Publications by authors named "Hulya Azakli"

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Is immune effector cell-associated enterocolitis a CAR T-cell lymphoproliferative disorder?
Kayra Somay, Hulya Azakli, Joeffrey J Chahine, Thomas M Loughney, Metin Ozdemirli

Blood Cancer J· July 2025

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Expanding the spectrum of syndromic PPP2R3C-related XY gonadal dysgenesis to XX gonadal dysgenesis.
Umut Altunoglu, Esra Börklü, Anju Shukla, Nathalie Escande-Beillard, Susanne Ledig

Clin Genet· February 2022

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MEFV mutation frequencies in a Turkish cohort with low prevalence of familial Mediterranean fever.
Necati Çakır, Hülya Azaklı, Duran Üstek, Ömer Uysal, Eren Gözke

Turk J Med Sci· August 2021

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Terminal osseous dysplasia with pigmentary defects (TODPD) in a Turkish girl with new skin findings.
Hülya Azakli, Ayse Deniz Akkaya, Murat Serhat Aygün, Cüyan Demirkesen, Serpil Eraslan

Am J Med Genet A· January 2019

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Origin and spread of human mitochondrial DNA haplogroup U7.
Hovhannes Sahakyan, Baharak Hooshiar Kashani, Rakesh Tamang, Alena Kushniarevich, Amirtharaj Francis, Hülya Azakli

Sci Rep· April 2017

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Mitochondrial DNA profiling via genomic analysis in mesial temporal lobe epilepsy patients with hippocampal sclerosis.
Candan Gurses, Hulya Azakli, Ahmet Alptekin, Aris Cakiris, Neslihan Abaci

Gene· April 2014

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Whole mitochondrial DNA variations in hippocampal surgical specimens and blood samples with high-throughput sequencing: a case of mesial temporal lobe epilepsy with hippocampal sclerosis.
Hulya Azakli, Candan Gurses, Muzaffer Arikan, Aydın Aydoseli, Yavuz Aras

Gene· October 2013

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The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still's disease.
Fulya Cosan, Zeliha Emrence, Gokhan Erbag, Hulya Azakli, Baris Yilmazer

Rheumatol Int· July 2013

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A genome-wide analysis of lentivector integration sites using targeted sequence capture and next generation sequencing technology.
Duran Ustek, Sema Sirma, Ergun Gumus, Muzaffer Arikan, Aris Cakiris, Hulya Azakli

Infect Genet Evol· October 2012

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Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.
Elaine F Remmers, Fulya Cosan, Yohei Kirino, Michael J Ombrello, Neslihan Abaci, Hulya Azakli

Nat Genet· August 2010

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