cinaz, M. Çamurdan +3 more
2007Clinical Endocrinology83 citations
Semantic Scholar
Frequency of vitamin D insufficiency in healthy children between 1 and 16 years of age in Turkey
Alkım Öden Akman, L. Tumer, A. Hasanoğlu, M. Ilhan +1 more
2011Pediatrics International63 citations
Semantic Scholar
Bone Mineral Density in Childhood Obesity
A. Hasanoğlu, A. Bideci, P. Cinaz, L. Tümer +1 more
2000Journal of Pediatric Endocrinology & Metabolism (JPEM)59 citations
Semantic Scholar
Endomysium antibodies in the diagnosis of celiac disease in short‐statured children with no gastrointestinal symptoms
L. Tümer, A. Hasanoğlu, C. Aybay
2001Pediatrics International51 citations
Semantic Scholar
Continuous glucose monitoring in children with glycogen storage disease type I
Ç. Kasapkara, G. Demir, A. Hasanoğlu, L. Tümer
2014European Journal of Clinical Nutrition44 citations
Semantic Scholar
Screening for Fabry disease in patients undergoing dialysis for chronic renal failure in Turkey: identification of new case with novel mutation.
I. Okur, F. Ezgü, G. Biberoğlu, L. Tumer +4 more
2013Gene44 citations
Semantic Scholar
Endothelial activation and inflammation in prepubertal obese Turkish children.
Fatih Süheyl Ezgü, A. Hasanoğlu, L. Tümer, Ferda Ozbay +2 more
2005Metabolism: Clinical and Experimental43 citations
Semantic Scholar
N-carbamylglutamate treatment for acute neonatal hyperammonemia in isovaleric acidemia
Ç. Kasapkara, F. Ezgü, I. Okur, L. Tumer +2 more
2011European Journal of Pediatrics41 citations
Semantic Scholar
Asymmetrical dimethylarginine level in atrial fibrillation
A. Çengel, A. Şahinarslan, G. Biberoğlu, A. Hasanoğlu +3 more
2008Acta Cardiologica38 citations
Semantic Scholar
Adjuvant effect of vitamin A on recurrent lower urinary tract infections
A. Yılmaz, E. Bahat, G. Yilmaz, A. Hasanoğlu +2 more
2007Pediatrics International35 citations
Semantic Scholar
SRD5A3-CDG: a patient with a novel mutation.
Ç. Kasapkara, L. Tümer, F. Ezgü, A. Hasanoğlu +3 more
2012European journal of paediatric neurology33 citations
Semantic Scholar
Vitamin D intoxication and hypercalcaemia in an infant treated with pamidronate infusions
F. Ezgü, N. Buyan, Mehmet Gündüz, L. Tümer +2 more
2004European Journal of Pediatrics31 citations
Semantic Scholar
Quality of life in children treated with restrictive diet for inherited metabolic disease
T. Eminoglu, Ş. Soysal, L. Tumer, I. Okur +1 more
2013Pediatrics International29 citations
Semantic Scholar
Plasma homocysteine and lipoprotein (a) levels as risk factors for atherosclerotic vascular disease in epileptic children taking anticonvulsants
L. Turner, A. Serdaroğlu, A. Hasanoğlu, G. Biberoğlu +1 more
2002Acta paediatrica29 citations
Semantic Scholar
Zinc deficiency in the pediatric age group is common but underevaluated
D. Vurallı, L. Tumer, A. Hasanoğlu
2017World Journal of Pediatrics27 citations
Semantic Scholar
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): case report with a new mutation
Z. Barış, T. Eminoglu, B. Dalgıç, L. Tümer +1 more
2010European Journal of Pediatrics27 citations
Semantic Scholar
Assessment of atherosclerosis risk due to the homocysteine-asymmetric dimethylarginine-nitric oxide cascade in children taking antiepileptic drugs.
H. Emeksiz, A. Serdaroğlu, G. Biberoğlu, O. Gulbahar +4 more
2013Seizure25 citations Open access
Semantic Scholar
Evaluation of oxidant stress in Wilson's disease and non-Wilsonian chronic liver disease in childhood.
B. Dalgıç, Nesrin Sönmez, G. Biberoğlu, A. Hasanoğlu +1 more
2005The Turkish Journal of Gastroenterology25 citations
Semantic Scholar
Severe renal tubulopathy in a newborn due to BCS1L gene mutation: effects of different treatment modalities on the clinical course.
F. Ezgü, Sara Senaca, M. Gunduz, L. Tumer +4 more
2013Gene24 citations
Semantic Scholar
