Genetic screening and public health

Contrasting biogeographical patterns in Margarella (Gastropoda: Calliostomatidae: Margarellinae) across the Antarctic Polar Front.

Molecular phylogenetics and evolution·2020

Valve microstructure and phylomineralogy of New Zealand chitons.

Journal of structural biology·2016

Non-conflict theories for the evolution of genomic imprinting.

Heredity·2014

Evolutionary consequences of microhabitat: population-genetic structuring in kelp- vs. rock-associated chitons.

Molecular ecology·2011

Molecular systematics of the marine gastropod families Trochidae and Calliostomatidae (Mollusca: Superfamily Trochoidea).

Molecular phylogenetics and evolution·2009

Phylogeographical disjunction in abundant high-dispersal littoral gastropods.

Molecular ecology·2005

Systematic and proactive evaluation of AIRE missense variant effects.

American journal of human genetics·2026

Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.

American journal of human genetics·2026

Cell villages and Dirichlet modeling map human cell fitness genetics.

American journal of human genetics·2026

Mismapping of sequencing reads from polymorphic duplications generates spurious trans-eQTLs.

American journal of human genetics·2026

Position effect at the SOX3 locus by an interchromosomal insertion causes hereditary spastic paraplegia.

American journal of human genetics·2026

Allele frequency trajectories across age groups reveal ongoing natural selection shaping disease susceptibility.

American journal of human genetics·2026

Multi-omics identification of ZFPM2 and CD44 as key candidates for testicular size in sheep.

Theriogenology·2026

Complex epilepsy phenotype associated with chromosome 2q24.2-q24.3 deletion involving sodium channel gene cluster.

Annals of the Child Neurology Society·2026

Purine Metabolism-Related Pathogenic Genes in Trigeminal Neuralgia: A Multiomics Mendelian Randomization Study.

Pain research & management·2026

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Frontiers in genetics·2026

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

European journal of human genetics : EJHG·2026

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

Nature communications·2026

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Genetic screening and public health

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Contrasting biogeographical patterns in Margarella (Gastropoda: Calliostomatidae: Margarellinae) across the Antarctic Polar Front.

Valve microstructure and phylomineralogy of New Zealand chitons.

Non-conflict theories for the evolution of genomic imprinting.

Evolutionary consequences of microhabitat: population-genetic structuring in kelp- vs. rock-associated chitons.

Molecular systematics of the marine gastropod families Trochidae and Calliostomatidae (Mollusca: Superfamily Trochoidea).

Phylogeographical disjunction in abundant high-dispersal littoral gastropods.

Systematic and proactive evaluation of AIRE missense variant effects.

Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.

Cell villages and Dirichlet modeling map human cell fitness genetics.

Mismapping of sequencing reads from polymorphic duplications generates spurious trans-eQTLs.

Position effect at the SOX3 locus by an interchromosomal insertion causes hereditary spastic paraplegia.

Allele frequency trajectories across age groups reveal ongoing natural selection shaping disease susceptibility.

Multi-omics identification of ZFPM2 and CD44 as key candidates for testicular size in sheep.

Complex epilepsy phenotype associated with chromosome 2q24.2-q24.3 deletion involving sodium channel gene cluster.

Purine Metabolism-Related Pathogenic Genes in Trigeminal Neuralgia: A Multiomics Mendelian Randomization Study.

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

Related Experiment Videos

Genetic screening and public health

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