Hakkımda
Fırat Üniversitesi Tıp Fakültesi'ni bitirdi. Uludağ Üniversitesi Tıp Fakültesinde Çocuk Sağlığı ve Hastalıkları ihtisası, Hacettepe Tıp Fakültesi Çocuk İmmunoloji bölümünde İmmünoloji yan dal ihtisası yaptı. 2000 yılında Uludağ Üniversitesi Tıp Fakültesi Çocuk İmmünoloji Bilim Dalı'nı kurdu. 2000 yılında doçent, 2006 yılında profesör oldu. 2007 yılında University College of London, Royal Free Hospital'da Yaygın değişken immün yetmezlikler, Lenfoproliferatif hastalıklar ve Konjenital nötropeni konularında immünogenetik çalışmalar yapmıştır. Halen Uludağ Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları AD 'nda Çocuk İmmunoloji Bilim Dalı Başkanı olarak görev yapmaktadır.

Üniversite Adres: Uludağ Üniversitesi Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, İmmünoloji Bilim Dalı, Görükle-Bursa.
Telefon: 0224 295 04 41
Faks: 0224 442 81 43

Şu anki görev pozisyonu
Profesör Doktor. Uludağ Üniversitesi Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, İmmünoloji Ünitesi.
Üye olduğu dernek ve kuruluşlar
  • Milli Pediatri Derneği
  • ÇOSAD: Çocuk Sağlığı ve Hastalıkları Derneği
  • Türk İmmünoloji Derneği
  • Alerji ve Klinik İmmünoloji Derneği
  • ESID (European society for immunodeficiencies)
  • ESPID (European society for pediatric infection disease)
  • EAACI European Academy of Allergology and Clinical Immunology
Kitap Bölüm Yazarlığı
  1. Kilic SS. Recurrent respiratory tract infection. Recent Advances in Pediatrics, Jaypee Brothers Medical Publishers, New Delhi, ISBN 81-8061-297-X , pp1-18, 2004
  2. Kilic SS. Recurrent aphthous stomatitis. Recent Advances in Pediatrics, Jaypee Brothers Medical Publishers, New Delhi, ISBN 81-8061-297-X, pp 63-75 , 2004
  3. Kilic SS. The child with fever. Recent Advances in Pediatrics, Jaypee Brothers Medical Publishers, New Delhi, 441 ISBN 81-8061-297-X , pp261-275, 2004
  4. Kilic SS. Sigara ve immünite. Sigara ve Sağlık, Bursa, 463 (Bölüm sayfa: 6), 2002.
  5. Kilic SS. Takayasu arteritis. Recent Advances in Pediatrics, Jaypee Brothers Medical Publishers, New Delhi, ISBN 81-8061-297-X , pp 338-354, 2006.
Yayınlar
  1. Hacımustafaoğlu M, Ener B, Tarım Ö, Kılıç S, Tanrıtanır A, Ildırım İ. Systemic candidiasis with acute Epstein-Barr virus infection. Acta Paediatrica 1997; 86:1267-1270.
  2. Kılıç S, Köksal N, Hacımustafaoğlu M. Varicella arthritis. The New Journal of Medicine 1998; 15(1): 51-52.
  3. Tezcan İ, Sanal Ö, Ersoy F, Uçkan D, Kılıç S, Metin A, Çetin M, Akın R, Öner C ve Tuncer A.M. Successful bone marrow transplantation in a case with Griscelli disease who presented with neurological manifestations. Bone Marrow Transplantation 1999; 24: 931-933.
  4. Kılıç S, Tarım Ö, Eralp Ö. Serum prolactin in neonatal seizures. Pediatrics International 1999:41 (1):61-64.
  5. Kılıç S.S, Ersoy F, Sanal Ö, Türkbay D ve Tezcan İ. Alopecia Universalis in a patient with common variable immunodeficiency. Pediatric Dermatology 1999; 16(4): 305-307.
  6. Çelebi S, Kılıç S.S ve Okan M. Psoriasis in a patient with neurofibromatosis. The Turkish Journal of Pediatrics 1999; 41(4): 545-549.
  7. Kılıç S.S, Ersoy F, Sanal Ö, Tezcan İ. Dermatomyositis-like syndrome in a patient with X-linked Agammaglobulinemia. Turkish Journal of Immunology. 1999; 4: 25-27.
