Öğr. Gör. MUSTAFA YILMAZ

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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

DÜNDAR M., FAHRİOGLU U., Yildiz S. H., Bakir-Gungor B., TEMEL Ş. G., AKIN H., et al.

FUNCTIONAL & INTEGRATIVE GENOMICS , cilt.22, sa.3, ss.291-315, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

The cumulative effects of MEFV gene polymorphisms and mutations in patients with inflammatory bowel diseases

AĞIN M., BİŞGİN A., YILMAZ M., KONT ÖZHAN A., Mammadov F., TÜMGÖR G.

JOURNAL OF THE PAKISTAN MEDICAL ASSOCIATION , cilt.71, sa.2, ss.479-483, 2021 (SCI-Expanded)

Altered expression of apoptosis-related, circulating cell-free miRNAs in children with familial Mediterranean fever: a cross-sectional study

Karpuzoglu E. M., KIŞLA EKİNCİ R. M., Balci S., BİŞGİN A., YILMAZ M.

RHEUMATOLOGY INTERNATIONAL , cilt.41, sa.1, ss.103-111, 2021 (SCI-Expanded)

Twenty-Year Experience of a Single Referral Center on Pediatric Familial Mediterranean Fever What Has Changed Over the Last Decade?

KIŞLA EKİNCİ R. M., Balci S., Dogruel D., ALTINTAŞ D. U., YILMAZ M.

JCR-JOURNAL OF CLINICAL RHEUMATOLOGY , cilt.27, sa.1, ss.18-24, 2021 (SCI-Expanded)

Clinical manifestations and outcomes of 420 children with Henoch Schonlein Purpura from a single referral center from Turkey: A three-year experience

KIŞLA EKİNCİ R. M., Balci S., MELEK E., KARABAY BAYAZIT A., DOĞRUEL D., ALTINTAŞ D. U., et al.

MODERN RHEUMATOLOGY , cilt.30, sa.6, ss.1039-1046, 2020 (SCI-Expanded)

Retrospective Analysis of the Factors Affecting Growth Parameters in Turkish Children With Systemic Lupus Erythematosus

Balci S., KIŞLA EKİNCİ R. M., MELEK E., KARABAY BAYAZIT A., Dogruel D., ALTINTAŞ D. U., et al.

ARCHIVES OF RHEUMATOLOGY , cilt.35, sa.3, ss.357-365, 2020 (SCI-Expanded)

Growth Parameters of Turkish Children With an Autoinflammatory Disease Before and After Canakinumab Treatment

Balci S., KIŞLA EKİNCİ R. M., Dogruel D., ALTINTAŞ D. U., YILMAZ M.

INDIAN PEDIATRICS , cilt.57, sa.7, ss.637-640, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

Pre-Pulseless Takayasu Arteritis in a Child Represented With Prolonged Fever of Unknown Origin and Successful Management With Concomitant Mycophenolate Mofetil and Infliximab

KIŞLA EKİNCİ R. M., Balci S., Piskin F. C., Varan C., ALINÇ ERDEM S., YILMAZ M.

ARCHIVES OF RHEUMATOLOGY , cilt.35, sa.2, ss.278-282, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

Unicentric Castleman Disease Mimicking an Autoinflammatory Disorder: A Diagnostic Challenge in a Pediatric Patient With Recurrent Fever

KIŞLA EKİNCİ R. M., Balci S., ERGİN M., KÜPELİ S., BAYRAM İ., YILMAZ M., et al.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.42, sa.3, ss.204-207, 2020 (SCI-Expanded)

Phenotypic variability in two patients with tumor necrosis factor receptor associated periodic fever syndrome emphasizes a rare manifestation: Immunoglobulin A nephropathy

Balci S., KIŞLA EKİNCİ R. M., MELEK E., ATMIŞ B., BİŞGİN A., YILMAZ M.

EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.63, sa.4, 2020 (SCI-Expanded)

Baricitinib experience on STING-associated vasculopathy with onset in infancy: A representative case from Turkey

Balci S., KIŞLA EKİNCİ R. M., de Jesus A. A., Goldbach-Mansky R., YILMAZ M.

CLINICAL IMMUNOLOGY , cilt.212, ss.113-116, 2020 (SCI-Expanded)

Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey

KIŞLA EKİNCİ R. M., Balci S., Hershfield M., BİŞGİN A., DOĞRUEL D., ALTINTAŞ D. U., et al.

