Prof. DENİZ ASLAN

Publication Network

Published journal articles indexed by SCI, SSCI, and AHCI

HbA2 levels in children with β-thalassemia trait associated with iron deficiency: A perspective for pediatricians

Degermenci S., ASLAN D.

AMERICAN JOURNAL OF CLINICAL PATHOLOGY , 2024 (SCI-Expanded)

DNAJC21-related thrombocytopenia in a young adult female

Aslan D., Akgün Doğan Ö., Ay B., Çamurdan M. O., Mancılar H., Alanay Y.

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics , vol.193, no.2, pp.193-197, 2023 (SCI-Expanded)

Fresh Frozen Plasma Plus Iron Therapy in Congenital Hypotransferrinemia in the Second Decade: A Dynamic Approach to Maintaining Hematological Stability

Aslan D.

TURKISH JOURNAL OF HEMATOLOGY , vol.39, no.1, pp.72-74, 2022 (SCI-Expanded)

Novel Mutation p.Asp374Val of SERPINC1 in a Turkish Family with Inherited Antithrombin Deficiency

ASLAN D.

TURKISH JOURNAL OF HEMATOLOGY , vol.38, no.2, pp.161-163, 2021 (SCI-Expanded)

Is Hemoglobin D Trait Hematologically Silent: Comparison With Healthy Controls and beta-thalassemia Carriers

Aslan D.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , vol.42, no.7, 2020 (SCI-Expanded)

Elevated serum ferritin level with cataract of spectacular morphology: Hyperferritinemia-cataract syndrome

ASLAN D.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.36, no.6, pp.390-393, 2019 (SCI-Expanded)

Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes

Tummala H., Collopy L. C., Walne A. J., Ellison A., Cardoso S., Aksu T., et al.

BLOOD , vol.132, no.12, pp.1349-1353, 2018 (SCI-Expanded)

The search for new approaches to treating type 1 plasminogen deficiency

ASLAN D., AKATA R. F.

PEDIATRIC BLOOD & CANCER , vol.65, no.4, 2018 (SCI-Expanded)

Formulas for the Detection beta-Thalassemia Carriers Are Affected by Changes in Red Cell Parameters

Aslan D.

MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES , vol.10, 2018 (SCI-Expanded)

Addition of oral iron to plasma transfusion in human congenital hypotransferrinemia: A 10-year observational follow-up with the effects on hematological parameters and growth

ASLAN D.

PEDIATRIC BLOOD & CANCER , vol.65, no.2, 2018 (SCI-Expanded)

Fanconi Anemia: A Rarely Considered Cause of Macrocytosis During Childhood

ASLAN D.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , vol.39, no.7, pp.570-572, 2017 (SCI-Expanded) Sustainable Development

Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia

Casini A., Vilar R., Beauverd Y., Aslan D., Devreese K., Mondelaers V., et al.

HAEMOPHILIA , vol.23, no.4, pp.583-589, 2017 (SCI-Expanded)

Maternal serum alpha-fetoprotein levels are normal in Fanconi anemia: Can it be a lack of postnatal inhibition of AFP gene resulting in the elevation?

ASLAN D., KARABACAK R. O., Aslan O. D.

PEDIATRIC BLOOD & CANCER , vol.64, no.4, 2017 (SCI-Expanded)

Harris Platelet Syndrome in Patients of Non-Indian Origin

ASLAN D.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , vol.38, no.8, 2016 (SCI-Expanded)

Pericardial effusion and cardiac tamponade: a sudden and unexpected deterioration in a newborn in the neonatal intensive care unit

AKTAS S., Gumustas M., Onal E., KULA S., ASLAN D.

TURK GOGUS KALP DAMAR CERRAHISI DERGISI-TURKISH JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY , vol.24, no.4, pp.777-778, 2016 (SCI-Expanded)

Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis

Boppudi S., Boegershausen N., Hove H. B., Percin E. F., Aslan D., Dvorsky R., et al.

CLINICAL GENETICS , vol.90, no.4, pp.334-342, 2016 (SCI-Expanded)

"Silent" beta-thalassemia mutation (promoter nt-101 C > T) with increased hemoglobin A(2)

ASLAN D.

TURKISH JOURNAL OF PEDIATRICS , vol.58, no.3, pp.305-308, 2016 (SCI-Expanded)

Recessive congenital methemoglobinemia in immediate generations

ASLAN D., Turkoz-Sucak G., Percy M. J.

TURKISH JOURNAL OF PEDIATRICS , vol.58, no.1, pp.113-115, 2016 (SCI-Expanded)

Molecular diagnosis of Fanconi anemia with next-generation sequencing in a case with subtle signs and a negative chromosomal breakage test

ASLAN D., Ameziane N., De Winter J. P.

