Prof.PINAR ATA


School of Medicine, Internal Medical Sciences

Department of Medical Genetics


Research Areas: Health Sciences, Natural Sciences


Names in Publications: PINAR ATA EREN, PINAR EREN

Metrics

Publication

201

Citation (WoS)

254

H-Index (WoS)

10

Citation (Scopus)

286

H-Index (Scopus)

10

Project

6

Thesis Advisory

3

Open Access

2
UN Sustainable Development Goals

Education Information

2000 - 2006

2000 - 2006

Doctorate

Marmara University, Institute Of Health Sciences, Department Of Medical Genetics, Turkey

1997 - 2001

1997 - 2001

Expertise In Medicine

Ministry of Health, University of Health Sciences , Haydarpaşa Numune Research and Education Hospital, Department of Internal Sciences, Turkey

1988 - 1994

1988 - 1994

Undergraduate

Marmara University, School Of Medicine, Turkey

Dissertations

2006

2006

Doctorate

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

2001

Expertise 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 Mastery

English

Certificates, Courses and Trainings

2019

2019

Herediter 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 - Continues

Professor

Marmara University, School Of Medicine, Internal Medical Sciences

Taught Courses And Trainings

2016 - 2016

2016 - 2016

Myelodisplastik 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

2022

CLINICAL 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) identifier

2022

2022

Etiological 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) identifier

2022

2022

Two 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) identifier

2021

2021

A 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) identifier

2020

2020

Expanding 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) identifier

2019

2019

Fibrodysplasia 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) identifier identifier identifier

2019

2019

A 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) identifier

2019

2019

Challenges 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) Sustainable Development identifier identifier identifier

2018

2018

THE 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) identifier

2018

2018

Intraoperative 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) identifier

2017

2017

Cytotoxic 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) identifier identifier identifier

2015

2015

A 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) identifier identifier identifier

2014

2014

Proteinuria 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) identifier identifier

2012

2012

The 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) identifier identifier identifier

2011

2011

Ramsay 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) identifier identifier identifier

2011

2011

Pyoderma 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) identifier identifier identifier

2011

2011

Effects 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) Creative Commons License identifier identifier identifier

2009

2009

Determination 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) identifier identifier identifier identifier

Articles Published in Other Journals

2022

2022

A 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) identifier identifier identifier

2021

2021

Türkiye’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) Sustainable Development

2019

2019

Association 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)

Refereed Congress / Symposium Publications in Proceedings

2021

2021

Toplumumuzda 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

2020

Çocukluk 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

2019

A 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

2019

GENETIC 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

2019

Schaaf 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

2019

Rare 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

2019

Genotype 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

2019

A 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

2018

FGF3 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 identifier

2018

2018

The 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 identifier

2018

2018

A 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 identifier

2018

2018

The 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 identifier

2019

2019

Fokal 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

2019

Otozomal 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

2019

Çocukluk 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

2019

Von 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

2019

Ankilozan Spondilit’te Mikrorna Ekspresyonu

TÜRKYILMAZ A., AKBAŞ F., ATA P., YAĞCI İ.

Uluslararası Katılımlı Türk Romatoloji Kongresi, Antalya, Turkey, 20 - 24 March 2019

2018

2018

İki 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

2018

ANKİLOZAN 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

2018

REVERSE 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

2018

NÖROMOTOR 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

2018

İKİ 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

2018

PEDİATRİK 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

2018

FARKLI 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

2018

The 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

2018

Novel 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

2017

A 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 identifier

2017

2017

BBS10 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 identifier

2017

2017

Inversion 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 identifier

2017

2017

Evaluation 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 Sustainable Development identifier

2017

2017

Novel 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 identifier

2018

2018

Hepatosellüler karsinom gelişiminde moleküleryolaklar

ATA P.

M.Ü. Tıp Fakültesi III. Uluslararası Onkolojive Cerrahi Günleri Sempozyumu, 3 - 04 May 2018

2018

2018

Hepatosellüler 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

2017

Does 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

2017

A 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

2017

BBS10 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

2017

A 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

2017

BBS10 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

2017

Novel 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

2017

Largest 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

2017

May 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 identifier

2016

2016

A 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

2016

BREAST 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 Sustainable Development

2016

2016

Silver 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

2016

Clinical 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

2016

Yaşlanma 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

2016

Analysis 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

2015

2015

PROGRESİVA 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

2014

2014

Assessment 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 Sustainable Development

2014

2014

Evaluation 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

2014

Evaluation 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

2014

Assessment 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

2014

Determination 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

2014

Evaluation 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

2014

Kronik 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

2014

KADAVRA 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

2014

Kadavradan 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

2014

Pretransplant 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

2013

2013

Is 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 identifier

2013

2013

Association 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

2012

Anti 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

2011

Early 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 identifier

2005

2005

Impact 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 identifier

Books & Book Chapters

2017

2017

Bölüm 1. İmmunolojik Terimler Sözlüğü

ATA P.

in: Laboratuvardan Kliniğe Transplantasyon Pratiği, ATA PINAR, Editor, NAMIK KEMAL ÜNİVERSİTESİ, pp.17-20, 2017

2017

2017

Bölüm 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

2010

Transplantasyon Antijenleri ve Genetiği

ATA P.

in: Renal Transplantasyona Pratik Yaklaşım, MESUT İZZET TİTİZ, Editor, NOON TANITIM, İstanbul, pp.47-58, 2010

2010

2010

Transplantasyon İmmünolojisine Giriş,

ATA P.

in: Renal Transplantasyona PratikYaklaşım, Mesut İzzet Titiz, Editor, NOON TANITIM, İstanbul, pp.29-42, 2010

Scientific Refereeing

September 2019

September 2019

TUBITAK Project

1001 - Program for Supporting Scientific and Technological Research Projects, Marmara University, Turkey

June 2019

June 2019

TUBITAK 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 2021

1. HEMATOONCOGENETICS CONGRESS

Invited Speaker

Antalya-Turkey

Citations

Total Citations (WOS): 254

h-index (WOS): 10

Jury Memberships

August-2020

August 2020

Associate Professor Exam

Associate Professor Exam - Marmara Üniversitesi

July-2020

July 2020

Post Graduate

Post Graduate - Marmara Üniversitesi

July-2020

July 2020

Appointment Academic Staff

Appointment Academic Staff - Sağlık Bilimleri Üniversitesi

June-2020

June 2020

Associate Professor Exam

Associate Professor Exam - Çukurova Üniversitesi