Arslan Bayram (Ruslan Bayramov)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2021
Publications (10 Years): 4

Top Topics

Bioinformatics Analysis

Attention Deficit Hyperactivity Disorder

Top Venues

Journal of neurogenetics

Scientific reports

Fetal and pediatric pathology

Movement disorders clinical practice

Ankara Etlik Zübeyde Hanım Kadın Hastalıkları Eğitim ve Araştırma Hastanesi

Azerbaijan Medical University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Ankara Etlik Zübeyde Hanım Kadın Hastalıkları Eğitim ve Araştırma Hastanesi May 11 2020

Turkey

M.D. :: Medical Genetics

Haseki Education Research Hospital Oct 07 2019 - Apr 30 2020

Turkey

Medical Genetics Doctor :: Medical Genetics

DETA-GEN Genetic Diagnosis Center Sep 20 2018 - Oct 06 2019

Turkey

Medical Genetics Doctor :: Medical Genetics

Erciyes Universitesi Tip Fakultesi Sep 01 2014 - Sep 10 2018

Turkey

Medical Doctor :: Medical Genetics

Education History

Azerbaijan Medical University Sep 15 2003 - Jun 18 2009

Azerbaijan

PHD :: Pediatry

Publications

Meltem Cerrah Gunes, Murat Salih Gunes, Alperen Vural, Fatma Aybuga, Arslan Bayram, Keziban Korkmaz Bayram, Mehmet Ilhan Sahin, Muhammet Ensar Dogan, Sevda Yesim Ozdemir, Yusuf Ozkul
Change in gene expression levels of GABA, glutamate and neurosteroid pathways due to acoustic trauma in the cochlea. Journal of neurogenetics 35 (1) (2021)
Mehmet Serdar Kutuk, Taha Takmaz, Arslan Bayram, Sule Ozturk
Prenatal Sonographic Detection of Monochorionic Twins with Bipartite Placenta. Fetal and pediatric pathology 40 (6) (2020)
Yusuf Ozkul, Serpil Taheri, Kezban Korkmaz Bayram, Elif Funda Sener, Ecmel Mehmetbeyoglu, Didem Behice Öztop, Fatma Aybuga, Esra Tufan, Arslan Bayram, Nazan Dolu, Gokmen Zararsiz, Leila Kianmehr, Feyzullah Beyaz, Züleyha Doganyigit, François Cuzin, Minoo Rassoulzadegan
A heritable profile of six miRNAs in autistic patients and mouse models. Scientific reports 10 (1) (2020)
Murat Gultekin, Neha Prakash, Christos Ganos, Meral Mirza, Arslan Bayram, Kailash P Bhatia, Niccolò E Mencacci
A Novel SGCE Nonsense Variant Associated With Marked Intrafamilial Variability in a Turkish Family With Myoclonus-Dystonia. Movement disorders clinical practice 6 (6) (2019)