Dr. Öğr. Üyesi
Hande Kaymakçalan ÇELEBİLER

Dr. Öğr. Üyesi
Hande Kaymakçalan ÇELEBİLER

Randevu Al
Ataşehir Florence Nightingale Hastanesi
İstanbul Florence Nightingale Hastanesi
Kadıköy Florence Nightingale Tıp Merkezi
    • 2014

      TC Demiroğlu Bilim Üniversitesi / Şişli Florence Nightingale Hastanesi
      Çocuk Sağlığı ve Hastalıkları / Çocuk Genetik Birimi

      2009 - 2014
      Bahçeşehir Üniversitesi
      Genetik ve Biyoinformatik Bölümü Kurucusu ve Bölüm Başkanı

      2009
      Yale Üniversitesi, New Haven, Anabilim Dalı
      Nörogenetik Laboratuarı Araştırma Görevlisi

      2007 - 2009
      Yale Universitesi
      Nörogenetik Laboratuarı Araştırma Görevlisi

      2007 - 2009
      Yale Üniversitesi, New Haven, Anabilim Dalı
      Klinik Genetik Yan Dal Uzmanlık İhtisası

      2005 - 2006
      Imperial College/ St. Mary's Hospital, Londra
      İngiltere Çocuk Allerji ve Immunoloji Bölümü Genel Pediatrist

      2000 - 2003
      Cook County Hastanesi
      Çocuk Sağlığı ve Hastalıkları Uzmanlık Şikago, Anabilim Dalı Uzmanlık İhtisası

      1993 - 1996
      Marmara Üniversitesi Tıp Fakültesi
      Tıp Eğitimi

      • Türk Tabipler Birliği
      • Türk Pediatri Kurumu
      • American Society of Human Genetics
      • European Society of Human Genetics
      • American Academy of Pediatrics

       