RHEUMATOLOGY , cilt.59, sa.1, ss.254-256, 2020 (SCI-Expanded)

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency

Kiykim A., Öğülür İ., Dursun E., Charbonnier L. M., Nain E., Çekiç Ş., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE , cilt.7, ss.2790-2815, 2019 (SCI-Expanded)

Canakinumab in Children with Familial Mediterranean Fever: A Single-Center, Retrospective Analysis

KIŞLA EKİNCİ R. M., Balci S., DOĞRUEL D., ALTINTAŞ D. U., YILMAZ M.

PEDIATRIC DRUGS , cilt.21, sa.5, ss.389-395, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

Etanercept for the Treatment of Chronic Arthritis Related to Chronic Granulomatous Disease: A Case

Balci S., KIŞLA EKİNCİ R. M., SERBES M., DOĞRUEL D., ALTINTAŞ D. U., YILMAZ M.

PEDIATRIC ALLERGY IMMUNOLOGY AND PULMONOLOGY , cilt.32, sa.3, ss.131-134, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

Disease Severity and Genotype Affect Physical Growth in Children With Familial Mediterranean Fever

KIŞLA EKİNCİ R. M., Balci S., Akay E., DOĞRUEL D., ALTINTAŞ D. U., YILMAZ M.

ARCHIVES OF RHEUMATOLOGY , cilt.34, sa.3, ss.288-293, 2019 (SCI-Expanded)

Hyperimmunoglobulinemia D syndrome with recurrent perianal abscess successfully treated with canakinumab

KIŞLA EKİNCİ R. M., Balci S., BİŞGİN A., TÜMGÖR G., DOĞRUEL D., YILMAZ M.

SCOTTISH MEDICAL JOURNAL , cilt.64, sa.3, ss.103-107, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

Unusual and early onset IPEX syndrome: a case report

DOĞRUEL D., GÜRBÜZ F., TURAN İ., ALTINTAŞ D. U., YILMAZ M., YÜKSEL B.

TURKISH JOURNAL OF PEDIATRICS , cilt.61, sa.4, ss.580-584, 2019 (SCI-Expanded)

Two years of newborn screening for cystic fibrosis in Turkey: Cukurova experience

Sasihuseyinoglu A. S., ALTINTAŞ D. U., BİŞGİN A., DOĞRUEL D., YILMAZ M., SERBES M.

TURKISH JOURNAL OF PEDIATRICS , cilt.61, sa.4, ss.505-512, 2019 (SCI-Expanded)

Concomitance of Familial Mediterranean Fever and Gitelman syndrome in an adolescent

ATMIŞ B., KIŞLA EKİNCİ R. M., MELEK E., BİŞGİN A., YILMAZ M., Anarat A., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.61, sa.3, ss.444-448, 2019 (SCI-Expanded)

Recurrent Henoch Schonlein purpura without renal involvement successfully treated with methotrexate

KIŞLA EKİNCİ R. M., Balci S., SERBES M., Aycin G. D., DOĞRUEL D., ALTINTAŞ D. U., et al.

SCOTTISH MEDICAL JOURNAL , cilt.64, sa.2, ss.74-77, 2019 (SCI-Expanded)

Clinical findings and genetic analysis of the patients with IL-12R beta 1 deficiency from southeast Turkey

DOĞRUEL D., ÖZGÜR GÜNDEŞLİOĞLU Ö., YILMAZ M., Alabaz D., ALTINTAŞ D. U., KOCABAŞ E.

TURKISH JOURNAL OF PEDIATRICS , cilt.61, sa.2, ss.174-179, 2019 (SCI-Expanded)

Evaluation of high resolution computed tomography findings of cystic fibrosis

Sasihuseyinoglu A. S., ALTINTAŞ D. U., SOYUPAK S., DOĞRUEL D., YILMAZ M., SERBES M., et al.

KOREAN JOURNAL OF INTERNAL MEDICINE , cilt.34, sa.2, ss.335-343, 2019 (SCI-Expanded)

Autoimmune Manifestations in Heterozygote Type I Complement 2 Deficiency: A Child Eventually Diagnosed With Systemic Lupus Erythematosus

KIŞLA EKİNCİ R. M., Balci S., BİŞGİN A., ATMIŞ B., DOĞRUEL D., YILMAZ M.

