Prof.Dr. MERAL ÖZGÜÇ

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Identification of two novel PNPLA1 mutations in Turkish families with autosomal recessive congenital ichthyosis.

Dökmeci-Emre S., TAŞKıRAN Z. E., YÜZBAŞıOĞLU A., ÖNAL G., AKARSU A. N., KARADUMAN A., et al.

The Turkish journal of pediatrics , cilt.59, ss.475-482, 2017 (SCI-Expanded)

Discovery of biomarkers in rare diseases: innovative approaches by predictive and personalized medicine

GÜLBAKAN B., ÖZGÜL R. K., YÜZBAŞIOĞLU A., Kohl M., Deigner H., ÖZGÜÇ M.

EPMA JOURNAL , cilt.7, 2016 (SCI-Expanded)

Bioethical Challenges of the Ebola Outbreak

Unsal C. Z., Akcay D., BÜKEN N., Ozguc M.

JOURNAL OF BIOETHICAL INQUIRY , cilt.12, sa.2, ss.173-175, 2015 (SCI-Expanded)

Biobanking: sample acquisition and quality assurance for 'omics' research

YÜZBAŞIOĞLU A., Ozguc M.

NEW BIOTECHNOLOGY , cilt.30, sa.3, ss.339-342, 2013 (SCI-Expanded)

Novel mutations of the MLC1 gene in Turkish patients

YÜZBAŞIOĞLU A., TOPÇU M., KOCAEFE Y. Ç., ÖZGÜÇ M.

EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.54, sa.3, ss.281-283, 2011 (SCI-Expanded)

TAP1 and TAP2 gene polymorphisms in childhood cystic echinococcosis

Kiper N., Gerceker F., Utine E., Yalcin E., Pekcan S., Cobanoglu N., et al.

PARASITOLOGY INTERNATIONAL , cilt.59, sa.2, ss.283-285, 2010 (SCI-Expanded)

Changes in the expression of selenoproteins in mesial temporal lobe epilepsy patients

YÜZBAŞIOĞLU A., Karatas H., GURSOY-OZDEMIR Y., Saygi S., Akalan N., Soylemezoglu F., et al.

Cellular and Molecular Neurobiology , cilt.29, sa.8, ss.1223-1231, 2009 (SCI-Expanded)

Statin potentiates human platelet eNOS activity without enhancing eNOS mRNA and protein levels

Yemisci M., AY H., Kocaefe C., Qui J., Topalkara K., ÖZGÜÇ M., et al.

CEREBROVASCULAR DISEASES , cilt.26, sa.2, ss.190-198, 2008 (SCI-Expanded)

Application of medical genetics in Turkey

Tuncbilek E., ÖZGÜÇ M.

TURKISH JOURNAL OF PEDIATRICS , cilt.49, sa.4, ss.353-359, 2007 (SCI-Expanded)

Report of an international survey of molecular genetic testing laboratories

McGovern M. M., Elles R., Beretta I., Somerville M. J., Hoefler G., Keinanen M., et al.

COMMUNITY GENETICS , cilt.10, sa.3, ss.123-131, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma

Liposome-mediated intraperitoneal interleukin 10 gene transfer increases survival in cecal ligation and puncture model of sepsis

Kabay B., Kocaefe Y. C., Baykal A., Ozguc M., SAYEK I.

SHOCK , cilt.26, sa.1, ss.37-40, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

Androgen receptor immunostaining and androgen receptor messenger ribonucleic acid expression are increased in cremaster muscles associated with undescended testis

Tanyel F. C., Yuzbasioglu A., Kocaefe C., Orhan D., Ozguc M.

UROLOGY , cilt.67, sa.4, ss.855-858, 2006 (SCI-Expanded)

Myogenic program induction in mature fat tissue (with MyoD expression)

Kocaefe Y. Ç., ISRAELI D., Ozguc M., DANOS O., GARCIA L.

