Meijian Guan

发表

Genome‐wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans

Nicholette D. Palmer, Chuan Gao, Adolfo Correa, 2018, Genetic epidemiology.

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

Jacob M. Keaton, Latchezar Dimitrov, D. Bowden, 2016, Human Genetics.

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

Nicholette D. Palmer, Chuan Gao, N. Palmer, 2016, Clinical journal of the American Society of Nephrology : CJASN.

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

Nicholette D. Palmer, Jacob M. Keaton, Latchezar Dimitrov, 2018, Kidney international reports.

Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata

John D. Eicher, M. Obeidat, K. Kristiansson, 2023, Nature Communications.

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

G. Schroth, W. Xiao, J. Zook, 2022, Genome biology.

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

David P. Kreil, Paweł P. Łabaj, Jeff S. Jasper, 2021, Genome biology.

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.

Nicholette D. Palmer, Latchezar Dimitrov, C. Langefeld, 2018, Kidney international.

The TLR 9 Ligand , CpG-ODN , Induces Protection against Cerebral Ischemia / Reperfusion Injury via Activation of PI 3 K / Akt Signaling

T. Ha, Chuanful Li, Chen Lu, 2014 .

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

Paul M. Rindler, David P. Kreil, Paweł P. Łabaj, 2021, Genome biology.

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

J. Kalbfleisch, T. Ha, Chuanful Li, 2014, Journal of the American Heart Association.

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

Nicholette D. Palmer, Jacob M. Keaton, Latchezar Dimitrov, 2021, PloS one.

Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans

Nicholette D. Palmer, Jacob M. Keaton, M. Fornage, 2019, Human Genomics.

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

Nicholette D. Palmer, Jacob M. Keaton, C. Langefeld, 2014, Human molecular genetics.

Deceased donor multidrug resistance protein 1 and caveolin 1 gene variants may influence allograft survival in kidney transplantation

Nicholette D. Palmer, A. Israni, C. Langefeld, 2015, Kidney international.

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing

Thomas M. Blomquist, Daoud M. Meerzaman, S. Sherry, 2021, Nature Biotechnology.

Genomic analysis of early-stage lung cancer reveals a role for TP53 mutations in distant metastasis

Allison P. Heath, Marilyn M. Li, Jena V. Lilly, 2022, Scientific Reports.

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

Christina Y. Yu, S. Sridhar, Kubra Karagoz, 2023, ArXiv.

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

Umit Topaloglu, Wei Zhang, Samuel Cho, 2019, JAMIA open.

A FinnGen pilot clinical recall study for Alzheimer’s disease

Pietro Della Briotta Parolo, John D. Eicher, M. Obeidat, 2023, medRxiv.