Citation Impact
Citing Papers
Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans
2009
Ribosome Profiling of Mouse Embryonic Stem Cells Reveals the Complexity and Dynamics of Mammalian Proteomes
2011 Standout
lincRNAs: Genomics, Evolution, and Mechanisms
2013 Standout
The mitophagy activator urolithin A is safe and induces a molecular signature of improved mitochondrial and cellular health in humans
2019 Standout
Oxidative stress, aging, and diseases
2018 Standout
Clinical Course of Genetic Diseases of the Insulin Receptor (Type A and Rabson-Mendenhall Syndromes)
2004
Zinc Fortification of Cereal Flours: Current Recommendations and Research Needs
2010
Protein-bound molybdenum cofactor is bioavailable and rescues molybdenum cofactor-deficient C. elegans
2021 StandoutNobel
Newborn Hearing Screening — A Silent Revolution
2006 Standout
Coenzyme Q<sub>10</sub> Therapy
2014
Polycystic ovary syndrome: definition, aetiology, diagnosis and treatment
2018 Standout
Cell and Molecular Aspects of Human Intestinal Biotin Absorption
2008
Predicting the sequence specificities of DNA- and RNA-binding proteins by deep learning
2015 Standout
The mechanism of eukaryotic translation initiation and principles of its regulation
2010 Standout
The genetics of deafness
2003
Molybdenum cofactor deficiency: Mutations in GPHN, MOCS1, and MOCS2
2010
Genome-Scale Identification of SARS-CoV-2 and Pan-coronavirus Host Factor Networks
2020 StandoutNobel
Structure of sulfamidase provides insight into the molecular pathology of mucopolysaccharidosis IIIA
2014
New hypotheses for the health-protective mechanisms of whole-grain cereals: what is beyond fibre?
2010 Standout
Biochemistry of Mitochondrial Coenzyme Q Biosynthesis
2017
Targeting ferroptosis as a vulnerability in cancer
2022 Standout
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
<p>Reactive Oxygen Species: Drivers of Physiological and Pathological Processes</p>
2020 Standout
Interpreting neural networks for biological sequences by learning stochastic masks
2022 StandoutNobel
A review on the oxidative and nitrosative stress (O&NS) pathways in major depression and their possible contribution to the (neuro)degenerative processes in that illness
2010 Standout
Coenzyme Q deficiency triggers mitochondria degradation by mitophagy
2009
Molybdenum cofactor transfer from bacteria to nematode mediates sulfite detoxification
2019 StandoutNobel
The role of inflammation in depression: from evolutionary imperative to modern treatment target
2015 Standout
Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue
2019 Standout
Characterization of a transcriptional TPP riboswitch in the human pathogen Neisseria meningitidis
2020 StandoutNobel
Regulation Mechanisms and Signaling Pathways of Autophagy
2009 Standout
Agronomic biofortification of cereals with zinc: a review
2017 Standout
Mitochondrial Disorders in the Nervous System
2008
CoQ10 and Aging
2019
Maintaining order: COG complex controls Golgi trafficking, processing, and sorting
2019
The in-depth evaluation of suspected mitochondrial disease
2008
Formylglycine, a Post-Translationally Generated Residue with Unique Catalytic Capabilities and Biotechnology Applications
2014 StandoutNobel
BIOTIN IN METABOLISM AND MOLECULAR BIOLOGY
2002
Host-Gut Microbiota Metabolic Interactions
2012 StandoutScience
Insulin Resistance and the Polycystic Ovary Syndrome Revisited: An Update on Mechanisms and Implications
2012 Standout
Functional analysis of LDLR promoter and 5′ UTR mutations in subjects with clinical diagnosis of familial hypercholesterolemia
2011
Zinc deficiency and human health: etiology, health consequences, and future solutions
2012
Tunable protein synthesis by transcript isoforms in human cells
2016 StandoutNobel
Intestinal absorption of water-soluble vitamins in health and disease
2011
Works of Ayşegül Tokatlı being referenced
Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and B
2002
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene
2007
The molecular basis of familial hypercholesterolaemia in Turkish patients
2005
A Turkish Case with Molybdenum Cofactor Deficiency
2006
The Effect of Zinc-Supplemented Bread Consumption on School Children with Asymptomatic Zinc Deficiency
1998
Key features and clinical variability of COG6-CDG
2015
Secondary Hemophagocytosis in 3 Patients With Organic Acidemia Involving Propionate Metabolism
2011
Fine Mapping of the Human Biotinidase Gene and Haplotype Analysis of Five Common Mutations
1999
Leprechaunism (Donohue's syndrome): a case report.
1994
Novel mutations cause biotinidase deficiency in Turkish children
2000