  8. Tezcan İ, Ersoy F, Sanal Ö, Uçkan D, Kılıç S, Tuncer M, Berkel Aİ. Allogeneic bone marrow transplantation for children with severe combined immunodeficiency. Bone Marrow Transplantation 1999; 23 supp 1: S109.
  9. Gerçeker FÖ, Tezcan İ, Berkel Aİ, Özcan ÖA, Özkara OS, Ersoy F, Sanal Ö, Kılıç S, Metin A, Özgüç M. The frequency of Mannose Binding Protein gene mutations in Turkish patients with different infections and healthy individuals. European Journal of Human Genetics 1999; 7 (supp 1): p586.
  10. Kılıç S.S, Tezcan İ, Sanal Ö, Metin A, Ersoy F. Transient hypogammaglobulinemia of infancy. Pediatrics International 2000; 42: 647-650.
  11. Sanal Ö, Özçelik U, Kuyucu N, Tezcan İ, Kütükçüler N, Kiper N, Metin A, Kılıc SS, Anadol D, Göçmen A, Berkel Aİ, Yalçın I, Ersoy F, de Boer A, Verhagen C, Ottenhoff THM. Heterogeneity in phenotypic features in ptients with IL12b1 deficiency: Clinical and laboratory features and response to therapy in five patients. International Proceedings Division, 2000.
  12. Kılıç S.S, Hacımustafaoğlu M, Çelebi S, Karadeniz A, Ildırım İ. Low dose cyclosporin A treatment in generalized pustular psoriasis. Pediatric Dermatology 2001;18(3):246-248.
  13. Kılıç S.S, Talim B, Tezcan İ, Sanal Ö, Çağlar M, Ersoy F. Herpes Simplex virus hepatitis in a patient with severe combined immunodeficiency. International Pediatrics 2001; 16(3): 155-157.
  14. Kılıç S.S, Bostan Ö, Çil E. Juvenile rheumatoid arthritis in a patient with common variable immunodeficiency. International Pediatrics 2001; 16-1: 94-95.
  15. Kılıç S.S.,Tezcan İ, Sanal Ö, Ersoy F. Common variable immunodeficiency in a patient with neurofibromatosis. Pediatrics International 2001;43-6: 691-693.
  16. Düzova A, Topaloğlu R, Sanal O, Kilic S, Mazza C, Besbas N, Bakkaloglu. Henoch-Schonlein purpura in Wiskott-Aldrich syndrome. Pediatr Nephrol. 2001 Jun;16(6):500-2.
  17. Kılıç S.S, Bostan Ö, Çil E. Takayasu arteritis in a case with low CD4 T+ lymphopenia without evidence of HIV infection. Annals of the Rheumatic Diseases 2002; 61(1): 92-93
  18. Kılıç S.S, Sanal Ö, Tezcan İ, Ersoy F. Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome. The Turkish Journal of Pediatrics. 2002 ;44(4):357-9
  19. Kılıç S.S. Leukocyte Adhesion Deficiency in a Case Presenting as Septic Arthritis. International Pediatrics 2002;17(2):96-97.
  20. Kılıç S.S. Omenn’s Syndrome. International Pediatrics 2003; 18(1):41-42.
  21. Kılıc SS, Gürpınar A, Yakut T, Egeli Ü, Dogruyol H. Esophageal atresia and tracheo-esophageal fistula in a patient with DiGeorge Syndrome. J Pediatr Surg 2003 ;38(8):E21-3.
  22. Kılıc SS, Oral HB, Budak F, Yavascaoglu B, Goral G. Immunoglobulin subclasses and HLA alleles in immunoglobulin A deficiency. Indian J Pediatr 2003; 70: 389-392.
  23. Kılıç S.S, Kose H, Ozturk H. Pulmonary involvement in a patient with dyskeratosis congenita. Pediatrics International (2003) 45, 740-742.
  24. Kılıc SS, Kezer EY, Ozarda YI, Yakut T, Aydin S, Ulus IH. Vitamin A deficiency in patients with common variable immunodeficiency. J Clin Immunol 2005; 25(3):275-80.
  25. Kılıc SS. Anti-tumour necrosis factor alpha treatment of juvenil idiopathic arthritis in a patient with common variable immunodeficiency. J Tropic Pediatr 2005; 51(3):194-5. Epub 2005 Apr 26.
