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Publications by Rafał Płoski
NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals With Leigh-Like Encephalomyopathy
American Journal of Human Genetics
Genetics
Bi-Allelic ADPRHL2 Mutations Cause Neurodegeneration With Developmental Delay, Ataxia, and Axonal Neuropathy
American Journal of Human Genetics
Genetics
Author Correction: Hybrid De Novo Whole-Genome Assembly and Annotation of the Model Tapeworm Hymenolepis Diminuta
Scientific data
Statistics
Probability
Information Sciences
Uncertainty
Library
Information Systems
Computer Science Applications
Education
Variants in theATM-CHEK2-BRCA1axis Determine Genetic Predisposition and Clinical Presentation of Papillary Thyroid Carcinoma
Genes Chromosomes and Cancer
Cancer Research
Genetics
Molecular Bases of Metachromatic Leukodystrophy in Polish Patients
Journal of Human Genetics
Genetics
New Perspective in Diagnostics of Mitochondrial Disorders: Two Years’ Experience With Whole-Exome Sequencing at a National Paediatric Centre
Journal of Translational Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
DISC1as a Possible Genetic Contribution to Opioid Dependence in a Polish Sample
Journal of Studies on Alcohol and Drugs
Psychiatry
Toxicology
Mental Health
Health
Possible Association Between Suicide Committed Under Influence of Ethanol and a Variant in the AUTS2 Gene
PLoS ONE
Multidisciplinary
The Association Between 38 Previously Reported Polymorphisms and Psoriasis in a Polish Population: High Predicative Accuracy of a Genetic Risk Score Combining 16 Loci
PLoS ONE
Multidisciplinary
State of the Art Paper Contemporary Role of Medical Genetics in Internal Medicine
Archives of Medical Science
Medicine
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