Yayınlar & Eserler

Yayın Ağı
Makaleler 19
Tümü (19)
SCI-E, SSCI, AHCI (15)
SCI-E, SSCI, AHCI, ESCI (16)
ESCI (1)
Scopus (19)
TRDizin (1)

1. 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, Scopus, TRDizin) Creative Commons License identifier identifier identifier

2. 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, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

3. 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, SSCI, Scopus) identifier identifier identifier

4. 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, Scopus) identifier identifier identifier

5. 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, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier

6. 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, Scopus) identifier identifier identifier

7. 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, Scopus) identifier identifier identifier

8. 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, Scopus) identifier identifier identifier

9. 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, Scopus) identifier identifier identifier

10. Application of medical genetics in Turkey

Tuncbilek E., ÖZGÜÇ M.
TURKISH JOURNAL OF PEDIATRICS , cilt.49, sa.4, ss.353-359, 2007 (SCI-Expanded, Scopus) identifier identifier identifier

11. 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, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

12. 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, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

13. 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, Scopus) identifier identifier identifier

14. 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, Scopus) identifier identifier identifier

15. 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, Scopus) identifier identifier identifier

16. 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, Scopus) Creative Commons License identifier identifier identifier

17. 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) identifier identifier

18. 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) identifier identifier

19. 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) identifier identifier
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 6

1. 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, (Tam Metin Bildiri)

2. 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, (Özet Bildiri)

3. 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, (Özet Bildiri)

4. 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, (Özet Bildiri)

5. Rare Disease Biobanks For Personalized Medicine

YÜZBAŞIOĞLU A., ÖZGÜÇ M.
EPMA World Congress 2015, Bonn, Almanya, 3 - 05 Eylül 2015, (Tam Metin Bildiri)

6. 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, (Özet Bildiri) identifier
Metrikler

Yayın

25

Yayın (WoS)

17

Yayın (Scopus)

19

Atıf (WoS)

213

H-İndeks (WoS)

9

Atıf (Scopus)

181

H-İndeks (Scopus)

8

Atıf (Scholar)

8

H-İndeks (Scholar)

1

Proje

5

Tez Danışmanlığı

6

Açık Erişim

4
BM Sürdürülebilir Kalkınma Amaçları