Metrics
Publication
20
Open Access
1
Education
2009 - 2015
2009 - 2015Expertise In Medicine
Hacettepe University, Tıp Fakültesi, Tıp Pr., Turkey
Academic Positions
2016 - Continues
2016 - ContinuesResearch Assistant
Eskisehir Osmangazi University, TIP FAKÜLTESİ, Dahili Tıp Bilimleri Bölümü
Articles
All (6)
SCI-E, SSCI, AHCI (5)
SCI-E, SSCI, AHCI, ESCI (6)
ESCI (1)
Scopus (6)
2022
20221. NDE1-related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly
BAŞ H., ŞAYLISOY S., ÇİLİNGİR O., Gokalp E., KOCAGİL S., YARAR C., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, vol.188, no.1, pp.326-331, 2022 (SCI-Expanded, Scopus)
2021
20212. Frequency of frontotemporal dementia-related gene variants in Turkey
Artan S., Erzurumluoğlu Gökalp E., Samancı B., Ozbabalik Adapinar D., Bas H., Tepgec F., et al.
Neurobiology of Aging
, vol.106, 2021 (SCI-Expanded)
2021
20213. Extra Chromosome, Extra Love
Aras B., Işık S., Baş H., Ocal E. E., Gokalp E., Çilingir O., et al.
GAZI MEDICAL JOURNAL
, vol.32, no.1, pp.83-87, 2021 (ESCI)
2020
20204. A Turkish patient with novel AHCY variants and presumed diagnosis of S-adenosylhomocysteine hydrolase deficiency
BAŞ H., ÇİLİNGİR O., TEKİN N., ŞAYLISOY S., DURAK ARAS B., Uzay E., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, vol.182, no.4, pp.740-745, 2020 (SCI-Expanded)
2019
20195. Clinical use of chromosomal microarray analysis in detection of fetal chromosomal abnormalities
ARTAN S., BAŞ H., Tanir M., ERZURUMLUOĞLU GÖKALP E., VELİPAŞAOĞLU M., Kocagil S., et al.
MOLECULAR CYTOGENETICS
, vol.12, 2019 (SCI-Expanded)
2017
20176. An interstitial deletion at 8q22.3 q24.11 associated with the Tricho Rhino Phalangeal Syndrome (TRPS) type I
ARTAN S., ÇİLİNGİR O., ERZURUMLUOĞLU GÖKALP E., BAŞ H., DURAK ARAS B., Aynaci S., et al.
MOLECULAR CYTOGENETICS
, vol.10, 2017 (SCI-Expanded)
Papers Presented at Peer-Reviewed Scientific Conferences
2020
20201. Prenatal tanıda kromozomal mikroarrayin kullanımı: 423 olgu üzerinden merkezimizin deneyimi
BAŞ H., ERZURUMLUOĞLU GÖKALP E., BÜTÜN Z., SUMAN K., KHADEM ANSARİ S., ARTAN S.
14. ULUSAL TIBBİ GENETİK KONGRESİ, Turkey, 20 - 22 November 2020, vol.31, pp.12, (Summary Text)
2020
20202. Prenatal Tanıda QF-PCR’ın Kullanımı: Kendi Tanı Merkezimizdeki Nadir Vakalar Üzerinden Avantaj ve Dezavantajlarının Örneklendirilmesi
KHADEM ANSARİ S., TEMENA A., BAŞ H., DURAK ARAS B., ÇİLİNGİR O., ERZURUMLUOĞLU GÖKALP E., et al.
14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Turkey, 20 - 22 November 2020, vol.31, pp.12, (Summary Text)
2019
20193. Assessment of genes known to be associated with MODY by next-generation sequencing
ÇİLİNGİR O., DURAK ARAS B., ŞİMŞEK E., ÇINAR D., TEMENA M. A., ARSLAN S., et al.
ESHG 2019, 15 - 19 June 2019, vol.27, (Summary Text)
2019
20194. A rare case of severe microcephaly caused by pathogenic variant of NDE1
BAŞ H., ÇİLİNGİR O., DURAK ARAS B., KOCAGİL S., ARTAN S.
