Rong Mao

Biochemistry, Genetics and Molecular Biology

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 5%percentile

0.572Author 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 →

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

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

European Journal of Human Genetics(2024)10.1038/s41431-024-01701-z

Top 34%

0.572DataRank

Top 34%16 citations

Felice D’Arco, Kimberly A. Aldinger, Constance Smith‐Hicks, Christiane Zweier, Gyri Aasland Gradek +69 more

Papers

Driven by 25 papers — median percentile 66. Top paper: “Characterising the autoantibody repertoire in systemic sclerosis following myeloablative haematopoietic stem cell transplantation”.

Characterising the autoantibody repertoire in systemic sclerosis following myeloablative haematopoietic stem cell transplantation

Annals of the Rheumatic Diseases(2023)10.1136/ard-2021-221926

N/A

0.795DataRank · unranked

22 citations

Michele Donato, Daniel E. Furst, Leslie J. Crofford, Ellen Goldmuntz, Lynette Keyes-Elstein +13 more

Specifications of the ACMG/AMP standards and guidelines for mitochondrial DNA variant interpretation

Human Mutation(2020)10.1002/humu.24107

N/A

0.789DataRank · unranked

192 citations

Marie T. Lott, Matthew C. Dulik, Li Shen, Marcella Attimonelli, Ornella Vitale +16 more

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

European Journal of Human Genetics(2024)10.1038/s41431-024-01701-z

Top 34%

0.572DataRank

Top 34%16 citations

Felice D’Arco, Kimberly A. Aldinger, Constance Smith‐Hicks, Christiane Zweier, Gyri Aasland Gradek +69 more

New-onset IgG autoantibodies in hospitalized patients with COVID-19

Nature Communications(2021)10.1038/s41467-021-25509-3

N/A

0DataRank · unranked

474 citations

Allan Feng, Wenzhao Meng, Sokratis A. Apostolidis, Elisabeth Mack, Maja Artandi +44 more

Effective variant filtering and expected candidate variant yield in studies of rare human disease

npj Genomic Medicine(2021)10.1038/s41525-021-00227-3

N/A

0DataRank · unranked

132 citations

Joe Brown, Harriet Dashnow, Amelia D. Wallace, Matt Velinder, Martin Tristani‐Firouzi +7 more

New-Onset IgG Autoantibodies in Hospitalized Patients with COVID-19

medRxiv(2021)10.1101/2021.01.27.21250559

N/A

0DataRank · unranked

91 citations

Allan Feng, Wenzhao Meng, Sokratis A. Apostolidis, Elisabeth Mack, Maja Artandi +44 more

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

medRxiv(2021)10.1101/2021.09.06.21262776

N/A

0DataRank · unranked

8 citations

Felice D’Arco, Kimberly A. Aldinger, Constance Smith‐Hicks, Christiane Zweier, Gyri Aasland Gradek +64 more

High incidence of proliferative and membranous nephritis in SLE patients with low proteinuria in the Accelerating Medicines Partnership

Lara D. Veeken(2022)10.1093/rheumatology/keac067

N/A

0DataRank · unranked

32 citations

Jessica Li, Andrea Fava, Kristina Deonaraine, David Wofsy, Judith A. James +95 more

Comprehensive variant calling from whole‐genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.1888

N/A

0DataRank · unranked

8 citations

Najla Al‐Sweel, Andrew Farrell, Rong Mao, Pınar Bayrak‐Toydemir, Christine E. Miller +22 more

Rapid genome sequencing identifies a novel de novoSNAP25variant for neonatal congenital myasthenic syndrome

Molecular Case Studies(2022)10.1101/mcs.a006242

N/A

0DataRank · unranked

15 citations

Ting Wen, Andrew Farrell, Rong Mao, Barry Moore, Steven E. Boyden +14 more

Autoantibodies targeting cytokines and connective tissue disease autoantigens are common in acute non-SARS-CoV-2 infections.

