Education Information
2000 - 2006
2000 - 2006Doctorate
Marmara University, Institute Of Health Sciences, Department Of Medical Genetics, Turkey
1997 - 2001
1997 - 2001Expertise In Medicine
Ministry of Health, University of Health Sciences , Haydarpaşa Numune Research and Education Hospital, Department of Internal Sciences, Turkey
1988 - 1994
1988 - 1994Undergraduate
Marmara University, School Of Medicine, Turkey
Dissertations
2006
2006Doctorate
Düşük dereceli gliomalarda egfr, pten, pdgfr-alfa, MGMT ifadelerindeki, TP53 ve P53 yolağı (MDM-2 ve P14arf) genlerindeki düzensizlikler ve klinik etkileri
Marmara Üniversitesi, Tıp Fakültesi
2001
2001Expertise In Medicine
Trisomi 21’in ve Nöral Tüp Defektinin Prenatal Tanısında İkinci Trimester AFP, hCG, uE3 Testlerinin Klinik Sonuçları
University Of Health Sciences, Ankara Keçiören Educatıon And Research Hospıtal, Department Of Internal Medıcıne
Foreign Languages
C2 Mastery
C2 MasteryEnglish
Certificates, Courses and Trainings
2019
2019Herediter Kanser Hastalıklarında Aileye Yaklaşım
Health&Medicine
Marmara Üniversitesi Tıp Fakültesi Pendik EĞİTİM VE ARAŞTIRMA HASTANESİ
Research Areas
Health Sciences
Natural Sciences
Academic Titles / Tasks
2018 - Continues
2018 - ContinuesProfessor
Marmara University, School Of Medicine, Internal Medical Sciences
Advising Theses
2018
2018Expertise In Medicine
Ankilozan spondilit'te mikrorna ekspresyonu ve etklili epigenetik mekanizmaların incelenmesi
ATA P. (Consultant)
A.TÜRKYILMAZ(Student)
2013
2013Postgraduate
Kronik böbrek yetersizliği hastalarında idrar bulundurmayan mesane dokusunda IL-8, CXR1 ve CXR2 nin gen ifadelerinin araştırılması
ATA P. (Consultant)
K.GÜNDOĞDU(Student)
2013
2013Postgraduate
Kronik böbrek yetersizliği hastalarında idrar bulundurmayan mesane dokusunda apoptotik bulguların incelenmesi
ATA P. (Consultant)
H.FINDIK(Student)
Taught Courses And Trainings
2016 - 2016
2016 - 2016Myelodisplastik sendrom: patogenezden tedaviye yenilikler sempozyumu
Academic Units - Training
Türköz H. K. , Atagündüz I., Bozkurt S., Ata P., Toptaş T.
Published journal articles indexed by SCI, SSCI, and AHCI
2022
2022CLINICAL SPECTRUM OF CUBULIN MUTATIONS
Cicek N., ALPAY H., Guven S., Turkkan O. N. , Polat S., DEMİRCİ BODUR E., et al.
PEDIATRIC NEPHROLOGY, vol.37, no.11, pp.2845-2846, 2022 (SCI-Expanded)
2022
2022GENETIC TESTS IN NON-NEUROGENIC NEUROGENIC BLADDER: TWO SIBLINGS WITH OCHOA SYNDROME
Pul S., GÖKCE İ., ALAVANDA C., ŞEKERCİ Ç. A. , DEMİRCİ BODUR E., Turkkan O. N. , et al.
PEDIATRIC NEPHROLOGY, vol.37, no.11, pp.2911, 2022 (SCI-Expanded)
2022
2022Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS-CoV-2 from 946 whole-exome sequencing data in the Turkish population
DUMAN N., Tuncel G., BİŞGİN A., TUĞ BOZDOĞAN S., Sag S. O. , GÜL Ş., et al.
JOURNAL OF MEDICAL VIROLOGY, vol.94, no.11, pp.5225-5243, 2022 (SCI-Expanded)
2022
2022Etiological analysis of hypophosphatemia: A single-center experience
Eltan M., Alavanda C., Abali Z. Y. , Bayramoglu E., Kaygusuz S. B. , Helvacioglu D., et al.
HORMONE RESEARCH IN PAEDIATRICS, vol.95, no.SUPPL 2, pp.141-142, 2022 (SCI-Expanded)
2022
2022Alloreactive memory B cell detection by flow cytometric cross match using polyclonally activated memory B cell culture supernatants
Akalan H., Sirin D. Y. , Yilmaz I., ATA P., Kara V. M. , Tasdemir N., et al.
TRANSPLANT IMMUNOLOGY, vol.73, 2022 (SCI-Expanded)
2022
2022First Patient Diagnosed as Feingold Syndrome Type 2 with Alport Syndrome and Review of the Current Literature
Demir S., SÖYLEMEZ M. A. , ARMAN A., ATA P.
MOLECULAR SYNDROMOLOGY, 2022 (SCI-Expanded)
2022
2022Two new cases diagnosed with Hermansky-Pudlak Syndrome
ALAVANDA C., Ates E. A. , GEÇKİNLİ B. B. , Demir S., Polat H., UĞUZDOĞAN F., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS, vol.30, no.SUPPL 1, pp.223, 2022 (SCI-Expanded)
2022
2022Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency
TÜRKYILMAZ A., ALAVANDA C., Ates E. A. , GEÇKİNLİ B. B. , Polat H., GÖKCÜ M., et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, vol.39, pp.695-710, 2022 (SCI-Expanded)
2021
2021Effects of vitamin D receptor gene polymorphisms on the prognosis of COVID-19.
Apaydin T., Polat H., Dincer Yazan C., Ilgin C., Elbasan O., Dashdamirova S., et al.
Clinical endocrinology, 2021 (SCI-Expanded)
2021
2021CLINICAL-GENETIC CHARACTERISTICS AND PREDICTORS OF DISEASE PROGRESSION IN PATIENTS WITH AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE
ALPAY H., Cicek N., ALAVANDA C., Guven S., SAK M., Turkkan O. N. , et al.
PEDIATRIC NEPHROLOGY, vol.36, no.10, pp.3422, 2021 (SCI-Expanded)
2021
2021KIDNEY DIMENSION IS THE MOST IMPORTANT PARAMETER ASSOCIATED WITH DETERIORATION IN KIDNEY FUNCTION IN CHILDREN WITH AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE
Cicek N., GÖKCE İ., ALAVANDA C., Guven S., SAK M., Turkkan O. N. , et al.
PEDIATRIC NEPHROLOGY, vol.36, no.10, pp.3421, 2021 (SCI-Expanded)
2021
2021THE FIRST CASE OF AMYLOIDOSIS DUE TO HOMOZYGOUS P.V377I MUTATION IN A PATIENT WITH HYPERIMMUNOGLOBULIN D SYNDROME
Bodur E. D. , GÖKCE İ., Sozeri B., Alavanda C., Farmanli O., Ata P., et al.
PEDIATRIC NEPHROLOGY, vol.36, no.10, pp.3448, 2021 (SCI-Expanded)
2021
2021PHENOTYPIC AND GENOTYPIC CHARACTERISTICS OF CHILDREN WITH BARTTER SYNDROME
Guven S., GÖKCE İ., ALAVANDA C., Bodur E. D. , Cicek N., SAK M., et al.
PEDIATRIC NEPHROLOGY, vol.36, no.10, pp.3430, 2021 (SCI-Expanded)
2021
2021A rare cause of hypercalcemia: Congenital Lactase Deficiency
Eltan M., Alavanda C., Abalı S., Abali Z. Y. , Kaygusuz S. B. , Gürpınar Tosun B., et al.
HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.75, 2021 (SCI-Expanded)
2021
2021The Spectrum of Low-Density Lipoprotein Receptor Mutations in a Large Turkish Cohort of Patients with Familial Hypercholesterolemia
Türkyılmaz A., Kurnaz E., Alavanda C., Yarali O., Kartal Baykan E., Yavuz D., et al.
METABOLIC SYNDROME AND RELATED DISORDERS, vol.19, pp.340-346, 2021 (SCI-Expanded)
2021
2021Can urinary HNF1B expression be a biomarker for multicystic dysplastic kidney?
Urer A., Ata P., Alpay H., Yilmaz I., Arslan E.
FEBS OPEN BIO, vol.11, pp.140, 2021 (SCI-Expanded)
2021
2021Secondary findings in 622 Turkish clinical exome sequencing data
Ates E. A. , TÜRKYILMAZ A., Yildirim O., ALAVANDA C., Polat H., Demir S., et al.
JOURNAL OF HUMAN GENETICS, 2021 (SCI-Expanded)
2021
2021Biallelic Mutations in DNAJB11are Associated with Prenatal Polycystic Kidney Disease in a Turkish Family
Ates E. A. , TÜRKYILMAZ A., DELİL K., ALAVANDA C., SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , et al.
