Personal information

Türkiye

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Employment (4)

Ankara Etlik Zübeyde Hanım Kadın Hastalıkları Eğitim ve Araştırma Hastanesi: Ankara, Ankara, TR

2020-05-11 to present | M.D. (Medical Genetics)
Employment
Source: Self-asserted source
Arslan Bayram

Haseki Education Research Hospital: İstanbul, TR

2019-10-07 to 2020-04-30 | Medical Genetics Doctor (Medical Genetics)
Employment
Source: Self-asserted source
Arslan Bayram

DETA-GEN Genetic Diagnosis Center: Kayseri, TR

2018-09-20 to 2019-10-06 | Medical Genetics Doctor (Medical Genetics)
Employment
Source: Self-asserted source
Arslan Bayram

Erciyes Universitesi Tip Fakultesi: Kayseri, TR

2014-09-01 to 2018-09-10 | Medical Doctor (Medical Genetics)
Employment
Source: Self-asserted source
Arslan Bayram

Education and qualifications (1)

Azerbaijan Medical University: Baku, Baku, AZ

2003-09-15 to 2009-06-18 | Medical Doctor (Pediatry)
Education
Source: Self-asserted source
Arslan Bayram

Works (41)

Unravelling the maternal stress-induced orchestrations: Fndc5 gene expression dynamics across duodenum, stomach, and whole blood in offspring

Acta Medica
2024-09-30 | Journal article
Contributors: Keziban Korkmaz Bayram; Aida Nurul Barokah; Merve Hilal Dönmez; Şevval Nebahat Işıktan; Arslan Bayram
Source: check_circle
Crossref

Coexistence of Neonatal Bartter Syndrome and Congenital Cutis Laxa, in which a new mutation in SLC12A1 was identified

Medical Science and Discovery
2023-10-30 | Journal article
Contributors: Fatih İşleyen; Dilek Ulubaş Işık; Ayşen Sumru Kavurt; Arslan Bayram; Ahmet Yağmur Baş; Nihal Demirel
Source: check_circle
Crossref

Prenatal Sonographic Detection of Monochorionic Twins with Bipartite Placenta

Fetal and Pediatric Pathology
2021-11-02 | Journal article
Contributors: Mehmet Serdar Kutuk; Taha Takmaz; Arslan Bayram; Sule Ozturk
Source: check_circle
Crossref

Investigation of the Relationship Between Inherited Thrombophilia and Novel Coronavirus Pneumonia

Future Virology
2021-05 | Journal article
Contributors: Aslihan Kiraz; Seda Guzeldag; Esma Eren; Musa Goksu; Arslan Bayram
Source: check_circle
Crossref

Gene Expression of Mouse Hippocampal Stem Cells Grown in a Galactose-Derived Molecular Gel Compared to In Vivo and Neurospheres

Processes
2021-04-18 | Journal article
Contributors: Keziban Korkmaz Bayram; Juliette Fitremann; Arslan Bayram; Zeynep Yılmaz; Ecmel Mehmetbeyoğlu; Yusuf Özkul; Minoo Rassoulzadegan
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

Change in gene expression levels of GABA, glutamate and neurosteroid pathways due to acoustic trauma in the cochlea

Journal of Neurogenetics
2021-01-02 | Journal article
Contributors: 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
Source: check_circle
Crossref

Comparing expression levels of PERIOD genes PER1, PER2 and PER3 in chronic insomnia patients and medical staff working in the night shift

Sleep Medicine
2020-09 | Journal article
Contributors: Rabia Emeklİ; Sevda İsmaİloğullari; Arslan Bayram; Hilal Akalin; Gülten Tuncel; Munis Dündar
Source: check_circle
Crossref

The Investigation of the Relationship Between the Inherited Thrombophilia and Novel Coronavirus Pneumonia

2020-09-22 | Preprint
Contributors: Aslihan Kiraz; Seda Guzeldag; Esma Eren; Musa Goksu; Arslan Bayram
Source: check_circle
Crossref

A heritable profile of six miRNAs in autistic patients and mouse models

Scientific Reports
2020-06-09 | Journal article
Contributors: Yusuf Ozkul; Serpil Taheri; Kezban Korkmaz Bayram; Elif Funda Sener; Ecmel Mehmetbeyoglu; Didem Behice Öztop; Fatma Aybuga; Esra Tufan; Arslan Bayram; Nazan Dolu et al.
Source: check_circle
Crossref

