Search for a schizophrenia susceptibility gene on chromosome 13

Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families.

Journal of neurodevelopmental disorders·2017

Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma.

Translational psychiatry·2014

SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking.

Translational psychiatry·2014

Genetic risk factors in two Utah pedigrees at high risk for suicide.

Translational psychiatry·2013

Differential expression of the rat homeobox genes in neural cell lines.

Molecular and cellular neurosciences·2009

Genome-wide linkage in Utah autism pedigrees.

Molecular psychiatry·2009

Contrasting outcomes of 16p11.2 microdeletion and microduplication in prenatal diagnosis: phenotypic variability and genetic counseling strategies.

Psychiatric genetics·2026

Dissecting causal and putative mechanistic pathways from lifestyle factors to neurological diseases via the glymphatic system: a Mendelian randomization study.

Psychiatric genetics·2026

A rare missense variant in Bruton's tyrosine kinase is associated with bipolar disorder accompanied by psychosis.

Psychiatric genetics·2026

Identification of rare missense variants of ionotropic glutamate receptor N-methyl- D -aspartate 2 genes in patients with schizophrenia.

Psychiatric genetics·2026

Expression and function of miR-218-5p in the pathogenesis of postpartum depression.

Psychiatric genetics·2026

Case report of a boy with autism spectrum disorder and lysinuric protein intolerance.

Psychiatric genetics·2026

Successful radiofrequency catheter ablation of right-sided focal atrial tachycardia in a patient with Holt-Oram syndrome: a case report.

Frontiers in cardiovascular medicine·2026

SNP genotyping in Pseudotsuga menziesii and Pinus radiata using targeted genotyping-by-sequencing (GBS): improved Bayesian SNP calling using a beta-binomial distribution and other optimized input parameters.

BMC genomics·2026

Causal Effects of Lipoproteins and Lipids on Atrial Fibrillation: A Mendelian Randomization Study.

Lipids·2026

Dissecting the shared genetic architecture and biological mechanisms linking sleep traits and suicide attempts: from variants to genes.

Molecular psychiatry·2026

Different properties of loss-of-function between variants in the LIPH gene responsible for autosomal recessive woolly hair and further characterization of C3orf52.

Journal of dermatological science·2026

Genetic Dissection of Wheat Heterosis Identifies Candidate Genes in Biparental and Diverse Hybrid Populations.

Plant biotechnology journal·2026

Related Experiment Videos

Search for a schizophrenia susceptibility gene on chromosome 13

Related Concept Videos

Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families.

Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma.

SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking.

Genetic risk factors in two Utah pedigrees at high risk for suicide.

Differential expression of the rat homeobox genes in neural cell lines.

Genome-wide linkage in Utah autism pedigrees.

Contrasting outcomes of 16p11.2 microdeletion and microduplication in prenatal diagnosis: phenotypic variability and genetic counseling strategies.

Dissecting causal and putative mechanistic pathways from lifestyle factors to neurological diseases via the glymphatic system: a Mendelian randomization study.

A rare missense variant in Bruton's tyrosine kinase is associated with bipolar disorder accompanied by psychosis.

Identification of rare missense variants of ionotropic glutamate receptor N-methyl- D -aspartate 2 genes in patients with schizophrenia.

Expression and function of miR-218-5p in the pathogenesis of postpartum depression.

Case report of a boy with autism spectrum disorder and lysinuric protein intolerance.

Successful radiofrequency catheter ablation of right-sided focal atrial tachycardia in a patient with Holt-Oram syndrome: a case report.

SNP genotyping in Pseudotsuga menziesii and Pinus radiata using targeted genotyping-by-sequencing (GBS): improved Bayesian SNP calling using a beta-binomial distribution and other optimized input parameters.

Causal Effects of Lipoproteins and Lipids on Atrial Fibrillation: A Mendelian Randomization Study.

Dissecting the shared genetic architecture and biological mechanisms linking sleep traits and suicide attempts: from variants to genes.

Different properties of loss-of-function between variants in the LIPH gene responsible for autosomal recessive woolly hair and further characterization of C3orf52.

Genetic Dissection of Wheat Heterosis Identifies Candidate Genes in Biparental and Diverse Hybrid Populations.

Related Experiment Videos

Search for a schizophrenia susceptibility gene on chromosome 13

Related Concept Videos

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