MOLECULAR SYNDROMOLOGY, 2021 (SCI-Expanded)
2021
2021Does Genotype–Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the Literature
Kaygusuz S. B. , Alavanda C., Kırkgöz T., Eltan M., Yavas Abali Z., Helvacioglu D., et al.
Calcified Tissue International, 2021 (SCI-Expanded)
2020
2020Expanding of mutation spectrum in Muscular Dystrophies: A Turkish Cohort
ALAVANDA C., Polat H., Ilker A., Ates E. A. , SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , et al.
EUROPEAN JOURNAL OF HUMAN GENETICS, vol.28, no.SUPPL 1, pp.435-436, 2020 (SCI-Expanded)
2020
2020Progesterone Receptivity and Expression of Progesterone Triggered Genes at the Decidual Tissue in Patients with Recurrent Pregnancy Loss.
ATA P., YILMAZ İ. T. , Karakas N., Eren A., ESİM BÜYÜKBAYRAK E.
EUROPEAN JOURNAL OF HUMAN GENETICS, vol.28, no.SUPPL 1, pp.804, 2020 (SCI-Expanded)
2020
2020Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation
Gulcan-Kersin S., Kirkgoz T., Eltan M., Rzayev T., Ata P., Bilgen H. S. , et al.
HORMONE RESEARCH IN PAEDIATRICS, vol.93, no.5, pp.313-321, 2020 (SCI-Expanded)
2020
2020A large Turkish pedigree with multiple endocrine neoplasia type 1 syndrome carrying a rare mutation: c.1680_1683 del TGAG
Demirtaş C. Ö. , Ata P., Çetin A., Turkyilmaz A., Duman D.
TURKISH JOURNAL OF GASTROENTEROLOGY, vol.31, pp.508-514, 2020 (SCI-Expanded)
2020
2020A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age
Eltan M., Alavanda C., Yavas Abali Z., Ergenekon P., Yalindag Ozturk N., Sakar M., et al.
CALCIFIED TISSUE INTERNATIONAL, vol.107, pp.96-103, 2020 (SCI-Expanded)
2020
2020THE EXPRESSION LEVELS OF microRNAs ASSOCIATED WITH T AND B CELL DIFFERENTIATION/STIMULATION IN ANKYLOSING SPONDYLITIS
Turkyilmaz A., Ata P., Akbas F., Yagci I.
BALKAN JOURNAL OF MEDICAL GENETICS, vol.23, no.1, pp.25-31, 2020 (SCI-Expanded)
2019
2019Fibrodysplasia ossificans progressiva: lessons learned from a rare disease.
Akyuz G. D. , Gencer-Atalay K., Ata P.
Current opinion in pediatrics, vol.31, pp.716-722, 2019 (SCI-Expanded)
2019
2019A rare cause of hypophosphatemia: Raine Syndrome
Eltan M., Ata P., Kırkgöz T., Alavanda C., Kaygusuz S. B. , Menevse T. S. , et al.
HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.384, 2019 (SCI-Expanded)
2019
2019Genotype and Phenotype Characterization of Turkish Patients with Vitamin D Dependent Rickets Type IA
Kaygusuz S. B. , Ata P., Kırkgöz T., Abali Z. Y. , Eltan M., Tosun B. G. , et al.
HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.215, 2019 (SCI-Expanded)
2019
2019Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees
Kaygusuz S. B. , Arman A., Abalı S., Ata P., Kırkgöz T., Eltan M., et al.
HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.214, 2019 (SCI-Expanded)
2019
2019Novel mutations and deletions in cystic fibrosis in a tertiary cystic fibrosis center in Istanbul.
Atag E., Bas I., Ergenekon A., Gokdemir Y., Eralp E., Ata P., et al.
Pediatric pulmonology, vol.54, pp.743-750, 2019 (SCI-Expanded)
2019
2019Association between occurrence of ossicular chain defect and osteoprotegerin gene expression in patients with chronic otitis media
Keskin S., Tatlipinar A., ATA P., Uzun S., Kinal M. E. , Erkal B.
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, vol.276, no.5, pp.1321-1325, 2019 (SCI-Expanded)
2019
2019Challenges in the treatment of fibrodysplasia ossificans progressiva
Gencer-Atalay K., Ozturk E. C. , YAĞCI İ., ATA P., DELİL K., Ozgen Z., et al.
Rheumatology International, vol.39, no.3, pp.569-576, 2019 (SCI-Expanded)
2018
2018NOVEL MUTATIONS AND VARIATIONS IN TURKISH CHILDREN WITH ALPORT SYNDROME: ARE THE BENIGN VARIATIONS ALWAYS HARMLESS?
Cicek N., YILDIZ N., ATA P., GÖKCE İ., SAK M., KAYA H., et al.
PEDIATRIC NEPHROLOGY, vol.33, no.10, pp.1918-1919, 2018 (SCI-Expanded)
2018
2018THE CO-EXISTENCE OF TWO RARE DISEASES: A CASE REPORT
Saki M., KIRKGÖZ T., GÖKCE İ., Cicek N., ATA P., Turan S., et al.
PEDIATRIC NEPHROLOGY, vol.33, no.10, pp.1881, 2018 (SCI-Expanded)
2018
2018Intraoperative Tissue-Immunosuppressive Therapy Reduces Rejection Episodes in Heart Transplant Recipients.
Rabus M., Cekmecelioglu D., Ata P., Salihi S., Selcuk E., Balkanay M.
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, 2018 (SCI-Expanded)
2017
2017THE INFLUENCE OF PREFORMED HLA CLASS I AND II PANEL REACTIVE ANTIBODIES ON CLINICAL AND PATHOLOGICAL OUTCOMES OF KIDNEY ALLOGRAFT
Ruhi C., Tugcu M., Kasapoglu U., Boynuegri B., Gumrukcu G., ATA P., et al.
TRANSPLANT INTERNATIONAL, vol.30, pp.318, 2017 (SCI-Expanded)
2017
2017DOES C.3979 G > A/P.VAL1327MET VARIANT OF COL4A4 HAS ANY PATHOGENIC EFFECT IN TURKISH PATIENTS WITH ALPORT SYNDROME?
YILDIZ N., ATA P., ALPAY H., GÖKCE İ., ÖZALTIN F.
PEDIATRIC NEPHROLOGY, vol.32, no.9, pp.1773, 2017 (SCI-Expanded)
2017
2017THE ROLE OF SOLUBLE CTLA-4 AS A NON-INVASIVE BIOMARKER FOR DIAGNOSIS OF KIDNEY ALLOGRAFT REJECTION: A PRELIMINARY STUDY
Ruhi C. B. , ATA P., Titiz I. M.
TRANSPLANT INTERNATIONAL, vol.30, pp.303, 2017 (SCI-Expanded)
2017
2017COMPARISON OF THE TREATMENT EFFICACY OF RITUXIMAB AND PLASMAPHERESIS/INTRAVENOUS IMMUNOGLOBULIN COMBINATION WITH HISTORICAL CONTROL IN CHRONIC ANTIBODY MEDIATED REJECTION
Ruhi C., TugCu M., KasapogLu U., Gokce A. M. , ATA P., Titiz I. M.
TRANSPLANT INTERNATIONAL, vol.30, pp.300-301, 2017 (SCI-Expanded)
2017
2017Cytotoxic Antibody Detection by Means of Flow-Cytometric Cross-Match
Bilgen T., Ata P., Tozkir J., Tozkir H., Titiz M. I.
TRANSPLANTATION PROCEEDINGS, vol.49, no.3, pp.440-444, 2017 (SCI-Expanded)
2016
2016Evaluation of Pre-Transplant Panel Reactive Antibody Levels and Sensitization: A Single-Center Study
Can O., Gokce A. M. , Canbakan M., ATA P., Sahin G. M. , TİTİZ M. İ. , et al.
ANNALS OF TRANSPLANTATION, vol.21, 2016 (SCI-Expanded)
2016
2016Determination of CYP2C19 Polymorphism, Side Effects, and Medication Adherence in Patients Who have Utilized Selective Serotonin Reuptake Inhibitors
Deniz S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., Talas A., et al.
KLINIK PSIKOFARMAKOLOJI BULTENI-BULLETIN OF CLINICAL PSYCHOPHARMACOLOGY, vol.26, no.2, pp.152-160, 2016 (SCI-Expanded)
2015
2015A Rare Reason of Ileus in Renal Transplant Patients With Peritoneal Dialysis History: Encapsulated Peritoneal Sclerosis.
Gökçe A., Özel L., İbişoğlu S., Ata P., Şahin G., Gücün M., et al.
