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

door Bezold, Katherine Y, Karjalainen, Minna K, Hallman, Mikko, Teramo, Kari, Muglia, Louis J
Gepubliceerd in 2013

Mitochondrial hearing loss mutations among Finnish preterm and term-born infants

door Soini, Heidi K., Karjalainen, Minna K., Hinttala, Reetta, Rautio, Arja, Hallman, Mikko, Uusimaa, Johanna
Gepubliceerd in Audiol Res (2017)

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

door Korppi, Matti, Teräsjärvi, Johanna, Liehu-Martiskainen, Milla, Lauhkonen, Eero, Vuononvirta, Juho, Nuolivirta, Kirsi, Kröger, Liisa, Pöyhönen, Laura, Karjalainen, Minna K., He, Qiushui
Gepubliceerd in Sci Rep (2017)

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

door Tiensuu, Heli, Haapalainen, Antti M., Karjalainen, Minna K., Pasanen, Anu, Huusko, Johanna M., Marttila, Riitta, Ojaniemi, Marja, Muglia, Louis J., Hallman, Mikko, Rämet, Mika
Gepubliceerd in PLoS Genet (2019)

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

door 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
Gepubliceerd in BMC Med Genet (2014)

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

door 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
Gepubliceerd in 2012

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

door Haapalainen, Antti M., Karjalainen, Minna K., Daddali, Ravindra, Ohlmeier, Steffen, Anttonen, Julia, Määttä, Tomi A., Salminen, Annamari, Mahlman, Mari, Bergmann, Ulrich, Mäkikallio, Kaarin, Ojaniemi, Marja, Hallman, Mikko, Rämet, Mika
Gepubliceerd in J Cell Mol Med (2017)

Genome-Wide Association Study of Polymorphisms Predisposing to Bronchiolitis

door Pasanen, Anu, Karjalainen, Minna K., Bont, Louis, Piippo-Savolainen, Eija, Ruotsalainen, Marja, Goksör, Emma, Kumawat, Kuldeep, Hodemaekers, Hennie, Nuolivirta, Kirsi, Jartti, Tuomas, Wennergren, Göran, Hallman, Mikko, Rämet, Mika, Korppi, Matti
Gepubliceerd in Sci Rep (2017)

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

door Haataja, Ritva, Karjalainen, Minna K., Luukkonen, Aino, Teramo, Kari, Puttonen, Hilkka, Ojaniemi, Marja, Varilo, Teppo, Chaudhari, Bimal P., Plunkett, Jevon, Murray, Jeffrey C., McCarroll, Steven A., Peltonen, Leena, Muglia, Louis J., Palotie, Aarno, Hallman, Mikko
Gepubliceerd in 2011

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

door Mahlman, Mari, Karjalainen, Minna K., Huusko, Johanna M., Andersson, Sture, Kari, M. Anneli, Tammela, Outi K. T., Sankilampi, Ulla, Lehtonen, Liisa, Marttila, Riitta H., Bassler, Dirk, Poets, Christian F., Lacaze-Masmonteil, Thierry, Danan, Claude, Delacourt, Christophe, Palotie, Aarno, Muglia, Louis J., Lavoie, Pascal M., Hadchouel, Alice, Rämet, Mika, Hallman, Mikko
Gepubliceerd in Sci Rep (2017)

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

door 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, Christensen, Kaare, Williams, Scott M., Rämet, Mika, Kingsmore, Stephen F., Ryckman, Kelli K., Hallman, Mikko, Muglia, Louis J.
Gepubliceerd in PLoS Genet (2018)

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

door 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, Christensen, Kaare, Williams, Scott M., Rämet, Mika, Kingsmore, Stephen F., Ryckman, Kelli K., Hallman, Mikko, Muglia, Louis J.
Gepubliceerd in PLoS Genet (2018)

Genetic Associations with Gestational Length and Spontaneous Preterm Birth

door Zhang, Ge, Feenstra, Bjarke, Bacelis, Jonas, Liu, Xueping, Muglia, Lisa M., Juodakis, Julius, Miller, Daniel E., Litterman, Nadia, Jiang, Pan-Pan, Russell, Laura, Hinds, David A., Hu, Youna, Weirauch, Matthew T., Chen, Xiaoting, Chavan, Arun R., Wagner, Günter P., Pavličev, Mihaela, Nnamani, Mauris C., Maziarz, Jamie, Karjalainen, Minna K., Rämet, Mika, Sengpiel, Verena, Geller, D Frank, Boyd, Heather A., Palotie, Aarno, Momany, Allison, Bedell, Bruce, Ryckman, Kelli K., Huusko, Johanna M., Forney, Carmy R., Kottyan, Leah C., Hallman, Mikko, Teramo, Kari, Nohr, Ellen A., Davey-Smith, George, Melbye, Mads, Jacobsson, Bo, Muglia, Louis J.
Gepubliceerd in N Engl J Med (2017)