P. Sistonen

3.4k citations
51 papers · 2.0k · h-index 24

Impact in

Papers in

    • Forensic and Genetic Research 8
    • Hemoglobinopathies and Related Disorders 5
    • Genetic diversity and population structure 3
    • Blood groups and transfusion 13

P. Sistonen

51 papers receiving 1.9k citations

Peers

P. Sistonen
Comparison fields: 5 of 108
  • Gastroenterology 177
  • Hematology 348
  • Genetics 752
  • Sensory Systems 79
  • Genetics 119
Replace Marco Forni with:
Marco Forni Italy
Ishwar C. Verma India
S Go Japan
Julie Wheway Australia
Benedicte A. Lie Norway
Peter K. Gregersen United States
Buhm Han South Korea
P. Lucarelli Italy
Danielle Degenne France
Max P. Baur Germany
P. Sistonen relative to Marco Forni Italy Marco Forni's profile →
Citations per field
00.5×5.0×
Marco Forni · 1×
Citations per year

Countries citing papers authored by P. Sistonen

Since Specialization
Citations

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

Fields of papers citing papers by P. Sistonen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside P. Sistonen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with P. Sistonen Line = papers co-authored together P. Sistonen links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1995200
2 1995119
3 1991118
4 2004114
5 2002111
6 1999104
7
The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA.
199691
8 199585
9 201280
10
Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer.
199675
11
Classification principles and genetics of chronic gastritis.
198770
12 199468
13 199367
14
Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.
199551
15 199148
16
High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia gene.
199446
17 199238
18
On the heritability of serum high density lipoprotein in twins.
198036
19 199735
20 199535

About P. Sistonen

P. Sistonen is a scholar working on Genetics, Hematology, Physiology, Molecular Biology and Immunology, having authored 51 papers that have together received 2.0k indexed citations. Recurring topics across this work include Blood groups and transfusion (13 papers), Erythrocyte Function and Pathophysiology (12 papers), Forensic and Genetic Research (8 papers), Helicobacter pylori-related gastroenterology studies (6 papers), Celiac Disease Research and Management (5 papers), Hemoglobinopathies and Related Disorders (5 papers), Immunodeficiency and Autoimmune Disorders (4 papers) and Genetic diversity and population structure (3 papers). The work is most often cited by research in Gastroenterology (177 citations), Hematology (348 citations), Genetics (752 citations), Sensory Systems (79 citations) and Genetics (119 citations). P. Sistonen has collaborated with scholars based in Finland, United Kingdom and Sweden. Frequent co-authors include Albert de la Chapelle, Antti Sajantila, Matti Lukka, H. R. Nevanlinna, P Aula, A.-E. Lehesjoki, M.-L. Savontaus, Päivi Lahermo, Reijo Norio and Jukka Partanen. Their work appears in journals such as Vox Sanguinis, Human Heredity, Blood, Annals of Human Genetics and Proceedings of the National Academy of Sciences.

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