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2020
Mark Dyslexia Candidate Gene and Ciliary Gene Expression Dynamics During Human Neuronal Differentiation
Bieder, Andrea ; Yoshihara, Masahito ; Katayama, Shintaro ; Krjutškov, Kaarel ; Falk, Anna ^LU ; Kere, Juha and Tapia-Páez, Isabel (2020) In Molecular Neurobiology 57(7). p.2944-2958
- Contribution to journal › Article
2017
Mark Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation
Purhonen, Janne ; Rajendran, Jayasimman ; Mörgelin, Matthias ^LU ; Uusi-Rauva, Kristiina ; Katayama, Shintaro ; Krjutskov, Kaarel ; Einarsdottir, Elisabet ; Velagapudi, Vidya ; Kere, Juha and Jauhiainen, Matti , et al. (2017) In Scientific Reports 7(1).
- Contribution to journal › Article
Mark Acute doses of caffeine shift nervous system cell expression profiles toward promotion of neuronal projection growth
Yu, Nancy Y ; Bieder, Andrea ; Raman, Amitha ; Mileti, Enrichetta ; Katayama, Shintaro ; Einarsdottir, Elisabet ; Fredholm, Bertil B ; Falk, Anna ^LU ; Tapia-Páez, Isabel and Daub, Carsten O , et al. (2017) In Scientific Reports 7(1).
- Contribution to journal › Article
Mark CELSR2 is a candidate susceptibility gene in idiopathic scoliosis
Einarsdottir, Elisabet ; Grauers, Anna ; Wang, Jingwen ; Jiao, Hong ; Escher, Stefan A. ; Danielsson, Aina ; Simony, Ane ; Andersen, Mikkel ; Christensen, Steen Bach and Åkesson, Kristina ^LU , et al. (2017) In PLoS ONE 12(12).
- Contribution to journal › Article
2015
Mark Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus
Acevedo, Nathalie ; Reinius, Lovisa E ; Greco, Dario ; Gref, Anna ; Orsmark-Pietras, Christina ^LU ; Persson, Helena ^LU ; Pershagen, Göran ; Hedlin, Gunilla ; Melén, Erik and Scheynius, Annika , et al. (2015) In Human Molecular Genetics 24(3). p.90-875
- Contribution to journal › Article
Mark Polymorphisms in DCDC2 and S100B associate with developmental dyslexia
Matsson, Hans ; Huss, Mikael ; Persson, Helena ^LU ; Einarsdottir, Elisabet ; Tiraboschi, Ettore ; Nopola-Hemmi, Jaana ; Schumacher, Johannes ; Neuhoff, Nina ; Warnke, Andreas and Lyytinen, Heikki , et al. (2015) In Journal of Human Genetics 60(7). p.399-401
- Contribution to journal › Article
Mark Transcriptome analysis of controlled and therapy-resistant childhood asthma reveals distinct gene expression profiles
Persson, Helena ^LU ; Kwon, Andrew T ; Ramilowski, Jordan A ; Silberberg, Gilad ; Söderhäll, Cilla ; Orsmark-Pietras, Christina ^LU ; Nordlund, Björn ; Konradsen, Jon R ; de Hoon, Michiel J L and Melén, Erik , et al. (2015) In Journal of Allergy and Clinical Immunology 136(3). p.48-638
- Contribution to journal › Article
Mark Helsinki alert of biodiversity and health
von Hertzen, Leena ; Beutler, Bruce ; Bienenstock, John ; Blaser, Martin ; Cani, Patrice D. ; Eriksson, Johan ; Farkkila, Martti ; Haahtela, Tari ; Hanski, Ilkka and Jenmalm, Maria C. , et al. (2015) In Annals of Medicine 47(3). p.218-225
- Contribution to journal › Scientific review
2014
Mark The Roots of Autism and ADHD Twin Study in Sweden (RATSS)
Bölte, Sven ; Willfors, Charlotte ; Berggren, Steve ; Norberg, Joakim ; Poltrago, Lina ; Mevel, Katell ; Coco, Christina ; Fransson, Peter ; Borg, Jacqueline and Sitnikov, Rouslan , et al. (2014) In Twin Research and Human Genetics 17(3). p.76-164
- Contribution to journal › Article
Mark Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease.
Flanagan, Sarah E ; Haapaniemi, Emma ; Russell, Mark A ; Caswell, Richard ; Lango Allen, Hana ; De Franco, Elisa ; McDonald, Timothy J ; Rajala, Hanna ; Ramelius, Anita ^LU and Barton, John , et al. (2014) In Nature Genetics 46(8). p.812-814
- Contribution to journal › Article

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