TURKISH JOURNAL OF PEDIATRICS , vol.57, no.3, pp.282-285, 2015 (SCI-Expanded) Sustainable Development

Oculoectodermal Syndrome: Report of a New Case With a Broad Clinical Spectrum

ASLAN D., AKATA R. F., Schroeder J., Happle R., Moog U., Bartsch O.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.164, no.11, pp.2947-2951, 2014 (SCI-Expanded)

The X chromosome: does it have a role in Bloom syndrome, a genomic instability disorder?

Aslan D.

TURKISH JOURNAL OF PEDIATRICS , vol.56, no.3, pp.327-329, 2014 (SCI-Expanded)

Leukopenia in Familial Mediterranean Fever: Case Series and Literature Review with Special Emphasis on Pathogenesis

Aslan D.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.31, no.2, pp.120-128, 2014 (SCI-Expanded)

Failure or delay in diagnosing Fanconi anemia - a well-defined genetic disorder

Aslan D.

TURKISH JOURNAL OF PEDIATRICS , vol.55, no.4, pp.462-464, 2013 (SCI-Expanded)

Use of Serum Iron Status and Hemoglobin A2 Levels for Discrimination Between Iron Deficiency and Thalassemia Minor

Aslan D.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.30, no.2, pp.113-115, 2013 (SCI-Expanded)

The MEFV gene and clonal myeloid disorders

Aslan D.

TURKISH JOURNAL OF PEDIATRICS , vol.54, no.5, pp.558-560, 2012 (SCI-Expanded)

A665G Mutation in PRF1 in a Turkish Infant With Familial Hemophagocytic Lymphohistiocytosis

Aslan D.

PEDIATRIC BLOOD & CANCER , vol.56, no.2, pp.319-320, 2011 (SCI-Expanded)

Familial Mediterranean fever with a single MEFV mutation: can a deletion resulting in alpha-thalassemia be the cause?

Aslan D.

JOURNAL OF HUMAN GENETICS , vol.56, no.2, pp.169-171, 2011 (SCI-Expanded)

Dyskeratosis congenita and limbal stem cell deficiency

Aslan D., Akata R. F.

EXPERIMENTAL EYE RESEARCH , vol.90, no.3, pp.472-473, 2010 (SCI-Expanded)

The Gene of Bloom's Syndrome: An Autosomal Recessive Disorder with Male Dominance

ASLAN D., EZGÜ F. S.

GENETIC TESTING AND MOLECULAR BIOMARKERS , vol.13, no.4, pp.443-444, 2009 (SCI-Expanded)

Dyskeratosis Congenita With Corneal Limbal Insufficiency

ASLAN D., ÖZDEK Ş., Camurdan O., BİDECİ A., CİNAZ P.

PEDIATRIC BLOOD & CANCER , vol.53, no.1, pp.95-97, 2009 (SCI-Expanded) Sustainable Development

Emperipolesis in immune thrombocytopenic purpura

Aslan D.

INDIAN JOURNAL OF PATHOLOGY AND MICROBIOLOGY , vol.52, no.2, pp.289-290, 2009 (SCI-Expanded)

The mode of inheritance' in differentiation of Fanconi anemia from Dyskeratosis congenita

Aslan D.

MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL , vol.13, no.11, 2008 (SCI-Expanded)

NADH-cytochrome b5 reductase in a Turkish family with recessive congenital methaemoglobinaemia type I

Percy M. J., Aslan D.

JOURNAL OF CLINICAL PATHOLOGY , no.10, pp.1122-1123, 2008 (SCI-Expanded) Sustainable Development

Automated blood counts and identification of thalassemia carriers

Asian D.

JOURNAL OF POSTGRADUATE MEDICINE , vol.54, no.3, pp.242-243, 2008 (SCI-Expanded)

Dysplasia and disorder of cell membrane entirety in iron-deficiency anemia

Yetgin S., ASLAN D., ÜNAL S., Tavil B., KUŞKONMAZ B. B., Elmas S. A., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.25, no.6, pp.492-501, 2008 (SCI-Expanded)

A new case of human atransferrinemia with a previously undescribed mutation in the transferrin gene

ASLAN D., Crain K., Beutler E.

ACTA HAEMATOLOGICA , vol.118, no.4, pp.244-247, 2007 (SCI-Expanded)

Fanconi anemia (FA) and squamous cell carcinoma in childhood

Aslan D.

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , vol.70, no.11, pp.1995-1997, 2006 (SCI-Expanded)

Griscelli syndrome: Description of a case with Rab27A mutation

Aslan D., Sari S., Derinoz O., Dalgic B.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.23, no.3, pp.255-261, 2006 (SCI-Expanded)

Gastric angiodysplasia in a child with Bernard-Soulier syndrome: efficacy of octreotide in long-term management.