Disregulation of Autophagy in the Transgenerational Cc2d1a Mouse Model of Autism

NeuroMolecular Medicine
2019 | Journal article
EID:

2-s2.0-85074996168

Contributors: Dana, H.; Bayramov, K.K.; Delibaşı, N.; Tahtasakal, R.; Bayramov, R.; Hamurcu, Z.; Sener, E.F.
Source: Self-asserted source
Arslan Bayram via Scopus - Elsevier

Multiple urinary tract infections are associated with genotype and phenotype in adult polycystic kidney disease

Clinical and Experimental Nephrology
2019 | Journal article
EID:

2-s2.0-85067019477

Contributors: Eroglu, E.; Kocyigit, I.; Cetin, M.; Zararsiz, G.; Imamoglu, H.; Bayramov, R.; Tastan, S.; Sipahioglu, M.H.; Tokgoz, B.; Oymak, O.
Source: Self-asserted source
Arslan Bayram via Scopus - Elsevier

NPHS2 gene sequencing results in children of the Azerbaijani population with different types of nephrotic syndrome caused by chronic glomerulonephritis

Bratislava Medical Journal
2019 | Journal article
EID:

2-s2.0-85061671425

Contributors: Baylarov, R.; Baylarova, R.; Berdeli, A.; Bayramov, R.; Haziyev, E.
Source: Self-asserted source
Arslan Bayram via Scopus - Elsevier

The association of endothelin-1 levels with renal survival in polycystic kidney disease patients

Journal of Nephrology
2019 | Journal article
EID:

2-s2.0-85050195280

Contributors: Kocyigit, I.; Eroglu, E.; Kaynar, A.S.; Kocer, D.; Kargi, S.; Zararsiz, G.; Bayramov, R.; Imamoglu, H.; Sipahioglu, M.H.; Tokgoz, B. et al.
Source: Self-asserted source
Arslan Bayram via Scopus - Elsevier

A Novel SGCE Nonsense Variant Associated With Marked Intrafamilial Variability in a Turkish Family With Myoclonus‐Dystonia

Movement Disorders Clinical Practice
2019-07 | Journal article
Contributors: Murat Gultekin; Neha Prakash; Christos Ganos; Meral Mirza; Ruslan Bayramov; Kailash P. Bhatia; Niccolò E. Mencacci
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

Dysmetabolic markers predict outcomes in autosomal dominant polycystic kidney disease.

Clinical and experimental nephrology
2019-05-27 | Journal article
Source: Self-asserted source
Arslan Bayram
grade
Preferred source (of 2)‎

Effects of post-learning REM sleep deprivation on hippocampal plasticity-related genes and microRNA in mice

Behavioural Brain Research
2019-04 | Journal article
Contributors: Sebahattin Karabulut; Keziban Korkmaz Bayramov; Ruslan Bayramov; Fadime Ozdemir; Tugba Topaloglu; Ergul Ergen; Kamile Yazgan; Ahmet Sevki Taskiran; Asuman Golgeli
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

The molecular basis and genotype–phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population

2019-04-20 | Journal article
Part of ISSN: 0301-4851
Part of ISSN: 1573-4978
Source: Self-asserted source
Arslan Bayram
grade
Preferred source (of 2)‎

A rare cause of male infertility: 45,X/46,XY mosaicism

Urologia Internationalis
2018 | Journal article
EID:

2-s2.0-85034827045

Contributors: Akinsal, E.C.; Baydilli, N.; Bayramov, R.; Ekmekcioglu, O.
Source: Self-asserted source
Arslan Bayram via Scopus - Elsevier

Effect of the allopregnanolone and allotetrahydrodeoxycorticosteron on spike-wave discharges in the EEG of absence epilepsy rat models

General Physiology and Biophysics
2018 | Journal article
EID:

2-s2.0-85045001998

Contributors: Karabulut, S.; Bayramov, R.; Bayramov, K.K.; Filiz, A.K.; Taskiran, A.S.; Ozdemir, E.
Source: Self-asserted source
Arslan Bayram via Scopus - Elsevier

