Berta Santesson

539 total citations
23 papers, 410 citations indexed

About

Berta Santesson is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Berta Santesson has authored 23 papers receiving a total of 410 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Plant Science. Recurrent topics in Berta Santesson's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Chromosomal and Genetic Variations (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Berta Santesson is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Chromosomal and Genetic Variations (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Berta Santesson collaborates with scholars based in Sweden, United States and Norway. Berta Santesson's co-authors include J.A. Böök, PER ZETTERQVIST, Kerstin Lindahl‐Kiessling, Anita Mattsson, K. H. Gustavson, L. Atkins, Hartmut Voss, Valdemar Skoog, Theodor Weber and Bengt Hagberg and has published in prestigious journals such as The Lancet, Journal of Cell Science and Experimental Cell Research.

In The Last Decade

Berta Santesson

21 papers receiving 347 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Berta Santesson Sweden	12	171	160	82	78	60	23	410
Cantú Jm Mexico	12	259 1.5×	165 1.0×	83 1.0×	104 1.3×	15 0.3×	67	405
P Colombiès France	12	150 0.9×	127 0.8×	75 0.9×	93 1.2×	12 0.2×	64	438
J Philip Denmark	6	183 1.1×	129 0.8×	56 0.7×	53 0.7×	9 0.1×	13	302
Drew Duckett United Kingdom	9	249 1.5×	142 0.9×	63 0.8×	128 1.6×	14 0.2×	23	353
J. P. M. Geraedts Netherlands	11	153 0.9×	104 0.7×	77 0.9×	105 1.3×	16 0.3×	22	422
Rina Schmidt United States	12	257 1.5×	164 1.0×	74 0.9×	109 1.4×	17 0.3×	20	430
Paolo Guanciali Franchi Italy	14	298 1.7×	220 1.4×	71 0.9×	80 1.0×	22 0.4×	31	484
Roberto Coco Argentina	12	401 2.3×	213 1.3×	143 1.7×	156 2.0×	9 0.1×	45	531
V. Sele Denmark	13	212 1.2×	136 0.8×	24 0.3×	60 0.8×	34 0.6×	26	477
Sugandhi A. Tharapel United States	10	215 1.3×	83 0.5×	94 1.1×	142 1.8×	21 0.3×	19	337

Countries citing papers authored by Berta Santesson

Since Specialization

Citations

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

Fields of papers citing papers by Berta Santesson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Berta Santesson

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

All Works

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20 of 20 papers shown

Atkins, Leonard & Berta Santesson. (2009). THE PATTERN OF DNA SYNTHESIS IN THE CHOMOSOMES OF HUMAN CELLS CONTAINING AN ISOCHROMOSOME FOR THE LONG ARM OF AN X CHROMOSOME. Hereditas. 51(1). 67–73. 2 indexed citations

Atkins, Leonard, J.A. Böök, & Berta Santesson. (2009). CHROMOSOME DNA SYNTHESIS IN THE CELLS OF A HUMAN TRIPLOID/DIPLOID MOSAIC. Hereditas. 55(1). 55–67.

Atkins, Leonard & Berta Santesson. (2009). CHROMOSOME DNA SYNTHESIS IN CULTURED NORMAL HUMAN FEMALE SKIN CELLS. Hereditas. 55(1). 39–46. 1 indexed citations

Santesson, Berta, Jon Jonasson, Kenneth Nilsson, & Kerstin Lindahl‐Kiessling. (2008). Modulation of SCE frequencies in cell lines derived from human B and T lymphocytes. Hereditas. 98(2). 175–180.

Santesson, Berta, et al.. (1985). The gene cluster for human U2 RNA is located on chromosome 17q21. Experimental Cell Research. 159(2). 473–478. 12 indexed citations

Jonasson, Jon, Berta Santesson, & Amy R. Strom. (1980). Analysis of sister-chromatid exchanges and tumorigenicity in cell hybrids. Journal of Cell Science. 42(1). 117–126. 3 indexed citations

Santesson, Berta, Kerstin Lindahl‐Kiessling, & Anita Mattsson. (1979). SCE in B and T lymphocytes. Possible implications for Bloom's syndrome. Clinical Genetics. 16(2). 133–135. 68 indexed citations

Bengtsson, B., et al.. (1974). Male pseudohermaphroditism with 45X/46XYq‐ mosaicism in a pair of monozygotic twins. Clinical Genetics. 5(2). 133–143. 7 indexed citations

Weber, Theodor, Berta Santesson, & Valdemar Skoog. (1973). The Activation of Fetal Lymphocytes. Scandinavian Journal of Haematology. 11(3). 177–183. 15 indexed citations

10.

Santesson, Berta, J.A. Böök, & B. Kjessler. (1973). THE MORTALITY OF HUMAN XO EMBRYOS. Reproduction. 34(1). 51–55. 2 indexed citations

11.

Santesson, Berta, J.A. Böök, & K.‐H. Gustavson. (1972). DNA synthesis of human XYY cells. Clinical Genetics. 3(1). 73–81. 4 indexed citations

12.

Gustavson, K. H., et al.. (1972). Three non‐mongoloid patients of similar phenotype with an extra G‐like chromosome. Clinical Genetics. 3(2). 135–146. 24 indexed citations

13.

Lindahl‐Kiessling, Kerstin, et al.. (1970). Chromosome and chromatid-type aberrations induced by cobalt60 irradiation and tritiated uridine in human leukocyte cultures. Chromosoma. 31(3). 280–284. 8 indexed citations

14.

Santesson, Berta, et al.. (1969). KARYOTYPING HUMAN AMNIOTIC-FLUID CELLS. The Lancet. 294(7629). 1067–1068. 16 indexed citations

15.

Böök, J.A., B. Kjessler, & Berta Santesson. (1968). Karyotypes of cultured cells from foetal membranes of normal newborns.. Journal of Medical Genetics. 5(3). 224–226. 8 indexed citations

16.

Gustavson, K. H., Bengt Hagberg, & Berta Santesson. (1967). Mosaic Trisomy of an Autosome in the 6–12 Group in a Patient With Multiple Congenital Anomalies. Acta Paediatrica. 56(6). 681–686. 11 indexed citations

17.

Atkins, L., Berta Santesson, & Hartmut Voss. (1965). Partial deletion of an X chromosome. Annals of Human Genetics. 29(1). 89–95. 24 indexed citations

18.

Böök, J.A., et al.. (1962). Malformation Syndrome Associated with Triploidy – Further Chromosome Studies of the Patient and his Family. Human Heredity. 12(3-4). 193–201. 22 indexed citations

19.

Böök, J.A., Berta Santesson, & PER ZETTERQVIST. (1961). TRANSLOCATION HETEROZYGOSITY IN MAN. The Lancet. 277(7169). 167–167. 22 indexed citations

20.

Böök, J.A., K. H. Gustavson, & Berta Santesson. (1961). Chromosomal Abnormality in a Mongolism‐Like Syndrome1. Acta Paediatrica. 50(3). 240–248. 7 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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