Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

ISL2 is a putative tumor suppressor whose epigenetic silencing reprograms the metabolism of pancreatic cancer

Ozturk H., Cingoz H., Tufan T., Yang J., Adair S. J., Tummala K. S., et al.
DEVELOPMENTAL CELL , cilt.57, sa.11, ss.1331-1356, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

The Role of Rat Hypothalamus Kisspeptin, Neurokinin and their respective Receptors in the Prolactin-Infertility Interaction

Isik E., USLU İ. N., AY G., Cetinel N., CÖMERTPAY G., Oksuz H., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.185, 2019 (SCI-Expanded) identifier

ATP sensitive K+ channel subunits (Kir6.1, Kir6.2) are the candidate mediators regulating ameliorating effects of pulsed magnetic field on aortic contractility in diabetic rats

ÖCAL I., YILMAZ M., Kocaturk-Sel S., Tufan T., Erkoc M. A., CÖMERTPAY G., et al.
BIOELECTROMAGNETICS , cilt.39, sa.4, ss.299-311, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Population structure of rice varieties used in Turkish rice breeding programs determined using simple-sequence repeat and inter-primer binding site-retrotransposon data

COMERTPAY G., Baloch F. S., DERYA M., Andeden E. E., ALSALEH A., SUREK H., et al.
GENETICS AND MOLECULAR RESEARCH , cilt.15, sa.1, 2016 (SCI-Expanded) identifier identifier identifier

REPORT OF A NEW CASE WITH PENTASOMY X AND NOVEL CLINICAL FINDINGS

DEMİRHAN O., TANRIVERDİ N., YILMAZ M., Kocaturk-Sel S., INANDIKLIOGLU N., Luleyap U., et al.
BALKAN JOURNAL OF MEDICAL GENETICS , cilt.18, sa.1, ss.85-92, 2015 (SCI-Expanded) Creative Commons License identifier identifier identifier

Development of end-stage renal disease at a young age in two cases with Joubert syndrome

Soenmez F., Guezuenler-Sen M., YILMAZ D., CÖMERTPAY G., Heise M., Cirak S., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.56, sa.4, ss.458-461, 2014 (SCI-Expanded) identifier identifier identifier

Clinical, Radiological, and Genetic Survey of Patients With Muscle-Eye-Brain Disease Caused by Mutations in POMGNT1

YİŞ U., Uyanik G., Rosendahl D. M., Carman K. B., BAYRAM E., Heise M., et al.
PEDIATRIC NEUROLOGY , cilt.50, sa.5, ss.491-497, 2014 (SCI-Expanded) identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

Role of endoplasmic reticulum stress response in tumorogenesis

Evyapan G., AY G., CÖMERTPAY G., LÜLEYAP H. Ü.
CUKUROVA MEDICAL JOURNAL , cilt.44, sa.1, ss.241-248, 2019 (ESCI) Sürdürülebilir Kalkınma identifier

Investigation of the effects of nicotine and resveratrol on expression levels of Sox2 and Sox4 genes in human amniotic cell culture by real time PCR

CÖMERTPAY G., Luleyap U., YILMAZ M. B., Tufan T., PAZARCI P.
CUKUROVA MEDICAL JOURNAL , cilt.43, sa.1, ss.7-12, 2018 (ESCI) identifier

The analysis of the phenylalanine hydroxylase gene mutations by sequencing and ARMS techniques in Turkish patients

Luleyap U., PAZARCI P., CÖMERTPAY G., Onenli H. N., PAZARBAŞI A., ALPTEKİN D., et al.
CUKUROVA MEDICAL JOURNAL , cilt.41, sa.4, ss.702-708, 2016 (ESCI) identifier

Association between pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections disease and tumor necrosis factor-? gene-308 g/a, -850 c/t polymorphisms in 4-12-year-old children in Adana/Turkey

Luleyap U., Onatoglu D., Yılmaz M., Alptekin D., Tahiroglu A., Çetiner S., et al.
Indian Journal of Human Genetics , cilt.19, sa.2, ss.196-201, 2013 (Hakemli Dergi)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Results of karyotype analysis of 8475 pregnancies in prenataly identified cases with amniocentesis from south of Turkey

PAZARBAŞI A., ALPTEKİN D., ILGAZ N. S., USLU İ. N., CÖMERTPAY G., AY G., et al.
16. Tıbbi Biyoloji ve Genetik Kongresi (Uluslararası Katılımlı), Muğla Bodrum, Türkiye, 27 - 30 Ekim 2019, ss.146

Result of karyotype analysis of 8475 pregnancies in prenataly identified cases with amniosentesis from south of Turkey.

