Evren Gumus
15PUBLICATIONS
38CO-AUTHORS
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Publications (15)
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|Dec 19, 2025
<i>CHEK2</i> Germline Variants and Their Clinical Implications: Experience from a Turkish Hereditary Cancer Cohort.Zehra Manav Yigit, Osman Semih Dikbas, Fatih Mergen
|Dec 01, 2023
Correction: Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.Jiyong Wang, Aidin Foroutan, Ellen Richardson
|Jan 07, 2022
Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.Jiyong Wang, Aidin Foroutan, Ellen Richardson
|Nov 20, 2021
Congenital insensitivity to pain: a novel mutation affecting a U12-type intron causes multiple aberrant splicing of SCN9A.Margherita Marchi, Ilaria D'Amato, Mirna Andelic
|Apr 05, 2021
Response to Letter to the Editor: "Atrioventricular canal defect is an infrequent congenital heart disease that can be observed in Bardet-Biedl syndrome".Evren Gumus, Ebru Tuncez, Ozlem Oz
|Mar 13, 2021
A novel homozygous RIPK4 variant in a family with severe Bartsocas-Papas syndrome.Tuba Dinçer, Evren Gümüş, Bayram Toraman
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Frequent Collaborators
2 joint publications
Matthew L Tedder
2 joint publications
Charles E Schwartz
2 joint publications
Phillis Lakeman
2 joint publications
Roger E Stevenson
2 joint publications
Stephen P Robertson
2 joint publications
Jennifer Kerkhof
1 joint publications
N Weaver
1 joint publications
Gokay Bozkurt
1 joint publications
M Zenker
1 joint publications
F Hildebrandt
