Sotabase

Career

· Co-Founder and CEO, Onboarded2022–
· VP of Sales and Partnerships, Check2021–2022
· Director, Strategic Sales and Platform Partnerships, Checkr, Inc.2020–
· Founder, Michael Johnson Performance2007–

Publications (85)

De novo mutations in the classic epileptic encephalopathies
Nature · 2013
1,071
cited
HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans.
New England Journal of Medicine · 2011
817
cited
Improved heritability estimation from genome-wide SNPs.
American Journal of Human Genetics · 2012
750
cited
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
Human Molecular Genetics · 2009
493
cited
Re-evaluation of SNP heritability in complex human traits
Nature Genetics · 2016
438
cited
Faciobrachial dystonic seizures: the influence of immunotherapy on seizure control and prevention of cognitive impairment in a broadening phenotype.
Brain : a journal of neurology · 2013
397
cited
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
American Journal of Human Genetics · 2010
257
cited
De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.
American Journal of Human Genetics · 2016
256
cited
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
bioRxiv · 2019
250
cited
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study
Lancet Neurology · 2017
207
cited
Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus
Nature Communications · 2015
181
cited
p21CIP1 attenuates Ras- and c-Myc-dependent breast tumor epithelial mesenchymal transition and cancer stem cell-like gene expression in vivo
Proceedings of the National Academy of Sciences of the United States of America · 2009
176
cited
Intrinsic Severity as a Determinant of Antiepileptic Drug Refractoriness
Epilepsy Currents · 2008
151
cited
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
Brain : a journal of neurology · 2010
150
cited
Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease
Nature Neuroscience · 2015
136
cited
MicroRNA profiles in hippocampal granule cells and plasma of rats with pilocarpine-induced epilepsy – comparison with human epileptic samples
Scientific Reports · 2015
110
cited
Adjunctive Lanicemine (AZD6765) in Patients with Major Depressive Disorder and History of Inadequate Response to Antidepressants: A Randomized, Placebo-Controlled Study
Neuropsychopharmacology · 2016
102
cited
Focal CA3 hippocampal subfield atrophy following LGI1 VGKC-complex antibody limbic encephalitis
Brain : a journal of neurology · 2017
99
cited
A Genome-Wide Association Study of Neuroticism in a Population-Based Sample
PLoS ONE · 2010
91
cited
Describing the genetic architecture of epilepsy through heritability analysis
Brain : a journal of neurology · 2014
89
cited
Sotabase
Michael Johnson | Researcher Profile | Sotabase | Sotabase