Management Practices During Perinatal Respiratory Transition of Very Premature Infants door Mikko Hallman, Mikko Hallman, Eveliina Ronkainen, Eveliina Ronkainen, Timo V. Saarela, Timo V. Saarela, Riitta H. Marttila, Riitta H. Marttila

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CPPED1-targeting microRNA-371a-5p expression in human placenta associates with spontaneous delivery. door Ravindra Daddali, Marja Ojaniemi, Mikko Hallman, Mika Rämet, Antti M Haapalainen

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Eustachian tube surfactant is different from alveolar surfactant: determination of phospholipid composition of porcine eustachian tube lavage fluid door Reija Paananen, Anthony D. Postle, Graeme Clark, Virpi Glumoff, Mikko Hallman

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Mitochondrial hearing loss mutations among Finnish preterm and term-born infants door Heidi K. Soini, Minna K. Karjalainen, Reetta Hinttala, Arja Rautio, Mikko Hallman, Johanna Uusimaa

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Maternal serum alpha-1 antitrypsin levels in spontaneous preterm and term pregnancies door Pinja Tissarinen, Heli Tiensuu, Antti M. Haapalainen, Eveliina Ronkainen, Liisa Laatio, Marja Vääräsmäki, Hanna Öhman, Mikko Hallman, Mika Rämet

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Influence of common non-synonymous Toll-like receptor 4 polymorphisms on bronchopulmonary dysplasia and prematurity in human infants. door Pascal M Lavoie, Mihoko Ladd, Aaron F Hirschfeld, Johanna Huusko, Mari Mahlman, David P Speert, Mikko Hallman, Thierry Lacaze-Masmonteil, Stuart E Turvey

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Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2. door Heli Tiensuu, Antti M Haapalainen, Minna K Karjalainen, Anu Pasanen, Johanna M Huusko, Riitta Marttila, Marja Ojaniemi, Louis J Muglia, Mikko Hallman, Mika Rämet

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Assessing the Causal Relationship of Maternal Height on Birth Size and Gestational Age at Birth: A Mendelian Randomization Analysis. door Ge Zhang, Jonas Bacelis, Candice Lengyel, Kari Teramo, Mikko Hallman, Øyvind Helgeland, Stefan Johansson, Ronny Myhre, Verena Sengpiel, Pål Rasmus Njølstad, Bo Jacobsson, Louis Muglia

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A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers. door Minna K Karjalainen, Johanna M Huusko, Johanna Ulvila, Jenni Sotkasiira, Aino Luukkonen, Kari Teramo, Jevon Plunkett, Verneri Anttila, Aarno Palotie, Ritva Haataja, Louis J Muglia, Mikko Hallman

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Human placental proteomics and exon variant studies link AAT/SERPINA1 with spontaneous preterm birth door Heli Tiensuu, Antti M. Haapalainen, Pinja Tissarinen, Anu Pasanen, Tomi A. Määttä, Johanna M. Huusko, Steffen Ohlmeier, Ulrich Bergmann, Marja Ojaniemi, Louis J. Muglia, Mikko Hallman, Mika Rämet

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Variant in NHLRC2 leads to increased hnRNP C2 in developing neurons and the hippocampus of a mouse model of FINCA disease door Anniina E. Hiltunen, Salla M. Kangas, Steffen Ohlmeier, Ilkka Pietilä, Jori Hiltunen, Heikki Tanila, Colin McKerlie, Subashika Govindan, Hannu Tuominen, Riitta Kaarteenaho, Mikko Hallman, Johanna Uusimaa, Reetta Hinttala

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Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. door Anu Pasanen, Minna K Karjalainen, FinnGen, Ge Zhang, Heli Tiensuu, Antti M Haapalainen, Marja Ojaniemi, Bjarke Feenstra, Bo Jacobsson, Aarno Palotie, Hannele Laivuori, Louis J Muglia, Mika Rämet, Mikko Hallman

