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

Chad A. Shaw

Baylor College of Medicine

ORCID: 0000-0001-7267-5398

Also affiliated with Neurological Research Institute, Texas Children's Hospital

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 3%percentile
1.1Author DataRank

Indexed papers

4in 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 4 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 →

Top data-sharing exemplar

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

A Renewable Tissue Resource of Phenotypically Stable, Biologically and Ethnically Diverse, Patient-Derived Human Breast Cancer Xenograft Models

UNC Libraries(2020)10.17615/43yk-w772
Top 31%
0.649DataRank
Top 31%17 citations

Qing Lai, Pavel Zuloaga, Amber M. Froehlich, Edward S. Chen, Jian Huang +24 more

Papers

Driven by 22 papers — median percentile 64. Top paper: “Low-level parental somatic mosaic SNVs in exomes from a large cohort of trios with diverse suspected Mendelian conditions”.

Low-level parental somatic mosaic SNVs in exomes from a large cohort of trios with diverse suspected Mendelian conditions

Genetics in Medicine(2020)10.1038/s41436-020-0897-z
N/A
1.8DataRank · unranked
63 citations

Qian Liu, Justyna A. Karolak, Christopher M. Grochowski, Nina Guanyi Xie, Lucia R. Wu +16 more

Detection of clinically relevant exonic copy-number changes by array CGH

Human Mutation(2010)10.1002/humu.21360
N/A
0.824DataRank · unranked
242 citations

Carlos A. Bacino, Chad A. Shaw, Patricia A. Eng, Patricia M. Hixson, Amber N. Pursley +29 more

A Renewable Tissue Resource of Phenotypically Stable, Biologically and Ethnically Diverse, Patient-Derived Human Breast Cancer Xenograft Models

UNC Libraries(2020)10.17615/43yk-w772
Top 31%
0.649DataRank
Top 31%17 citations

Qing Lai, Pavel Zuloaga, Amber M. Froehlich, Edward S. Chen, Jian Huang +24 more

Hematopoietic stem and progenitor cells confer cross-protective trained immunity in mouse models

iScience(2023)10.1016/j.isci.2023.107596
N/A
0.546DataRank · unranked
37 citations

Brandon T. Tran, Pamela N. Luna, Ruoqiong Cao, Duy T. Le, Marcus A. Florez +11 more

Targeted accurate RNA consensus sequencing (tARC-seq) reveals mechanisms of replication error affecting SARS-CoV-2 divergence

Nature Microbiology(2024)10.1038/s41564-024-01655-4
N/A
0.464DataRank · unranked
21 citations

Chen Wang, Alasdair J.E. Gordon, Alice X Wen, Pamela N. Luna, Matthew Cooke +9 more

Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62919
Top 41%
0.461DataRank
Top 41%9 citations

Aliska M. Berry, Ian M. Campbell, Xiaonan Zhao, Pengfei Liu, Amanda Gerard +41 more

Sox7‐positive endothelial progenitors establish coronary arteries and govern ventricular compaction

EMBO Reports(2023)10.15252/embr.202255043
N/A
0.385DataRank · unranked
8 citations

David Humphrey, Richard J. Mills, Peter Kaltzis, Shikha Pachauri, Matthew S. Graus +16 more

Exome sequencing efficacy and phenotypic expansions involving esophageal atresia/tracheoesophageal fistula plus

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62976
N/A
0.385DataRank · unranked
12 citations

Jaynee Chauhan, Katrina Prescott, Aliza Imam, Alison Kraus, Ana Beleza‐Meireles +48 more

FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia

Journal of Pediatric Genetics(2023)10.1055/s-0043-1767731
N/A
0.269DataRank · unranked
5 citations

Andrés Hernández, Jennifer M. Lyu, Ian M. Campbell, Chad A. Shaw, Julie Vogt +5 more

Two lysosomal genes ATP13A2 and GBA1 interact to drive neurodegeneration

Molecular Neurodegeneration(2026)10.1186/s13024-025-00923-z
N/A
0.208DataRank · unranked
3 citations

