Astrid Thilén

1.3k total citations
17 papers, 926 citations indexed

About

Astrid Thilén is a scholar working on Molecular Biology, Hematology and Clinical Biochemistry. According to data from OpenAlex, Astrid Thilén has authored 17 papers receiving a total of 926 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Hematology and 4 papers in Clinical Biochemistry. Recurrent topics in Astrid Thilén's work include Sexual Differentiation and Disorders (8 papers), Metabolism and Genetic Disorders (4 papers) and Urological Disorders and Treatments (3 papers). Astrid Thilén is often cited by papers focused on Sexual Differentiation and Disorders (8 papers), Metabolism and Genetic Disorders (4 papers) and Urological Disorders and Treatments (3 papers). Astrid Thilén collaborates with scholars based in Sweden, Canada and United Kingdom. Astrid Thilén's co-authors include Anna Wedell, E. Martin Ritzén, Agne Larsson, Holger Luthman, Anna Nordenström, Ulrika von Döbeln, Lars Hagenfeldt, Claes Guthenberg, Henrik Falhammar and Sebastian Gidlöf and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, PEDIATRICS and Annals of the Rheumatic Diseases.

In The Last Decade

Astrid Thilén

17 papers receiving 871 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Astrid Thilén Sweden	12	751	491	295	224	171	17	926
Ahmed Khattab United States	11	247 0.3×	127 0.3×	44 0.1×	106 0.5×	67 0.4×	36	450
Kei Takasawa Japan	13	247 0.3×	116 0.2×	33 0.1×	187 0.8×	24 0.1×	64	456
David Rodriguez‐Buritica United States	12	161 0.2×	52 0.1×	31 0.1×	227 1.0×	23 0.1×	37	429
M. Furbetta Italy	15	243 0.3×	29 0.1×	19 0.1×	158 0.7×	2 0.0×	48	1.1k
I. Phocas Greece	13	106 0.1×	42 0.1×	9 0.0×	26 0.1×	10 0.1×	46	504
Andrea Luczay Hungary	9	86 0.1×	82 0.2×	8 0.0×	68 0.3×	5 0.0×	32	321
E Neumann Austria	11	77 0.1×	95 0.2×	16 0.1×	77 0.3×		37	422
Schindler Am Switzerland	13	161 0.2×	36 0.1×	3 0.0×	63 0.3×	13 0.1×	31	431
Daphna Marom Israel	11	227 0.3×	26 0.1×	86 0.3×	65 0.3×	1 0.0×	26	510
E Konova Bulgaria	11	31 0.0×	75 0.2×	52 0.2×	69 0.3×		50	482

Countries citing papers authored by Astrid Thilén

Since Specialization

Citations

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

Fields of papers citing papers by Astrid Thilén

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Astrid Thilén

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

All Works

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17 of 17 papers shown

Gidlöf, Sebastian, Henrik Falhammar, Astrid Thilén, et al.. (2013). One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study. The Lancet Diabetes & Endocrinology. 1(1). 35–42. 139 indexed citations

Nordenström, Anna, Astrid Thilén, Lars Hagenfeldt, Agne Larsson, & Anna Wedell. (1999). Genotyping Is a Valuable Diagnostic Complement to Neonatal Screening for Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency¹. The Journal of Clinical Endocrinology & Metabolism. 84(5). 1505–1509. 86 indexed citations

Thilén, Astrid, Anna Nordenström, Lars Hagenfeldt, et al.. (1998). Benefits of Neonatal Screening for Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) in Sweden. PEDIATRICS. 101(4). e11–e11. 117 indexed citations

Thilén, Astrid, et al.. (1995). Early growth is not increased in untreated moderately severe 21‐hydroxylase deficiency. Acta Paediatrica. 84(8). 894–898. 39 indexed citations

Wedell, Anna, et al.. (1994). Mutational Spectrum of the Steroid 21-Hydroxylase Gene In Sweden. Obstetrical & Gynecological Survey. 49(10). 695–697. 4 indexed citations

Wedell, Anna, et al.. (1994). Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation.. The Journal of Clinical Endocrinology & Metabolism. 78(5). 1145–1152. 308 indexed citations

Larsson, Agne, Astrid Thilén, Lars Hagenfeldt, Ulrika von Döbeln, & Claes Guthenberg. (1992). Screening of half a million Swedish newborn infants for congenital adrenal hyperplasia. 1(3). 159–166. 16 indexed citations

Thilén, Astrid & Agne Larsson. (1990). Congenital Adrenal Hyperplasia in Sweden 1969‐1986 Prevalence, Symptoms and Age at Diagnosis. Acta Paediatrica. 79(2). 168–175. 56 indexed citations

Gäre, Boel Andersson, Anders Fasth, Jacob Andersson, et al.. (1987). Incidence and prevalence of juvenile chronic arthritis: a population survey.. Annals of the Rheumatic Diseases. 46(4). 277–281. 45 indexed citations

10.

Eeg‐Olofsson, Orvar, et al.. (1981). [Neurofibromatosis in children].. PubMed. 78(35). 2940–2. 3 indexed citations

11.

Ljung, Rolf, et al.. (1979). Fanconi's anaemia associated with haemophilia A. Clinical Genetics. 16(5). 364–368. 1 indexed citations

12.

Olofsson, Tor, et al.. (1976). Granulopoiesis in Infantile Genetic Agranulocytosis In vitro Cloning of Marrow Cells in Agar Culture. Scandinavian Journal of Haematology. 16(1). 18–24. 18 indexed citations

13.

Thilén, Astrid, et al.. (1967). Familial Leukaemia — Three Cases of Acute Leukaemia in Four Siblings. Acta Paediatrica. 56(S173). 200–205. 4 indexed citations

14.

Sterky, G & Astrid Thilén. (1960). A Study on the Onset and Prognosis of Acute Vascular Purpura (the Schönlein‐Henoch Syndrome) in Children. Acta Paediatrica. 49(3). 217–229. 34 indexed citations

15.

Nilsson, Inga Marie, et al.. (1959). Carriers of Hemophilia A. Acta Medica Scandinavica. 165(5). 357–370. 41 indexed citations

16.

BERGSTRAND, C. G., T Fahlén, & Astrid Thilén. (1957). A Follow‐up Study of Children Treated for Acute Purulent Meningitis. Acta Paediatrica. 46(1). 10–17. 12 indexed citations

17.

Herrlin, K. & Astrid Thilén. (1955). Antihemophilic Activity in Cohn's Fraction I Prepared from Postpartum Serum. Scandinavian Journal of Clinical and Laboratory Investigation. 7(3). 218–224. 3 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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