Related Experiment Videos
Perils of gene mapping with microsatellite markers
American Journal of Human Genetics
|October 1, 1992
Summary
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology·2017
Genetic effects influencing risk for major depressive disorder in China and Europe.
Translational psychiatry·2017
Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder.
Translational psychiatry·2017
Dependent personality, separation anxiety disorder and other anxiety disorders in OCD.
Personality and mental health·2015
Effectiveness of the Kids in Control of Food (KICk-OFF) structured education course for 11-16 year olds with Type 1 diabetes.
Diabetic medicine : a journal of the British Diabetic Association·2015
Systematic and proactive evaluation of AIRE missense variant effects.
American journal of human genetics·2026
Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.
American journal of human genetics·2026
Cell villages and Dirichlet modeling map human cell fitness genetics.
American journal of human genetics·2026
Mismapping of sequencing reads from polymorphic duplications generates spurious trans-eQTLs.
American journal of human genetics·2026
Position effect at the SOX3 locus by an interchromosomal insertion causes hereditary spastic paraplegia.
American journal of human genetics·2026
Allele frequency trajectories across age groups reveal ongoing natural selection shaping disease susceptibility.
American journal of human genetics·2026
Complex epilepsy phenotype associated with chromosome 2q24.2-q24.3 deletion involving sodium channel gene cluster.
Annals of the Child Neurology Society·2026
Purine Metabolism-Related Pathogenic Genes in Trigeminal Neuralgia: A Multiomics Mendelian Randomization Study.
Pain research & management·2026
Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.
Frontiers in genetics·2026
Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.
European journal of human genetics : EJHG·2026
Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.
Nature communications·2026