Doç. Dr. AYÇA KIYKIM

Yayın Ağı

Makaleler 163

1. Genomic Dissection of Pediatric Protein-Losing Enteropathy and Related Disorders: Clinical, Immunologic, and Therapeutic Insights

Sefer A. P., ERMAN B., BARIŞ S., Karakoc-Aydiner E., Aydogdu E. S., Cevahir S., et al.

Gastroenterology , cilt.170, sa.4, ss.821-825, 2026 (SCI-Expanded, Scopus)

2. A Survey on Environmental Protective and Risk Factors and Awareness Related to Epithelial Barrier Integrity, Microbiome and Allergic Diseases

BAKIRTAŞ A., KIYKIM A., BASKIN A. K., ANIL H., Bozkurt H. B., Cimen S. S., et al.

Allergy: European Journal of Allergy and Clinical Immunology , cilt.81, sa.3, ss.930-933, 2026 (SCI-Expanded, Scopus)

3. The Skin Tells the Story: Early Signs of Inborn Errors of Immunity.

Meric Z., Kosa B., Karaaslan B. G., Aydemir S., Aydin M., Gumus D. D., et al.

The journal of allergy and clinical immunology. In practice , cilt.14, sa.2, ss.464, 2026 (SCI-Expanded, Scopus)

4. A Comprehensive Assessment of Health-Related Quality of Life in Hereditary Angioedema as a Patient-Centered Approach

Yalcin Gungoren E., Karabiber E., YORĞUN ALTUNBAŞ M., CAN S., Tusuz Onata E., Atik O., et al.

INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY , 2026 (SCI-Expanded, Scopus)

5. Immunodeficiency-Associated Childhood Interstitial Lung Diseases: Data from Türkiye chILD Registry

Kekeç H., Eyüboğlu T. Ş., ASLAN A. T., MEDENİ V., ZİREK F., Tekin M., et al.

Balkan Medical Journal , cilt.43, sa.3, ss.125-135, 2026 (SCI-Expanded, Scopus, TRDizin)

6. Identification of nonsense variants in the ATM gene mimicking SCID phenotype: a brief report

FIRTINA S., Saritas M., Ng Y. Y., Nepesov S., KIYKIM A., Bozkurt S., et al.

Immunologic Research , cilt.73, sa.1, 2025 (SCI-Expanded, Scopus)

7. Granulomatous and Lymphocytic Interstitial Lung Disease in Hyper-IgM Syndrome.

Aydin M., Aydemir S., Meric Z., Gumus D. D., Karaaslan B. G., Aykut A., et al.

Scandinavian journal of immunology , cilt.102, sa.6, 2025 (SCI-Expanded, Scopus)

8. Diverse Clinical and Immunological Profiles in Patients with IPEX Syndrome: a Multicenter Analysis from Turkey

BEKİS BOZKURT H., Catak F. B., Sahin A., Gungoren E. Y., Karaarslan B. G., YAKICI N., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.45, sa.1, 2025 (SCI-Expanded, Scopus)

9. Diagnostic Challenges in Pediatric Fever of Unknown Origin: Combined Role of Ferritin and Fever Duration

Önal P., Sever G. A., Eren B. A., Kes G., Yücel E. Ö., Ocak S., et al.

CHILDREN-BASEL , cilt.12, sa.11, 2025 (SCI-Expanded, Scopus)

10. Expansion of Myeloid-Derived Suppressor Cells and Lymphocyte Apoptosis Beyond B-Cell Deficiency in X-Linked Agammaglobulinemia

Ceylan A., Kulhas Celik I., KELEŞ S., Celebi Celik F., SAĞLAM H., Meric Z., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , cilt.102, sa.5, 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

11. Phenotypes of Food Allergies in Patients with Atopic Dermatitis Aged Under 24 Months: A Multicenter Study

Cogurlu M. T., Aydoğan M., Cavkaytar O., Uysal P., Çulpan H. C., Yıldız N., et al.

DIAGNOSTICS , cilt.15, sa.20, 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

12. Clinical and Immunological Prognostic Factors With Novel Variants in a Large Cohort of Diacylglycerol Acyltransferase 1 Deficiency

Yorgun Altunbas M., Kogler H., Abolhassani H., Akkus E., Basturk A., Akkelle E., et al.

Journal of Allergy and Clinical Immunology: In Practice , cilt.13, sa.9, ss.2449, 2025 (SCI-Expanded, Scopus)

13. Monocyte plasticity and HLA-DR expression in patients with X-linked agammaglobulinemia

Artac H., Ceylan A., Celik I. K., Celik F. C., KARALI Y., Meric Z., et al.

IMMUNOLOGIC RESEARCH , cilt.73, sa.1, 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

14. Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry

Chavoshzadeh Z., Fallah S., Zeinali V., Sharafian S., Delavari S., Mesdaghi M., et al.

FRONTIERS IN GENETICS , cilt.16, 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

15. Unmasking Beta-Lactam Allergies in Children: A Closer Look at Diagnosis and Risk Factors

Meric Z., Karaaslan B. G., Aydemir S., Aydin M., Gumus D. D., Demirel S. O., et al.

INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY , 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

16. Patients With IgA Vasculitis and Kawasaki Disease Show Dysregulated Interferon Signature

Varol S. E., Cinar C., Burtecene N., Sahin S., Yildiz M., Barut K., et al.

INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES , cilt.28, sa.7, 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

17. Type 2 Immunity and Its Role in Allergic Disorders

Gao Y., Wang Z., Ogulur I., Li S., Yazici D., Li X., et al.

Allergy: European Journal of Allergy and Clinical Immunology , cilt.80, sa.7, ss.1848-1877, 2025 (SCI-Expanded, Scopus)

18. Invasive Mould Infections in Chronic Granulomatous Disease: A Multicenter Study From Türkiye

Ergenc Z., Eltan S. B., Karaaslan B. G., KIYKIM A., Tuncay S. A., Yilmaz S., et al.

Mycoses , cilt.68, sa.7, 2025 (SCI-Expanded, Scopus)

19. Evaluating the Humoral Immune Response to Sinovac-Coronavac in a Pediatric Patient with Propionic Acidemia: A Case Study.

Ergün İ., Dinç H. Ö., Burtecene N., Kıykım E., Aktuğlu-Zeybek Ç., Cansever M. Ş., et al.

Turkish archives of pediatrics , cilt.60, sa.4, ss.440-442, 2025 (ESCI, Scopus, TRDizin)

20. Role of IgG4 Antibodies in Human Health and Disease

Shi L., Xiong P., Yang M., Ardicli O., Schneider S. R., Funch A. B., et al.

Cells , cilt.14, sa.9, 2025 (SCI-Expanded, Scopus)

21. Determinants of Exercise Capacity in Children and Adolescents with Asthma: A Comparative Case-Control Study

Kaya M., Ucgun H., Karaaslan B. G., KIYKIM A., Kulli H. D.

NIGERIAN JOURNAL OF CLINICAL PRACTICE , cilt.28, sa.4, ss.531-538, 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

22. Breath of relief: Transforming pediatric asthma care with telemedicine-guided exercises.

Karaaslan B. G., Ucgun H., Kaya M., Cengiz G. N., Ozturk S., Barut O., et al.

Clinical and translational allergy , cilt.15, sa.3, 2025 (SCI-Expanded, Scopus)

23. Type 2 immunity in allergic diseases

Ogulur I., Mitamura Y., Yazici D., Pat Y., ARDIÇLI S., Li M., et al.

Cellular and Molecular Immunology , cilt.22, sa.3, ss.211-242, 2025 (SCI-Expanded, Scopus)

24. Amino Acid Metabolism and Immune Dysfunction in Urea Cycle Disorders: T and B Cell Perspectives.

Gemici Karaaslan B., Kiykim A., Burtecene N., Gokden M., Cansever M. S., Hopurcuoglu D., et al.

Journal of inherited metabolic disease , cilt.48, sa.2, 2025 (SCI-Expanded, Scopus)

25. Ruxolitinib treatment ameliorates clinical, immunologic, and transcriptomic aberrations in patients with STAT3 gain-of-function disease

Bayram Catak F., Catak M. C., Babayeva R., Toubia J., Warnock N. I., Celmeli F., et al.