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, vol.13, pp.588-92, 2015 (SCI-Expanded)
2015
2015Factors Affecting the Selection of Patients on Waiting List: A Single Center Study.
Can Ö., Kasapoğlu U., Boynueğri B., Tuğcu M., Çağlar R., Canbakan M., et al.
Transplantation proceedings, vol.47, pp.1265-8, 2015 (SCI-Expanded)
2015
2015Cancer Screening of Renal Transplant Patients Undergoing Long-Term Immunosuppressive Therapy
Demir T., Ozel L., Gokce A. M. , Ata P., Kara M., Eris C., et al.
TRANSPLANTATION PROCEEDINGS, vol.47, no.5, pp.1413-1417, 2015 (SCI-Expanded)
2015
2015Relationship of Urothelial Gene Expressions in Urine-Deprived Bladders of Renal Recipients With Posttransplant Urinary Infections
Gokce A. M. , Findik H., Ata P., Gumrukcu G., Ozel L., Gundogdu K., et al.
TRANSPLANTATION PROCEEDINGS, vol.47, no.5, pp.1331-1335, 2015 (SCI-Expanded)
2015
2015Determination of CYP2C19 polymorphisms, adverse drug reaction, and medication adherence in patients utilized selective serotonin reuptake inhibitors
Deniz S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., Talas A., et al.
INTERNATIONAL JOURNAL OF CLINICAL PHARMACY, vol.37, no.1, pp.231-232, 2015 (SCI-Expanded)
2014
2014Proteinuria associated with mTOR inhibitors after kidney transplant.
Guney M., Sahin G., Yilmaz B., Canbakan M., Gucun M., Kayatas K., et al.
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, vol.12, pp.539-42, 2014 (SCI-Expanded)
2014
2014The GABA(A) Receptor gamma 2 Subunit (R43Q) Mutation in Febrile Seizures
Hancili S., Onal Z. E. , Ata P., Karatoprak E. Y. , Gurbuz T., Bostanci M., et al.
PEDIATRIC NEUROLOGY, vol.50, no.4, pp.353-356, 2014 (SCI-Expanded)
2014
2014TLR4 gene polymorphism in patients with nonalcoholic fatty liver disease in comparison to healthy controls.
Kiziltas S., Ata P., Colak Y., Mesçi B., Senates E., Enc F., et al.
Metabolic syndrome and related disorders, vol.12, pp.165-70, 2014 (SCI-Expanded)
2013
2013EFFECTIVENESS OF PLASMAPHERESIS AS A TREATMENT OF CHOICE IN SENSITIZED RENAL RECIPIENTS
Ata P., Ibisoglu S., Canbakan M., Gucun M., Gokce A. M. , Kara M., et al.
TRANSPLANT INTERNATIONAL, vol.26, pp.79, 2013 (SCI-Expanded)
2013
2013Association of COL1A1 polymorphism in Turkish patients with otosclerosis.
Ertugay O., Ata P., Kalaycik E., Kaya K., Tatlipinar A., Kulekci S.
American journal of otolaryngology, vol.34, pp.403-6, 2013 (SCI-Expanded)
2013
2013Monitoring of CD3(+) T-cell count in patients receiving antithymocyte globulin induction after cadaveric renal transplantation.
Ata P., Kara M., Özdemir E., Canbakan M., Gökçe A., Bayraktar F., et al.
Transplantation proceedings, vol.45, pp.929-31, 2013 (SCI-Expanded)
2012
2012The impact of preoperative immunonutrition and other nutrition models on tumor infiltrative lymphocytes in colorectal cancer patients.
Caglayan K., Oner I., Gunerhan Y., Ata P., Koksal N., Ozkara S.
American journal of surgery, vol.204, pp.416-21, 2012 (SCI-Expanded)
2012
2012Serum flow cytometric C1q binding antibody analysis of renal recipients with low levels of sensitization.
Ata P., Canbakan M., Kara M., Özel L., Ünal E., Titiz M.
Transplantation proceedings, vol.44, pp.1652-5, 2012 (SCI-Expanded)
2012
2012The impact of C4d staining as a humoral injury marker.
Kara M., Demir F., Ata P., Ozel L., Gumrukcu G., Unal E., et al.
Transplantation proceedings, vol.44, pp.1694-6, 2012 (SCI-Expanded)
2012
2012Flow Cytometric Detection of Anti-AB Antibody Titers in Blood Group O Recipients of Blood Group A2 Donor Kidneys
Ata P., Cetinkaya F., Ozgezer T., Ozel L., Tulunay A., Eksioglu E., et al.
TRANSPLANTATION PROCEEDINGS, vol.44, no.6, pp.1706-1709, 2012 (SCI-Expanded)
2011
2011Ramsay Hunt syndrome with atypical progress in a renal transplant recipient: a case report.
Ozel L., Toros S., Unal E., Kara M., Eren P., Canbakan M., et al.
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, vol.9, pp.413-6, 2011 (SCI-Expanded)
2011
2011Pyoderma gangrenosum in a renal transplantation patient having immunosuppressive treatment for 5 years.
Serdar Z., Ata P., Titiz M.
Transplant international : official journal of the European Society for Organ Transplantation, vol.24, 2011 (SCI-Expanded)
2011
2011Risk factors for osteoporosis after renal transplantation and effect of vitamin D receptor Bsm I polymorphism.
Ozel L., Ata P., Ozel M., Toros A., Kara M., Unal E., et al.
Transplantation proceedings, vol.43, pp.858-62, 2011 (SCI-Expanded)
2011
2011Elective and emergency surgery in chronic hemodialysis patients.
Ozel L., Krand O., Ozel M., Toros A., Sağıroğlu J., Kara M., et al.
Renal failure, vol.33, pp.672-6, 2011 (SCI-Expanded)
2011
2011Effects of intra- and extracellular factors on anti-aging klotho gene expression
Turan K., Ata P.
GENETICS AND MOLECULAR RESEARCH, vol.10, pp.2009-2023, 2011 (SCI-Expanded)
2010
2010Dermatologic Findings in Renal Transplant Recipients: Possible Effects of Immunosuppression Regimen and p53 Mutations
Serdar Z. A. , Eren P., Canbakan M., Turan K., Tellioglu G., Gulle S., et al.
TRANSPLANTATION PROCEEDINGS, vol.42, no.7, pp.2538-2541, 2010 (SCI-Expanded)
2010
2010Evaluation of intraoperative parathormone measurement for predicting successful surgery in patients undergoing subtotal/total parathyroidectomy due to secondary hyperparathyroidism.
Kara M., Tellioglu G., Bugan U., Krand O., Berber I., Seymen P., et al.
The Laryngoscope, vol.120, pp.1538-44, 2010 (SCI-Expanded)
2009
2009Determination of the Risk Group in Patients with Venous Thrombosis
Eren P., Denizli N., Sokmen H. M. , Erdem S., Solak M.
TURKIYE KLINIKLERI TIP BILIMLERI DERGISI, vol.29, no.6, pp.1430-1434, 2009 (SCI-Expanded)
2009
2009The clinical significance of parathyroid tissue calcium sensing receptor gene polymorphisms and expression levels in end-stage renal disease patients
ATA EREN P., TURAN K., BERBER İ., CANBAKAN M.
CLINICAL NEPHROLOGY, vol.72, no.2, pp.114-121, 2009 (SCI-Expanded)
2009
2009The clinical significance of parathyroid tissue calcium sensing receptor gene polymorphisms and expression levels in end-stage renal disease patients.
Eren P., Turan K., Berber I., Canbakan M., Kara M., Tellioglu G., et al.
Clinical nephrology, vol.72, pp.114-21, 2009 (SCI-Expanded)
2009
2009Calcium-sensing receptor gene polymorphisms and cardiac valvular calcification in patients with chronic renal failure: a pilot study.
Turkmen F., Ozdemir A., Sevinc C., Eren P., Demiral S.
Hemodialysis international. International Symposium on Home Hemodialysis, vol.13, pp.176-80, 2009 (SCI-Expanded)
2009
2009Evaluation of Gadolinium Pre-Treatment with or without Splenectomy in the Setting of Renal Ischemia Reperfusion Injury in Rats
Kara M., Tellioglu G., Sehirli O., Yildar M., Krand O., Berber I., et al.
RENAL FAILURE, vol.31, no.10, pp.956-963, 2009 (SCI-Expanded)
2005
2005Cerebellar liponeurocytoma/lipidized medulloblastoma - Case report and review of the literature
Aker F., Ozkara S., Eren P., Peker O., Armagan S., Hakan T.