  26. Kılıc SS, Cil E, Meral A, Villa A. Cardiac Thrombus in Omenn Syndrome. J Pediatr Cardiol 2005; 26(5):694-7.
  27. Kilic SS, Donmez O, Sloan EA, Elizondo LI, Huang C, Andre JL, Bogdanovic R, Cockfield S, Cordeiro I, Deschenes G, Frund S, Kaitila I, Lama G, Lamfers P, Lucke T, Milford DV, Najera L, Rodrigo F, Saraiva JM, Schmidt B, Smith GC, Stajic N, Stein A, Taha D, Wand D, Armstrong D, Boerkoel CF. Association of migraine-like headaches with Schimke immunoosseous dysplasia. Am J Med Genet 2005; 135(2):206-10.
  28. Bayrakci B, Ersoy F, Sanal O, Kilic S, Metin A, Tezcan I. The efficacy of immunoglobulin replacement therapy in the long-term follow-up of the B-cell deficiencies (XLA, HIM, CVID). Turk J Pediatr. 2005 ;47(3):239-46.
  29. Yakut T, Kılıc SS , Cil E, Yapici E, Egeli Ü. Use of FISH technique in the diagnosis of DiGeorge syndrome/chromosome 22q11.2 deletion syndrome. Pediatr Surg Int 2006; 22(4):380-3.
  30. Kilic SS, Kilicbay F. Interferon- alpha treatment of molluscum contagiosum in a patient with hyper Ig E syndrome. Pediatrics 2006; 117(6): 1253-1255.
  31. Giambra V, Martinez-Labarga C, Giufre' M, Modiano D, Simpore' J, Gisladottir BK, Francavilla R, Zhelezova G, Kilic SS, Crawford M, Biondi G, Rickards O, Frezza D. Immunoglobulin Enhancer HS1,2 polymorphism: a new powerful anthropogenetic marker. Ann Hum Genet. 2006 ;70(Pt 6):946-50.
  32. Kilic SS. A small girl with a bird-like face. Acta Paediatr. 2006 Nov;95(11):1505-8.
  33. Clewing JM, Fryssira H, Goodman D, Smithson SF, Sloan EA, Lou S, Huang Y, Choi K, Lucke T, Alpay H, Andre JL, Asakura Y, Biebuyck-Gouge N, Bogdanovic R, Bonneau D, Cancrini C, Cochat P, Cockfield S, Collard L, Cordeiro I, Cormier-Daire V, Cransberg K, Cutka K, Deschenes G, Ehrich JH, Frund S, Georgaki H, Guillen-Navarro E, Hinkelmann B, Kanariou M, Kasap B, Kilic SS, Lama G, Lamfers P, Loirat C, Majore S, Milford D, Morin D, Ozdemir N, Pontz BF, Proesmans W, Psoni S, Reichenbach H, Reif S, Rusu C, Saraiva JM, Sakallioglu O, Schmidt B, Shoemaker L, Sigaudy S, Smith G, Sotsiou F, Stajic N, Stein A, Stray-Pedersen A, Taha D, Taque S, Tizard J, Tsimaratos M, Wong NA, Boerkoel CF. Schimke immunoosseous dysplasia: suggestions of genetic diversity. Hum Mutat. 2007 Mar;28(3):273-83.
  34. Recio MJ, Moreno-Pelayo MA, Kilic SS, Guardo AC, Sanal O, Allende LM, Perez-Flores V, Mencia A, Modamio-Hoybjor S, Seoane E, Regueiro JR. Differential biological role of CD3 chains revealed by human immunodeficiencies. J Immunol. 2007 15;178(4):2556-64.
  35. Kilic SS, Giraud M, Schmitt S, Bezieau S, Kury S. A novel mutation of the SLC39A4 gene causing acrodermatitis enteropathica. Br J Dermatol. 2007; 157(2):386-7.
  36. Pasvolsky R, Feigelson SW, Kilic SS, Simon AJ, Tal-Lapidot G, Grabovsky V, Crittenden JR, Amariglio N, Safran M, Graybiel AM, Rechavi G, Ben-Dor S, Etzioni A, Alon R. A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and platelets. J Exp Med. 2007 Jul 9;204(7):1571-82.
  37. Yeganeh M, Henneke P, Rezaei N, Ehl S, Thiel D, Matamoros N, Pietrogrande C, Espanol T, Litzman J, Franco JL, Sanal O, Kilic SS, Breborowicz A, Plebani A, Renner E, Rothenfusser S, Hawn TR, Woellner C, Grimbacher B. Toll-Like Receptor Stimulation Induces Higher TNF-alpha Secretion in Peripheral Blood Mononuclear Cells from Patients with Hyper IgE Syndrome. Int Arch Allergy Immunol. 2008;146(3):190-194 .
