Ingegerd Fransson

3.1k total citations
22 papers, 1.2k citations indexed

About

Ingegerd Fransson is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Ingegerd Fransson has authored 22 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Neurology. Recurrent topics in Ingegerd Fransson's work include interferon and immune responses (3 papers), Signaling Pathways in Disease (3 papers) and Craniofacial Disorders and Treatments (3 papers). Ingegerd Fransson is often cited by papers focused on interferon and immune responses (3 papers), Signaling Pathways in Disease (3 papers) and Craniofacial Disorders and Treatments (3 papers). Ingegerd Fransson collaborates with scholars based in Sweden, United States and Finland. Ingegerd Fransson's co-authors include Jan P. Dumanski, Darek Kedra, Juha Kere, Ian Dunham, Myriam Peyrard, Nikolaus Blin, Josiane Grosgeorge, Nicolas Sirvent, Nils Mandahl and Gabriella Sozzi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Ingegerd Fransson

22 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
Ingegerd Fransson Sweden 18 520 352 312 220 170 22 1.2k
A.M.W. van den Ouweland Netherlands 17 327 0.6× 422 1.2× 147 0.5× 140 0.6× 148 0.9× 27 1.0k
Hiroshi Kawame Japan 23 1.1k 2.2× 634 1.8× 214 0.7× 163 0.7× 139 0.8× 66 2.1k
Paolo Simi Italy 22 633 1.2× 571 1.6× 201 0.6× 243 1.1× 64 0.4× 82 1.4k
Eul‐Ju Seo South Korea 24 796 1.5× 417 1.2× 157 0.5× 285 1.3× 98 0.6× 116 1.9k
Trijnie Dijkhuizen Netherlands 24 801 1.5× 677 1.9× 382 1.2× 196 0.9× 82 0.5× 62 1.6k
Jeroen Knijnenburg Netherlands 22 473 0.9× 578 1.6× 151 0.5× 153 0.7× 150 0.9× 47 1.4k
Jennifer Ivanovich United States 17 622 1.2× 377 1.1× 247 0.8× 311 1.4× 58 0.3× 34 1.8k
J.G. Seidman United States 20 634 1.2× 244 0.7× 169 0.5× 114 0.5× 61 0.4× 35 1.3k
Shirley Soukup United States 23 774 1.5× 556 1.6× 366 1.2× 177 0.8× 138 0.8× 66 1.7k
Luba Trakhtenbrot Israel 19 1.1k 2.1× 284 0.8× 87 0.3× 232 1.1× 86 0.5× 54 1.8k

Countries citing papers authored by Ingegerd Fransson

Since Specialization
Citations

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

Fields of papers citing papers by Ingegerd Fransson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingegerd Fransson