JOURNAL OF NEURO-ONCOLOGY, vol.71, no.1, pp.53-59, 2005 (SCI-Expanded)
Articles Published in Other Journals
2022
2022Molecular Aspects of Distal Kidney Tubular Acidosis in Children, Its Long-Term Outcome, and Relationship with Hyperammonemia.
Güven S., Gökçe İ., Alavanda C., Öztürk Hişmi B., Çiçek N., Bodur Demirci E., et al.
Turkish archives of pediatrics, vol.57, no.4, pp.432-440, 2022 (ESCI)
2022
2022A New Biomarker on Bone Resorption in Chronic Otitis Media: Osteoprotegerin and NLRP3 Inflammasome Gene Polymorphisms
Keskin S., Tatlipinar A., ATA P.
INDIAN JOURNAL OF OTOLARYNGOLOGY AND HEAD & NECK SURGERY, vol.74, no.2, pp.205-211, 2022 (ESCI)
2021
2021Türkiye’de Tıbbi Yardımla Üreme Tedavisine Erişim ve Üreme Hakları
MEGA E., YENENER ÇAKMUT Ö., SERT G., ATA P., GÖNENÇ F. İ.
İstanbul Medipol Üniversitesi Hukuk Fakültesi Dergisi, vol.8, no.1, 2021 (Peer-Reviewed Journal)
2021
2021Differential diagnosis of classical Bartter syndrome and Gitelman syndrome: Do we need genetic analysis?
Guven S., GÖKCE İ., ALAVANDA C., Cicek N., Demirci E. B. , SAK M., et al.
MARMARA MEDICAL JOURNAL, vol.34, no.3, pp.254-259, 2021 (ESCI)
2019
2019Association of TBX21 gene polymorphism with nasal polyposis
KAYA K. S. , ATA P., ERTUGAY Ö. Ç. , KÜLEKÇİ S., ZER TOROS S.
Praxis of ORL, vol.7, no.3, pp.145-150, 2019 (Peer-Reviewed Journal)
2017
2017Comparison of the Treatment Efficacy of Rituximab and Plasmapheresis/Intravenous Immunoglobulin Combination with Historical Control in Chronic Antibody Mediated Rejection
Ruhi C., Tugcu M., Kasapoglu U., Gokce A. M. , ATA P., Titiz M. I.
TURKISH NEPHROLOGY DIALYSIS AND TRANSPLANTATION JOURNAL, vol.26, no.1, pp.48-54, 2017 (ESCI)
2016
2016The Influence of Preformed HLA Class I and II Panel Reactive Antibodies on Clinical and Pathological Outcomes of Kidney Allograft
Ruhi C., Tugcu M., Kasapoglu U., Boynuegri B., Gumrukcu G., ATA P., et al.
TURKISH NEPHROLOGY DIALYSIS AND TRANSPLANTATION JOURNAL, vol.25, no.1, pp.73-78, 2016 (ESCI)
Refereed Congress / Symposium Publications in Proceedings
2021
2021Toplumumuzda Osteogenezis İmperfektada Genetik Nedenler ve Genotip Fenotip İlişkisi
Kaygusuz S. B. , Alavanda C., Eltan M., Seven Menevse T., Abalı S., Yavaş Abalı Z., et al.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Turkey, 06 October 2021
2020
2020Expression Profile Of Complement Activation At Decidual Tissue In Patients With Recurrent Pregnancy Loss
YILMAZ İ., ATA P., gürkan karakaş n., ESİM BÜYÜKBAYRAK E.
European Human Genetics Virtual Conference 2020, 6 - 09 June 2020
2020
2020Çocukluk çağında otozomal dominant polikistik böbrek hastalığı
Çiçek N., Gökce İ., Güven S., Sak M., Bodur E., Yıldız N., et al.
7. Marmara Pediatri Kongresi, İstanbul, Turkey, 20 - 22 February 2020, pp.174
2019
2019A NOVEL MUTATION IN ATP6V0A4 GENE IN APATIENT WITH DISTAL RENAL TUBULAR ACIDOSIS
SAK M., YILDIZ N., Çiçek N., GÜVEN S., ATA P., GÖKCE İ., et al.
18 th Congress of the International Pediatric Nephrology Association-IPNA, 17 - 21 October 2019
2019
2019GENETIC ANALYSIS IN TURKISH CHILDRENWITH ALPORT SYNDROME: NOVEL MUTATIONS AND VARIATIONS
çiçek n., YILDIZ N., ATA P., GÖKCE İ., KAYA H., ALPAY H.
18 th Congress of the International Pediatric Nephrology Association-IPNA, Italy, 17 - 21 October 2019, vol.34, pp.1821-2260
2019
2019Nadir bir iskelet displazisi: Piknodizostoz tanısı alan iki kız kardeş
ALAVANDA C., GEÇKİNLİ B. B. , ARSLAN ATEŞ E., POLAT H., SÖYLEMEZ M. A. , GÜNEY A. İ. , et al.
4. Ulusal Çocuk genetik kongresi, Turkey, 25 - 27 September 2019
2019
2019Schaaf Yang sendromu
Alavanda C., Arslan Ateş E., Polat H., Geçkinli B. B. , Söylemez M. A. , Güney A. İ. , et al.
4. Ulusal Çocuk Genetik kongresi, İstanbul, Turkey, 25 - 27 September 2019
2019
2019Rare Causes of Osteogenesis Imperfecta are Commonin Consanguineous Pedigrees
KAYGUSUZ S. B. , ARMAN A., ABALI S., ATA P., KIRKGÖZ T., YAVAŞ ABALI Z., et al.
European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019
2019
2019Genotype and Phenotype Characterization ofTurkish Patients with Vitamin D Dependent RicketsType IA
KAYGUSUZ S. B. , ATA P., KIRKGÖZ T., YAVAŞ ABALI Z., ELTAN M., GÜRPINAR T. B. , et al.
European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, vol.91
2019
2019A rare cause of hypophosphatemia: Raine Syndrome
ELTAN M., ATA P., KIRKGÖZ T., ALAVANDA C., KAYGUSUZ S. B. , SEVEN M. T. , et al.
European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, vol.91
2018
2018FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia
Turkyilmaz A., GEÇKİNLİ B. B. , Ates E. A. , SÖYLEMEZ M. A. , GÜNEY A. İ. , ATA P., et al.
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.893
2018
2018The relationship between defects at the middle ear bone chain and NLRP3 and OPG gene polymorphisms at chronic otitis media patients
Keskin S., ATA P., Erkal B., Dogan T., Eren A., Tatlipinar A.
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.46
2018
2018A novel intronic ATM gene mutation affecting splicing in a patient with Ataxia-Telangiectasia
Ates E. A. , Turkyilmaz A., SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , ATA P., ARMAN A., et al.
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.255-256
2018
2018The effects of calcium-sensing receptor CASR genotypes, treatment duration, gender bone health and mineral metabolism in chronic renal failure patients
ATA P., Erkal B., Gultekin D., Altas B., ÇELİK B., Kayir D., et al.
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.97
2019
2019The prevalence in coeliac related hla haplotypes in paediatric IBD patients
Ertem Şahinoğlu D., Akkelle B., Şengül Ö., Volkan B., Tutar E., Ata P.
52. ESPGHAN, Glasgow, United Kingdom, 5 - 08 June 2019, vol.68, no.1, pp.592
2019
2019Fokal Segmental Glomeruloskleroz, son tanı mı?
Çiçek N., Yıldız N., Ata P., Gökce İ., Güven S., Sak M., et al.
10.Uluslararası katılımlı Çocuk Nefroloji Kongresi, Muğla, Turkey, 1 - 04 May 2019, pp.194
2019
2019Otozomal dominant polikistik böbrek hastalığında iki yeni mutasyon
Çiçek N., Gökce İ., Ata P., Güven S., Sak M., Yıldız N., et al.
10.Uluslararası katılımlı Çocuk Nefroloji Kongresi, Muğla, Turkey, 1 - 04 May 2019, pp.195
2019
2019Çocukluk çağında Otozomal dominant polikistik böbrek hastalığı
Çiçek N., Gökce İ., Güven S., Sak M., Ata P., Yıldız N., et al.
10.Uluslararası katılımlı Çocuk Nefroloji Kongresi, Muğla, Turkey, 1 - 04 May 2019, pp.196
2019
2019Alport Sendromu Tanılı Hastalarda Genetik Analiz ve Yeni Mutasyonlar: Varyasyonlar Her Zaman Masum Mu?
çiçek n., YILDIZ N., ATA P., GÖKCE İ., SAK M., KAYA H., et al.
Uluslararası katılımlı 10. Çocuk Nefroloji Kongresi, Turkey, 1 - 04 May 2019
2019
2019TWO NOVEL MUTATIONS IN THREE DIFFERENT GENES ASSOCIATED WITHRETINITIS PIGMENTOSA/LEBER CONGENITAL AMAROSIS IN ONE PATIENT
ALAVANDA C., ATA P., YILMAZ Ö., POLAT H., GEÇKİNLİ B. B. , ARMAN A.