  38. Guerrini MM, Sobacchi C, Cassani B, Abinun M, Kilic SS, Pangrazio A, Moratto D, Mazzolari E, Clayton-Smith J, Orchard P, Coxon FP, Helfrich MH, Crockett JC, Mellis D, Vellodi A, Tezcan I, Notarangelo LD, Rogers MJ, Vezzoni P, Villa A, Frattini A. Human Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia due to TNFRSF11A (RANK) Mutations. Am J Hum Genet. 2008 Jul;83(1):64-76.
  39. Turul Özgür T, Türkkanı Asal G, Cetinkaya D, Orhan D, Kılıç SS, Usta Y, Ozen H, Tezcan I. Hematopoietic stem cell transplantation in a CD3gamma-deficient infant with inflammatory bowel disease. Pediatr Transplant. 2008; 12: 910-913.
  40. Kilic SS, Etzioni A. The Clinical Spectrum of Leukocyte Adhesion Deficiency (LAD) III due to Defective CalDAG-GEF1. J Clin Immunol. 2008 Aug 16. [Epub ahead of print]
  41. Mory A, Feigelson SW, Yarali N, Kilic SS, Bayhan GI, Gershoni-Baruch R, Etzioni A, Alon R. Kindlin-3: a new gene involved in the pathogenesis of LAD-III. Blood. 2008;112(6):2591.
  42. Kilic SS, Ozturk R, Sarisozen B, Rotthier A, Baets J, Timmerman V. Humoral immunodeficiency in congenital insensitivity to pain with anhidrosis. Neurogenetics. 2008 Dec 17. [Epub ahead of print]
  43. Conley ME, Dobbs AK, Farmer DM, Kilic S, Paris K, Grigoriadou S, Coustan-Smith E, Howard V, Campana D. Primary B cell immunodeficiencies: comparisons and contrasts. Annu Rev Immunol. 2009;27:199-227
  44. Manevich-Mendelson E, Feigelson SW, Pasvolsky R, Aker M, Grabovsky V, Shulman Z, Kilic SS, Rosenthal-Allieri MA, Ben-Dor S, Mory A, Bernard A, Moser M, Etzioni A, Alon R. Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions. Blood. 2009 Jul 17. [Epub ahead of print]
  45. Rotthier A, Baets J, Vriendt ED, Jacobs A, Auer-Grumbach M, Lévy N, Bonello-Palot N, Kilic SS, Weis J, Nascimento A, Swinkels M, Kruyt MC, Jordanova A, De Jonghe P, Timmerman V. Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Brain. 2009 Aug 3. [Epub ahead of print]
  46. Elhasid R, Kilic SS, Ben-Arush M, Etzioni A, Rowe JM. Prompt recovery of recipient hematopoiesis after two consecutive haploidentical peripheral blood SCTs in a child with leukocyte adhesion defect III syndrome. Bone Marrow Transplant. 2009 Jul 6.
  47. Hanada R, Leibbrandt A, Hanada T, Kitaoka S, Furuyashiki T, Fujihara H, Trichereau J, Paolino M, Qadri F, Plehm R, Klaere S, Komnenovic V, Mimata H, Yoshimatsu H, Takahashi N, von Haeseler A, Bader M, Kilic SS, Ueta Y, Pifl C, Narumiya S, Penninger JM. Central control of fever and female body temperature by RANKL/RANK. Nature. 2009;462(7272):505-9.