Journal of Allergy and Clinical Immunology , cilt.155, sa.3, ss.784-791, 2025 (SCI-Expanded, Scopus)

26. Evaluation of T-cell repertoire by flow cytometric analysis in primary immunodeficiencies with DNA repair defects

Karaaslan B. G., Demirkale Z. H., Turan I., Aydemir S., Meric Z., Taskin Z., et al.

Scandinavian Journal of Immunology , cilt.101, sa.2, 2025 (SCI-Expanded, Scopus)

27. Beyond Dermatological Findings: Multisystem Involvement in Prolidase Deficiency.

Yalcin Gungoren E., Meric Z., Pinar Sefer A., Ozkan A. D., CAN S., Babayeva R., et al.

Turkish archives of pediatrics , cilt.60, sa.1, ss.48-56, 2025 (ESCI, TRDizin)

28. Allergen-specific B cell responses in oral immunotherapy-induced desensitization, remission, and natural outgrowth in cow's milk allergy.

Satitsuksanoa P., van de Veen W., Tan G., Lopez J., Wirz O., Jansen K., et al.

Allergy , cilt.80, sa.1, ss.161-180, 2025 (SCI-Expanded, Scopus)

29. **Molecular investigations on T cell subsets in patients affected by hypomorphic DCLRE1C mutation**

KARASELEK M. A., DURAN T., Kuccukturk S., Hazar E., Dogar O., Kiykim A., et al.

EXPERT REVIEW OF CLINICAL IMMUNOLOGY , cilt.21, sa.3, ss.393-399, 2025 (SCI-Expanded, Scopus)

30. Understanding and Managing Hyper IgE Syndromes

Meric Z., Aydin M., Gumus D. D., YÜCEL E., KIYKIM A.

IMMUNOTARGETS AND THERAPY , cilt.14, ss.1233-1245, 2025 (ESCI, Scopus)

31. Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signature

Bosticardo M., Dobbs K., Delmonte O. M., Martins A. J., Pala F., Kawai T., et al.

Science Immunology , cilt.10, sa.103, 2025 (SCI-Expanded, Scopus)

32. Children With Type I Interferonopathy: Commonalities and Diversities in a Large Patient Cohort

Haslak F., Kilic H., Sahin S., Hotaman B., Cebi N. M., Yildiz M., et al.

JOURNAL OF RHEUMATOLOGY , cilt.51, sa.12, ss.1208-1217, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

33. Insights into Patient Experiences with Facilitated Subcutaneous Immunoglobulin Therapy in Primary Immune Deficiency: A Prospective Observational Cohort

Gungoren E. Y., YORĞUN ALTUNBAŞ M., Dikici U., Meric Z., ESER ŞİMŞEK I., KIYKIM A., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.44, sa.8, 2024 (SCI-Expanded, Scopus)

34. The epithelial barrier theory and its associated diseases

Sun N., Ogulur I., Mitamura Y., Yazici D., Pat Y., Bu X., et al.

ALLERGY , cilt.79, sa.12, ss.3192-3237, 2024 (SCI-Expanded, Scopus)

35. LTβR deficiency causes lymph node aplasia and impaired B cell differentiation

Ransmayr B., Bal S. K., Thian M., Svaton M., van de Wetering C., Hafemeister C., et al.

SCIENCE IMMUNOLOGY , cilt.9, sa.101, 2024 (SCI-Expanded, Scopus)

36. Atypical Mycobacterial Pneumonia in 2 Siblings with a Novel Hypomorphic NEMO/IKBKG Mutation

Meric Z., Aydemir S., Kilic Baskan A., Gemici Karaaslan B., Kendir Demirkol Y., KILINÇ SAKALLI A. A., et al.

Turkish Archives of Pediatrics , cilt.59, sa.6, ss.605-607, 2024 (ESCI, Scopus, TRDizin)

37. OUTCOME OF PATIENTS WITH SIGNAL-TRANSDUCER AND ACTIVATOR OF OF TRANSCRIPTION 1 MUTATIONS (STAT1) GAIN-OF-FUNCTION VARIANTS AFTER HAEMATOPOIETIC STEM CELL TRANSPLANTATION - AN IEWP/PIDTC STUDY

Buddingh E. P., Slatter M., Aldave Becerra J. C., Alonso Garcia L., von Asmuth E., BARIŞ S., et al.

BONE MARROW TRANSPLANTATION , ss.94-95, 2024 (SCI-Expanded, Scopus)

38. Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye

ERMAN B., Aba U., Ipsir C., Pehlivan D., Aytekin C., Cildir G., et al.

Journal of Clinical Immunology , cilt.44, sa.7, 2024 (SCI-Expanded, Scopus)

39. Interferon Gamma in Sickness Predisposing to Mycobacterial Infectious Diseases

GEMİCİ KARAASLAN H. B., Rosain J., Bustamante J., KIYKIM A.

BALKAN MEDICAL JOURNAL , cilt.41, sa.5, ss.326-332, 2024 (SCI-Expanded, Scopus)

40. Immunodeficiencies in childhood interstitial lung diseases: First data from the Turkish National chILD registry

ŞİŞMANLAR EYÜBOĞLU T., KEKEÇ H., Hangul M., Ozturk G. K., Hizal M., Zirek F., et al.

EUROPEAN RESPIRATORY JOURNAL , 2024 (SCI-Expanded, Scopus)

41. MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort

Gulec Koksal Z., BİLGİÇ ELTAN S., Topyildiz E., Sezer A., Keles S., Celebi Celik F., et al.

Journal of Allergy and Clinical Immunology: In Practice , cilt.12, sa.9, ss.2490, 2024 (SCI-Expanded, Scopus)

42. Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variants

Aykut A., Durmaz A., Karaca N., Gulez N., Genel F., Celmeli F., et al.

Immunologic Research , cilt.72, sa.4, ss.714-726, 2024 (SCI-Expanded, Scopus)

43. Rapid Drug Desensitization and Management of Breakthrough Reactions in Pediatric Patients

GEMİCİ KARAASLAN H. B., AYDEMİR S., Meric Z., KARABAĞ YILMAZ E., BİBİNOĞLU AMIROV C., Dilek T. D., et al.

ASTHMA ALLERGY IMMUNOLOGY , sa.2, ss.170-180, 2024 (ESCI)

44. Neurocognitive Impairment in Patients With Ataxia Telangiectasia and Their Unaffected Parents: Is It Similar?

Uyar E., Akturk H., Usanmaz S., KIYKIM A., Tufan A. E., Alibas H., et al.

Pediatric Neurology , cilt.156, ss.85-90, 2024 (SCI-Expanded, Scopus)

45. Artemis deficiency: A large cohort including a novel variant with increased radiosensitivity.

Meric Z., Gemici Karaaslan B., Yalcin Gungoren E., Bektas Hortoglu M., Cavas T., Aydemir S., et al.

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology , cilt.35, sa.6, 2024 (SCI-Expanded, Scopus)

46. Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency

Rosain J., KIYKIM A., Michev A., Kendir-Demirkol Y., Rinchai D., Peel J. N., et al.

Journal of Clinical Immunology , cilt.44, sa.3, 2024 (SCI-Expanded, Scopus)

47. Perioperative hypersensitivity in children: A prospective multidisciplinary study.

Aydemir S., Gemici Karaaslan H. B., Mustu U., Tin O., Hakalmaz A. E., Ozcan R., et al.

Acta anaesthesiologica Scandinavica , cilt.68, sa.3, ss.321-327, 2024 (SCI-Expanded, Scopus)

48. GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway

Park A. Y., Leney-Greene M., Lynberg M., Gabrielski J. Q., Xu X., Schwarz B., et al.

NATURE IMMUNOLOGY , cilt.25, sa.2, ss.282-293, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

49. Evaluation of Clinical and Immunological Alterations Associated with ICF Syndrome

Bilgic Eltan S., Nain E., Catak M. C., Ezen E., Sefer A. P., Karimi N., et al.

