Hannele Pihlaja - Concepedia

Author

Hannele Pihlaja

Also Known As

H Pihlaja, H. Pihlaja, Hannele Pihlaja

Publications

234

Citations

H-Index

Concepts

All Affiliations

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

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	194
2	Biology	2	2	132
3	Natural Sciences	1	1	104
4	Public Health	1	1	32
5	Biochemistry	1	1	104

Hannele Pihlaja

Publications

228

Citations

H-Index

Page 1

	Year	Citations
Acute intermittent porphyria in Finland: 19 mutations in the porphobilinogen deaminase gene Raili Kauppinen, Sami Mustajoki, Hannele Pihlaja, Human Molecular Genetics BiologyGenetic AnalysisBiochemistryFamily MembersMedicine	1995	104
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, Genes and Immunity Linkage DisequilibriumNeurological DisorderMedicineNeuroepidemiologyGenetic Disorder	2003	32
Three splicing defects, an insertion, and two missense mutations responsible for acute intermittent porphyria Sami Mustajoki, Hannele Pihlaja, Helena Ahola, Human Genetics Missense MutationsGeneticsPathogenesisPathologyMolecular Genetics	1998	30
Four Novel Mutations in the Ferrochelatase Gene among Erythropoietic Protoporphyria Patients Matti Henriksson, Kaisa Timonen, Pertti Mustajoki, Journal of Investigative Dermatology BiologyErythropoietic Protoporphyria PatientsIron MetabolismGeneticsNovel Mutations	1996	28
Mild familial neurofibromatosis 2 associates with expression of merlin with altered COOH-terminus Markku Sainio, J Jääskeläinen, Hannele Pihlaja, Neurology	2000	19
CRIM-positive mutations of acute intermittent porphyria in Finland Raili Kauppinen, Leena Peltonen, Hannele Pihlaja, Human Mutation	1992	15

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