Harriet von Koskull

2.0k total citations
52 papers, 1.1k citations indexed

About

Harriet von Koskull is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Harriet von Koskull has authored 52 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 17 papers in Pediatrics, Perinatology and Child Health and 14 papers in Molecular Biology. Recurrent topics in Harriet von Koskull's work include Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Harriet von Koskull is often cited by papers focused on Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Harriet von Koskull collaborates with scholars based in Finland, United States and Germany. Harriet von Koskull's co-authors include Perttì Aula, Ismo Virtanen, Pirkko Ämmälä, Riitta Salonen, Jean‐Louis Mandel, Maarit Peippo, Jaakko Leisti, T Vartio, Peter Steinbach and V.-P. Lehto and has published in prestigious journals such as Journal of Clinical Investigation, FEBS Letters and Annals of the New York Academy of Sciences.

In The Last Decade

Harriet von Koskull

52 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Harriet von Koskull Finland 19 689 465 272 225 106 52 1.1k
Jean‐Pierre Fryns Belgium 18 635 0.9× 664 1.4× 185 0.7× 182 0.8× 249 2.3× 72 1.3k
Arie P.T. Smits Netherlands 21 858 1.2× 612 1.3× 283 1.0× 279 1.2× 45 0.4× 43 1.2k
Giovanni Sorge Italy 22 553 0.8× 486 1.0× 153 0.6× 60 0.3× 150 1.4× 75 1.3k
A. Moseley United States 5 890 1.3× 834 1.8× 92 0.3× 100 0.4× 133 1.3× 10 1.6k
Ursula G. Froster Germany 23 886 1.3× 900 1.9× 371 1.4× 201 0.9× 334 3.2× 79 2.0k
C.D. DeLozier-Blanchet Switzerland 21 1.3k 1.8× 807 1.7× 305 1.1× 409 1.8× 184 1.7× 38 1.8k
Jaakko Leisti Finland 27 873 1.3× 1.1k 2.4× 267 1.0× 183 0.8× 151 1.4× 82 2.1k
Gholamali Tariverdian Germany 18 812 1.2× 721 1.6× 212 0.8× 77 0.3× 103 1.0× 64 1.3k
A L Beaudet United States 16 678 1.0× 688 1.5× 312 1.1× 96 0.4× 86 0.8× 23 1.8k
Shivanand R. Patil United States 24 1.2k 1.7× 1.2k 2.5× 418 1.5× 150 0.7× 172 1.6× 77 2.2k

Countries citing papers authored by Harriet von Koskull

Since Specialization
Citations

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

Fields of papers citing papers by Harriet von Koskull

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Harriet von Koskull. 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 Harriet von Koskull. The network helps show where Harriet von Koskull may publish in the future.

