Ania Fiksinski

1.4k total citations
14 papers, 214 citations indexed

About

Ania Fiksinski is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Ania Fiksinski has authored 14 papers receiving a total of 214 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Epidemiology. Recurrent topics in Ania Fiksinski's work include Congenital heart defects research (13 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Congenital Heart Disease Studies (6 papers). Ania Fiksinski is often cited by papers focused on Congenital heart defects research (13 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Congenital Heart Disease Studies (6 papers). Ania Fiksinski collaborates with scholars based in Netherlands, Canada and United States. Ania Fiksinski's co-authors include Jacob Vorstman, Elemi Breetvelt, René S. Kahn, Anne S. Bassett, Maude Schneider, Janneke Zinkstok, Sasja N. Duijff, Carrie E. Bearden, Gil D. Hoftman and Celso Arango and has published in prestigious journals such as Human Molecular Genetics, The British Journal of Psychiatry and Psychological Medicine.

In The Last Decade

Ania Fiksinski

13 papers receiving 213 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ania Fiksinski Netherlands	9	164	93	81	60	53	14	214
L. Scutt Canada	6	269 1.6×	180 1.9×	103 1.3×	34 0.6×	84 1.6×	7	336
Elfi Vergaelen Belgium	8	125 0.8×	73 0.8×	52 0.6×	26 0.4×	38 0.7×	18	185
Louise K. Hoeffding Denmark	6	68 0.4×	61 0.7×	28 0.3×	34 0.6×	18 0.3×	12	142
Jananne Khuri United States	7	203 1.2×	69 0.7×	54 0.7×	27 0.5×	63 1.2×	7	245
Malgorzata Lamacz United States	3	240 1.5×	219 2.4×	60 0.7×	57 0.9×	49 0.9×	5	356
Christine Hinard Switzerland	6	325 2.0×	194 2.1×	123 1.5×	109 1.8×	126 2.4×	8	435
Sailaja Golla United States	8	78 0.5×	127 1.4×	16 0.2×	86 1.4×	13 0.2×	11	242
A Curtis United Kingdom	6	137 0.8×	62 0.7×	30 0.4×	30 0.5×	15 0.3×	7	201
Eugene Yu United States	6	89 0.5×	112 1.2×	18 0.2×	40 0.7×	8 0.2×	7	303
Jin Szatkiewicz United States	11	125 0.8×	220 2.4×	7 0.1×	40 0.7×	24 0.5×	30	321

Countries citing papers authored by Ania Fiksinski

Since Specialization

Citations

This map shows the geographic impact of Ania Fiksinski'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 Ania Fiksinski with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ania Fiksinski more than expected).

Fields of papers citing papers by Ania Fiksinski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ania Fiksinski. 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 Ania Fiksinski. The network helps show where Ania Fiksinski may publish in the future.

Co-authorship network of co-authors of Ania Fiksinski

This figure shows the co-authorship network connecting the top 25 collaborators of Ania Fiksinski. A scholar is included among the top collaborators of Ania Fiksinski 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 Ania Fiksinski. Ania Fiksinski is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Boerma, Tessel, A. A. A. Manik J. Djelantik, Marlies Houben, et al.. (2024). A comprehensive overview of neuropsychiatric symptoms in adolescents with 22q11.2 deletion syndrome. Journal of Intellectual Disability Research. 69(2). 113–126.

Fiksinski, Ania, Gil D. Hoftman, Jacob Vorstman, & Carrie E. Bearden. (2022). A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome. Molecular Psychiatry. 28(1). 341–353. 27 indexed citations

Boks, Marco P., Ania Fiksinski, Jacob Vorstman, et al.. (2022). Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome. Translational Psychiatry. 12(1). 97–97. 5 indexed citations

Lin, Amy, Jennifer K. Forsyth, Gil D. Hoftman, et al.. (2021). Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression. Brain Behavior & Immunity - Health. 18. 100386–100386. 5 indexed citations

Fiksinski, Ania, Maude Schneider, Janneke Zinkstok, et al.. (2021). Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome. Current Psychiatry Reports. 23(3). 13–13. 25 indexed citations

Fiksinski, Ania, Tracy Heung, Maria Corral, et al.. (2021). Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model. Psychological Medicine. 52(14). 3184–3192. 9 indexed citations

Namavar, Yasmin, et al.. (2021). Psychiatric phenotypes associated with hyperprolinemia: A systematic review. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 186(5). 289–317. 16 indexed citations

Zinkstok, Janneke, Fleur P. Velders, Marlies Houben, et al.. (2020). [Psychosis and movement disorders in an adolescent with 22q11.2 deletion syndrome].. Tijdschrift voor psychiatrie. 62(3). 229–233. 1 indexed citations

Vingerhoets, Claudia, Oswald Bloemen, Erik Boot, et al.. (2019). Low prevalence of substance use in people with 22q11.2 deletion syndrome. The British Journal of Psychiatry. 215(5). 661–667. 12 indexed citations

10.

Vergaelen, Elfi, Matthew S. Hestand, Jeroen Breckpot, et al.. (2019). Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins. Human Molecular Genetics. 28(22). 3724–3733. 6 indexed citations

11.

Fiksinski, Ania, Elemi Breetvelt, Erik Boot, et al.. (2018). Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia. Psychological Medicine. 49(6). 1047–1054. 13 indexed citations

12.

Fiksinski, Ania, Maude Schneider, Clodagh M. Murphy, et al.. (2018). Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 176(10). 2182–2191. 42 indexed citations

13.

Nuninga, Jasper O., Marc M. Bohlken, Sanne Koops, et al.. (2017). White matter abnormalities in 22q11.2 deletion syndrome patients showing cognitive decline. Psychological Medicine. 48(10). 1655–1663. 11 indexed citations

14.

Fiksinski, Ania, Elemi Breetvelt, Sasja N. Duijff, et al.. (2017). Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study. Schizophrenia Research. 188. 59–62. 42 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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