Prof. HATİCE ASUMAN ÖZKARA

Publication Network

Journal articles indexed in SCI, SSCI, and AHCI

Myelin oligodendrocyte glycoprotein antibodies in genetic leukodystrophies

EROĞLU ERTUĞRUL N. G., Yousefi M., Pekguel F., Doran T., Guenbey C., TOPÇU M., et al.

JOURNAL OF NEUROIMMUNOLOGY , vol.369, 2022 (SCI-Expanded)

Comprehensive clinical, biochemical, radiological and genetic analysis of 28 Turkish cases with suspected metachromatic leukodystrophy and their relatives

Pekgul F., Eroglu-Ertugrul N. G., Bekircan-Kurt C. E., Erdem-Ozdamar S., Cetinkaya A., Tan E., et al.

MOLECULAR GENETICS AND METABOLISM REPORTS , vol.25, 2020 (SCI-Expanded)

A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2

Ozen S., Bilginer Y., Batu E., Taşkıran E., Özkara H. A., Ünal Ş., et al.

JOURNAL OF RHEUMATOLOGY , vol.47, no.1, pp.117-125, 2020 (SCI-Expanded)

Prenatal enzymatic diagnosis of lysosomal storage diseases using cultured amniotic cells, uncultured chorionic villus samples, and fetal blood cells: Hacettepe experience

ÜNAL C., ÖZKARA H. A., TANAÇAN A., FADILOĞLU E., LAY İ., TOPÇU M., et al.

PRENATAL DIAGNOSIS , vol.39, no.12, pp.1080-1085, 2019 (SCI-Expanded)

Inflammatory response and its relation to sphingolipid metabolism proteins: Chaperones as potential indirect anti-inflammatory agents

Yagci Z. B., Esvap E., ÖZKARA H. A., Ulgen K. O., ÖZKIRIMLI ÖLMEZ E.

MOLECULAR CHAPERONES IN HUMAN DISORDERS , vol.114, pp.153-219, 2019 (SCI-Expanded)

Evaluating the effects of cardiac resynchronization therapy on pathophysiological pathways of heart failure using surrogate biomarkers

SUNMAN H., ÖZKAN A., YORGUN H., CANPOLAT U., KARABULUT E., Bayrak T., et al.

CARDIOLOGY JOURNAL , vol.25, no.1, pp.42-51, 2018 (SCI-Expanded)

Four novel mutations in the beta-galactosidase gene identified in infantile type of GM1 gangliosidosis

CELTIKCI B., AYDIN H. I., Sivri S., Sonmez M., TOPÇU M., ÖZKARA H. A.

CLINICAL BIOCHEMISTRY , vol.45, pp.571-574, 2012 (SCI-Expanded)

Two novel alpha-galactosidase A mutations causing Fabry disease: A missense mutation M11V in a heterozygote woman and a nonsense mutation R190X in a hemizygote man.

CELTIKCI B., TOPÇU M., ÖZKARA H. A.

Clinical biochemistry , vol.44, pp.809-12, 2011 (SCI-Expanded)

Why are they having infant colic? A nested case-control study

YALÇIN Ş., ORUN E., MUTLU B., MADENDAG Y., Sinici İ., DURSUN A., et al.

PAEDIATRIC AND PERINATAL EPIDEMIOLOGY , vol.24, no.6, pp.584-596, 2010 (SCI-Expanded)

Effectiveness of topical zinc oxide application on hypertrophic scar development in rabbits

AKSOY B., Atakan N., AKSOY H. M., Tezel G. G., RENDA N., ÖZKARA H. A., et al.

BURNS , vol.36, no.7, pp.1027-1035, 2010 (SCI-Expanded)

Establishment of Green Fluorescent Protein Expressing CHO Cells by Stable Transfection Using Activated Dendrimers and G418 Selection

CELTIKCI B., PURALI N., ÖZKARA H. A.

TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , vol.35, no.4, pp.340-343, 2010 (SCI-Expanded)

Identification of two novel arylsulfatase A mutations with a polymorphism as a cause of metachromatic leukodystrophy

Oender E., Sinici I., Soenmez F. M., TOPÇU M., Oezkara H. A.

NEUROLOGICAL RESEARCH , vol.31, no.1, pp.60-66, 2009 (SCI-Expanded)

Inhibition of Endoplasmic Reticulum Associated Degradation of Mutant Pro-beta Subunits of beta-Hexosaminidase by Kifunensine and Lactacystin

SINICI I., Tropak M. B., Oezkara H. A., Mahuran D. J.

TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , vol.34, no.3, pp.160-166, 2009 (SCI-Expanded)

Protective role of 27bp repeat polymorphism in intron 4 of eNOS gene in lacunar infarction

Yemisci M., Sinici I., ÖZKARA H. A., Hayran M., AY H., CELTIKCI B., et al.

FREE RADICAL RESEARCH , vol.43, no.3, pp.272-279, 2009 (SCI-Expanded)

Increased hexosaminidase activity in antipsychotic-induced extrapyramidal side effects: Possible association with higher occurrence in bipolar disorder patients

Tunca Z., RESMI H., ÖZKARA H. A., Ciliv G., CELTIKCI B., ALPTEKIN K., et al.

PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY , vol.32, no.5, pp.1214-1220, 2008 (SCI-Expanded)

Identification of 7th hexosaminidase A mutation of Tay-Sachs disease in the Turkish population

Sinici I., OENDER E., Topcu M., Oezkara H. A.

TURKISH JOURNAL OF PEDIATRICS , vol.49, no.3, pp.337-338, 2007 (SCI-Expanded)

Comparison of HCMV IE and EF-1 alpha promoters for the stable expression of beta-subunit of hexosaminidase in CHO cell lines

SINICI I., ZARGHOONI M., TROPAK M. B., MAHURAN D. J., Ozkara H. A.

BIOCHEMICAL GENETICS , vol.44, pp.173-180, 2006 (SCI-Expanded)

Serum ribonuclease activity in the diagnosis of prostate cancer in men with serum prostate-specific antigen levels between 2.5 and 20 ng/mL

ESKICORAPCI S., Ozkara H. A., ONDER E., AKDOGAN B., ERKAN İ., CILIV G., et al.

CLINICAL BIOCHEMISTRY , vol.39, no.4, pp.363-366, 2006 (SCI-Expanded) Sustainable Development

Recent advances in the biochemistry and genetics of sphingolipidoses

Ozkara H. A.

BRAIN & DEVELOPMENT , vol.26, no.8, pp.497-505, 2004 (SCI-Expanded)

Does serum hexosaminidase activity play a role in the diagnosis of strangulated bowel obstruction? An experimental study

ORUC M., OZMEN M., KAZAN O., DUZGUN A., Ozkara H. A., ARIK D., et al.

DIGESTIVE DISEASES AND SCIENCES , vol.49, no.10, pp.1681-1686, 2004 (SCI-Expanded)

Sphingolipidoses in Turkey

Ozkara H. A., Topca M.

BRAIN & DEVELOPMENT , vol.26, no.6, pp.363-366, 2004 (SCI-Expanded)

Assessing the severity of the small inframe deletion mutation in the alpha-subunit of beta-hexosaminidase A found in the Turkish population by reproducing it in the more stable beta-subunit

Sinici I., Tropak M., Mahuran D., Ozkara H.

JOURNAL OF INHERITED METABOLIC DISEASE , vol.27, no.6, pp.747-756, 2004 (SCI-Expanded)

Characterization of two Turkish beta-hexosaminidase mutations causing Tay-Sachs disease

Ozkara H. A., SANDHOFF K.

BRAIN & DEVELOPMENT , vol.25, no.3, pp.191-194, 2003 (SCI-Expanded)

A new point mutation (G412 to A) at the last nucleotide of exon 3 of hexosaminidase at-subunit gene affects splicing

Ozkara H. A., SANDHOFF K.

BRAIN & DEVELOPMENT , vol.25, no.3, pp.203-206, 2003 (SCI-Expanded)

Biochemical and molecular characterization of mutant hexosaminidase A in a Turkish family

Sinici İ., Ozkara H., Topcu M., Ciliv G.

PEDIATRICS INTERNATIONAL , vol.45, no.1, pp.16-22, 2003 (SCI-Expanded)

Propofol anaesthesia and metabolic acidosis in children

OZLU O., Ozkara H. A., ERIS S., OCAL T.

PAEDIATRIC ANAESTHESIA , vol.13, no.1, pp.53-57, 2003 (SCI-Expanded)

Amplification of the c-myc oncogene in non-small cell lung cancer

Ozkara H. A., OZKARA S., TOPCU S., CRISS W.

