Jacob Vorstman

Also affiliated with Hospital for Sick Children, SickKids Foundation

Biochemistry, Genetics and Molecular BiologyNeuroscience

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 6%percentile

0.208Author 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.

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

medRxiv(2022)10.1101/2022.05.05.22274031

Top 65%

0.208DataRank

Top 65%3 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Papers

Driven by 17 papers — median percentile 35. 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

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Nature Genetics(2022)10.1038/s41588-022-01203-y

N/A

1.3DataRank · unranked

55 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +94 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

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

medRxiv(2022)10.1101/2022.05.05.22274031

Top 65%

0.208DataRank

Top 65%3 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 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

Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels

Genetics in Medicine(2022)10.1016/j.gim.2022.05.001

N/A

0DataRank · unranked

25 citations

Taylor I. Bingaman, Carrie-Ann Barry, Andrea Behlmann, Krista Bluske, Bret L. Bostwick +36 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

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

Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

Molecular Psychiatry(2023)10.1038/s41380-023-02009-y

N/A

0DataRank · unranked

5 citations

Yingjie Zhao, M. Reza Jabalameli, Nha Nguyen, Joydeep Mitra, Ann Swillen +15 more

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

Penetrance of Neurodevelopmental Copy Number Variants Is Associated With Variations in Cortical Morphology

Biological Psychiatry Cognitive Neuroscience and Neuroimaging(2025)10.1016/j.bpsc.2025.05.010

N/A

0DataRank · unranked

1 citations

Ida E. Sønderby, George Kirov, Abdel Abdellaoui, Ingrid Agartz, David Ames +95 more

Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia

Brain(2025)10.1093/brain/awaf273

N/A

0DataRank · unranked

1 citations

Ny Hoang, Jamie C Stark, Sunny Cui, Emanuela Pannia, Chung Ting Tsoi +36 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

Diagnostic genetic testing for neurodevelopmental psychiatric disorders: closing the gap between recommendation and clinical implementation

Current Opinion in Genetics & Development(2021)10.1016/j.gde.2020.12.016

N/A

0DataRank · unranked

52 citations

David H. Ledbetter, Jacob Vorstman, Brenda Finucane

Harnessing rare variants in neuropsychiatric and neurodevelopment disorders—a Keystone Symposia report

Annals of the New York Academy of Sciences(2021)10.1111/nyas.14658

N/A

0DataRank · unranked

7 citations

Ryan H. Purcell, Elise Robinson, Jacob Vorstman, Wendy K. Chung, John N. Constantino +9 more

Genomic architecture of autism from comprehensive whole-genome sequence annotation

Cell(2022)10.1016/j.cell.2022.10.009

N/A

0DataRank · unranked

280 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Jacob Vorstman

Indexed papers

Top data-sharing exemplar

Papers