FP049THE ASSOCIATION OF ENDOTHELIN-1 LEVELS WITH RENAL SURVIVAL IN POLYCYSTIC KIDNEY DISEASE PATIENTS

Nephrology Dialysis Transplantation
2018 | Journal article
Contributors: Eroglu, Eray; Kocyigit, Ismail; Kaynar, Ahmet; Kocer, Derya; Zararsiz, Gokmen; Bayramov, Ruslan; Imamoglu, Hakan; Sipahioglu, Murat; Tokgoz, Bulent; Dundar, Munis et al.
Source: Self-asserted source
Arslan Bayram via ResearcherID

Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorder

Molecular Biology Reports
2018 | Journal article
EID:

2-s2.0-85047145197

Contributors: Balta, B.; Gumus, H.; Bayramov, R.; Korkmaz Bayramov, K.; Erdogan, M.; Oztop, D.B.; Dogan, M.E.; Taheri, S.; Dundar, M.
Source: Self-asserted source
Arslan Bayram via Scopus - Elsevier

PEX10-related autosomal recessive cerebellar ataxia with hearing loss

Acta Neurologica Belgica
2018 | Journal article
EID:

2-s2.0-85050248838

Contributors: Kaya Özçora, G.D.; Miyatake, S.; Matsumoto, N.; Canpolat, M.; Erdoğan, M.; Bayramov, R.; Kumandaş, S.
Source: Self-asserted source
Arslan Bayram via Scopus - Elsevier

Sialidosis type I presenting with a novel mutation and advanced neuroimaging features

Neurosciences
2018 | Journal article
EID:

2-s2.0-85041081120

Contributors: Gultekin, M.; Bayramov, R.; Karaca, C.; Acer, N.
Source: Self-asserted source
Arslan Bayram via Scopus - Elsevier

A Rare Cause of Male Infertility: 45,X/46,XY Mosaicism.

Urologia internationalis
2017-11 | Journal article
Source: Self-asserted source
Arslan Bayram via Europe PubMed Central

Association of the thrombophilia factors with breast and/or ovarian cancer risk

Journal of Biotechnology
2017-08 | Journal article
Contributors: Damla Badur Mermer; Nuriye Coskun; Hilal Akalin; Ruslan Bayramov; Muge Gulcihan Onal; Cetin Saatci; Yusuf Ozkul; Munis Dundar
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

Frequency of chromosome variants in families with recurrent pregnancy loss and statistical analysis of infertility

Journal of Biotechnology
2017-08 | Journal article
Contributors: Beyzanur Gunsili; Ruslan Bayramov; Sercan Kenanoglu; Muhammet Ensar Dogan; Meltem Cerrah Gunes; Çetin Saatçi; Yusuf Ozkul; Munis Dundar
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

NF1 gene variant allele frequencies comparison of Turkish population with databases

Journal of Biotechnology
2017-08 | Journal article
Contributors: Ruslan Bayramov; Muhammet Ensar Dogan; Meltem Cerrah Gunes; Muge Gulcihan Unal; Mehmet Boz; Yasin Ada; Havva Nur Eryılmaz; Keziban Korkmaz Bayramov; Çetin Saatçı; Yusuf Ozkul et al.
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

Prenatal diagnosis of a foetus with partial monosomy 4p and partial trisomy 13q

Journal of Biotechnology
2017-08 | Journal article
Contributors: Muhammet E. Dogan; Mehmet Serdar Kutuk; Ruslan Bayramov; Cetin Saatci; Yusuf Ozkul; Munis Dundar
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

Retrospective results of 18 years prenatal diagnosis cases and its evaluation

Journal of Biotechnology
2017-08 | Journal article
Contributors: Ruslan Bayramov; Mehmet Serdar Kutuk; Sercan Kenanoglu; Meltem Cerrah Gunes; Muhammet Ensar Dogan; Yusuf Ozkul; Çetin Saatçi; Munis Dundar
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

The correlation of genotype–phenotype of FMF disease and its review of statistical data

Journal of Biotechnology
2017-08 | Journal article
Contributors: Fatih Yavuz; Ruslan Bayramov; Sercan Kenanoglu; Muhammet Ensar Dogan; Meltem Cerrah Gunes; Mehmet Boz; Çetin Saatci; Yusuf Ozkul; Munis Dundar
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