13. BALKAN GENETİK KONGRESİ, Edirne, Turkey, 16 - 20 April 2019
2019
2019Acute Pancreatitis Severity Related With Macrophage Migration Inhibitory FactorGene - 173 G/C Polymorphism and Serum MIF Level
UZUN M. A. , erkal b., ATA P., DOĞAN T., BERK OCAK S., ALKAN KAYAOĞLU S., et al.
13. balkan genetik kongresi, Edirne, Turkey, 16 - 20 April 2019
2019
2019Von Hippel Lindau Patients
ALAVANDA C., TÜRKYILMAZ A., POLAT H., GEÇKİNLİ B. B. , GÜNEY A. İ. , ATA P., et al.
13. BALKAN GENETİK KONGRESİ, Edirne, Turkey, 16 - 20 April 2019
2019
2019Yenidoğanda Nadir Bir Hiperkalsemi nedeni : Kalsiyum Duyarlı Reseptör Mutasyonuna bağlı Ağır neonatal Hiperparatiroidizm
Rzayev T., KIRKGÖZ T., Özdemir H., ATA P., BİLGEN H. S. , MEMİŞOĞLU A., et al.
27. Ulusal Neonatoloji Kongresi, Antalya, Turkey, 3 - 07 April 2019
2019
2019Ankilozan Spondilit’te Mikrorna Ekspresyonu
TÜRKYILMAZ A., AKBAŞ F., ATA P., YAĞCI İ.
Uluslararası Katılımlı Türk Romatoloji Kongresi, Antalya, Turkey, 20 - 24 March 2019
2019
2019Alport sendromu tanılı hastalarda yeni mutasyon ve varyasyonlar: Varyasyonlar her zaman zararsız mı?
Çiçek N., Yıldız N., Ata P., Gökce İ., Sak M., Kaya H., et al.
6. Marmara Pediatri Kongresi, İstanbul, Turkey, 21 - 23 February 2019, pp.144
2018
2018İki nadir hastalığın birlikteliği:olgu sunumu
Atalah Y., Sak M., Kırkgöz T., Gökce İ., Çiçek N., Ata P., et al.
4. Genç Pediatristler Kongresi, İstanbul, Turkey, 30 November - 02 December 2018, pp.124
2018
2018ANKİLOZAN SPONDİLİT’xxTE MİKRO RNA EKSPRESYONU
TÜRKYILMAZ A., AKBAŞ F., YAĞCI İ., ATA P.
Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018
2018
2018Chromosomal array-CGH analysisin patients having neurodevelopmental delay and dysmorphic features
ALAVANDA C., ARSLAN ATEŞ E., TÜRKYILMAZ A., GEÇKİNLİ B. B. , ATA P., GÜNEY A. İ. , et al.
13 ULUSAL TIBBİ GENETİK KONGRESİ, Turkey, 7 - 11 November 2018
2018
2018REVERSE GENETİK İLE TANI KOYULAN NADİR BİR SPASTİK PARAPLEJİ AİLESİ
ALAVANDA C., ates e., TÜRKYILMAZ A., GÜNEY A. İ. , GEÇKİNLİ B. B. , ATA P., et al.
13.ULUSLARARASI KATILIMLI ULUSAL TIBBİ GENETİK ANABİLİM DALI, Turkey, 7 - 11 November 2018
2018
2018NÖROMOTOR GELİŞME GERİLİĞİ VE DİSMORFİK BULGULARI OLAN HASTALARDA ARRAY-CGH ANALİZİ
ATA P., ALAVANDA C., ATEŞ E., GEÇKİNLİ B. B. , GÜNEY A. İ. , SÖYLEMEZ M. A. , et al.
Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 7 - 11 November 2018
2018
2018İKİ LAMİNOPATİ OLGUSU: LMNA GENİ MUTASYONLARI İLE İLİŞKİLİ FENOTİPLER
GEÇKİNLİ B. B. , TÜRKYILMAZ A., SÖYLEMEZ M. A. , ATES E., YILDIRIM Ö., ATA P., et al.
Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 07 November 2018 - 11 November 1918
2018
2018GENETİK KLİNİĞİNE PSÖDOBARTTER SENDROMU BULGULARIYLA BAŞVURAN KİSTİK FİBROZLU İKİ KIZ KARDEŞ
ALAVANDA C., ATA P., TÜRKYILMAZ A., Arslan E., YILDIZ N., ALPAY H.
Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018
2018
2018PEDİATRİK AKUT LENFOBLASTİK LÖSEMİDE TEŞHİSSEL TESTLERİN GEÇERLİLİĞİ
Yılmaz İ., ATA P., ALAVANDA C., Arslan E., Eren R., Yılmaz B., et al.
13. Uluslararası Katılımlı Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 7 - 11 November 2018
2018
2018FARKLI GENLER,FARKLI MUTASYONLAR,FENOTİPTE FARKLILIK YARATIYOR MU ?: ALPORT SENDROMU
ATA P., ALAVANDA C., TÜRKYILMAZ A., YILDIZ N., ALPAY H.
Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018
2018
2018Genotype and phenotype correlation in Turkish Alport syndrome patients with different COL4A3, COL4A4 and COL4A5 mutations.
ATA P., CELİK T., PAK T., ISIK A., YILDIRIM S., TÜRKYILMAZ A.
ASHG 2018, 16 October 2018 - 20 January 2019
2018
2018The co-existence of two rare diseases: a case report
SAK M., kırkgöz t., Gökçe İ., Çiçek N., ata P., turan S., et al.
51th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Antalya, Turkey, 3 - 06 October 2018
2018
2018Novel mutations and variations in turkish children with Alport syndrome: are the benign variations always harmless?
Çiçek N., YILDIZ N., ATA P., Gökçe İ., SAK M., KAYA H., et al.
51th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Antalya, Turkey, 3 - 06 October 2018
2017
2017A novel HNF1B mutation in a family with two MODY patients
Ates E. A. , Turkyilmaz A., GEÇKİNLİ B. B. , SÖYLEMEZ M. A. , Delil K., ATA P., et al.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.863
2017
2017BBS10 frameshift mutation in a turkish girl with bardet biedl syndrome
SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , Delil K., Ates E., Turkyilmaz A., AVŞAR M., et al.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.457
2017
2017Inversion Y Having Different Phenotypic Expressions at Three Brothers
Turkyilmaz A., ATA P., DELİL K., SOYSAL S., Ates E. A. , GÜNEY A. İ.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.829
2017
2017Evaluation of BRCA1/BRCA2 test results for Turkish breast cancer families
Ates E. A. , Turkyilmaz A., GEÇKİNLİ B. B. , Ozgumus G. G. , SÖYLEMEZ M. A. , Delil K., et al.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.966
2017
2017Novel Large CFTR Gene Deletions in Turkish Patients with Increased Morbidity
ATA P., Atag E., GÖKDEMİR Y., Ikizoglu N. B. , DELİL K., Eralp E., et al.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.980
2018
2018A novel intronic ATM genemutation a×ecting splicing in a patient withAtaxia-Telangiectasia
ATES E., TÜRKYILMAZ A., ATA P., GEÇKİNLİ B. B. , SÖYLEMEZ M. A. , GÜNEY A. İ. , et al.
ESHG2018, 16 - 19 June 2018
1918
1918The relationship betweendefects at the middle ear bone chain andNLRP3 and OPG gene polymorphisms atchronic otitis media patients
KESKIN S., ATA P., erkal b., DOGAN T., EREN A., TATLIPINAR A.
ESHG 2018, 16 June 1918 - 19 June 2018
2018
2018HLA and non-HLA genetic predisposing factors and environmental effects at Celiac Disease pathogenesis
ATA P., erkal b., ŞAHİN AKKELLE B., SİSKO S., ERTEM ŞAHİNOĞLU D.
EUROPEAN SOCIETY OF HUMAN GENETICS, 16 - 19 June 2018
2018
2018Herediter parapleji hastalık ailesine olgularla yaklaşım
SAĞER S. G. , ÖZTÜRK THOMAS G., TÜRKYILMAZ A., ATA P., ÜNVER O., TÜRKDOĞAN D.
20. Çocuk Ulusal Nörolojisi Kongresi, Cyprus (Kktc), 2 - 06 May 2018
2018
2018Hepatosellüler karsinom gelişiminde moleküleryolaklar
ATA P.
M.Ü. Tıp Fakültesi III. Uluslararası Onkolojive Cerrahi Günleri Sempozyumu, 3 - 04 May 2018
2018
2018Hepatosellüler karsinom tanısında genetikbiyobelirteçler
ATA P.
