Gamze Guven
Overview
Explore the profile of Gamze Guven including associated specialties, affiliations and a list of published articles.
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Articles
23
Citations
411
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Recent Articles
1.
Atasu B, Simon-Sanchez J, Hanagasi H, Bilgic B, Hauser A, Guven G, et al.
J Med Genet
. 2024 Mar;
61(5):443-451.
PMID: 38458754
Background: Dystonia is one of the most common movement disorders. To date, the genetic causes of dystonia in populations of European descent have been extensively studied. However, other populations, particularly...
2.
Guclu-Geyik F, Koseoglu P, Guven G, Can G, Kaya A, Coban N, et al.
Biochem Genet
. 2023 Apr;
61(6):2276-2292.
PMID: 37020118
The anti-inflammatory adipokine intelectin-1, which is encoded by the ITLN1 gene, is hypothesized to be linked to the pathogenesis of type 2 diabetes (T2DM) and obesity. The purpose of this...
3.
Foddis M, Blumenau S, Holtgrewe M, Paquette K, Westra K, Alonso I, et al.
Neurobiol Aging
. 2022 Dec;
123:208-215.
PMID: 36586737
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and retinal vasculopathy with cerebral leukodystrophy and systemic manifestations (RVCL-S) are the most common forms of rare monogenic early-onset cerebral...
4.
Atasu B, Ozdag Acarli A, Bilgic B, Baykan B, Demir E, Ozluk Y, et al.
BMC Neurol
. 2022 Mar;
22(1):122.
PMID: 35346091
Background: Biallelic pathogenic variants in the SCARB2 gene have been associated with action myoclonus-renal failure (AMRF) syndrome. Even though SCARB2 associated phenotype has been reported to include typical neurological characteristics,...
5.
Dehghani N, Guven G, Kun-Rodrigues C, Gouveia C, Foster K, Hanagasi H, et al.
Hum Genomics
. 2021 Jul;
15(1):48.
PMID: 34321086
Background: Copy number variants (CNVs) include deletions or multiplications spanning genomic regions. These regions vary in size and may span genes known to play a role in human diseases. As...
6.
Samanci B, Bilgic B, Gelisin O, Tepgec F, Guven G, Tufekcioglu Z, et al.
Eur J Neurol
. 2021 May;
28(8):2603-2613.
PMID: 33969597
Background And Purpose: Nasu-Hakola disease (NHD) is a rare, autosomal recessive disorder characterized by skeletal and neurological symptoms. Behavioral symptoms with cognitive impairment may mimic the behavioral variant of frontotemporal...
7.
Guven G, Samanci B, Gulec C, Hanagasi H, Gurvit H, Gokalp E, et al.
Neurol Sci
. 2021 Apr;
42(6):2497-2504.
PMID: 33855622
Alzheimer's disease (AD) can be either sporadic or familial, and familial forms of AD accounts for only 5% of the cases. So far, autosomal dominantly inherited mutations in "Presenilin 1"...
8.
Messerschmidt C, Foddis M, Blumenau S, Muller S, Bentele K, Holtgrewe M, et al.
Sci Rep
. 2021 Mar;
11(1):6072.
PMID: 33727568
Recently, several genome-wide association studies identified PHACTR1 as key locus for five diverse vascular disorders: coronary artery disease, migraine, fibromuscular dysplasia, cervical artery dissection and hypertension. Although these represent significant...
9.
Guven G, Bilgic B, Samanci B, Gurvit H, Hanagasi H, Donmez C, et al.
Mol Biol Rep
. 2020 Jul;
47(8):5903-5909.
PMID: 32681391
'Triggering receptor expressed on myeloid cells 2' (TREM2) gene is involved in Alzheimer's disease (AD) and TREM2 mRNA expression is known to be increased in the peripheral blood cells of...
10.
Guven G, Erginel-Unaltuna N, Samanci B, Gulec C, Hanagasi H, Bilgic B
Neurobiol Aging
. 2019 Jul;
84:238.e1-238.e4.
PMID: 31296348
"Presenilin 1" (PSEN1) gene mutations are the major known genetic cause of early-onset Alzheimer's disease. Herein, we report a novel heterozygous PSEN1 mutation (p.Leu424Pro) in a Turkish patient presenting with...