Man to mouse--lessons learned from the distal end of the human X chromosome

Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm control.

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Identification and functional characterization of rare SHANK2 variants in schizophrenia.

Molecular psychiatry·2015

Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour.

Molecular psychiatry·2014

5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual Disability.

Molecular syndromology·2013

New roles of SHOX as regulator of target genes.

Pediatric endocrinology reviews : PER·2012

Human mesenchymal stem cells derived from bone marrow display a better chondrogenic differentiation compared with other sources.

Connective tissue research·2007

CircExor enables interpretable prediction of circRNA localization into extracellular vesicles.

Genome research·2026

Unifying multimodal single-cell data with a mixture-of-experts β-variational autoencoder framework.

Genome research·2026

SwinePan for pig graph-based pangenome and multiomics data mining.

Genome research·2026

Combined effects of Ret coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous system.

Genome research·2026

Dual-contrastive learning for spatial domain identification in spatial transcriptomics with STAMGC.

Genome research·2026

k-mer-based Upstream Preprocessing of long reads for Isoform Discovery.

Genome research·2026

Delving into the clinical and genetic spectrum of NLSDM: A case study.

Journal of neuromuscular diseases·2026

Mutation Spectrum and Novel Rare Variants in a Han Chinese Hearing Loss Cohort Using a Tiered Sequencing Strategy.

Molecular genetics & genomic medicine·2026

Further delineation of 2p13.2-p11.2 deletion syndrome by optical genome mapping.

Neurogenetics·2026

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Medicine·2026

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Medicine·2026

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Medicine·2026

Related Experiment Videos

Man to mouse--lessons learned from the distal end of the human X chromosome

Related Concept Videos

Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm control.

Identification and functional characterization of rare SHANK2 variants in schizophrenia.

Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour.

5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual Disability.

New roles of SHOX as regulator of target genes.

Human mesenchymal stem cells derived from bone marrow display a better chondrogenic differentiation compared with other sources.

CircExor enables interpretable prediction of circRNA localization into extracellular vesicles.

Unifying multimodal single-cell data with a mixture-of-experts β-variational autoencoder framework.

SwinePan for pig graph-based pangenome and multiomics data mining.

Combined effects of Ret coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous system.

Dual-contrastive learning for spatial domain identification in spatial transcriptomics with STAMGC.

k-mer-based Upstream Preprocessing of long reads for Isoform Discovery.

Delving into the clinical and genetic spectrum of NLSDM: A case study.

Mutation Spectrum and Novel Rare Variants in a Han Chinese Hearing Loss Cohort Using a Tiered Sequencing Strategy.

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Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

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Man to mouse--lessons learned from the distal end of the human X chromosome

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