Journal of Clinical Immunology , cilt.44, sa.1, 2024 (SCI-Expanded, Scopus)

50. STAT1/STAT3 Gain of Function and Mechanisms of Immune Dysregulation

KIYKIM A.

TURKISH JOURNAL OF IMMUNOLOGY , cilt.12, ss.47-52, 2024 (ESCI, Scopus, TRDizin)

51. JAK-inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID and EBMT IEWP retrospective study.

Fischer M., Olbrich P., Hadjadj J., Aumann V., Bakhtiar S., Barlogis V., et al.

The Journal of allergy and clinical immunology , cilt.153, 2024 (SCI-Expanded, Scopus)

52. Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency.

Taghizade N., Babayeva R., Kara A., Karakus I. S., Catak M. C., Bulutoglu A., et al.

The Journal of allergy and clinical immunology , cilt.152, sa.6, ss.1634-1645, 2023 (SCI-Expanded, Scopus)

53. Neurologic Status of Patients with Purine Nucleoside Phosphorylase Deficiency Before and After Hematopoetic Stem Cell Transplantation

Karaaslan B. G., Turan I., Aydemir S., Meric Z. A., ATAY D., AKÇAY A., et al.

Journal of Clinical Immunology , cilt.43, sa.8, ss.2062-2075, 2023 (SCI-Expanded, Scopus)

54. Activated phosphoinositide 3-kinase d syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

Maccari M. E., Wolkewitz M., Schwab C., Lorenzini T., Leiding J. W., Aladjdi N., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , sa.4, 2023 (SCI-Expanded, Scopus)

55. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.

Maccari M. E., Wolkewitz M., Schwab C., Lorenzini T., Leiding J. W., Aladjdi N., et al.

The Journal of allergy and clinical immunology , cilt.152, 2023 (SCI-Expanded, Scopus)

56. Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients.

Yakici N., Kreins A. Y., Catak M. C., Babayeva R., Erman B., Kenney H., et al.

Clinical immunology (Orlando, Fla.) , cilt.255, ss.109757, 2023 (SCI-Expanded, Scopus)

57. JAK-inhibitor treatment for inborn errors of JAK/ STAT signalling: An ESID and EBMT IEWP retrospective study

Fischer M., Olbrich P., Hadjadj J., Aumann V., Bakhtiar S., Barlogis V., et al.

SWISS MEDICAL WEEKLY , cilt.153, 2023 (SCI-Expanded, Scopus)

58. **Immune Reconstitution Inflammatory Syndrome After Hematopoietic Stem Cell Transplantation in a FOXN1-deficient Patient**

Corbali O., Gemici Karaaslan H. B., Aydemir S., Onal P., Kendir Demirkol Y., Nepesov S., et al.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.45, sa.5, ss.275-277, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

59. Humoral and cellular immune response to SARS-CoV-2 mRNA BNT162b2 vaccine in pediatric kidney transplant recipients compared with dialysis patients and healthy children.

Gulmez R., Ozbey D., Agbas A., Aksu B., Yildiz N., Uckardes D., et al.

Pediatric nephrology (Berlin, Germany) , cilt.38, sa.7, ss.2199-2208, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

60. Evaluation of pediatric patients with suspected polyethylene glycol and polysorbate allergy before mRNA SARS-CoV2 vaccination.

Karaaslan B. G., Burtecene N., Mustu U., Ocak S., Kasapcopur Ö., Kıykım A., et al.

Allergologia et immunopathologia , cilt.51, sa.3, ss.174-180, 2023 (SCI-Expanded, Scopus)

61. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.

Leiding J. W., Vogel T. P., Santarlas V. G. J., Mhaskar R., Smith M. R., Carisey A., et al.

The Journal of allergy and clinical immunology , cilt.151, sa.4, ss.1081-1095, 2023 (SCI-Expanded, Scopus)

62. Epithelial Barrier Hypothesis and Its Comparison with the Hygiene Hypothesis

KIYKIM A., Ogulur I., Yazici D., ÇOKUĞRAŞ H. C., Akdis M., Akdis C. A.

TURKISH ARCHIVES OF PEDIATRICS , cilt.58, sa.2, ss.122-128, 2023 (ESCI, Scopus, TRDizin)

63. Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.

Lévy R., Gothe F., Momenilandi M., Magg T., Materna M., Peters P., et al.

The Journal of experimental medicine , cilt.220, sa.2, 2023 (SCI-Expanded, Scopus)

64. Natural history and genetic spectrum of the Turkish metaphyseal dysplasia cohort, including rare types caused by biallelic COL10A1, COL2A1, and LBR variants

Tüysüz B., Kasap B., Sarıtaş M., Alkaya D., Bozlak S., Kıykım A., et al.

BONE , cilt.167, 2023 (SCI-Expanded, Scopus)

65. Comparison of mitogen-induced proliferation in child and adult healthy groups by flow cytometry revealed similarities

Elshari Z. S., NEPESOV S., Tahrali I., KIYKIM A., CAMCIOĞLU Y., Deniz G., et al.

IMMUNOLOGIC RESEARCH , cilt.71, sa.1, ss.51-59, 2023 (SCI-Expanded, Scopus)

66. The Notch1/CD22 signaling axis disrupts Treg function in SARS-CoV-2-associated multisystem inflammatory syndrome in children

Benamar M., Chen Q., Chou J., Julé A. M., Boudra R., Contini P., et al.

JOURNAL OF CLINICAL INVESTIGATION , cilt.133, sa.1, 2023 (SCI-Expanded, Scopus)

67. The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity.

Baris S., Abolhassani H., Massaad M. J., Al-Nesf M., Chavoshzadeh Z., Keles S., et al.

The journal of allergy and clinical immunology. In practice , cilt.11, sa.1, ss.158, 2023 (SCI-Expanded, Scopus)

68. [Analysis of IFN-γR1 (CD119) and IL-12Rβ1 (CD212) Deficiency by Flow Cytometry].

Gelmez M. Y., Köksalan K., Çınar S., Hatipoğlu N., Coşkuner T., Topkarcı Z., et al.

Mikrobiyoloji bulteni , cilt.57, sa.1, ss.83-96, 2023 (SCI-Expanded, Scopus, TRDizin)

69. Chronic Rhinosinusitis in Patients with Primary Immunodeficiency.

Karadeniz E. B., Aliyeva C., Aydemir S., Karaaslan B. G., Mustu U., Ada M., et al.

International archives of allergy and immunology , cilt.184, sa.3, ss.302-310, 2023 (SCI-Expanded, Scopus)

70. Serving Healthy (?) Food on Toxic Plates

KIYKIM A.

TURKISH ARCHIVES OF PEDIATRICS , cilt.58, sa.1, ss.1-2, 2023 (ESCI, TRDizin)

71. HUMORAL AND CELLULAR IMMUNITY TO SARS-COV-2 VACCINATION WITH BNT162B2 MRNA VACCINE IN PEDIATRIC KIDNEY TRANSPLANT AND DIALYSIS PATIENTS

Gulmez R., Ozbey D., AĞBAŞ A., Aksu B., YILDIZ N., ÜÇKARDEŞ D., et al.

PEDIATRIC NEPHROLOGY , sa.11, ss.2816, 2022 (SCI-Expanded, Scopus)

72. IMPAIRED T CELL RECEPTOR REPERTOIRE IN CHILDREN WITH CHRONIC KIDNEY DISEASE

Ulgen E., KIYKIM A., Saygili S. K., BURTECENE N., ÇOKUĞRAŞ H. C., ÇALIŞKAN S., et al.

PEDIATRIC NEPHROLOGY , cilt.37, sa.11, ss.2843, 2022 (SCI-Expanded, Scopus)

73. Successful Rapid Desensitization of a Pediatric Multiple Sclerosis Patient with Anaphylaxis to Ocrelizumab.

Karaaslan H. B., Aydemir S., Amirov C. B., Dilek T. D., Bayramli Z., Saltik S., et al.

