Y family study: heritable variation in the length of the human Y chromosome

Familial dyslexia: genetic and medical findings in eleven three-generation families.

Annals of dyslexia·2013

Renpenning syndrome comes into focus.

American journal of medical genetics. Part A·2005

Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene.

Clinical genetics·2002

A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25.

Journal of medical genetics·2000

A new gene (DYX3) for dyslexia is located on chromosome 2.

Journal of medical genetics·1999

X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.

American journal of medical genetics·1999

Integrating clinical diagnostics with interventional genetics for neurodevelopmental disorders.

American journal of human genetics·2026

Effect heterogeneity reveals complex pleiotropic effects of rare coding variants.

American journal of human genetics·2026

Monoallelic variants in BRSK1 are associated with a neurodevelopmental disorder with or without epilepsy.

American journal of human genetics·2026

Genetic data sharing by clinical laboratories in Canada: A position statement by the Canadian College of Medical Geneticists.

American journal of human genetics·2026

Robust cis-by-trans epistasis in the human plasma proteome highlights an ABO-centered interaction network.

American journal of human genetics·2026

International experiences of genomic newborn screening: Lessons from over 10,800 newborns.

American journal of human genetics·2026

Age-specific genomic and transcriptomic variation reveals limited evidence for cis-regulatory interactions modulating aging in Saccharomyces cerevisiae.

G3 (Bethesda, Md.)·2026

Herd immunity underlies homologous recombination in stationary phase bacteria.

Molecular biology and evolution·2026

Full-length transcriptomics and proteomics reveal how genome minimization reshapes gene expression in synthetic bacteria.

bioRxiv : the preprint server for biology·2026

Inversion characterization in Timema stick insects: from local PCA to pangenome approaches.

bioRxiv : the preprint server for biology·2026

Population genetics of active transposable elements: overdispersion arises naturally from transposition-deletion-selection balance.

Genome biology and evolution·2026

How mutagenic are transposable elements?

Trends in genetics : TIG·2026

Related Experiment Videos

Y family study: heritable variation in the length of the human Y chromosome

Related Concept Videos

Familial dyslexia: genetic and medical findings in eleven three-generation families.

Renpenning syndrome comes into focus.

Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene.

A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25.

A new gene (DYX3) for dyslexia is located on chromosome 2.

X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.

Integrating clinical diagnostics with interventional genetics for neurodevelopmental disorders.

Effect heterogeneity reveals complex pleiotropic effects of rare coding variants.

Monoallelic variants in BRSK1 are associated with a neurodevelopmental disorder with or without epilepsy.

Genetic data sharing by clinical laboratories in Canada: A position statement by the Canadian College of Medical Geneticists.

Robust cis-by-trans epistasis in the human plasma proteome highlights an ABO-centered interaction network.

International experiences of genomic newborn screening: Lessons from over 10,800 newborns.

Age-specific genomic and transcriptomic variation reveals limited evidence for cis-regulatory interactions modulating aging in Saccharomyces cerevisiae.

Herd immunity underlies homologous recombination in stationary phase bacteria.

Full-length transcriptomics and proteomics reveal how genome minimization reshapes gene expression in synthetic bacteria.

Inversion characterization in Timema stick insects: from local PCA to pangenome approaches.

Population genetics of active transposable elements: overdispersion arises naturally from transposition-deletion-selection balance.

How mutagenic are transposable elements?

Related Experiment Videos

Y family study: heritable variation in the length of the human Y chromosome

Related Concept Videos

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