R. Kenana

The Role of 3′ to 5′ Reverse RNA Polymerization in tRNA Fidelity and Repair

Ilka U. Heinemann, Malith Jayasinghe, J. Jackman, 2019, Genes.

ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder

Olfat Al-Harazi, N. Kaya, D. Çolak, 2014, Journal of Medical Genetics.

A novel anti-IL4Rα nanoparticle efficiently controls lung inflammation during asthma

S. Al‐Muhsen, R. Halwani, Sibtain Afzal, 2016, Experimental & Molecular Medicine.

Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly

N. Kaya, D. Çolak, E. Faqeih, 2014, American journal of medical genetics. Part A.

Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay.

N. Kaya, D. Çolak, Y. Lakmache, 2013, American journal of human genetics.

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability

N. Kaya, D. Çolak, M. D’Adamo, 2016, Journal of Medical Genetics.

A Systematic Genetic Assessment of ARFGEF2 Mutations in Periventricular Heterotopia

N. Kaya, D. Çolak, M. Daghestani, 2018 .

Association of IL-13 rs20541 and rs1295686 variants with symptomatic asthma in a Saudi Arabian population

S. Al‐Muhsen, R. Halwani, Z. Shakoor, 2018, The Journal of asthma : official journal of the Association for the Care of Asthma.

Towards a Cure for HARS Disease

Ilka U. Heinemann, P. O'Donoghue, R. Kenana, 2023, Genes.

Histidine supplementation can escalate or rescue HARS deficiency in a Charcot–Marie–Tooth disease model

Martin L. Duennwald, Ilka U. Heinemann, V. Siu, 2022, Human molecular genetics.