R. Haataja

发表

Data mining and multiparameter analysis of lung surfactant protein genes in bronchopulmonary dysplasia.

V. Ollikainen, M. Hallman, O. Tammela, 2004, Human molecular genetics.

Association between the Asp299Gly Polymorphisms in the Toll-like Receptor 4 and Premature Births in the Finnish Population

D. Schwartz, M. Hallman, E. Lorenz, 2002, Pediatric Research.

Surfactant Protein D Gene Polymorphism Associated with Severe Respiratory Syncytial Virus Infection

M. Rämet, M. Hallman, M. Renko, 2002, Pediatric Research.

An Evolutionary Genomic Approach to Identify Genes Involved in Human Birth Timing

Leena Peltonen, Edward Kuczynski, Scott Doniger, 2011, PLoS genetics.

Genetic influences and neonatal lung disease.

M. Hallman, R. Haataja, 2003, Seminars in neonatology : SN.

A study of collectin genes in spontaneous preterm birth reveals an association with a common surfactant protein D gene polymorphism

M. Hallman, R. Haataja, M. Karjalainen, 2012, Pediatric Research.

Genes Encoding Vascular Endothelial Growth Factor A (VEGF-A) and VEGF Receptor 2 (VEGFR-2) and Risk for Bronchopulmonary Dysplasia

M. Rämet, M. Ojaniemi, M. Hallman, 2015, Neonatology.

Surfactant protein A and B genetic variants in respiratory distress syndrome in singletons and twins.

M. Hallman, S. Guttentag, R. Haataja, 2003, American journal of respiratory and critical care medicine.

Surfactant protein A gene locus and respiratory distress syndrome in Finnish premature twin pairs

M. Rämet, M. Hallman, O. Tammela, 2003, Annals of medicine.

Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission.

R. Haataja, J. Leisti, M. Väisänen, 1996, American journal of human genetics.

Associate with Spontaneous Preterm Birth CXCR3 Polymorphism and Expression

A. Palotie, M. Rämet, L. Muglia, 2015 .

Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis

L. Peltonen, S. Mccarroll, A. Palotie, 2011, PLoS genetics.

Genetic association of SP-C with duration of preterm premature rupture of fetal membranes and expression in gestational tissues

M. Ojaniemi, R. Haataja, S. Glasser, 2009, Annals of medicine.

Association between the surfactant protein A (SP-A) gene locus and respiratory-distress syndrome in the Finnish population.

M. Rämet, M. Hallman, J. Floros, 2000, American journal of human genetics.

Surfactant proteins and genetic predisposition to respiratory distress syndrome.

R. Haataja, R. Marttila, M. Hallman, 2002, Seminars in perinatology.

Mannose-binding lectin as a risk factor for acute coronary syndromes

L. Truedsson, S. Meri, S. Sarna, 2009, Annals medicus.

Genes and Environment in Common Neonatal Lung Disease

M. Ojaniemi, M. Hallman, R. Haataja, 2007, Neonatology.

Surfactant protein B polymorphism and respiratory distress syndrome in premature twins

M. Rämet, M. Hallman, R. Haataja, 2002, Human Genetics.

Surfactant proteins as genetic determinants of multifactorial pulmonary diseases

M. Hallman, R. Haataja, 2002, Annals of medicine.

Uridine enhances expression of the fragile X chromosome in human lymphocytes

R. Haataja, M. Kähkönen, J. Leisti, 2005, Human Genetics.

CXCR3 Polymorphism and Expression Associate with Spontaneous Preterm Birth

S. Kingsmore, A. Palotie, M. Rämet, 2015, The Journal of Immunology.

Polymorphisms of the gene encoding Kit ligand are associated with bronchopulmonary dysplasia

S. Kingsmore, M. Rämet, M. Hallman, 2015, Pediatric pulmonology.

A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia

M. Rämet, M. Hallman, O. Tammela, 2014, BMC Medical Genetics.

A Potential Novel Spontaneous Preterm Birth Gene, AR, Identified by Linkage and Association Analysis of X Chromosomal Markers

Louis J. Muglia, Aarno Palotie, Jevon Plunkett, 2012, PloS one.

Surfactant protein polymorphisms and neonatal lung disease.

M. Hallman, R. Haataja, 2006, Seminars in perinatology.

The role of surfactant protein A and B genes in heritable susceptibility to neonatal respiratory distress syndrome

R. Haataja, 2001 .

Genetic basis of respiratory distress syndrome.

M. Hallman, R. Haataja, 2007, Frontiers in bioscience : a journal and virtual library.

G protein‐coupled receptor for asthma susceptibility associates with respiratory distress syndrome

C. Lindgren, J. Kere, V. Pulkkinen, 2006, Annals of medicine.

Haplotype analysis of ABCA3: association with respiratory distress in very premature infants

M. Hallman, R. Haataja, M. Karjalainen, 2008, Annals of medicine.

Surfactant proteins A and B as interactive genetic determinants of neonatal respiratory distress syndrome.

M. Rämet, M. Hallman, R. Haataja, 2000, Human molecular genetics.

Mother’s Genome or Maternally-Inherited Genes Acting in the Fetus Influence Gestational Age in Familial Preterm Birth

Michael F. Wangler, L. Peltonen, I. Borecki, 2009, Human Heredity.

Respiratory distress syndrome: evaluation of genetic susceptibility and protection by transmission disequilibrium test

M. Rämet, M. Hallman, P. Uimari, 2001, Human Genetics.

Human Surfactant Protein – A Gene Locus for Genetic Studies in the Finnish Population

M. Knip, M. Rämet, M. Hallman, 2002, Disease markers.

Allele-specific N-glycosylation delays human surfactant protein B secretion in vitro and associates with decreased protein levels in vivo

M. Hallman, S. Guttentag, U. Petäjä-Repo, 2013, Pediatric Research.

Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth

Justin C. Fay, L. Peltonen, I. Borecki, 2010, BMC Medical Genomics.