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F. Ozaltin · SciRah

Researcher profile · Semantic Scholar

F. Ozaltin

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F. Ozaltin — researcher profile on SciRah

h-index: 44
Works: 220
Citations: 7,749

Most-cited papers

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
Jillian K. Warejko, Wei-Zhen Tan, Ankana Daga, D. Schapiro +57 more
2018American Society of Nephrology. Clinical Journal209 citations Open access
Semantic Scholar
Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children.
A. Trautmann, S. Schnaidt, B. Lipska-Ziętkiewicz, M. Bodria +38 more
2017Journal of the American Society of Nephrology202 citations Open access
Semantic Scholar
Mutations in nuclear pore genes NUP93, NUP205, and XPO5 cause steroid resistant nephrotic syndrome
Daniela A. Braun, C. E. Sadowski, Stefan Kohl, S. Lovric +23 more
2016Nature Genetics195 citations Open access
Semantic Scholar
Mutations in the evolutionarily highly conserved KEOPS complex genes cause nephrotic syndrome with microcephaly
Daniela A. Braun, Jia Rao, G. Mollet, D. Schapiro +98 more
2017Nature Genetics191 citations Open access
Semantic Scholar
Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group
O. Boyer, F. Schaefer, D. Haffner, D. Bockenhauer +8 more
2021Nature Reviews Nephrology84 citations Open access
Semantic Scholar
Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment
Mustafa Atmaca, B. Gülhan, E. Korkmaz, Mihriban Inozu +9 more
2017Pediatric nephrology (Berlin, West)69 citations
Semantic Scholar
Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD.
R. Shroff, H. Aitkenhead, N. Costa, A. Trivelli +11 more
2016Journal of the American Society of Nephrology66 citations Open access
Semantic Scholar
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency.
S. Drovandi, B. Lipska-Ziętkiewicz, F. Ozaltin, F. Emma +42 more
2022Kidney International62 citations Open access
Semantic Scholar
An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis.
F. Emma, W. Hoff, K. Hohenfellner, R. Topaloğlu +22 more
2021Kidney International60 citations Open access
Semantic Scholar
Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children.
K. Ažukaitis, W. Ju, M. Kirchner, V. Nair +112 more
2019Kidney International57 citations Open access
Semantic Scholar
Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients
N. Beşbaş, B. Gülhan, O. Soylemezoglu, Z. Ozcakar +3 more
2017BMC Nephrology48 citations Open access
Semantic Scholar
Extra-Renal manifestations of atypical hemolytic uremic syndrome in children
K. Fidan, Nilüfer Göknar, B. Gülhan, E. Melek +7 more
2018Pediatric nephrology (Berlin, West)46 citations
Semantic Scholar
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.
S. Drovandi, B. Lipska-Ziętkiewicz, F. Ozaltin, F. Emma +40 more
2022Kidney International43 citations Open access
Semantic Scholar
Anti-nephrin autoantibodies in steroid-resistant nephrotic syndrome may inform treatment strategy.
Felicitas E. Hengel, Silke Dehde, A. Yilmaz, A. Bayazıt +9 more
2025Kidney International37 citations Open access
Semantic Scholar
Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia
B. Lipska-Ziętkiewicz, J. Gellermann, O. Boyer, O. Gribouval +20 more
2017PLoS ONE37 citations Open access
Semantic Scholar
Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet–ESPN inherited glomerulopathy working group
B. Lipska-Ziętkiewicz, F. Ozaltin, T. Hölttä, D. Bockenhauer +7 more
2020European Journal of Human Genetics34 citations Open access
Semantic Scholar
LONG TERM RENAL SURVIVAL OF PEDIATRIC PATIENTS WITH LUPUS NEPHRITIS.
S. Demir, B. Gülhan, Seza Özen, Kübra Çeleğen +7 more
2021Nephrology, Dialysis and Transplantation32 citations
Semantic Scholar
Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation.
