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S57 Impact of the HLA-DQA105 Allele on Ustekinumab Loss of Response, Anti-drug Antibodies, and Concentration in Patients With Inflammatory Bowel Disease

The American journal of gastroenterology, 2022-12, Vol.117 (12S), p.S15-S15

2022

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153 High expression of tertiary lymphoid structure gene signatures is associated with improved survival in head and neck squamous cell carcinoma patients treated with immune checkpoint blockade

Journal for immunotherapy of cancer, 2023-11, Vol.11 (Suppl 1), p.A173-A173

2023

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Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study

PloS one, 2021-05, Vol.16 (5), p.e0251423-e0251423

2021

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1288 Characterization of tertiary lymphoid structure in pancreatic ductal adenocarcinoma tumors: insights from gene expression and pathology images, and identification using a deep learning approach

Journal for immunotherapy of cancer, 2023-11, Vol.11 (Suppl 1), p.A1429-A1429

2023

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The TLR9 Ligand, CpG‐ODN, Induces Protection against Cerebral Ischemia/Reperfusion Injury via Activation of PI3K/Akt Signaling

Journal of the American Heart Association, 2014-04, Vol.3 (2), p.e000629-n/a

2014

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Improving accuracy of GPT-3/4 results on biomedical data using a retrieval-augmented language model

PLOS digital health, 2024-08, Vol.3 (8), p.e0000568

2024

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An Exome-wide Association Study for Type 2 Diabetes-Attributed End-Stage Kidney Disease in African Americans

Kidney international reports, 2018-07, Vol.3 (4), p.867-878

2018

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HLA-DQA105 Not Associated With Ustekinumab Loss of Response and Antidrug Antibodies in Ulcerative Colitis and Crohn's Disease Patients

Inflammatory bowel diseases, 2023-11

2023

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Decoding atopic dermatitis: patient heterogeneity and genetic variation contributing to immune-mediated dermatologic disease in the UK Biobank

The Journal of immunology (1950), 2022-05, Vol.208 (1_Supplement), p.60-60.03

2022

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Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1–second gene interactions

Kidney international, 2018-09, Vol.94 (3), p.599-607

2018

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Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing

Nature biotechnology, 2021-09, Vol.39 (9), p.1151-1160

2021

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Abstract A012: Stratifying immune subtypes in real-world HNSCC cohort to identify those with better outcomes to standard treatment regimens

Cancer immunology research, 2024-10, Vol.12 (10_Supplement), p.A012-A012

2024

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Assessing reproducibility of inherited variants detected with short-read whole genome sequencing

Genome Biology, 2022-01, Vol.23 (1), p.2-26, Article 2

2022

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Natural language processing and recurrent network models for identifying genomic mutation-associated cancer treatment change from patient progress notes

JAMIA open, 2019-04, Vol.2 (1), p.139-149

2019

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A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency

Genome Biology, 2021-04, Vol.22 (1), p.111-38, Article 111

2021

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Better together: Extending JMP® with open‐source software

Stat (International Statistical Institute), 2021-12, Vol.10 (1), p.n/a

2021

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Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions

Genome Biology, 2021-04, Vol.22 (1), p.109-23, Article 109

2021

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Incorporating EMR and Genomic Data Using NLP and Machine Learning to Refine Cancer Treatment

Guan, Meijian

2018

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Association of kidney structure-related gene variants with type 2 diabetes-attributed end-stage kidney disease in African Americans

Human genetics, 2016-11, Vol.135 (11), p.1251-1262

2016

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Machine Learning and Deep Learning in Computational Toxicology

Hong, Huixiao

1, 2023

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Implications of Selection Bias Due to Delayed Study Entry in Clinical Genomic Studies

JAMA oncology, 2022-02, Vol.8 (2), p.287

2022

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Evaluation of Genetic Variants for Type 2 Diabetes Associated Kidney Disease in African Americans

Guan, Meijian

2017

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Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans

Clinical journal of the American Society of Nephrology, 2016-06, Vol.11 (6), p.1034-1043

2016

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Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with non-diabetic nephropathy than strong APOL1-second gene interactions

Kidney international, 2018-06, Vol.94 (3), p.599-607

2018

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The ras responsive transcription factor RREB1 is a novel candidate gene for type 2 diabetes associated end-stage kidney disease

Human molecular genetics, 2014-12, Vol.23 (24), p.6441-6447

2014

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S57 Impact of the HLA-DQA105 Allele on Ustekinumab Loss of Response, Anti-drug Antibodies, and Concentration in Patients With Inflammatory Bowel Disease

153 High expression of tertiary lymphoid structure gene signatures is associated with improved survival in head and neck squamous cell carcinoma patients treated with immune checkpoint blockade

Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study

1288 Characterization of tertiary lymphoid structure in pancreatic ductal adenocarcinoma tumors: insights from gene expression and pathology images, and identification using a deep learning approach

The TLR9 Ligand, CpG‐ODN, Induces Protection against Cerebral Ischemia/Reperfusion Injury via Activation of PI3K/Akt Signaling

Improving accuracy of GPT-3/4 results on biomedical data using a retrieval-augmented language model

An Exome-wide Association Study for Type 2 Diabetes-Attributed End-Stage Kidney Disease in African Americans

HLA-DQA105 Not Associated With Ustekinumab Loss of Response and Antidrug Antibodies in Ulcerative Colitis and Crohn's Disease Patients

Decoding atopic dermatitis: patient heterogeneity and genetic variation contributing to immune-mediated dermatologic disease in the UK Biobank

Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1–second gene interactions

Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing

Abstract A012: Stratifying immune subtypes in real-world HNSCC cohort to identify those with better outcomes to standard treatment regimens

Assessing reproducibility of inherited variants detected with short-read whole genome sequencing

Natural language processing and recurrent network models for identifying genomic mutation-associated cancer treatment change from patient progress notes

A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency

Better together: Extending JMP® with open‐source software

Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions

Incorporating EMR and Genomic Data Using NLP and Machine Learning to Refine Cancer Treatment

Association of kidney structure-related gene variants with type 2 diabetes-attributed end-stage kidney disease in African Americans

Machine Learning and Deep Learning in Computational Toxicology

Implications of Selection Bias Due to Delayed Study Entry in Clinical Genomic Studies

Evaluation of Genetic Variants for Type 2 Diabetes Associated Kidney Disease in African Americans

Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans

Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with non-diabetic nephropathy than strong APOL1-second gene interactions

The ras responsive transcription factor RREB1 is a novel candidate gene for type 2 diabetes associated end-stage kidney disease

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