Author

Dalin Li

Cedars-Sinai Medical CenterORCID 0000-0003-4738-0074Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biochemistry· 2 Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Research Focus:differential expression· 3 Approach:statistical model· 3 Research Focus:benchmarking· 2 Approach:benchmark study· 1 Approach:deep learning· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Dermot P.B. McGoverniD· 3 shared Christopher I. MurrayiD· 2 shared Emebet MengeshaiD· 2 shared Jennifer E. Van EykiD· 2 shared Manasa Vegesna· 2 shared Philip DebbasiD· 2 shared Sandy Y. JoungiD· 2 shared Susan C. ChengiD· 2 shared

Activity by Year

2016-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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3 shared papersBiochemistry

Dermot P.B. McGovernORCID

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4 papers

Recent·Most cited

BiochemistryAngewandte Chemie International EditionPeer-reviewedSep 22, 2025

Development and Clinical Evaluation of a Multiplexed Health Surveillance Panel Using Ultra High-Throughput PRM-MS in an Inflammatory Bowel Disease Cohort.

Qin Fu, Philip M. Remes, Jihyeon Lee…·Jennifer E. Van Eyk

The paper develops and evaluates a multiplexed PRM-MS assay for quantifying plasma proteins in an IBD cohort, demonstrating high quantifiability and consistent data acquisition.

2 citations

humanproteomics

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BiochemistryAngewandte ChemiePeer-reviewedOct 21, 2024

Paradigm shift in biomarker translation: a pipeline to generate clinical grade biomarker candidates from DIA-MS discovery

Qin Fu, Manasa Vegesna, Niveda Sundararaman…·Jennifer E. Van Eyk

This paper introduces TEAQ, a software tool that selects clinical-grade biomarker candidates from DIA-MS data by evaluating protein quantification metrics in a discovery cohort.

8 citations

humanmetabolomics

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Genetic & Genomic MedicinemedRxivPreprintJul 1, 2020

Identifying novel high-impact rare disease-causing mutations, genes and pathways in exomes of Ashkenazi Jewish inflammatory bowel disease patients

Yiming Wu, Kyle Gettler, Mamta Giri…·Yuval Itan

The paper identifies 7 novel IBD-causing genes in Ashkenazi Jewish IBD patients using exome sequencing and analyzes their overlap with early-onset IBD and other diseases.

DOI 10.1101/2020.07.01.20143750

humanwhole-exome sequencing

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GeneticsNature CommunicationsPeer-reviewedAug 9, 2016

A protein truncating R179X variant in RNF186 confers protection against ulcerative colitis

Manuel A Rivas, Daniel Graham, Patrick Sulem…·Steve

The paper identifies a protein truncating variant in RNF186 that protects against ulcerative colitis by reducing disease risk.

DOI 10.1038/ncomms12342

humanGWAS summary statistics

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