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Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease door Antti Tallgren, Leo Kager, Leo Kager, Leo Kager, Gina O’Grady, Hannu Tuominen, Jarmo Körkkö, Outi Kuismin, Outi Kuismin, Martha Feucht, Callum Wilson, Jana Behunova, Eleina England, Mitja I. Kurki, Mitja I. Kurki, Mitja I. Kurki, Aarno Palotie, Aarno Palotie, Aarno Palotie, Aarno Palotie, Aarno Palotie, Mikko Hallman, Mikko Hallman, Riitta Kaarteenaho, Riitta Kaarteenaho, Franco Laccone, Kaan Boztug, Kaan Boztug, Kaan Boztug, Kaan Boztug, Reetta Hinttala, Reetta Hinttala, Johanna Uusimaa, Johanna Uusimaa

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Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis. door Ritva Haataja, Minna K Karjalainen, Aino Luukkonen, Kari Teramo, Hilkka Puttonen, Marja Ojaniemi, Teppo Varilo, Bimal P Chaudhari, Jevon Plunkett, Jeffrey C Murray, Steven A McCarroll, Leena Peltonen, Louis J Muglia, Aarno Palotie, Mikko Hallman

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Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth door Johanna M. Huusko, Heli Tiensuu, Antti M. Haapalainen, Anu Pasanen, Pinja Tissarinen, Minna K. Karjalainen, Ge Zhang, Kaare Christensen, Kelli K. Ryckman, Bo Jacobsson, Jeffrey C. Murray, Stephen F. Kingsmore, Mikko Hallman, Louis J. Muglia, Mika Rämet

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Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype... door Jing Chen, Jonas Bacelis, Pol Sole-Navais, Amit Srivastava, Julius Juodakis, Amy Rouse, Mikko Hallman, Kari Teramo, Mads Melbye, Bjarke Feenstra, Rachel M Freathy, George Davey Smith, Deborah A Lawlor, Jeffrey C Murray, Scott M Williams, Bo Jacobsson, Louis J Muglia, Ge Zhang

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An evolutionary genomic approach to identify genes involved in human birth timing. door Jevon Plunkett, Scott Doniger, Guilherme Orabona, Thomas Morgan, Ritva Haataja, Mikko Hallman, Hilkka Puttonen, Ramkumar Menon, Edward Kuczynski, Errol Norwitz, Victoria Snegovskikh, Aarno Palotie, Leena Peltonen, Vineta Fellman, Emily A DeFranco, Bimal P Chaudhari, Tracy L McGregor, Jude J McElroy, Matthew T Oetjens, Kari Teramo, Ingrid Borecki, Justin Fay, Louis Muglia

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Effects of repeat prenatal corticosteroids given to women at risk of preterm birth: An individual participant data meta-analysis. door Caroline A Crowther, Philippa F Middleton, Merryn Voysey, Lisa Askie, Sasha Zhang, Tanya K Martlow, Fariba Aghajafari, Elizabeth V Asztalos, Peter Brocklehurst, Sourabh Dutta, Thomas J Garite, Debra A Guinn, Mikko Hallman, Pollyanna Hardy, Men-Jean Lee, Kimberley Maurel, Premasish Mazumder, Cindy McEvoy, Kellie E Murphy, Outi M Peltoniemi, Elizabeth A Thom, Ronald J Wapner, Lex W Doyle, PRECISE Group

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Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth. door Johanna M Huusko, Minna K Karjalainen, Britney E Graham, Ge Zhang, Emily G Farrow, Neil A Miller, Bo Jacobsson, Haley R Eidem, Jeffrey C Murray, Bruce Bedell, Patrick Breheny, Noah W Brown, Frans L Bødker, Nadia K Litterman, Pan-Pan Jiang, Laura Russell, David A Hinds, Youna Hu, 23andMe Research Team, Antonis Rokas, Kari Teramo, Kaare Christensen, Scott M Williams, Mika Rämet, Stephen F Kingsmore, Kelli K Ryckman, Mikko Hallman, Louis J Muglia

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Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth. door Johanna M Huusko, Minna K Karjalainen, Britney E Graham, Ge Zhang, Emily G Farrow, Neil A Miller, Bo Jacobsson, Haley R Eidem, Jeffrey C Murray, Bruce Bedell, Patrick Breheny, Noah W Brown, Frans L Bødker, Nadia K Litterman, Pan-Pan Jiang, Laura Russell, David A Hinds, Youna Hu, 23andMe Research Team, Antonis Rokas, Kari Teramo, Kaare Christensen, Scott M Williams, Mika Rämet, Stephen F Kingsmore, Kelli K Ryckman, Mikko Hallman, Louis J Muglia

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