Annals of Indian Academy of Neurology , cilt.25, sa.6, ss.1210-1213, 2022 (SCI-Expanded, Scopus)

74. GENETIC AND CLINICAL PROFILING OF MENDELIAN SUSCEPTIBILITY TO MYCOBACTERIAL DISEASE PATIENTS; SINGLECENTER EXPERIENCE

NEPESOV S., FIRTINA S., AYGÜN D., Işıkgil B., ÇAMCIOĞLU Y., KIYKIM A., et al.

Sabiad , cilt.5, sa.3, ss.140-146, 2022 (TRDizin)

75. Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency.

Ogishi M., Arias A. A., Yang R., Han J., Zhang P., Rinchai D., et al.

The Journal of experimental medicine , cilt.219, sa.10, 2022 (SCI-Expanded, Scopus)

76. Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency

Catak M. C., Akcam B., Eltan S. B., Babayeva R., KARAKUŞ İ. H., Akgun G., et al.

ALLERGY , cilt.77, sa.10, ss.3108-3123, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

77. A Stk4-Foxp3-NF-κB p65 transcriptional complex promotes Treg cell activation and homeostasis

Cui Y., Benamar M., Schmitz-Abe K., Poondi-Krishnan V., Chen Q., Jugder B., et al.

Science Immunology , cilt.7, sa.75, 2022 (SCI-Expanded, Scopus)

78. Clinical, Genetic, and Outcome Characteristics of Pediatric Patients with Primary Hemophagocytic Lymphohistiocytosis

Nepesov S., Yaman Y., Elli M., Bayram N., Ozdilli K., KIYKIM A., et al.

TURKISH ARCHIVES OF PEDIATRICS , cilt.57, sa.4, ss.398-405, 2022 (ESCI, Scopus, TRDizin)

79. Clinical and Laboratory Factors Affecting the Prognosis of Severe Combined Immunodeficiency

ÖZTÜRK E., Catak M. C., KIYKIM A., Baser D., Bilgic Eltan S., Yalcin K., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.42, sa.5, ss.1036-1050, 2022 (SCI-Expanded, Scopus)

80. Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia

Zhang Q., Matuozzo D., Le Pen J., Lee D., Moens L., Asano T., et al.

JOURNAL OF EXPERIMENTAL MEDICINE , cilt.219, sa.8, 2022 (SCI-Expanded, Scopus)

81. Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants

AYKUT A., DURMAZ A., KARACA N., Gulez N., Genel F., Celmeli F., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , cilt.95, sa.6, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

82. Omalizumab may facilitate drug desensitization in patients failing standard protocols

Gemici Karaaslan H. B., Karabağ Yılmaz E., Gulmez R., Canpolat N., Kıykım A., Çokuğraş H. C.

PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.33, sa.5, 2022 (SCI-Expanded, Scopus)

83. Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO Deficiency

Yilmaz N. S., Eltan S. B., KAYAOĞLU B., Geckin B., Heredia R. J., Sefer A. P., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.42, ss.582-596, 2022 (SCI-Expanded, Scopus)

84. Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency

Sefer A. P., Abolhassani H., Ober F., KAYAOĞLU B., Eltan S. B., Kara A., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.42, ss.634-652, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

85. Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency

KOCAMIŞ B., Baser D., Akcam B., Danielson J., Eltan S. B., Haliloglu Y., et al.

ALLERGY , cilt.77, sa.3, ss.1004-1019, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

86. Determining T and B Cell development by TREC/KREC analysis in primary immunodeficiency patients and healthy controls

Şentürk G., Ng Y. Y., Eltan S. B., Başer D., Ogulur I., Altındirek D., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , cilt.95, sa.3, 2022 (SCI-Expanded, Scopus)

87. Primary antibody deficiencies in Turkey: molecular and clinical aspects

Firtina S., Ng Y. Y., HATIRNAZ NG Ö., KIYKIM A., Ozek E., Kara M., et al.

IMMUNOLOGIC RESEARCH , cilt.70, sa.1, ss.44-55, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

88. Therapeutic options for CTLA-4 insufficiency.

Egg D., Rump I. C., Mitsuiki N., Rojas-Restrepo J., Maccari M., Schwab C., et al.

The Journal of allergy and clinical immunology , cilt.149, ss.736-746, 2022 (SCI-Expanded, Scopus)

89. Adverse COVID-19 outcomes in immune deficiencies: Inequality exists between subclasses

AYDINER E., Eltan S. B., Babayeva R., Aydiner O., KEPENEKLİ KADAYİFCİ E., KOLUKISA B., et al.

ALLERGY , cilt.77, sa.1, ss.282-295, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

90. Altered immune response in organic acidemia.

Altun İ., Kiykim A., Zubarioglu T., Burtecene N., Hopurcuoglu D., Topcu B., et al.

Pediatrics international : official journal of the Japan Pediatric Society , cilt.64, sa.1, 2022 (SCI-Expanded, Scopus)

91. Hematopoietic Stem Cell Transplantation in Patients with Severe Combined Immunodeficiency: A Single-Center Experience

Nepesov S., YAMAN Y., ELLİ M., BAYRAM N., ÖZDİLLİ K., KIYKIM A., et al.

Experimed , cilt.12, sa.1, ss.24-28, 2022 (Scopus, TRDizin)

92. Functions of NK and iNKT cells in pediatric and adult CVID, ataxia telangiectasia and agammaglobulinemia patients

Adin-Cinar S., Gelmez M. Y., Akdeniz N., Ozcit-Gurel G., KIYKIM A., Karakoc-Aydiner E., et al.

IMMUNOLOGY LETTERS , cilt.240, ss.46-55, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

93. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

Thalhammer J., Kindle G., Nieters A., Rusch S., Seppänen M. R., Fischer A., et al.

Journal of Allergy and Clinical Immunology , cilt.148, sa.5, ss.1332, 2021 (SCI-Expanded, Scopus)

94. Primary immunodeficiencies: HSCT experiences of a single center in Turkey

Erol Cipe F., Adakli Aksoy B., Aydogdu S., Dikme G., Kiykim A., Aydogmus C., et al.

PEDIATRIC TRANSPLANTATION , cilt.25, sa.7, 2021 (SCI-Expanded, Scopus)

95. Telemedicine Applications in a Tertiary Pediatric Hospital in Turkey During COVID-19 Pandemic

Aydemir S., Ocak S., Saygılı S. K., Hopurcuoğlu D., Haşlak F., Kıykım E., et al.

TELEMEDICINE AND E-HEALTH , cilt.27, sa.10, ss.1180-1187, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

96. Food-induced anaphylaxis in early childhood and factors associated with its severity.

Aydogan M., Topal E., Yakıcı N., Acar H. C., Demirkale Z. H., Arga M., et al.

Allergy and asthma proceedings , cilt.42, sa.5, 2021 (SCI-Expanded, Scopus)

97. Impaired respiratory burst contributes to infections in PKC-deficient patients

Neehus A., Moriya K., Nieto-Patlan A., Le Voyer T., Levy R., Ozen A., et al.

JOURNAL OF EXPERIMENTAL MEDICINE , cilt.218, sa.9, 2021 (SCI-Expanded, Scopus)

98. Adverse COVID outcomes in youngsters with immune deficiencies; inequality exists between subclasses

AYDINER E., Eltan S. B., Babayeva R., Aydiner O., KEPENEKLİ KADAYİFCİ E., Kolukisa B., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.285, 2021 (SCI-Expanded, Scopus)

99. Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency

Aydemir S., Islek A., Nepesov S., Yaman Y., Baysoy G., Beser O. F., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.6, ss.1406-1410, 2021 (SCI-Expanded, Scopus)

100. Autoinflammatory manifestations as a result of an elevated type I IFN signature in a case of NEMO deficiency

Yilmaz N. S., Eltan S. B., KAYAOĞLU B., Geckin B., Sozeri B., KIYKIM A., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.370, 2021 (SCI-Expanded, Scopus)

101. Reversal clinical and immunological effects of abatacept in patients with LRBA and CTLA4 deficiencies

BARIŞ S., Babayeva R., Catak M. C., Baser D., Eltan S. B., Akgun G., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.77, 2021 (SCI-Expanded, Scopus)

102. Two patients with chronic mucocutaneous candidiasis caused by TRAF3IP2 deficiency.

Shafer S., Yao Y., Comrie W., Cook S., Zhang Y., Yesil G., et al.

