Publications & Works

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

PHENOTYPIC AND GENOTYPIC CHARACTERISTICS OF CHILDREN WITH BARTTER SYNDROME

PEDIATRIC NEPHROLOGY, vol.36, no.10, pp.3430, 2021 (Journal Indexed in SCI) identifier

A rare cause of hypercalcemia: Congenital Lactase Deficiency

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.75, 2021 (Journal Indexed in SCI) identifier

Fibrodysplasia ossificans progressiva: lessons learned from a rare disease.

Current opinion in pediatrics, vol.31, pp.716-722, 2019 (Journal Indexed in SCI) identifier identifier identifier

Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.214, 2019 (Journal Indexed in SCI) identifier

A rare cause of hypophosphatemia: Raine Syndrome

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.384, 2019 (Journal Indexed in SCI) identifier

Challenges in the treatment of fibrodysplasia ossificans progressiva

RHEUMATOLOGY INTERNATIONAL, vol.39, no.3, pp.569-576, 2019 (Journal Indexed in SCI) identifier identifier identifier

THE CO-EXISTENCE OF TWO RARE DISEASES: A CASE REPORT

PEDIATRIC NEPHROLOGY, vol.33, no.10, pp.1881, 2018 (Journal Indexed in SCI) identifier

Intraoperative Tissue-Immunosuppressive Therapy Reduces Rejection Episodes in Heart Transplant Recipients.

Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, 2018 (Journal Indexed in SCI Expanded) identifier

Cytotoxic Antibody Detection by Means of Flow-Cytometric Cross-Match

TRANSPLANTATION PROCEEDINGS, vol.49, no.3, pp.440-444, 2017 (Journal Indexed in SCI) identifier identifier identifier

A Rare Reason of Ileus in Renal Transplant Patients With Peritoneal Dialysis History: Encapsulated Peritoneal Sclerosis.

Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, vol.13, pp.588-92, 2015 (Journal Indexed in SCI Expanded) identifier identifier identifier

Factors Affecting the Selection of Patients on Waiting List: A Single Center Study.

Transplantation proceedings, vol.47, pp.1265-8, 2015 (Journal Indexed in SCI Expanded) identifier identifier identifier

Cancer Screening of Renal Transplant Patients Undergoing Long-Term Immunosuppressive Therapy

TRANSPLANTATION PROCEEDINGS, vol.47, no.5, pp.1413-1417, 2015 (Journal Indexed in SCI) identifier identifier identifier

Proteinuria associated with mTOR inhibitors after kidney transplant.

Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, vol.12, pp.539-42, 2014 (Journal Indexed in SCI Expanded) identifier identifier

TLR4 gene polymorphism in patients with nonalcoholic fatty liver disease in comparison to healthy controls.

Metabolic syndrome and related disorders, vol.12, pp.165-70, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

Association of COL1A1 polymorphism in Turkish patients with otosclerosis.

American journal of otolaryngology, vol.34, pp.403-6, 2013 (Journal Indexed in SCI Expanded) identifier identifier identifier

The impact of C4d staining as a humoral injury marker.

Transplantation proceedings, vol.44, pp.1694-6, 2012 (Journal Indexed in SCI Expanded) identifier identifier identifier

Ramsay Hunt syndrome with atypical progress in a renal transplant recipient: a case report.

Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, vol.9, pp.413-6, 2011 (Journal Indexed in SCI Expanded) identifier identifier identifier

Pyoderma gangrenosum in a renal transplantation patient having immunosuppressive treatment for 5 years.

Transplant international : official journal of the European Society for Organ Transplantation, vol.24, 2011 (Journal Indexed in SCI) identifier identifier identifier

Effects of intra- and extracellular factors on anti-aging klotho gene expression

GENETICS AND MOLECULAR RESEARCH, vol.10, pp.2009-2023, 2011 (Journal Indexed in SCI) Creative Commons License identifier identifier identifier

Determination of the Risk Group in Patients with Venous Thrombosis

TURKIYE KLINIKLERI TIP BILIMLERI DERGISI, vol.29, no.6, pp.1430-1434, 2009 (Journal Indexed in SCI) identifier identifier identifier

Calcium-sensing receptor gene polymorphisms and cardiac valvular calcification in patients with chronic renal failure: a pilot study.

