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Publications by Jonathan Berg

Bi-Allelic Loss-Of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

American Journal of Human Genetics
Genetics
2019English

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

American Journal of Human Genetics
Genetics
2019English

Why Do Women Not Return Family History Forms When Referred to Breast Cancer Genetics Services? A Mixed-Method Study

Health Expectations
EnvironmentalPublic HealthOccupational Health
2014English

GCH1 Heterozygous Mutation Identified by Whole-Exome Sequencing as a Treatable Condition in a Patient Presenting With Progressive Spastic Paraplegia

Journal of Neurology
Neurology
2014English

Refining the Primrose Syndrome Phenotype: A Study of Five Patients With ZBTB20 De Novo Variants and a Review of the Literature

American Journal of Medical Genetics, Part A
Genetics
2019English

Nomenclature for Alleles of the Thiopurine Methyltransferase Gene

Pharmacogenetics and Genomics
Molecular MedicineGeneticsMolecular Biology
2013English

Field Test Results From the Sandia SMART Rotor

2013English

Impact of Higher Fidelity Models on Active Aerodynamic Load Control for Fatigue Damage Reduction

2010English

Model Validation and Simulated Fatigue Load Alleviation of SNL SMART Rotor Experiment

2013English

Interpreting Arguments

Informal Logic
Philosophy
1987English

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