Sigrid Sahlén

688 total citations
21 papers, 466 citations indexed

About

Sigrid Sahlén is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Sigrid Sahlén has authored 21 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Plant Science. Recurrent topics in Sigrid Sahlén's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (6 papers) and Prenatal Screening and Diagnostics (3 papers). Sigrid Sahlén is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (6 papers) and Prenatal Screening and Diagnostics (3 papers). Sigrid Sahlén collaborates with scholars based in Sweden, Belgium and Denmark. Sigrid Sahlén's co-authors include Elisabeth Blennow, Jacqueline Schoumans, Magnus Nordenskjöld, Ann Nordgren, Britt‐Marie Anderlid, Göran Annerén, Mihailo Vujic, Mårten Kyllerman, Bengt Hagberg and Helena Malmgren and has published in prestigious journals such as British Journal of Haematology, Genomics and Mutation research. Fundamental and molecular mechanisms of mutagenesis.

In The Last Decade

Sigrid Sahlén

21 papers receiving 444 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sigrid Sahlén Sweden 11 327 243 148 115 52 21 466
G. Bourrouillou France 14 398 1.2× 279 1.1× 95 0.6× 146 1.3× 71 1.4× 40 587
Paolo Guanciali Franchi Italy 14 298 0.9× 220 0.9× 71 0.5× 80 0.7× 36 0.7× 31 484
Franca Bernardi Italy 10 246 0.8× 116 0.5× 128 0.9× 93 0.8× 34 0.7× 13 367
Jean‐Louis Taillemite France 12 247 0.8× 193 0.8× 98 0.7× 80 0.7× 23 0.4× 15 368
Rina Schmidt United States 12 257 0.8× 164 0.7× 74 0.5× 109 0.9× 40 0.8× 20 430
Steven Schonberg United States 13 147 0.4× 247 1.0× 39 0.3× 111 1.0× 32 0.6× 19 422
G. R. Stalder Switzerland 12 256 0.8× 146 0.6× 87 0.6× 98 0.9× 19 0.4× 21 387
Berta Santesson Sweden 12 171 0.5× 160 0.7× 82 0.6× 78 0.7× 49 0.9× 23 410
I. López Pajares Spain 12 316 1.0× 286 1.2× 94 0.6× 106 0.9× 16 0.3× 27 493
Rethoré Mo France 14 460 1.4× 190 0.8× 150 1.0× 212 1.8× 40 0.8× 63 561

Countries citing papers authored by Sigrid Sahlén

Since Specialization
Citations

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

Fields of papers citing papers by Sigrid Sahlén

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sigrid Sahlén

This figure shows the co-authorship network connecting the top 25 collaborators of Sigrid Sahlén. A scholar is included among the top collaborators of Sigrid Sahlén 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 Sigrid Sahlén. Sigrid Sahlén 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.
Zucchelli, Marco, Susanne Ström, Frida Holm, et al.. (2012). In Vivo Differentiated Human Embryonic Stem Cells Can Acquire Chromosomal Aberrations More Frequently Than In Vitro During the Same Period. Stem Cells and Development. 21(18). 3363–3371. 5 indexed citations
2.
3.
Lindstrand, Anna, H Malmgren, Sigrid Sahlén, et al.. (2009). Detailed molecular and clinical characterization of three patients with 21q deletions. Clinical Genetics. 77(2). 145–154. 52 indexed citations
4.
Iwarsson, Erik, Sigrid Sahlén, & Ann Nordgren. (2009). Jumping translocation in a phenotypically normal male: A study of mosaicism in spermatozoa, lymphocytes, and fibroblasts. American Journal of Medical Genetics Part A. 149A(8). 1706–1711. 19 indexed citations
5.
Blennow, Elisabeth, et al.. (2008). Concurrent microdeletion and duplication of 22q11.2. Clinical Genetics. 74(1). 61–67. 11 indexed citations
6.
Lindstrand, Anna, H Malmgren, Sigrid Sahlén, et al.. (2008). Molecular cytogenetic characterization of a constitutional, highly complex intrachromosomal rearrangement of chromosome 1, with 14 breakpoints and a 0.5 Mb submicroscopic deletion. American Journal of Medical Genetics Part A. 146A(24). 3217–3222. 8 indexed citations
7.
Malmgren, Helena, et al.. (2007). Distal 3p deletion syndrome: Detailed molecular cytogenetic and clinical characterization of three small distal deletions and review. American Journal of Medical Genetics Part A. 143A(18). 2143–2149. 46 indexed citations
8.
Malmgren, H, Gunilla Malm, Sigrid Sahlén, Markus Karlsson, & Elisabeth Blennow. (2005). Molecular cytogenetic characterization of an insertional translocation, ins(6;7)(p25;q33q34): Deletion/duplication of 7q33‐34 and clinical correlations. American Journal of Medical Genetics Part A. 139A(1). 25–31. 5 indexed citations
9.
Nordgren, Ann, Mats Heyman, Sigrid Sahlén, et al.. (2002). Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G‐banding. European Journal Of Haematology. 68(1). 31–41. 45 indexed citations
10.
Malmgren, H, Sigrid Sahlén, José Inzunza, et al.. (2002). O-12. Single-cell comparative genomic hybridization analysis of human preimplantation embryos from patients with balanced structural chromosome aberrations undergoing PGD. Reproductive BioMedicine Online. 4. 14–15. 2 indexed citations
11.
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
12.
Anderlid, Britt‐Marie, Jacqueline Schoumans, Göran Annerén, et al.. (2001). Subtelomeric rearrangements detected in patients with idiopathic mental retardation. American Journal of Medical Genetics. 107(4). 275–284. 107 indexed citations
13.
Tapia‐Páez, Isabel, Kevin P. O'Brien, Maria Kost‐Alimova, et al.. (2000). Fine mapping of the constitutional translocation t(11;22)(q23;q11). Human Genetics. 106(5). 506–516. 18 indexed citations
14.
Nordgren, Ann, Filip Farnebo, Magnus Björkholm, et al.. (2000). Detailed characterization of a complex karyotype in a patient with primary plasma cell leukaemia using multicolour spectral karyotyping and micro-FISH. The Hematology Journal. 1(2). 95–101. 3 indexed citations
15.
16.
Peyrard, Myriam, et al.. (1998). Cloning, Expression Pattern, and Chromosomal Assignment to 16q23 of the Human γ-Adaptin Gene (ADTG). Genomics. 50(2). 275–280. 7 indexed citations
17.
Sahlén, Sigrid, et al.. (1993). Hprt activities and RNA phenotypes in 6-thioguanine resistant human T-lymphocytes. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 286(2). 209–215. 7 indexed citations
18.
Sahlén, Sigrid, et al.. (1993). A missense mutation in the hypoxanthine phosphoribosyltransferase gene in a pediatric patient with hyperuricemia. Acta Paediatrica. 82(10). 758–763. 4 indexed citations
19.
Hellgren, Dennis, Sigrid Sahlén, & Bo Lambert. (1990). Unequal SCE is a rare event in homologous recombination between duplicated neo gene fragments in CHO cells. Mutation Research Letters. 243(1). 75–80. 10 indexed citations
20.
Hellgren, Dennis, Sigrid Sahlén, & B. Lambert. (1989). Mutagen-induced recombination between stably integrated neo gene fragments in CHO and EM9 cells. Mutation Research Letters. 226(1). 1–8. 19 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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