Sverre Heim

896 total citations
16 papers, 706 citations indexed

About

Sverre Heim is a scholar working on Genetics, Pathology and Forensic Medicine and Hematology. According to data from OpenAlex, Sverre Heim has authored 16 papers receiving a total of 706 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Pathology and Forensic Medicine and 4 papers in Hematology. Recurrent topics in Sverre Heim's work include Genomic variations and chromosomal abnormalities (4 papers), Cancer Genomics and Diagnostics (4 papers) and Genetic factors in colorectal cancer (3 papers). Sverre Heim is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Cancer Genomics and Diagnostics (4 papers) and Genetic factors in colorectal cancer (3 papers). Sverre Heim collaborates with scholars based in Sweden, Denmark and Norway. Sverre Heim's co-authors include Felix Mitelman, Rolf Lundgren, Nils Mandahl, Janusz Limon, Nils Mandahl, Ulf Kristoffersson, Nikos Pandis, Georgia Bardi, Ragnhild A. Lothe and A.L. Børresen-Dale and has published in prestigious journals such as International Journal of Cancer, British Journal of Haematology and Genes Chromosomes and Cancer.

In The Last Decade

Sverre Heim

16 papers receiving 687 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sverre Heim Sweden	14	278	217	200	175	143	16	706
Bertil Johansson Sweden	10	297 1.1×	104 0.5×	126 0.6×	172 1.0×	207 1.4×	12	633
Montserrat Domènech Spain	17	317 1.1×	250 1.2×	117 0.6×	121 0.7×	259 1.8×	70	882
Ilse Chudoba Germany	16	436 1.6×	171 0.8×	91 0.5×	149 0.9×	410 2.9×	36	858
Max M. van Noesel Netherlands	16	445 1.6×	232 1.1×	137 0.7×	169 1.0×	68 0.5×	44	1.0k
S. Jani-Sait United States	11	406 1.5×	96 0.4×	189 0.9×	73 0.4×	69 0.5×	12	664
TS Ganesan United Kingdom	14	319 1.1×	91 0.4×	215 1.1×	75 0.4×	70 0.5×	23	942
Stéphanie Struski France	16	264 0.9×	76 0.4×	171 0.9×	84 0.5×	106 0.7×	30	596
Tarja Niini Finland	10	323 1.2×	122 0.6×	114 0.6×	92 0.5×	35 0.2×	15	567
T Flores Spain	9	232 0.8×	143 0.7×	124 0.6×	90 0.5×	36 0.3×	21	570
Nils Mandahl Sweden	15	253 0.9×	328 1.5×	94 0.5×	111 0.6×	137 1.0×	18	745

Countries citing papers authored by Sverre Heim

Since Specialization

Citations

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

Fields of papers citing papers by Sverre Heim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sverre Heim

This figure shows the co-authorship network connecting the top 25 collaborators of Sverre Heim. A scholar is included among the top collaborators of Sverre Heim 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 Sverre Heim. Sverre Heim is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Forestier, Erik, Bertil Johansson, Göran Gustafsson, et al.. (2000). Prognostic impact of karyotypic findings in childhood acute lymphoblastic leukaemia: a Nordic series comparing two treatment periods. British Journal of Haematology. 110(1). 147–153. 51 indexed citations

Pandis, Nikos, et al.. (1999). Karyotypic Evolution in Breast Carcinomas with i(1)(q10) and der(1;16)(q10;p10) as the Primary Chromosome Abnormality. Cancer Genetics and Cytogenetics. 113(2). 156–161. 23 indexed citations

Schrøder, Henrik Daa, et al.. (1999). Simple Numerical Chromosome Aberrations Characterize Pituitary Adenomas. Cancer Genetics and Cytogenetics. 114(2). 144–149. 17 indexed citations

Heim, Sverre, Georgia Bardi, Claus Fenger, et al.. (1998). Allelic imbalance and cytogenetic deletion of 1p in colorectal adenomas: A target region identified between DIS199 and DIS234. Genes Chromosomes and Cancer. 21(3). 185–194. 20 indexed citations

Fadl-Elmula, Imad, Ludmila Gorunova, Nils Mandahl, Peter Elfving, & Sverre Heim. (1998). Chromosome abnormalities in squamous cell carcinoma of the urethra. Genes Chromosomes and Cancer. 23(1). 72–73. 1 indexed citations

Bardi, Georgia, Luis A. Parada, Nikos Pandis, et al.. (1997). Cytogenetic findings in metastases from colorectal cancer. International Journal of Cancer. 72(4). 604–607. 16 indexed citations

Pejović, Tanja, Constantin S. Iosif, Felix Mitelman, & Sverre Heim. (1996). Karyotypic characteristics of borderline malignant tumors of the ovary: Trisomy 12, trisomy 7, and r(1) as nonrandom features. Cancer Genetics and Cytogenetics. 92(2). 95–98. 25 indexed citations

Lothe, Ragnhild A., Ritva Karhu, Nils Mandahl, et al.. (1996). Gain of 17q24-qter detected by comparative genomic hybridization in malignant tumors from patients with von Recklinghausen's neurofibromatosis.. PubMed. 56(20). 4778–81. 65 indexed citations

Johansson, Bertil, Georgia Bardi, Nikos Pandis, et al.. (1994). Karyotypic pattern of pancreatic adenocarcinomas correlates with survival and tumour grade. International Journal of Cancer. 58(1). 8–13. 26 indexed citations

10.

Dietrich, Claudia U., Nikos Pandis, P. Bjerre, Henrik Daa Schrøder, & Sverre Heim. (1993). Simple numerical chromosome aberrations in two pituitary adenomas. Cancer Genetics and Cytogenetics. 69(2). 118–121. 17 indexed citations

11.

Higashi, Koichiro, et al.. (1992). Supernumerary ring marker chromosome as a secondary rearrangement in a parapharyngeal lipoma with t(10;12)(q25;q15) as the primary karyotypic abnormality. Cancer Genetics and Cytogenetics. 64(2). 163–165. 9 indexed citations

12.

Mitelman, Felix & Sverre Heim. (1992). Quantitative acute leukemia cytogenetics. Genes Chromosomes and Cancer. 5(1). 57–66. 104 indexed citations

13.

Lundgren, Rolf, et al.. (1992). Cytogenetic analysis of 57 primary prostatic adenocarcinomas. Genes Chromosomes and Cancer. 4(1). 16–24. 145 indexed citations

14.

Heim, Sverre. (1992). Cytogenetic findings in primary and secondary MDS. Leukemia Research. 16(1). 43–46. 81 indexed citations

15.

Bardi, Georgia, Nikos Pandis, Nils Mandahl, et al.. (1991). Chromosomal abnormalities in giant cell tumors of bone. Cancer Genetics and Cytogenetics. 57(2). 161–167. 27 indexed citations

16.

Lundgren, Rolf, Ulf Kristoffersson, Sverre Heim, Nils Mandahl, & Felix Mitelman. (1988). Multiple structural chromosome rearrangements, including del(7q) and del(10q), in an adenocarcinoma of the prostate. Cancer Genetics and Cytogenetics. 35(1). 103–108. 79 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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