Pages that link to "Q29417097"
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The following pages link to Genome-wide association study in German patients with attention deficit/hyperactivity disorder (Q29417097):
Displaying 50 items.
- attention deficit hyperactivity disorder (Q181923) (← links)
- GRM5 (Q18026547) (← links)
- BCL11A (Q18040602) (← links)
- Decoding the non-coding genome: elucidating genetic risk outside the coding genome (Q26777924) (← links)
- Advances in molecular genetic studies of attention deficit hyperactivity disorder in China (Q26995422) (← links)
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (Q28296286) (← links)
- Paternal Aging Affects Behavior in Pax6 Mutant Mice: A Gene/Environment Interaction in Understanding Neurodevelopmental Disorders (Q30368285) (← links)
- BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations (Q30657341) (← links)
- DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder (Q31059827) (← links)
- Neuroanatomical abnormalities and cognitive impairments are shared by adults with attention-deficit/hyperactivity disorder and their unaffected first-degree relatives (Q34281470) (← links)
- Results of genome-wide analyses on neurodevelopmental phenotypes at four-year follow-up following cardiac surgery in infancy (Q34438599) (← links)
- Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients (Q34926767) (← links)
- Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder (Q35089391) (← links)
- Genome-wide analysis of attention deficit hyperactivity disorder in Norway (Q35393713) (← links)
- A common genetic network underlies substance use disorders and disruptive or externalizing disorders (Q35957593) (← links)
- Family-based association study of DRD4 gene in methylphenidate-responded Attention Deficit/Hyperactivity Disorder (Q36304489) (← links)
- Gene-set and multivariate genome-wide association analysis of oppositional defiant behavior subtypes in attention-deficit/hyperactivity disorder (Q36470865) (← links)
- ADHD-associated dopamine transporter, latrophilin and neurofibromin share a dopamine-related locomotor signature in Drosophila (Q36719177) (← links)
- Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder (Q37414540) (← links)
- Attention-deficit/hyperactivity disorder genomics: update for clinicians (Q38030489) (← links)
- Genetics of attention-deficit/hyperactivity disorder: current findings and future directions. (Q38094814) (← links)
- Nutrition, immunological mechanisms and dietary immunomodulation in ADHD. (Q38184947) (← links)
- Applying imaging genetics to ADHD: the promises and the challenges (Q38200975) (← links)
- Assessment of potential cardiovascular risks of methylphenidate in comparison with sibutramine: do we need a SCOUT (trial)? (Q38242438) (← links)
- Should we keep on? Looking into pharmacogenomics of ADHD in adulthood from a different perspective. (Q38243174) (← links)
- The molecular genetic architecture of attention deficit hyperactivity disorder. (Q38323555) (← links)
- Long-term prenatal exposure to paracetamol is associated with DNA methylation differences in children diagnosed with ADHD. (Q38430269) (← links)
- Genetics of attention-deficit/hyperactivity disorder: an update (Q38664320) (← links)
- Separating the wheat from the chaff: systematic identification of functionally relevant noncoding variants in ADHD. (Q38809774) (← links)
- A new locus regulating MICALL2 expression was identified for association with executive inhibition in children with attention deficit hyperactivity disorder (Q38833493) (← links)
- Cdh13 and AdipoQ gene knockout alter instrumental and Pavlovian drug conditioning. (Q38848009) (← links)
- A current snapshot of common genomic variants contribution in psychiatric disorders (Q38916885) (← links)
- Common and specific genes and peripheral biomarkers in children and adults with attention-deficit/hyperactivity disorder (Q39093319) (← links)
- Brain imaging genetics in ADHD and beyond - Mapping pathways from gene to disorder at different levels of complexity. (Q39118764) (← links)
- Bipolar disorder risk alleles in children with ADHD. (Q39411928) (← links)
- Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach (Q40838440) (← links)
- Converging evidence does not support GIT1 as an ADHD risk gene (Q40849309) (← links)
- New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder (Q41586761) (← links)
- Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014. (Q45022135) (← links)
- Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. (Q46511619) (← links)
- Dopamine receptor DRD4 gene and stressful life events in persistent attention deficit hyperactivity disorder (Q50440522) (← links)
- Variation in Latent Classes of Adult Attention-Deficit Hyperactivity Disorder by Sex and Environmental Adversity (Q50683828) (← links)
- Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder. (Q54441345) (← links)
- Genetic variant for behavioral regulation factor of executive function and its possible brain mechanism in attention deficit hyperactivity disorder. (Q54967408) (← links)
- Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan (Q57317051) (← links)
- Imaging genetics in neurodevelopmental psychopathology (Q57317054) (← links)
- Genetics of attention deficit hyperactivity disorder (Q57399674) (← links)
- CK1δ over-expressing mice display ADHD-like behaviors, frontostriatal neuronal abnormalities and altered expressions of ADHD-candidate genes (Q58074510) (← links)
- The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta-analysis (Q59543897) (← links)
- A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene (Q60301494) (← links)