Genetic mapping of facioscapulohumeral muscular dystrophy

Synergy between culturomics and metagenomics of health status-associated gut bacteria originating from non-IBD and IBD populations.

Scientific reports·2025

Gut feelings: the relations between depression, anxiety, psychotropic drugs and the gut microbiome.

Gut microbes·2023

Facioscapulohumeral Disease as a myodevelopmental disease: Applying Ockham's razor to its various features.

Journal of neuromuscular diseases·2023

Environmental factors shaping the gut microbiome in a Dutch population.

Nature·2022

A combination of fecal calprotectin and human beta-defensin 2 facilitates diagnosis and monitoring of inflammatory bowel disease.

Gut microbes·2021

Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations.

Journal of neurology·2019

DNA-based immunization.

Molecular and cell biology of human diseases series·1995

Molecular biology of schizophrenia.

Molecular and cell biology of human diseases series·1994

Spatial Genetic Mapping of Normal Human Prostate Tissue Identifies Epithelial Compartments Enriched for Prostate Cancer Association.

Molecular carcinogenesis·2026

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

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Genetic mapping of facioscapulohumeral muscular dystrophy

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Synergy between culturomics and metagenomics of health status-associated gut bacteria originating from non-IBD and IBD populations.

Gut feelings: the relations between depression, anxiety, psychotropic drugs and the gut microbiome.

Facioscapulohumeral Disease as a myodevelopmental disease: Applying Ockham's razor to its various features.

Environmental factors shaping the gut microbiome in a Dutch population.

A combination of fecal calprotectin and human beta-defensin 2 facilitates diagnosis and monitoring of inflammatory bowel disease.

Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations.

DNA-based immunization.

Molecular biology of schizophrenia.

Spatial Genetic Mapping of Normal Human Prostate Tissue Identifies Epithelial Compartments Enriched for Prostate Cancer Association.

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Related Experiment Videos

Genetic mapping of facioscapulohumeral muscular dystrophy

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