The role of teacher characteristics for student achievement in mathematics and student perceptions of instructional quality

by Anna Toropova, Stefan Johansson, Eva Myrberg
Published 2019-10-01

Inter-pregnancy Weight Change and Risks of Severe Birth-Asphyxia-Related Outcomes in Singleton Infants Born at Term: A Nationwide Swedish Cohort Study.

by Martina Persson, Stefan Johansson, Sven Cnattingius
Published 2016-06-01

Are future renewable energy targets consistent with current planning perspectives?

by Jon Rytterbro, Markus Robert, Stefan Johansson, Nils Brandt
Published 2011-07-01

Maternal overweight and obesity and risks of severe birth-asphyxia-related complications in term infants: a population-based cohort study in Sweden.

by Martina Persson, Stefan Johansson, Eduardo Villamor, Sven Cnattingius
Published 2014-05-01

Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients.

by Thegna Mavroconstanti, Stefan Johansson, Ingeborg Winge, Per M Knappskog, Jan Haavik
Published 2013-01-01

Novel SACS mutations identified by whole exome sequencing in a norwegian family with autosomal recessive spastic ataxia of Charlevoix-Saguenay.

by Charalampos Tzoulis, Stefan Johansson, Bjørn Ivar Haukanes, Helge Boman, Per Morten Knappskog, Laurence A Bindoff
Published 2013-01-01

Surge of immune cell formation at birth differs by mode of delivery and infant characteristics-A population-based cohort study.

by Titus Schlinzig, Stefan Johansson, Olof Stephansson, Lennart Hammarström, Rolf H Zetterström, Ulrika von Döbeln, Sven Cnattingius, Mikael Norman
Published 2017-01-01

Chip Protein U-Box Domain Truncation Affects Purkinje Neuron Morphology and Leads to Behavioral Changes in Zebrafish

by Yasaman Pakdaman, Yasaman Pakdaman, Yasaman Pakdaman, Elsa Denker, Eirik Austad, William H. J. Norton, Hans O. Rolfsnes, Laurence A. Bindoff, Laurence A. Bindoff, Charalampos Tzoulis, Charalampos Tzoulis, Ingvild Aukrust, Ingvild Aukrust, Per M. Knappskog, Per M. Knappskog, Stefan Johansson, Stefan Johansson, Ståle Ellingsen
Published 2021-09-01

Transcriptional Changes in Regulatory T Cells From Patients With Autoimmune Polyendocrine Syndrome Type 1 Suggest Functional Impairment of Lipid Metabolism and Gut Homing

by Amund Holte Berger, Amund Holte Berger, Amund Holte Berger, Eirik Bratland, Eirik Bratland, Eirik Bratland, Thea Sjøgren, Thea Sjøgren, Thea Sjøgren, Marte Heimli, Marte Heimli, Marte Heimli, Torgeir Tyssedal, Torgeir Tyssedal, Øyvind Bruserud, Øyvind Bruserud, Øyvind Bruserud, Stefan Johansson, Stefan Johansson, Stefan Johansson, Eystein Sverre Husebye, Eystein Sverre Husebye, Eystein Sverre Husebye, Bergithe Eikeland Oftedal, Bergithe Eikeland Oftedal, Bergithe Eikeland Oftedal, Anette Susanne Bøe Wolff, Anette Susanne Bøe Wolff, Anette Susanne Bøe Wolff
Published 2021-08-01

The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey)

by Øyvind Helgeland, Jens K. Hertel, Anders Molven, Helge Ræder, Carl G. P. Platou, Kristian Midthjell, Kristian Hveem, Ottar Nygård, Pål R. Njølstad, Stefan Johansson
Published 2015-01-01

Assessing the Causal Relationship of Maternal Height on Birth Size and Gestational Age at Birth: A Mendelian Randomization Analysis.

by 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
Published 2015-08-01

Novel SLC19A3 Promoter Deletion and Allelic Silencing in Biotin-Thiamine-Responsive Basal Ganglia Encephalopathy.

by Irene Flønes, Paweł Sztromwasser, Kristoffer Haugarvoll, Christian Dölle, Maria Lykouri, Thomas Schwarzlmüller, Inge Jonassen, Hrvoje Miletic, Stefan Johansson, Per M Knappskog, Laurence A Bindoff, Charalampos Tzoulis
Published 2016-01-01

Exome sequencing and genetic testing for MODY.

by Stefan Johansson, Henrik Irgens, Kishan K Chudasama, Janne Molnes, Jan Aerts, Francisco S Roque, Inge Jonassen, Shawn Levy, Kari Lima, Per M Knappskog, Graeme I Bell, Anders Molven, Pål R Njølstad
Published 2012-01-01

