Akademisyen
HÜSEYİN YÜCE
PROFESÖR
DÜZCE ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.
- Makale 78
- Proje 0
- Kitap 0
- Bildiri 0
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
3
Q2
9
Q3
4
Q4
31
WoS (JCR)
Q1
2
Q2
3
Q3
13
Q4
32
TR Index
41
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
0
Ort. yüzdelik
46.5%
Üst %1 payı
0.0%
Üst %10 payı
0.0%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2022 Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium YÖKSİS SJR Q2 JCR Q3 OpenAlex 75.1%
- 2022 Study of ten causal genes in Turkish patients with clinically suspected maturity-onset diabetes of the young (MODY) using a targeted next-generation sequencing panel YÖKSİS SJR Q2 JCR Q3 OpenAlex 83.6%
- 2021 Effects of Epigenetic Regulation on Cancer YÖKSİS OpenAlex 4.3%
- 2018 A Case of Schmid Type Metaphyial Dysplasia YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 7.6%
- 2018 Results of BTD Gene Molecular Analysis with Clinical Findings in Three Individuals from the Same Family YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 14.3%
- 2017 A Novel p.Arg179Ser (c.537 G>T) Heterozygotes Mutation on Exon 3 Of SRD5A2 Gene Accompany With Biotidinase Deficiency In Case With Ambiguous External Genitalia YÖKSİS TR Index JCR Q3 OpenAlex 11.1%
- 2016 Vascular endothelial growth factor 936 CT and 2578 CA single nucleotide polymorphisms and postmenopausal osteoporosis. YÖKSİS OpenAlex 9.8%
- 2016 Polymorphisms of kappa casein gene and their effects on milk production traits in Holstein Jersey and Brown Swiss cattle YÖKSİS OpenAlex 89.7%
- 2012 Determination of Kappa Casein Gene Polymorphisms and Their Effects on Milk Composition in Some Native Cattle Breeds of Turkey YÖKSİS SJR Q3 JCR Q4 OpenAlex 73.4%
- 2011 Serotonin transporter gene polymorphism implicates reduced orbito frontal cortex in obsessive compulsive disorder YÖKSİS SJR Q1 JCR Q1 OpenAlex 87.4%
- 2010 The association of myelin oligodendrocyte glycoprotein gene and white matter volume in obsessive compulsive disorder YÖKSİS SJR Q1 JCR Q1 OpenAlex 74.7%
- 2019 Distal 10p duplication at distal 18qdeletion syndrome YÖKSİS TR Index SJR Q4 JCR Q3 OpenAlex 47.8%
- 2019 45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine sahip unikornuat uteruslu olgu YÖKSİS TR Index
- 2019 A case with 45,X[34]/46,X,i(X)(q10)[5] karyotype YÖKSİS TR Index SJR Q4 JCR Q3 OpenAlex 47.8%
- 2019 A family with rare E167D mutationfrom Turkey with a total of fourmembers clinically diagnosed asFMF YÖKSİS TR Index SJR Q4 JCR Q3 OpenAlex 47.8%
- 2018 Polymorphisms of kappa-casein gene and their effects on milkproduction traits in Holstein, Jersey and Brown Swiss cattle YÖKSİS SJR Q2 JCR Q2
- 2018 A Case Consistent With Type 2b of Limb-Girdle Muscular Dystrophy Determined as Homozygous c.3166CT Mutation in The DYSF Gene YÖKSİS TR Index SJR Q4 JCR Q4
- 2018 Evaluation of Karyotype Composition of Our Turner Syndrome Patients with Their Application Complaints and Anthropometric Data YÖKSİS TR Index JCR Q3 OpenAlex 7.6%
- 2018 A Case with Recurrent Fetal Loss, 46,XX,T(26) (q33pP25) Karyotype and Her Thrombophilia Panel YÖKSİS TR Index SJR Q4 JCR Q4
- 2018 Clinical Findings and Molecular Genetic Analysis Results in Patients with Hemochromatosis YÖKSİS TR Index SJR Q4 JCR Q4