Ricardo P. Schnekenberg
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 20 publications
Gene-Pseudogene Inversions as a Hidden Source of Missing Heritability.
Journal: medRxiv : the preprint server for health sciences
Published: November 24, 2025
Regional and national estimates of children affected by all-cause and COVID-19-associated orphanhood and caregiver death in Brazil, by age and family circumstance: a modeling study.
Journal: Lancet regional health. Americas
Published: May 05, 2025
CGG repeat expansions in Charcot-Marie-Tooth disease: insights from the 100 000 Genomes Project.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: April 24, 2025
Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.
Journal: The Journal of clinical investigation
Published: July 08, 2024
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.
Journal: Nature communications
Published: September 29, 2023
Optical Genome Mapping Enables Detection and Accurate Sizing of RFC1 Repeat Expansions.
Journal: Biomolecules
Published: August 14, 2023
Report 46: Factors driving extensive spatial and temporal fluctuations in COVID-19 fatality rates in Brazilian hospitals.
Journal: medRxiv : the preprint server for health sciences
Published: November 09, 2021
Spatial and temporal fluctuations in COVID-19 fatality rates in Brazilian hospitals.
Journal: Nature medicine
Published: November 04, 2021
Autosomal Recessive Cerebellar Atrophy and Spastic Ataxia in Patients With Pathogenic Biallelic Variants in GEMIN5.
Journal: Frontiers in cell and developmental biology
Published: October 20, 2021
Estimating the COVID-19 infection fatality ratio accounting for seroreversion using statistical modelling.
Journal: Communications medicine
Published: August 13, 2021
Last Updated: 09/26/2026