Sotabase

Career

· Mechanical Engineer II, Backburner Labs Inc.2026–
· Electrical Mechanical Engineer II, Lema2025–2025
· Manufacturing Engineer, Lema Technology2023–2023
· Mechanical Engineer II, Lema Technology2023–2025
· Contract Manufacturing Engineer, Lema Technology2021–2022
· Contract Manufacturing Engineer, Next Inflexion LLC2021–2022
· Campus Tour Guide, University of St. Thomas2020–2020
· Incoming First Year Student Orientation Leader, University of St. Thomas2020–2020
· Bachelor's of Science, Mechanical Engineering, University of St. Thomas2019–2023
· Sales Associate Service Coordinator, Discount Tire2018–2022
· Kitchen Staff, Luci Ancora2015–2018

Publications (40)

Chronic Ankle Instability Leads to Lower Extremity Kinematic Changes During Landing Tasks: A Systematic Review
International Journal of Exercise Science · 2019
266
cited
Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication
Molecular Cytogenetics · 2008
234
cited
Use of targeted array‐based CGH for the clinical diagnosis of chromosomal imbalance: Is less more?
American Journal of Medical Genetics. Part A · 2005
204
cited
A comprehensive laboratory‐based program for classification of variants of uncertain significance in hereditary cancer genes
Clinical Genetics · 2014
181
cited
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome
Genetics in Medicine · 2007
165
cited
Comparison of microarray‐based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens
Prenatal Diagnosis · 2008
126
cited
High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44
Human Genetics · 2011
121
cited
Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems
Genetics in Medicine · 2011
115
cited
The clinical utility of enhanced subtelomeric coverage in array CGH
American Journal of Medical Genetics. Part A · 2007
103
cited
Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalities.
American Journal of Human Genetics · 2010
98
cited
Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2
Clinical Genetics · 2008
95
cited
Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure
European Journal of Human Genetics · 2005
72
cited
Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.
Human Molecular Genetics · 2009
71
cited
Case series: 2q33.1 microdeletion syndrome—further delineation of the phenotype
Journal of Medical Genetics · 2011
62
cited
Comparison of locus-specific databases for BRCA1 and BRCA2 variants reveals disparity in variant classification within and among databases
Journal of Community Genetics · 2015
56
cited
Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH
Genetics in Medicine · 2007
56
cited
Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate
American Journal of Medical Genetics. Part A · 2011
47
cited
Array-based comparative genomic hybridization in clinical diagnosis
Expert Review of Molecular Diagnostics · 2005
41
cited
The Application of Clinical Genetics Dovepress Disorders Caused by Chromosome Abnormalities
41
cited
aCGH detects partial tetrasomy of 12p in blood from Pallister–Killian syndrome cases without invasive skin biopsy
American Journal of Medical Genetics. Part A · 2009
38
cited
Sotabase
Andrew Theisen | Researcher Profile | Sotabase | Sotabase