Publications by authors named "Bayram Toraman"

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A synonymous single nucleotide variant on the FAM20C gene causes non-lethal Raine syndrome.
Bayram Toraman, İdris Er, Burak Kaan Kasap, Ümit Uzun, Tuba Dinçer

Hum Mol Genet· October 2025

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A novel homozygous RIPK4 variant in a family with severe Bartsocas-Papas syndrome.
Tuba Dinçer, Evren Gümüş, Bayram Toraman, İdris Er, Gokhan Yildiz

Am J Med Genet A· June 2021

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Finding underlying genetic mechanisms of two patients with autism spectrum disorder carrying familial apparently balanced chromosomal translocations.
Bayram Toraman, Samiye Çilem Bilginer, Selma Tural Hesapçıoğlu, Zeynep Göker, Hüseyin Okan Soykam

J Gene Med· April 2021

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[Investigation of Plasmid Mediated mcr Colistin Resistance Gene in Clinical Enterobacterales Isolates].
Esra Özkaya, Celal Kurtuluş Buruk, İlknur Tosun, Bayram Toraman, Neşe Kaklıkkaya

Mikrobiyol Bul· April 2020

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RIPK4 suppresses the TGF-β1 signaling pathway in HaCaT cells.
Tuba Dinçer, Asiye Büşra Boz Er, İdris Er, Bayram Toraman, Gokhan Yildiz

Cell Biol Int· March 2020

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Analysis of centrosome and DNA damage response in PLK4 associated Seckel syndrome.
Tuba Dinçer, Gülden Yorgancıoğlu-Budak, Akgün Ölmez, İdris Er, Yavuz Dodurga, Bayram Toraman

Eur J Hum Genet· October 2017

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HLA-E*0101/0103X is Associated with Susceptibility to Pemphigus Vulgaris: A Case-control Study.
Ece Altun, Savas Yayli, Bayram Toraman, Deniz Aksu Arica, Ersan Kalay

Acta Dermatovenerol Croat· October 2017

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Novel splice-site and missense mutations in the ALDH1A3 gene underlying autosomal recessive anophthalmia/microphthalmia.
C Nur Semerci, Ersan Kalay, Cem Yıldırım, Tuba Dinçer, Akgün Olmez, Bayram Toraman

Br J Ophthalmol· June 2014

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Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation.
Bayram Toraman, Ayşenur Ökten, Ersan Kalay, Gülay Karagüzel, Tuba Dinçer

Gene· January 2013

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Mutations in RIPK4 cause the autosomal-recessive form of popliteal pterygium syndrome.
Ersan Kalay, Orhan Sezgin, Vasant Chellappa, Mehmet Mutlu, Heba Morsy, Bayram Toraman

Am J Hum Genet· January 2012

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CEP152 is a genome maintenance protein disrupted in Seckel syndrome.
Ersan Kalay, Gökhan Yigit, Yakup Aslan, Karen E Brown, Esther Pohl, Bayram Toraman

Nat Genet· January 2011

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Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.
Rob W J Collin, Ersan Kalay, Jaap Oostrik, Refik Caylan, Bernd Wollnik, Bayram Toraman

Hum Mutat· July 2007

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