Gudrun Nygren

8.2k total citations
31 papers, 1.4k citations indexed

About

Gudrun Nygren is a scholar working on Cognitive Neuroscience, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Gudrun Nygren has authored 31 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Cognitive Neuroscience, 12 papers in Genetics and 12 papers in Psychiatry and Mental health. Recurrent topics in Gudrun Nygren's work include Autism Spectrum Disorder Research (22 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Family and Disability Support Research (9 papers). Gudrun Nygren is often cited by papers focused on Autism Spectrum Disorder Research (22 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Family and Disability Support Research (9 papers). Gudrun Nygren collaborates with scholars based in Sweden, France and Russia. Gudrun Nygren's co-authors include Christopher Gillberg, Elena V. Orekhova, Mikael Elam, Tatiana A. Stroganova, M. M. Tsetlin, I. N. Posikera, Bibbi Hagberg, Marion Leboyer, Catalina Betancur and Maria Råstam and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Biological Psychiatry.

In The Last Decade

Gudrun Nygren

31 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gudrun Nygren Sweden 19 990 428 297 294 272 31 1.4k
Maretha Jonge Netherlands 19 969 1.0× 527 1.2× 224 0.8× 333 1.1× 300 1.1× 41 1.3k
Roberto Canitano Italy 23 1.0k 1.0× 772 1.8× 376 1.3× 474 1.6× 294 1.1× 46 1.7k
Stephen J. Guter United States 18 988 1.0× 725 1.7× 283 1.0× 365 1.2× 155 0.6× 26 1.3k
Pauline Chaste France 13 1.3k 1.3× 763 1.8× 465 1.6× 429 1.5× 488 1.8× 20 1.9k
Taina Nieminen‐von Wendt Finland 23 1.3k 1.3× 360 0.8× 216 0.7× 434 1.5× 238 0.9× 35 1.7k
Xiu Xu China 21 626 0.6× 377 0.9× 286 1.0× 196 0.7× 251 0.9× 71 1.3k
Mark D. Shen United States 17 769 0.8× 390 0.9× 166 0.6× 180 0.6× 126 0.5× 35 1.1k
Donna M. Werling United States 12 978 1.0× 735 1.7× 383 1.3× 230 0.8× 254 0.9× 18 1.6k
Raija Vanhala Finland 23 1.5k 1.5× 889 2.1× 464 1.6× 317 1.1× 209 0.8× 46 2.1k
Lonnie Zwaigenbaum Canada 11 1.6k 1.6× 921 2.2× 395 1.3× 338 1.1× 442 1.6× 16 2.0k

Countries citing papers authored by Gudrun Nygren

Since Specialization
Citations

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

Fields of papers citing papers by Gudrun Nygren

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gudrun Nygren

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

All Works

20 of 20 papers shown
1.
Nygren, Gudrun, et al.. (2025). Bridging gaps in healthcare: child health services and specialist care collaboration for young children with autism and coexisting conditions. Frontiers in Pediatrics. 13. 1501650–1501650. 1 indexed citations
2.
Nygren, Gudrun, et al.. (2024). Intervention in autism based on Early Start Denver Model in a multiethnic immigrant setting—experiences of preschool staff involved in its implementation. SHILAP Revista de lepidopterología. 3. 1341729–1341729. 2 indexed citations
3.
Nygren, Gudrun, et al.. (2024). “The package has been opened”- parents' perspective and social validity of an Early Start Denver Model intervention for young children with autism. SHILAP Revista de lepidopterología. 3. 1509828–1509828. 1 indexed citations
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6.
Nygren, Gudrun, et al.. (2021). Feeding Problems Including Avoidant Restrictive Food Intake Disorder in Young Children With Autism Spectrum Disorder in a Multiethnic Population. Frontiers in Pediatrics. 9. 780680–780680. 34 indexed citations
7.
Gillberg, Christopher, et al.. (2019). <p>Experiences Of Immigrant Parents In Sweden Participating In A Community Assessment And Intervention Program For Preschool Children With Autism</p>. Neuropsychiatric Disease and Treatment. Volume 15. 3397–3410. 17 indexed citations
8.
Scheid, Isabelle, Anna Maruani, Guillaume Huguet, et al.. (2013). Heterozygous FA2H mutations in autism spectrum disorders. BMC Medical Genetics. 14(1). 124–124. 7 indexed citations
9.
Nygren, Gudrun, et al.. (2012). A new screening programme for autism in a general population of Swedish toddlers. Research in Developmental Disabilities. 33(4). 1200–1210. 82 indexed citations
10.
Nygren, Gudrun, et al.. (2011). The Prevalence of Autism Spectrum Disorders in Toddlers: A Population Study of 2-Year-Old Swedish Children. Journal of Autism and Developmental Disorders. 42(7). 1491–1497. 77 indexed citations
11.
Delorme, Richard, Catalina Betancur, Isabelle Scheid, et al.. (2010). Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls. BMC Medical Genetics. 11(1). 108–108. 30 indexed citations
12.
Henningsson, Susanne, Lina Jönsson, Lars Westberg, et al.. (2009). Possible association between the androgen receptor gene and autism spectrum disorder. Psychoneuroendocrinology. 34(5). 752–761. 48 indexed citations
13.
Orekhova, Elena V., et al.. (2009). The right hemisphere fails to respond to temporal novelty in autism: Evidence from an ERP study. Clinical Neurophysiology. 120(3). 520–529. 50 indexed citations
14.
Nygren, Gudrun, et al.. (2009). The Swedish Version of the Diagnostic Interview for Social and Communication Disorders (DISCO-10). Psychometric Properties. Journal of Autism and Developmental Disorders. 39(5). 730–741. 63 indexed citations
15.
Stroganova, Tatiana A., Gudrun Nygren, M. M. Tsetlin, et al.. (2007). Abnormal EEG lateralization in boys with autism. Clinical Neurophysiology. 118(8). 1842–1854. 112 indexed citations
16.
Miniscalco, Carmela, Gudrun Nygren, Bibbi Hagberg, Björn Kadesjö, & Christopher Gillberg. (2006). Neuropsychiatric and neurodevelopmental outcome of children at age 6 and 7 years who screened positive for language problems at 30 months. Developmental Medicine & Child Neurology. 48(5). 361–366. 110 indexed citations
17.
Delorme, Richard, Christelle M. Durand, Catalina Betancur, et al.. (2006). No Human Tryptophan Hydroxylase-2 Gene R441H Mutation in a Large Cohort of Psychiatric Patients and Control Subjects. Biological Psychiatry. 60(2). 202–203. 43 indexed citations
18.
Chaste, Pauline, Gudrun Nygren, Henrik Anckarsäter, et al.. (2006). Mutation screening of the ARX gene in patients with autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(2). 228–230. 22 indexed citations
19.
Orekhova, Elena V., Tatiana A. Stroganova, Gudrun Nygren, et al.. (2006). P21.5 High frequency activity in ongoing EEG from young children with autism: A two sample study. Clinical Neurophysiology. 117. 218–218. 2 indexed citations
20.
Durand, Christelle M., Caroline Kappeler, Catalina Betancur, et al.. (2005). Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(1). 67–70. 40 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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