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Publications by Erica E. Davis

Identification of Cis-Suppression of Human Disease Mutations by Comparative Genomics

Nature
Multidisciplinary
2015English

Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome

American Journal of Human Genetics
Genetics
2017English

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy With Contractures, Macrocephaly, and Dyskinesias

American Journal of Human Genetics
Genetics
2019English

Germline-Activating RRAS2 Mutations Cause Noonan Syndrome

American Journal of Human Genetics
Genetics
2019English

Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome That Expands the Phenotypic Spectrum of Condensinopathies

American Journal of Human Genetics
Genetics
2019English

Loss of Function Mutations inNNTAre Associated With Left Ventricular NoncompactionCLINICAL PERSPECTIVE

Circulation: Cardiovascular Genetics
2015English

The Vertebrate Primary Cilium in Development, Homeostasis, and Disease

Cell
BiochemistryGeneticsMolecular Biology
2009English

An Essential Role for DYF-11/MIP-T3 in Assembling Functional Intraflagellar Transport Complexes

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2008English

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