Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Spatial analysis of paraneoplastic cerebellar degeneration in ovarian cancer with anti-Yo syndrome and SCA1.

Journal of neurology·2026

Biallelic ATG9B Variants Define a Novel Autophagy-Related Neurodevelopmental Disorder with Cerebellar Ataxia.

Genes·2026

Transitional Life Events in Friedreich Ataxia: Differential Age at Onset Perspectives.

Cerebellum (London, England)·2026

Cerebellar cognitive-affective syndrome in Friedreich Ataxia.

Journal of neurology·2026

A Patient-Reported Outcome Measure of Communication Difficulties in Friedreich Ataxia: COMATAX.

Cerebellum (London, England)·2026

Short-term outcomes of a randomized, mixed-methods trial to improve hereditary cancer test results disclosure and follow-up communication with family.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Development of a simple clinical score to prioritize detection of severe alpha-1 antitrypsin deficiency with PiZZ genotype.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Genomics-first association of pharmacogenomic risk phenotypes with adverse drug reactions in a healthcare-based population.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Current Status of Genetic Testing and Mosaic Variant Assessment in Somatic Overgrowth and Vascular Anomalies: Insights from the Cancer Genomics Consortium Working Group.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Hospital-wide implementation of inpatient first-tier rapid genome sequencing.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Disease characteristics of SEPSECS deficiency: an international, retrospective, multicenter cohort study.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Using classification and regression trees (CART) to investigate unknown ethnicity records in NHS emergency care data.

BMJ open·2026

Autopsied foreign national deaths in Edirne, Türkiye.

Medicine, science, and the law·2026

Genetic diversity and geographical distribution of Trypanosoma cruzi DTUs in Mexico: A Systematic Review.

Revista da Sociedade Brasileira de Medicina Tropical·2026

[Interculturality, protagonism and diversity: narratives of indigenous mediators of the Introduction to the Indigenous People's Health course].

Ciencia & saude coletiva·2026

International differences in the technical qualities of place of death classifications and data: A survey of researchers' perspectives.

Palliative medicine·2026

18th GCC Closed Forum: Compliance with FDA Biomarkers Guidance, Novel ELN/LIMS Platforms, Sample Reconciliation, Emerging Technologies, Improvements in ELISpot, Post-extraction Sample Stability, LBA Singlicate, Regulatory Inspections, Chicken anti-Human IgG, Cross-validation Harmonization.

Bioanalysis·2026

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Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study

Related Concept Videos

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Spatial analysis of paraneoplastic cerebellar degeneration in ovarian cancer with anti-Yo syndrome and SCA1.

Biallelic ATG9B Variants Define a Novel Autophagy-Related Neurodevelopmental Disorder with Cerebellar Ataxia.

Transitional Life Events in Friedreich Ataxia: Differential Age at Onset Perspectives.

Cerebellar cognitive-affective syndrome in Friedreich Ataxia.

A Patient-Reported Outcome Measure of Communication Difficulties in Friedreich Ataxia: COMATAX.

Short-term outcomes of a randomized, mixed-methods trial to improve hereditary cancer test results disclosure and follow-up communication with family.

Development of a simple clinical score to prioritize detection of severe alpha-1 antitrypsin deficiency with PiZZ genotype.

Genomics-first association of pharmacogenomic risk phenotypes with adverse drug reactions in a healthcare-based population.

Current Status of Genetic Testing and Mosaic Variant Assessment in Somatic Overgrowth and Vascular Anomalies: Insights from the Cancer Genomics Consortium Working Group.

Hospital-wide implementation of inpatient first-tier rapid genome sequencing.

Disease characteristics of SEPSECS deficiency: an international, retrospective, multicenter cohort study.

Using classification and regression trees (CART) to investigate unknown ethnicity records in NHS emergency care data.

Autopsied foreign national deaths in Edirne, Türkiye.

Genetic diversity and geographical distribution of Trypanosoma cruzi DTUs in Mexico: A Systematic Review.

[Interculturality, protagonism and diversity: narratives of indigenous mediators of the Introduction to the Indigenous People's Health course].

International differences in the technical qualities of place of death classifications and data: A survey of researchers' perspectives.

18th GCC Closed Forum: Compliance with FDA Biomarkers Guidance, Novel ELN/LIMS Platforms, Sample Reconciliation, Emerging Technologies, Improvements in ELISpot, Post-extraction Sample Stability, LBA Singlicate, Regulatory Inspections, Chicken anti-Human IgG, Cross-validation Harmonization.

Related Experiment Videos

Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study...

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Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study