Kaya Z., Gursel T., Dalgic B., Aslan D.

Pediatric hematology and oncology , vol.22, no.3, pp.223-7, 2005 (SCI-Expanded) Sustainable Development

An unusual ocular manifestation in Fanconi anemia: Congenital glaucoma

Aslan D., Ozdogan S., Onol M., Kaya Z., Gursel T.

AMERICAN JOURNAL OF HEMATOLOGY , vol.78, no.1, pp.64-66, 2005 (SCI-Expanded)

Temporary dysplastic hematological features due to iron deficiency in a case of Poland syndrome

Aslan D., Balci S.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.21, no.8, pp.711-715, 2004 (SCI-Expanded)

Parvovirus 1319 infection presenting as pre-B-cell acute lymphoblastic leukemia:: A transient and progressive course in two children

Yetgin S., Çetin M., Aslan D., Özyürek E., Anlar B., Uçkan D.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , vol.26, no.10, pp.689-692, 2004 (SCI-Expanded) Sustainable Development

Supernumerary nipples in children with hematologic disorders

Aslan D., Gursel T., Kaya Z.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.21, no.5, pp.461-463, 2004 (SCI-Expanded)

Red blood cell count and rapid discrimination between thalassemia trait and iron deficiency anemia

Aslan D.

PEDIATRICS INTERNATIONAL , vol.46, no.3, pp.384, 2004 (SCI-Expanded)

Metamizole sodium-induced severe aplastic anemia and its recovery with a short-course steroid therapy

Yetgin S., Ozyurek E., Aslan D., Cetin M.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.21, no.4, pp.343-347, 2004 (SCI-Expanded)

The prognosis and survival of childhood acute lymphoblastic leukemia with central nervous system relapse

ÜNAL S., Yetgin S., Cetin M., Gumruk F., Arslan D., Ozyurek E., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.21, no.3, pp.279-289, 2004 (SCI-Expanded)

Early-onset drusen in a girl with bloom syndrome: probable clinical importance of an ocular manifestation.

Aslan D., Ozturk G., Kaya Z., Bideci A., Ozdogaan S., Gursel T.

Journal of pediatric hematology/oncology , vol.26, no.4, pp.256-7, 2004 (SCI-Expanded) Sustainable Development

Parvovirus B19 infection associated with severe aplastic anemia in an immunocompetent patient

Yetgin S., Çetin M., Özyürek E., Aslan D., ÇETİNKAYA F. D.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.21, no.3, pp.223-226, 2004 (SCI-Expanded) Sustainable Development

Children with acute myeloblastic leukemia presenting with extramedullary infiltration: The effects of high-dose steroid treatment

Hiçsönmez G., Çetin M., TUNCER A., Yenicesu I., Aslan D., Özyürek E., et al.

Leukemia Research , vol.28, no.1, pp.25-34, 2004 (SCI-Expanded)

The role of short course of high-dose methylprednisolone in children with acute myeloblastic leukemia (FAB M2) presented with myeloid tumor

Hicsonmez G., Cetin M., Aslan D., Ozyurek E.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.20, no.5, pp.373-379, 2003 (SCI-Expanded)

Primary hemophagocytic lymphohistiocytosis in Turkish children

Gurgey A., Gogus S., Ozyurek E., Aslan D., Gumruk F., Cetin M., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.20, no.5, pp.367-371, 2003 (SCI-Expanded) Sustainable Development

Incidence of high erythrocyte count in infants and young children with iron deficiency anemia: Re-evaluation of an old parameter

Aslan D., Altay C.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , vol.25, no.4, pp.303-306, 2003 (SCI-Expanded)

Trauma as a risk factor for thrombosis in children: a report of three cases.

Ozyürek E., Beşbaş N., Aslan D., Gürgey A.

The Turkish journal of pediatrics , vol.45, no.2, pp.167-9, 2003 (SCI-Expanded)

Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up

Yetgin S., Tuncer M., Cetin M., Gumruk F., Yenicesu I., Tunc B., et al.

LEUKEMIA , vol.17, no.2, pp.328-333, 2003 (SCI-Expanded)

Serum α-fetoprotein level in Fanconi's anemia: Evaluation of 33 Turkish patients

Aslan D., GÜMRÜK F., ALİKAŞİFOĞLU M., Altay Ç.

American Journal of Hematology , vol.71, no.4, pp.275-278, 2002 (SCI-Expanded) Sustainable Development

Virus-associated immune thrombocytopenic purpura in childhood

Yenicesu I., Yetgin S., Ozyurek E., Aslan D.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.19, no.6, pp.433-437, 2002 (SCI-Expanded) Sustainable Development

Importance of RDW value in differential diagnosis of hypochrome anemias

Aslan D., Gumruk F., Gurgey A., Altay C.

