Britt‐Marie Anderlid

4.2k total citations
56 papers, 1.3k citations indexed

About

Britt‐Marie Anderlid is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Britt‐Marie Anderlid has authored 56 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 23 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Britt‐Marie Anderlid's work include Genomic variations and chromosomal abnormalities (27 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Genomics and Rare Diseases (9 papers). Britt‐Marie Anderlid is often cited by papers focused on Genomic variations and chromosomal abnormalities (27 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Genomics and Rare Diseases (9 papers). Britt‐Marie Anderlid collaborates with scholars based in Sweden, United Kingdom and France. Britt‐Marie Anderlid's co-authors include Magnus Nordenskjöld, Elisabeth Blennow, Jacqueline Schoumans, Ann Nordgren, Anna Lindstrand, Daniel Nilsson, Göran Annerén, Sigrid Sahlén, Maria Pettersson and Tommy Stödberg and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Experimental Cell Research.

In The Last Decade

Britt‐Marie Anderlid

55 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Britt‐Marie Anderlid Sweden 22 813 607 209 200 179 56 1.3k
Míriam Guitart Spain 23 914 1.1× 625 1.0× 348 1.7× 153 0.8× 170 0.9× 58 1.4k
Anne Moncla France 24 1.3k 1.6× 1.1k 1.7× 185 0.9× 343 1.7× 94 0.5× 38 1.9k
Jyotsna Sudi United States 13 1.0k 1.2× 705 1.2× 189 0.9× 451 2.3× 104 0.6× 14 1.5k
Kiran K. Mantripragada United Kingdom 22 853 1.0× 773 1.3× 100 0.5× 274 1.4× 178 1.0× 41 1.8k
Bai-Lin Wu United States 21 1.4k 1.7× 1.0k 1.7× 209 1.0× 646 3.2× 154 0.9× 43 2.2k
María Clara Bonaglia Italy 25 1.1k 1.3× 891 1.5× 422 2.0× 226 1.1× 364 2.0× 61 1.8k
Katherine Lachlan United Kingdom 19 659 0.8× 869 1.4× 82 0.4× 122 0.6× 84 0.5× 45 1.4k
Katherina Walz United States 26 965 1.2× 1.1k 1.8× 90 0.4× 193 1.0× 146 0.8× 59 1.7k
Laia Rodríguez‐Revenga Spain 23 1.4k 1.7× 873 1.4× 356 1.7× 455 2.3× 141 0.8× 87 1.9k
Abdul Noor Canada 20 620 0.8× 823 1.4× 118 0.6× 145 0.7× 35 0.2× 42 1.4k

Countries citing papers authored by Britt‐Marie Anderlid

Since Specialization
Citations

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

Fields of papers citing papers by Britt‐Marie Anderlid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Britt‐Marie Anderlid

