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JPM, Vol. 12, Pages 1111: Modeling a Novel Variant of Glycogenosis IXa Using a Clonal Inducible Reprogramming System to Generate “Diseased” Hepatocytes for Accurate Diagnosis

Preimplantation genetic testing for structural rearrangement based on low-coverage next-generation sequencing accurately discriminates between normal and carrier embryos for patients with translocations

Genetic testing in severe aplastic anemia is required for optimal hematopoietic cell transplant outcomes

Nutrients, Vol. 14, Pages 2702: Genetic Variants in Folate and Cobalamin Metabolism-Related Genes in Pregnant Women of a Homogeneous Spanish Population: The Need for Revisiting the Current Vitamin Supplementation Strategies

Comprehensive epithelial tubo-ovarian cancer risk prediction model incorporating genetic and epidemiological risk factors

Cancers, Vol. 14, Pages 3113: Solute Carrier Nucleoside Transporters in Hematopoiesis and Hematological Drug Toxicities: A Perspective

Genes, Vol. 13, Pages 505: MicroRNA-17-92a-1 Host Gene (MIR17HG) Expression Signature and rs4284505 Variant Association with Alopecia Areata: A Case–Control Study

The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

Differential associations between apolipoprotein E alleles and cerebral myelin content in normative aging

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.

Comparison of clinical rating scales in genetic frontotemporal dementia within the GENFI cohort

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 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 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 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 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

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

Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease Database

Genetic testing in women with early-onset breast cancer: a Traceback pilot study

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

Genetic Variations in the α2A-Adrenoreceptor Are Associated with Blood Pressure Response to the Agonist Dexmedetomidine.

Genetic risk-factors for anxiety in healthy individuals: polymorphisms in genes important for the HPA axis

Carriers of Either of Two Genetic Mutations Causing Alpha-1 Antitrypsin Deficiency at Greater Risk for Illness & Death from COVID-19; Mutations Found Less Frequently in East and Southeast Asia and Sub-Saharan Africa, Which Have Suffered Less from

Genetic factors associated with treatment response to reduced-fluence photodynamic therapy for chronic central serous chorioretinopathy