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The economics of renewable CaC2 and C2H2 production from biomass and CaO

Biomass & bioenergy, 2019-01, Vol.120, p.40-48

2019

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Concomitant head or neck injury increases risk of traumatic brain injury in facial fracture patients

British journal of oral & maxillofacial surgery, 2024-10, Vol.62 (8), p.704-709

2024

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The Collagenopathies: Review of Clinical Phenotypes and Molecular Correlations

Current rheumatology reports, 2014, Vol.16 (1), p.394-394, Article 394

2014

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Avascular necrosis of the femoral head due to a novel C propeptide mutation in COL2A1

American journal of medical genetics. Part A, 2011-07, Vol.155A (7), p.1759-1762

2011

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Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis

Osteoarthritis and cartilage, 2016-04, Vol.24 (4), p.655-663

2016

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Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis

Annals of the rheumatic diseases, 2003-12, Vol.62 (12), p.1208-1214

2003

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Genome-wide scan for schizophrenia in the Finnish population : evidence for a locus on chromosome 7q22

Human molecular genetics, 2000-04, Vol.9 (7), p.1049-1057

2000

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A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders

The Journal of clinical investigation, 2005-05, Vol.115 (5), p.1250-1257

2005

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Phenotypic and population differences in the association between CILP and lumbar disc disease

Journal of medical genetics, 2007-04, Vol.44 (4), p.285-288

2007

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The role of sequence variations within the genes encoding collagen II, IX and XI in non-syndromic, early-onset osteoarthritis

Osteoarthritis and cartilage, 2005-06, Vol.13 (6), p.497-507

2005

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The effect of age and density of the breast on the sensitivity of breast cancer diagnostic by mammography and ultasonography

Breast cancer research and treatment, 2001-05, Vol.67 (2), p.117-123

2001

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Clinical assessment of spinal mobility measurements in ankylosing spondylitis: a compact set for follow-up and trials?

Clinical rheumatology, 2000-01, Vol.19 (2), p.131-137

2000

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First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q

European journal of human genetics : EJHG, 1998-03, Vol.6 (2), p.151-157

1998

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Association between sequence variations in genes encoding human zona pellucida glycoproteins and fertilization failure in IVF

Human reproduction (Oxford), 2005-06, Vol.20 (6), p.1578-1585

2005

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Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditions

Journal of medical genetics, 2002-01, Vol.39 (1), p.34-41

2002

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Linkage analysis of putative schizophrenia gene candidate regions on chromosomes 3p, 5q, 6p, 8p, 20p and 22q in a population-based sampled Finnish family set

Molecular psychiatry, 1998-09, Vol.3 (5), p.452-457

1998

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A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci

American journal of human genetics, 1999-10, Vol.65 (4), p.1114-1124

1999

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Aggrecan core protein of a certain length is protective against hand osteoarthritis

Osteoarthritis and cartilage, 2006-10, Vol.14 (10), p.1075-1080

2006

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Genetic risk factors for lumbar disc disease

Annals of medicine (Helsinki), 2002, Vol.34 (1), p.42-47

Ala-Kokko, Leena

2002

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Mapping the Ligand-binding Sites and Disease-associated Mutations on the Most Abundant Protein in the Human, Type I Collagen

The Journal of biological chemistry, 2002-02, Vol.277 (6), p.4223-4231

2002

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Missense mutations in the β strands of the single A-domain of matrilin-3 result in multiple epiphyseal dysplasia

Journal of medical genetics, 2004-01, Vol.41 (1), p.52-59

2004

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Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity

BMC medical genetics, 2012-04, Vol.13 (1), p.26-26, Article 26

2012

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Correlation between mobility restrictions and radiologic changes in ankylosing spondylitis

Spine (Philadelphia, Pa. 1976), 1995-02, Vol.20 (4), p.492-496

1995

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Homogeneous Noncompetitive Immunoassay for 17β-Estradiol Based on Fluorescence Resonance Energy Transfer

Analytical chemistry (Washington), 2007-08, Vol.79 (15), p.5935-5940

2007

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Stop Codon in the Procollagen II Gene (COL2A1) in a Family with the Stickler Syndrome (Arthro-Ophthalmopathy)

Proceedings of the National Academy of Sciences - PNAS, 1991-08, Vol.88 (15), p.6624-6627

1991

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The economics of renewable CaC2 and C2H2 production from biomass and CaO

Concomitant head or neck injury increases risk of traumatic brain injury in facial fracture patients

The Collagenopathies: Review of Clinical Phenotypes and Molecular Correlations

Avascular necrosis of the femoral head due to a novel C propeptide mutation in COL2A1

Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis

Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis

Genome-wide scan for schizophrenia in the Finnish population : evidence for a locus on chromosome 7q22

A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders

Phenotypic and population differences in the association between CILP and lumbar disc disease

The role of sequence variations within the genes encoding collagen II, IX and XI in non-syndromic, early-onset osteoarthritis

The effect of age and density of the breast on the sensitivity of breast cancer diagnostic by mammography and ultasonography

Clinical assessment of spinal mobility measurements in ankylosing spondylitis: a compact set for follow-up and trials?

First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q

Association between sequence variations in genes encoding human zona pellucida glycoproteins and fertilization failure in IVF

Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditions

Linkage analysis of putative schizophrenia gene candidate regions on chromosomes 3p, 5q, 6p, 8p, 20p and 22q in a population-based sampled Finnish family set

A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci

Aggrecan core protein of a certain length is protective against hand osteoarthritis

Genetic risk factors for lumbar disc disease

Mapping the Ligand-binding Sites and Disease-associated Mutations on the Most Abundant Protein in the Human, Type I Collagen

Missense mutations in the β strands of the single A-domain of matrilin-3 result in multiple epiphyseal dysplasia

Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity

Correlation between mobility restrictions and radiologic changes in ankylosing spondylitis

Homogeneous Noncompetitive Immunoassay for 17β-Estradiol Based on Fluorescence Resonance Energy Transfer

Stop Codon in the Procollagen II Gene (COL2A1) in a Family with the Stickler Syndrome (Arthro-Ophthalmopathy)

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