EXPERIMENTAL CELL RESEARCH , cilt.308, sa.2, ss.300-308, 2005 (SCI-Expanded)

Expression of matrix metalloproteinases in vasculitic neuropathy

Gurer G., Erdern S., Kocaefe C., Ozguc M., Tan E.

RHEUMATOLOGY INTERNATIONAL , cilt.24, sa.5, ss.255-259, 2004 (SCI-Expanded)

Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients

Kocaefe Y. Ç., Erdem S., Ozguc M., Tan E.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.11, sa.1, ss.102-104, 2003 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

Genetic testing: predictive value of genotyping for diagnosis and management of disease

ÖZGÜÇ M.

EPMA JOURNAL , cilt.2, sa.2, ss.173-179, 2011 (ESCI)

Mutational analysis of Turkish galactosaemia patients

Coskun T., ERKUL E., Seyrantepe V., ÖZGÜÇ M., TOKATLI A., Özalp I.

Journal of Inherited Metabolic Disease , cilt.18, sa.3, ss.368-369, 1995 (Scopus)

Genetic and neurological evaluation of untreated and late-treated patients with phenylketonuria

Özalp I., Coskun T., ÖZGÜÇ M., TOKATLI A., Yalaz K., Vanli L., et al.

Journal of Inherited Metabolic Disease , cilt.17, sa.3, ss.371, 1994 (Scopus)

Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients

ÖZGÜÇ M., YILMAZ E., Erdem H., Coskun T., TOKATLI A., Özalp I.

Journal of Inherited Metabolic Disease , cilt.17, sa.3, ss.373-374, 1994 (Scopus)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Analysis of genetic background in Turkish early onset Parkinson’s disease patients

AKBABA T. H., ÖNAL G., YÜZBAŞIOĞLU A., YALÇIN ÇAKMAKLI G., PEYNİRCİOĞLU B., ÖZGÜÇ M., et al.

6th International Congress of the Molecular Biology Association of Turkey, İzmir, Türkiye, 05 Eylül 2018, ss.46

Analysis of genomic rearrangements in aTurkish cohort of early onset Parkinson’sdisease

ÖNAL G., YÜZBAŞIOĞLU A., YALÇIN ÇAKMAKLI G., PEYNİRCİOĞLU B., DÖKMECİ S., ÖZGÜÇ M., et al.

42nd FEBS Congress, 10 - 14 Eylül 2017

How common are the genomic rearrangements among possiblyautosomal recessive PD cases in Turkey?

YALÇIN ÇAKMAKLI G., YÜZBAŞIOĞLU A., ÖNAL G., PEYNİRCİOĞLU B., ÖZGÜÇ M., DÖKMECİ S., et al.

International Congress of Parkinson’xxs Disease and Movement Disorders, 4 - 08 Haziran 2017

Analysis of Genomic Rearrangements in a Turkish cohort of early onset Pwarkinso s Disease

YÜZBAŞIOĞLU A., ÖNAL G., YALÇIN ÇAKMAKLI G., PEYNİRCİOĞLU B., ÖZGÜÇ M., ELİBOL B., et al.

^rd International Parkinson Disease Symposium, 6 - 08 Ekim 2016

Rare Disease Biobanks For Personalized Medicine

YÜZBAŞIOĞLU A., ÖZGÜÇ M.

EPMA World Congress 2015, Bonn, Almanya, 3 - 05 Eylül 2015

Influence of monocyte chemoattractant protein-1-2518A > G polymorphism on childhood focal segmental glomerulosclerosis

Kalyoncu M., Besbas N., Ozgul K., Ozaltin F., Duzova A., Topaloglu R., et al.

43rd ERA-EDTA Congress, Glasgow, Birleşik Krallık, 15 - 18 Temmuz 2006, cilt.21, ss.328

Metrikler

Yayın

Atıf (WoS)

203

H-İndeks (WoS)

Atıf (Scopus)

180

H-İndeks (Scopus)

Proje

Tez Danışmanlığı

Açık Erişim

BM Sürdürülebilir Kalkınma Amaçları

Yayınlar & Eserler