Pelle Sahlin

893 total citations
20 papers, 651 citations indexed

About

Pelle Sahlin is a scholar working on Surgery, Genetics and Molecular Biology. According to data from OpenAlex, Pelle Sahlin has authored 20 papers receiving a total of 651 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Surgery, 9 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Pelle Sahlin's work include Craniofacial Disorders and Treatments (8 papers), Cleft Lip and Palate Research (8 papers) and Ear and Head Tumors (5 papers). Pelle Sahlin is often cited by papers focused on Craniofacial Disorders and Treatments (8 papers), Cleft Lip and Palate Research (8 papers) and Ear and Head Tumors (5 papers). Pelle Sahlin collaborates with scholars based in Sweden, United States and Finland. Pelle Sahlin's co-authors include Göran Stenman, Claes Lauritzen, Michael Oldridge, Steven A. Wall, Andrew O.M. Wilkie, Dominique M. Moloney, Joachim Mark, Claire Sanger, Charles R. Davis and Jyri Hukki and has published in prestigious journals such as Nature Genetics, Molecular and Cellular Biology and Journal of neurosurgery.

In The Last Decade

Pelle Sahlin

19 papers receiving 619 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pelle Sahlin Sweden 12 371 245 203 74 61 20 651
Tony Huynh Australia 14 184 0.5× 252 1.0× 137 0.7× 97 1.3× 31 0.5× 42 608
Marie‐Ange Delrue France 15 258 0.7× 291 1.2× 106 0.5× 28 0.4× 75 1.2× 30 590
C Lecointre France 10 203 0.5× 336 1.4× 55 0.3× 27 0.4× 35 0.6× 15 506
J.R. Korenberg United States 10 155 0.4× 385 1.6× 52 0.3× 38 0.5× 56 0.9× 19 590
Pilar Magoulas United States 15 290 0.8× 383 1.6× 73 0.4× 41 0.6× 53 0.9× 24 727
Claire Deloche France 11 192 0.5× 123 0.5× 67 0.3× 116 1.6× 69 1.1× 14 818
Luc Lemli United States 9 243 0.7× 500 2.0× 407 2.0× 44 0.6× 44 0.7× 12 822
Frederick V. Schaefer United States 13 130 0.4× 231 0.9× 30 0.1× 65 0.9× 45 0.7× 29 506
E. Vámos Belgium 11 205 0.6× 156 0.6× 78 0.4× 17 0.2× 20 0.3× 23 420
Esperanza Berensztein Argentina 14 236 0.6× 316 1.3× 116 0.6× 15 0.2× 19 0.3× 34 598

Countries citing papers authored by Pelle Sahlin

Since Specialization
Citations

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

Fields of papers citing papers by Pelle Sahlin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pelle Sahlin

