Anna Hammarsjö

1.5k total citations
21 papers, 264 citations indexed

About

Anna Hammarsjö is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anna Hammarsjö has authored 21 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anna Hammarsjö's work include Congenital heart defects research (5 papers), Genomics and Rare Diseases (3 papers) and Renal and related cancers (3 papers). Anna Hammarsjö is often cited by papers focused on Congenital heart defects research (5 papers), Genomics and Rare Diseases (3 papers) and Renal and related cancers (3 papers). Anna Hammarsjö collaborates with scholars based in Sweden, Japan and United States. Anna Hammarsjö's co-authors include Giedré Grigelioniené, Gen Nishimura, Ann Nordgren, Anna Lindstrand, Atsuhiko Handa, Eva Horemuzova, Helena Malmgren, Tatsuya Kobayashi, Kristina Lagerstedt‐Robinson and Hiroshi Suzuki and has published in prestigious journals such as Nature Medicine, PLoS ONE and Scientific Reports.

In The Last Decade

Anna Hammarsjö

20 papers receiving 262 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Hammarsjö Sweden 9 164 115 59 30 27 21 264
Sabina Benko France 5 273 1.7× 146 1.3× 103 1.7× 20 0.7× 12 0.4× 6 353
Glenda M. Beaman United Kingdom 9 129 0.8× 86 0.7× 26 0.4× 19 0.6× 34 1.3× 20 278
Dagmar Kruspe Germany 7 163 1.0× 65 0.6× 23 0.4× 23 0.8× 5 0.2× 8 225
Marina Manvelyan Germany 13 190 1.2× 228 2.0× 43 0.7× 93 3.1× 23 0.9× 22 402
Sara Benito‐Sanz Spain 14 395 2.4× 501 4.4× 53 0.9× 29 1.0× 14 0.5× 22 637
Vera Riehmer Germany 7 142 0.9× 54 0.5× 46 0.8× 23 0.8× 5 0.2× 11 229
Antti Railo Finland 8 244 1.5× 68 0.6× 16 0.3× 26 0.9× 3 0.1× 13 305
Essam Al Ageeli Saudi Arabia 11 237 1.4× 110 1.0× 169 2.9× 18 0.6× 9 0.3× 29 388
Kristen L. Sund United States 9 193 1.2× 171 1.5× 19 0.3× 56 1.9× 11 0.4× 15 326
Anna Sowińska‐Seidler Poland 13 254 1.5× 237 2.1× 23 0.4× 74 2.5× 34 1.3× 38 409

