Publications by authors named "Erhan Pariltay"

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Detection of copy number variations by chromosomal microarray analysis in disorders of sex development of unexplained molecular etiology and association with clinical findings.
Murat Çağlar Karataş, Ferda Evin, Tahir Atik, Aysun Ata, Eren Er

Endocrine· December 2025

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Identifying a rare mechanism: double parallel trisomy rescue leading to combined segmental and whole-chromosome mosaicism in an IVF-derived embryo.
Elif Kubar, Alp Peker, İrem Oflaz, Erhan Parıltay, Aslı Ece Solmaz

J Assist Reprod Genet· December 2025

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The anticancer potential of Origanum onites L. in gastric cancer through epigenetic alterations.
Fatma Sogutlu, Mert Pekerbas, Gulsum Boztas, Emine Bayram, Erhan Pariltay

BMC Complement Med Ther· July 2025

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Uniparental Disomy of Chromosome 4: A Case of Whole Chromosome UPD Presenting with LRBA Deficiency.
Bilgesu Ak, Erhan Parıltay, Reyhan Gümüşburun, Ceyda Tunakan Dalgıç, Ayça Aykut

J Clin Immunol· September 2024

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Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiency.
Merve Yoldas Celik, Ebru Canda, Havva Yazici, Fehime Erdem, Ayse Yuksel Yanbolu, Erhan Pariltay

Nutr Metab Cardiovasc Dis· July 2024

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A unique case of thrombophilia: the role of F9 gene duplication and increased factor IX activity in cerebral venous thrombosis.
Turkan Turkut Tan, Erhan Pariltay, Enise Avci Durmusaliogu, Esra Isik, Ozgur Cogulu

J Thromb Haemost· October 2023

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Investigation of possible associations of the and genes with the neurocognitive measures: and genes might be involved in attention domain, gene in executive function.
Hilmi Bolat, Gül Ünsel-Bolat, Semiha Özgül, Erhan Parıltay, Akın Tahıllıoğlu

Nord J Psychiatry· November 2022

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Association between clinical variations and copy number variations in cases with Turner syndrome.
Ezgi Aksoy, Ozgur Cogulu, Erhan Pariltay, Samim Ozen, Aysun Ata

J Pediatr Endocrinol Metab· September 2022

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Propolis Extract Regulates microRNA Expression in Glioblastoma and Brain Cancer Stem Cells.
Ugur C Yilmaz, Bakiye Goker Bagca, Emin Karaca, Asude Durmaz, Burak Durmaz, Erhan Pariltay

Anticancer Agents Med Chem· March 2022

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A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case report.
Asli Ece Solmaz, Erhan Pariltay, Beril Talim, Huseyin Onay

Clin Neurol Neurosurg· January 2022

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Prenatal diagnosis of a case with tetrasomy 9p confirmed by cytogenetics, FISH, microarray analysis and review.
Gizem Kok Kilic, Erhan Pariltay, Emin Karaca, Burak Durmaz, Huseyin Ekici

Taiwan J Obstet Gynecol· January 2022

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20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey.
Burak Durmaz, Hilmi Bolat, Zehra Cengisiz, Fuat Akercan, Tuba Sözen Türk

Turk J Med Sci· August 2021

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DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo.
Hilmi Bolat, Eyüp S Ercan, Gül Ünsel-Bolat, Akin Tahillioğlu, Kemal U Yazici, Erhan Pariltay

Braz J Psychiatry· November 2020

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Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure.
Yasemin Karaca, Erhan Pariltay, Lamiya Mardan, Emin Karaca, Asude Durmaz

Reprod Biol· March 2020

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Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages.
Necil Kutukculer, Ayca Aykut, Neslihan E Karaca, Asude Durmaz, Guzide Aksu, Erhan Pariltay

Scand J Immunol· February 2019

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Profile Templates to Use during Surgery in Precision Rhinoplasty.
Fazil Apaydin, Rodrigo Fortunato Fernández-Pellón Garcia, Erhan Pariltay

Facial Plast Surg· February 2019

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An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation.
Necil Kutukculer, Neslihan Edeer Karaca, Guzide Aksu, Ayca Aykut, Erhan Pariltay

Case Reports Immunol· October 2018

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A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel.
Erhan Parıltay, Filiz Hazan, Esra Ataman, Korcan Demir, Özdal Etlik

J Pediatr Endocrinol Metab· September 2016

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, Selma Düzenli, Robert P Marshall

J Hum Genet· January 2015

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, Selma Düzenli, Robert P Marshall

J Hum Genet· January 2015

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Demonstration of uniparental-isodisomy on chromosome 22q11.2 in a patient with childhood schizophrenia and facial dysmorphology by whole-genome analysis.
Ozgur Cogulu, Erhan Pariltay, Asude Alpman Durmaz, Ayca Aykut, Cumhur Gunduz

J Neuropsychiatry Clin Neurosci· August 2012

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Reasons for adult referrals for genetic counseling at a genetics center in Izmir, Turkey: analysis of 8965 cases over an eleven-year period.
Ozgur Cogulu, Ferda Ozkinay, Haluk Akin, Huseyin Onay, Emin Karaca, Erhan Pariltay

J Genet Couns· June 2011

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The evaluation of the referral reasons of patients at a tertiary pediatric genetic center in Izmir, Turkey.
Burak Durmaz, Asude Alpman, Erhan Pariltay, Mehmet Akgul, Esra Ataman

Genet Test Mol Biomarkers· April 2009

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Seckel syndrome with Morgagni hernia.
Asan Onder, Ozgur Cogulu, Aslihan Ekmekci, Erhan Pariltay, Ozgur Kirbiyik

Clin Dysmorphol· July 2007

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