J.A.S. Vorstman

416 total citations
4 papers, 298 citations indexed

About

J.A.S. Vorstman is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, J.A.S. Vorstman has authored 4 papers receiving a total of 298 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Cognitive Neuroscience. Recurrent topics in J.A.S. Vorstman's work include Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers) and Autism Spectrum Disorder Research (2 papers). J.A.S. Vorstman is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers) and Autism Spectrum Disorder Research (2 papers). J.A.S. Vorstman collaborates with scholars based in Netherlands, United States and Belgium. J.A.S. Vorstman's co-authors include Wouter Staal, Hermán van Engeland, Emma van Daalen, Ron Hochstenbach, Jacobine E. Buizer‐Voskamp, Roel A. Ophoff, Lude Franke, Joris Vermeesch, Eva W.C. Chow and Stephen T. Warren and has published in prestigious journals such as Molecular Psychiatry and Cytogenetic and Genome Research.

In The Last Decade

J.A.S. Vorstman

4 papers receiving 291 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
J.A.S. Vorstman Netherlands	4	225	141	133	29	25	4	298
Barbara Wiśniowiecka‐Kowalnik Poland	8	306 1.4×	214 1.5×	155 1.2×	21 0.7×	71 2.8×	11	445
Chelsea Lowther Canada	8	245 1.1×	191 1.4×	45 0.3×	17 0.6×	16 0.6×	8	330
Sailaja Golla United States	8	127 0.6×	78 0.6×	86 0.6×	16 0.6×	11 0.4×	11	242
Wei‐Hsien Chien Taiwan	8	145 0.6×	72 0.5×	145 1.1×	31 1.1×	14 0.6×	14	257
Tracie C. Rosser United States	10	205 0.9×	260 1.8×	86 0.6×	33 1.1×	7 0.3×	13	444
Mihoko Shimada Japan	12	77 0.3×	128 0.9×	175 1.3×	25 0.9×	20 0.8×	27	386
Amy Lawson‐Yuen United States	6	223 1.0×	154 1.1×	172 1.3×	21 0.7×	13 0.5×	7	363
Teresa Lim United States	5	215 1.0×	127 0.9×	161 1.2×	5 0.2×	14 0.6×	6	299
Marie‐Christine de Blois France	8	352 1.6×	182 1.3×	96 0.7×	14 0.5×	65 2.6×	10	455
Tess Levy United States	10	156 0.7×	137 1.0×	93 0.7×	13 0.4×	6 0.2×	23	293

Countries citing papers authored by J.A.S. Vorstman

Since Specialization

Citations

This map shows the geographic impact of J.A.S. Vorstman's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by J.A.S. Vorstman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J.A.S. Vorstman more than expected).

Fields of papers citing papers by J.A.S. Vorstman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.A.S. Vorstman. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by J.A.S. Vorstman. The network helps show where J.A.S. Vorstman may publish in the future.

Co-authorship network of co-authors of J.A.S. Vorstman

This figure shows the co-authorship network connecting the top 25 collaborators of J.A.S. Vorstman. A scholar is included among the top collaborators of J.A.S. Vorstman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with J.A.S. Vorstman. J.A.S. Vorstman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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4 of 4 papers shown

1.

Gur, Raquel E., Anne S. Bassett, Donna M. McDonald‐McGinn, et al.. (2017). A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium. Molecular Psychiatry. 22(12). 1664–1672. 56 indexed citations

2.

Hochstenbach, Ron, Jacobine E. Buizer‐Voskamp, J.A.S. Vorstman, & Roel A. Ophoff. (2011). Genome Arrays for the Detection of Copy Number Variations in Idiopathic Mental Retardation, Idiopathic Generalized Epilepsy and Neuropsychiatric Disorders: Lessons for Diagnostic Workflow and Research. Cytogenetic and Genome Research. 135(3-4). 174–202. 80 indexed citations

3.

Vorstman, J.A.S., Emma van Daalen, G R Jalali, et al.. (2010). A double hit implicates DIAPH3 as an autism risk gene. Molecular Psychiatry. 16(4). 442–451. 51 indexed citations

4.

Vorstman, J.A.S., et al.. (2005). Overview of cytogenetic regions of interest (CROIs) associated with the autism phenotype across the human genome. Molecular Psychiatry. 11(1). 1–1. 111 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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