Publications by authors named "Elif Everest"

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Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.
Furkan Büyükgöl, Berk Gürdamar, Mehmet Ufuk Aluçlu, Yeşim Beckmann, Kaya Bilguvar, Elif Everest

Sci Rep· April 2025

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The Canadian collaborative project on genetic susceptibility to multiple sclerosis cohort population structure and disease etiology.
Alison M Pagalilauan, Elif Everest, Suzanna Rachimi, Daniel S Reich, Alex D Waldman

Front Neurol· March 2025

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Letter to the Editor Regarding "Spinocerebellar ataxia masquerading as multiple sclerosis, a case report".
Bade Gulec, Elif Everest, Ugur Uygunoglu

J Neuroimmunol· February 2025

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Investigation of multiple sclerosis-related pathways through the integration of genomic and proteomic data.
Elif Everest, Ege Ülgen, Ugur Uygunoglu, Melih Tutuncu, Sabahattin Saip

PeerJ· November 2024

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HLA-B gene methylation and expression in Behçet's syndrome: a potential role of epigenetics in the pathogenesis.
Merve Özkılınç Önen, Elif Everest, Turna Demirci, Pelinsu Köprülü Şen, Esra Kızıltepe Kısakesen

Clin Exp Rheumatol· October 2024

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A Case of Coexistent Spinocerebellar Ataxia Type 2 and Primary Progressive Multiple Sclerosis-Coincidental or Associated?
Elif Everest, Bade Gulec, Ugur Uygunoglu

Cerebellum· June 2024

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The Canadian Collaborative Project on Genetic Susceptibility to Multiple Sclerosis cohort population structure and disease etiology.
Alison M Pagalilauan, Elif Everest, Suzanna Rachimi, Daniel Reich, Alex D Waldman

medRxiv· April 2024

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Erdheim-Chester disease of brain parenchyma without any systemic involvement: A case report and review of literature.
Merve Aktan Suzgun, Elif Everest, Selin Kucukyurt, Melih Tutuncu, Ugur Uygunoglu

Neuropathology· February 2024

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Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype.
Merve Özkılınç Önen, Umut I Onat, Serdal Uğurlu, Ahmet C Timuçin, Devrim Öz Arslan, Elif Everest

Rheumatology (Oxford)· September 2023

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Comparison of multiple sclerosis patients with or without rebound activity after fingolimod cessation: Five-year clinical outcomes.
Bade Gulec, Elif Everest, Ogeday Derin Gorkey, Metehan Koc, Melih Tutuncu

Eur J Neurol· September 2023

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Prospective outcome analysis of multiple sclerosis cases reveals candidate prognostic cerebrospinal fluid markers.
Elif Everest, Ugur Uygunoglu, Melih Tutuncu, Alper Bulbul, Umut Inci Onat

PLoS One· June 2023

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Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation.
Elif Everest, Mohammad Ahangari, Ugur Uygunoglu, Melih Tutuncu, Alper Bulbul

Sci Rep· October 2022

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Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effects.
Mohammad Ahangari, Elif Everest, Tan-Hoang Nguyen, Brian C Verrelli, Bradley T Webb

Brain Behav Immun· August 2022

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MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia.
Ece Selçuk, Koray Kırımtay, Benan Temizci, Şeyma Akarsu, Elif Everest

Mol Genet Genomics· July 2022

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Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study.
İlker Karacan, Ayşe Balamir, Serdal Uğurlu, Aslı Kireçtepe Aydın, Elif Everest

Rheumatol Int· May 2019

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Correction to: Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study.
İlker Karacan, Ayşe Balamir, Serdal Uğurlu, Aslı Kireçtepe Aydın, Elif Everest

Rheumatol Int· May 2019

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Gene Defects in Familial Form of Juvenile Arthritis.
Ilker Karacan, Serdal Uğurlu, Sezgin Şahin, Elif Everest, Özgür Kasapçopur

J Rheumatol· May 2018

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Role of genetics in pediatric rheumatology.
Eda Tahir Turanlı, Elif Everest, Ayşe Balamir, Aslı Kireçtepe Aydın, Özgür Kasapçopur

Turk Pediatri Ars· September 2017

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Alternatively spliced MEFV transcript lacking exon 2 and its protein isoform pyrin-2d implies an epigenetic regulation of the gene in inflammatory cell culture models.
Gokce Celikyapi Erdem, Sule Erdemir, Irem Abaci, Asli K Kirectepe Aydin, Elif Everest

Genet Mol Biol· August 2017

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