AMERICAN JOURNAL OF HEMATOLOGY , vol.69, no.1, pp.31-33, 2002 (SCI-Expanded)

Outcome of noncatheter-related thrombosis in children: Influence of underlying or coexisting factors

Gurgey A., Aslan D.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , vol.23, no.3, pp.159-164, 2001 (SCI-Expanded)

Articles Published in Other Journals

Epistaxis-related hemolacria in a 6-year-old female after midfacial trauma: Epistaxis-related hemolacria

Demirer Çelik M., Aslan D.

Indian Journal of Case Reports , vol.9, no.9, 2023 (Peer-Reviewed Journal)

Peripheral Blood Erythrocyte Parameters in B-Thalassemia Minor with Coexistent Iron Deficiency: Comparisons between Iron-Deficient and -Sufficient Carriers

Aslan D., Degermenci S.

THALASSEMIA REPORTS , vol.12, no.2, pp.34-38, 2022 (ESCI)

Limbal stem cell deficiency in patients with inherited stem cell disorder of dyskeratosis congenita

ASLAN D., AKATA R. F., Holme H., Vulliamy T., Dokal I.

International Ophthalmology , vol.32, no.6, pp.615-622, 2012 (Scopus)

Refereed Congress / Symposium Publications in Proceedings

USP9X-related intellectual disability in a female with anemia: further delineation of phenotype or dual diagnosis?

Ay B., Akgül T., AKGÜN DOĞAN Ö., ASLAN D., ALANAY Y.

11th Conference on Rare and Undiagnosed Diseases, Vienna, Austria, 7 - 08 November 2022

Kalıtsal Antitrombin Eksikliği: Ulusal Verilerimiz

ÜNÜVAR A., SARPER N., DEMİRSOY U., EROĞLU N., EKER İ., KAYA Z., et al.

13. Ulusal Pediatrik Hematoloji Kongresi, Antalya, Turkey, 14 - 17 October 2021, pp.38-39

Miks Anemilerin Eritrosit Parametreleri Üstüne Etkisi

UYSAL A. E., ASLAN D.

56. Türk Pediatri Kongresi, Antalya, Turkey, 17 October 2021

8p 11.2 delesyonu: FGFR1 ve ANK1 komşu gen sendromu

Bideci A., Döğer E., Küpçü Z., Aslan D., Arhan E., Perçin F. E., et al.

XXIV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Ankara, Turkey, 30 October - 01 November 2020, vol.1, no.1, pp.205

Genotoxicity assessment of children with B-thalassemia minor by use of micronucleus assay in peripheral blood lymphocytes

Özel Babacanoğlu E., Emerce E., Kargın D., Arslan U., Aslan D., Çakmak G.

2nd International Gazi Pharma Symposium, Ankara, Turkey, 11 - 13 October 2017

Genotoxicity Assessment of Children with Β-Thalassemia Minor by Use of Micronucleus Assay in Peripheral Blood Lymphocytes

Özel Babacanoğlu E., EMERCE GÜRSEL E., Kargın D., ARSLAN U., ASLAN D., ÇAKMAK G.

2nd International Gazi Pharma Symposium Series (GPSS-2017), Ankara, Turkey, 11 - 13 October 2017, pp.181

Yenidoğanlarda Santral Venöz Katater İlişkili Yaşamı Tehdit Eden Komplikasyonlar

GÜMÜŞTAŞ M., KULA S., TOKGÖZ S., Aktaş S., ASLAN D., ÖNAL E. E.

12. Ulusal Pediatrik Kardiyoloji ve Kalp Damar Cerrahisi Kongresi, Turkey, 1 - 05 May 2013

Books & Book Chapters

Eye Disorders Caused by Limbal Stem Cell Deficiency

Aslan D., Akata R. F.

in: Stem Cells and Cancer Stem Cells, M.A. Hayat, Editor, Springer, London/Berlin , New Jersey, pp.173-188, 2012 Sustainable Development

Metrics

Publication

Citation (WoS)

564

H-Index (WoS)

Citation (Scopus)

698

H-Index (Scopus)

Project

Thesis Advisory

Open Access

UN Sustainable Development Goals

Publications & Works

Published journal articles indexed by SCI, SSCI, and AHCI

Articles Published in Other Journals

Refereed Congress / Symposium Publications in Proceedings

Books & Book Chapters

Metrics

Publication

Citation (WoS)

H-Index (WoS)

Citation (Scopus)

H-Index (Scopus)

Project

Thesis Advisory

Open Access