The Journal of allergy and clinical immunology , cilt.148, ss.256-263, 2021 (SCI-Expanded, Scopus)

103. LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency

Kardelen A. D., Kara M., Guller D., Ozturan E. K., Abali Z. Y., Ceylaner S., et al.

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM , cilt.20, sa.2, ss.389-394, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

104. Notch4 signaling limits regulatory T-cell-mediated tissue repair and promotes severe lung inflammation in viral infections

Harb H., Benamar M., Lai P. S., Contini P., Griffith J. W., Crestani E., et al.

IMMUNITY , cilt.54, sa.6, ss.1186-1206, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

105. Parents of ataxia-telangiectasia patients display a distinct cellular immune phenotype mimickingATM-mutated patients

ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., Uyar E., KIYKIM A., et al.

PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.32, sa.2, ss.349-357, 2021 (SCI-Expanded, Scopus)

106. Reference values for T and B lymphocyte subpopulations in Turkish children and adults

BESCİ Ö., BaSer D., Ogulur I., Berberoglu A. C., KIYKIM A., BescI T., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.51, sa.4, ss.1814-1824, 2021 (SCI-Expanded, Scopus, TRDizin)

107. Proven Food-Induced Acute Urticaria and Predictive Factors for Definitive Diagnosis in Childhood.

Aydoğan M., Topal E., Uysal P., Acar H. C., Cavkaytar O., Hızlı Demirkale Z., et al.

International archives of allergy and immunology , cilt.182, sa.7, ss.607-614, 2021 (SCI-Expanded, Scopus)

108. Novel Frameshift Autosomal Recessive Loss-of-Function Mutation inSMARCD2Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis

YÜCEL E., Karakus I. S., Krolo A., KIYKIM A., Heredia R. J., TAMAY Z. Ü., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.1, ss.59-65, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

109. A set of clinical and laboratory markers differentiates hyper-IgE syndrome from severe atopic dermatitis.

Kasap N., Celik V., Isik S., Cennetoglu P., Kiykim A., Eltan S. B., et al.

Clinical immunology (Orlando, Fla.) , cilt.223, ss.108645, 2020 (SCI-Expanded, Scopus)

110. Mutational landscape of severe combined immunodeficiency patients from Turkey

Firtina S., Ng Y. Y., Ng O. H., KIYKIM A., ÖZEN A. O., ÖZEN A. O., et al.

INTERNATIONAL JOURNAL OF IMMUNOGENETICS , cilt.47, sa.6, ss.529-538, 2020 (SCI-Expanded, Scopus)

111. Diagnostic Modalities Based on Flow Cytometry for Chronic Granulomatous Disease: A Multicenter Study in a Well-Defined Cohort

BARIŞ H. E., Ogulur I., Akcam B., KIYKIM A., Karagoz D., SARAYMEN B., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE , cilt.8, sa.10, ss.3525-3535, 2020 (SCI-Expanded, Scopus)

112. Immunization practices in children with a history of allergies

Baris H. E., BORAN P., Kiykim A., BARIŞ S., Ozen A., AYDINER E.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.55, sa.3, ss.244-250, 2020 (ESCI, Scopus, TRDizin) Sürdürülebilir Kalkınma

113. Lymphoma Predisposing Gene in an Extended Family: CD70 Signaling Defect

Khodzhaev K., Bay S. B., Kebudi R., ALTINDİREK D., Kaya A., Erbilgin Y., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.40, sa.6, ss.883-892, 2020 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

114. Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty

ÖZEN A. O., ÖZEN A. O., Bugrul F., ÖZEN A. O., ÖZEN A. O., KIYKIM A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.93, sa.1, ss.66-72, 2020 (SCI-Expanded, Scopus)

115. The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study

ÇEKİÇ Ş., ÖZEN A. O., ÖZEN A. O., Karaca N. E., BARIŞ S., ÖZEN A. O., et al.

PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.31, sa.5, ss.528-536, 2020 (SCI-Expanded, Scopus)

116. Genetic Characteristics, Infectious, and Noninfectious Manifestations of 32 Patients with Chronic Granulomatous Disease

Aygun D., KÖKER M. Y., NEPESOV S., KÖKER M. Y., van Leeuwen K., de Boer M., et al.

International Archives of Allergy and Immunology , cilt.181, sa.7, ss.540-550, 2020 (SCI-Expanded, Scopus)

117. ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients

ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., et al.

ALLERGY , cilt.75, sa.4, ss.921-933, 2020 (SCI-Expanded, Scopus)

118. Lymphocyte Subset Abnormalities in Pediatric-Onset Common Variable Immunodeficiency

ÖZEN A. O., KIYKIM A., ÖZEN A. O., ÖZEN A. O., Ozen A., ÖZEN A. O.

INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY , cilt.181, sa.3, ss.228-237, 2020 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

119. Immediate adverse reactions to intravenous immunoglobulin in primary immune deficiencies: a single center experience.

Nain E., Kıykım A., Kasap N. A., Barış S., Özen A., Aydıner E. K.

The Turkish journal of pediatrics , cilt.62, ss.379-386, 2020 (SCI-Expanded, Scopus, TRDizin)

120. Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype

ÖZEN A. O., ÖZEN A. O., KIYKIM A., ÖZEN A. O., Ozen A., BARIŞ S.

CLINICAL IMMUNOLOGY , cilt.210, 2020 (SCI-Expanded, Scopus)

121. Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat

KIYKIM A., EKER N., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., et al.

PEDIATRIC BLOOD & CANCER , 2019 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

122. Immune system defects in DiGeorge syndrome and association with clinical course

ÖZEN A. O., KIYKIM A., ÖZEN A. O., ÖZEN A. O., AYDINER E., Ozen A., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , cilt.90, sa.5, 2019 (SCI-Expanded, Scopus)

123. Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency

KIYKIM A., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., ÇEKİÇ Ş., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE , cilt.7, sa.8, ss.2790-2815, 2019 (SCI-Expanded, Scopus)

124. Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry

YILMAZ KARAPINAR D., PATIROĞLU T., Metin A., Caliskan U., Celkan T., YILMAZ B., et al.

PEDIATRIC BLOOD & CANCER , cilt.66, sa.10, 2019 (SCI-Expanded, Scopus)

125. Polymerase delta deficiency causes syndromic immunodeficiency with replicative stress

Conde C. D., Petronczki O. Y., BARIŞ S., Willmann K. L., Girardi E., Salzer E., et al.

JOURNAL OF CLINICAL INVESTIGATION , cilt.129, sa.10, ss.4194-4206, 2019 (SCI-Expanded, Scopus)

126. How to Approach Systemic Hypersensitivity reactions to Gonadotropin Releasing Hormone Analogues during treatment of Central Precocious Puberty

KIRKGÖZ T., Karakoc E. A., KIYKIM A., Bugrul F., Helvacioglu D., Eltan S. B., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.185, 2019 (SCI-Expanded, Scopus)

127. Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency

Farmer J. R., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE , cilt.7, sa.6, ss.1970-1989, 2019 (SCI-Expanded, Scopus)

128. A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency

FIRTINA S., CIPE F., NG Y., Kiykim A., NG O., SUDUTAN T., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.39, sa.2, ss.144-147, 2019 (SCI-Expanded, Scopus)

129. Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation

KIYKIM A., Charbonnier L. M., Akcay A., Karakoc-Aydiner E., Ozen A., Ozturk G., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.39, sa.1, ss.37-44, 2019 (SCI-Expanded, Scopus)

130. Lymphocyte Functions in Patients with Chronic Granulomatous Disease and Carrier Individuals

ÖĞÜLÜR İ., Baris E., KIYKIM A., Baser D., Akgun G., Ozen A., et al.

