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Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2

PLoS genetics, 2019-06, Vol.15 (6), p.e1008107-e1008107

2019

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Apolipoprotein A-I concentrations and risk of coronary artery disease: A Mendelian randomization study

Atherosclerosis, 2020-04, Vol.299, p.56-63

2020

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Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci

PLoS genetics, 2023-10, Vol.19 (10), p.e1010982-e1010982

2023

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Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth

Scientific reports, 2021-08, Vol.11 (1), p.17115-17115, Article 17115

2021

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A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers

PloS one, 2012-12, Vol.7 (12), p.e51378

2012

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The genomics of preterm birth: from animal models to human studies

Genome medicine, 2013-04, Vol.5 (4), p.34-34

2013

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Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis

PLoS genetics, 2011-02, Vol.7 (2), p.e1001293-e1001293

2011

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IL10 polymorphisms, rhinovirus-induced bronchiolitis, and childhood asthma

Journal of allergy and clinical immunology, 2013-01, Vol.131 (1), p.249-250

2013

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Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

PLoS genetics, 2018-09, Vol.14 (9), p.e1007673-e1007673

2018

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Circulating anti-Müllerian hormone levels in pre-menopausal women: novel genetic insights from a genome-wide association meta-analysis

Human reproduction (Oxford), 2024-05, Vol.39 (7), p.1564-1572

2024

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Spontaneous premature birth as a target of genomic research

Pediatric research, 2019-03, Vol.85 (4), p.422-431

2019

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Immature surfactant protein-B impairs the antioxidant capacity of HDL

International journal of cardiology, 2019-06, Vol.285, p.53-58

2019

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Mitochondrial Hearing Loss Mutations among Finnish Preterm and Term-Born Infants

Audiology research (Pavia, Italy), 2017-11, Vol.7 (2), p.189

2017

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Genome-wide characterization of circulating metabolic biomarkers

Nature (London), 2024-04, Vol.628 (8006), p.130-138

2024

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Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

PLoS genetics, 2018-07, Vol.14 (7), p.e1007394

2018

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Genetic and observational evidence: No independent role for cholesterol efflux over static high‐density lipoprotein concentration measures in coronary heart disease risk assessment

Journal of internal medicine, 2022-07, Vol.292 (1), p.146-153

2022

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Genome-Wide Association Study of Polymorphisms Predisposing to Bronchiolitis

Scientific reports, 2017-01, Vol.7 (1), p.41653-41653, Article 41653

2017

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CDHR3 gene variation and childhood bronchiolitis

Journal of allergy and clinical immunology, 2017-11, Vol.140 (5), p.1469-1471.e7

2017

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Haplotype of the Interleukin 17A gene is associated with osteitis after Bacillus Calmette-Guerin vaccination

Scientific reports, 2017-09, Vol.7 (1), p.11691-5, Article 11691

2017

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Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene

Scientific reports, 2017-08, Vol.7 (1), p.9271-10, Article 9271

2017

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CXCR3 Polymorphism and Expression Associate with Spontaneous Preterm Birth

The Journal of immunology (1950), 2015-09, Vol.195 (5), p.2187-2198

2015

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NKG2D gene variation and susceptibility to viral bronchiolitis in childhood

Pediatric research, 2018-09, Vol.84 (3), p.451-457

2018

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Expression of CPPED1 in human trophoblasts is associated with timing of term birth

Journal of cellular and molecular medicine, 2018-02, Vol.22 (2), p.968-981

2018

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Low and high serum IgG associates with respiratory infections in a young and working age population

EBioMedicine, 2023-08, Vol.94, p.104712-104712, Article 104712

2023

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Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2

Apolipoprotein A-I concentrations and risk of coronary artery disease: A Mendelian randomization study

Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci

Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth

A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers

The genomics of preterm birth: from animal models to human studies

Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis

IL10 polymorphisms, rhinovirus-induced bronchiolitis, and childhood asthma

Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

Circulating anti-Müllerian hormone levels in pre-menopausal women: novel genetic insights from a genome-wide association meta-analysis

Spontaneous premature birth as a target of genomic research

Immature surfactant protein-B impairs the antioxidant capacity of HDL

Mitochondrial Hearing Loss Mutations among Finnish Preterm and Term-Born Infants

Genome-wide characterization of circulating metabolic biomarkers

Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth

Genetic and observational evidence: No independent role for cholesterol efflux over static high‐density lipoprotein concentration measures in coronary heart disease risk assessment

Genome-Wide Association Study of Polymorphisms Predisposing to Bronchiolitis

CDHR3 gene variation and childhood bronchiolitis

Haplotype of the Interleukin 17A gene is associated with osteitis after Bacillus Calmette-Guerin vaccination

NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease

Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene

CXCR3 Polymorphism and Expression Associate with Spontaneous Preterm Birth

NKG2D gene variation and susceptibility to viral bronchiolitis in childhood

Expression of CPPED1 in human trophoblasts is associated with timing of term birth

Low and high serum IgG associates with respiratory infections in a young and working age population

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