13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.67, (Summary Text)
2019
20195. A RARE CASE OF FRONTOTEMPORAL LOBAR DEGENERATION CAUSED BY VARIANTS OF GRN AND CHMP2B GENES
ARTAN S., ERZURUMLUOĞLU GÖKALP E., ÖZBABALIK ADAPINAR B. D., BAŞ H., ÇİLİNGİR O., DURAK ARAS B.
FENS Regional Meeting 2019, Belgrade, Serbia, 10 - 13 July 2019, (Summary Text)
2019
20196. Clinical use of chromosomal microarray analysis in detection of fetal chromosomal abnormalities
ARTAN S., BAŞ H., ERZURUMLUOĞLU GÖKALP E., VELİPAŞAOĞLU M., KOCAGİL S., DURAK ARAS B., et al.
12th EuropeanCytogenomics Conference 2019, Salzburg, Austria, 6 - 09 July 2019, vol.12, (Summary Text)
2019
20197. Assesment of Genes Known to be Assosiated with MODY by Next Generation Sequencing.
ÇİLİNGİR O., DURAK ARAS B., ŞİMŞEK E., ÇINAR D., TEMENA M. A., ARSLAN S., et al.
European Human Genetics Conference, Gothenburg, Sweden, 15 June 2019, vol.27, pp.1260, (Summary Text)
2019
20198. A patient with a balanced inversion of chromosome 11 and unbalanced inversion of chromosome 2
SUSAM E., ÇİLİNGİR O., BAŞ H., DURAK ARAS B., ERZURUMLUOĞLU GÖKALP E., ARTAN S.
Erciyes Meidcal Genetics Days 2019, Kayseri, Turkey, 21 - 23 February 2019, vol.41, pp.20, (Summary Text)
2019
20199. A Patient with a Balanced Inversion of Chromosome 11 and Unbalancded Inversion of Chromosome 2.
SUSAM E., ÇİLİNGİR O., BAŞ H., DURAK ARAS B., ERZURUMLUOĞLU GÖKALP E., ARTAN S.
Erciyes Medical Genetics Days, Kayseri, Turkey, 21 February 2019, vol.21, pp.20, (Summary Text)
2018
201810. Assesment of candidate genes in patients with frontotemporal lobar degeneration spectrum: preliminary findings
ARTAN S., ERZURUMLUOĞLU E., ÇİLİNGİR O., ÖZBABALIK ADAPINAR B. D., TEPGEÇ F., BAŞ H., et al.
European Human Genetics Conference 2018, Milan, Italy, 16 - 19 June 2018, (Summary Text)
2018
201811. SEVERE PELIZAEUS - MERZBACHER DISEASE ON A CASE WITH DEVELOPMENTAL DELAY AND ABNORMAL MYELINATION
BAŞ H., YARAR C., ERZURUMLUOĞLU E., DURAK ARAS B., KOCAGİL S., ARTAN S.
Erciyes Medical Genetics Days 2018, Turkey, 7 - 10 March 2018, (Summary Text)
2017
201712. A New Mutation Associated With Bannayan Riley Ruvalcaba Syndrome
ÇİLİNGİR O., ÖZDEMİR M., YARAR C., ERZURUMLUOĞLU E., DURAK ARAS B., KOCAGİL S., et al.
Erciyes Tıp Genetik Günleri, Turkey, 11 - 13 May 2017, vol.39, (Summary Text)
2017
201713. A NOVEL INDEL MUTATION IN THE TCOF1 GENE FOUND IN ANEWBORN WITH TREACHER COLLINS SYNDROME
KOCAGİL S., ÇİLİNGİR O., ÇARMAN K. B., AYNACI S., DURAK ARAS B., BAŞ H., et al.
Erciyes Medical Genetics Days, Turkey, 11 - 13 May 2017, (Summary Text)
2017
201714. Diagnosis rate of DNA fragment analysisi for patients with SMA symptomes
ÖZDEMİR M., ARTAN S., YARAR C., DURAK ARAS B., ÇARMAN K. B., BAŞ H., et al.
European Human Genetic Conference, Denmark, 27 - 30 May 2017, (Summary Text)