| NO |
AD |
YIL |
| 1 | An API for dynamic estimation of reference intervals for functional abundances of gut microbiota... | 2023 |
| 2 | Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Stu... | 2023 |
| 3 | Editorial: Mental health: cell models to mechanisms... | 2023 |
| 4 | Whole Genome Analysis of Dizygotic Twins With Autism Reveals Prevalent Transposon Insertion Within N... | 2023 |
| 5 | An in silico approach to the identification of diagnostic and prognostic markers in low-grade glioma... | 2023 |
| 6 | Associations Between Blood Levels of NLRP3 Inflammasome Components and Obsessive Compulsive Disorder... | 2023 |
| 7 | Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects... | 2022 |
| 8 | High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases... | 2021 |
| 9 | Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, ep... | 2021 |
| 10 | Different selection dynamics of S and RdRp between SARS-CoV-2 genomes with and without the dominant ... | 2021 |
| 11 | Alternative splicing and gene co-expression network-based analysis of dizygotic twins with autism-sp... | 2021 |
| 12 | Current mutatome of SARS-CoV-2 in Turkey reveals mutations of interest.... | 2021 |
| 13 | Autosomal recessive variants in TUBGCP2 alter the gamma-tubulin ring complex leading to neurodevelop... | 2021 |
| 14 | Mutations and Copy Number Alterations in IDH Wild-Type Glioblastomas Are Shaped by Different Oncogen... | 2020 |
| 15 | Mutations of SARS-CoV-2 nsp14 exhibit strong association with increased genome-wide mutation load... | 2020 |
| 16 | Mutation density changes in SARS-CoV-2 are related to the pandemic stage but to a lesser extent in t... | 2020 |
| 17 | Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDG... | 2020 |
| 18 | RdRp mutations are associated with SARS-CoV-2 genome evolution... | 2020 |
| 19 | Confirmation of TACO1 as a Leigh syndrome disease gene in two additional families... | 2020 |
| 20 | COL4A1-related autosomal recessive encephalopathy in 2 Turkish children... | 2020 |
| 21 | Severe neurodevelopmental disease caused by a homozygous TLK2 variant.... | 2019 |
| 22 | Dihydropyridine Receptor Congenital Myopathy In A Consangineous Turkish Family.... | 2019 |
| 23 | Whole exome sequencing-based analysis to identify DNA damage repair deficiency as a major contributo... | 2019 |
| 24 | Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical beh... | 2017 |
| 25 | Gliom Gelişiminde Genetik Yatkınlığın Rolü
... | 2017 |
| 26 | Determinants of resistance to chemotherapy and ionizing radiation in breast cancer stem cells... | 2016 |
| 27 | Determinants of resistance to chemotherapy and radiation in breast cancer stem cells... | 2016 |
| 28 | IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation... | 2016 |
| 29 | Gliomların patolojisi ve moleküler biyolojik özellikleri... | 2014 |
| 30 | UCP2 regulates energy metabolism and differentiation potential of human pluripotent stem cells... | 2011 |
| 31 | PNPASE Regulates RNA Import into Mitochondria... | 2010 |
| 32 | Cardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner ... | 2008 |
| 33 | Hypoxia-inducible factor 2 alpha regulates expression of the mitochondrial aconitase chaperone prote... | 2007 |
| 34 | HIF-2alpha regulates murine hematopoietic development in an erythropoietin-dependent manner... | 2005 |
| 35 | Multiple organ pathology, metabolic abnormalities and impaired homeostasis of reactive oxygen specie... | 2003 |
| 36 | The HIF family member EPAS1/HIF-2alpha is required for normal hematopoiesis in mice... | 2003 |