MARMARA ÜNİVERSİTESİ TIP FAKÜLTESİIII. ULUSLARARASI ONKOLOJİ VE CERRAHİ GÜNLERİHEPATO-PANKREATO-BİLİYER ve GASTROİNTESTİNAL KANSERLERDESİSTEMİK VE CERRAHİ TEDAVİLERDE GELİŞMELER, 3 - 05 May 2018
2017
2017Makrofaj migrasyon inhibitör faktör -173 G/C gen polimorfizmi ile akut pankreatit gelişimi ve şiddeti arasındaki ilişki
UZUN M. A. , ALKAN KAYAOĞLU S., ATA P., TİLKİ M., BERK OCAK S., DOĞAN T., et al.
13. Türk Hepatopankreatobilier Cerrahi Kongresi, Antalya, Turkey, 1 - 04 November 2017, vol.33, pp.1-92
2017
2017COMPARISON OF THE TREATMENT EFFICACY OFRITUXIMAB AND PLASMAPHERESIS/INTRAVENOUSIMMUNOGLOBULIN COMBINATION WITH HISTORICALCONTROL IN CHRONIC ANTIBODY MEDIATEDREJECTION
Ruhi Borçak ç., ATA P., TİTİZ M. İ.
18th Congressof the European Society for Organ Transplantation, 24 - 27 September 2017
2017
2017THE ROLE OF SOLUBLE CTLA-4 AS A NON-INVASIVEBIOMARKER FOR DIAGNOSIS OF KIDNEY ALLOGRAFTREJECTION: A PRELIMINARY STUDY
Ruhi Borçak ç., ATA P., TİTİZ M. İ.
18th Congressof the European Society for Organ Transplantation, 24 - 27 September 2017
2017
2017THE INFLUENCE OF PREFORMED HLA CLASS I AND II PANEL REACTIVE ANTIBODIES ON CLINICAL AND PATHOLOGICAL OUTCOMES OF KIDNEY ALLOGRaft
RUHİ Ç., TUĞCU M., KASAPOĞLU U., BOYNUEĞRİ B., GÜMRÜKÇÜ G., ATA P., et al.
ESOT, 15 - 18 September 2017, vol.30, pp.318
2017
2017Does C.3979 G A/P.VAL1327MET variant of COL4A4 has any pathogenic effect in Turkish patients with Alport Syndrome ?
YILDIZ N., ATA P., ALPAY H., GÖKCE İ., ÖZALTIN F.
48th Anniversary Meeting of the European Society for Paediatric Nephrology, 6 - 09 September 2017
2017
2017Evaluation of BRCA1/BRCA2 test results for Turkish breast cancer families.
ARSLAN ATEŞ E., TÜRKYILMAZ A., GEÇKİNLİ B. B. , GİRGİN ÖZGÜMÜŞ G., SÖYLEMEZ M. A. , DELİL K., et al.
The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 May 2017
2017
2017A Novel HNF1B mutation in a family with two MODY patients
ARSLAN ATEŞ E., TÜRKYILMAZ A., GEÇKİNLİ B. B. , SÖYLEMEZ M. A. , DELİL K., ATA P., et al.
The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 May 2017
2017
2017BBS10 frameshift mutation in a Turkish girl with Bardet Biedl Syndrome.
SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , DELİL K., ARSLAN ATEŞ E., TÜRKYILMAZ A., AVŞAR M., et al.
The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 May 2017
2017
2017A novel HNF1B mutation in a family with two MODY patients
ARSLAN ATEŞ E., TÜRKYILMAZ A., GEÇKİNLİ B. B. , DELİL K., SÖYLEMEZ M. A. , ATA P., et al.
The European Society of Human Genetics 2017., KOPENHAGEN, Denmark, 25 - 28 May 2017
2017
2017BBS10 frameshift mutation in a turkish girl with bardet biedl syndrome
SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , DELİL K., TÜRKYILMAZ A., AVŞAR M., GİRGİN G., et al.
The European Society of Human Genetics 2017, KOPENHAGEN, Denmark, 25 - 30 May 2017
2017
2017Evaluation of BRCA1/2 test results for Turkish breast cancer families.
ARSLAN ATEŞ E., TÜRKYILMAZ A., GEÇKİNLİ B. B. , SÖYLEMEZ M. A. , ÖZGÜMÜŞ GİRGİN G., DELİL K., et al.
The European Society of Human Genetics 2017, KOPENHAGEN, Denmark, 25 - 30 May 2017
2017
2017Inversion Y Having Different Phenotypic Expressions at Three Brothers
TÜRKYILMAZ A., ATA P., DELİL K., SOYSAL S., ARSLAN ATEŞ E., GÜNEY A. İ.
The European Society of Human Genetics, KOPENHAGEN, Denmark, 25 - 30 May 2017
2017
2017Novel Large CFTR Gene Deletions in Turkish Patients with Increased Morbidity,
ATA P., ATAG E., GOKDEMİR Y., NE B. I. , DELİL K., ERALP E., et al.
The European Society of Human Genetics, KOPENHAGEN, Denmark, 26 - 30 May 2017
2017
2017BBS-10 frameshift mutation in a Turkish girl with bardet biedl syndrome
GEÇKİNLİ B. B. , SÖYLEMEZ M. A. , TÜRKYILMAZ A., ARSLAN ATEŞ E., DELİL K., ATA P., et al.
ERCİYES TIP GÜNLERİ 2017, Kayseri, Turkey, 11 - 13 May 2017
2017
2017EVALUATION OF THE BRCA1/BRCA2 MUTATIONS AT BREAST CANCER PATIENTS
ARSLAN ATEŞ E., TÜRKYILMAZ A., GEÇKİNLİ B. B. , SÖYLEMEZ M. A. , GİRGİN ÖZGÜMÜŞ G., DELİL K., et al.
ERCİYES TIP GÜNLERİ, Kayseri, Turkey, 11 - 13 May 2017
2017
2017Largest family in Turkey with multiple endocrine neoplasia-type 1 and a newly discovered mutation.
DUMAN D., ÇETİN A., Tütüncü Y., Şimşek H., ATA P.
16. Eurasian Congress of Gastrtoenterology and Surgery, Mostar, Bosnia And Herzegovina, 27 - 30 April 2017, vol.7, pp.117-118
2017
2017May Intraoperative Immunosuppressive Therapy Reduce the Rejection Episodes at Cardiac Transplant Recipients?
Rabus M. B. , Cekmecelioglu D., Ata P., Salihi S., Selcuk E., Balkanay M.
37th Annual Meeting and Scientific Sessions of the International-Society-for-Heart-and-Lung-Transplantation (ISHLT), California, United States Of America, 5 - 08 April 2017, vol.36
2016
2016A New Flowcytometric crossmatch Technique with 7AAD For Cytotoxic Antibody Detection
BİLGEN T., ATA P., TOZKIR J., TOZKIR H., TİTİZ M. İ.
TÜRKİYE ORGAN NAKLİ KOORDİNATÖRLERİ KONGRESİ, Konya, Turkey, 13 - 15 October 2016
2016
2016BREAST CANCER INHERITANCE FAMILY PATIENTS POINT OF VIEW
DASTAN B., ERGİN Z., GÜLTEKİN H. D. , AKIN S., HELVACI M. S. , NAZLI Y., et al.
International Istanbul Breast Cancer Conference - BREASTANBUL 2016, İstanbul, Turkey, 10 - 12 October 2016
2016
2016RAB3GAP1 geninde bilinen bir splice-site mutasyonunun fonksiyonel değerlendirilmesi
TÜRKYILMAZ A., SÖYLEMEZ M. A. , ARSLAN ATEŞ E., ERGÜNER B., ŞİMŞEK H., KARAKAYA T., et al.
12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016
2016
2016Nadir görülen bir genetik sendrom: Meacham sendromu
DELİL K., TÜRKYILMAZ A., ŞİMŞEK H., KARAKAYA T., ARSLAN ATEŞ E., SÖYLEMEZ M. A. , et al.
12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016
2016
2016Geç tanı almış Williams sendromlu üç olgunun klinik değerlendirmesi
ARSLAN ATEŞ E., GEÇKİNLİ B. B. , KARAKAYA T., TÜRKYILMAZ A., ŞİMŞEK H., SÖYLEMEZ M. A. , et al.
12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016
2016
2016Von Hippel -Lindau sendromu ailesindeki asemptomatik 3 çocoğun genetik test sonuçlarının değerlendirilmesi
DELİL K., GEÇKİNLİ B. B. , ŞİMŞEK H., TÜRKYILMAZ A., ARSLAN ATEŞ E., SÖYLEMEZ M. A. , et al.
