Salih Tuna
Cambridge, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 17 publications
Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders.
Journal: American journal of human genetics
Published: March 13, 2023
Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans.
Journal: Nature communications
Published: July 10, 2019
Craniometric Analysis of Skullbase With Magnetic Resonance Imaging in Patients With Chiari Malformation.
Journal: The Journal of craniofacial surgery
Published: May 03, 2019
Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy.
Journal: Journal of the American Society of Nephrology : JASN
Published: April 30, 2019
Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responses.
Journal: The Journal of experimental medicine
Published: February 22, 2019
Whole-genome sequencing of patients with rare diseases in a national health system.
Journal: Nature
Published: December 23, 2018
Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.
Journal: The Journal of allergy and clinical immunology
Published: April 13, 2017
Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding.
Journal: Blood
Published: March 30, 2017
Platelet function is modified by common sequence variation in megakaryocyte super enhancers.
Journal: Nature communications
Published: March 29, 2017
Last Updated: 09/26/2026