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Genome Research, ISSN 1088-9051, 09/2014, Volume 24, Issue 9, pp. 1455 - 1468
Journal Article
Nature, ISSN 0028-0836, 08/2016, Volume 536, Issue 7615, pp. 205 - 209
Journal Article
Nature Methods, ISSN 1548-7091, 05/2010, Volume 7, Issue 5, pp. 365 - 371
The extent of human genomic structural variation suggests that there must be portions of the genome yet to be discovered, annotated and characterized at the... 
FINE-SCALE | STRUCTURAL VARIATION | MAP | BIOCHEMICAL RESEARCH METHODS | Biotechnology | Chromosome mapping | Human genome | Genomics | Research | Nucleotide sequencing | Identification and classification | Methods | Genetic polymorphisms | Genotype & phenotype | Molecular structure | Population genetics | Research methodology
Journal Article
Human Mutation, ISSN 1059-7794, 02/2018, Volume 39, Issue 2, pp. 281 - 291
Journal Article
BIO Web of Conferences, ISSN 2117-4458, 2016, Volume 7, p. 1016
Grapevine is one of the most important crop plants in the world. Recently there was great expansion of genomics resources about grapevine genome, thus... 
Cultivation | Breeding | Copy number | Cross-breeding | Genes | Genomics | Phenotypic variations | Genomes | Single-nucleotide polymorphism | Molecular chains | Fruit cultivation | Inbreeding | Bioinformatics | Cultivars
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 10/2017, Volume 101, Issue 4, pp. 564 - 577
Copy-number changes in 16p11.2 contribute significantly to neuropsychiatric traits. Besides the 600 kb BP4-BP5 CNV found in 0.5%–1% of individuals with autism... 
epistasis | 16p11.2 | zebrafish | head size | autism | obesity | genome architecture | CHROMOSOME 16P11.2 | INTELLECTUAL DISABILITY | MAJOR VAULT PROTEIN | OBESITY | AUTISM | GENETICS & HEREDITY | BRAIN-DEVELOPMENT | DEVELOPMENTAL DELAY | MUTATIONS | COPY-NUMBER VARIANT | PREFRONTAL CORTEX | Microcephaly - genetics | Humans | Middle Aged | Child, Preschool | Male | DNA Copy Number Variations | Brain - metabolism | Young Adult | Membrane Proteins - physiology | Aged, 80 and over | Child | Chromosomes, Human, Pair 16 - genetics | Autistic Disorder - genetics | Chromosome Deletion | Signal Transduction | Embryo, Nonmammalian - pathology | Membrane Proteins - genetics | Intellectual Disability - pathology | Chromosome Disorders - immunology | Zebrafish - genetics | Mice, Knockout | Phenotype | Adolescent | Brain - pathology | Mice | Zebrafish Proteins - genetics | Cohort Studies | Autistic Disorder - pathology | Intellectual Disability - immunology | Embryo, Nonmammalian - metabolism | Autistic Disorder - immunology | Infant | Zebrafish - embryology | Intellectual Disability - genetics | Gene Expression Regulation, Developmental | Microcephaly - pathology | Adult | Female | Membrane Proteins - metabolism | Phosphoproteins - physiology | Chromosome Disorders - pathology | Zebrafish Proteins - metabolism | Mice, Inbred C57BL | Chromosomes, Human, Pair 16 - immunology | Adaptor Proteins, Signal Transducing - physiology | Animals | Adaptor Proteins, Signal Transducing - genetics | Aged | Adaptor Proteins, Signal Transducing - metabolism | Chromosome Disorders - genetics | Cell proliferation | Obesity | Zebra fish | Genetic aspects | Research | Health aspects | Genetic epistasis | Immune system
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 2017, Volume 22, Issue 6, pp. 836 - 849
Journal Article