ARCHIVES OF RHEUMATOLOGY , cilt.34, sa.1, ss.96-99, 2019 (SCI-Expanded)

Is Henoch-Schonlein purpura a susceptibility factor for functional gastrointestinal disorders in children?

KIŞLA EKİNCİ R. M., Balci S., Mart O. O., TÜMGÖR G., Yavuz S., Celik H., et al.

RHEUMATOLOGY INTERNATIONAL , cilt.39, sa.2, ss.317-322, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

Dendritic cell activation is blunted in patients with coronary artery disease and diabetes mellitus

Yetkin G. I., YÜCEL A. A., TEKİN İ. Ö., YILMAZ M., Atalay H., Yetkin E.

JOURNAL OF DIABETES AND ITS COMPLICATIONS , cilt.33, sa.2, ss.134-139, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

Renal Amyloidosis in Deficiency of Adenosine Deaminase 2: Successful Experience With Canakinumab

Kışla Ekinci R. M., Balci S., Bişgin A., Hershfield M., Atmış B., Doğruel D., et al.

PEDIATRICS , cilt.142, sa.5, 2018 (SCI-Expanded)

Coexistence of 2 rare autosomal recessively inherited disorders manifesting with immune deficiency; IL-12 receptor beta 1 and biotinidase deficiencies

DOĞRUEL D., BULUT F. D., YILMAZ M., Onenli-Mungan N., ALTINTAŞ D. U.

TURKISH JOURNAL OF PEDIATRICS , cilt.60, sa.5, ss.584-587, 2018 (SCI-Expanded)

Squamous Cell Carcinoma With Hyper-IgE Syndrome: A Case Report

Sasihuseyinoglu A. S., YILMAZ M., ALTINTAŞ D. U., DOĞRUEL D., SERBES M., Uguz A. H., et al.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.40, sa.6, 2018 (SCI-Expanded)

Ataxia-Telangiectasia Clinical and Laboratory Features: Single Center Results

Sasihuseyinoglu A. S., YILMAZ M., BİŞGİN A., DOĞRUEL D., ALTINTAŞ D. U., Duyuler G., et al.

PEDIATRIC ALLERGY IMMUNOLOGY AND PULMONOLOGY , cilt.31, sa.1, ss.9-14, 2018 (SCI-Expanded)

Hematopoietic stem cell transplantation from unrelated donors in children with DOCK8 deficiency

Uygun D. F. K., Uygun V., REİSLİ İ., KELEŞ S., Ozen A., YILMAZ M., et al.

PEDIATRIC TRANSPLANTATION , cilt.21, sa.7, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

Engelhardt K. R., Gertz M. E., Keles S., Schaeffer A. A., Sigmund E. C., Glocker C., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.136, sa.2, ss.402-412, 2015 (SCI-Expanded)

Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion

YILMAZ M., Cagdas D., Grandin V., ALTINTAŞ D. U., Tezcan I., de Saint Basile G., et al.

PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.25, sa.8, ss.817-819, 2014 (SCI-Expanded)

A Novel Mutation in Leukocyte Adhesion Deficiency Type II/CDGIIc

Cagdas D., YILMAZ M., KANDEMİR N., Tezcan I., Etzioni A., Sanal O.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.34, sa.8, ss.1009-1014, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

AUTOIMMUNE HEPATITIS AND SCLERODERMA IN A PATIENT WITH X-LINKED AGAMMAGLOBULINAEMIA

YILMAZ M., BİNGÖL KARAKOÇ G., ALTINTAŞ D. U., Kotil A.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.34, sa.6, ss.723, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

EFFECTS OF ANTIDOTAL THERAPY ON TESTIS TISSUE IN ORGANOPHOSPHATE POISONING

GUMUSAY U., SEBE A., SATAR D. A., AY M. O., Yilmaz M., METE U. Ö.

ACTA MEDICA MEDITERRANEA , cilt.30, sa.2, ss.435-439, 2014 (SCI-Expanded)

Correlation between nasal eosinophils and nasal airflows in children with asthma and/or rhinitis monosensitised to house dust mites

Yukselen A., Kendirli S. G., YILMAZ M., ALTINTAŞ D. U., BİNGÖL KARAKOÇ G.

