Max M. He
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Comparison of RNA-seq and microarray-based models for clinical endpoint prediction
W Zhang, Y Yu, F Hertwig, J Thierry-Mieg, W Zhang, D Thierry-Mieg, ...
Genome biology 16 (1), 1-12, 2015
Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants
ML Markert, BH Devlin, MJ Alexieff, J Li, EA McCarthy, SE Gupton, ...
Blood 109 (10), 4539-4547, 2007
Association of arrhythmia-related genetic variants with phenotypes documented in electronic medical records
SL Van Driest, QS Wells, S Stallings, WS Bush, A Gordon, DA Nickerson, ...
Jama 315 (1), 47-57, 2016
Big data analytics for genomic medicine
KY He, D Ge, MM He
International journal of molecular sciences 18 (2), 412, 2017
Exome Sequencing Followed by Large-Scale Genotyping Fails to Identify Single Rare Variants of Large Effect in Idiopathic Generalized Epilepsy
EL Heinzen, C Depondt, GL Cavalleri, EK Ruzzo, NM Walley, AC Need, ...
The American Journal of Human Genetics, 2012
Using ERDS to Infer Copy-Number Variants in High-Coverage Genomes
M Zhu, AC Need, Y Han, D Ge, JM Maia, Q Zhu, EL Heinzen, ET Cirulli, ...
The American Journal of Human Genetics, 2012
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia
The American Journal of Human Genetics 91 (2), 303-312, 2012
Some experiences and opportunities for big data in translational research
CG Chute, M Ullman-Cullere, GM Wood, SM Lin, M He, J Pathak
Genetics in Medicine 15 (10), 802-809, 2013
Traditional Chinese medicine database and application on the Web
M He, X Yan, J Zhou, G Xie
Journal of chemical information and computer sciences 41 (2), 273-277, 2001
Sparktext: Biomedical text mining on big data framework
Z Ye, AP Tafti, KY He, K Wang, MM He
PloS one 11 (9), e0162721, 2016
Tumoral expression of drug and xenobiotic metabolizing enzymes in breast cancer patients of different ethnicities with implications to personalized medicine
Y Li, A Steppi, Y Zhou, F Mao, PC Miller, MM He, T Zhao, Q Sun, J Zhang
Scientific reports 7 (1), 1-11, 2017
Statistical analysis of antigen receptor spectratype data
TB Kepler, M He, JK Tomfohr, BH Devlin, M Sarzotti, ML Markert
Bioinformatics 21 (16), 3394-3400, 2005
3DSEM++: Adaptive and intelligent 3D SEM surface reconstruction
AP Tafti, JD Holz, A Baghaie, HA Owen, MM He, Z Yu
Micron 87, 33-45, 2016
Challenges of identifying clinically actionable genetic variants for precision medicine
TC Carter, MM He
Journal of healthcare engineering 2016, 2016
Longitudinal analysis of T-cell receptor variable β chain repertoire in patients with acute graft-versus-host disease after allogeneic stem cell transplantation
C Liu, M He, B Rooney, TB Kepler, NJ Chao
Biology of blood and marrow transplantation 12 (3), 335-345, 2006
Prevalence estimation for monogenic autosomal recessive diseases using population-based genetic data
SJ Schrodi, A DeBarber, M He, Z Ye, P Peissig, JJ Van Wormer, R Haws, ...
Human genetics 134 (6), 659-669, 2015
Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants
MM He, Q Li, M Yan, H Cao, Y Hu, KY He, K Cao, MM Li, K Wang
Genome Medicine 11 (1), 53, 2019
SeqHBase: a big data toolset for family based sequencing data analysis
M He, TN Person, SJ Hebbring, E Heinzen, Z Ye, SJ Schrodi, ...
Journal of Medical Genetics, doi: 10.1136/jmedgenet-2014-102907, 2015
Prioritizing Genetic Variants for Causality on the Basis of Preferential Linkage Disequilibrium
Q Zhu, D Ge, EL Heinzen, SP Dickson, TJ Urban, M Zhu, JM Maia, M He, ...
The American Journal of Human Genetics, 2012
SpA: web-accessible spectratype analysis: data management, statistical analysis and visualization
M He, JK Tomfohr, BH Devlin, M Sarzotti, ML Markert, TB Kepler
Bioinformatics 21 (18), 3697-3699, 2005
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