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Serotonergic 5HTTLPR/rs25531 s-allele homozygosity associates with violent suicides in male citalopram users

Recessive MYH3 variants cause "Contractures, pterygia, and variable skeletal fusions syndrome 1B" mimicking Escobar variant multiple pterygium syndrome

Recessive MED With Auricular Swelling Due to Compound Heterozygosity Arg279Tpr/Thr512Lys in the SLC26A2 Gene.

Recessive MED With Auricular Swelling Due to Compound Heterozygosity Arg279Tpr/Thr512Lys in the SLC26A2 Gene.

Recessive MED with auricular swelling due to compound heterozygosity Arg279Tpr/Thr512Lys in the SLC26A2 gene

Genetic linkage findings for DSM-IV nicotine withdrawal in two populations.

Genetic linkage findings for DSM-IV nicotine withdrawal in two populations.

PAK3 related mental disability: Further characterization of the phenotype.

PAK3 related mental disability: Further characterization of the phenotype.

Speech characteristics in neurofibromatosis type 1.

Speech characteristics in neurofibromatosis type 1.

Trilateral retinoblastoma in a patient with Peutz-Jeghers syndrome.

Rare SUZ12 variants commonly cause an overgrowth phenotype.

Linkage analysis of schizophrenia controlling for population substructure.

Linkage analysis of schizophrenia controlling for population substructure.

Linkage analysis of schizophrenia controlling for population substructure.

Linkage analysis of schizophrenia controlling for population substructure.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

The association study between DHCR24 polymorphisms and Alzheimer's disease.

The association study between DHCR24 polymorphisms and Alzheimer's disease.

The influence of urban/rural residency on depressive symptoms is moderated by the serotonin receptor 2A gene.

No association of migraine to the GABA-A receptor complex on chromosome 15.

No association of migraine to the GABA-A receptor complex on chromosome 15.

No association between common variants in glyoxalase 1 and autism spectrum disorders.

No association between common variants in glyoxalase 1 and autism spectrum disorders.

Genetics of tension-type headache: A population based twin study.

Heritability of cognitive functions in families with bipolar disorder.

Heritability of cognitive functions in families with bipolar disorder.

Association of the cannabinoid receptor gene (CNR1) with ADHD and post-traumatic stress disorder.

Association of the cannabinoid receptor gene (CNR1) with ADHD and post-traumatic stress disorder.

Analysis of X chromosome inactivation in autism spectrum disorders.

5-HTTLPR genotype and anxiety-related personality traits: A meta-analysis and new data.

5-HTTLPR genotype and anxiety-related personality traits: A meta-analysis and new data.

DRD2 C32806T modifies the effect of child-rearing environment on adulthood novelty seeking.

DRD2 C32806T modifies the effect of child-rearing environment on adulthood novelty seeking.

DRD2 C32806T modifies the effect of child-rearing environment on adulthood novelty seeking.

No association between common variants in glyoxalase 1 and autism spectrum disorders.

An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population.

An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population.

Allelic variants in HTR3C show association with autism.