A genetic map of chromosome 19 based on family linkage data

Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.

Human reproduction (Oxford, England)·2015

Association between telomere length and chromosome 21 nondisjunction in the oocyte.

Human genetics·2015

Animal models of cartilage repair.

Bone & joint research·2014

Clinical outcomes of revision biceps tenodesis.

International journal of shoulder surgery·2012

Intra-individual stability over time of standardized anti-Mullerian hormone in FMR1 premutation carriers.

Human reproduction (Oxford, England)·2011

Associations of progesterone receptor polymorphisms with age at menarche and menstrual cycle length.

Hormone research in paediatrics·2010

Decoding the Genetic and Phenotypic Spectrum of MT-TI Mitochondrial Diseases.

Annals of human genetics·2026

Ancestry-Stratified Variant Classification in Monogenic Diabetes Genes: Annotation Coverage and Differential Curation Burden.

Annals of human genetics·2026

Population-Level Nucleotide Diversity and Genetic Differentiation at SOD1 Across Global Human Populations.

Annals of human genetics·2026

Structural Variations of Alu Elements in the Kuwaiti Population: Laying the Foundations for Forensic Medicine.

Annals of human genetics·2026

Trans-Ancestry Psychiatric Genomics in Admixed Populations: Advances, Challenges, and Future Directions.

Annals of human genetics·2026

Evidence of a Protective Effect of Metformin on Abdominal Aortic Aneurysm Risk: Insights From an Observational Study and Mendelian Randomisation Analysis Using Putative Metformin Targets.

Annals of human genetics·2026

Genome-wide candidate signatures of divergent selection between broody Silkie and White Leghorn chickens revealed by high-density SNP genotyping.

British poultry science·2026

Successful radiofrequency catheter ablation of right-sided focal atrial tachycardia in a patient with Holt-Oram syndrome: a case report.

Frontiers in cardiovascular medicine·2026

SNP genotyping in Pseudotsuga menziesii and Pinus radiata using targeted genotyping-by-sequencing (GBS): improved Bayesian SNP calling using a beta-binomial distribution and other optimized input parameters.

BMC genomics·2026

Causal Effects of Lipoproteins and Lipids on Atrial Fibrillation: A Mendelian Randomization Study.

Lipids·2026

Dissecting the shared genetic architecture and biological mechanisms linking sleep traits and suicide attempts: from variants to genes.

Molecular psychiatry·2026

Different properties of loss-of-function between variants in the LIPH gene responsible for autosomal recessive woolly hair and further characterization of C3orf52.

Journal of dermatological science·2026

Related Experiment Videos

A genetic map of chromosome 19 based on family linkage data

Related Concept Videos

Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.

Association between telomere length and chromosome 21 nondisjunction in the oocyte.

Animal models of cartilage repair.

Clinical outcomes of revision biceps tenodesis.

Intra-individual stability over time of standardized anti-Mullerian hormone in FMR1 premutation carriers.

Associations of progesterone receptor polymorphisms with age at menarche and menstrual cycle length.

Decoding the Genetic and Phenotypic Spectrum of MT-TI Mitochondrial Diseases.

Ancestry-Stratified Variant Classification in Monogenic Diabetes Genes: Annotation Coverage and Differential Curation Burden.

Population-Level Nucleotide Diversity and Genetic Differentiation at SOD1 Across Global Human Populations.

Structural Variations of Alu Elements in the Kuwaiti Population: Laying the Foundations for Forensic Medicine.

Trans-Ancestry Psychiatric Genomics in Admixed Populations: Advances, Challenges, and Future Directions.

Evidence of a Protective Effect of Metformin on Abdominal Aortic Aneurysm Risk: Insights From an Observational Study and Mendelian Randomisation Analysis Using Putative Metformin Targets.

Genome-wide candidate signatures of divergent selection between broody Silkie and White Leghorn chickens revealed by high-density SNP genotyping.

Successful radiofrequency catheter ablation of right-sided focal atrial tachycardia in a patient with Holt-Oram syndrome: a case report.

SNP genotyping in Pseudotsuga menziesii and Pinus radiata using targeted genotyping-by-sequencing (GBS): improved Bayesian SNP calling using a beta-binomial distribution and other optimized input parameters.

Causal Effects of Lipoproteins and Lipids on Atrial Fibrillation: A Mendelian Randomization Study.

Dissecting the shared genetic architecture and biological mechanisms linking sleep traits and suicide attempts: from variants to genes.

Different properties of loss-of-function between variants in the LIPH gene responsible for autosomal recessive woolly hair and further characterization of C3orf52.

Related Experiment Videos

A genetic map of chromosome 19 based on family linkage data

Abstract:

Related Concept Videos

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