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

Xi Luo

Southern Medical University

ORCID: 0000-0002-1941-2318

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 16 papers. Top paper: “ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines”.

ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines

Genome Medicine(2022)10.1186/s13073-021-01004-8

N/A

2.6DataRank · unranked

85 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

Optimising clinical care through CDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelines

Journal of Medical Genetics(2022)10.1136/jmg-2022-108807

N/A

0.745DataRank · unranked

24 citations

Jamie L. Maciaszek, Bryony A. Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa +19 more

ClinGen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria from ACMG/AMP Guidelines

medRxiv(2021)10.1101/2021.02.12.21251663

N/A

0DataRank · unranked

5 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

Drosophila functional screening of de novo variants in autism uncovers deleterious variants and facilitates discovery of rare neurodevelopmental diseases

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2020.12.30.424813

N/A

0DataRank · unranked

3 citations

Samantha L. Deal, Jonathan C. Andrews, J. Michael Harnish, Venkata Hemanjani Bhavana, Hillary K. Graves +39 more

ClinGen CDH1 specifications for the ACMG/AMP guidelines: improvement of germline variant clinical assertions and updated curation guidelines

medRxiv(2021)10.1101/2021.11.01.21265332

N/A

0DataRank · unranked

0 citations

Jamie L. Maciaszek, Bryony A. Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa +19 more

Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases

Cell Reports(2022)10.1016/j.celrep.2022.110517

N/A

0DataRank · unranked

52 citations

Samantha L. Deal, Jonathan C. Andrews, J. Michael Harnish, Venkata Hemanjani Bhavana, Hillary K. Graves +56 more

Revision of RUNX1 variant curation rules

Blood Advances(2022)10.1182/bloodadvances.2022008017

N/A

0DataRank · unranked

15 citations

Xi Luo, Mancy Shah, Taylor Walker, Nikita Mehta, David Wu +2 more

Reliable detection of generalized convulsive seizures using an off‐the‐shelf digital watch: A multisite phase 2 study

Epilepsia(2024)10.1111/epi.17974

N/A

0DataRank · unranked

9 citations

Xiaojin Li, Jaison S. Hampson, Yan Huang, John C. Mosher, Yuri Dabaghian +9 more

Detection of diffusely abnormal white matter in multiple sclerosis on multiparametric brain MRI using semi-supervised deep learning

Scientific Reports(2024)10.1038/s41598-024-67722-2

N/A

0DataRank · unranked

3 citations

Refaat E. Gabr, Yanyu Yang, Arash Kamali, John A. Lincoln, Michael A. Jacobs +6 more

Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function

eLife(2024)10.7554/elife.95887

N/A

0DataRank · unranked

2 citations

Yiming Zheng, Mingxi Deng, Shenzhao Lu, Xueyang Pan, Xi Luo +25 more

Risk markers for sudden unexpected death in epilepsy: an observational, prospective, multicentre cohort study

The Lancet(2025)10.1016/s0140-6736(25)01636-8

N/A

0DataRank · unranked

27 citations

Xi Luo, Laura Vilella, Nuria Lacuey, Shirin Jamal Omidi, Norma J. Hupp +28 more

The ClinGen Severe Combined Immunodeficiency Disease Variant Curation Expert Panel: Specifications for classification of variants in ADA, DCLRE1C, IL2RG, IL7R, JAK3, RAG1, and RAG2

Genetics in Medicine(2025)10.1016/j.gim.2025.101613

N/A

0DataRank · unranked

5 citations

Michelle Zelnick, Shannon McNulty, Justyne E Ross, Namrata Khurana, Xueyang Pan +38 more

Concurrent TB and HIV therapies control TB reactivation during co-infection but not chronic immune activation

Nature Communications(2025)10.1038/s41467-025-67188-4

N/A

0DataRank · unranked

2 citations

Yi Zou, Bindu Singh, Vinay Shivanna, Edward J. Dick, Shannan Hall-Ursone +10 more

How I curate: applying American Society of Hematology-Clinical Genome Resource Myeloid Malignancy Variant Curation Expert Panel rules for RUNX1 variant curation for germline predisposition to myeloid malignancies

Haematologica(2020)10.3324/haematol.2018.214221

N/A

0DataRank · unranked

32 citations

Xi Luo, Simone Feurstein, Chimene Kesserwan, Shruthi Mohan, Daniel Pineda‐Alvarez +2 more

Single nucleotide variants in UNC13C associated with neurodevelopmental disorders affect ethanol sensitivity in Drosophila

Biochemistry and Biophysics Reports(2025)10.1016/j.bbrep.2025.102375

N/A

0DataRank · unranked

0 citations

Sonja Neuser, Gaurav Shrestha, Netra Prasad Neupane, Katharina J. Götze, Nicola Brunetti‐Pierri +26 more

Rare deleterious de novo missense variants in Rnf2/Ring2 are associated with a neurodevelopmental disorder with unique clinical features

Human Molecular Genetics(2021)10.1093/hmg/ddab110

N/A

0DataRank · unranked

29 citations

Kelly Schoch, Sharayu Jangam, Venkata Hemanjani Bhavana, Hillary K. Graves, Sujay Kansagra +11 more