TURKISH JOURNAL OF IMMUNOLOGY , cilt.7, sa.2, ss.93-101, 2019 (ESCI, Scopus, TRDizin)

131. Evaluation of a Standardized Bakery Product (SUTMEK) as a Potential Tool for Baked-Milk Tolerance and Immunotherapy Research Studies

KIYKIM A., Karakoc-Aydiner E., Gunes E., Nain E., ÖĞÜLÜR İ., Yazici D., et al.

INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY , cilt.178, sa.1, ss.1-9, 2019 (SCI-Expanded, Scopus)

132. Primary Immunodeficiency and Cancer in Children; A Review of the Literature

Kebudi R., Kiykim A., Sahin M. K.

CURRENT PEDIATRIC REVIEWS , cilt.15, sa.4, ss.245-250, 2019 (ESCI, Scopus) Sürdürülebilir Kalkınma

133. The Diagnostic Value of Flow Cytometry in DOCK8 Deficiency

ÖĞÜLÜR İ., KIYKIM A., Nain E., Kasap N., Akgun G., Karakoc-Aydiner E., et al.

TURKISH JOURNAL OF IMMUNOLOGY , cilt.7, sa.2, ss.102-106, 2019 (ESCI, Scopus, TRDizin)

134. Disease evolution and response to rapamycin in Activated Phosphoinositide 3-Kinase delta syndrome: the european society for immunodeficiencies-Activated Phosphoinositide 3-Kinase d syndrome registry

Maccari M. E., Abolhassani H., Aghamohammadi A., Aiuti A., Aleinikova O., Bangs C., et al.

FRONTIERS IN IMMUNOLOGY , cilt.9, 2018 (SCI-Expanded, Scopus)

135. Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study

Barzaghi F., Hernandez L. C. A., Neven B., Ricci S., Kucuk Z. Y., Bleesing J. J., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.141, sa.3, ss.1036-1054, 2018 (SCI-Expanded, Scopus)

136. Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation

Alroqi F. J., Charbonnier L., BARIŞ S., KIYKIM A., Chou J., Platt C. D., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.141, sa.3, ss.1050-1069, 2018 (SCI-Expanded, Scopus)

137. Diagnostic Usage of Intracellular Protein Staining by Flow Cytometer in Primary Immune Deficiencies; Marmara Experience

ÖĞÜLÜR İ., BARIŞ S., Ozen A., Nain E., Kiykim A., Karakoc-Aydiner E.

ASTIM ALLERJI IMMUNOLOJI , cilt.16, sa.2, ss.81-89, 2018 (ESCI, TRDizin)

138. Effects of Vitamin D on House Dust Mite Sensitized Children with Atopic Dermatitis

Nain E., KIYKIM A., Yasoz C., Bayramli R., BARIŞ S., Ozen A., et al.

ASTIM ALLERJI IMMUNOLOJI , cilt.16, sa.1, ss.40-46, 2018 (ESCI, TRDizin)

139. Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

PETERSEN B., AUGUST D., ABT R., ALDDAFARI M., ATAROD L., BARIS S., et al.

Inflammatory bowel diseases , cilt.23, ss.2109-2120, 2017 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

140. Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2

van den Boogaard M., Thijssen P., Aytekin C., Licciardi F., KIYKIM A., Spossito L., et al.

Clinical Genetics , cilt.92, sa.4, ss.380-387, 2017 (SCI-Expanded, Scopus)

141. CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis.

OZEN A., COMRIE W., ARDY R., Domínguez C., DALGIC B., BESER Ö. F., et al.

The New England journal of medicine , cilt.377, ss.52-61, 2017 (SCI-Expanded, Scopus)

142. Patients with primary immunodeficiencies are a reservoir of poliovirus and a risk to polio eradication

Aghamohammadi A., Abolhassani H., Kutukculer N., Wassilak S. G., Pallansch M. A., Kluglein S., et al.

Frontiers in Immunology , cilt.8, sa.JUN, 2017 (SCI-Expanded, Scopus)

143. Basophil activation test for inhalant allergens in pediatric patients with allergic rhinitis.

OGULUR I., Kiykim A., BARIS S., OZEN A., YUCE E., KARAKOC-AYDINER E.

International journal of pediatric otorhinolaryngology , cilt.97, ss.197-201, 2017 (SCI-Expanded, Scopus)

144. Could Sublingual Immunotherapy Affect Oral Health in Children with Asthma and/or Allergic Rhinitis Sensitized to House Dust Mite?

KIYKIM A., MUMCU G., ÖĞÜLÜR İ., Karakoc-Aydiner E., DİRESKENELİ R. H., BARIŞ S., et al.

INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY , cilt.174, sa.1, ss.52-56, 2017 (SCI-Expanded, Scopus)

145. The plethora, clinical manifestations and treatment options of autoimmunity in patients with primary immunodeficiency

Baris H. E., KIYKIM A., Nain E., ÖZEN A. O., Karakoc-Aydiner E., BARIŞ S.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.51, sa.4, ss.186-192, 2016 (ESCI, Scopus, TRDizin)

146. Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1

BARIŞ S., Alroqi F., KIYKIM A., Karakoc-Aydiner E., ÖĞÜLÜR İ., Ozen A., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.36, sa.7, ss.641-648, 2016 (SCI-Expanded, Scopus)

147. Nijmegen-Breakage Syndrome; Two Siblings Presenting with Different Phenotypes

KIYKIM A., AYDINER E., ÖĞÜLÜR İ., BARIŞ S., Ozen A., Serifov K., et al.

ASTIM ALLERJI IMMUNOLOJI , cilt.14, sa.2, ss.98-102, 2016 (ESCI, TRDizin)

148. Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia.

Kiykim A., GARNCARZ W., Karakoc-Aydiner E., Ozen A., Kiykim E., YEŞİL G., et al.

Clinical immunology (Orlando, Fla.) , cilt.165, ss.1-3, 2016 (SCI-Expanded, Scopus)

149. Use of subcutaneous immunoglobulin in primary immune deficiencies

AYDINER E., KIYKIM A., BARIŞ S., Ozen A., Barlan I.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.51, sa.1, ss.8-14, 2016 (ESCI, Scopus, TRDizin)

150. Two patients with novel missense mutation in the purine nucleoside phosphorylase gene without serious or recurrent infections

KIYKIM A., Simsek I. E., KIYKIM E., Karakoc-Aydiner E., BARIŞ S., ÖZEN A. O., et al.

Clinical and Experimental Neuroimmunology , cilt.7, sa.1, ss.79-82, 2016 (Scopus)

151. Primary catastrophic antiphospholipid syndrome in an 8 year-old-girl

Baris H. E., Aksu Limon C., Vural I., KEPENEKLİ KADAYİFCİ E., KOÇ A., Kiykim A., et al.

MARMARA MEDICAL JOURNAL , cilt.29, sa.1, ss.41-44, 2016 (ESCI, Scopus, TRDizin)

152. G6PC3 Deficiency: Primary Immune Deficiency Beyond Just Neutropenia

KIYKIM A., BARIŞ S., Karakoc-Aydiner E., ÖZEN A. O., ÖĞÜLÜR İ., BOZKURT S., et al.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.37, sa.8, ss.616-622, 2015 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

153. Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: A double-blind, double-dummy study

ÖZEN A. O., ÖZEN A. O., KIYKIM A., ÖZEN A. O., ÖZEN A. O., ÖZEN A. O., et al.

RESPIRATORY MEDICINE , cilt.109, sa.9, ss.1120-1125, 2015 (SCI-Expanded, Scopus)

154. The Effect of Vitamin D Supplementation on Subcutaneous Allergen Immunotherapy in House Dust Mite Sensitive Asthmatic Children

BARIŞ S., Ozen A., Cagan H., KIYKIM A., Tulunay A., Karakoc-Aydiner E., et al.

TURKISH JOURNAL OF IMMUNOLOGY , cilt.3, sa.2, ss.54-63, 2015 (ESCI, Scopus)

155. Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase C delta Deficiency

KIYKIM A., ÖĞÜLÜR İ., BARIŞ S., Salzer E., Karakoc-Aydiner E., ÖZEN A. O., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.35, sa.6, ss.523-526, 2015 (SCI-Expanded, Scopus)

156. Oxidative Burst with Dihydrorhodamine Test: Reference Values in Healthy Controls

Cicekkoku D., ÖĞÜLÜR İ., Karakoc-Aydiner E., BARIŞ S., KIYKIM A., Ozen A., et al.