Countries citing papers authored by Anna Hammarsjö

Since Specialization
Citations

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

Fields of papers citing papers by Anna Hammarsjö

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Hammarsjö

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Hammarsjö. A scholar is included among the top collaborators of Anna Hammarsjö 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 Anna Hammarsjö. Anna Hammarsjö 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.
Hammarsjö, Anna, Peter Conner, Nikos Papadogiannakis, et al.. (2025). Genome sequencing in a cohort of 32 fetuses with genetic skeletal disorders. European Journal of Human Genetics. 33(11). 1474–1483. 1 indexed citations
2.
3.
Swolin‐Eide, Diana, Anna Hammarsjö, Jesper Eisfeldt, et al.. (2024). Structural Variants in COL1A1 and COL1A2 in Osteogenesis Imperfecta. American Journal of Medical Genetics Part A. 197(3). e63935–e63935. 1 indexed citations
4.
Gregersen, Pernille Axél, Anna Hammarsjö, Nis Brix, et al.. (2024). Compound heterozygosity for two variants in BMP5 in human skeletal dysostosis with atrioventricular septal defect. Clinical Genetics. 107(1). 78–82. 1 indexed citations
5.
Pettersson, Maria, Dora Dias‐Santagata, Daniel Nilsson, et al.. (2023). Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome. Frontiers in Genetics. 14. 1174046–1174046. 5 indexed citations
6.
Pettersson, Maria, Anna Hammarsjö, Ann Nordgren, et al.. (2023). The cost-effectiveness of whole genome sequencing in neurodevelopmental disorders. Scientific Reports. 13(1). 6904–6904. 17 indexed citations
7.
Nilsson, Daniel, Martin Engvall, Helena Malmgren, et al.. (2023). Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders. Frontiers in Neurology. 14. 1170005–1170005. 4 indexed citations
8.
Hammarsjö, Anna, Ritsuko K. Pooh, Osamu Shimokawa, et al.. (2023). Compound heterozygous variants in RAB34 in a rare skeletal ciliopathy syndrome. Clinical Genetics. 105(1). 87–91. 2 indexed citations
9.
Krstić, Jelena, Fatemah Rezayee, Leonie Saft, et al.. (2023). Case Report: Whole genome sequencing identifies CCDC88C as a novel JAK2 fusion partner in pediatric T-cell acute lymphoblastic leukemia. Frontiers in Pediatrics. 10. 1082986–1082986. 1 indexed citations
10.
Jacob, Prince, Cecilie F. Rustad, V. Reid Sutton, et al.. (2023). Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13. npj Genomic Medicine. 8(1). 39–39. 1 indexed citations
11.
Muñoz, Daniel Martín, Anne K. Örtqvist, Maria Pettersson, et al.. (2023). Polymicrogyria: epidemiology, imaging, and clinical aspects in a population-based cohort. Brain Communications. 5(4). fcad213–fcad213. 5 indexed citations
12.
Shvedova, Maria, Yutaro Mihara, Jun Akiba, et al.. (2022). A hypomorphic variant in the translocase of the outer mitochondrial membrane complex subunit TOMM7 causes short stature and developmental delay. Human Genetics and Genomics Advances. 4(1). 100148–100148. 12 indexed citations
13.
Horemuzova, Eva, et al.. (2022). Case Report: Inversion of LMX1B - A Novel Cause of Nail-Patella Syndrome in a Swedish Family and a Longtime Follow-Up. Frontiers in Endocrinology. 13. 862908–862908. 1 indexed citations
14.
Handa, Atsuhiko, et al.. (2020). Skeletal ciliopathies: a pattern recognition approach. Japanese Journal of Radiology. 38(3). 193–206. 33 indexed citations
15.
Grigelioniené, Giedré, Hiroshi Suzuki, Fulya Taylan, et al.. (2019). Gain-of-function mutation of microRNA-140 in human skeletal dysplasia. Nature Medicine. 25(4). 583–590. 70 indexed citations
16.
Pettersson, Maria, Raquel Vaz, Anna Hammarsjö, et al.. (2018). Alu-Alu mediated intragenic duplications in IFT81 and MATN3 are associated with skeletal dysplasias. Human Mutation. 39(10). 1456–1467. 11 indexed citations
17.
Tham, Emma, Erik A. Eklund, Anna Hammarsjö, et al.. (2015). A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach–Nishimura skeletal dysplasia due to pathogenic variants in ALG9. European Journal of Human Genetics. 24(2). 198–207. 26 indexed citations
18.
Lagerstedt‐Robinson, Kristina, Helena Malmgren, Anna Hammarsjö, et al.. (2013). GSTM1 Gene Expression Correlates to Leiomyoma Volume Regression in Response to Mifepristone Treatment. PLoS ONE. 8(12). e80114–e80114. 24 indexed citations
19.
Lundin, Johanna, Cilla Söderhäll, Anna Hammarsjö, et al.. (2010). 22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment. European Journal of Medical Genetics. 53(2). 61–65. 32 indexed citations
20.
Nordenskjöld, Agneta, Johanna Lundin, Cilla Söderhäll, et al.. (2010). 22q11.2 Microduplication in Two Patients with Bladder Exstrophy and Hearing Impairment. Journal of Pediatric Urology. 6. S20–S21. 1 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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