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

Ania Fiksinski

Utrecht University

ORCID: 0000-0002-8169-7721

Also affiliated with University Medical Center Utrecht

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 7 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

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Molecular Psychiatry(2020)10.1038/s41380-020-0654-3

N/A

0.738DataRank · unranked

136 citations

Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston +95 more

Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression

Brain Behavior & Immunity - Health(2021)10.1016/j.bbih.2021.100386

N/A

0.373DataRank · unranked

11 citations

Jennifer K. Forsyth, Gil D. Hoftman, Leila Kushan, Maria Jalbrzikowski, Deepika Dokuru +7 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

A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome

Molecular Psychiatry(2022)10.1038/s41380-022-01783-5

N/A

0DataRank · unranked

50 citations

Gil D. Hoftman, Jacob Vorstman, Carrie E. Bearden, Ania Fiksinski

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

Human Brain Mapping(2024)10.1002/hbm.26553

N/A

0DataRank · unranked

6 citations

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

Multicenter retrospective study on effectiveness, reported side effects, and cognitive outcomes of SSRIs in 22q11.2 deletion syndrome

Research Square(2025)10.21203/rs.3.rs-8286229/v1

N/A

0DataRank · unranked

0 citations

Valentina Mancini, Marija Dvojakovska, Leila Kushan, Fatouma Mchangama, Feryal Tairi +21 more