Works by Hallman, Mikko

Results: 136
    1

    Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother-infant pairs.

    Published in:
    2020
    By:
    • Chen, Jing;
    • Bacelis, Jonas;
    • Sole-Navais, Pol;
    • Srivastava, Amit;
    • Juodakis, Julius;
    • Rouse, Amy;
    • Hallman, Mikko;
    • Teramo, Kari;
    • Melbye, Mads;
    • Feenstra, Bjarke;
    • Freathy, Rachel M.;
    • Smith, George Davey;
    • Lawlor, Deborah A.;
    • Murray, Jeffrey C.;
    • Williams, Scott M.;
    • Jacobsson, Bo;
    • Muglia, Louis J.;
    • Zhang, Ge
    Publication type:
    journal article
    2
    3
    4
    5
    6
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16

    Development and behaviour of 5-year-old very low birthweight infants.

    Published in:
    European Child & Adolescent Psychiatry, 2010, v. 19, n. 8, p. 669, doi. 10.1007/s00787-010-0104-x
    By:
    • Rautava, Liisi;
    • Andersson, Sture;
    • Gissler, Mika;
    • Hallman, Mikko;
    • Häkkinen, Unto;
    • Korvenranta, Emmi;
    • Korvenranta, Heikki;
    • Leipälä, Jaana;
    • Tammela, Outi;
    • Lehtonen, Liisa
    Publication type:
    Article
    17
    18
    19
    20

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

    Published in:
    Journal of Cellular & Molecular Medicine, 2018, v. 22, n. 2, p. 968, doi. 10.1111/jcmm.13402
    By:
    • 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
    Publication type:
    Article
    21
    22
    23

    Cerebral palsy is characterized by protein mediators in cord serum.

    Published in:
    Annals of Neurology, 2004, v. 55, n. 2, p. 186
    By:
    • Tuula Kaukola;
    • Ebenezer Satyaraj;
    • Dhavalkumar D. Patel;
    • Velizar T. Tchernev;
    • Brian G. Grimwade;
    • Stephen F. Kingsmore;
    • Pentti Koskela;
    • Outi Tammela;
    • Leena Vainionpää;
    • Helena Pihko;
    • Tuula Äärimaa;
    • Mikko Hallman
    Publication type:
    Article
    24
    25
    26
    27
    28
    29
    30
    31

    TREOCAPA: prophylactic treatment of the ductus arteriosus in preterm infants by acetaminophen—statistical analysis plan for the randomized phase III group sequential trial.

    Published in:
    Trials, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s13063-025-08751-8
    By:
    • Ursino, Moreno;
    • Alberti, Corinne;
    • Cambonie, Gilles;
    • Kemp, Ruth;
    • Vanhecke, Aure;
    • Levoyer, Lea;
    • Diallo, Alpha;
    • Hallman, Mikko;
    • Rozé, Jean-Christophe;
    • Alberti, Corine;
    • Carbajal, Ricardo;
    • Kuhn, Pierre;
    • Baruteau, Alban;
    • Morgan, Andrei;
    • Ancel, Pierre-Yves;
    • Zeilin, Jennifer;
    • Bouazza, Naim;
    • Baud, Olivier;
    • Claris, Olivier;
    • Picaud, Jean-Charles
    Publication type:
    Article
    32

    Identification of SPOCK2 As a Susceptibility Gene for Bronchopulmonary Dysplasia.

    Published in:
    American Journal of Respiratory & Critical Care Medicine, 2011, v. 184, n. 10, p. 1164, doi. 10.1164/rccm.201103-0548OC
    By:
    • Hadchouel, Alice;
    • Durrmeyers, Xavier;
    • Bouzigon, Emmanuelle;
    • Incitti, Roberto;
    • Huusko, Johanna;
    • Jarreau, Pierre-Henri;
    • Demenais, Florence;
    • Franco-Montoyal, Marie-Laure;
    • Layouni, Inès;
    • Patkai, Juliana;
    • Bourbon, Jacques;
    • Hallman, Mikko;
    • Danan, Claude;
    • Delacourt, Christophe
    Publication type:
    Article
    33
    34
    35

    Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease.

    Published in:
    Frontiers in Neuroscience, 2023, p. 01, doi. 10.3389/fnins.2023.1123327
    By:
    • Tallgren, Antti;
    • Kager, Leo;
    • O'Grady, Gina;
    • Tuominen, Hannu;
    • Körkkö, Jarmo;
    • Kuismin, Outi;
    • Feucht, Martha;
    • Wilson, Callum;
    • Behunova, Jana;
    • England, Eleina;
    • Kurki, Mitja I.;
    • Palotie, Aarno;
    • Hallman, Mikko;
    • Kaarteenaho, Riitta;
    • Laccone, Franco;
    • Boztug, Kaan;
    • Hinttala, Reetta;
    • Uusimaa, Johanna
    Publication type:
    Article
    36
    37
    38
    39
    40
    41
    42
    43
    44

    Differences in the length of initial hospital stay in very preterm infants.

    Published in:
    Acta Paediatrica, 2007, v. 96, n. 10, p. 1416, doi. 10.1111/j.1651-2227.2007.00471.x
    By:
    • Korvenranta, Emmi;
    • Linna, Miika;
    • Häkkinen, Unto;
    • Peltola, Mikko;
    • Andersson, Sture;
    • Gissler, Mika;
    • Hallman, Mikko;
    • Korvenranta, Heikki;
    • Leipälä, Jaana;
    • Rautava, Liisi;
    • Tammela, Outi;
    • Lehtonen, Liisa
    Publication type:
    Article
    45
    46
    47
    48
    49
    50

    Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study.

    Published in:
    BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-77
    By:
    • Kim, Jinsil;
    • Stirling, Kara J.;
    • Cooper, Margaret E.;
    • Ascoli, Mario;
    • Momany, Allison M.;
    • McDonald, Erin L.;
    • Ryckman, Kelli K.;
    • Rhea, Lindsey;
    • Schaa, Kendra L.;
    • Cosentino, Viviana;
    • Gadow, Enrique;
    • Saleme, Cesar;
    • Shi, Min;
    • Hallman, Mikko;
    • Plunkett, Jevon;
    • Kari A.;
    • Muglia, Louis J.;
    • Feenstra, Bjarke;
    • Geller, Frank;
    • Boyd, Heather A.
    Publication type:
    Article