Anuradha Karunanidhi

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 11 papers. Top paper: “ACAD10 protein expression and Neurobehavioral assessment of Acad10-deficient mice”.

ACAD10 protein expression and Neurobehavioral assessment of Acad10-deficient mice

PLoS ONE(2020)10.1371/journal.pone.0242445

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0DataRank · unranked

2 citations

Anuradha Karunanidhi, Kimimasa Tobita, Charles L. Hoppel, Edda Thiels, Eloise Peet +4 more

Development and characterization of a mouse model for Acad9 deficiency

Molecular Genetics and Metabolism(2021)10.1016/j.ymgme.2021.09.002

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0DataRank · unranked

12 citations

Al‐Walid Mohsen, Kailyn Bloom, Anuradha Karunanidhi, Sivakama S. Bharathi, Yijen Wu +6 more

Characterization of variants of uncertain significance in isovaleryl-CoA dehydrogenase identified through newborn screening: An approach for faster analysis

Molecular Genetics and Metabolism(2021)10.1016/j.ymgme.2021.08.012

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0DataRank · unranked

10 citations

Erik Koppes, Ahmad Alodaib, Catherine Kochersperger, Anuradha Karunanidhi, Al‐Walid Mohsen +2 more

Mitochondrial dysfunction associated with TANGO2 deficiency

Scientific Reports(2022)10.1038/s41598-022-07076-9

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0DataRank · unranked

48 citations

Al‐Walid Mohsen, Anuradha Karunanidhi, Claudette M. St. Croix, Simon C. Watkins, Erik Koppes +4 more

Synthetic mRNA rescues very long-chain acyl-CoA dehydrogenase deficiency in patient fibroblasts and a murine model

Molecular Genetics and Metabolism(2022)10.1016/j.ymgme.2022.106982

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0DataRank · unranked

16 citations

Al‐Walid Mohsen, Stephanie J. Mihalik, Keaton J. Solo, Ermal Aliu, Huifang Shi +13 more

ITCH deficiency clinical phenotype expansion and mitochondrial dysfunction

Molecular Genetics and Metabolism Reports(2022)10.1016/j.ymgmr.2022.100932

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0DataRank · unranked

5 citations

Paige Heiman, Olivia D’Annibale, Anuradha Karunanidhi, Alyssa Powers, Marianne McGuire +8 more

Treatment of VLCAD deficient patient fibroblasts with peroxisome-proliferator activated receptor δ agonist improves cellular bioenergetics

Research Square(2022)10.21203/rs.3.rs-1530711/v1

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0DataRank · unranked

2 citations

Yu Leng Phua, Clinton Van’t Land, Anuradha Karunanidhi, Alejandro Dorenbaum, Al‐Walid Mohsen +2 more

Messenger RNA rescues medium-chain acyl-CoA dehydrogenase deficiency in fibroblasts from patients and a murine model

Human Molecular Genetics(2023)10.1093/hmg/ddad076

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0DataRank · unranked

13 citations

Al‐Walid Mohsen, Stephanie J. Mihalik, Keaton J. Solo, Shakuntala Basu, Ermal Aliu +14 more

Heptanoic and medium branched-chain fatty acids as anaplerotic treatment for medium chain acyl-CoA dehydrogenase deficiency

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107689

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0DataRank · unranked

7 citations

Shakuntala Basu, Xuejun Zhao, Olivia D’Annibale, Clinton Van’t Land, Jerry Vockley +2 more

A multiomics approach to understanding pathology of Combined D,L-2- Hydroxyglutaric Aciduria and phenylbutyrate as potential treatment

The Knowledge Bank (The Ohio State University)(2023)10.1101/2023.02.02.526527

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0DataRank · unranked

0 citations

Olivia D’Annibale, Anuradha Karunanidhi, Al‐Walid Mohsen, Brian Kirmse, Steven F. Dobrowolski +2 more

A multiomics approach reveals evidence for phenylbutyrate as a potential treatment for combined D,L-2- hydroxyglutaric aciduria

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108495

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0DataRank · unranked

6 citations

Olivia D’Annibale, Anuradha Karunanidhi, Al‐Walid Mohsen, Brian Kirmse, Steven F. Dobrowolski +2 more