Author

Madhur Singh

King's College London

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Amanda Elswick GentryiD· 1 shared Ananda B. AmstadteriD· 1 shared Bradley Todd WebbiD· 1 shared Brien Riley· 1 shared Chris ChatzinakosiD· 1 shared Christina M. SheeriniD· 1 shared Hermine H. Maes· 1 shared Jonathan R. I. ColemaniD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Amanda Elswick GentryORCID

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1 paper

Recent·Most cited

Rare copy number variation in Post-traumatic stress disorder using whole genome sequencing and biobank data

Sydney Kramer, Saeed Farajzadeh Valilou, Madhur Singh, Stephen Vieno, Roseann E. Peterson, Chris Chatzinakos, Bradley Todd Webb, Jonathan R. I. Coleman, Ananda B. Amstadter, Amanda Elswick Gentry, Hermine H. Maes, Brien Riley, Kenneth S. Kendler, Christina M. Sheerin, Tan-Hoang Nguygen

This study investigates rare copy number variants in PTSD using whole-genome sequencing and biobank data, finding significant associations in specific ancestry groups and gene-sets.

medRxiv · Sep 17, 2026 · PreprintGenetic & Genomic Medicine