ALLERGOLOGIA ET IMMUNOPATHOLOGIA , cilt.42, sa.1, ss.50-55, 2014 (SCI-Expanded)

Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients

KÖKER M. Y., Camcioglu Y., van Leeuwen K., KILIÇ S. Ş., Barlan I., YILMAZ M., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.132, sa.5, ss.1156-1168, 2013 (SCI-Expanded)

Evaluation of efficacy of immunotherapy in children with asthma monosensitized to Alternaria

Kilic M., ALTINTAŞ D. U., YILMAZ M., BİNGÖL KARAKOÇ G., Burgut R., Guneser-Kendirli S.

TURKISH JOURNAL OF PEDIATRICS , cilt.53, sa.3, ss.285-294, 2011 (SCI-Expanded)

Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling

LI Y., LAUE K., TEMTAMY S., AGLAN M., KOTAN L. D., YIGIT G., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , cilt.87, sa.6, ss.757-767, 2010 (SCI-Expanded)

Exhaled Breath Condensate MMP-9 Levels in Children With Bronchiectasis

BİNGÖL KARAKOÇ G., Inal A., YILMAZ M., ALTINTAŞ D. U., Kendirli S. G.

PEDIATRIC PULMONOLOGY , cilt.44, sa.10, ss.1010-1016, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

The clinical and genetical features of 124 children with Familial Mediterranean fever: experience of a single tertiary center

Inal A., YILMAZ M., Kendirli S. G., ALTINTAŞ D. U., BİNGÖL KARAKOÇ G.

RHEUMATOLOGY INTERNATIONAL , cilt.29, sa.11, ss.1279-1285, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

Al Khatib S., Keles S., Garcia-Lioret M., Koc-Aydiner E. K., Reisli I., ARTAÇ H., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.124, sa.2, ss.342-348, 2009 (SCI-Expanded)

Exposure to house dust endotoxin and allergic sensitization in allergic and nonallergic children living in Adana, Turkey

YILMAZ M., ALTINTAŞ D. U., BİNGÖL KARAKOÇ G., Inal A., Kilic M., Sutolukta Z., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.51, sa.3, ss.225-231, 2009 (SCI-Expanded)

Effect of outdoor fungus concentrations on symptom severity of children with asthma and/or rhinitis monosensitized to molds

Inal A., BİNGÖL KARAKOÇ G., ALTINTAŞ D. U., Pinar M., Ceter T., YILMAZ M., et al.

ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY , cilt.26, sa.1, ss.11-17, 2008 (SCI-Expanded)

T helper, cytotoxic T, and natural killer T cell profiles and their association with clinical prognosis in children with sickle cell anemia

ATMIŞ B., KILINÇ Y., YILMAZ M., Atmis A., Karagun B. S., ŞAŞMAZ H. İ.

CUKUROVA MEDICAL JOURNAL , cilt.43, sa.4, ss.1002-1007, 2018 (ESCI)

Yenidoğan döneminde sağlık bakımı ile ilişkili enfeksiyon geçirmiş ve geniş spektrumlu antibiyotik kullanmış olmanın erken çocukluk döneminde gözlenen astma, allerjik rinit ve atopik dermatit üzerine etkisi

YAPICIOĞLU YILDIZDAŞ H., ÖZCAN A., YILMAZ M., SERTDEMİR Y.

CUKUROVA MEDICAL JOURNAL , cilt.42, sa.1, ss.132-139, 2017 (Hakemli Dergi)

Effect of healthcare associated infections and broad spectrum antibiotic use in newborn period on development of asthma, allergic rhinitis and atopic dermatitis in early childhood

YILDIZDAS H. Y., OEZCAN A., Sertdemir Y., Yilmaz M.

CUKUROVA MEDICAL JOURNAL , cilt.42, sa.1, ss.132-139, 2017 (ESCI)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

The evaluation of rare and low-frequency genetic variants in common variable immune deficiency (CVID) patients together with CV/RVCD (common variant/rare variant, common disease) hypothesis for final interpretation

BİŞGİN A., SÖNMEZLER Ö., BOGA İ., YILMAZ M.

6. Uluslararası Katılımlı Erciyes Tıp Tibbi Genetik Kongresi, Türkiye, 16 Eylül 2021

Metrikler

Yayın

Atıf (WoS)

483

H-İndeks (WoS)

Atıf (Scopus)

533

H-İndeks (Scopus)

Açık Erişim

BM Sürdürülebilir Kalkınma Amaçları

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