TUMORI J , vol.85, no.6, pp.508-511, 1999 (SCI-Expanded)

At least six different mutations in HEXA gene cause Tay-Sachs disease among the Turkish population

Ozkara H. A., NAVON R.

MOLECULAR GENETICS AND METABOLISM , vol.65, no.3, pp.250-253, 1998 (SCI-Expanded)

Comparison of three different primer pairs for the detection of Mycobacterium tuberculosis by polymerase chain reaction in paraffin-embedded tissues

Ozkara H. A., Kocagöz T., Ozcelik U., Akcoren Z., GOCMEN A.

INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE , vol.2, no.6, pp.451-455, 1998 (SCI-Expanded) Sustainable Development

Sandhoff disease in the Turkish population

Ozkara H. A., TOPCU M., RENDA Y.

BRAIN & DEVELOPMENT , vol.19, no.7, pp.469-472, 1997 (SCI-Expanded)

Detection of Mycobacterium tuberculosis DNA in tissue samples of children with sarcoidosis

Ozcelik U., Ozkara H. A., GOCMEN A., Akcoren Z., KOCAGOZ T., Kiper N., et al.

PEDIATRIC PULMONOLOGY , vol.24, no.2, pp.122-124, 1997 (SCI-Expanded) Sustainable Development

A STUDY ON ENZYME-ACTIVITIES OF SOME SPHINGOLIPIDOSES

OZKARA H. A., ARIKAN M., TOPCU M., EMRE S., RENDA Y.

TURKISH JOURNAL OF PEDIATRICS , vol.36, no.3, pp.215-221, 1994 (SCI-Expanded)

Articles Published in Other Journals

Association between reverse electrical remodeling and cardiac fibrosis markers in patients with cardiac resynchronization therapy.

Sunman H., Canpolat U., Yorgun H., Özkan A., Yalçın M., Bayrak T., et al.

Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir , vol.46, pp.84-91, 2018 (ESCI)

Vitamin D levels predict the response to cardiac resynchronization therapy in patients with systolic heart failure

Sunman H., Ozkan A., YORGUN H., CANPOLAT U., Maharjan N., Asil S., et al.

TURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGY , vol.44, no.8, pp.670-676, 2016 (ESCI)

Metachromatic leukodystrophy: Biochemical characterization of two (p.307Glu→Lys, p.318Trp→Cys) arylsulfatase A mutations.

ÖZKAN A., Özkara H. A.

Intractable & rare diseases research , vol.5, pp.280-283, 2016 (ESCI)

Gelişen Klinik Biyokimya Metabolomik

ÖZKARA H. A.

Hacettepe Tıp Dergisi , vol.39, no.1, pp.4-8, 2008 (Peer-Reviewed Journal)

Prenatal enzymatic diagnosis of Tay Sachs and Sandhoff diseases using chorionic villus and fetal blood sampling

ÖZKARA H. A., TOPÇU M., ÇAKAR A. N., BEKSAÇ M. S.

Gynecology, Obstetrics and Reproductive Medicine (GORM) , vol.3, no.1, pp.251-254, 1997 (Peer-Reviewed Journal)

Sfingolipit depo hastalıklarının enzimatik tanısı

ÖZKARA H. A., TOPÇU M., BEKSAÇ M. S.

Klinik Bilimler ve Doktor , vol.3, pp.431-439, 1997 (Peer-Reviewed Journal)

Donor splice site mutation in intron 5 of the HEXA gene in a Turkish infant with Tay‐Sachs disease

ÖZKARA H. A., Akerman B., Ciliv G., TOPÇU M., Renda Y., Gravel R.

Human Mutation , vol.5, no.2, pp.186-187, 1995 (Scopus)

Çocukluk çağı Metakromatik lökodistrofi tanısı alan olgularda Arilsülfataz A enzim aktivite değerleri klinik ve laboratuvar bulguları

EMRE S., TOPÇU M., SEYRANTEPE V., ÖZKARA H. A., RENDA Y.

Çocuk Sağlığı ve Hastalıkları Dergisi , vol.38, no.4, pp.575-582, 1995 (Peer-Reviewed Journal)

Tay Sachs hastalığının moleküler temeli 1

ÖZKARA H. A., CİLİV G.

Doktor , vol.2, no.3-4, pp.243-245, 1994 (Peer-Reviewed Journal)

Gangliosides in cell cell interaction differentiation and oncogenesis a review

ÖZKARA H. A., CRİSS W. E.