TURKISH JOURNAL OF IMMUNOLOGY , cilt.3, sa.2, ss.49-53, 2015 (ESCI, Scopus)

157. Biotinidase deficiency mimicking primary immune deficiencies.

Kiykim E., Kiykim A., Cansever M. Ş., Aktuglu Zeybek C. A.

BMJ case reports , cilt.2015, 2015 (Scopus)

158. JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family

BARIŞ S., Karakoc-Aydiner E., ÖZEN A. O., DELİL K., KIYKIM A., ÖĞÜLÜR İ., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.35, sa.4, ss.339-343, 2015 (SCI-Expanded, Scopus)

159. TURKISH NATIONAL SEVERE CONGENITAL NEUTROPENIA REGISTRY

Karapinar D. Y., Patiroglu T., Metin A., Caliskan U., CELKAN T. T., YILMAZ B., et al.

HAEMATOLOGICA , cilt.100, ss.11, 2015 (SCI-Expanded, Scopus)

160. Profile of the patients who present to immunology outpatient clinics because of frequent infections.

Aldırmaz S., Yücel E., KIYKIM A., ÇOKUĞRAŞ H. C., Akçakaya N., Camcioğlu Y.

Turk pediatri arsivi , cilt.49, sa.3, ss.210-6, 2014 (ESCI, Scopus, TRDizin)

161. Vitamin D as an adjunct to subcutaneous allergen immunotherapy in asthmatic children sensitized to house dust mite.

BARIS S., Kiykim A., OZEN A., TULUNAY A., KARAKOC-AYDINER E., BARLAN I.

Allergy , cilt.69, ss.246-53, 2014 (SCI-Expanded, Scopus)

162. Comparison of oral microflora in selective IgA deficiency and X linked agammaglobulinemia cases with control group Selektif IgA eksikliǧi ve X'e baǧlı agammaglobülinemi olgularında aǧız mikroflorasının saǧlam grupla karşılaştırılması

KIYKIM A., Topçuoǧlu N., Külekçi G., ÇOKUĞRAŞ H. C., Akçakaya N., Camcioǧlu Y.

Turk Pediatri Arsivi , cilt.48, sa.3, ss.204-209, 2013 (SCI-Expanded, ESCI, Scopus, TRDizin)

163. The phenotype-genotype relationship in severe congenital neutropenia patients

BARIŞ S., Aydiner E. K., KIYKIM A., Cagan H. H., Boztug K., Barlan I.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.47, sa.4, ss.272-277, 2012 (SCI-Expanded, Scopus, TRDizin)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 47

1. Type I interferon response in MSMD patients: evaluation of IFN signature score as a biomarker

Karacan A., Suleyman A., Hatipoglu N., YÜCEL E., KIYKIM A., Yucesoy M. A., et al.

58th Conference of the European-Society-of-Human-Genetics (ESHG), Milan, İtalya, 24 - 27 Mayıs 2025, cilt.33, ss.731-732, (Özet Bildiri)

2. Preclinical Applications of Lentiviral Gene Therapy in X-linked Agammaglobulinemia (XLA)

ŞAHİN İ., KIYKIM A., OCAK S., EKEN Y., ÖNDER G., Gundogdu M., et al.

58th Conference of the European-Society-of-Human-Genetics (ESHG), Milan, İtalya, 24 - 27 Mayıs 2025, cilt.33, ss.1179, (Özet Bildiri)

3. Exploring Germline Variations and Predisposition in Childhood Lymphoma

Sudutan T., Khidzhaev K., ERBİLGİN Y., ALTINDİREK D., Kocaaga S., Saritas M., et al.

57th Conference of the European-Society-of-Human-Genetics (ESHG), Berlin, Almanya, 1 - 04 Haziran 2024, cilt.32, ss.1246, (Özet Bildiri)

4. Comparison of respiratory function, exercise capacity, fatigue, and perception of dyspnea in asthmatic children with and without respiratory dysfunction

Kulli H. D., Ucgun H., Kaya M., Karaaslan H. B. G., KIYKIM A.

European-Respiratory-Society Congress (ERS), Vienna, Avusturya, 7 - 11 Eylül 2024, (Özet Bildiri)

5. Do pulmonary and extrapulmonary characteristics differ between asthmatic and healthy children?

Kaya M., Ucgun H., Karaaslan B. G., KIYKIM A., Kulli H. D.

European-Respiratory-Society Congress (ERS), Vienna, Avusturya, 7 - 11 Eylül 2024, (Özet Bildiri)

6. Evaluation of hypersensitivity reactions in children with rheumatologic diseases during treatment with biological agents

Karaaslan H. B. G., Meric Z., Aydemir S., Papagan S., Kaynar O., Taskin Z., et al.

Annual Hybrid Congress of the European-Academy-of-Allergy-and-Clinical-Immunology (EAACI), Hamburg, Almanya, 9 - 11 Haziran 2023, cilt.78, ss.37-38, (Özet Bildiri)

7. OUTCOME OF PATIENTS WITH SIGNAL-TRANSDUCER AND ACTIVATOR OF OF TRANSCRIPTION 1 (STAT1) GAIN-OF-FUNCTION VARIANTS AFTER HAEMATOPOIETIC STEM CELL TRANSPLANTATION

Buddingh E. P., Slatter M. A., Kiykim A., Alonso Garcia L., Leahy T. R., Chellapandian D., et al.

49th Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation, ELECTR NETWORK, 23 - 26 Nisan 2023, ss.392-393, (Özet Bildiri)

8. Geç tanınmış bir Gaucher Hastalığı disiplinler arası iletişimin önemi

KIYKIM E., AKTUĞLU ZEYBEK A. Ç., AYDIN A., KIYKIM A.

III. Uluslararası Katılımlı Lizozomal Depo Hastalıkları Kongresi, Girne, Kıbrıs (Kktc), 26 - 29 Nisan 2012, cilt.4, ss.56, (Özet Bildiri)

9. PRİMER İMMÜN YETMEZLİK HASTA VE SAĞLIKLI BİREYLERDE TREC/KREC KOPYA SAYILARININ ANALİZİ VE KULLANIMI

Şentürk G., NG Y. Y., ERTAN S. B., ÖĞÜLÜR İ., KIYKIM A., ÖZEN A. O., et al.

1st Bursa International Genetics Days: Dermatogenetics Symposium, Türkiye, 09 Ocak 2020, (Özet Bildiri)

10. Primer İmmün Yetmezlik hastaları ve sağlıklı bireylerde TREC/KREC kopya sayılarının analizi ve kullanımı: Pilot çalışma

Şentürk G., NG Y. Y., ERTAN S. B., YİLMAZ H., ÖĞÜLÜR İ., FIRTINA S., et al.

45. Ulusal Hematoloji Kongresi, Türkiye, 30 Ekim 2019, (Özet Bildiri)

11. MMR immunisation practices in children with a history of egg allergy

Baris E., Boran P., Kiykim A., Safa B., Ahmet O., Karakoc-Aydiner E.

Congress of the European-Academy-of-Allergy-and-Clinical-Immunology (EAACI), Lisbon, Portekiz, 1 - 05 Haziran 2019, cilt.74, ss.895, (Özet Bildiri)

12. Immunological Evaluation of Patients with Organic Acidemia

USLU İ., AYDEMİR S., KIYKIM A., KIYKIM E., AKTUĞLU ZEYBEK A. Ç., ÇOKUĞRAŞ H. C.

INTERNATIONAL INBORN ERRORS OF METABOLISM AND NUTRITION CONGRESS, İstanbul, Türkiye, 10 - 14 Nisan 2019, (Tam Metin Bildiri)

13. Evaluation of a standardized bakery product (SUTMEK) as a potential tool for baked milk tolerance and immunotherapy research studies

KIYKIM A., Karakoc-Aydiner E., Gunes E., Nain E., ÖĞÜLÜR İ., AKTAÇ Ş., et al.

