A. Nyström

440 total citations
8 papers, 345 citations indexed

About

A. Nyström is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, A. Nyström has authored 8 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Pediatrics, Perinatology and Child Health and 6 papers in Genetics. Recurrent topics in A. Nyström's work include Genetic Syndromes and Imprinting (6 papers), Prenatal Screening and Diagnostics (6 papers) and Epigenetics and DNA Methylation (5 papers). A. Nyström is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Prenatal Screening and Diagnostics (6 papers) and Epigenetics and DNA Methylation (5 papers). A. Nyström collaborates with scholars based in Sweden, United Kingdom and Switzerland. A. Nyström's co-authors include Paul N. Schofield, Tomas J. Ekström, Fredrik Hedborg, Virpi Töhönen, F Flam, Rolf Ohlsson, Susan Pfeifer‐Ohlsson, Janet Cheetham, Wilhelm Engström and Ulf Hesser and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Cancer Letters.

In The Last Decade

A. Nyström

8 papers receiving 339 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. Nyström Sweden	7	268	237	163	63	38	8	345
Kailash Daryanani United States	7	118 0.4×	140 0.6×	59 0.4×	97 1.5×	35 0.9×	10	250
R Gracia Spain	7	234 0.9×	250 1.1×	63 0.4×	26 0.4×	129 3.4×	8	353
Emile Hendriks United Kingdom	13	142 0.5×	125 0.5×	43 0.3×	107 1.7×	116 3.1×	23	313
William C. Deamer United States	6	203 0.8×	210 0.9×	131 0.8×	36 0.6×	71 1.9×	16	378
Tanja Knüppel Germany	5	245 0.9×	89 0.4×	140 0.9×	60 1.0×	11 0.3×	5	310
Marian Krawczyński Poland	6	136 0.5×	165 0.7×	64 0.4×	113 1.8×	8 0.2×	31	322
J.M. Wilhelm France	3	166 0.6×	204 0.9×	35 0.2×	216 3.4×	85 2.2×	5	304
R H Khoury United States	8	183 0.7×	59 0.2×	20 0.1×	57 0.9×	102 2.7×	9	366
Kristina Uvebrant Sweden	7	73 0.3×	101 0.4×	36 0.2×	59 0.9×	52 1.4×	9	256
C. Steinkamm Germany	5	225 0.8×	280 1.2×	68 0.4×	48 0.8×	3 0.1×	11	322

Countries citing papers authored by A. Nyström

Since Specialization

Citations

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

Fields of papers citing papers by A. Nyström

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Nyström

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Nyström, A., M.-L. Bondeson, Johan Mårtensson, et al.. (2004). A Novel Nonsense Mutation of the Mineralocorticoid Receptor Gene in a Swedish Family with Pseudohypoaldosteronism Type I (PHA1). The Journal of Clinical Endocrinology & Metabolism. 89(1). 227–231. 18 indexed citations

2.

Ekström, Tomas J., Hengmi Cui, A. Nyström, Eeva‐Marja Rutanen, & Rolf Ohlsson. (1995). Monoallelic expression of IGF2 at the human fetal/maternal boundary. Molecular Reproduction and Development. 41(2). 177–183. 9 indexed citations

3.

Schofield, Paul N., et al.. (1995). Expression of a high molecular weight form of insulin-like growth factor II in a Beckwith-Wiedemann syndrome associated adrenocortical adenoma. Cancer Letters. 94(1). 71–77. 6 indexed citations

4.

Nyström, A., et al.. (1994). Insulin-like growth factor 2 cannot be linked to a familial form of Beckwith-Wiedemann syndrome. European Journal of Pediatrics. 153(8). 574–580. 15 indexed citations

5.

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

6.

Hesser, Ulf, et al.. (1993). Gray-scale sonography in torsion of the testicular appendages. Pediatric Radiology. 23(7). 529–532. 32 indexed citations

7.

Nyström, A., Wilhelm Engström, Janet Cheetham, & Paul N. Schofield. (1992). Molecular analysis of patients with Wiedemann-Beckwith syndrome I. Gene dosage on the short arm of chromosome 11. European Journal of Pediatrics. 151(7). 504–510. 7 indexed citations

8.

Nyström, A., Janet Cheetham, Wilhelm Engström, & Paul N. Schofield. (1992). Molecular analysis of patients with Wiedemann-Beckwith syndrome II. Paternally derived disomies of chromosome 11. European Journal of Pediatrics. 151(7). 511–514. 24 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.

Explore authors with similar magnitude of impact