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

Wendy R. Kates

SUNY Upstate Medical University

ORCID: 0000-0003-3358-2572
Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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: “Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness”.

Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness

American Journal of Psychiatry(2020)10.1176/appi.ajp.2019.19060583
N/A
1.4DataRank · unranked
89 citations

Boris A. Gutman, Daqiang Sun, Julio E. Villalón‐Reina, Anjanibhargavi Ragothaman, Dmitry Isaev +50 more

Source‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome

Human Brain Mapping(2024)10.1002/hbm.26553
N/A
0.385DataRank · unranked
6 citations

Christopher R. K. Ching, Anne S. Bassett, Leila Kushan, Kevin M. Antshel, Thérèse van Amelsvoort +42 more

Unique Functional Neuroimaging Signatures of Genetic Versus Clinical High Risk for Psychosis

Biological Psychiatry(2024)10.1016/j.biopsych.2024.08.010
N/A
0.320DataRank · unranked
5 citations

Sarah Chang, Carolyn Amir, Kathleen O’Hora, Hoki Fung, Jee Won Diane Kang +23 more

Inter-rater reliability of subthreshold psychotic symptoms in individuals with 22q11.2 deletion syndrome

Journal of Neurodevelopmental Disorders(2021)10.1186/s11689-021-09372-3
N/A
0DataRank · unranked
1 citations

Deby Salzer, Carrie E. Bearden, Monica E. Calkins, Wendy R. Kates, Leila Kushan +7 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.30.507111
N/A
0DataRank · unranked
0 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +45 more

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

medRxiv(2020)10.1101/2020.01.14.20017426
N/A
0DataRank · unranked
14 citations

Joanne Doherty, Richard Anney, Kevin M. Antshel, Carrie E. Bearden, Raphael Bernier +26 more

Brief Report: Sensory Features Associated with Autism After Controlling for ADHD Symptoms

Journal of Autism and Developmental Disorders(2023)10.1007/s10803-023-06046-y
N/A
0DataRank · unranked
3 citations

Kevin M. Antshel, Wendy R. Kates, Natalie Russo, Ellen C. Masters

Abnormalities in white matter tracts in the fronto-striatal-thalamic circuit are associated with verbal performance in 22q11.2DS

Schizophrenia Research(2020)10.1016/j.schres.2020.09.008
N/A
0DataRank · unranked
10 citations

Saskia Steinmann, James J. Levitt, Nikos Makris, Kevin M. Antshel, Wanda Fremont +8 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS

npj Genomic Medicine(2023)10.1038/s41525-023-00363-y
N/A
0DataRank · unranked
12 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +47 more