V Kartik Chundru

12PUBLICATIONS
135CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Gene mappingEpigenetics (incl. genome methylation and epigenomics)Medical molecular engineering of nucleic acids and proteinsNeurogenetics
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Publications (12)

|Sep 24, 2026
AlphaGenome Atlas: in silico mutagenesis of the entire human genome improves prioritization and interpretation of non-coding variants.

|May 25, 2026
A genome-wide deletion map in 125,730 individuals for novel rare disease gene and variant discovery.

|Mar 18, 2026
Polygenic background contributes to GCK-MODY clinical presentation and glycaemic variability.

Jacques Murray Leech, Ankit M Arni, V Kartik Chundru

|Feb 06, 2026
Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations.

Gareth Hawkes, Harrison I W Wright, Robin N Beaumont

|Jan 23, 2026
Modulating splicing in 5' untranslated regions to treat rare haploinsufficient disease.

Eloise S Beer Wells, Laura De Conti, Hyung Chul Kim

|Sep 09, 2025
Common genetic variants modify disease risk and clinical presentation in monogenic diabetes.

Jacques Murray Leech, Robin N Beaumont, Ankit M Arni

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Frequent Collaborators

5 joint publications

Caroline F Wright

5 joint publications

Michael N Weedon

4 joint publications

Kashyap Patel

4 joint publications

Robin N Beaumont