12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016
2016
2016Nöromotor gelişme geriliği ve distonili Xq28 duplikasyon sendromu
GEÇKİNLİ B. B. , ŞİMŞEK H., DELİL K., TÜRKDOĞAN D., GÜNEŞ SAĞER S., SÖYLEMEZ M. A. , et al.
12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016
2016
2016Chromosome 17p11.2 deletion in a Turkish girl with Smith -Magenis Syndrome
GEÇKİNLİ B. B. , DELİL K., TÜRKYILMAZ A., SÖYLEMEZ M. A. , ŞİMŞEK H., KARAKAYA T., et al.
12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016
2016
2016Silver Russel Sendromlu bir olgu
GEÇKİNLİ B. B. , DELİL K., ŞİMŞEK H., SÖYLEMEZ M. A. , TÜRKYILMAZ A., ARSLAN ATEŞ E., et al.
12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016
2016
2016Beckwith Wiedemann sendromlu olgunun klinik bulguları ve moleküler tanısı
KARAKAYA T., SÖYLEMEZ M. A. , ARSLAN ATEŞ E., TÜRKYILMAZ A., ŞİMŞEK H., DELİL K., et al.
12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016
2016
2016Clinical Evaluation of a MDC1A Case Carrying LAMA2 Mutation
SÖYLEMEZ M. A. , TÜRKYILMAZ A., ŞİMŞEK H., DELİL K., GEÇKİNLİ B. B. , ARMAN A., et al.
ULUSAL TIBBİ GENETİK KONGRESİ, İZMİR ÇEŞME, Turkey, 5 - 09 October 2016
2016
2016Yaşlanma ile İlişkili Klotho Geni ve Bu Genin Ekspresyonunda Epigenetik Faktörlerin Rolü
TURAN K., Çağlayan E., ATA P.
Ulusal Moleküler Tıp Sempozyumu: Moleküler Bakıştan Kliniğe, İstanbul, Turkey, 1 - 03 June 2016
2016
2016Recurrent miscarriage and implantation failure Could the etiology be maternal intolerance itself
ATA P., SOYSAL S., TÜRKYILMAZ A., DELİL K., ANIK İLHAN G., GEÇKİNLİ B. B.
European Society of Human Genetics Congress, BARSELONA, Spain, 21 - 24 May 2016
2016
2016Analysis of The Molecular Markers in 49 AML Patients
TÜRKYILMAZ A., SÖYLEMEZ M. A. , DELİL K., ŞİMŞEK H., GÜNEY A. İ. , ATA P.
European Society of Human Genetics Congress, Barcelona, Spain, 21 - 24 May 2016
2016
2016A case of Weaver Syndrome caused by a novel frameshift EZH2 mutation
TÜRKYILMAZ A., KARAKAYA T., ŞİMŞEK H., SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , ARMAN A., et al.
European Society of Human Genetics, 21 - 24 May 2016
2016
2016A novel splice site JAG1 mutation in a Turkish girl with Alagille Syndrome
TÜRKYILMAZ A., GEÇKİNLİ B. B. , DELİL K., SÖYLEMEZ M. A. , GÜNEY A. İ. , ARMAN A., et al.
European Society Of Human Genetics Congress, Barcelona, Spain, 21 - 24 May 2016
2016
2016A case of Weaver Syndrome caused by a novel frameshift EZH2mutation
ŞİMŞEK H., GEÇKİNLİ B. B. , DELİL K., SÖYLEMEZ M. A. , TÜRKYILMAZ A., Arslan Ateş E., et al.
ESHG 2016 | BARCELONA, SPAIN, 21 - 24 May 2016
2015
2015Evaluation of Potentially Inappropriate Medication Use and Drug Burden Index in Elderly Patients with Cancer
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
44th European Symposium on Clinical Pharmacy, LİZBON, Portugal, 28 - 30 October 2015
2015
2015Determination of Potential Drug Drug Interactions by Using Various Software Programs at Community Pharmacy Setting
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
44th European Symposium on Clinical Pharmacy, LİZBON, Portugal, 28 - 30 October 2015
2015
2015Determination of Potential Drug Drug Interactions by Using Various Drug Interaction Software Programs at Hospital Pharmacy Setting
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
44th European Symposium on Clinical Pharmacy, LİZBON, Portugal, 28 - 30 October 2015
2015
2015Implementation of Medication Reconciliation and Medication Review Services Conducted by Pharmacist in Hospitalized COPD Patients
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
44th European Symposium on Clinical Pharmacy, LİZBON, Portugal, 28 - 30 October 2015
2015
2015Assessment of Attitude and Knowledge in Patients Utilized Disposable Insulin Pens at Community Pharmacy Setting
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
44th European Symposium on Clinical Pharmacy, LİZBON, Portugal, 28 - 30 October 2015
2015
2015Recurrent Fetal Loss Family with Translocation t 18 19 p11 2 p13 1 and its Clinical İmplications
TURKYILMAZ A., ŞİMSEK H., MAMADOV e., DELİL K., GEÇKİNLİ B. B. , SÖYLEMEZ M. A. , et al.
European Society of Human Genetics, 6 - 09 June 2015
2015
2015A Case of Sotos Syndrome with a Novel Mutation of NSD1 Gene
ŞİMŞEK H., GEÇKİNLİ B. B. , DELİL K., SÖYLEMEZ M. A. , TURKYILMAZ A., ATA P., et al.
European Society ofHuman Genetics, 6 - 09 June 2015
2015
2015Hereditary Heterotopic Ossification Syndromes Effect of GNAS inactivation in progressive osseousheteroplasia A case report
ATA P., TURKYILMAZ A., DELIL K., YAĞCI İ., GENCER K., OZTURK E., et al.
European Society of Human Genetics, Milan, Italy, 6 - 09 June 2015
2015
2015Translocation t 18 19 p11 2 p13 1 and its Clinical Implications Case report and Mechanism of Pathogenesis
TÜRKYILMAZ A., ŞİMŞEK H., Mamadov E., DELİL K., GEÇKİNLİ B. B. , SÖYLEMEZ M. A. , et al.
ESHG Congress 2015, 6 - 09 June 2015
2015
2015PROGRESİVA ANKİLOZAN SPONDİLİT İLE KARIŞAN NADİR BİR HASTALIK
AKYÜZ G. D. , GENCER K., YAĞCI İ., ÖZTÜRK E., DELİL K., TÜRKYILMAZ A., et al.
25.UlusalFiziksel TipveRehabilitasyonKongresi, Turkey, 22 - 26 April 2015
2015
2015KALITIMSAL HETEROTOPI K OSSI FI KASYON SENDROMLARI FI BRODI SPLAZI A OSSI FI KANS PROGRESSI VAMI PROGRESI F OSSÖZ HETEROPLAZI MI OLGU SUNUMU
YAĞCI İ., GENCER K., AKYÜZ G. D. , DELİL K., TÜRKYILMAZ A., ATA P.
25.UlusalFizikselTipveRehabilitasyonKongresi, Turkey, 22 - 26 April 2015
2015
2015KALITIMSAL HETEROTOPİK OSSİFİKASYON SENDROMLARI FİBRODİSPLAZİA OSSİFİKANS PROGRESSİVA MI PROGRESİF OSSÖZ HETEROPLAZİ Mİ OLGU SUNUMU
YAĞCI İ., GENÇER Z. K. , AKYÜZ G. D. , DELİL K., TÜRKYILMAZ A., ATA P.
24. Ulusal Fiziksel Tıp ve Rehabilitasyon Kongresi, Turkey, 23 - 26 April 2015
2014
2014Assessment of knowledge and attitude towards osteoporosis among women attending community pharmacy settings
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.213
2014
2014Evaluation of drug burden index in elderly patients utilized inhaler
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.205
2014
2014Evaluation of drug burden index and medication utilization in geriatric patients at community pharmacy
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.206-207
2014
2014Assessment of patients knowledge and attitude towards methotrexate utilization
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.256
2014
2014Determination of drug related problem and drug burden index in elderly patients
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.208-209
2014
2014The role of pharmacist in detecting angiotensin converting enzyme inhibitors induced dry cough at community pharmacy setting
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.207
2014
2014Evaluation of drug burden index in elderly patients utilized disposable insulin pen
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.203-204
2014
2014Kronik Antikor Aracılı Rejeksiyonda Rituksimab ve Plazmaferez/İntravenöz İmmünglobulin Kombinasyonun Etkinliğinin
RUHİ B. Ç. , KASAPOĞLU U., TUĞCU M., CAN Ö., ATA P., Gümrükçü G., et al.
