Daman Kumari

National Institute of Diabetes and Digestive and Kidney Diseases

Biochemistry, Genetics and Molecular BiologyNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 6 papers. Top paper: “Molecular analysis of FMR1 alleles for fragile X syndrome diagnosis and patient stratification”.

Molecular analysis of FMR1 alleles for fragile X syndrome diagnosis and patient stratification

Expert Review of Molecular Diagnostics(2020)10.1080/14737159.2020.1729744

N/A

0DataRank · unranked

11 citations

Karen Usdin, Daman Kumari

Common Threads: Aphidicolin-Inducible and Folate-Sensitive Fragile Sites in the Human Genome

Frontiers in Genetics(2021)10.3389/fgene.2021.708860

N/A

0DataRank · unranked

13 citations

Daman Kumari, Karen Usdin, Rachel Lokanga

All three MutL complexes are required for repeat expansion in a human stem cell model of CAG-repeat expansion mediated glutaminase deficiency

Scientific Reports(2024)10.1038/s41598-024-64480-z

N/A

0DataRank · unranked

9 citations

Daman Kumari, Saikat Santra, Clara van Karnebeek, André B. P. Kuilenburg, Karen Usdin +1 more

The fragile X locus is prone to spontaneous DNA damage that is preferentially repaired by nonhomologous end-joining to preserve genome integrity

iScience(2024)10.1016/j.isci.2024.108814

N/A

0DataRank · unranked

5 citations

Rachel Lokanga, Cai McCann, Thomas Ried, Karen Usdin, Daman Kumari

Intersection of the fragile X-related disorders and the DNA damage response

DNA repair(2024)10.1016/j.dnarep.2024.103785

N/A

0DataRank · unranked

2 citations

Jessalyn Grant-Bier, Farid A. Kadyrov, Karen Usdin, Daman Kumari

MSH2 is not required for either maintenance of DNA methylation or repeat contraction at the FMR1 locus in fragile X syndrome or the FXN locus in Friedreich’s ataxia

Epigenetics & Chromatin(2025)10.1186/s13072-025-00588-4

N/A

0DataRank · unranked

1 citations

Kathryn Ruppert, Bruce E. Hayward, Karen Usdin, Daman Kumari, Jessalyn Grant-Bier