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Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth.
Published in:
Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-96374-9
By:
- Huusko, Johanna M.;
- Tiensuu, Heli;
- Haapalainen, Antti M.;
- Pasanen, Anu;
- Tissarinen, Pinja;
- Karjalainen, Minna K.;
- Zhang, Ge;
- Christensen, Kaare;
- Ryckman, Kelli K.;
- Jacobsson, Bo;
- Murray, Jeffrey C.;
- Kingsmore, Stephen F.;
- Hallman, Mikko;
- Muglia, Louis J.;
- Rämet, Mika
Publication type:
Article
Cerebral Palsy and Polymorphism of the Chemokine CCL18 in Very Preterm Children.
Published in:
Neonatology (16617800), 2015, v. 108, n. 2, p. 124, doi. 10.1159/000430765
By:
- Kallankari, Hanna;
- Huusko, Johanna M.;
- Kaukola, Tuula;
- Ojaniemi, Marja;
- Mahlman, Mari;
- Marttila, Riitta;
- Kingsmore, Stephen F.;
- Haataja, Leena;
- Lavoie, Pascal M.;
- Synnes, anne;
- Hallman, Mikko
Publication type:
Article
Genes Encoding Vascular Endothelial Growth Factor A (VEGF-A) and VEGF Receptor 2 (VEGFR-2) and Risk for Bronchopulmonary Dysplasia.
Published in:
Neonatology (16617800), 2015, v. 108, n. 1, p. 53, doi. 10.1159/000381279
By:
- Mahlman, Mari;
- Huusko, Johanna M.;
- Karjalainen, Minna K.;
- Kaukola, Tuula;
- Marttila, Riitta;
- Ojaniemi, Marja;
- Haataja, Ritva;
- Lavoie, Pascal M.;
- Rämet, Mika;
- Hallman, Mikko
Publication type:
Article
Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.
Published in:
PLoS Genetics, 2019, v. 15, n. 6, p. 1, doi. 10.1371/journal.pgen.1008107
By:
- Tiensuu, Heli;
- Haapalainen, Antti M.;
- Karjalainen, Minna K.;
- Pasanen, Anu;
- Huusko, Johanna M.;
- Marttila, Riitta;
- Ojaniemi, Marja;
- Muglia, Louis J.;
- Hallman, Mikko;
- Rämet, Mika
Publication type:
Article
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Published in:
2018
By:
- Huusko, Johanna M.;
- Karjalainen, Minna K.;
- Graham, Britney E.;
- Zhang, Ge;
- Farrow, Emily G.;
- Miller, Neil A.;
- Jacobsson, Bo;
- Eidem, Haley R.;
- Murray, Jeffrey C.;
- Bedell, Bruce;
- Breheny, Patrick;
- Brown, Noah W.;
- Bødker, Frans L.;
- Litterman, Nadia K.;
- Jiang, Pan-Pan;
- Russell, Laura;
- Hinds, David A.;
- Hu, Youna;
- Rokas, Antonis;
- Teramo, Kari
Publication type:
Correction Notice
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Published in:
PLoS Genetics, 2018, v. 14, n. 7, p. 1, doi. 10.1371/journal.pgen.1007394
By:
- Huusko, Johanna M.;
- Karjalainen, Minna K.;
- Graham, Britney E.;
- Zhang, Ge;
- Farrow, Emily G.;
- Miller, Neil A.;
- Jacobsson, Bo;
- Eidem, Haley R.;
- Murray, Jeffrey C.;
- Bedell, Bruce;
- Breheny, Patrick;
- Brown, Noah W.;
- Bødker, Frans L.;
- Litterman, Nadia K.;
- Jiang, Pan-Pan;
- Russell, Laura;
- Hinds, David A.;
- Hu, Youna;
- null, null;
- Rokas, Antonis
Publication type:
Article
Polymorphisms of the gene encoding Kit ligand are associated with bronchopulmonary dysplasia.
Published in:
Pediatric Pulmonology, 2015, v. 50, n. 3, p. 260, doi. 10.1002/ppul.23018
By:
- Huusko, Johanna M.;
- Mahlman, Mari;
- Karjalainen, Minna K.;
- Kaukola, Tuula;
- Haataja, Ritva;
- Marttila, Riitta;
- Toldi, Gergely;
- Szabó, Miklós;
- Kingsmore, Stephen F.;
- Rämet, Mika;
- Lavoie, Pascal M.;
- Hallman, Mikko
Publication type:
Article
A Potential Novel Spontaneous Preterm Birth Gene, AR, Identified by Linkage and Association Analysis of X Chromosomal Markers.
Published in:
PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051378
By:
- Karjalainen, Minna K.;
- Huusko, Johanna M.;
- Ulvila, Johanna;
- Sotkasiira, Jenni;
- Luukkonen, Aino;
- Teramo, Kari;
- Plunkett, Jevon;
- Anttila, Verneri;
- Palotie, Aarno;
- Haataja, Ritva;
- Muglia, Louis J.;
- Hallman, Mikko
Publication type:
Article
Human placental proteomics and exon variant studies link AAT/SERPINA1 with spontaneous preterm birth.
Published in:
BMC Medicine, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12916-022-02339-8
By:
- Tiensuu, Heli;
- Haapalainen, Antti M.;
- Tissarinen, Pinja;
- Pasanen, Anu;
- Määttä, Tomi A.;
- Huusko, Johanna M.;
- Ohlmeier, Steffen;
- Bergmann, Ulrich;
- Ojaniemi, Marja;
- Muglia, Louis J.;
- Hallman, Mikko;
- Rämet, Mika
Publication type:
Article
Human placental proteomics and exon variant studies link AAT/SERPINA1 with spontaneous preterm birth.
Published in:
2022
By:
- Tiensuu, Heli;
- Haapalainen, Antti M.;
- Tissarinen, Pinja;
- Pasanen, Anu;
- Määttä, Tomi A.;
- Huusko, Johanna M.;
- Ohlmeier, Steffen;
- Bergmann, Ulrich;
- Ojaniemi, Marja;
- Muglia, Louis J.;
- Hallman, Mikko;
- Rämet, Mika
Publication type:
journal article
Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
Published in:
2022
By:
- Scocchia, Alicia;
- Kangas-Kontio, Tiia;
- Irving, Melita;
- Hero, Matti;
- Saarinen, Inka;
- Pelttari, Liisa;
- Gall, Kimberly;
- Valo, Satu;
- Huusko, Johanna M.;
- Tallila, Jonna;
- Sistonen, Johanna;
- Koskenvuo, Juha;
- Alastalo, Tero-Pekka
Publication type:
corrected article
Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
Published in:
2021
By:
- Scocchia, Alicia;
- Kangas-Kontio, Tiia;
- Irving, Melita;
- Hero, Matti;
- Saarinen, Inka;
- Pelttari, Liisa;
- Gall, Kimberly;
- Valo, Satu;
- Huusko, Johanna M.;
- Tallila, Jonna;
- Sistonen, Johanna;
- Koskenvuo, Juha;
- Alastalo, Tero-Pekka
Publication type:
journal article
A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia
Published in:
BMC Medical Genetics, 2014, v. 15, n. 1, p. 120, doi. 10.1186/s12881-014-0120-7
By:
- Huusko, Johanna M;
- Karjalainen, Minna K;
- Mahlman, Mari;
- Haataja, Ritva;
- Kari, M Anneli;
- Andersson, Sture;
- Toldi, Gergely;
- Tammela, Outi;
- Rämet, Mika;
- Lavoie, Pascal M;
- Hallman, Mikko
Publication type:
Article

Found: 13