  • Uluslararası Hakemli Dergilerde Yayımlanan Makaleler

      • 1: Caglayan AO, Baranoski JF, Aktar F, Han W, Tuysuz B, Guzel A, Guclu B, Kaymakcalan H, Aktekin B, Akgumus GT, Murray PB, Erson-Omay EZ, Caglar C, Bakircioglu M, Sakalar YB, Guzel E, Demir N, Tuncer O, Senturk S, Ekici B, Minja FJ, Šestan N, Yasuno K, Bilguvar K, Caksen H, Gunel M. Brain malformations associated with Knobloch syndrome--review of literature, expanding clinical spectrum, and identification of novel mutations. Pediatr Neurol. 2014
      • Dec;51(6):806-813.e8. doi: 10.1016/j.pediatrneurol.2014.08.025. Epub 2014 Sep 4.
      • PubMed PMID: 25456301.
      • 2: Fox AT, Kaymakcalan H, Perkin M, du Toit G, Lack G. Changes in peanut allergy prevalence in different ethnic groups in 2 time periods. J Allergy Clin Immunol. 2015 Feb;135(2):580-2. doi: 10.1016/j.jaci.2014.09.022. Epub 2014 Oct 29. PubMed PMID: 25441289.
      • 3: Caglayan AO, Comu S, Baranoski JF, Parman Y, Kaymakçalan H, Akgumus GT, Caglar C, Dolen D, Erson-Omay EZ, Harmanci AS, Mishra-Gorur K, Freeze HH, Yasuno K, Bilguvar K, Gunel M. NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy. Eur J Med Genet. 2015 Jan;58(1):39-43. doi: 10.1016/j.ejmg.2014.08.008. Epub 2014 Sep 9. PubMed PMID: 25220016.
      • 4:Radmanesh F, Caglayan AO, Silhavy JL, Yilmaz C, Cantagrel V, Omar T, Rosti B, Kaymakcalan H, Gabriel S, Li M, Sestan N, Bilguvar K, Dobyns WB, Zaki MS, Gunel M, Gleeson JG : Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalities. Am J Hum Genet. 2013 Mar 7;92(3):468-74
      • 5:Clark VE, Erson-Omay EZ, Serin A, Yin J, Cotney J, Ozduman K, Avşar T, Li J, Murray PB, Henegariu O, Yilmaz S, Günel JM, Carrión-Grant G, Yilmaz B, Grady C, Tanrikulu B, Bakircioğlu M, Kaymakçalan H, Caglayan AO, Sencar L, Ceyhun E, Atik AF, Bayri Y, Bai H, Kolb LE, Hebert RM, Omay SB, Mishra-Gorur K, Choi M, Overton JD, Holland EC, Mane S, State MW, Bilgüvar K, Baehring JM, Gutin PH, Piepmeier JM, Vortmeyer A, Brennan CW, Pamir MN, Kiliç T, Lifton RP, Noonan JP, Yasuno K, Günel M : Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO. Science. 2013Mar 1; 339(6123):1077-80
      • 6:Juho Harkonen, Hande Kaymakçalan, Pirjo Maki, Anja Taanila: Prenatal Health, Educational Attainment, and Intergenerational Inequality: The Northern Finland Birth Cohort 1966 Study. Demography (2012) 49: 525-552
      • 7:Barak T, Kwan KY, Louvi A, Demirbilek V, Saygı S, Tüysüz B, Choi M, Boyacı H, Doerschner K, Zhu Y, Kaymakçalan H, Yılmaz S, Bakırcıoğlu M, Cağlayan AO, Oztürk AK, Yasuno K, Brunken WJ, Atalar E, Yalçınkaya C, Dinçer A, Bronen RA, Mane S, Ozçelik T, Lifton RP, Sestan N, Bilgüvar K, Günel M: Recessive LAMC3 mutations cause malformations of occipital cortical development. Nat Genet. 2011 Jun; 43(6):590-4.
      • 8:Kaya Bilguvar , Ali Ozturk , Angeliki Louvi , Murim Choi , Burak Tatli , Dilek Yalnizoglu , Beyhan Tuysuz , Ahmet Caglayan , Sarenur Gokben , Hande Kaymakçalan , Tanyeri Barak , Mehmet Bakircioglu , Katsuhito Yasuno , Winson Ho , Stephan Sanders , Sanem Yilmaz , Alp Dincer , Michele Johnson , Richard Bronen , Naci Kocer , Huseyin Per , Shrikant Mane , M Necmettin Pamir , Cengiz Yalcinkaya , Sefer Kumandas , Meral Topcu , Meral Ozmen , Richard Lifton , Matthew State , Kenneth Kwan , Ying Zhu , Nenad Sestan, Murat Gunel: Whole exome sequencing identifies recessive WDR62 mutations in severe brain malformations.Nature.2010 September 09.
      • 9:Li Peining, Rossi Michael, DiMaio Miriam, Xiang Bixia, Lu Kangmo, Kaymakçalan Hande
      • Seashore Margreta, Mahoney Maurice. Clinical and Genomic Characterization of Distal Duplications and Deletions of Chromosome 4q: Study of Two Cases and Review of
      • Literature. Am J Med Genet A. 2009 Dec; 149A (12):2788-94
      • 10:Issever H, Hapcioglu B, Ozdilli K, Kocyigit E, Kaymakçalan H, Yegenoglu Y, Ozturk O: Assessment of Nasal Flora and Respiratory Function Tests of bakery workers working under modern conditions in Istanbul, Turkey. Indoor and Built Environment Journal.2006.Volume 15:1.197-202
      • 11:Hapcioglu B, Yegenoglu Y, Disci R, Erturan Z, Kaymakçalan H: Epidemiology of Superficial Mycosis (Tinea Pedis, Onychomycosis) in Elementary School Children in Istanbul, Turkey.Collegium Antropologicum, 30(2006) 1: 119-124
      • 12:Kaymakçalan H, Rao S. 10-month-old female with progressive abdominal distention. Hospital Physician. 2003 October. Volume 39.Number 10. 20-26
      • Kitap ve Bölüm Yazarlığı
      • Kaymakçalan H, State Matthew: Rare genetic variants and autism spectrum disorders. Geswind Autism Spectrum Disorders Book. Chapter 41. 722-736 
      • Uluslararası Bilimsel Toplantılarda Sunulan ve Bildiri Kitabında Basılan Bildiriler
      • 1.Hande Kaymakçalan, Margreta Seashore, Peining Li: Chromosome 1q21.1 deletion and duplication in the patient with psychiatric problems. European Society of Human Genetics Annual Meeting. Wien, Austria 2009
      • 2.H Kaymakçalan, A Bale, J McGrath: ALL and multiple congenital anomalies. Pediatric Cancer Genetics Meeting. Houston, USA 2009
      • Juho Harkönen, Hande Kaymakçalan, Anja Taanila: Prenatal Health, Family Background and Educational Attainment: Results from the 1966 Northern Finland Birth Cohort Study .Population Association of America Annual Meeting. Detroit, USA 2009
      • 3.H Kaymakçalan, AT Fox, M Perkin, G Lack: Changing ethnicity in Peanut Allergy. American Academy of Allergy Asthma and Immunology Annual Meeting. Miami, USA 2006
      • 4.K.M. Schroederus, H.Kaymakçalan, J.Moy and B.Yu: Correlation of cockroach and dust mite specific IgE levels and medication requirements among inner-city astmatic children. American Academy of Allergy Asthma and Immunology Annual Meeting. San Francisco, USA 2004
      • Ulusal Kongreler
      • Otizmde son genetik çalışmalar: Konya Otizm Günleri, 2013 
      • Katıldığı Kongre/sempozyum ve kurslar
      • Ulusal Kongreler
      • 26. Çocuk ve Ergen Ruh sağlığı ve hasstalıkları kongresi, 2016: 21. yy'da Otizm Kliniği. Yale Deneyimi ve Simons Simplex Araştırması 
      • Aldığı Ödüller ve Sertifikalar
      • 49. European Society of Human Genetics  Konferansında ' Story Telling in Genetics' konuşmacı ödülü
      •