F. K. Eroğlu, F. Ozaltin, Nazlı Gönç, H. Nalcacioglu +9 more
2018Pediatric Neurology27 citations
Semantic Scholar
Loss of diacylglycerol kinase epsilon in mice causes endothelial distress and impairs glomerular Cox-2 and PGE2 production.
Ji-Li Zhu, M. Chaki, Dongmei Lu, Chongyu Ren +17 more
2016AJP - Renal Physiology23 citations Open access
Semantic Scholar
The Clinical and Mutational Spectrum of Turkish Patients with Cystinosis.
R. Topaloğlu, B. Gülhan, Mihriban İnözü, N. Canpolat +14 more
2017American Society of Nephrology. Clinical Journal22 citations Open access
Semantic Scholar
An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues
Aytekin Akyol, Güneş Güner, Havva Solak Özşeker, A. Işık +7 more
2018Laboratory Investigation20 citations Open access
Semantic Scholar
Mitochondria-Targeted CoQ10 Loaded PLGA-b-PEG-TPP Nanoparticles: Their Effects on Mitochondrial Functions of COQ8B-/- HK-2 cells.
Hamide Sena Ozbay, S. Yabanoğlu-Ciftci, İ. Baysal, Merve Gultekinoglu +5 more
2022European journal of pharmaceutics and biopharmaceutics15 citations
Semantic Scholar
Cystinosis beyond kidneys: gastrointestinal system and muscle involvement
R. Topaloğlu, Ayse Gultekingil, B. Gülhan, F. Ozaltin +6 more
2020BMC Gastroenterology15 citations Open access
Semantic Scholar
Rituximab for Children With Difficult-to-Treat Nephrotic Syndrome: Its Effects on Disease Progression and Growth
R. Topaloğlu, B. Gülhan, Kübra Çeleğen, Mihriban İnözü +3 more
2019Frontiers in Pediatrics15 citations Open access
Semantic Scholar
Predictors of kidney complications and analysis of hypertension in children with allogeneic hematopoietic stem cell transplantation
A. Gurbanov, B. Gülhan, B. Kuşkonmaz, F. Okur +4 more
2022Pediatric nephrology (Berlin, West)13 citations
Semantic Scholar
Atypical Hemolytic Uremic Syndrome in Children Aged <2 Years
N. Çakar, Z. Özçakar, F. Ozaltin, M. Koyun +8 more
2018Nephron13 citations
Semantic Scholar
A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome
N. Canpolat, Ding-Xiao Liu, E. Atayar, S. Saygılı +16 more
2021Clinical Genetics12 citations Open access
Semantic Scholar
COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome
G. Ozdemir, B. Gülhan, E. Atayar, S. Saygılı +13 more
2020Pediatric nephrology (Berlin, West)12 citations
Semantic Scholar
CD80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood
F. K. Eroğlu, D. Orhan, Mihriban İnözü, A. Duzova +3 more
2019Pediatrics International12 citations
Semantic Scholar
Epidermolysis Bullosa with Pyloric Atresia and Aplasia Cutis in a Newborn Due to Homozygous Mutation in ITGB4
Gozdem Kaykı, D. Bozkaya, F. Ozaltin, D. Orhan +3 more
2017Fetal and Pediatric Pathology12 citations
Semantic Scholar
A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature
Tugba Tastemel Ozturk, N. Canpolat, S. Saygılı, U. Bayrakçı +3 more
2022Pediatric nephrology (Berlin, West)11 citations
Semantic Scholar
Eculizumab treatment and discontinuation in pediatric patients with atypical hemolytic uremic syndrome: a multicentric retrospective study
E. Baskın, K. Fidan, B. Gülhan, K. Gulleroglu +6 more
2022JN. Journal of Nephrology (Milano. 1992)10 citations
Semantic Scholar
COVID‐19 associated thrombotic microangiopathy
Esra Karabağ Yılmaz, M. N. Cebi, I. Karahan, S. Saygılı +7 more
2023Nephrology9 citations
Semantic Scholar
Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression
A. Trautmann, S. Seide, B. Lipska-Ziętkiewicz, F. Ozaltin +24 more
2022Pediatric nephrology (Berlin, West)8 citations Open access
Semantic Scholar
Childhood-onset Takayasu arteritis and immunodeficiency: case-based review
S. Şener, Ozge Basaran, E. D. Batu, E. Atalay +9 more
2022Clinical Rheumatology8 citations
Semantic Scholar
