Shridhar Parthasarathy

Also affiliated with University of Pennsylvania

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 2%percentile

4.0Author DataRank

Indexed papers

2in 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 2 indexed papers 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Assessing the landscape of STXBP1-related disorders in 534 individuals

Brain(2021)10.1093/brain/awab327

Top 9%

2.3DataRank

Top 9%125 citations

Shridhar Parthasarathy, Sarah M. Ruggiero, Ganna Balagura, Eryn Fitch, Katherine L. Helbig +48 more

Papers

Driven by 13 papers — median percentile 89. Top paper: “Assessing the landscape of STXBP1-related disorders in 534 individuals”.

Assessing the landscape of STXBP1-related disorders in 534 individuals

Brain(2021)10.1093/brain/awab327

Top 9%

2.3DataRank

Top 9%125 citations

Shridhar Parthasarathy, Sarah M. Ruggiero, Ganna Balagura, Eryn Fitch, Katherine L. Helbig +48 more

Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders

Genetics in Medicine(2021)10.1038/s41436-021-01120-1

Top 12%

1.7DataRank

Top 12%69 citations

Julie Xian, Katherine L. Helbig, Peter D. Galer, Shridhar Parthasarathy, David Lewis‐Smith +11 more

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Nature Communications(2023)10.1038/s41467-023-39539-6

N/A

1.2DataRank · unranked

56 citations

David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj, Shridhar Parthasarathy, Julie Xian +94 more

SCN1A gain‐of‐function mutation causing an early onset epileptic encephalopathy

Epilepsia(2022)10.1111/epi.17444

N/A

0.550DataRank · unranked

38 citations

Shridhar Parthasarathy, Stacey Cohen, Jillian L. McKee, Shavonne L. Massey, Ala Somarowthu +3 more

A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.11.002

N/A

0.529DataRank · unranked

33 citations

Sarah M. Ruggiero, A. Gélot, Fernanda Caroline Soardi, Bethânia FR Ribeiro, Douglas E. V. Pires +21 more

Pathogenic paralogous variants can be used to apply the ACMG PS1 and PM5 variant interpretation criteria

medRxiv(2023)10.1101/2023.08.22.23294353

N/A

0.269DataRank · unranked

5 citations

Alina Ivaniuk, Eduardo Pérez‐Palma, Ludovica Montanucci, Stacey Cohen, Lacey Smith +6 more

Early life seizures and epileptic spasms in STXBP1‐related disorders

Epilepsia(2024)10.1111/epi.17886

N/A

0DataRank · unranked

18 citations

Julie Xian, Danielle de Campo, Shridhar Parthasarathy, Jan Magielski, Katie Rose Sullivan +8 more

Conserved missense variant pathogenicity and correlated phenotypes across paralogous genes

Research Square(2024)10.21203/rs.3.rs-5434140/v1

N/A

0DataRank · unranked

0 citations

Alina Ivanuk, Eduardo Pérez‐Palma, Ludovica Montanucci, Stacey Cohen, Lacey Smith +6 more

Child neurology telemedicine: Analyzing 14 820 patient encounters during the first year of the COVID ‐19 pandemic

Developmental Medicine & Child Neurology(2022)10.1111/dmcn.15406

N/A

0DataRank · unranked

7 citations

Julie Xian, Peter D. Galer, Shridhar Parthasarathy, Alexander K. Gonzalez, Jillian L. McKee +4 more

A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.06.02.492389

N/A

0DataRank · unranked

1 citations

Sarah M. Ruggiero, A. Gélot, Fernanda Caroline Soardi, Bethânia FR Ribeiro, Douglas E. V. Pires +20 more

The SCN1A Philadelphia variant – a gain-of-function mutation causing an early-onset epileptic encephalopathy

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.06.29.498154

N/A

0DataRank · unranked

1 citations

Shridhar Parthasarathy, Stacey Cohen, Jillian L. McKee, Shavonne L. Massey, Ala Somarowthu +3 more

Enriching representation learning using 53 million patient notes through human phenotype ontology embedding

Artificial Intelligence in Medicine(2023)10.1016/j.artmed.2023.102523

N/A

0DataRank · unranked

25 citations

Peter D. Galer, David Lewis‐Smith, Shridhar Parthasarathy, Edward Kim, Dario D. Salvucci +4 more

Early life seizures and epileptic spasms in STXBP1 -related disorders

medRxiv(2023)10.1101/2023.06.26.23291892

N/A

0DataRank · unranked

1 citations

Julie Xian, Danielle deCampo, Shridhar Parthasarathy, Jan Magielski, Katie Rose Sullivan +8 more

Shridhar Parthasarathy

Indexed papers

Top data-sharing exemplar

Papers