Author

Harald H.H. Göring

The University of Texas Rio Grande ValleyORCID 0000-0002-0507-088XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Adithya BalasubramanianiD· 1 shared Adolfo CorreaiD· 1 shared Agustı́n RuiziD· 1 shared Alanna C. MorrisoniD· 1 shared Alex P. ReineriD· 1 shared Alisa Knodle ManningiD· 1 shared Allison E. Ashley‐KochiD· 1 shared Álvaro AlonsoiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

Adithya BalasubramanianORCID

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2 papers

Recent·Most cited

Identification of a specific APOE transcript and functional elements associated with Alzheimer's disease

Qiang Chen, Luis Aguirre, Guoming Liang, Huanhuan Zhao, Tao Dong, Felix Borrego, Itziar de Rojas, Qichan Hu, Christopher Reyes, Ling‐Yan Su, Bao Zhang, James Donald Lechleiter, Harald H.H. Göring, Philip L. De Jager, Joel E. Kleinman, , Liang Ma

The paper identifies a specific APOE transcript and functional SNP associated with Alzheimer's disease using integrated genomic data from human postmortem brains.

Molecular Neurodegeneration · Aug 29, 2024Peer-reviewedGenetic & Genomic Medicine

A framework for detecting noncoding rare variant associations of large-scale whole-genome sequencing studies

Zilin Li, Xihao Li, Hufeng Zhou, Sheila M. Gaynor, Margaret Sunitha Selvaraj, Theodore Arapoglou, Corbin Quick, Yaowu Liu, Han Chen, Ryan Sun, Rounak Dey, Donna K. Arnett, Paul Livermore Auer, Lawrence F. Bielak, Joshua C. Bis, , Deborah Brown

The paper introduces a framework for detecting noncoding rare variant associations using whole-genome sequencing data, applying it to lipid traits in the TOPMed program.

Nature Methods · Oct 27, 2022Peer-reviewedGenetics