A. Arman

发表

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

A. Caglayan, O. Ozdemır, S. Artan, 2022, Functional & Integrative Genomics.

Enostosis in a patient with KBG syndrome caused by a novel missense ANKRD11 variant.

A. Arman, B. Geckinli, Ceren Alavanda, 2022, Clinical dysmorphology.

Biallelic Mutations in DNAJB11are Associated with Prenatal Polycystic Kidney Disease in a Turkish Family

E. Ateş, P. Ata, A. Arman, 2021, Molecular Syndromology.

Association between sporadic Parkinson disease and interleukin-1 beta -511 gene polymorphisms in the Turkish population.

E. List, A. Arman, N. Işık, 2010, European cytokine network.

Interleukin 1 Activates STAT3/Nuclear Factor-κB Cross-talk via a Unique TRAF6- and p65-dependent Mechanism*

P. Auron, Hai-bing Peng, Y. Yoshida, 2004, Journal of Biological Chemistry.

Lack of association between IL-6 gene polymorphisms and rheumatoid arthritis in Turkish population

A. Çoker, N. Inanç, H. Direskeneli, 2012, Rheumatology International.

Interleukin 1 (IL-1) induces the activation of Stat3.

P. Auron, A. Arman, 2003, Advances in experimental medicine and biology.

Vitamin D Receptor Polymorphisms in the Turkish Population are associated with Multiple Sclerosis

E. List, A. Arman, N. Işık, 2020 .

Vitamin D Receptor Polymorphisms in the Turkish Population are not associated with Multiple Sclerosis

E. List, A. Arman, N. Işık, 2020 .

Novel clinical features and pleiotropic effect in three unrelated patients with LMNA variant.

E. Ateş, A. Arman, B. Geckinli, 2020, Clinical dysmorphology.

Lack of association between IL‐1 and IL‐6 gene polymorphisms and myocardial infarction in Turkish population

A. Çoker, O. Soylu, T. Tezel, 2011, International journal of immunogenetics.

Interleukin-1 receptor antagonist (IL-1RN) and interleukin-1B gene polymorphisms in Turkish patients with rheumatoid arthritis.

A. Çoker, N. Inanç, H. Direskeneli, 2006, Clinical and experimental rheumatology.

Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity

S. Duan, S. Mumm, M. Whyte, 2022, JBMR plus.

Interleukin-1 receptor antagonist (IL-1RN) and interleukin-1B gene polymorphisms in Turkish patients with rheumatoid arthritis.

A. Çoker, N. Inanç, H. Direskeneli, 2006, Clinical and experimental rheumatology.

Concentrations of Serum Cyclophilin A in Patients With Bell Palsy.

B. Demir, Burak Kerşin, A. Binnetoğlu, 2020, The Journal of craniofacial surgery.

VITAMIN D RECEPTOR GENE POLYMORPHISMS IN PEDIATRIC PATIENTS WITH LEUKEMIA-LYMPHOMA: DOES IT HAVE AN IMPACT ON MALIGNANCY?

A. Arman, G. Tokuç, B. Yilmaz, 2020, Marmara Medical Journal.

Novel Growth Hormone-Releasing Hormone Receptor Gene Mutations in Turkish Children with Isolated Growth Hormone Deficiency

A. Büyükgebiz, B. Dündar, A. Arman, 2014, Journal of clinical research in pediatric endocrinology.

Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features

B. Özkan, T. Akçay, Y. Alanay, 2014, Orphanet Journal of Rare Diseases.

Vitreoscilla hemoglobin renders Enterobacter aerogenes highly susceptible to heavy metals

Hikmet Geçkil, S. Gencer, B. Ateş, 2004, Biometals.

Multiple sclerosis: association with the interleukin-1 gene family polymorphisms in the Turkish population

E. List, O. Duz, A. Arman, 2013, The International journal of neuroscience.

Characterization of GH-1 Mutations in Children with Isolated Growth Hormone Deficiency in the Turkish Population

Z. Şıklar, A. Arman, B. Dundar, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Association Between IL7R Promoter Polymorphisms and Multiple Sclerosis in Turkish Population

E. List, A. Arman, H. Simsek, 2018, Journal of Molecular Neuroscience.

Secondary findings in 622 Turkish clinical exome sequencing data

Ö. Yildirim, P. Ata, A. Arman, 2021, Journal of Human Genetics.

Assessment of Interleukin‐1 Gene Cluster Polymorphisms in Lone Atrial Fibrillation: New Insight into the Role of Inflammation in Atrial Fibrillation

T. Tezel, E. Uçer, A. Alper, 2013, Pacing and clinical electrophysiology : PACE.

Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features

I. Gokce, A. Bereket, S. Turan, 2021, Calcified Tissue International.

Novel Splice Site Mutation in the Growth Hormone Receptor Gene in Turkish Patients with Laron-type Dwarfism

I. Peker, N. Yordam,, A. Ozon, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Interleukin-1 receptor antagonist gene VNTR polymorphism is associated with coronary artery disease.

O. Soylu, T. Tezel, H. Aydoǧan, 2008, Arquivos brasileiros de cardiologia.

Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency

M. Gokcu, E. Ateş, P. Ata, 2022, Journal of Assisted Reproduction and Genetics.

Novel Growth Hormone Receptor Gene Mutation in a Patient with Laron Syndrome

A. Topaloğlu, F. Temiz, B. Yüksel, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

First Patient Diagnosed as Feingold Syndrome Type 2 with Alport Syndrome and Review of the Current Literature

P. Ata, A. Arman, M. A. Söylemez, 2022, Molecular Syndromology.

Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty

A. Bereket, S. Turan, T. Guran, 2023, Journal of pediatric endocrinology & metabolism : JPEM.

Novel, homozygous RAB3GAP1 c.2606 + 1G>A, p.Glu830ValfsTer9 variant and chromosome 3q29 duplication in a Turkish individual with Warburg micro syndrome

G. Sager, A. Arman, B. Geckinli, 2023, Clinical dysmorphology.

Two new cases with novel pathogenic variants reflecting the clinical diversity of Schaaf‐Yang syndrome

S. Turan, A. Arman, B. Geckinli, 2023, Clinical genetics.

Human growth hormone

A. Arman, A. Çoker, 2009 .