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Generation and characterization of Ccdc28b mutant mice links the Bardet-Biedl associated gene with social behavioral phenotypes

Frailty and the risk of dementia: is the association explained by shared environmental and genetic factors?

Life, Vol. 11, Pages 1110: Genetics and Cognitive Vulnerability to Sleep Deprivation in Healthy Subjects: Interaction of ADORA2A, TNF-α and COMT Polymorphisms

Genetic polymorphisms of chemokine (C-X-C motif) ligand 10 gene associated with hepatitis B virus infection in a Chinese Han population

Behavioural and molecular characterisation of the Dlg2 haploinsufficiency rat model of genetic risk for psychiatric disorder

Identifying carrier status for thalassaemia, sickle cell disease, cystic fibrosis, or Tay-Sachs disease in non-pregnant women and their partners

Lifetime risk of rheumatoid arthritis-associated interstitial lung disease in <em>MUC5B</em> mutation carriers

Interactions between dietary patterns and genetic factors in relation to incident dementia among 70-year-olds

Novel Models of Genetic Education and Testing for Pancreatic Cancer Interception: Preliminary Results from the GENERATE Study

Heterozygous Arrhythmogenic Cardiomyopathy-<em>desmoplakin</em> Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion

Do Brain-Derived Neurotrophic Factor Genetic Polymorphisms Modulate the Efficacy of Motor Cortex Plasticity Induced by Non-invasive Brain Stimulation? A Systematic Review

Pathogens, Vol. 10, Pages 1299: Revisiting Persistent Salmonella Infection and the Carrier State: What Do We Know?

Association of Agenesis of the Dorsal Pancreas With HNF1B Heterozygote Mutation: A Case Report

Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease

Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease

Homozygous <em>SHBG</em> Variant (<em>rs6258</em>) Linked to Gonadotropin-Independent Precocious Puberty in a Young Girl

Genes, Vol. 12, Pages 1601: Impact of ABCG2 Gene Polymorphism on the Predisposition to Psoriasis

The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

Effect of carriers' sex on meiotic segregation patterns and chromosome stability of reciprocal translocations

A variation in the infant oxytocin receptor gene modulates infant hippocampal volumes in association with sex and prenatal maternal anxiety

Carrier Frequencies of Mutations/Polymorphisms in the Connexin 26 Gene (GJB2) in the Moroccan Population

A genetic study of Wilson's disease in the United Kingdom.

Genetic Counselors’ Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings

Genetic Susceptibility to Nonsteroidal Anti-Inflammatory Drug-Related Gastroduodenal Bleeding: Role of Cytochrome P450 2C9 Polymorphisms.

Carrier frequency of HLA-DQB1*02 allele in patients affected with celiac disease: A systematic review assessing the potential rationale of a targeted allelic genotyping as a first-line screening.

Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease

Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers.

Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers.

Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in C9orf72 expansion carriers in the GENFI cohort

Genetic variations of leptin and leptin receptor are associated with body composition changes in response to physical training.

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk.

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk.

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk.

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk.

Genetic variation in bone morphogenetic proteins family members (BMPs 2 and 4) and hypertension risk in middle-aged men: The TAMRISK study.

Genetic variation in bone morphogenetic proteins family members (BMPs 2 and 4) and hypertension risk in middle-aged men: The TAMRISK study.

Genetic polymorphism of sterol transporters in children with future gallstones.

Genetic polymorphism of sterol transporters in children with future gallstones.

Genetic polymorphism of sterol transporters in children with future gallstones.

Genetic polymorphism of sterol transporters in children with future gallstones.

Genetic polymorphism of sterol transporters in children with future gallstones.

Genetic polymorphism of sterol transporters in children with future gallstones.

Genetic Modulation of Brugada Syndrome by a Common Polymorphism.

Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.

Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.

Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia.

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk