Karen Usdin

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 24 papers. Top paper: “High-Throughput Screening to Identify Compounds That Increase Fragile X Mental Retardation Protein Expression in Neural Stem Cells Differentiated From Fragile X Syndrome Patient-Derived Induced Pluripotent Stem Cells”.

High-Throughput Screening to Identify Compounds That Increase Fragile X Mental Retardation Protein Expression in Neural Stem Cells Differentiated From Fragile X Syndrome Patient-Derived Induced Pluripotent Stem Cells

Stem Cells Translational Medicine(2015)10.5966/sctm.2014-0278

N/A

0.659DataRank · unranked

80 citations

Manju Swaroop, Noel Southall, Wenwei Huang, Wei Zheng, Karen Usdin +1 more

S1-END-seq reveals DNA secondary structures in human cells

Molecular Cell(2022)10.1016/j.molcel.2022.08.007

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0.628DataRank · unranked

65 citations

Niek van Wietmarschen, Wei Wu, Veenu Tripathi, Natasha C. Koussa, Raphael Pavani +10 more

A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus

Nature Genetics(2024)10.1038/s41588-024-01808-5

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0.533DataRank · unranked

34 citations

Giulia Gobbo, Madeline Couse, Egor Dolzhenko, Sathiji Nageshwaran, Warren Cheung +95 more

FAN1’s protection against CGG repeat expansion requires its nuclease activity and is FANCD2-independent

Nucleic Acids Research(2021)10.1093/nar/gkab899

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0.494DataRank · unranked

26 citations

Huiyan Lü, Karen Usdin, Xiao-Nan Zhao

Clinical implications of somatic allele expansion in female FMR1 premutation carriers

Scientific Reports(2023)10.1038/s41598-023-33528-x

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0.425DataRank · unranked

16 citations

Ye Hyun Hwang, Ellery Santos, Bruce E. Hayward, Karen Usdin, Blythe Durbin‐Johnson +3 more

Somatic instability of the FGF14 -SCA27B GAA•TTC repeat reveals a marked expansion bias in the cerebellum

Brain(2024)10.1093/brain/awae312

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0.425DataRank · unranked

16 citations

Jean‐Loup Méreaux, Susana Boluda, Matt C. Danzi, Marie-Josée Dicaire, Claire-Sophie Davoine +32 more

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

Expert Review of Molecular Diagnostics(2020)10.1080/14737159.2020.1729744

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0.373DataRank · unranked

11 citations

Karen Usdin, Daman Kumari

CGG Repeat Expansion, and Elevated Fmr1 Transcription and Mitochondrial Copy Number in a New Fragile X PM Mouse Embryonic Stem Cell Model

Frontiers in Cell and Developmental Biology(2020)10.3389/fcell.2020.00482

N/A

0.345DataRank · unranked

9 citations

Carson J. Miller, Geum-Yi Kim, Karen Usdin, Inbal Gazy

Linking Dynamic DNA Secondary Structures to Genome Instability

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.01.19.476973

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0.229DataRank · unranked

3 citations

Niek van Wietmarschen, Wei Wu, Veenu Tripathi, Natasha C. Koussa, Raphael Pavani +9 more

Stool is a sensitive and noninvasive source of DNA for monitoring expansion in repeat expansion disease mouse models

Disease Models & Mechanisms(2022)10.1242/dmm.049453

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0DataRank · unranked

6 citations

Cassandra McHugh, Sydney R. Coffey, Diego Antonio Jimenez, Elizabeth Adams, Jeffrey B. Carroll +2 more

A point mutation in the nuclease domain of MLH3 eliminates repeat expansions in a mouse stem cell model of the Fragile X-related disorders

Nucleic Acids Research(2020)10.1093/nar/gkaa573

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0DataRank · unranked

34 citations

Peter Steinbach, Karen Usdin, Bruce E. Hayward

Repeat expansions confer WRN dependence in microsatellite-unstable cancers

Nature(2020)10.1038/s41586-020-2769-8

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0DataRank · unranked

200 citations

Sriram Sridharan, William J. Nathan, Anthony Tubbs, Edmond M. Chan, Elsa Callén +28 more

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

Frontiers in Genetics(2021)10.3389/fgene.2021.708860

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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

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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

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0DataRank · unranked

5 citations

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

Assessment of the Clinical Interactions of GAA Repeat Expansions in FGF14 and FXN

Neurology Genetics(2024)10.1212/nxg.0000000000200210

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0DataRank · unranked

4 citations

David Pellerin, Matt C. Danzi, Stephan Züchner, Bernard Brais, Gabriel Matos‐Rodrigues +7 more

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

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

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0DataRank · unranked

2 citations

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

Reconciling the effects of PMS2 in different repeat expansion disease models supports a common expansion mechanism

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.08.13.607839

N/A

0DataRank · unranked

5 citations

Carson J. Miller, Alexandra K. Walker, Kusala Anupindi, Bruce E. Hayward, Hernán Lorenzi +3 more

Somatic instability of the FGF14 -SCA27B GAA•TTC repeat reveals a marked expansion bias in the cerebellum

medRxiv(2024)10.1101/2024.07.01.24309777

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0DataRank · unranked

3 citations

Jean‐Loup Méreaux, Susana Boluda, Matt C. Danzi, Marie-Josée Dicaire, Claire-Sophie Davoine +32 more

Repeat expansion in a Fragile X model is independent of double strand break repair mediated by Pol θ, Rad52, Rad54l or Rad54b

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.11.05.621911

N/A

0DataRank · unranked

1 citations

Geum-Yi Kim, Carson J. Miller, Cai McCann, Megan G. Lowery, Richard D. Wood +2 more

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

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0DataRank · unranked

1 citations

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

3A or not 3A: Cytidine deaminases in the etiology of the CAG-repeat expansion diseases

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2426776122

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0DataRank · unranked

0 citations

Karen Usdin

Repeat expansions nested within tandem CNVs: a unique structural change in GLS exemplifies the diagnostic challenges of non-coding pathogenic variation

Human Molecular Genetics(2022)10.1093/hmg/ddac173

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0DataRank · unranked

13 citations

Matt C. Danzi, André B. P. Kuilenburg, Selina Reich, Andreas Traschütz, Benjamin Bender +13 more

All three mammalian MutL complexes are required for repeat expansion in a mouse cell model of the Fragile X-related disorders

PLoS Genetics(2020)10.1371/journal.pgen.1008902

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0DataRank · unranked

59 citations

Geum-Yi Kim, Xiao-Nan Zhao, Karen Usdin, Carson J. Miller