  48. Giambra V, Cianci R, Lolli S, Mattioli C, Tampella G, Cattalini M, Kilic SS, Pandolfi F, Plebani A, Frezza D. Allele *1 of HS1.2 Enhancer Associates with Selective IgA Deficiency and IgM Concentration. J Immunol. 2009 Dec 15;183(12):8280-5
  49. Kilic SS, Mustafayeva S, Ipek K, Adim SB. Leukocytoclastic Vasculitis in Patients with Severe Congenital Neutropenia. J Trop Pediatr. 2010 Jan 25. [Epub ahead of print]
  50. Woellner C, Gertz EM, Schäffer AA, Lagos M, Perro M, Glocker EO, Pietrogrande MC, Cossu F, Franco JL, Matamoros N, Pietrucha B, Heropolitanska-Pliszka E, Yeganeh M, Moin M, Español T, Ehl S, Gennery AR, Abinun M, Breborowicz A, Niehues T, Kilic SS, Junker A, Turvey SE, Plebani A, Sánchez B, Garty BZ, Pignata C, Cancrini C, Litzman J, Sanal O, Baumann U, Bacchetta R, Hsu AP, Davis JN, Hammarström L, Davies EG, Eren E, Arkwright PD, Moilanen JS, Viemann D, Khan S, Maródi L, Cant AJ, Freeman AF, Puck JM, Holland SM, Grimbacher B.Mutations in the signal transducer and activator of transcription 3 (STAT3) and diagnostic guidelines for the Hyper-IgE Syndrome. The Journal of Allergy and Clinical Immunology 2010;125(2):424-432.
  51. Tanir S, Karkucak M, Yakut T, Kilic SS . Toll-like Receptor-9 Gene Polymorphism in Common Variable Immunodefi ciency. J Investig Allergol Clin Immunol. 2010;20(3):267-8.
  52. Kilic SS, Kavurt S, Balaban Adim S. Transfusion-associated graft-versus-host disease in severe combined immunodeficiency. J Investig Allergol Clin Immunol. 2010;20(2):153-6.
  53. de Paus RA, Kilic SS, van Dissel JT, van de Vosse E. Effect of amino acid substitutions in the human IFN-GR2 on IFN-G responsiveness. Genes Immun. 2011;12(2):136-44.
  54. Mazza C, Buzi F, Ortolani F, Vitali A, Notarangelo LD, Weber G, Bacchetta R, Soresina A, Lougaris V, Greggio NA, Taddio A, Pasic S, de Vroede M, Pac M, Kilic SS, Ozden S, Rusconi R, Martino S, Capalbo D, Salerno M, Pignata C, Radetti G, Maggiore G, Plebani A, Notarangelo LD, Badolato R. Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome. Clin Immunol. 2011;139(1):6-11
  55. Karali Y, Saglam H, Karali Z, Kilic SS. The use of complementary and alternative medicine in patients with common variable immunodeficiency. Investig Allergol Clin Immunol. 2011;21(6):480-3.
  56. Meyers G, Ng YS, Bannock JM, Lavoie A, Walter JE, Notarangelo LD, Kilic SS, Aksu G, Debré M, Rieux-Laucat F, Conley ME, Cunningham-Rundles C, Durandy A, Meffre E. Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans. Proc Natl Acad Sci U S A. 2011;108(28):11554-9.
  57. Grant AV, Boisson-Dupuis S, Herquelot E, de Beaucoudrey L, Filipe-Santos O, Nolan DK, Feinberg J, Boland A, Al-Muhsen S, Sanal O, Camcioglu Y, Palanduz A, Kilic SS, Bustamante J, Casanova JL, Abel L. Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease. J Med Genet. 2011;48(8):567-71.
  58. Liu L, Okada S, Kong XF, Kreins AY, Cypowyj S, Abhyankar A, Toubiana J, Itan Y, Audry M, Nitschke P, Masson C, Toth B, Flatot J, Migaud M, Chrabieh M, Kochetkov T, Bolze A, Borghesi A, Toulon A, Hiller J, Eyerich S, Eyerich K, Gulácsy V, Chernyshova L, Chernyshov V, Bondarenko A, Grimaldo RM, Blancas-Galicia L, Beas IM, Roesler J, Magdorf K, Engelhard D, Thumerelle C, Burgel PR, Hoernes M, Drexel B, Seger R, Kusuma T, Jansson AF, Sawalle-Belohradsky J, Belohradsky B, Jouanguy E, Bustamante J, Bué M, Karin N, Wildbaum G, Bodemer C, Lortholary O, Fischer A, Blanche S, Al-Muhsen S, Reichenbach J, Kobayashi M, Rosales FE, Lozano CT, Kilic SS, Oleastro M, Etzioni A, Traidl-Hoffmann C, Renner ED, Abel L, Picard C, Maródi L, Boisson-Dupuis S, Puel A, Casanova JL. Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis. J Exp Med. 2011 1;208(8):1635-48
  59. Karali Z, Basaranoglu ST, Karali Y, Oral B, Kilic SS. Autoimmunity and hepatitis A vaccine in children. J Investig Allergol Clin Immunol. 2011;21(5):389-93.