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Targeted next generation sequencing identifies a genetic spectrum of DNA variants in patients with hemiplegic migraine.
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- Cephalalgia Reports, 2019, v. 2, p. N.PAG, doi. 10.1177/2515816319881630
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- Article
Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity.
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- International Journal of Molecular Sciences, 2018, v. 19, n. 10, p. 3113, doi. 10.3390/ijms19103113
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- Article
BDNF Variants May Modulate Long-Term Visual Memory Performance in a Healthy Cohort.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 3, p. 655, doi. 10.3390/ijms18030655
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- Article
Exonic mutations in cell–cell adhesion may contribute to CADASIL-related CSVD pathology.
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- Human Genetics, 2023, v. 142, n. 9, p. 1361, doi. 10.1007/s00439-023-02584-8
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- Article
Association of KCNJ6 rs2070995 and methadone response for pain management in advanced cancer at end-of-life.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-21180-w
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- Article
Psip1/Ledgf p75 restrains Hox gene expression by recruiting both trithorax and polycomb group proteins.
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- Nucleic Acids Research, 2014, v. 42, n. 14, p. 9021, doi. 10.1093/nar/gku647
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- Article
Exploring the Hereditary Nature of Migraine.
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- Neuropsychiatric Disease & Treatment, 2021, v. 17, p. 1183, doi. 10.2147/NDT.S282562
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- Article
Tiered analysis of whole-exome sequencing for epilepsy diagnosis.
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- Molecular Genetics & Genomics, 2020, v. 295, n. 3, p. 751, doi. 10.1007/s00438-020-01657-x
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- Article
Exome Sequencing Diagnoses X-Linked Moesin-Associated Immunodeficiency in a Primary Immunodeficiency Case.
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- Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.00420
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- Article
Alterations in DNA methylation associate with reduced migraine and headache days after medication withdrawal treatment in chronic migraine patients: a longitudinal study.
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- Clinical Epigenetics, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13148-023-01604-8
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- Article
Using Monozygotic Twins to Dissect Common Genes in Posttraumatic Stress Disorder and Migraine.
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- Frontiers in Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnins.2021.678350
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- Article
Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine.
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- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.892820
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- Article
Long-Term Consumption of Anthocyanin-Rich Fruit Juice: Impact on Gut Microbiota and Antioxidant Markers in Lymphocytes of Healthy Males.
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- Antioxidants, 2021, v. 10, n. 1, p. 27, doi. 10.3390/antiox10010027
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- Article
Gene-centric analysis implicates nuclear encoded mitochondrial protein gene variants in migraine susceptibility.
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- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 2, p. 157, doi. 10.1002/mgg3.270
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- Article
Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes.
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- Frontiers in Genetics, 2018, p. 1, doi. 10.3389/fgene.2018.00020
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- Article
Genetics of Migraine: Insights into the Molecular Basis of Migraine Disorders.
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- Headache: The Journal of Head & Face Pain, 2017, v. 57, n. 4, p. 537, doi. 10.1111/head.13053
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- Article
Reactivation of heritably silenced gene expression in mice.
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- Mammalian Genome, 2000, v. 11, n. 5, p. 347, doi. 10.1007/s003350010066
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- Article
The <italic>NRP1</italic> migraine risk variant shows evidence of association with menstrual migraine.
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- Journal of Headache & Pain, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s10194-018-0857-z
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- Article
Case-control study of ADARB1 and ADARB2 gene variants in migraine.
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- Journal of Headache & Pain, 2015, v. 16, p. 1, doi. 10.1186/s10194-015-0511-y
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- Article
Comprehensive Exonic Sequencing of Known Ataxia Genes in Episodic Ataxia.
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- Biomedicines, 2020, v. 8, n. 5, p. 134, doi. 10.3390/biomedicines8050134
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- Article
Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants.
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- Cells (2073-4409), 2020, v. 9, n. 11, p. 2368, doi. 10.3390/cells9112368
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- Article
Epigenetic Regulation of miR-92a and TET2 and Their Association in Non-Hodgkin Lymphoma.
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- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.768913
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- Article
Psip1/Ledgf p52 Binds Methylated Histone H3K36 and Splicing Factors and Contributes to the Regulation of Alternative Splicing.
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- PLoS Genetics, 2012, v. 8, n. 5, p. 1, doi. 10.1371/journal.pgen.1002717
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- Article
Discriminating head trauma outcomes using machine learning and genomics.
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- Journal of Molecular Medicine, 2022, v. 100, n. 2, p. 303, doi. 10.1007/s00109-021-02158-z
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- Article
An emerging role for epigenetic factors in relation to executive function.
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- Briefings in Functional Genomics, 2018, v. 17, n. 3, p. 170, doi. 10.1093/bfgp/elx032
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- Article
Identification of Polymorphisms in EAAT1 Glutamate Transporter Gene SLC1A3 Associated with Reduced Migraine Risk.
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- Genes, 2024, v. 15, n. 6, p. 797, doi. 10.3390/genes15060797
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- Article
Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging Approaches.
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- Genes, 2024, v. 15, n. 4, p. 443, doi. 10.3390/genes15040443
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- Article
Association Study of a Comprehensive Panel of Neuropeptide-Related Polymorphisms Suggest Potential Roles in Verbal Learning and Memory.
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- Genes, 2024, v. 15, n. 1, p. 30, doi. 10.3390/genes15010030
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- Article
Single Nucleotide Polymorphisms in MIR143 Contribute to Protection against Non-Hodgkin Lymphoma (NHL) in Caucasian Populations.
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- Genes, 2019, v. 10, n. 3, p. 185, doi. 10.3390/genes10030185
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Dysregulated MicroRNA Expression Profiles and Potential Cellular, Circulating and Polymorphic Biomarkers in Non-Hodgkin Lymphoma.
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- Genes, 2016, v. 7, n. 12, p. 130, doi. 10.3390/genes7120130
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- Article
Genome-wide allele-specific methylation is enriched at gene regulatory regions in a multi-generation pedigree from the Norfolk Island isolate.
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- Epigenetics & Chromatin, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13072-019-0304-7
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- Article
A CREB1 Gene Polymorphism (rs2253206) Is Associated with Prospective Memory in a Healthy Cohort.
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- Frontiers in Behavioral Neuroscience, 2017, p. 1, doi. 10.3389/fnbeh.2017.00086
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- Article
Can Genetic Markers Predict the Sporadic Form of Alzheimer's Disease? An Updated Review on Genetic Peripheral Markers.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 17, p. 13480, doi. 10.3390/ijms241713480
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- Article
Investigating a Genetic Link Between Alzheimer's Disease and CADASIL-Related Cerebral Small Vessel Disease.
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- Molecular Neurobiology, 2022, v. 59, n. 12, p. 7293, doi. 10.1007/s12035-022-03039-3
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- Article
Advances in genetics of migraine.
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- Journal of Headache & Pain, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s10194-019-1017-9
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- Article
Evaluating the suitability of current mitochondrial DNA interpretation guidelines for multigenerational whole mitochondrial genome comparisons.
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- Journal of Forensic Sciences, 2022, v. 67, n. 5, p. 1766, doi. 10.1111/1556-4029.15097
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- Article
Association Study of MTHFD1 Coding Polymorphisms R134 K and R653 Q With Migraine Susceptibility.
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- Headache: The Journal of Head & Face Pain, 2014, v. 54, n. 9, p. 1506, doi. 10.1111/head.12428
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- Article
Investigation of Brain-Derived Neurotrophic Factor ( BDNF) Gene Variants in Migraine.
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- Headache: The Journal of Head & Face Pain, 2014, v. 54, n. 7, p. 1184, doi. 10.1111/head.12351
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- Article
Genetic Analysis of GRIA2 and GRIA4 Genes in Migraine.
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- Headache: The Journal of Head & Face Pain, 2014, v. 54, n. 2, p. 303, doi. 10.1111/head.12234
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- Article