The effect of CYP2C19 * 2 polymorphism on clopidogrel resistance in COPD patients

Journal of Biotechnology
2017-08 | Journal article
Contributors: Zeliha Funda Kılık; Hilal Akalın; Ruslan Bayramov; Yakut Erdem; Munis Dundar
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

Effect of sodium benzoate on DNA breakage, micronucleus formation and mitotic index in peripheral blood of pregnant rats and their newborns

Biotechnology & Biotechnological Equipment
2016-09-09 | Journal article
Contributors: Cetin Saatci; Yagut Erdem; Ruslan Bayramov; Hilal Akalın; Nazife Tascioglu; Yusuf Ozkul
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search
grade
Preferred source (of 3)‎

A case of XYY male patient with micropenis

Journal of Biotechnology
2016-08 | Journal article
Contributors: Ruslan Bayramov; Meltem Cerrah Gunes; Muhammet Ensar Dogan; Ruksan Boyukoglan; Keziban Korkmaz Bayramov; Munis Dundar
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

A novel nonsense mutation in GALNS gene in family with MPS4A diagnosed child

Journal of Biotechnology
2016-08 | Journal article
Contributors: Meltem Cerrah Gunes; Ruslan Bayramov; Ruksan Boyukoglan; Muhammet Ensar Dogan; Keziban Korkmaz Bayramov; Munis Dundar
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

A case of SRY positive 46, XX male with speaking disorder

Journal of Biotechnology
2015-08 | Journal article
Contributors: Ruslan Bayramov; Meltem Cerrah Güneş; Yagut Erdem; Munis Dündar
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

Novel FBN1 gene frameshift mutation in patient with type 1 Chiari malformation

Journal of Biotechnology
2015-08 | Journal article
Contributors: Meltem Cerrah Güneş; Ruslan Bayramov; Yagut Erdem; Munis Dündar
Source: Self-asserted source
Arslan Bayram via Crossref Metadata Search

THE EXPRESSION LEVEL OF BRMS1 IN COLON CANCER PATIENTS AND ITS CLINICAL SIGNIFICANCE

CIÊNCIA E TÉCNICA VITIVINÍCOLA
2015-05-01 | Journal article
Source: Self-asserted source
Arslan Bayram

Effect of the allopregnanolone and allotetrahydrodeoxycorticosteron on spike-wave discharges in the EEG of absence epilepsy rat models

Journal article
SOURCE-WORK-ID:

0415180423639-35

Contributors: Karabulut, S.; Bayramov R Fau - Korkmaz Bayramov, Keziban; Korkmaz Bayramov K Fau - Filiz, Ahmet K.; Filiz Ak Fau - Taskiran, Ahmet S.; Taskiran As Fau - Ozdemir, Ercan; Ozdemir, E.
Source: Self-asserted source
Arslan Bayram via ResearcherID

Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorder. LID - 10.1007/s11033-018-4191-y [doi]

Journal article
SOURCE-WORK-ID:

0521181349638-36

Contributors: Balta, B.; Gumus, H.; Bayramov, R.; Korkmaz Bayramov, K.; Erdogan, M.; Oztop, D. B.; Dogan, M. E.; Taheri, S.; Dundar, M.
Source: Self-asserted source
Arslan Bayram via ResearcherID

NPHS2 gene sequencing results in children of the Azerbaijani population with different types of nephrotic syndrome caused by chronic glomerulonephritis

Journal article
SOURCE-WORK-ID:

0223191125521-41

Contributors: Baylarov R Fau - Baylarova, R.; Baylarova R Fau - Berdeli, A.; Berdeli A Fau - Bayramov, R.; Bayramov R Fau - Haziyev, E.; Haziyev, E.
Source: Self-asserted source
Arslan Bayram via ResearcherID

Sialidosis type I presenting with a novel mutation and advanced neuroimaging features

Journal article
SOURCE-WORK-ID:

0521181349638-37

Contributors: Gultekin, M.; Bayramov R Fau - Karaca, Cagatay; Karaca C Fau - Acer, Niyazi; Acer, N.
Source: Self-asserted source
Arslan Bayram via ResearcherID

Peer review (1 review for 1 publication/grant)

Review activity for SN Comprehensive Clinical Medicine (1)