Jinghan Zhao, Mingxi Deng, Guang Lin, Xueyang Pan, Wenwen Lin +13 more

Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return

European Journal of Human Genetics(2023)10.1038/s41431-023-01451-4
N/A
0DataRank · unranked
8 citations

Xiaonan Zhao, Nichole Owen, Pamela N. Luna, Ida Vogel, Inger Lily Hjuler Dorf +27 more

CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels

Genetics in Medicine(2020)10.1038/s41436-020-0864-8
N/A
0DataRank · unranked
71 citations

Lei Wang, Pengfei Liu, Chad A. Shaw, Hongzheng Dai, Lance Cooper +25 more

Analysis of 13 cell types reveals evidence for the expression of numerous novel primate- and tissue-specific microRNAs

UNC Libraries(2020)10.17615/jbap-cx13
N/A
0DataRank · unranked
0 citations

Charles J. Yeo, L. Jay Katz, Clay E.S. Comstock, George L. Spaeth, Lisa Hark +22 more

High Clinical Exome Sequencing Diagnostic Rates and Novel Phenotypic Expansions for Nonisolated Microphthalmia, Anophthalmia, and Coloboma

Investigative Ophthalmology & Visual Science(2024)10.1167/iovs.65.3.25
N/A
0DataRank · unranked
8 citations

Bailey A. Martin‐Giacalone, Xiaonan Zhao, Pamela N. Luna, Brian P. Brooks, Robert B. Hufnagel +6 more

Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)

European Journal of Human Genetics(2025)10.1038/s41431-025-01929-3
N/A
0DataRank · unranked
4 citations

Xiaonan Zhao, Jill A. Rosenfeld, Pamela N. Luna, Chad A. Shaw, Jennifer E. Posey +2 more

Non-isolated tetralogy of fallot (TOF+): exome sequencing efficacy and phenotypic expansions

European Journal of Human Genetics(2025)10.1038/s41431-025-01916-8
N/A
0DataRank · unranked
2 citations

Xiaonan Zhao, Nichole Owen, Tom Evans, Muriel Holder‐Espinasse, Nayana Lahiri +28 more

Revealing the nervous system requirements of Alzheimer’s disease risk genes in Drosophila

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.07.24.666383
N/A
0DataRank · unranked
0 citations

Shabab B. Hannan, Mingxue Gu, Colleen E Strohlein, Lindsey D. Goodman, Sasidhar Pasupuleti +14 more

WNT4 deficiency impacts heart, diaphragm, and palate development: Insights from human genetics, machine learning, and mouse models

Developmental Biology(2025)10.1016/j.ydbio.2025.09.016
N/A
0DataRank · unranked
0 citations

Bum‐Joon Kim, David Chitayat, Patrick Shannon, Stephanie Hedges, Maria Al Bandari +10 more

Revealing the nervous system requirements of Alzheimer disease risk genes in Drosophila

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.10.003
N/A
0DataRank · unranked
0 citations

Shabab B. Hannan, Mingxue Gu, Colleen E Strohlein, Lindsey D. Goodman, Sasidhar Pasupuleti +14 more

Phase Separation Contributes to Pathogenicity for Nonsense Mediated Decay-Escaping Variant Alleles

medRxiv(2025)10.64898/2025.12.01.25341387
N/A
0DataRank · unranked
0 citations

Jacob Schmidt, Tugce Bozkurt‐Yozgatli, Iman Egab, Luisa Mestroni, Matthew Taylor +12 more

Human Genome-Wide Association and Mouse Knockout Approaches Identify Platelet Supervillin as an Inhibitor of Thrombus Formation Under Shear Stress

UNC Libraries(2020)10.17615/b6de-6048
N/A
0DataRank · unranked
0 citations

Wolfgang Bergmeier, Altaf A. Kondkar, Ying Jin, Elizabeth J. Luna, Moritz Stolla +14 more

Bayesian modelling of high-throughput sequencing assays with malacoda

PLoS Computational Biology(2020)10.1371/journal.pcbi.1007504
N/A
0DataRank · unranked
3 citations

Xianguo Kong, Ed Chen, Leonard C. Edelstein, Chad A. Shaw, Andrew R. Ghazi