| scholarly article | Q13442814 |
| P2093 | author name string | Choong Yi Fong | |
| Zahurin Mohamed | |||
| Batoul Sadat Haerian | |||
| Azman Ali Raymond | |||
| Hui Jan Tan | |||
| Chong Tin Tan | |||
| Sau Wei Wong | |||
| Lai Choo Ong | |||
| Hidayati Mohd Sha'ari | |||
| P2860 | cites work | Overlapping microdeletions involving 15q22.2 narrow the critical region for intellectual disability to NARG2 and RORA | Q59659985 |
| Genetic variation, classification and 'race' | Q22122050 | ||
| Coordination of circadian timing in mammals | Q27860673 | ||
| Epileptic seizures and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE) | Q28243974 | ||
| Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009 | Q28274778 | ||
| Genome-wide association scan of trait depression | Q28943415 | ||
| Positive natural selection in the human lineage | Q29614585 | ||
| A functional genomics strategy reveals Rora as a component of the mammalian circadian clock | Q29616297 | ||
| Linking neural activity and molecular oscillations in the SCN. | Q30416917 | ||
| Circadian pacemaking in cells and circuits of the suprachiasmatic nucleus. | Q30581156 | ||
| Evidence for genetic association of RORB with bipolar disorder | Q30883555 | ||
| High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy | Q34084054 | ||
| A Simple and Computationally Efficient Approach to Multifactor Dimensionality Reduction Analysis of Gene-Gene Interactions for Quantitative Traits | Q34353866 | ||
| Epistasis analysis using multifactor dimensionality reduction | Q34448239 | ||
| Retinoid-related orphan receptors (RORs): critical roles in development, immunity, circadian rhythm, and cellular metabolism | Q34976906 | ||
| Alternative splicing modulates inactivation of type 1 voltage-gated sodium channels by toggling an amino acid in the first S3-S4 linker | Q35378377 | ||
| Na(V)1.1 channels are critical for intercellular communication in the suprachiasmatic nucleus and for normal circadian rhythms | Q35750926 | ||
| Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia | Q36108124 | ||
| Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism. | Q37332233 | ||
| Molecular genetics of Dravet syndrome | Q37866829 | ||
| Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia | Q37956490 | ||
| Circadian profiles of focal epileptic seizures: a need for reappraisal. | Q38005790 | ||
| Clock gene variants in mood and anxiety disorders | Q38005900 | ||
| Evidence for shared susceptibility to epilepsy and psychosis: a population-based family study. | Q42637791 | ||
| Synchronization of cellular clocks in the suprachiasmatic nucleus | Q44664187 | ||
| RORA, a large common fragile site gene, is involved in cellular stress response | Q46931410 | ||
| Power and sample size calculations for studies involving linear regression | Q47273484 | ||
| SCN1A, SCN2A and SCN3A gene polymorphisms and responsiveness to antiepileptic drugs: a multicenter cohort study and meta-analysis. | Q47998164 | ||
| GABA is the principal neurotransmitter of the circadian system | Q48333442 | ||
| PER2 variantion is associated with depression vulnerability | Q48390922 | ||
| Diurnal rhythms in seizures detected by intracranial electrocorticographic monitoring: an observational study | Q48401094 | ||
| The neural circadian system of mammals. | Q48961472 | ||
| Nav1.1 is predominantly expressed in nodes of Ranvier and axon initial segments. | Q49092166 | ||
| Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy. | Q54441071 | ||
| Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese | Q57233954 | ||
| P433 | issue | 4 | |
| P921 | main subject | Malaysia | Q833 |
| P304 | page(s) | 229-236 | |
| P577 | publication date | 2015-02-07 | |
| P1433 | published in | Genomics | Q5533503 |
| P1476 | title | RORA gene rs12912233 and rs880626 polymorphisms and their interaction with SCN1A rs3812718 in the risk of epilepsy: a case-control study in Malaysia | |
| P478 | volume | 105 |
| Q50124176 | DNA methylation alterations induced by transient exposure of MCF-7 cells to maghemite nanoparticles. |
| Q35814413 | Determination of the Optimal Concentration of Valproic Acid in Patients with Epilepsy: A Population Pharmacokinetic-Pharmacodynamic Analysis |
| Q36571294 | Retinoic Acid-Related Orphan Receptors (RORs): Regulatory Functions in Immunity, Development, Circadian Rhythm, and Metabolism |
| Q47668992 | The association of RAR-related orphan receptor A (RORA) gene polymorphisms with the risk of asthma |
Search more.