Author

Kathryn A Lawrence

Stanford MedicineORCID 0000-0002-7304-8318Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:benchmarking· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:CRISPR screen· 1 Research Focus:database / resource· 1 Research Focus:eQTL / molecular QTL mapping· 1 Approach:experimental assay· 1

Frequent Co-Authors

Anshul Bharat KundajeiD· 2 shared Daniel C. NachuniD· 2 shared Kelly CochraniD· 2 shared Stephen B. MontgomeryiD· 2 shared Adam FrankishiD· 1 shared Andrea Tanzer AiD· 1 shared Andrew E. BerryiD· 1 shared Anusri PampariiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenetics

Anshul Bharat KundajeORCID

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3 papers

Recent·Most cited

GeneticsThe American Journal of Human GeneticsPeer-reviewedMar 23, 2026

Focus on single gene effects limits discovery and interpretation of complex trait-associated variants

Kathryn A Lawrence, Tamara Gjorgjieva, Daniel C. Nachun, Stephen B. Montgomery

The paper introduces a multi-gene eQTL mapping framework to detect variants influencing multiple neighboring genes, finding novel loci and improving colocalization with GWAS variants.

3 citationstop 3%

humanbulk RNA-seq

GeneticsCellPeer-reviewedJun 1, 2025

Rewriting regulatory DNA to dissect and reprogram gene expression

Gabriella E. Martyn, Michael T. Montgomery, Hank Jones…·J Engreitz

The paper introduces Variant-FlowFISH to measure the effects of DNA sequence variants on gene expression, identifies regulatory mechanisms, and benchmarks predictive models.

49 citationstop 3%

humanCRISPR screen

GenomicsbioRxivPreprintOct 29, 2024

The GENCODE CLS project: massively expanding the lncRNA catalog through capture long-read RNA sequencing

Tamara Perteghella, Gazaldeep Kaur, Sílvia Carbonell Sala…·Roderic Guigó

The paper expands the lncRNA catalog using capture long-read RNA sequencing, significantly increasing the number of annotated transcripts in human and mouse genomes.

26 citations

humanmouse