Anne‐Marie Bisgaard

2.4k total citations
31 papers, 924 citations indexed

About

Anne‐Marie Bisgaard is a scholar working on Genetics, Cognitive Neuroscience and Clinical Psychology. According to data from OpenAlex, Anne‐Marie Bisgaard has authored 31 papers receiving a total of 924 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 11 papers in Cognitive Neuroscience and 10 papers in Clinical Psychology. Recurrent topics in Anne‐Marie Bisgaard's work include Genetics and Neurodevelopmental Disorders (18 papers), Genomic variations and chromosomal abnormalities (14 papers) and Autism Spectrum Disorder Research (11 papers). Anne‐Marie Bisgaard is often cited by papers focused on Genetics and Neurodevelopmental Disorders (18 papers), Genomic variations and chromosomal abnormalities (14 papers) and Autism Spectrum Disorder Research (11 papers). Anne‐Marie Bisgaard collaborates with scholars based in Denmark, Australia and Germany. Anne‐Marie Bisgaard's co-authors include Maria Kirchhoff, Zeynep Tümer, Karen Brøndum‐Nielsen, Cathrine Jespersgaard, Thue Bryndorf, Jenny Downs, Tommy Gerdes, Helen Leonard, Reinhard Ullmann and Flemming Skovby and has published in prestigious journals such as PLoS ONE, PEDIATRICS and Gene.

In The Last Decade

Anne‐Marie Bisgaard

30 papers receiving 888 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne‐Marie Bisgaard Denmark 15 680 378 203 135 124 31 924
Theresa A. Grebe United States 16 458 0.7× 449 1.2× 102 0.5× 92 0.7× 41 0.3× 34 879
Bhooma Thiruvahindrapuram Canada 14 500 0.7× 420 1.1× 147 0.7× 123 0.9× 34 0.3× 47 880
Cinzia Galasso Italy 13 367 0.5× 250 0.7× 63 0.3× 163 1.2× 31 0.3× 37 651
Shay Ben‐Shachar Israel 18 700 1.0× 592 1.6× 238 1.2× 145 1.1× 27 0.2× 41 1.0k
Marzia Pollazzon Italy 14 494 0.7× 368 1.0× 143 0.7× 43 0.3× 37 0.3× 31 692
Deborah Barbouth United States 11 412 0.6× 285 0.8× 183 0.9× 85 0.6× 24 0.2× 32 678
Silvia Souza da Costa Brazil 17 397 0.6× 370 1.0× 77 0.4× 94 0.7× 29 0.2× 64 740
Melissa T. Carter Canada 16 326 0.5× 320 0.8× 103 0.5× 75 0.6× 41 0.3× 34 616
A. Moncla France 17 748 1.1× 633 1.7× 121 0.6× 174 1.3× 17 0.1× 29 1.1k
Rossella Caselli Italy 15 607 0.9× 401 1.1× 139 0.7× 68 0.5× 31 0.3× 20 796

Countries citing papers authored by Anne‐Marie Bisgaard

Since Specialization
Citations

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

Fields of papers citing papers by Anne‐Marie Bisgaard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anne‐Marie Bisgaard. 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 Anne‐Marie Bisgaard. The network helps show where Anne‐Marie Bisgaard may publish in the future.

