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Profile

Full Name
Karaer, Kadri
Variants
Karaer, K.
K. Karaer
Karaer, Kadri.
 
Main Affiliation
14.02. Internal Medicine
 
Email
kkaraer@pau.edu.tr
 
Link to YOK Profile
YOK Profile
ORCID
0000-0003-1415-9103
Source ID
383270
Starting Date
16-07-2020
 
Interests
Tıbbi Genetik
 
Country
Turkey
Status
Current staff
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Publications
(Articles)

Author

  • 9 Karaer, Kadri
  • 5 Karaer, Derya
  • 3 Şahinoğlu, Bahtiyar
  • 2 Gürler, Abdullah İhsan
  • 1 Cetin, Gokhan Ozan
  • 1 Dogan, Berat
  • 1 Durak, T.
  • 1 Durak, Taner
  • 1 Duz, Senem Arda
  • 1 Erdogan, Ali
  • . next >

Subject

  • 1 AXIN2
  • 1 Beta-Globin gene
  • 1 Blepharophimosis
  • 1 calcium binding protein
  • 1 Calcium-Binding Proteins
  • 1 case report
  • 1 CCBE1 protein, human
  • 1 cerebellum
  • 1 child
  • 1 clinical article
  • . < previous next >

Date issued

  • 11 2020 - 2025

Type

  • 11 Article
  • 1 Article; Early Access

Fulltext

  • 7 No Fulltext
  • 4 With Fulltext


Results 1-11 of 11 (Search time: 0.006 seconds).

Issue DateTitleAuthor(s)
12024A case report of Hennekam syndrome with a mutation in the CCBE1 geneDurak, T. ; Karaer, D. ; Karaer, K. 
22022Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64, a very rare form of hereditary spastic paraplegiasOlmez, Akgun; Cetin, Gokhan Ozan ; Karaer, Kadri 
32023Evaluation of the frequency of MEFV gene variants in patients with a pre-diagnosis of Familial Mediterranean Fever (FMF) in southeast TürkiyeKaraer, Derya ; Şahinoğlu, Bahtiyar; Gürler, Abdullah İhsan; Karaer, Kadri 
42021İnfertil erkek hastalarda karyotip analizi ve Y kromozom mikrodelesyon analiz sonuçlarıKaraer, Derya ; Şahinoğlu, Bahtiyar; Gürler, Abdullah İhsan; Karaer, Kadri 
52023The Molecular Spectrum of Beta Thalassemia Mutations in Southeastern, TurkeyKaraer, Derya ; Şahinoğlu, Bahtiyar; Şahinoğlu, Esra Pekpak; Gürler, Abdullah I.; Kirat, Emre; Karaer, Kadri 
62025Multi-omics analysis of placental metabolomics and transcriptomics datasets reveals comprehensive insights into the pathophysiology of preeclampsiaMumcu, Akin; Saridogan, Erdinc; Duz, Senem Arda; Tuncay, Gorkem; Erdogan, Ali; Karaer, Kadri ; Dogan, Berat
72022Neurodevelopmental disorder with microcephaly, ataxia, and seizures syndrome: expansion of the clinical spectrumKaraer K. ; Karaer D. ; Yüksel Z.; Işikay S.
82024Noonan syndrome: molecular and clinical findings in individuals with PTPN11 pathogenic variantsKaraer, Derya ; Durak, Taner ; Karaer, Kadri 
92024Presentation of Pallister-Hall-Like Syndrome in a Girl with a Homozygous Rare Variant in the SMO GeneTan, Mertcan ; Turgut, Musa ; Ozdemir, Ozmert Muhammed Ali ; Karaer, Kadri 
102022Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes Analysis of a Turkish cohortKeskin, Gul; Karaer, Kadri ; Ucar Gundogar, Zubeyde
112022Two novel variants in SCARF2 gene underlie van den Ende-Gupta syndromeKaraer, Derya ; Karaer, Kadri 

 

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