Author

Antti Levo

Observed names: A Levo, A. Levo

Observed institutions: University of Helsinki, Finnish Red Cross

OpenAlex ID: A5026909336

Population-Wide Evaluation of Disease Manifestation in Relation to Molecular Genotype in Steroid 21-Hydroxylase (CYP21) Deficiency: Good Correlation in a Well Defined Population

1997 · Jarmo Jääskeläinen, Antti Levo, et al. · The Journal of Clinical Endocrinology & Metabolism · 160

Post-mortem SNP analysis of CYP2D6 gene reveals correlation between genotype and opioid drug (tramadol) metabolite ratios in blood

2003 · Antti Levo, Anna Koski, et al. · Forensic Science International · 107

CYP2D6 Genotyping by a Multiplex Primer Extension Reaction

2005 · Johanna Sistonen, Silvia Fuselli, et al. · Clinical Chemistry · 100

A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interaction

1997 · Svetlana Lajic, Antti Levo, et al. · Human Genetics · 66

Mutation-haplotype analysis of steroid 21-hydroxylase (CYP21) deficiency in Finland. Implications for the population history of defective alleles

1997 · Antti Levo, Jukka Partanen · Human Genetics · 62

Molecular screening of selected long QT syndrome (LQTS) mutations in 165 consecutive bodies found in water

2003 · Philippe Lunetta, Antti Levo, et al. · International Journal of Legal Medicine · 34

Major histocompatibility complex (MHC)‐ linked microsatellite markers in a founder population

2000 · K. Karell, N. Klinger, et al. · Tissue Antigens · 20

Tracing past population migrations: genealogy of steroid 21-hydroxylase (CYP21) gene mutations in Finland

1999 · Antti Levo, Jarmo Jääskeläinen, et al. · European Journal of Human Genetics · 18

Novel mutations in the human CYP21 gene

2001 · Antti Levo, Jukka Partanen · Prenatal Diagnosis · 15

Single Founder Mutation (W380G) in Type II Protein C Deficiency in Finland

2000 · Kristiina Kuismanen, Päivi Holopainen, et al. · Thrombosis and Haemostasis · 14

Death in bathtub revisited with molecular genetics: a victim with suicidal traits and a LQTS gene mutation

2002 · P Lunetta, A Levo, et al. · Forensic Science International · 13

The natural history of an HLA haplotype and its recombinants

1998 · S. D'Alfonso, Iolanda Borelli, et al. · Immunogenetics · 10

An approach to mapping haplotype-specific recombination sites in human MHC class III

1996 · Antti Levo, Pia Westman, et al. · Immunogenetics · 10

Genetic background of type I protein C deficiency in Finland

2005 · Kristiina Kuismanen, Antti Levo, et al. · Thrombosis Research · 6

A rare neutral polymorphism in 21-hydroxylase genes as HLA haplotype marker

1995 · Kirsi Narko, Antti Levo, et al. · Human Immunology · 3

Predicting Pilot Fatigue in Commercial Air Transportation

2016 · Antti Levo

[Prenatal dexamethasone treatment of 21-hydroxylase deficiency].

1996 · J Jääskeläinen, J Partanen, et al. · PubMed

21-hydroksylaasin geenivirheet Suomessa : kolme yleisintä mutaatiota selittää 90% tautitapauksista

1995 · Antti Levo · Työväentutkimus Vuosikirja

Works count: 18

Citation count: 638

H-index: 11

I10-index: 13