Research Square(2022)10.21203/rs.3.rs-1233038/v1

N/A

0DataRank · unranked

9 citations

Emily Yu-Ann Yang, A. R. Moore, Shaurya Dhingra, Sarah E. Chang, Xihui Yin +38 more

Autoantibodies are highly prevalent in non–SARS-CoV-2 respiratory infections and critical illness

JCI Insight(2023)10.1172/jci.insight.163150

N/A

0DataRank · unranked

28 citations

Emily Yu-Ann Yang, A. R. Moore, Shaurya Dhingra, Sarah E. Chang, Xihui Yin +38 more

Specifications of the ACMG/AMP guidelines for ACADVL variant interpretation

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107668

N/A

0DataRank · unranked

10 citations

Alexa Dickson, Marcus J. Miller, Elaine Spector, Gregory M. Enns, Heather Baudet +11 more

Open-Source Artificial Intelligence System Supports Diagnosis of Mendelian Diseases in Acutely Ill Infants

Children(2023)10.3390/children10060991

N/A

0DataRank · unranked

4 citations

Pablo Botas, Christine E. Miller, Jian Zhao, Sabrina Malone Jenkins, Hunter Best +5 more

SON -Related Zhu-Tokita-Takenouchi-Kim Syndrome With Recurrent Hemiplegic Migraine

Neurology Genetics(2023)10.1212/nxg.0000000000200062

N/A

0DataRank · unranked

4 citations

Lana Vukadin, John C. Carey, Lorenzo D. Botto, Matt Velinder, Rong Mao +4 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

Novel molecular mechanism in Malan syndrome uncovered through genome sequencing reanalysis, exon‐level Array, and RNA sequencing

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63516

N/A

0DataRank · unranked

2 citations

Nicola Longo, Robert G. Lewis, Thomas J. Nicholas, Steven E. Boyden, Ashley Andrews +6 more

Developing a scoring system for gene curation prioritization in lysosomal diseases

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108572

N/A

0DataRank · unranked

1 citations

Jennifer L Goldstein, Emily Groopman, Shruthi Mohan, Amber Waddell, Raquel Fernandez +10 more

Assessment of genes involved in lysosomal diseases using the ClinGen clinical validity framework

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108593

N/A

0DataRank · unranked

1 citations

Shruthi Mohan, Amber Waddell, Matheus Vernet Machado Bressan Wilke, Raquel Fernández, Meredith Weaver +13 more

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

UNC Libraries(2024)10.17615/2254-fj45

N/A

0DataRank · unranked

0 citations

Rolph Pfundt, Birgit Elisabeth Kristiansen, Mary J. Green, Sally Ann Lynch, Amanda Openshaw +67 more

RNA sequencing provides functional insights and diagnostic resolution in previously unsolved rare disease cases

BMC Medical Genomics(2025)10.1186/s12920-025-02227-z

N/A

0DataRank · unranked

4 citations

John M. O’Shea, Lucilla Pizzo, Ting Wen, Makenzie Fulmer, Jian Zhao +20 more

Identification of 2 novel noncoding variants in patients with Diamond-Blackfan anemia syndrome by whole genome sequencing

Blood Advances(2025)10.1182/bloodadvances.2024015347

N/A

0DataRank · unranked

3 citations

Steven E. Boyden, Caleb M. Hocutt, Robert G. Lewis, Erin E. Baldwin, Jennie Vagher +9 more

Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64108

N/A

0DataRank · unranked

0 citations

Jian Zhao, Steven E. Boyden, Rong Mao, Pınar Bayrak‐Toydemir, A. Pflaum +9 more

Integrated, multicohort analysis reveals unified signature of systemic lupus erythematosus

JCI Insight(2020)10.1172/jci.insight.122312

N/A

0DataRank · unranked

54 citations

D. James Haddon, Vivian K. Diep, Avani Khatri, Erika Bongen, Gloria Yiu +6 more

Characterization of Reference Materials for Spinal Muscular Atrophy Genetic Testing

Journal of Molecular Diagnostics(2020)10.1016/j.jmoldx.2020.10.011

N/A

0DataRank · unranked

9 citations

Pınar Bayrak‐Toydemir, Ty C. Lynnes, Rong Mao, James D. Metcalf, Kasinathan Muralidharan +9 more

Rong Mao

Indexed papers

Top data-sharing exemplar

Papers