Publications by authors named "Gamze Guven"

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FBXO7 Pathogenic Variants in Early-Onset Parkinsonism: Insights from a Neuroimaging Perspective and Review of the Literature.
Erdi Şahin, Bedia Samanci, Gül Yalçın Çakmaklı, Ebba Lohmann, Gamze Güven

Mov Disord Clin Pract· November 2025

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Cross-cultural adaptation, reliability, and validity of the Turkish version of moral courage scale for physicians.
Şerife Yılmaz, Gamze Özbek Güven, Feyza İnceoğlu

PLoS One· October 2025

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Unravelling the plasma proteome: Pioneering biomarkers for differential dementia diagnosis.
Haşim Gezegen, Merve Alaylıoğlu, Erdi Şahin, Owen Swann, Elena Veleva

Alzheimers Dement· July 2025

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Development of an Assessment Tool to Measure Hand Hygiene Compliance and Competency in Health Care Services.
Muhdedir Caner, Fatma Kartaloğlu Agay, Gamze Özbek Güven

J Nurs Meas· April 2025

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Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights.
Burcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, Basar Bilgic, Ann-Kathrin Hauser, Gamze Guven

J Med Genet· April 2024

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Association of Intelectin 1 Gene rs2274907 A > T Polymorphism with Obesity, Type 2 Diabetes, Serum Intelectin-1 Levels and Lipid Profiles in Turkish Adults.
Filiz Guclu-Geyik, Pınar Koseoglu, Gamze Guven, Gunay Can, Aysem Kaya

Biochem Genet· December 2023

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TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients.
Marco Foddis, Sonja Blumenau, Manuel Holtgrewe, Kimberly Paquette, Kaitlyn Westra, Gamze Guven

Neurobiol Aging· March 2023

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Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review.
Burcu Atasu, Ayse Nur Ozdag Acarlı, Basar Bilgic, Betül Baykan, Erol Demir, Gamze Guven

BMC Neurol· March 2022

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TREM2 variants as a possible cause of frontotemporal dementia with distinct neuroimaging features.
Bedia Samanci, Başar Bilgiç, Özlem Gelişin, Fatih Tepgeç, Gamze Guven

Eur J Neurol· August 2021

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A comprehensive analysis of copy number variation in a Turkish dementia cohort.
Nadia Dehghani, Gamze Guven, Celia Kun-Rodrigues, Catarina Gouveia, Kalina Foster

Hum Genomics· July 2021

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A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer's disease.
Gamze Guven, Bedia Samanci, Cagri Gulec, Hasmet Hanagasi, Hakan Gurvit

Neurol Sci· June 2021

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PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice.
Clemens Messerschmidt, Marco Foddis, Sonja Blumenau, Susanne Müller, Kajetan Bentele, Gamze Guven

Sci Rep· March 2021

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Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease's patients.
Gamze Guven, Basar Bilgic, Bedia Samanci, Hakan Gurvit, Hasmet Hanagasi

Mol Biol Rep· August 2020

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Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia.
Gamze Guven, Başar Bilgic, Zeynep Tufekcioglu, Nihan Erginel Unaltuna, Hasmet Hanagasi

J Alzheimers Dis· March 2020

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A patient with early-onset Alzheimer's disease with a novel PSEN1 p.Leu424Pro mutation.
Gamze Guven, Nihan Erginel-Unaltuna, Bedia Samanci, Cagri Gulec, Hasmet Hanagasi

Neurobiol Aging· December 2019

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Association between selected cholesterol-related gene polymorphisms and Alzheimer's disease in a Turkish cohort.
Gamze Guven, Eren Vurgun, Basar Bilgic, Hasmet Hanagasi, Hakan Gurvit

Mol Biol Rep· April 2019

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HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype.
Burcu Atasu, Hasmet Hanagasi, Basar Bilgic, Meltem Pak, Nihan Erginel-Unaltuna, Gamze Guven

Mov Disord· August 2018

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Mutations in TYROBP are not a common cause of dementia in a Turkish cohort.
Lee Darwent, Susana Carmona, Ebba Lohmann, Gamze Guven, Celia Kun-Rodrigues

Neurobiol Aging· October 2017

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Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients.
Gamze Guven, Ebba Lohmann, Jose Bras, J Raphael Gibbs, Hakan Gurvit

PLoS One· August 2017

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Unilateral complex syngnathia of the maxilla, mandible, and zygomatic complex in a newborn baby.
Abdullah Özel, Gamze Şenol Güven, Emrah Dilaver, Sina Uçkan

Br J Oral Maxillofac Surg· February 2017

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A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family.
Hasmet A Hanagasi, Anamika Giri, Ece Kartal, Gamze Guven, Başar Bilgiç

Parkinsonism Relat Disord· August 2016

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Histologic and Histomorphometric Comparison of Bone Regeneration Between Bone Morphogenetic Protein-2 and Platelet-Derived Growth Factor-BB in Experimental Groups.
Gokhan Guven, B Alper Gultekin, Gamze Senol Guven, Elif Guzel, Selenay Furat

J Craniofac Surg· May 2016

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PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism.
Anamika Giri, Gamze Guven, Hasmet Hanagasi, Ann-Kathrin Hauser, Nihan Erginul-Unaltuna

Tremor Other Hyperkinet Mov (N Y)· April 2016

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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
Suzanne Lesage, Valérie Drouet, Elisa Majounie, Vincent Deramecourt, Maxime Jacoupy, Gamze Guven

Am J Hum Genet· March 2016

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A new F-box protein 7 gene mutation causing typical Parkinson's disease.
Ebba Lohmann, Anne-Sophie Coquel, Aurélie Honoré, Hakan Gurvit, Hasmet Hanagasi, Gamze Guven

Mov Disord· July 2015

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