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

Deborah Watson

University of San Diego

ORCID: 0000-0002-8044-8344

Also affiliated with University of California San Diego

MedicineNeuroscienceMaterials 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 9 papers. Top paper: “Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing”.

Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing

Biomarker Research(2022)10.1186/s40364-022-00431-y
N/A
0DataRank · unranked
8 citations

Hui‐Qi Qu, Xiao Chang, Frank Mentch, Haijun Qiu, Kenny Nguyen +6 more

A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63130
N/A
0DataRank · unranked
3 citations

Soumya Rao, Sandra von Hardenberg, Dong Li, Liza L. Cox, Paul C. Lee +34 more

Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development

Molecular Cancer(2023)10.1186/s12943-023-01828-5
N/A
0DataRank · unranked
1 citations

Hui‐Qi Qu, Xiao Chang, Frank Mentch, Haijun Qiu, Xiang Wang +5 more

High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations

Translational research(2023)10.1016/j.trsl.2023.11.004
N/A
0DataRank · unranked
1 citations

Joseph Glessner, Jingchun Qu, Yichuan Liu, Deborah Watson, Xiao Chang +6 more

Multiple independent gene disorders causing Bardet--Biedl syndrome, congenital hypothyroidism, and hearing loss in a single Indian consanguineous patient

(2023)10.22541/au.167722036.60770586/v1
N/A
0DataRank · unranked
0 citations

Dong Li, Deborah Watson, Elizabeth M. McCormick, Lisa M. Elden, Thomas Aleman +4 more

Multiple Independent Gene Disorders Causing Bardet–Biedl Syndrome, Congenital Hypothyroidism, and Hearing Loss in a Single Indian Patient

Brain Sciences(2023)10.3390/brainsci13081210
N/A
0DataRank · unranked
0 citations

Dong Li, Deborah Watson, Elizabeth M. McCormick, Lisa M. Elden, T. S. Aleman +4 more

Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome

Genetics in Medicine(2024)10.1016/j.gim.2024.101222
N/A
0DataRank · unranked
8 citations

Michael March, Christopher J. Cardinale, Yichuan Liu, Mark R. Battig, Lívia Sertori Finoti +15 more

Variants in BSN, encoding the presynaptic protein Bassoon, result in a distinct neurodevelopmental disorder with a broad phenotypic range

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.011
N/A
0DataRank · unranked
4 citations

Sarah M. Ruggiero, Shiva Ganesan, Colin A. Ellis, Abiola Harrison, Katie Rose Sullivan +32 more

Variants in BSN , encoding the presynaptic protein Bassoon, result in a novel neurodevelopmental disorder with a broad phenotypic range

medRxiv(2025)10.1101/2025.02.10.25321755
N/A
0DataRank · unranked
0 citations

Sarah M. Ruggiero, Shiva Ganesan, Colin A. Ellis, Abiola Harrison, Katie Rose Sullivan +34 more