GBA2 Mutations Cause a Marinesco-Sjögren-Like Syndrome: Genetic and Biochemical Studies.

by Kristoffer Haugarvoll, Stefan Johansson, Carlos E Rodriguez, Helge Boman, Bjørn Ivar Haukanes, Ove Bruland, Francisco Roque, Inge Jonassen, Maria Blomqvist, Wenche Telstad, Jan-Eric Månsson, Per Morten Knappskog, Laurence A Bindoff
Published 2017-01-01

Genome-wide analysis of attention deficit hyperactivity disorder in Norway.

by Tetyana Zayats, Lavinia Athanasiu, Ida Sonderby, Srdjan Djurovic, Lars T Westlye, Christian K Tamnes, Tormod Fladby, Heidi Aase, Pål Zeiner, Ted Reichborn-Kjennerud, Per M Knappskog, Gun Peggy Knudsen, Ole A Andreassen, Stefan Johansson, Jan Haavik
Published 2015-01-01

Genetic Dominant Variants in <i>STUB1,</i> Segregating in Families with SCA48, Display In Vitro Functional Impairments Indistinctive from Recessive Variants Associated with SCAR16

by Yasaman Pakdaman, Siren Berland, Helene J. Bustad, Sigrid Erdal, Bryony A. Thompson, Paul A. James, Kjersti N. Power, Ståle Ellingsen, Martin Krooni, Line I. Berge, Adrienne Sexton, Laurence A. Bindoff, Per M. Knappskog, Stefan Johansson, Ingvild Aukrust
Published 2021-05-01

Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth

by Øyvind Helgeland, Marc Vaudel, Petur B. Juliusson, Oddgeir Lingaas Holmen, Julius Juodakis, Jonas Bacelis, Bo Jacobsson, Haakon Lindekleiv, Kristian Hveem, Rolv Terje Lie, Gun Peggy Knudsen, Camilla Stoltenberg, Per Magnus, Jørn V. Sagen, Anders Molven, Stefan Johansson, Pål Rasmus Njølstad
Published 2019-10-01

Length of Variable Numbers of Tandem Repeats in the Carboxyl Ester Lipase (CEL) Gene May Confer Susceptibility to Alcoholic Liver Cirrhosis but Not Alcoholic Chronic Pancreatitis.

by Karianne Fjeld, Sebastian Beer, Marianne Johnstone, Constantin Zimmer, Joachim Mössner, Claudia Ruffert, Mario Krehan, Christian Zapf, Pål Rasmus Njølstad, Stefan Johansson, Peter Bugert, Fabio Miyajima, Triantafillos Liloglou, Laura J Brown, Simon A Winn, Kelly Davies, Diane Latawiec, Bridget K Gunson, David N Criddle, Munir Pirmohamed, Robert Grützmann, Patrick Michl, William Greenhalf, Anders Molven, Robert Sutton, Jonas Rosendahl
Published 2016-01-01

DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder.

by Bjarte Håvik, Franziska A Degenhardt, Stefan Johansson, Carla P D Fernandes, Anke Hinney, André Scherag, Helle Lybæk, Srdjan Djurovic, Andrea Christoforou, Kari M Ersland, Sudheer Giddaluru, Michael C O'Donovan, Michael J Owen, Nick Craddock, Thomas W Mühleisen, Manuel Mattheisen, Benno G Schimmelmann, Tobias Renner, Andreas Warnke, Beate Herpertz-Dahlmann, Judith Sinzig, Özgür Albayrak, Marcella Rietschel, Markus M Nöthen, Clive R Bramham, Thomas Werge, Johannes Hebebrand, Jan Haavik, Ole A Andreassen, Sven Cichon, Vidar M Steen, Stéphanie Le Hellard
Published 2012-01-01

GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibility

by Daniel Eriksson, Ellen Christine Røyrvik, Maribel Aranda-Guillén, Amund Holte Berger, Nils Landegren, Haydee Artaza, Åsa Hallgren, Marianne Aardal Grytaas, Sara Ström, Eirik Bratland, Ileana Ruxandra Botusan, Bergithe Eikeland Oftedal, Lars Breivik, Marc Vaudel, Øyvind Helgeland, Alberto Falorni, Anders Palmstrøm Jørgensen, Anna-Lena Hulting, Johan Svartberg, Olov Ekwall, Kristian Johan Fougner, Jeanette Wahlberg, Bjørn Gunnar Nedrebø, Per Dahlqvist, The Norwegian Addison Registry Study Group, The Swedish Addison Registry Study Group, Per Morten Knappskog, Anette Susanne Bøe Wolff, Sophie Bensing, Stefan Johansson, Olle Kämpe, Eystein Sverre Husebye
Published 2021-02-01