Probe KK5.33 (D5S85) improves indirect genotype analysis in familial adenomatous polyposis

Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder.

Translational psychiatry·2015

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.

Molecular psychiatry·2011

[Heterozygous alpha-1-antitrypsin deficiency (PiMZ): risk factor in the development of primary liver carcinoma in non-cirrhotic liver?].

Zeitschrift fur Gastroenterologie·2010

Peutz-Jeghers syndrome: a systematic review and recommendations for management.

Gut·2010

Susceptibility for alcoholism: DRD4 exon III polymorphism: a case-control and a family-based association approach.

Addiction biology·2010

Qualitative variation of photolabelled benzodiazepine receptors in different species.

Neurochemistry international·2010

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Human genetics·2026

Integrating genetic, historical, and demographic evidence to reconstruct Argentina's matrilineal ancestry.

Human genetics·2026

Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.

Human genetics·2026

From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

Human genetics·2026

Genomic characterization of historical Jinlingnan individuals: insights into genetic continuity and trans-Eurasian signals in eastern China.

Human genetics·2026

Clinical and zebrafish studies of truncating SF3B2-variants in craniofacial microsomia.

Human genetics·2026

Spatial isoform sequencing at single-cell resolution reveals cell-type-specific spatial isoform variability in multiple brain cell types.

Nature methods·2026

Large-scale single-molecule analysis of tau proteoforms.

Nature methods·2026

Gene-Chronos: parameter-efficient developmental time inference using a pretrained single-cell foundation model.

Briefings in bioinformatics·2026

Improving long-read somatic structural variant calling with pangenome and de novo personal genome assembly.

Cancer research communications·2026

Glycemic and bodyweight effects of GIPR coding variation reflect differences in surface expression and intrinsic functional impairment.

Science advances·2026

Upscaling Genotyping by Amplicon Sequencing With GBAS-GUI.

Molecular ecology resources·2026

Related Experiment Videos

Probe KK5.33 (D5S85) improves indirect genotype analysis in familial adenomatous polyposis

Related Concept Videos

Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder.

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.

[Heterozygous alpha-1-antitrypsin deficiency (PiMZ): risk factor in the development of primary liver carcinoma in non-cirrhotic liver?].

Peutz-Jeghers syndrome: a systematic review and recommendations for management.

Susceptibility for alcoholism: DRD4 exon III polymorphism: a case-control and a family-based association approach.

Qualitative variation of photolabelled benzodiazepine receptors in different species.

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Integrating genetic, historical, and demographic evidence to reconstruct Argentina's matrilineal ancestry.

Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.

From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

Genomic characterization of historical Jinlingnan individuals: insights into genetic continuity and trans-Eurasian signals in eastern China.

Clinical and zebrafish studies of truncating SF3B2-variants in craniofacial microsomia.

Spatial isoform sequencing at single-cell resolution reveals cell-type-specific spatial isoform variability in multiple brain cell types.

Large-scale single-molecule analysis of tau proteoforms.

Gene-Chronos: parameter-efficient developmental time inference using a pretrained single-cell foundation model.

Improving long-read somatic structural variant calling with pangenome and de novo personal genome assembly.

Glycemic and bodyweight effects of GIPR coding variation reflect differences in surface expression and intrinsic functional impairment.

Upscaling Genotyping by Amplicon Sequencing With GBAS-GUI.

Related Experiment Videos

Probe KK5.33 (D5S85) improves indirect genotype analysis in familial adenomatous polyposis

Related Concept Videos

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