Swetha Ramadesikan

Biochemistry, Genetics and Molecular BiologyMedicine

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: “Lowe syndrome patient cells display mTOR- and RhoGTPase-dependent phenotypes alleviated by rapamycin and statins”.

Lowe syndrome patient cells display mTOR- and RhoGTPase-dependent phenotypes alleviated by rapamycin and statins

Human Molecular Genetics(2020)10.1093/hmg/ddaa086

N/A

0DataRank · unranked

13 citations

Swetha Ramadesikan, W.‐C. Hsieh, Mariana C Aguilar, Claudia B. Hanna, Robert L. Bacallao +2 more

Genotype & Phenotype in Lowe Syndrome: Specific OCRL1 patient mutations differentially impact cellular phenotypes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.04.236612

N/A

0DataRank · unranked

0 citations

Lisette Skiba, Jennifer Lee, Kayalvizhi Madhivanan, Daipayan Sarkar, Agustina De La Fuente +6 more

Genotype & phenotype in Lowe Syndrome: specific OCRL1 patient mutations differentially impact cellular phenotypes

Human Molecular Genetics(2021)10.1093/hmg/ddab025

N/A

0DataRank · unranked

18 citations

Lisette Skiba, Jennifer Lee, Kayalvizhi Madhivanan, Daipayan Sarkar, Agustina De La Fuente +6 more

Heterogeneity in Lowe Syndrome: Mutations Affecting the Phosphatase Domain of OCRL1 Differ in Impact on Enzymatic Activity and Severity of Cellular Phenotypes

Biomolecules(2023)10.3390/biom13040615

N/A

0DataRank · unranked

8 citations

Swetha Ramadesikan, Adrianna F. Black, Charles Christoffer, Andrés Felipe Pacheco Pacheco, Sneha Subramanian +6 more

Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromes

npj Genomic Medicine(2024)10.1038/s41525-024-00454-4

N/A

0DataRank · unranked

12 citations

Maria Elena Hernandez‐Gonzalez, Swetha Ramadesikan, Mohammad Marhabaie, Allison C. Daley, Leeran Dublin-Ryan +11 more

Like father, like son: RNA-sequencing from a 30-year-old muscle biopsy identifies a novel splice variant in ACTA1 as the cause of an attenuated nemaline myopathy phenotype

Neuromuscular Disorders(2025)10.1016/j.nmd.2025.105416

N/A

0DataRank · unranked

0 citations

Sana Yousfi, Stefan Nicolau, Afrooz Rashnonejad, Jingting Zhu, Zarife Sahenk +6 more