Mitigation of portal fibrosis and cholestatic liver disease in ANKS6-deficient livers by macrophage depletion
Merlin Airik, B. McCourt, Tugba Tastemel Ozturk, Amy B. Huynh +10 more
2022The FASEB Journal8 citations Open access
Semantic Scholar
A homozygous HOXA11 variation as a potential novel cause of autosomal recessive CAKUT.
S. Saygılı, E. Atayar, N. Canpolat, M. Eliçevik +4 more
2020Clinical Genetics8 citations Open access
Semantic Scholar
Surgical management of renovascular hypertension in children and young adults: a 13-year experience.
O. Peker, F. T. Aki, U. Kumbasar, M. Guvener +7 more
2019Interactive Cardiovascular and Thoracic Surgery8 citations Open access
Semantic Scholar
Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers
S. Saygılı, N. Canpolat, L. Sever, S. Çalışkan +2 more
2018Pediatric nephrology (Berlin, West)7 citations
Semantic Scholar
Efficacy of Calcineurin Inhibition in Children With Steroid-Resistant Nephrotic Syndrome
A. Trautmann, J. Hofstetter, B. Lipska-Ziętkiewicz, A. Tsygin +25 more
2025Kidney International Reports6 citations Open access
Semantic Scholar
Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence
Jessica Kachmar, O. Boyer, B. Lipska-Ziętkiewicz, V. Moriniére +21 more
2024Kidney International Reports6 citations Open access
Semantic Scholar
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
K. Riedhammer, Thanh-Minh T. Nguyen, C. Koşukcu, J. Calzada-Wack +56 more
2023Kidney International6 citations Open access
Semantic Scholar
Renal Biopsy Prognostic Findings in Children With Atypical Hemolytic Uremic Syndrome
Selçuk Yüksel, İpek Işık Gönül, N. Canpolat, I. Gökçe +4 more
2020Pediatric and Developmental Pathology6 citations
Semantic Scholar
Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Questions
S. Saygılı, N. Canpolat, L. Sever, Salim Çalişkan +2 more
2018Pediatric nephrology (Berlin, West)6 citations
Semantic Scholar
Acute kidney injury in children with moderate-severe COVID-19 and multisystem inflammatory syndrome in children: a referral center experience
Tugba Tastemel Ozturk, A. Düzova, P. Oygar, Demet Baltu +12 more
2023Pediatric nephrology (Berlin, West)5 citations
Semantic Scholar
AGTR1-related Renal Tubular Dysgeneses May Not Be Fatal
E. Demirgan, S. Saygılı, N. Canpolat, L. Sever +4 more
2020Kidney International Reports5 citations Open access
Semantic Scholar
Nephropathic Cystinosis Mimicking Bartter Syndrome: a Novel Mutation.
Funda Baştuğ, H. Nalcacioglu, F. Ozaltin, E. Korkmaz +1 more
2018Iranian Journal of Kidney Diseases5 citations
Semantic Scholar
Calcineurin inhibitor‐related hyperkalemia is caused by hyporeninemic hypoaldosteronism and fludrocortisone is an effective treatment: Report of a case series and review of the literature
Yagmur Unsal, Demet Baltu, B. Gülhan, F. Okur +5 more
2024Pediatric Transplantation4 citations
Semantic Scholar
Hearing Loss Related to Gene Mutations in Distal Renal Tubular Acidosis
Ezgi Ay, Emre Gurses, F. Aslan, B. Gülhan +7 more
2023Audiology and Neurotology4 citations
Semantic Scholar
The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study
Ozum Tutal, B. Gülhan, E. Atayar, S. Yuksel +10 more
2023Nephron4 citations
Semantic Scholar

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R. Topaloğlu×20
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R. Topaloğlu — researcher profile on SciRah
B. Gülhan×18
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N. Canpolat×11
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S. Saygılı×10
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B. Lipska-Ziętkiewicz

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O. Soylemezoglu×8

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A. Trautmann×7

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E. Baskın — researcher profile on SciRah