🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Minjie Luo

Children's Hospital of Philadelphia

ORCID: 0000-0002-5788-3962

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 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 13 papers. Top paper: “Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma”.

Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma

Acta Neuropathologica Communications(2022)10.1186/s40478-022-01401-z

N/A

0.396DataRank · unranked

13 citations

Angela N. Viaene, Jenny Ruiz, Jeffrey Schubert, Jinhua Wu, Jiani Chen +16 more

Keratin-Positive Giant Cell Tumor of Bone and Soft Tissue With HMGA2::NCOR2 Fusion in Children Under 10 With Response to Imatinib Therapy: A Case Series

JCO Precision Oncology(2024)10.1200/po.23.00659

N/A

0.241DataRank · unranked

4 citations

Anne L. Ryan, Daniel D. Wong, Minjie Luo, Ken Kazahaya, Alexandre Arkader +8 more

Spatial and Single Cell Mapping of Castleman Disease Reveals Key Stromal Cell Types and Cytokine Pathways

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.09.609717

N/A

0.104DataRank · unranked

1 citations

Anna Eichinger, Andrew J. Rech, Julia Wang, Eduardo Esteva, Arta Seyedian +9 more

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

European Journal of Human Genetics(2021)10.1038/s41431-020-00790-w

N/A

0DataRank · unranked

17 citations

Chayada Tangshewinsirikul, Kevin T. Booth, Héla Azaiez, Devorah Yefet, Adina Quint +23 more

Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group

Genetics in Medicine(2023)10.1016/j.gim.2023.101036

N/A

0DataRank · unranked

70 citations

Marcie Steeves, Pınar Bayrak‐Toydemir, Katherine A. Benson, Bradley P. Coe, Laura K. Conlin +42 more

A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data

Genome Medicine(2020)10.1186/s13073-020-0712-0

N/A

0DataRank · unranked

68 citations

Jill R. Murrell, Minjie Luo, Laura K. Conlin, Ramakrishnan Rajagopalan

Spatial and single cell mapping of castleman disease reveals key stromal cell types and cytokine pathways

Nature Communications(2025)10.1038/s41467-025-61214-1

N/A

0DataRank · unranked

12 citations

Anna Eichinger, Éanna Fennell, Zijun Y. Xu‐Monette, Andrew J. Rech, Julia Wang +13 more

ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time

Genetics in Medicine(2025)10.1016/j.gim.2025.101392

N/A

0DataRank · unranked

1 citations

Marina T. DiStefano, Andrea M. Oza, Pamela Ajuyah, Ryan Webb, Enyonam Edoh +76 more

Genome-wide association study of childhood B-cell acute lymphoblastic leukemia reveals novel African ancestry-specific susceptibility loci

Nature Communications(2025)10.1038/s41467-025-64337-7

N/A

0DataRank · unranked

1 citations

Andrew R. Raduski, Lauren J. Mills, Kashi Raj Bhattarai, Robert J. Mobley, Kelly R. Barnett +38 more

Leveraging genomic diagnostics for prognostics and therapeutics in pediatric acute leukemia

HemaSphere(2025)10.1002/hem3.70269

N/A

0DataRank · unranked

0 citations

Derek Wong, Jinhua Wu, Jeffrey Schubert, Netta Golenberg, Natali S. Sobel Naveh +24 more

The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program Directors

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101820

N/A

0DataRank · unranked

2 citations

Vimla S. Aggarwal, A. Bale, Daniel B. Bellissimo, Jessica K. Booker, Yang Cao +30 more

A germline PALB2 pathogenic variant identified in a pediatric high-grade glioma

Molecular Case Studies(2020)10.1101/mcs.a005397

N/A

0DataRank · unranked

5 citations

Jeffrey Schubert, Jinhua Wu, Feng Xu, Fumin Lin, Kajia Cao +9 more

Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel

Blood Advances(2021)10.1182/bloodadvances.2020003712

N/A

0DataRank · unranked

37 citations

Bing Zhang, Kristy Lee, Shruthi Mohan, Brian R. Branchford, Paul F. Bray +14 more