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Author Details
Full Name
Heikki Lehv??slaiho
Affiliation
CSC-IT Center for Science
ORCID
Career Start Year
1987
Papers
58
H Index
32
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35705716
The GA4GH Phenopacket schema defines a computable representation of clinical data.
Nat Biotechnol
2022
31550514
3D cellular reconstruction of cortical glia and parenchymal morphometric analysis from Serial Block-Face Electron Microscopy of juvenile rat.
Prog Neurobiol
2019
30319342
A Process for Digitizing and Simulating Biologically Realistic Oligocellular Networks Demonstrated for the Neuro-Glio-Vascular Ensemble.
Front Neurosci
2018
30161133
Norepinephrine stimulates glycogenolysis in astrocytes to fuel neurons with lactate.
PLoS Comput Biol
2018
26179415
Three-dimensional immersive virtual reality for studying cellular compartments in 3D models from EM preparations of neural tissues.
J Comp Neurol
2016
24921648
Core microbial functional activities in ocean environments revealed by global metagenomic profiling analyses.
PLoS One
2014
20398331
Locus Reference Genomic sequences: an improved basis for describing human DNA variants.
Genome Med
2010
20727200
The DBCLS BioHackathon: standardization and interoperability for bioinformatics web services and workflows. The DBCLS BioHackathon Consortium*.
J Biomed Semantics
2010
19479963
The phenotype and genotype experiment object model (PaGE-OM): a robust data structure for information related to DNA variation.
Hum Mutat
2009
18157828
Recommendations for locus-specific databases and their curation.
Hum Mutat
2008
17726697
A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases.
Hum Mutat
2007
14681459
Ensembl 2004.
Nucleic Acids Res
2004
15078858
An overview of Ensembl.
Genome Res
2004
14681471
HGVbase: a curated resource describing human DNA variation and phenotype relationships.
Nucleic Acids Res
2004
12519943
Ensembl 2002: accommodating comparative genomics.
Nucleic Acids Res
2003
11752248
The Ensembl genome database project.
Nucleic Acids Res
2002
12368254
The Bioperl toolkit: Perl modules for the life sciences.
Genome Res
2002
11752345
HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources.
Nucleic Acids Res
2002
11480780
Databases of human hemoglobin variants and other resources at the globin gene server.
Hemoglobin
2001
10612816
Guidelines and recommendations for content, structure, and deployment of mutation databases: II. Journey in progress.
Hum Mutat
2000
12001454
[Genetic databases and their use].
Duodecim
2000
11465027
Human sequence variation and mutation databases.
Brief Bioinform
2000
10592273
HGBASE: a database of SNPs and other variations in and around human genes.
Nucleic Acids Res
2000
10612822
Sequence variation database project at the European Bioinformatics Institute.
Hum Mutat
2000
9847160
Update of the Human MitBASE database.
Nucleic Acids Res
1999
10338088
Guidelines and recommendations for content, structure, and deployment of mutation databases.
Hum Mutat
1999
9613206
Unified access to mutation databases.
Trends Genet
1998
9399843
The Androgen Receptor Gene Mutations Database.
Nucleic Acids Res
1998
9036873
Detection of squamous-cell carcinoma antigen-expressing tumour cells in blood by reverse transcriptase-polymerase chain reaction in cancer of the uterine cervix.
Int J Cancer
1997
9016530
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
Nucleic Acids Res
1997
8883363
Unique and conserved features of Tula hantavirus M gene encoding envelope glycoproteins G1 and G2.
Virus Genes
1996
8971044
Quasispecies in wild-type tula hantavirus populations.
J Virol
1996
8961625
BTKbase: XLA-mutation registry.
Immunol Today
1996
8887490
Distribution and genetic heterogeneity of Puumala virus in Sweden.
J Gen Virol
1996
7595404
Human B-cell epitopes of Puumala virus nucleocapsid protein, the major antigen in early serological response.
J Med Virol
1995
8837894
Nucleotide and deduced amino acid sequences of the M and S genome segments of a Swedish Puumala virus isolate.
Virus Res
1995
8837887
Genetic variation in Tula hantaviruses: sequence analysis of the S and M segments of strains from Central Europe.
Virus Res
1995
8546008
Genetic variation of wild Puumala viruses within the serotype, local rodent populations and individual animal.
Virus Res
1995
7553856
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure.
Cell
1995
7966573
Tula virus: a newly detected hantavirus carried by European common voles.
J Virol
1994
8113763
Sequences of wild Puumala virus genes show a correlation of genetic variation with geographic origin of the strains.
J Gen Virol
1994
8093406
Familial erythrocytosis genetically linked to erythropoietin receptor gene.
Lancet
1993
8406437
Genetic mapping of the erythropoietin receptor gene.
Hum Genet
1993
1360234
A chimeric EGFR/neu receptor in studies of neu function.
Cancer Treat Res
1992
1352454
A chimeric EGFR/neu receptor in functional analysis of the neu oncoprotein.
Acta Oncol
1992
1706346
Constitutively activated neu oncoprotein tyrosine kinase interferes with growth factor-induced signals for gene activation.
J Cell Biochem
1991
1670091
[Proto-oncogenes and the control of cell growth].
Duodecim
1990
1969420
Regulation by EGF is maintained in an overexpressed chimeric EGFR/neu receptor tyrosine kinase.
J Cell Biochem
1990
1970155
Similar early gene responses to ligand-activated EGFR and neu tyrosine kinases in NIH3T3 cells.
Oncogene
1990
1972791
Downregulation of the early genomic growth factor response in neu oncogene-transformed cells.
Oncogene
1990
1 - 50 of 58
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