Turkish J Cancer , vol.23, no.2, pp.53-58, 1993 (Peer-Reviewed Journal)

Akciğer tüberkülozunda bronş lavaj sıvısında ve serumda lizozim aktivitesi üzerine bir çalışma

ÖZKARA Ş., ÖZKARA H. A., ULUTÜRK S., ÖZAL N., ÖRÜÇ O.

Solunum Hastalıkları , vol.4, no.2, pp.191-196, 1993 (Peer-Reviewed Journal)

Bronş lavaj sıvısı ve serum adenozin deaminaz ADA aktivitesinin akciğer tüberkülozu tanısındaki rolü

ÖZKARA Ş., ÖZKARA H. A., KAHRAMAN M., ÖRÜÇ O., CİLİV G.

Solunum Hastalıkları , vol.4, no.2, pp.203-211, 1993 (Peer-Reviewed Journal)

Papers Presented at Peer-Reviewed Scientific Conferences

AB0574 A MONOGENIC DISEASE WITH WIDE RANGE OF SYMPTOMS: DEFICIENCY OF ADENOSINE DEAMINASE 2

BATU AKAL E. D., TAŞKIRAN Z. E., TEZCAN F. İ., ÖZKARA H. A., ÇAĞDAŞ AYVAZ D. N., ÖZEN S., et al.

Annual European Congress of Rheumatology (EULAR), Madrid, Spain, 12 - 15 June 2019, vol.78, pp.1748, (Full Text)

Association between reverse electrical remodeling and cardiac fibrosis markers in patients with cardiac resynchronization therapy

SUNMAN H., CANPOLAT U., YORGUN H., ÖZKAN A., YALÇIN M. U., BAYRAK T., et al.

33nd Turkish Cardiology Congress With International Participation, Antalya, Turkey, 5 - 08 October 2017, vol.18, pp.54, (Summary Text)

P3184 BEDSIDEThe in uence of cardiac resynchronization therapy on molecular pathways in pathophysiology of heart failure

SUNMAN H., ÖZKAN A., CANPOLAT U., YORGUN H., BAYRAK T., ŞAHİNER M. L., et al.

ESC Congress 2013, 31 August-4 September 2013, Amsterdam, Holland, 31 August - 04 September 2013

OP 125 PROGNOSTIC VALUE OF REVERSE REMODELLING BIOMARKERS AND BRAIN NATRIURETIC PEPTIDE IN THE MANAGEMENT OF PATIENTS RECEIVING CARDIAC RESYNCHRONIZATION THERAPY

SUNMAN H., YORGUN H., ÖZKAN A., CANPOLAT U., YALÇIN M. U., ŞAHİNER M. L., et al.

9th International Congress of Update in Cardiology and Cardiovascular Surgery, March 21-24, 2013, Antalya, Turkey, 21 - 24 March 2013

OP 126 USEFULNESS OF PREIMPLANTATION B TYPE NATRIURETIC PEPTIDE AND CARDIAC INJURY MARKERS LEVEL FOR PREDICTING RESPONSE TO CARDIAC RESYNCHRONIZATION THERAPY

SUNMAN H., ÖZKAN A., YORGUN H., CANPOLAT U., ÜLGEN A., ŞAHİNER M. L., et al.

9th International Congress of Update in Cardiology and Cardiovascular Surgery, March 21-24, 2013, Antalya, Turkey, 21 - 24 March 2013

OP 127 PREDICTION OF MAJOR CARDIOVASCULAR EVENTS IN CRT PATIENTS WITH INFLAMMATION MARKERS AND BNP LEVELS

SUNMAN H., ÖZKAN A., CANPOLAT U., YORGUN H., ŞAHİNER M. L., BAYRAK T., et al.

9th International Congress of Update in Cardiology and Cardiovascular Surgery, March 21-24, 2013, Antalya, Turkey, 21 - 24 March 2013

The establishment of Green Fluorescent Protein expressing CHO cells by stable transfection using activated dendrimers and G418 selection

ÇELTİKÇİ B., ÖZKARA H. A., PURALI N.

FEBS JOURNAL, Prague, 4 - 09 July 2009, vol.276, pp.215-216

Protective role of 27 bp deletion polymorphism in intron 4 of eNOS gene in cerebral small-vessel disease

Yemisci M., Sinici I., ÖZKARA H. A., HAYRAN K. M., ay h., ÇELTİKÇİ B., et al.

FEBS JOURNAL, İstanbul, Turkey, 24 - 29 June 2006

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