Concepedia

Hannele Pihlaja

HP

6

Publications

228

Citations

6

H-Index

1992

Active since

Affiliations

Institute for Molecular Medicine Finland(Current)

Helsinki University Hospital

University of Helsinki

Hannele Pihlaja is an author at Institute for Molecular Medicine Finland specializing in medicine, porphyrias, and genetics.

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Publications per year

1992–2003

6

Publications

6

Acute intermittent porphyria in Finland: 19 mutations in the porphobilinogen deaminase gene

Raili Kauppinen, Sami Mustajoki, Hannele Pihlaja et al. · Human Molecular Genetics · 1995 · 104 citations

, , +15

Linkage disequilibrium between the MBP tetranucleotide repeat and multiple sclerosis is restricted to a geographically defined subpopulation in Finland

Hannele Pihlaja, Terhi Rantamäki, J. Wikström et al. · Genes and Immunity · 2003 · 32 citations

, , +9

Three splicing defects, an insertion, and two missense mutations responsible for acute intermittent porphyria

Sami Mustajoki, Hannele Pihlaja, Helena Ahola et al. · Human Genetics · 1998 · 30 citations

, , +5

Four Novel Mutations in the Ferrochelatase Gene among Erythropoietic Protoporphyria Patients

Matti Henriksson, Kaisa Timonen, Pertti Mustajoki et al. · Journal of Investigative Dermatology · 1996 · 28 citations · Full text

, , +10

Mild familial neurofibromatosis 2 associates with expression of merlin with altered COOH-terminus

Markku Sainio, J Jääskeläinen, Hannele Pihlaja et al. · Neurology · 2000 · 19 citations

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