Congress of the European-Academy-of-Allergy-and-Clinical-Immunology (EAACI), Munich, Almanya, 26 - 30 Mayıs 2018, cilt.73, ss.122-123, (Özet Bildiri)

14. SOTI in IgE mediated cow's milk allergy, two case reports

Kasap N., KIYKIM A., Karakoc-Aydiner E., ÖZEN A. O., BARIŞ S.

Congress of the European-Academy-of-Allergy-and-Clinical-Immunology (EAACI), Munich, Almanya, 26 - 30 Mayıs 2018, cilt.73, ss.842, (Özet Bildiri)

15. The effect of high dose vitamin-D on lymphocytes in children with atopic dermatitis

ÖĞÜLÜR İ., ÖZEN A. O., Nain E., KIYKIM A., BARIŞ S., Karakoc-Aydiner E.

Congress of the European-Academy-of-Allergy-and-Clinical-Immunology (EAACI), Munich, Almanya, 26 - 30 Mayıs 2018, cilt.73, ss.798, (Özet Bildiri)

16. “Çıplak” Ağır Kombine İmmün Yetmezlikli 2 Kardeşte Tanımlanan Yeni Foxn1 Mutasyonu

FIRTINA S., ÇİPE F., KIYKIM A., HATIRNAZ N. Ö., SUDUTAN T., AYDOĞMUŞ Ç., et al.

4. Klinik İmmünoloji Kongresi, Türkiye, 11 - 14 Nisan 2018, (Özet Bildiri)

17. Detection of T-cell Receptor Excision Circles (TRECs) in Dried Blood Spot (DBS) Implementation of Routine Newborn Screening For The Diagnosis of SCID,

NG Y. Y., FIRTINA S., HATIRNAZ N. Ö., KIYKIM A., AYDINER E., ÖZEN A. O., et al.

4. Klinik İmmünoloji Kongresi, Türkiye, 11 - 14 Nisan 2018, (Özet Bildiri)

18. Hypomorfic JAK3 and IL2RG Mutations Presenting with a Predominantly Antibody DEficiency Phenotype

KIYKIM A., FIRTINA S., ye z., ee n., SAYİTOĞLU M., BARIŞ S., et al.

European Society for Immunodeficiencies (ESID) Meeting, 11 - 14 Kasım 2017, (Özet Bildiri)

19. Diagnostics Of Primary Antibody Deficiencies Through Targeted Next Generation Sequencing Panel

NG Y. Y., FIRTINA S., HATIRNAZ N. Ö., camcıoğlu y., AYDINER E., KIYKIM A., et al.

International Primary Immunodeficiencies Congress, 8 - 10 Kasım 2017, (Özet Bildiri)

20. Molecular Dıagnosıs Of Scıd Patıents By A Custom Desıgned Targeted Next Generatıon Sequencıng Panel

FIRTINA S., SAYİTOĞLU M., HATIRNAZ N. Ö., KIYKIM A., AYDINER E., BARIŞ S., et al.

International Primary Immunodeficiencies Congress, 8 - 10 Kasım 2017, (Özet Bildiri)

21. Primer Antikor Yetersizliği Olan Hastalarda Saptanan Bruton Tirozin Kinaz (BTK) Gen Varyasyonları

FIRTINA S., NG Y. Y., HATIRNAZ N. Ö., HASKOLOĞLU Z. Ş., KIYKIM A., AYDINER E., et al.

XXIV. Ulusal İmmünoloji Kongresi, Türkiye, 27 - 30 Nisan 2017, (Özet Bildiri)

22. Erişkin Yaşta Tanı Alan X’e Bağlı Hipomorfik İmmün Yetmezlik

KIYKIM A., FIRTINA S., NAİM E., BARIŞ S., SAYİTOĞLU M., AYDINER E., et al.

3. Klinik İmmünoloji Kongresi, Türkiye, 12 - 15 Nisan 2017, (Özet Bildiri)

23. Ağır Kombine İmmün Yetmezlik Hastalarında TREC/KREC Analizleri ve Klinik Uyumun Araştırılması

NG Y. Y., FIRTINA S., HATIRNAZ N. Ö., nepesov s., KIYKIM A., AYDINER E., et al.

3. Klinik İmmünoloji Kongresi, Türkiye, 12 - 15 Nisan 2017, (Özet Bildiri)

24. Turkish National Severe Congenital Neutropenia Registry

YILMAZ KARAPINAR D., Karakas Z., PATIROĞLU T., Metin A., Caliskan U., Celkan T., et al.

58th Annual Meeting and Exposition of the American-Society-of-Hematology (ASH), California, Amerika Birleşik Devletleri, 3 - 06 Aralık 2016, cilt.128, (Özet Bildiri)

25. Ağır Kombine İmmün Yetmezlik Hastalarında Yeni Varyasyonların Tespiti: CD3E örneği

FIRTINA S., NG Y. Y., HATIRNAZ N. Ö., nepesov s., CAMCIOĞLU Y., KIYKIM A., et al.

XXIII. Ulusal Allerji ve Klinik İmmünoloji Kongresi, Türkiye, 8 - 12 Ekim 2016, (Özet Bildiri)

26. IDENTIFICATION OF GENETIC VARIATION BY TARGETED NEXT GENERATION SEQUENCING IN TURKISH SCID PATIENTS

FIRTINA S., SAYİTOĞLU M., HATIRNAZ N. Ö., KIYKIM A., AYDINER E., nepesov s., et al.

17th Biennial Meeting of the European Society for Immunodeficiencies (ESID), 21 - 24 Eylül 2016, (Özet Bildiri)

27. Detection of genetic variations in severe combined immunodeficiency (SCID) patients by targeted amplicon sequencing

NG Y. Y., FIRTINA S., HATIRNAZ N. Ö., KIYKIM A., AYDINER E., nepesov s., et al.

Molecular Immunology Immunogenetics (MIMIC) Congress, 2016, 27 - 30 Nisan 2016, (Özet Bildiri)

28. Ağır Kombine İmmün Yetmezlik Hastalarında Yeni Nesil Dizileme Yöntemi ile Genetik Varyasyonların Saptanması

FIRTINA S., NG Y. Y., HATIRNAZ N. Ö., KIYKIM A., AYDINER E., NEPESOV S., et al.

2. Klinik İmmünoloji Kongresi, Türkiye, 31 Mart - 03 Nisan 2016, (Özet Bildiri)

29. A PATIENT WITH A MUTATION IN CD40L PRESENTING WITH PANHYPOGAMMAGLOBULINEMIA AND NATURAL KILLER CELL LYMPHOPENIA

BARIŞ S., Karakoc-Aydiner E., KIYKIM A., Nain E., Ozen A., Hoyos-Bachiloglu R., et al.

CIS Annual Meeting on Immune Deficiency and Dysregulation North American Conference, Massachusetts, Amerika Birleşik Devletleri, 14 - 17 Nisan 2016, cilt.36, ss.311, (Özet Bildiri)

30. DO CUT-OFF VALUES OF IgE AND EOSINOPHIL LEVELS HELP DISCRIMINATE HYPERIGE SYNDROME FROM ATOPIC DISEASES?

Karakoc-Aydiner E., KIYKIM A., Yuce E. G., Baris E., Nain E., Keles S., et al.

CIS Annual Meeting on Immune Deficiency and Dysregulation North American Conference, Massachusetts, Amerika Birleşik Devletleri, 14 - 17 Nisan 2016, cilt.36, ss.254, (Özet Bildiri)

31. MONOGENIC PRIMARY IMMUNE DEFICIENCIES IDENDIFIED IN A PEDIATRIC-ONSET CVID COHORT, IS THERE A PREDICTIVE MARKER?

Karakoc-Aydiner E., KIYKIM A., Nain E., Kacmaz M., Ogulur I., BARIŞ S., et al.

CIS Annual Meeting on Immune Deficiency and Dysregulation North American Conference, Massachusetts, Amerika Birleşik Devletleri, 14 - 17 Nisan 2016, cilt.36, ss.253-254, (Özet Bildiri)