Author

P. Sistonen

Observed names: P Sistonen, P. SISTONEN, Pertti Sistonen

Observed institutions: University of Helsinki, Inserm, University of Turku, University of Michigan, Finnish Red Cross, Institut National de la Transfusion Sanguine, Tampere University Hospital, Bristol Institute for Transfusion Sciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, University College London, Medical Research Council

OpenAlex ID: A5109970899

Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q

1995 · E.-M. Sankila, L. Pakarinen, et al. · Human Molecular Genetics · 188

Blood group terminology 2004: from the International Society of Blood Transfusion committee on terminology for red cell surface antigens

2004 · G. L. Daniels, A. Fletcher, et al. · Vox Sanguinis · 180

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Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.

1991 · A E Lehesjoki, M Koskiniemi, et al. · Proceedings of the National Academy of Sciences · 151

Frequent loss of SMAD4/DPC4 protein in colorectal cancers

2002 · R Salovaara, S Roth, et al. · Gut · 133

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Blood Group Terminology 1995: ISBT Working Party on Terminology for Red Cell Surface Antigens

1995 · G. L. Daniels, D. J. Anstee, et al. · Vox Sanguinis · 133

CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family‐based association study

1999 · P. Holopainen, M. Arvas, et al. · Tissue Antigens · 124

The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA.

1996 · P Lahermo, A Sajantila, et al. · PubMed Central · 117

Association study of FUT2 (rs601338) with celiac disease and inflammatory bowel disease in the Finnish population

2012 · A. S. Parmar, N. Alakulppi, et al. · Tissue Antigens · 100

Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer.

1996 · A L Moisio, P Sistonen, et al. · PubMed Central · 97

Familial erythrocytosis genetically linked to erythropoietin receptor gene

1993 · A. de la Chapelle, P. Sistonen, et al. · The Lancet · 93

Classification principles and genetics of chronic gastritis.

1987 · M Kekki, M Siurala, et al. · PubMed · 88

Blood Group Terminology 1990

1990 · M. Lewis, D.J. Anstee, et al. · Vox Sanguinis · 84

International Society of Blood Transfusion Committee on Terminology for Red Blood Cell Surface Antigens: Macao report

2008 · G. Daniels, L. Castilho, et al. · Vox Sanguinis · 83

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The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.

1994 · E Tahvanainen, S Ranta, et al. · Proceedings of the National Academy of Sciences · 83

Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22

2008 · K Pulli, K Karma, et al. · Journal of Medical Genetics · 82

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International Society of Blood Transfusion Committee on Terminology for Red Cell Surface Antigens: Cape Town report

2007 · G. Daniels, W. A. Flegel, et al. · Vox Sanguinis · 81

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Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.

1995 · P Höglund, P Sistonen, et al. · Europe PMC (PubMed Central) · 69

A Population Genetic Study in Finland: Comparison of the Finnish- and Swedish-Speaking Populations

1991 · K. Virtaranta-Knowles, P. Sistonen, et al. · Human Heredity · 60

High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia gene.

1994 · T Sulisalo, J Klockars, et al. · PubMed Central · 58

Donors with a rare pheno (geno) type

2008 · H. W. Reesink, C. P. Engelfriet, et al. · Vox Sanguinis · 56

Terminology for Red Cell Surface Antigens

1999 · G.L. Daniels, D.J. Anstee, et al. · Vox Sanguinis · 54

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Uniparental Disomy in Cartilage-Hair Hypoplasia

1997 · Tuija Sulisalo, Outi Mäkitie, et al. · European Journal of Human Genetics · 51

Finnish mitochondrial DNA HVS-I and HVS-II population data

2007 · M. Hedman, A. Brandstätter, et al. · Forensic Science International · 50

Molecular basis of the RhCW (Rh8) and RhCX (Rh9) blood group specificities

1995 · I Mouro, Y Colin, et al. · Blood · 48

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Linkage studies in progressive myoclonus epilepsy

1992 · A.-E. Lehesjoki, M. Koskiniemi, et al. · Neurology · 46

Works count: 64

Citation count: 3,050

H-index: 32

I10-index: 53