Hemodialysis international. International Symposium on Home Hemodialysis, vol.13, pp.176-80, 2009 (Journal Indexed in SCI Expanded) identifier identifier identifier

Articles Published in Other Journals

Refereed Congress / Symposium Publications in Proceedings

A NOVEL MUTATION IN ATP6V0A4 GENE IN APATIENT WITH DISTAL RENAL TUBULAR ACIDOSIS

18 th Congress of the International Pediatric Nephrology Association-IPNA, 17 - 21 October 2019

A NOVEL MUTATION IN ATP6V0A4 GENE IN APATIENT WITH DISTAL RENAL TUBULAR ACIDOSIS

18 th Congress of the International Pediatric Nephrology Association-IPNA, 17 - 21 October 2019

GENETIC ANALYSIS IN TURKISH CHILDRENWITH ALPORT SYNDROME: NOVEL MUTATIONS AND VARIATIONS

18 th Congress of the International Pediatric Nephrology Association-IPNA, Italy, 17 - 21 October 2019, vol.34, pp.1821-2260

Schaaf Yang sendromu

4. Ulusal Çocuk Genetik kongresi, İstanbul, Turkey, 25 - 27 September 2019

Rare Causes of Osteogenesis Imperfecta are Commonin Consanguineous Pedigrees

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019

Genotype and Phenotype Characterization ofTurkish Patients with Vitamin D Dependent RicketsType IA

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, vol.91

A rare cause of hypophosphatemia: Raine Syndrome

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, vol.91

A novel intronic ATM gene mutation affecting splicing in a patient with Ataxia-Telangiectasia

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

FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia

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

The effects of calcium-sensing receptor CASR genotypes, treatment duration, gender bone health and mineral metabolism in chronic renal failure patients

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

Fokal Segmental Glomeruloskleroz, son tanı mı?

10.Uluslararası katılımlı Çocuk Nefroloji Kongresi, Muğla, Turkey, 1 - 04 May 2019, pp.194

Von Hippel Lindau Patients

13. BALKAN GENETİK KONGRESİ, Edirne, Turkey, 16 - 20 April 2019

FARKLI GENLER,FARKLI MUTASYONLAR,FENOTİPTE FARKLILIK YARATIYOR MU ?: ALPORT SENDROMU

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018

İKİ LAMİNOPATİ OLGUSU: LMNA GENİ MUTASYONLARI İLE İLİŞKİLİ FENOTİPLER

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 07 November 2018 - 11 November 1918

PEDİATRİK AKUT LENFOBLASTİK LÖSEMİDE TEŞHİSSEL TESTLERİN GEÇERLİLİĞİ

13. Uluslararası Katılımlı Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 7 - 11 November 2018

REVERSE GENETİK İLE TANI KOYULAN NADİR BİR SPASTİK PARAPLEJİ AİLESİ

13.ULUSLARARASI KATILIMLI ULUSAL TIBBİ GENETİK ANABİLİM DALI, Turkey, 7 - 11 November 2018

ANKİLOZAN SPONDİLİT’xxTE MİKRO RNA EKSPRESYONU

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018

Novel mutations and variations in turkish children with Alport syndrome: are the benign variations always harmless?

51th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Antalya, Turkey, 3 - 06 October 2018

Novel Large CFTR Gene Deletions in Turkish Patients with Increased Morbidity

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.980 identifier

Inversion Y Having Different Phenotypic Expressions at Three Brothers

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.829 identifier

Hepatosellüler karsinom gelişiminde moleküleryolaklar

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

Hepatosellüler karsinom tanısında genetikbiyobelirteçler

MARMARA ÜNİVERSİTESİ TIP FAKÜLTESİIII. ULUSLARARASI ONKOLOJİ VE CERRAHİ GÜNLERİHEPATO-PANKREATO-BİLİYER ve GASTROİNTESTİNAL KANSERLERDESİSTEMİK VE CERRAHİ TEDAVİLERDE GELİŞMELER, 3 - 05 May 2018

A Novel HNF1B mutation in a family with two MODY patients

The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 May 2017

BBS10 frameshift mutation in a Turkish girl with Bardet Biedl Syndrome.

