Vijay Ganesh

ORCID: 0000-0002-6029-2047

Computer Science

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 19 papers. Top paper: “Beyond the exome: What’s next in diagnostic testing for Mendelian conditions”.

Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.009

N/A

2.2DataRank · unranked

123 citations

Chloe Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan +91 more

Metagenomic sequencing with spiked primer enrichment for viral diagnostics and genomic surveillance

Nature Microbiology(2020)10.1038/s41564-019-0637-9

N/A

0.794DataRank · unranked

198 citations

Asmeeta Achari, Scot Federman, Guixia Yu, Sneha Somasekar, Inês Bártolo +35 more

Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.008

N/A

0.489DataRank · unranked

25 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Enhanced virus detection and metagenomic sequencing in patients with meningitis and encephalitis

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.25.399394

N/A

0.230DataRank · unranked

2 citations

Shibani S. Mukerji, Simon Ye, Michael J. Leone, Lisa M. Freimark, Daniel Park +16 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

medRxiv(2024)10.1101/2024.12.22.24319370

N/A

0.104DataRank · unranked

1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +30 more

Diagnostic capabilities of nanopore long‐read sequencing in muscular dystrophy

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51612

N/A

0DataRank · unranked

40 citations

Hannah R. Littel, Audrey L. Daugherty, Seth A. Stafki, Elicia Estrella, Emily S. McGaughy +19 more

Variants in DTNA cause a mild, dominantly inherited muscular dystrophy

Acta Neuropathologica(2023)10.1007/s00401-023-02551-7

N/A

0DataRank · unranked

12 citations

Christine C. Bruels, Sandra Donkervoort, A. Reghan Foley, Anna Codina, José C. Milisenda +29 more

Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis

medRxiv(2023)10.1101/2023.08.08.23293829

N/A

0DataRank · unranked

8 citations

Gabrielle Lemire, Maha S. Zaki, Mariel Wissman, Wathone Win, S. White +70 more

Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease

medRxiv(2023)10.1101/2023.10.05.23296595

N/A

0DataRank · unranked

1 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Genome Sequencing for Diagnosing Rare Diseases

New England Journal of Medicine(2024)10.1056/nejmoa2314761

N/A

0DataRank · unranked

189 citations

Gabrielle Lemire, Eva Berger, Maha S. Zaki, Mariel Wissmann, Wathone Win +84 more

Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing alone

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.52041

N/A

0DataRank · unranked

23 citations

Samantha J. Bryen, Melanie Bahlo, Anita Cairns, Katherine R. Chao, Alastair Corbett +25 more

Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

Genetics in Medicine(2024)10.1016/j.gim.2024.101199

N/A

0DataRank · unranked

14 citations

Seth Berger, Samantha Baxter, Erica D. Smith, Changrui Xiao, Daniel G. Calame +89 more

Expert Panel Curation of 31 Genes in Relation to Limb Girdle Muscular Dystrophy

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.05.03.592369

N/A

0DataRank · unranked

0 citations

Shannon McNulty, Courtney L Thaxton, Marwa Elnagheeb, Emma Owens, May Flowers +25 more

Dominant stop‐loss HNRNPA1 variants in juvenile‐onset myopathy

Muscle & Nerve(2024)10.1002/mus.28214

N/A

0DataRank · unranked

0 citations

Christine C. Bruels, Audrey L. Daugherty, Elicia Estrella, Seth A. Stafki, Safoora B. Syeda +15 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100441

N/A

0DataRank · unranked

1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +31 more

Jamestown Canyon virus in Massachusetts: clinical case series and vector screening

Emerging Microbes & Infections(2020)10.1080/22221751.2020.1756697

N/A

0DataRank · unranked

36 citations

Molly L Paras, Sandra Smole, Samar Mehta, Vijay Ganesh, Lin H. Chen +9 more

Fatal Case of Chronic Jamestown Canyon Virus Encephalitis Diagnosed by Metagenomic Sequencing in Patient Receiving Rituximab

Emerging infectious diseases(2020)10.3201/eid2701.203448

N/A

0DataRank · unranked

34 citations

Vijay Ganesh, Guixia Yu, Xian Ding Deng, Michael R. Wilson, Steve Miller +13 more

Enhanced Virus Detection and Metagenomic Sequencing in Patients with Meningitis and Encephalitis

mBio(2021)10.1128/mbio.01143-21

N/A

0DataRank · unranked

123 citations

Shibani S. Mukerji, Simon Ye, Michael J. Leone, Lisa M. Freimark, Daniel Park +16 more

A form of muscular dystrophy associated with pathogenic variants in JAG2

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.03.020

N/A

0DataRank · unranked

41 citations

Alison M. Barnard, Sanna Puusepp, Sander Pajusalu, Katrin Õunap, Dorianmarie Vargas‐Franco +53 more