Plasma asymmetric dimethylarginine and L-arginine levels in patients with cardiac syndrome X
Kaan Okyay, A. Çengel, A. Şahinarslan, Y. Tavil +3 more
2007Coronary Artery Disease24 citations
Semantic Scholar
Cholesteryl ester storage disease in a young child presenting as isolated hepatomegaly treated with simvastatin.
B. Dalgıç, S. Sarı, Mehmet Gündüz, F. Ezgü +3 more
2006Turkish Journal of Pediatrics24 citations Open access
Semantic Scholar
Home sleep study characteristics in patients with mucopolysaccharidosis
Ç. Kasapkara, L. Tümer, A. Aslan, A. Hasanoğlu +4 more
2014Sleep and Breathing23 citations
Semantic Scholar
BCS1L gene mutation causing GRACILE syndrome: case report
Ç. Kasapkara, L. Tümer, F. Ezgü, Aynur Küçükçongar +1 more
2014Renal Failure22 citations Open access
Semantic Scholar
Free oxygen radical-induced lipid peroxidation and antioxidant in infants receiving total parenteral nutrition.
A. Hasanoğlu, N. Dalgıç, L. Tümer, Y. Atalay +4 more
2005Prostaglandins, Leukotrienes and Essential Fatty Acids22 citations
Semantic Scholar
The co-existence of Fabry and celiac diseases: a case report
L. Tümer, F. Ezgü, A. Hasanoğlu, B. Dalgıç +3 more
2004Pediatric nephrology (Berlin, West)21 citations
Semantic Scholar
HARDEROPORPHYRIA DUE TO HOMOZYGOSITY FOR COPROPORPHYRINOGEN OXIDASE MISSENSE MUTATION H327R
A. Hasanoğlu, M. Balwani, Ç. Kasapkara, F. Ezgü +8 more
2010Journal of Inherited Metabolic Disease20 citations Open access
Semantic Scholar
Crisponi syndrome: A new case with additional features and new mutation in CRLF1
I. Okur, L. Tumer, L. Crisponi, F. T. Eminoğlu +4 more
2008American Journal of Medical Genetics. Part A19 citations
Semantic Scholar
Clinical Case Report
F. Ezgü, Y. Atalay, A. Hasanoğlu, K. Gücüyener +2 more
2004Nutritional neuroscience19 citations
Semantic Scholar
Oxidized low-density lipoprotein levels and carotid intima-media thickness as markers of early atherosclerosis in prepubertal obese children
I. Okur, L. Tumer, F. Ezgü, E. Yeşilkaya +4 more
2013Journal of Pediatric Endocrinology & Metabolism (JPEM)18 citations
Semantic Scholar
Plasma asymmetric dimethylarginine level and extent of lesion at coronary angiography
A. Şahinarslan, A. Çengel, G. Biberoğlu, A. Hasanoğlu +2 more
2006Coronary Artery Disease18 citations
Semantic Scholar
Pattern of human leukocyte antigens in Turkish children with celiac disease
L. Tümer, B. Altuntaş, A. Hasanoğlu, O. Söylemezoğlu +1 more
2000Pediatrics International18 citations
Semantic Scholar
Asymmetric dimethylarginine and coronary collateral vessel development
S. Kocaman, A. Şahinarslan, G. Biberoğlu, A. Hasanoğlu +3 more
2008Coronary Artery Disease17 citations
Semantic Scholar
Cholesterol screening in school children: is family history reliable to choose the ones to screen?
O. Derinoz, L. Tumer, A. Hasanoğlu, H. Paşaoğlu +2 more
2007Acta paediatrica17 citations
Semantic Scholar
EFFECTS OF ORAL GLUTAMINE SUPPLEMENTATION ON CHILDREN WITH SOLID TUMORS RECEIVING CHEMOTHERAPY
Arzu Okur, F. Ezgü, L. Tümer, G. Cinasal +3 more
2006Pediatric Hematology & Oncology17 citations
Semantic Scholar
Vitamin A status and factors associated in healthy school-age children.
D. Vurallı, L. Tumer, A. Hasanoğlu, G. Biberoğlu +1 more
2014Clinical Nutrition16 citations
Semantic Scholar
3-Methylcrotonyl-CoA Carboxylase Deficiency: Phenotypic Variability in a Family
F. T. Eminoğlu, A. Ozcelik, I. Okur, L. Tumer +4 more
2009Journal of Child Neurology14 citations
Semantic Scholar
Vertebra and femur neck bone mineral density values in healthy Turkish children.
A. Hasanoğlu, L. Tümer, F. Ezgü
2004Turkish Journal of Pediatrics13 citations Open access
Semantic Scholar
Serum levels of vitamins A, C, and E, β-carotene, selenium, and zinc in patients with behçet’s disease
A. Erel, E. Özsoy, G. Biberoğlu, A. Bilgihan +4 more
2003Biological Trace Element Research13 citations