The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 May 2017

BBS10 frameshift mutation in a turkish girl with bardet biedl syndrome

The European Society of Human Genetics 2017, KOPENHAGEN, Denmark, 25 - 30 May 2017

A novel HNF1B mutation in a family with two MODY patients

The European Society of Human Genetics 2017., KOPENHAGEN, Denmark, 25 - 28 May 2017

Novel Large CFTR Gene Deletions in Turkish Patients with Increased Morbidity,

The European Society of Human Genetics, KOPENHAGEN, Denmark, 26 - 30 May 2017

Largest family in Turkey with multiple endocrine neoplasia-type 1 and a newly discovered mutation.

16. Eurasian Congress of Gastrtoenterology and Surgery, Mostar, Bosnia And Herzegovina, 27 - 30 April 2017, vol.7, pp.117-118

May Intraoperative Immunosuppressive Therapy Reduce the Rejection Episodes at Cardiac Transplant Recipients?

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

A New Flowcytometric crossmatch Technique with 7AAD For Cytotoxic Antibody Detection

TÜRKİYE ORGAN NAKLİ KOORDİNATÖRLERİ KONGRESİ, Konya, Turkey, 13 - 15 October 2016

BREAST CANCER INHERITANCE FAMILY PATIENTS POINT OF VIEW

International Istanbul Breast Cancer Conference - BREASTANBUL 2016, İstanbul, Turkey, 10 - 12 October 2016

Silver Russel Sendromlu bir olgu

12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016

Clinical Evaluation of a MDC1A Case Carrying LAMA2 Mutation

ULUSAL TIBBİ GENETİK KONGRESİ, İZMİR ÇEŞME, Turkey, 5 - 09 October 2016

Yaşlanma ile İlişkili Klotho Geni ve Bu Genin Ekspresyonunda Epigenetik Faktörlerin Rolü

Ulusal Moleküler Tıp Sempozyumu: Moleküler Bakıştan Kliniğe, İstanbul, Turkey, 1 - 03 June 2016

Analysis of The Molecular Markers in 49 AML Patients

European Society of Human Genetics Congress, Barcelona, Spain, 21 - 24 May 2016

PROGRESİVA ANKİLOZAN SPONDİLİT İLE KARIŞAN NADİR BİR HASTALIK

25.UlusalFiziksel TipveRehabilitasyonKongresi, Turkey, 22 - 26 April 2015

Determination of drug related problem and drug burden index in elderly patients

43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.208-209

Assessment of knowledge and attitude towards osteoporosis among women attending community pharmacy settings

43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.213

Evaluation of drug burden index in elderly patients utilized disposable insulin pen

43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.203-204

Assessment of patients knowledge and attitude towards methotrexate utilization

43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.256

Evaluation of drug burden index in elderly patients utilized inhaler

43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.205

Evaluation of drug burden index and medication utilization in geriatric patients at community pharmacy

43rd European Symposium on Clinical Pharmacy, KOPENHANG, Denmark, 22 - 24 October 2014, vol.37, pp.206-207

Is the TLR-4 Gene Polymorphism Play a Protective Role in the Development of NAFLD in Humans ?

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

Anti aging Klotho geni ekspresyonuna hücre içi ve hücreler arası faktörlerin etkisi

10.Ulusan Tıbbi Genetik Kongresi, Bursa, Turkey, 19 - 23 December 2012

Early posttransplant clinical status of desensitized live-donor kidney recipients sensitized with pregnancy and blood transfusions

25th Conference on European Immunogenetics and Histocompatibility, Prague, Czech Republic, 4 - 07 May 2011, vol.77, pp.453 identifier

Impact of sensitization to HLA antigens on receiving a second kidney transplant after a failed graft

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

Bölüm 1. İmmunolojik Terimler Sözlüğü

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

Bölüm 2. Bağışıklık Sistemi ve Antikorlar

in: Laboratuvardan Kliniğe Transplantasyon Pratiği, ATA PINAR, TİTİZ İZZET TİTİZ, Editor, NAMIK KEMAL ÜNİVERSİTESİ, pp.20-48, 2017

Transplantasyon Antijenleri ve Genetiği

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

Transplantasyon İmmünolojisine Giriş,

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