This figure shows the co-authorship network connecting the top 25 collaborators of Britt‐Marie Anderlid. A scholar is included among the top collaborators of Britt‐Marie Anderlid 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 Britt‐Marie Anderlid. Britt‐Marie Anderlid 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.
Nordenskjöld, Agneta, Kristina Lagerstedt‐Robinson, Britt‐Marie Anderlid, & Johanna Lundin. (2023). Tissue specific trisomy 15 mosaicism associated with urogenital malformations. European Journal of Medical Genetics. 66(10). 104824–104824. 2 indexed citations
2.
Tabet, Anne Claude, María Clara Bonaglia, Britt‐Marie Anderlid, et al.. (2023). Consensus recommendations on counselling in Phelan-McDermid syndrome, with special attention to recurrence risk and to ring chromosome 22. European Journal of Medical Genetics. 66(7). 104773–104773. 8 indexed citations
3.
Becker, Martin, Francesca Mastropasqua, Simon Maier, et al.. (2020). Presynaptic dysfunction in CASK-related neurodevelopmental disorders. Translational Psychiatry. 10(1). 312–312. 22 indexed citations
4.
Schuster, Jens, Maria Sobol, Ambrin Fatima, et al.. (2019). Mowat-Wilson syndrome: Generation of two human iPS cell lines (UUIGPi004A and UUIGPi005A) from siblings with a truncating ZEB2 gene variant. Stem Cell Research. 39. 101518–101518. 5 indexed citations
5.
Kvarnung, Malin, Mansoureh Shahsavani, Fulya Taylan, et al.. (2019). Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186. Frontiers in Genetics. 10. 896–896. 5 indexed citations
6.
Nordgren, Ann, et al.. (2018). Reversed gender ratio of autism spectrum disorder in Smith-Magenis syndrome. Molecular Autism. 9(1). 1–1. 33 indexed citations
7.
Anderlid, Britt‐Marie, Charlotte Willfors, Bhooma Thiruvahindrapuram, et al.. (2018). Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders. Twin Research and Human Genetics. 21(1). 1–11. 19 indexed citations
8.
Schoot, Vyne van der, Sonja de Munnik, Hanka Venselaar, et al.. (2018). Toward clinical and molecular understanding of pathogenic variants in the ZBTB18 gene. Molecular Genetics & Genomic Medicine. 6(3). 393–400. 18 indexed citations
9.
10.
Wales, Jeremy, et al.. (2016). X-linked Malformation and Cochlear Implantation. Otology & Neurotology. 38(1). 38–46. 24 indexed citations
11.
Breckpot, Jeroen, Britt‐Marie Anderlid, Yasemin Alanay, et al.. (2015). Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate. European Journal of Human Genetics. 24(1). 51–58. 20 indexed citations
12.
Anderlid, Britt‐Marie, et al.. (2013). Small mosaic deletion encompassing the snoRNAs and SNURF‐SNRPN results in an atypical Prader–Willi syndrome phenotype. American Journal of Medical Genetics Part A. 164(2). 425–431. 21 indexed citations
13.
Anderlid, Britt‐Marie, et al.. (2012). [Lactose intolerance in children is an overdiagnosed condition. Risk of missing intestinal diseases such as IBD and celiac disease].. PubMed. 109(5). 218–21. 4 indexed citations
14.
Vergult, Sarah, Bart Loeys, Stanislas Lyonnet, et al.. (2011). Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions. European Journal of Human Genetics. 19(10). 1032–1037. 8 indexed citations
15.
Gustavsson, Peter, Kristina Lagerstedt‐Robinson, Elisabeth Blennow, et al.. (2010). Chimerism resulting from parthenogenetic activation and dispermic fertilization. American Journal of Medical Genetics Part A. 152A(9). 2277–2286. 24 indexed citations
16.
Bremer, Anna, Jacqueline Schoumans, Magnus Nordenskjöld, Britt‐Marie Anderlid, & MaiBritt Giacobini. (2009). An interstitial deletion of 7.1 Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities. European Journal of Medical Genetics. 52(5). 358–362. 19 indexed citations
17.
Zhou, Xiaolei, MaiBritt Giacobini, Britt‐Marie Anderlid, et al.. (2007). Association of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD). American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(3). 351–354. 29 indexed citations
18.
Schoumans, Jacqueline, Johan Staaf, Göran Jönsson, et al.. (2005). Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith–Magenis syndrome minimum deletion to ~650 kb. European Journal of Medical Genetics. 48(3). 290–300. 11 indexed citations
19.
Anderlid, Britt‐Marie, Sigrid Sahlén, Jacqueline Schoumans, et al.. (2001). Detailed characterization of 12 supernumerary ring chromosomes using micro‐FISH and search for uniparental disomy. American Journal of Medical Genetics. 99(3). 223–233. 64 indexed citations
20.
Anderlid, Britt‐Marie, et al.. (1999). Subtelomeric rearrangements detected by FISH in patients with idiopatic mental retardation. The American Journal of Human Genetics. 65. 6 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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