10. Türkiye Organ Nakli Kuruluşları Kordinasyon Derneği Kongresi, Muğla, Turkey, 15 - 18 October 2014
2014
2014KADAVRA BÖBREK BESLEME LİSTESİNDEKİ HASTALARDA PRA DÜZEYİNİ BEKLEYEN FAKTÖRLER
CAN Ö., Daşkın N., CAN Ö., APAYDIN S., ATA P., CANBAKAN M., et al.
10. Türkiye Organ Nakli Kuruluşları Kordinasyon Derneği Kongresi, Muğla, Turkey, 15 - 18 October 2014
2014
2014Kadavradan Alıcı Seçimini Etkileyen Faktörler
CAN Ö., BOYNUEĞRİ B., TUĞCU M., CANBAKAN M., RUHİ B. Ç. , Daşkın N., et al.
10. Türkiye Organ Nakli Kuruluşları Kordinasyon Derneği Kongresi, Muğla, Turkey, 15 - 18 October 2014
2014
2014Pretransplant Gelişmiş Hla Sınıf I ve II Panel Reaktif Antikor Varlığının Graft Fonksiyonu ve Sağ Kalıma Etkisi
RUHİ B. Ç. , TUĞCU M., KASAPOĞLU U., BOYNUEĞRİ B., APAYDIN S., ATA P., et al.
10. Türkiye Organ Nakli Kuruluşları Kordinasyon Derneği Kongresi, Muğla, Turkey, 15 - 18 October 2014
2014
2014Alt extremite hemihipertrofisi olan bir Prader Willi Sendromu Olgusu
ŞİMŞEK H., DELİL K., GEÇKİNLİ B. B. , TÜRKYILMAZ A., AVŞAR M., SÖYLEMEZ M. A. , et al.
11. Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014
2014
2014Duchenne Musküler Distrofi DMD tipik klinik bulguları olan ve DMD geninde nonsense mutasyon saptanan olgu
TÜRKYILMAZ A., DELİL K., GEÇKİNLİ B. B. , ŞİMŞEK H., SÖYLEMEZ M. A. , AVŞAR M., et al.
11. Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014
2014
2014Recurrent fetal loss family with translocation t 18 19 p11 2 p13 1 and its clinical implications
TÜRKYILMAZ A., ŞİMŞEK H., MAMADOV E., DELİL K., GEÇKİNLİ B. B. , GÜNEY A. İ. , et al.
11. Ulusal Tıbbi Genetik Kongresi, 24-27 Eylül 2014, Turkey, 24 - 27 September 2014
2014
2014FBN1 mutasyonu ve tipik klinik bulguları olan Marfan sendromlu üç olgu
DELİL K., SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , AVŞAR M., ŞİMŞEK H., TÜRKYILMAZ A., et al.
11. Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014
2014
2014Determination of CYP2C19 polymorphisms adverse drug reaction and medication adherence in patients utilized selective serotonin reuptake inhibitors
DENİZ S., SANCAR M., OKUYAN B., ATA P., BİNGÖL ÖZAKPINAR Ö., TALAS A., et al.
Four International Meeting on Pharmacy and Pharmaceutical Sciences (IMPPS-4), 18 - 21 September 2014
2013
2013Is the TLR-4 Gene Polymorphism Play a Protective Role in the Development of NAFLD in Humans ?
Kiziltas S., Ata P., Colak Y., Mesci B., Senates E., Enc F., et al.
Digestive Disease Week / 28th Annual Residents and Fellows Research Conference of the Society-for-Surgery-of-the-Alimentary-Tract (SSAT), Florida, United States Of America, 18 - 21 May 2013, vol.144
2013
2013Association between toll-like receptor 4polymorphism and type 2 diabetes mellitus
MESCİ B., EREN P., KIZILTAŞ Ş., OĞUZ A., TUNCER İ., KÖSTEK O., et al.
15th European Congress of Endocrinology, 27 April - 01 May 2013, vol.32, pp.372
2012
2012Anti aging Klotho geni ekspresyonuna hücre içi ve hücreler arası faktörlerin etkisi
ATA P., TURAN K.
10.Ulusan Tıbbi Genetik Kongresi, Bursa, Turkey, 19 - 23 December 2012
2011
2011Early posttransplant clinical status of desensitized live-donor kidney recipients sensitized with pregnancy and blood transfusions
Ata P., Canbakan M., Ozel L., Kara M., Krand O., Unal E., et al.
25th Conference on European Immunogenetics and Histocompatibility, Prague, Czech Republic, 4 - 07 May 2011, vol.77, pp.453
2005
2005Impact of sensitization to HLA antigens on receiving a second kidney transplant after a failed graft
Eren P., Goral S., Bloom R., Doyle A., Grossman R., Israni A., et al.
42nd Annual Meeting of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), İstanbul, Turkey, 4 - 07 June 2005, vol.20
2005
2005Impact of sensitization to HLA class I and class II antigens (AG) on receiving a 2ND kidney transplant (tx) after a failed graft: Report from a transplant center using a stringent HLA crossmatching (XM) strategy
Goral S., Eren P., Bloom R., Doyle A., Grossman R., Israni A., et al.
6th American Transplant Congress, Washington, United States Of America, 21 - 25 May 2005, vol.5, pp.351
Books & Book Chapters
2017
2017Bölüm 1. İmmunolojik Terimler Sözlüğü
ATA P.
in: Laboratuvardan Kliniğe Transplantasyon Pratiği, ATA PINAR, Editor, NAMIK KEMAL ÜNİVERSİTESİ, pp.17-20, 2017
2017
2017Bölüm 2. Bağışıklık Sistemi ve Antikorlar
ATA P.
in: Laboratuvardan Kliniğe Transplantasyon Pratiği, ATA PINAR, TİTİZ İZZET TİTİZ, Editor, NAMIK KEMAL ÜNİVERSİTESİ, pp.20-48, 2017
2010
2010Transplantasyon Antijenleri ve Genetiği
ATA P.
in: Renal Transplantasyona Pratik Yaklaşım, MESUT İZZET TİTİZ, Editor, NOON TANITIM, İstanbul, pp.47-58, 2010
2010
2010Transplantasyon İmmünolojisine Giriş,
ATA P.
in: Renal Transplantasyona PratikYaklaşım, Mesut İzzet Titiz, Editor, NOON TANITIM, İstanbul, pp.29-42, 2010
Supported Projects
2018 - 2021
2018 - 2021DESİDUAL VE PLAZMA KOMPLEMAN DÜZENLEYİCİ GENLERİN EKSPRESYON DÜZEYLERİ İLE MATERNAL SERUM ANTİ-TROFOBLASTİK ANTİKOR (ATA) DÜZEYLERİNİN İDİOPATİK TEKRARLAYAN VE SPONTAN GEBELİK KAYIPLARINDA ARAŞTIRILMASI
Project Supported by Other Official Institutions
Esim Büyükbayrak E., Ata P. (Executive)
2018 - 2021
2018 - 2021İDİYOPATİK TEKRARLAYAN GEBELİK KAYIPLARINDA DESİDUAL DOKUDA PROGESTERON RESEPTİVİTESİNİ ETKİLEYEN PROGESTERON RESEPTÖR GENİ VE İLİŞKİLİ GENLERİN EKSPRESYON DÜZEYİNİN İNCELENMESİ
Project Supported by Other Official Institutions
Esim Büyükbayrak E., Ata P. (Executive)
2018 - 2020
2018 - 2020Transplantasyon Başarısında Etkili Olan Donöre ÖzgünAlloreaktif Hafıza B Hücre Rezervinin Değerlendirilmesi
TUBITAK Project
(Project Abstract)
Ata P., Bilgen T.(Executive), Titiz M. İ.
2018 - 2019
2018 - 2019
CAKUT Hastalarının Demografik Özellikleri ve Organogenezde Etkili Faktörlerinin Değerlendirilmesi
Project Supported by Higher Education Institutions
(Project Abstract)
Ata P., Alpay H. (Executive), Ürer A.
Scientific Refereeing
September 2019
September 2019TUBITAK Project
1001 - Program for Supporting Scientific and Technological Research Projects, Marmara University, Turkey
June 2019
June 2019TUBITAK Project
1001 - Program for Supporting Scientific and Technological Research Projects, Marmara University, Turkey
Congress and Symposium Activities
25 November 2021 - 28 November 2021
25 November 2021 - 28 November 20211. HEMATOONCOGENETICS CONGRESS
Invited Speaker
Antalya-Turkey
Citations
Total Citations (WOS): 254
h-index (WOS): 10
Jury Memberships
August-2020
August 2020Associate Professor Exam
Associate Professor Exam - Marmara Üniversitesi
July-2020
July 2020Post Graduate
Post Graduate - Marmara Üniversitesi
July-2020
July 2020Appointment Academic Staff
Appointment Academic Staff - Sağlık Bilimleri Üniversitesi
June-2020
June 2020