Co-authorship network of co-authors of Anne‐Marie Bisgaard

This figure shows the co-authorship network connecting the top 25 collaborators of Anne‐Marie Bisgaard. A scholar is included among the top collaborators of Anne‐Marie Bisgaard 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 Anne‐Marie Bisgaard. Anne‐Marie Bisgaard 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.
Cianci, Paola, Milena Mariani, Sylvia Huisman, et al.. (2024). SMC1A epilepsy syndrome: clinical data from a large international cohort. American Journal of Medical Genetics Part A. 194(7). e63577–e63577. 1 indexed citations
2.
Hansson, Helena, et al.. (2024). Psychological aspects of being a parent of an individual with Rett syndrome: A scoping review. Journal of Applied Research in Intellectual Disabilities. 37(2). e13188–e13188.
3.
Downs, Jenny, et al.. (2016). Validating the Rett Syndrome Gross Motor Scale. PLoS ONE. 11(1). e0147555–e0147555. 58 indexed citations
4.
Schönewolf‐Greulich, Bitten, et al.. (2016). Functional abilities in aging women with Rett syndrome – the Danish cohort. Disability and Rehabilitation. 39(9). 911–918. 19 indexed citations
5.
Downs, Jenny, et al.. (2016). Building the repertoire of measures of walking in Rett syndrome. Disability and Rehabilitation. 39(19). 1926–1931. 22 indexed citations
6.
Schönewolf‐Greulich, Bitten, Morten Dunø, Kirstine Ravn, Karen Brøndum‐Nielsen, & Anne‐Marie Bisgaard. (2015). [Clinical molecular genetics diagnostics of Rett syndrome in Denmark].. PubMed. 177(27). 1 indexed citations
7.
Bisgaard, Anne‐Marie, et al.. (2015). Is it possible to diagnose Rett syndrome before classical symptoms become obvious? Review of 24 Danish cases born between 2003 and 2012. European Journal of Paediatric Neurology. 19(6). 679–687. 12 indexed citations
9.
Grønskov, Karen, et al.. (2014). Mosaicism for c.431_454dup in ARX causes a mild Partington syndrome phenotype. European Journal of Medical Genetics. 57(6). 284–287. 4 indexed citations
10.
Kirchhoff, Maria, Anne‐Marie Bisgaard, Radka Stoeva, et al.. (2009). Phenotype and 244k array‐CGH characterization of chromosome 13q deletions: An update of the phenotypic map of 13q21.1‐qter. American Journal of Medical Genetics Part A. 149A(5). 894–905. 92 indexed citations
11.
Tzschach, Andreas, Anne‐Marie Bisgaard, Maria Kirchhoff, et al.. (2009). Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11. European Journal of Human Genetics. 18(3). 291–295. 17 indexed citations
12.
Hove, Hanne, et al.. (2008). Facial asymmetry associated with small and large intestinal atresia, and ipsilateral malformations of eye, skin, and extremities. Clinical Dysmorphology. 17(2). 121–122. 2 indexed citations
13.
Bisgaard, Anne‐Marie, et al.. (2007). Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata. Clinical Dysmorphology. 16(2). 109–112. 10 indexed citations
14.
Ullmann, Reinhard, Gillian Turner, Maria Kirchhoff, et al.. (2007). Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Human Mutation. 28(7). 674–682. 204 indexed citations
15.
Bisgaard, Anne‐Marie, Maria Kirchhoff, Jens Erik Nielsen, et al.. (2007). Transmitted cytogenetic abnormalities in patients with mental retardation: Pathogenic or normal variants?. European Journal of Medical Genetics. 50(4). 243–255. 30 indexed citations
16.
Kirchhoff, Maria, Anne‐Marie Bisgaard, Morten Dunø, Flemming Juul Hansen, & Marianne Schwartz. (2007). A 17q21.31 microduplication, reciprocal to the newly described 17q21.31 microdeletion, in a girl with severe psychomotor developmental delay and dysmorphic craniofacial features. European Journal of Medical Genetics. 50(4). 256–263. 48 indexed citations
17.
Cingöz, Sultan, Anne‐Marie Bisgaard, Iben Bache, et al.. (2006). 4q35 deletion and 10p15 duplication associated with immunodeficiency. American Journal of Medical Genetics Part A. 140A(20). 2231–2235. 9 indexed citations
18.
Bisgaard, Anne‐Marie, Maria Kirchhoff, Zeynep Tümer, et al.. (2006). Additional chromosomal abnormalities in patients with a previously detected abnormal karyotype, mental retardation, and dysmorphic features. American Journal of Medical Genetics Part A. 140A(20). 2180–2187. 47 indexed citations
19.
Kirchhoff, Maria, Anne‐Marie Bisgaard, Thue Bryndorf, & Tommy Gerdes. (2006). MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams–Beuren syndrome regions. European Journal of Medical Genetics. 50(1). 33–42. 79 indexed citations
20.
Anhøj, Jacob, Anne‐Marie Bisgaard, & Hans Bisgaard. (2002). Systemic Activity of Inhaled Steroids in 1- to 3-Year-Old Children With Asthma. PEDIATRICS. 109(3). e40–e40. 32 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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