This figure shows the co-authorship network connecting the top 25 collaborators of Ingegerd Fransson. A scholar is included among the top collaborators of Ingegerd Fransson 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 Ingegerd Fransson. Ingegerd Fransson 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.
Bruce, R. Douglas, Katariina Hannula‐Jouppi, Ingegerd Fransson, et al.. (2009). Submicroscopic genomic alterations in Silver–Russell syndrome and Silver–Russell-like patients. Journal of Medical Genetics. 47(12). 816–822. 52 indexed citations
2.
Pegelow, Marie, Myriam Peyrard‐Janvid, Marco Zucchelli, et al.. (2008). Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes. European Journal of Orthodontics. 30(2). 169–175. 37 indexed citations
3.
Salmela, Elina, Tuuli Lappalainen, Ingegerd Fransson, et al.. (2008). Genome-Wide Analysis of Single Nucleotide Polymorphisms Uncovers Population Structure in Northern Europe. PLoS ONE. 3(10). e3519–e3519. 98 indexed citations
4.
Anthoni, Heidi, Marco Zucchelli, Hans Matsson, et al.. (2007). A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Human Molecular Genetics. 16(6). 667–677. 91 indexed citations
5.
Peyrard‐Janvid, Myriam, Marie Pegelow, Hannele Koillinen, et al.. (2005). Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome. European Journal of Human Genetics. 13(12). 1261–1267. 18 indexed citations
6.
Ali, Haider, Carl E.G. Bruder, Ingegerd Fransson, et al.. (2003). Strong conservation of the human NF2 locus based on sequence comparison in five species. Mammalian Genome. 14(8). 526–536. 5 indexed citations
7.
Grigelioniené, Giedré, Jacqueline Schoumans, Sten A. Ivarsson, et al.. (2001). Analysis of short stature homeobox-containing gene ( SHOX ) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity. Human Genetics. 109(5). 551–558. 38 indexed citations
8.
Kiss, Hajnalka, Darek Kedra, Ying Yang, et al.. (1999). A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3. Human Genetics. 105(6). 552–559. 58 indexed citations
9.
Yang, Ying, Hajnalka Kiss, Maria Kost‐Alimova, et al.. (1999). A 1-Mb PAC Contig Spanning the Common Eliminated Region 1 (CER1) in Microcell Hybrid-Derived SCID Tumors. Genomics. 62(2). 147–155. 25 indexed citations
10.
Seroussi, Eyal, Darek Kedra, Maria Kost‐Alimova, et al.. (1999). TOM1Genes Map to Human Chromosome 22q13.1 and Mouse Chromosome 8C1 and Encode Proteins Similar to the Endosomal Proteins HGS and STAM. Genomics. 57(3). 380–388. 17 indexed citations
11.
Kedra, Darek, Huaqin Pan, Eyal Seroussi, et al.. (1998). Characterization of the human synaptogyrin gene family. Human Genetics. 103(2). 131–141. 52 indexed citations
12.
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
13.
Kedra, Darek, Eyal Seroussi, Ingegerd Fransson, et al.. (1997). The germinal center kinase gene and a novel CDC25-like gene are located in the vicinity of the PYGM gene on 11q13. Human Genetics. 100(5-6). 611–619. 26 indexed citations
14.
Peyrard, Myriam, Ingegerd Fransson, Sandra W. Clifton, et al.. (1997). Characterization of the mouse beta-prime adaptin gene; cDNA sequence, genomic structure, and chromosomal localization. Mammalian Genome. 8(9). 651–656. 6 indexed citations
15.
Pédeutour, Florence, Nicolas Sirvent, Josiane Grosgeorge, et al.. (1997). Deregulation of the platelet-derived growth factor β-chain gene via fusion with collagen gene COL1A1 in dermatof ibrosarcoma protuberans and giant-cell fibroblastoma. Nature Genetics. 15(1). 95–98. 364 indexed citations
16.
Peyrard, Myriam, Huaqin Pan, Darek Kedra, et al.. (1996). Structure of the Promoter and Genomic Organization of the Human β′-Adaptin Gene (BAM22) from Chromosome 22q12. Genomics. 36(1). 112–117. 19 indexed citations
17.
Peyrard, Myriam, Ingegerd Fransson, Ya‐Gang Xie, et al.. (1994). Characterization of a new member of the human /-adaptin gene family from chromosome 22q12, a candidate meningioma gene. Human Molecular Genetics. 3(8). 1393–1399. 81 indexed citations
18.
Ruttledge, Martin, Ya‐Gang Xie, Fei‐Yu Han, et al.. (1994). Physical Mapping of the NF2/Meningioma Region on Human Chromosome 22q12. Genomics. 19(1). 52–59. 11 indexed citations
19.
Rose, Timothy M., Ingegerd Fransson, Barbro Werelius, et al.. (1993). The Genes for Oncostatin M (OSM) and Leukemia Inhibitory Factor (LIF) Are Tightly Linked on Human Chromosome 22. Genomics. 17(1). 136–140. 39 indexed citations
20.
Han, Fei‐Yu, Martin Ruttledge, Ingegerd Fransson, et al.. (1993). Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12. Human Molecular Genetics. 2(9). 1361–1368. 22 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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