Rolf Ohlsson

699 total citations
8 papers, 571 citations indexed

About

Rolf Ohlsson is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rolf Ohlsson has authored 8 papers receiving a total of 571 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Rolf Ohlsson's work include Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (6 papers) and Prenatal Screening and Diagnostics (4 papers). Rolf Ohlsson is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (6 papers) and Prenatal Screening and Diagnostics (4 papers). Rolf Ohlsson collaborates with scholars based in Sweden, United Kingdom and France. Rolf Ohlsson's co-authors include Kristian Svensson, Fredrik Hedborg, Virpi Töhönen, F Flam, Tomas J. Ekström, Paul N. Schofield, Susan Pfeifer‐Ohlsson, A. Nyström, Andràs Páldi and Jennifer A. Marshall Graves and has published in prestigious journals such as Nature Genetics, Trends in Genetics and Mechanisms of Development.

In The Last Decade

Rolf Ohlsson

8 papers receiving 561 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rolf Ohlsson Sweden	6	461	425	205	45	28	8	571
Poustka Annemarie Germany	8	431 0.9×	287 0.7×	109 0.5×	16 0.4×	12 0.4×	9	514
J L Watt United Kingdom	13	191 0.4×	298 0.7×	161 0.8×	24 0.5×	42 1.5×	19	462
Judith Dagan Israel	12	231 0.5×	223 0.5×	96 0.5×	14 0.3×	18 0.6×	27	457
C. Mignon France	11	327 0.7×	176 0.4×	74 0.4×	13 0.3×	9 0.3×	14	434
B. Horsthemke Germany	9	326 0.7×	321 0.8×	135 0.7×	8 0.2×	7 0.3×	13	444
Anne Bergmann United States	10	394 0.9×	289 0.7×	124 0.6×	13 0.3×	20 0.7×	15	484
Anna Newlin United States	12	147 0.3×	210 0.5×	96 0.5×	19 0.4×	41 1.5×	17	425
Patricia Outeda United States	11	448 1.0×	472 1.1×	59 0.3×	28 0.6×	13 0.5×	20	672
Josef Davidsson Sweden	11	191 0.4×	165 0.4×	82 0.4×	15 0.3×	122 4.4×	16	442
Jovenal San Agustin United States	6	354 0.8×	311 0.7×	27 0.1×	13 0.3×	30 1.1×	6	469

Countries citing papers authored by Rolf Ohlsson

Since Specialization

Citations

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

Fields of papers citing papers by Rolf Ohlsson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rolf Ohlsson

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

All Works

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8 of 8 papers shown

1.

Ohlsson, Rolf, et al.. (2002). Allele-Specific In Situ Hybridization (ASISH). Humana Press eBooks. 181. 153–167. 4 indexed citations

2.

Ohlsson, Rolf, Andràs Páldi, & Jennifer A. Marshall Graves. (2001). Did genomic imprinting and X chromosome inactivation arise from stochastic expression?. Trends in Genetics. 17(3). 136–141. 63 indexed citations

3.

Frank, Dale, Cathy Mendelsohn, Emilio Ciccone, et al.. (1999). A novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1: tissue-specific expression, chromosomal location, and parental imprinting. Mammalian Genome. 10(12). 1150–1159. 86 indexed citations

4.

Lin, Weili, Xiaobing He, Kristian Svensson, et al.. (1999). The genotype and epigenotype synergize to diversify the spatial pattern of expression of the imprinted H19 gene. Mechanisms of Development. 82(1-2). 195–197. 10 indexed citations

5.

Pettersson, Katarina, Kristian Svensson, Ragnar Mattsson, et al.. (1996). Expression of a novel member of estrogen response element-binding nuclear receptors is restricted to the early stages of chorion formation during mouse embryogenesis. Mechanisms of Development. 54(2). 211–223. 115 indexed citations

6.

Ohlsson, Rolf, et al.. (1996). An improved protocol for purification of 35S-labelled oligonucleotide DNA probes for in situ hybridization applications. Trends in Genetics. 12(12). 506–507. 5 indexed citations

7.

Walsh, Colum P., Anna Glaser, Reinald Fundele, et al.. (1994). The non-viability of uniparental mouse conceptuses correlates with the loss of the products of imprinted genes. Mechanisms of Development. 46(1). 55–62. 54 indexed citations

8.

Ohlsson, Rolf, A. Nyström, Susan Pfeifer‐Ohlsson, et al.. (1993). IGF2 is parentally imprinted during human embryogenesis and in the Beckwith–Wiedemann syndrome. Nature Genetics. 4(1). 94–97. 234 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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