PAZARBAŞI A., ALPTEKİN D., ILGAZ N. S., USLU İ. N., CÖMERTPAY G., AY G., et al.
16. Tıbbi Biyoloji ve Genetik Kongresi (Uluslararası Katılımlı), Türkiye, 27 - 30 Ekim 2019

Nicotine and resveratrol alter sox2 and sox4 genes expression levels in human amniotic cell culture

CÖMERTPAY G., LÜLEYAP H. Ü., YILMAZ M. B., PAZARCI P.
European human genetics Conferenece, 15 - 18 Haziran 2019

Chromosomal Abnormalities identified at prenatal diagnosis

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., ÖZPAK L., ILGAZ N. S., USLU İ. N., et al.
Innovation in Medicine Meeting 4, Gaziantep, Türkiye, 11 - 13 Ekim 2018, ss.60-69

Bisphenol a triggers ER stress mediated autophagy in SH-SY5Y cell line.

LÜLEYAP H. Ü., YOLDAŞ A., CÖMERTPAY G., AY G., EVYAPAN G., PAZARBAŞI A., et al.
European Human Genetics Conference, Milan, İtalya, 16 - 19 Haziran 2018, cilt.9028

Low Dose Dexmethasone Decrease the Level of ATG5 in SH SY5Y cell line

ALPTEKİN D., LÜLEYAP H. Ü., YOLDAŞ A., CÖMERTPAY G., PAZARCI P., AY G., et al.
European Human Genetics Conference 2018, Milano, İtalya, 16 - 19 Haziran 2018

Low Dose Dexmethasone Decrease the Level of ATG5 in SH SY5Y cell line

ALPTEKİN D., LÜLEYAP H. Ü., YOLDAŞ A., CÖMERTPAY G., PAZARCI P., AY G., et al.
European Human Genetics Conference 2018, Milano, İtalya, 16 - 19 Haziran 2018

Low Dose Dexmethasone Decrease the Level of ATG5 in SH SY5Y cell line

ALPTEKİN D., LÜLEYAP H. Ü., YOLDAŞ A., CÖMERTPAY G., PAZARCI P., AY G., et al.
European Human Genetics Conference 2018, Milano, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.279

Amniyosentez iile prenatal tanı konulan 7821 olguda kromozom analizi sonuçları

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., ÖZPAK L., ILGAZ N. S., USLU İ. N., et al.
15.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Türkiye, 26 - 29 Ekim 2017

Effect of sodium butyrate on some alternative splicing genes and bace1 isoforms in SH-SY5Y

LÜLEYAP H. Ü., AY G., CÖMERTPAY G., ALPTEKİN D., PAZARBAŞI A.
European Human Genetics Conference, Kopenhag, Danimarka, 27 - 30 Mayıs 2017, cilt.P09

Rapid aneuplody testing in postnatal samples from Cukurova region

KOCATÜRK SEL S., YILMAZ M. B., LÜLEYAP H. Ü., PAZARBAŞI A., ALPTEKİN D., DEMİRHAN O., et al.
Innovation in Medicine Meeting 3, Gaziantep, Türkiye, 11 - 13 Mayıs 2017

Effects of neonatal ketamine and dexmedetomidine administration on NMDA receptor, alpha 2 adrenergic receptor and anxiety in mice

YILMAZ M. B., AKILLIOĞLU K., ÖZCENGİZ D., TÜRKTAN M., ILGAZ N. S., CÖMERTPAY G., et al.
17th congress of the european neuroendocrine association, 19 - 22 Ekim 2016

Analysis of maternal polymorphisms of RFC1 gene and risk of Down syndrome offspring

PAZARBAŞI A., ÖZPAK L., Keser N., KOCATÜRK SEL S., Cömertpay G., Özgünen F. T.
European Human Genetics Conference 2016, Barselona, İspanya, 21 - 24 Mayıs 2016, ss.581

Rapid Detection Of Fetal Aneuploidies By Quantitative Fluorence Pcr (Qf-Pcr) In Prenatal Dioagnosis

TUFAN T., PAZARBAŞI A., Erkoç M. A., CÖMERTPAY G., KOCATÜRK SEL S., OZGUNEN F. T., et al.
European Human Genetics Conference 2013, Paris, Fransa, 8 - 11 Haziran 2013, cilt.21, ss.18

The Presence Of One Trisomic Diallelic Marker Of A Fetus For D21s1411 With Normal Karyotype

ALPTEKİN D., PAZARBAŞI A., LÜLEYAP H. Ü., ERKOC M. A., YILMAZ M. B., CÖMERTPAY G., et al.
European Human Genetics Conference 2013, Paris, Fransa, 8 - 11 Haziran 2013, cilt.21, ss.57

Chromosomal Abnormalities Identified At Prenatal Diagnosis

PAZARBAŞI A., TUNÇ E., ALPTEKİN D., LÜLEYAP H. Ü., DEMİRHAN O., TANRIVERDI N., et al.
European Human Genetics Conference 2013, Paris, Fransa, 8 - 11 Haziran 2013, cilt.21, ss.78

Metrikler

Yayın

27

Atıf (WoS)

24

H-İndeks (WoS)

4

Atıf (Scopus)

24

H-İndeks (Scopus)

3

Proje

3

Açık Erişim

1
BM Sürdürülebilir Kalkınma Amaçları