Baboons as an animal model for genetic studies of common human disease

Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration.

Scientific reports·2021

Assessing the effects of candidate genes on quantitative traits in primate populations.

American journal of primatology·2020

Common variants in the Na(+)-coupled bicarbonate transporter genes and salt sensitivity of blood pressure: the GenSalt study.

Journal of human hypertension·2015

Associations of epithelial sodium channel genes with blood pressure: the GenSalt study.

Journal of human hypertension·2014

The PPAR alpha gene is associated with triglyceride, low-density cholesterol and inflammation marker response to fenofibrate intervention: the GOLDN study.

The pharmacogenomics journal·2012

Genetic correlation of blood pressure responses to dietary sodium and potassium intervention and cold pressor test in Chinese population.

Journal of human hypertension·2010

A highly prevalent lupus risk haplotype increases IRF7-dependent induction of IFN-α, enhancing antiviral defense and exacerbating autoimmunity.

American journal of human genetics·2026

CanVar-UK: A collaborative platform for germline interpretation in cancer susceptibility genes.

American journal of human genetics·2026

Distinct cochlear cell types associated with genetic susceptibility to sensory and metabolic hearing loss in older adults.

American journal of human genetics·2026

Functional characterization of the 9q34.13 locus identifies RAPGEF1 as a candidate gene modulating risk for melanoma and nevi via RAS activation.

American journal of human genetics·2026

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

American journal of human genetics·2026

Beyond exons: Linking noncoding heritability and polygenicity across complex human traits and disorders.

American journal of human genetics·2026

Molecular detection of Leptospira spp. in urinary and vaginal samples of domestic and free-roaming cats in Tehran, Iran.

Comparative immunology, microbiology and infectious diseases·2026

Molecular investigation of coronavirus and Leptospira spp. in bats (Chiroptera, Mammalia) from Brazil.

Veterinary research communications·2026

Hendra virus: research progress on a bat-borne threat lurking at the human-animal interface.

Frontiers in veterinary science·2026

Cryogenic Preservation of Xenopus Sperm.

Methods in molecular biology (Clifton, N.J.)·2026

Safeguarding biomedical AI: a critical scoping review of privacy-enhancing technologies, hybrid approaches, and deployment models.

Frontiers in digital health·2026

Obesity Induced by High-Fat Diet Affects Epididymal Sperm Motility by Regulating Macrophage Polarization.

Biomedicines·2026

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Baboons as an animal model for genetic studies of common human disease

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Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration.

Assessing the effects of candidate genes on quantitative traits in primate populations.

Common variants in the Na(+)-coupled bicarbonate transporter genes and salt sensitivity of blood pressure: the GenSalt study.

Associations of epithelial sodium channel genes with blood pressure: the GenSalt study.

The PPAR alpha gene is associated with triglyceride, low-density cholesterol and inflammation marker response to fenofibrate intervention: the GOLDN study.

Genetic correlation of blood pressure responses to dietary sodium and potassium intervention and cold pressor test in Chinese population.

A highly prevalent lupus risk haplotype increases IRF7-dependent induction of IFN-α, enhancing antiviral defense and exacerbating autoimmunity.

CanVar-UK: A collaborative platform for germline interpretation in cancer susceptibility genes.

Distinct cochlear cell types associated with genetic susceptibility to sensory and metabolic hearing loss in older adults.

Functional characterization of the 9q34.13 locus identifies RAPGEF1 as a candidate gene modulating risk for melanoma and nevi via RAS activation.

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

Beyond exons: Linking noncoding heritability and polygenicity across complex human traits and disorders.

Molecular detection of Leptospira spp. in urinary and vaginal samples of domestic and free-roaming cats in Tehran, Iran.

Molecular investigation of coronavirus and Leptospira spp. in bats (Chiroptera, Mammalia) from Brazil.

Hendra virus: research progress on a bat-borne threat lurking at the human-animal interface.

Cryogenic Preservation of Xenopus Sperm.

Safeguarding biomedical AI: a critical scoping review of privacy-enhancing technologies, hybrid approaches, and deployment models.

Obesity Induced by High-Fat Diet Affects Epididymal Sperm Motility by Regulating Macrophage Polarization.

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Baboons as an animal model for genetic studies of common human disease

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