Pages that link to "Q34236650"
The following pages link to Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism (Q34236650):
Displaying 50 items.
- Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing Technology (Q26744368) (← links)
- Moving from capstones toward cornerstones: successes and challenges in applying systems biology to identify mechanisms of autism spectrum disorders (Q26779153) (← links)
- Two-phase and family-based designs for next-generation sequencing studies (Q26828744) (← links)
- Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations (Q27325479) (← links)
- Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms (Q28087577) (← links)
- Human variants in the neuronal basic helix-loop-helix/Per-Arnt-Sim (bHLH/PAS) transcription factor complex NPAS4/ARNT2 disrupt function (Q28115497) (← links)
- Using whole-exome sequencing to identify inherited causes of autism (Q30418126) (← links)
- DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics (Q33592044) (← links)
- Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing. (Q33600262) (← links)
- MiR-2425-5p targets RAD9A and MYOG to regulate the proliferation and differentiation of bovine skeletal muscle-derived satellite cells (Q33671786) (← links)
- Whole genome and exome sequencing of monozygotic twins with trisomy 21, discordant for a congenital heart defect and epilepsy (Q33783876) (← links)
- Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism (Q33790438) (← links)
- Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approach. (Q33840498) (← links)
- A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder (Q33925250) (← links)
- Brain transcriptional and epigenetic associations with autism (Q34416063) (← links)
- Alkylation sensitivity screens reveal a conserved cross-species functionome (Q34434871) (← links)
- Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles (Q34586198) (← links)
- Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay (Q34631519) (← links)
- Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls (Q34672061) (← links)
- Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes (Q34961828) (← links)
- Whole-exome sequencing reveals overlap between macrophage activation syndrome in systemic juvenile idiopathic arthritis and familial hemophagocytic lymphohistiocytosis (Q35064189) (← links)
- Genomics in neurological disorders (Q35543494) (← links)
- No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins (Q35549243) (← links)
- Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders (Q35595321) (← links)
- Sex differences in brain plasticity: a new hypothesis for sex ratio bias in autism (Q35686555) (← links)
- Investigation of sex differences in the expression of RORA and its transcriptional targets in the brain as a potential contributor to the sex bias in autism (Q35694641) (← links)
- A novel disorder reveals clathrin heavy chain-22 is essential for human pain and touch development (Q35880735) (← links)
- The contribution of protein intrinsic disorder to understand the role of genetic variants uncovered by autism spectrum disorders exome studies. (Q35927955) (← links)
- Salivary miRNA profiles identify children with autism spectrum disorder, correlate with adaptive behavior, and implicate ASD candidate genes involved in neurodevelopment (Q35997185) (← links)
- Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes (Q36083196) (← links)
- Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome (Q36451459) (← links)
- Emerging evidence of coding mutations in the ubiquitin-proteasome system associated with cerebellar ataxias (Q36671121) (← links)
- Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders (Q36733238) (← links)
- The expanding genomic landscape of autism: discovering the 'forest' beyond the 'trees' (Q36799924) (← links)
- Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways (Q36915542) (← links)
- Intellectual disability is associated with increased runs of homozygosity in simplex autism (Q37010426) (← links)
- Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing (Q37083418) (← links)
- Genetic influences on alcohol use across stages of development: GABRA2 and longitudinal trajectories of drunkenness from adolescence to young adulthood (Q37198784) (← links)
- Power and Autistic Traits (Q37219831) (← links)
- The role of AUTS2 in neurodevelopment and human evolution (Q37296558) (← links)
- Next-generation sequencing in understanding complex neurological disease (Q37331388) (← links)
- Autism as the Early Closure of a Neuroplastic Critical Period Normally Seen in Adolescence (Q37394661) (← links)
- Current Perspectives in Autism Spectrum Disorder: From Genes to Therapy (Q37444926) (← links)
- Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders (Q37496956) (← links)
- Identifying essential cell types and circuits in autism spectrum disorders. (Q37500060) (← links)
- Impaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models (Q37564195) (← links)
- Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (Q37719319) (← links)
- Autism genetics: searching for specificity and convergence (Q38031004) (← links)
- Activity-dependent neuronal signalling and autism spectrum disorder (Q38074584) (← links)
- Modeling autism by SHANK gene mutations in mice (Q38098737) (← links)