Co-authorship network of co-authors of Harriet von Koskull

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

All Works

20 of 20 papers shown
1.
Koskull, Harriet von & Perttì Aula. (2009). Distribution of chromosome breaks in measles, Fanconi's anemia and controls. Hereditas. 87(1). 1–10. 2 indexed citations
2.
Mononen, Tarja, et al.. (2007). A novel duplication in the FMR1 gene: implications for molecular analysis in fragile X syndrome and repeat instability. Clinical Genetics. 72(6). 528–531. 10 indexed citations
3.
Rousseau, Frédéric, Helle Hjalgrim, Elke Holinski‐Feder, et al.. (2000). FMR1 CGG expansion to full mutation: What is the lower limit in premutation females?. The American Journal of Human Genetics. 67(4). 365–365. 2 indexed citations
4.
Salonen, Riitta, Ursula Turpeinen, Pirkko Ämmälä, et al.. (1997). Maternal serum screening for Down's syndrome on population basis. Acta Obstetricia Et Gynecologica Scandinavica. 76(9). 817–821. 14 indexed citations
5.
Koskull, Harriet von & Riitta Salonen. (1997). Genetic services in Finland.. PubMed. 5 Suppl 2. 69–75. 2 indexed citations
6.
Koskull, Harriet von, et al.. (1995). Fetal erythroblasts from maternal blood identified with 2,3‐bisphosphoglycerate (BPG) and in situ hybridization (ISH) using Y‐specific probes. Prenatal Diagnosis. 15(2). 149–154. 15 indexed citations
7.
Linnala, Auli, et al.. (1994). Isoforms of cellular fibronectin and tenascin in amniotic fluid. FEBS Letters. 337(2). 167–170. 15 indexed citations
8.
Ylinen, K, et al.. (1994). Nucleated Erythrocytes in Enriched and Unenriched Peripheral Venous Blood Samples from Pregnant and Nonpregnant Women. Fetal Diagnosis and Therapy. 9(5). 291–295. 9 indexed citations
9.
Koskull, Harriet von, et al.. (1994). Occurrence of Nucleated Erythrocytes in Peripheral Blood of Pregnant Women. Annals of the New York Academy of Sciences. 731(1). 226–228. 1 indexed citations
10.
Ämmälä, Pirkko, et al.. (1993). Randomized trial comparing first‐trimester transcervical chorionic villus sampling and second‐trimester amniocentesis. Prenatal Diagnosis. 13(10). 919–927. 31 indexed citations
11.
Oudet, C, et al.. (1993). Striking Founder Effect for the Fragile X Syndrome in Finland. European Journal of Human Genetics. 1(3). 181–189. 48 indexed citations
12.
Hydén‐Granskog, Christel, Riitta Salonen, & Harriet von Koskull. (1993). Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11. Human Genetics. 91(2). 185–189. 7 indexed citations
13.
Penttinen, Maila, et al.. (1992). Linkage to Xq28 in a family with nonspecific X-linked mental retardation. Human Genetics. 90(3). 263–266. 29 indexed citations
14.
Koskull, Harriet von, et al.. (1992). Prenatal diagnosis and carrier detection in fragile X. American Journal of Medical Genetics. 43(1-2). 174–180. 1 indexed citations
15.
Aula, P, et al.. (1989). First‐trimester prenatal diagnosis of aspartylglucosaminuria. Prenatal Diagnosis. 9(9). 617–620. 8 indexed citations
16.
Koskull, Harriet von & Ismo Virtanen. (1987). Induction of cytokeratin expression in human mesenchymal cells. Journal of Cellular Physiology. 133(2). 321–329. 38 indexed citations
17.
Aula, Perttì, Juhani Rapola, Harriet von Koskull, & Pirkko Ämmälä. (1984). Prenatal diagnosis and fetal pathology of aspartylglucosaminuria. American Journal of Medical Genetics. 19(2). 359–367. 14 indexed citations
18.
Aula, Perttì, Harriet von Koskull, Kari Teramo, et al.. (1980). Glial origin of rapidly adhering amniotic fluid cells.. BMJ. 281(6253). 1456–1457. 27 indexed citations
19.
Aula, Perttì, Jaakko Leisti, & Harriet von Koskull. (1973). Partial trisomy 21. Clinical Genetics. 4(3). 241–251. 56 indexed citations
20.
Koskull, Harriet von & Perttì Aula. (1973). Nonrandom distribution of chromosome breaks in Fanconi’s anemia. Cytogenetic and Genome Research. 12(6). 423–434. 44 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

Breakdown of academic impact, for papers by Jean‐Pierre Fryns Breakdown of academic impact, for papers by Arie P.T. Smits Breakdown of academic impact, for papers by Giovanni Sorge Breakdown of academic impact, for papers by A. Moseley Breakdown of academic impact, for papers by Ursula G. Froster Breakdown of academic impact, for papers by C.D. DeLozier-Blanchet Breakdown of academic impact, for papers by Jaakko Leisti Breakdown of academic impact, for papers by Gholamali Tariverdian Breakdown of academic impact, for papers by A L Beaudet Breakdown of academic impact, for papers by Shivanand R. Patil
Rankless by CCL
2026