Found: 33
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Interactions of genetic risks for autism and the broad autism phenotypes.
- Published in:
- Frontiers in Psychiatry, 2023, v. 14, p. 1, doi. 10.3389/fpsyt.2023.1110080
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- Publication type:
- Article
The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population.
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- Frontiers in Aging Neuroscience, 2021, v. 13, p. 1, doi. 10.3389/fnagi.2021.749109
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- Publication type:
- Article
PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population.
- Published in:
- 2021
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- Publication type:
- Letter
Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes.
- Published in:
- Life (2075-1729), 2021, v. 11, n. 3, p. 233, doi. 10.3390/life11030233
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- Publication type:
- Article
Minimized Delay with Reliability Guaranteed by Using Variable Width Tiered Structure Routing in WSNs.
- Published in:
- International Journal of Distributed Sensor Networks, 2015, v. 2015, p. 1, doi. 10.1155/2015/689504
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- Publication type:
- Article
Cat Swarm Optimization applied to alcohol use disorder identification.
- Published in:
- Multimedia Tools & Applications, 2018, v. 77, n. 17, p. 22875, doi. 10.1007/s11042-018-6003-8
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- Publication type:
- Article
Smart pathological brain detection by synthetic minority oversampling technique, extreme learning machine, and Jaya algorithm.
- Published in:
- Multimedia Tools & Applications, 2018, v. 77, n. 17, p. 22629, doi. 10.1007/s11042-017-5023-0
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- Publication type:
- Article
Exploring a smart pathological brain detection method on pseudo Zernike moment.
- Published in:
- Multimedia Tools & Applications, 2018, v. 77, n. 17, p. 22589, doi. 10.1007/s11042-017-4703-0
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- Publication type:
- Article
Cortical interactions during the resolution of information processing demands in autism spectrum disorders.
- Published in:
- Brain & Behavior, 2017, v. 7, n. 2, p. n/a, doi. 10.1002/brb3.596
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- Publication type:
- Article
Aberrant functional brain connectome in people with antisocial personality disorder.
- Published in:
- Scientific Reports, 2016, p. 26209, doi. 10.1038/srep26209
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- Publication type:
- Article
Severity of Autism Spectrum Disorder Symptoms Associated with de novo Variants and Pregnancy-Induced Hypertension.
- Published in:
- Journal of Autism & Developmental Disorders, 2024, v. 54, n. 2, p. 749, doi. 10.1007/s10803-022-05824-4
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- Publication type:
- Article
Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders.
- Published in:
- Journal of Autism & Developmental Disorders, 2022, v. 52, n. 3, p. 1299, doi. 10.1007/s10803-021-05031-7
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- Publication type:
- Article
Gene4PD: A Comprehensive Genetic Database of Parkinson's Disease.
- Published in:
- Frontiers in Neuroscience, 2021, v. 15, p. N.PAG, doi. 10.3389/fnins.2021.679568
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- Publication type:
- Article
Characterizing the Expression Patterns of Parkinson's Disease Associated Genes.
- Published in:
- Frontiers in Neuroscience, 2021, v. 15, p. N.PAG, doi. 10.3389/fnins.2021.629156
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- Publication type:
- Article
Association between ovarian reserve and spontaneous miscarriage and their shared genetic architecture.
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- Human Reproduction, 2023, v. 38, n. 11, p. 2247, doi. 10.1093/humrep/dead180
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- Publication type:
- Article
Verbal–spatial IQ discrepancies impact brain activation associated with the resolution of cognitive conflict in children and adolescents.
- Published in:
- Developmental Science, 2018, v. 21, n. 2, p. 1, doi. 10.1111/desc.12550
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- Publication type:
- Article
A Delay-Aware and Reliable Data Aggregation for Cyber-Physical Sensing.
- Published in:
- Sensors (14248220), 2017, v. 17, n. 2, p. 395, doi. 10.3390/s17020395
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- Publication type:
- Article
Risk factors associated with age at onset of Parkinson's disease in the UK Biobank.
- Published in:
- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-023-00623-9
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- Publication type:
- Article
Genetic landscape of human mitochondrial genome using whole-genome sequencing.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 11, p. 1747, doi. 10.1093/hmg/ddab358
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- Publication type:
- Article
Fractal Dimension Analysis of Subcortical Gray Matter Structures in Schizophrenia.
- Published in:
- PLoS ONE, 2016, v. 11, n. 5, p. 1, doi. 10.1371/journal.pone.0155415
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- Publication type:
- Article
Gene4MND: An Integrative Genetic Database and Analytic Platform for Motor Neuron Disease.
- Published in:
- Frontiers in Molecular Neuroscience, 2021, v. 13, p. N.PAG, doi. 10.3389/fnmol.2021.644202
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- Publication type:
- Article
ATP10B variants in Parkinson's disease: a large cohort study in Chinese mainland population.
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- Acta Neuropathologica, 2021, v. 141, n. 5, p. 805, doi. 10.1007/s00401-021-02280-9
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- Publication type:
- Article
Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read Sequencing.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.810595
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- Publication type:
- Article
Gene4HL: An Integrated Genetic Database for Hearing Loss.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.773009
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- Publication type:
- Article
VarCards2: an integrated genetic and clinical database for ACMG-AMP variant-interpretation guidelines in the human whole genome.
- Published in:
- Nucleic Acids Research, 2024, v. 52, n. D1, p. D1478, doi. 10.1093/nar/gkad1061
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- Publication type:
- Article
Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans.
- Published in:
- Nucleic Acids Research, 2020, v. 48, n. D1, p. D913, doi. 10.1093/nar/gkz923
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- Publication type:
- Article
De novo mutation of cancer-related genes associates with particular neurodevelopmental disorders.
- Published in:
- Journal of Molecular Medicine, 2020, v. 98, n. 12, p. 1701, doi. 10.1007/s00109-020-01991-y
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- Publication type:
- Article
A metabolomic profile of biological aging in 250,341 individuals from the UK Biobank.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-52310-9
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- Publication type:
- Article
Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.
- Published in:
- Molecular Autism, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13229-020-00382-x
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- Publication type:
- Article
Reduced structural complexity of the right cerebellar cortex in male children with autism spectrum disorder.
- Published in:
- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0196964
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- Publication type:
- Article
Casual associations between brain structure and sarcopenia: A large‐scale genetic correlation and mendelian randomization study.
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- Aging Cell, 2024, v. 23, n. 10, p. 1, doi. 10.1111/acel.14252
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- Publication type:
- Article
Two Pathogenic Gene Mutations Identified Associating with Congenital Cataract and Iris Coloboma Respectively in a Chinese Family.
- Published in:
- Journal of Ophthalmology, 2020, p. 1, doi. 10.1155/2020/7054315
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- Publication type:
- Article
Functional neural circuits that underlie developmental stuttering.
- Published in:
- PLoS ONE, 2017, v. 12, n. 7, p. 1, doi. 10.1371/journal.pone.0179255
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- Publication type:
- Article