This figure shows the co-authorship network connecting the top 25 collaborators of Pelle Sahlin. A scholar is included among the top collaborators of Pelle Sahlin 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 Pelle Sahlin. Pelle Sahlin 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.
Bergman, Annika, Pelle Sahlin, Monica Emanuelsson, et al.. (2009). Germline mutation screening of the Saethre-Chotzen-associated genes TWIST1 and FGFR3 in families with BRCA1/2-negative breast cancer. Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery. 1–5.
2.
Bergman, Annika, Pelle Sahlin, Monica Emanuelsson, et al.. (2009). Germline mutation screening of the Saethre-Chotzen-associated genesTWIST1andFGFR3in families withBRCA1/2-negative breast cancer. Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery. 43(5). 251–255. 1 indexed citations
3.
Davis, Charles R., et al.. (2008). Spring-Assisted Cranioplasty vs Pi-Plasty for Sagittal Synostosis-A Long Term Follow-Up Study. Journal of Craniofacial Surgery. 19(1). 59–64. 85 indexed citations
4.
Sahlin, Pelle, et al.. (2007). Women with Saethre‐Chotzen syndrome are at increased risk of breast cancer. Genes Chromosomes and Cancer. 46(7). 656–660. 29 indexed citations
5.
Gewalli, Fredrik, et al.. (2003). ORBITAL FRACTURES IN CRANIOFACIAL TRAUMA IN GÖTEBORG: TRAUMA SCORING, OPERATIVE TECHNIQUES, AND OUTCOME. Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery. 37(2). 69–74. 14 indexed citations
6.
Hukki, Jyri, Terhi Karaharju‐Suvanto, Kirsti Hurmerinta, & Pelle Sahlin. (2002). Pinhole osteotomy in distraction osteogenesis – a technical note. Journal of Cranio-Maxillofacial Surgery. 30(3). 144–147. 3 indexed citations
7.
Kushnerenko, Elena, et al.. (2002). Auditory ERPs Reveal Brain Dysfunction in Infants With Plagiocephaly. Journal of Craniofacial Surgery. 13(4). 520–525. 65 indexed citations
8.
Gewalli, Fredrik, Pelle Sahlin, Hans Friede, et al.. (2001). Dynamic cranioplasty for brachycephaly in Apert syndrome: long-term follow-up study. Journal of neurosurgery. 94(5). 757–764. 9 indexed citations
9.
Gewalli, Fredrik, et al.. (2001). Mental Development After Modified ?? Procedure: Dynamic Cranioplasty for Sagittal Synostosis. Annals of Plastic Surgery. 46(4). 415–420. 41 indexed citations
10.
Lauritzen, Claes, et al.. (1998). Reuse of Tumorous Calvarial Bone After Gamma Irradiation. Journal of Craniofacial Surgery. 9(5). 459–463. 5 indexed citations
11.
Sahlin, Pelle, et al.. (1997). Cytogenetic and fluorescence in situ hybridization analyses of a microcystic adnexal carcinoma with del(6)(q23q25). Cancer Genetics and Cytogenetics. 98(2). 106–110. 7 indexed citations
12.
Moloney, Dominique M., Michael Oldridge, Steven A. Wall, et al.. (1996). Exclusive paternal origin of new mutations in Apert syndrome. Nature Genetics. 13(1). 48–53. 217 indexed citations
13.
Sahlin, Pelle, Joachim Mark, & Göran Stenman. (1995). Detection of hidden structural rearrangements by fish in pleomorphic adenomas. Genes Chromosomes and Cancer. 12(2). 81–86. 8 indexed citations
14.
Sahlin, Pelle, Joachim Mark, & Göran Stenman. (1994). Submicroscopic deletions of 3p sequences in pleomorphic adenomas with t(3;8)(p21;q12). Genes Chromosomes and Cancer. 10(4). 256–261. 14 indexed citations
15.
Rüetschi, Ulla, Anita Dellsèn, Pelle Sahlin, et al.. (1993). Human 4‐hydroxyphenylpyruvate dioxygenase. European Journal of Biochemistry. 213(3). 1081–1089. 34 indexed citations
16.
Stenman, Göran, Pelle Sahlin, Joachim Mark, et al.. (1993). The 12q13‐q15 translocation breakpoints in pleomorphic adenoma and clear‐cell sarcoma of tendons and aponeuroses are different from that in myxoid liposarcoma. Genes Chromosomes and Cancer. 7(3). 178–180. 13 indexed citations
17.
Sahlin, Pelle, Joachim Mark, & Göran Stenman. (1992). INT1 and GLI genes are not rearranged or amplified in benign pleomorphic adenomas with chromosome abnormalities of 12q13–15. Cancer Genetics and Cytogenetics. 58(1). 85–88. 4 indexed citations
18.
19.
Stenman, Göran, Hiroaki Honda, Pelle Sahlin, et al.. (1991). Organization and Chromosomal Localization of the Human Platelet- Derived Endothelial Cell Growth Factor Gene. Molecular and Cellular Biology. 11(4). 2125–2132. 15 indexed citations
20.
Stenman, Göran, Jens Sandros, Anders Nordkvist, Joachim Mark, & Pelle Sahlin. (1991). Expression of the ERBB2 protein in benign and malignant salivary gland tumors. Genes Chromosomes and Cancer. 3(2). 128–135. 36 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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