Semantic Scholar
Rapid screening of 12 common mutations in Turkish GSD 1a patients using electronic DNA microarray.
T. Eminoglu, F. Ezgü, A. Hasanoğlu, L. Tumer
2013Gene11 citations
Semantic Scholar
Oxidant and antioxidant status in beta thalassemia major patients Beta talasemi major hastalarinda oksidan ve antioksidan düzeyleri
Filiz Şimşek, Gulyuz Ozturk, S. Kemahlı, D. Erbaş +1 more
200511 citations Open access
Semantic Scholar
Serum dipeptidyl peptidase-IV: a better screening test for early detection of mucopolysaccharidosis?
Í. Kurt, E. Sertoğlu, I. Okur, S. Tapan +5 more
2014Clinica chimica acta; international journal of clinical chemistry10 citations
Semantic Scholar
DGUOK-related mitochondrial DNA depletion syndrome in a child with an early diagnosis of glycogen storage disease.
Ç. Kasapkara, L. Tümer, Aynur Küçükçongar, A. Hasanoğlu +2 more
2013Journal of Pediatric Gastroenterology and Nutrition - JPGN10 citations
Semantic Scholar
The levels of asymmetric dimethylarginine, homocysteine and carotid intima-media thickness in hypercholesterolemic children.
A. Hasanoğlu, I. Okur, A. Oren, G. Biberoğlu +3 more
2011Turkish Journal of Pediatrics10 citations Open access
Semantic Scholar
An extremely rare case: osteosclerotic metaphyseal dysplasia.
Ç. Kasapkara, Aynur Küçükçongar, O. Boyunaga, T. Bedir +3 more
2013Genetic Counseling9 citations
Semantic Scholar
Rapid screening of 10 common mutations in Turkish Gaucher patients using electronic DNA microarray.
F. Ezgü, A. Hasanoğlu, I. Okur, G. Biberoğlu +3 more
2008Blood Cells, Molecules & Diseases9 citations
Semantic Scholar
Secondary Hemophagocytosis in Propionic Acidemia
Ç. Kasapkara, M. Kanğın, Banu Oflaz Ozmen, M. Ozbek +5 more
2015Iranian Journal of Pediatrics8 citations Open access
Semantic Scholar
Analysis of acylcarnitine levels by tandem mass spectrometry in epileptic children receiving valproate and oxcarbazepine
A. Cansu, A. Serdaroğlu, G. Biberoğlu, L. Tumer +3 more
2011Epileptic disorders8 citations
Semantic Scholar
Is oxidative damage in operation in patients with hereditary spastic paraparesis?
K. Gücüyener, F. Pınarlı, D. Erbaş, A. Hasanoğlu +2 more
2010Brain & development (Tokyo. 1979)8 citations
Semantic Scholar
Rapid Molecular Diagnosis of Genetic Diseases by High Resolution Melting Analysis: Fabry and Glycogen Storage 1A Diseases
F. Ezgü, Yoruk Divanoglu, M. Polat, S. Bahceci +2 more
2014Genetic Testing and Molecular Biomarkers7 citations
Semantic Scholar

Frequent co-authors

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F. Ezgü×20
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F. Ezgü — researcher profile on SciRah
L. Tümer×19
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L. Tümer — researcher profile on SciRah
G. Biberoğlu×16
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G. Biberoğlu — researcher profile on SciRah
L. Tumer×15
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L. Tumer — researcher profile on SciRah

×11

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I. Okur — researcher profile on SciRah

Ç. Kasapkara×9

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Ç. Kasapkara — researcher profile on SciRah

F. T. Eminoğlu×4

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F. T. Eminoğlu — researcher profile on SciRah

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A. Çengel — researcher profile on SciRah

A. Şahinarslan×4

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A. Şahinarslan — researcher profile on SciRah

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T. Eminoglu — researcher profile on SciRah

A. Serdaroğlu×4

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A. Serdaroğlu — researcher profile on SciRah

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B. Dalgıç — researcher profile on SciRah