Jonathan Badger
Jonathan Badger
Research Project Pharmacist, Marshfield Clinic
Verified email at mcrf.mfldclin.edu
Title
Cited by
Cited by
Year
Candidate gene analysis of 21q22: support for S100B as a susceptibility gene for bipolar affective disorder with psychosis
S Roche, F Cassidy, C Zhao, J Badger, E Claffey, L Mooney, C Delaney, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007
652007
Antibacterial fluoromicas: a novel delivery medium
B Dizman, JC Badger, MO Elasri, LJ Mathias
Applied Clay Science 38 (1-2), 57-63, 2007
472007
Genome‐wide scan of bipolar disorder and investigation of population stratification effects on linkage: Support for susceptibility loci at 4q21, 7q36, 9p21, 12q24, 14q24, and 16p13
F Cassidy, C Zhao, J Badger, E Claffey, S Dobrin, S Roche, P McKeon
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007
462007
Adverse drug event discovery using biomedical literature: a big data neural network adventure
AP Tafti, J Badger, E LaRose, E Shirzadi, A Mahnke, J Mayer, Z Ye, ...
JMIR medical informatics 5 (4), e51, 2017
252017
A new mutation in the Chr19p calcium channel gene CACNL1A4 causing hemiplegic migraine with ataxia
K Gardner, O Bernal, M Keegan, J Badger, O Gerber, N Lowry, E Hoffman
Neurology 52 (6), 1999
181999
Object detection to assist visually impaired people: A deep neural network adventure
FS Bashiri, E LaRose, JC Badger, RM D’Souza, Z Yu, P Peissig
International Symposium on Visual Computing, 500-510, 2018
152018
Cloudmatcher: A cloud/crowd service for entity matching
Y Govind, E Paulson, M Ashok, SGC Paul, A Hitawala, AH Doan, Y Park, ...
KDD Workshop on Big Data as a Service (BIGDAS-17), 2017
122017
bigNN: An open-source big data toolkit focused on biomedical sentence classification
AP Tafti, E Behravesh, M Assefi, E LaRose, J Badger, J Mayer, AH Doan, ...
2017 IEEE International Conference on Big Data (Big Data), 3888-3896, 2017
112017
Using machine learning algorithms to predict risk for development of calciphylaxis in patients with chronic kidney disease
RS Kleiman, ER LaRose, JC Badger, D Page, MD Caldwell, JA Clay, ...
AMIA Summits on Translational Science Proceedings 2018, 139, 2018
102018
Machine learning-as-a-service and its application to medical informatics
AP Tafti, E LaRose, JC Badger, R Kleiman, P Peissig
International Conference on Machine Learning and Data Mining in Pattern …, 2017
92017
Entity Matching Using Magellan: Matching Drug Reference Tables.
ER LaRose, JC Badger, P Konda, AH Doan, PL Peissig
CRI, 2017
62017
A two-locus FHM2 family with unique ATP1A2 mutation and comparative study in C. elegans showing regulation of tryptophan hydroxylase by EAT-6 and UNC-2, the orthologous FHM2 …
K Gardner, M Estevez, S Keryanov, A Estevez, M Barmada, J Badger, ...
Cephalalgia 24 (2), 149-150, 2004
62004
Expansion of the chromosome 1q31 locus for hemiplegic migraine
K Gardner, J Badger, MM Barmada, E Hoffman
Genetics of headache disorders. Lippincott Williams and Wilkins …, 2000
52000
A two locus model for hemiplegic migraine on Chr1q and candidate gene screening
K Gardner, J Badger, MM Barmada, J O'Connell, EP Hoffman
Neurology 51 (1), 311-311-a, 1998
31998
Machine learning for phenotyping opioid overdose events
J Badger, E LaRose, J Mayer, F Bashiri, D Page, P Peissig
Journal of biomedical informatics 94, 103185, 2019
22019
Big data deep neural network to analyze adverse vaccine reactions
AP Tafti, E LaRose, J Badger, Z Ye, N Shimpi, FS Bashiri, E Sagheb, ...
AMIA, 2018
12018
Lung Nodule Classification Using Combined Deep and Spectral 3D Shape Features
FS Bashiri, JC Badger, RM D'Souza, Z Yu, P Peissig
2019 IEEE EMBS International Conference on Biomedical & Health Informatics …, 2019
2019
SCCS for Detection of Differences in Brand and Generic Adverse Drug Events.
JC Badger, ER LaRose, R Kleiman, RL Berg, JG Linneman, R Hansen, ...
CRI, 2017
2017
A whole genome scan for linkage in 62 Irish pedigrees with bipolar disorder
F Cassidy, J Badger, C Zhao, S Dobrin, S Roche, P McKeon
American Journal Of Medical Genetics-A 138 (1), 74-75, 2009
2009
P12. Northern Irish pedigrees with familial phaechromocytoma/paraganglioma syndrome, demonstrate clinical heterogeneity and variable penetrance in addition to a founder mutation
L Tam, AS Kiang, A Kennan, P Humphries, A Reynolds, PF Kenna, ...
The Ulster Medical Society, 2007
2007
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