New insights in the genetic variant spectrum of SLC34A2 in pulmonary alveolar microlithiasis; a systematic review von Jönsson, Åsa Lina M, Hilberg, Ole, Simonsen, Ulf, Christensen, Jane Hvarregaard, Bendstrup, Elisabeth

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Impaired phosphate transport in SLC34A2 variants in patients with pulmonary alveolar microlithiasis von Jönsson, Åsa Lina M, Hernando, Nati, Knöpfel, Thomas, Mogensen, Susie, Bendstrup, Elisabeth, Hilberg, Ole, Christensen, Jane Hvarregaard, Simonsen, Ulf, Wagner, Carsten A

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Pulmonary Alveolar Microlithiasis-A Review von Enemark, Asbjorn, Jonsson, Asa Lina M., Kronborg-White, Sissel, Bendstrup, Elisabeth

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Eight novel variants in the SLC34A2 gene in pulmonary alveolar microlithiasis von Jonsson, Asa Lina M., Bendstrup, Elisabeth, Mogensen, Susie, Kopras, Elizabeth J., McCormack, Francis X., Campo, Ilaria, Mariani, Francesca, Escribano-Montaner, Amparo, Holm, Are M., del Mar Martinez-Colls, Maria, Pintos-Morell, Guillem, Taille, Camille, Crestani, Bruno, Hilberg, Ole, Christensen, Jane Hvarregaard, Simonsen, Ulf

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Pulmonary alveolar microlithiasis: no longer in the stone age von Bendstrup, Elisabeth, Jönsson, Åsa Lina M.

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Conformation traits and their genetic and phenotypic associations with health status in young Swedish warmblood riding horses von Jönsson, Lina, Näsholm, Anna, Roepstorff, Lars, Egenvall, Agneta, Dalin, Göran, Philipsson, Jan

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Pulmonary alveolar microlithiasis: two case reports and review of the literature von Jönsson, Åsa Lina M, Simonsen, Ulf, Hilberg, Ole, Bendstrup, Elisabeth

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SLC34A2 gene mutation may explain comorbidity of pulmonary alveolar microlithiasis and aortic valve sclerosis von Jönsson, Åsa Lina M, Hilberg, Ole, Bendstrup, Elisabeth M, Mogensen, Susie, Simonsen, Ulf

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MAP1B mutations cause intellectual disability and extensive white matter deficit von Walters, G. Bragi, Gustafsson, Omar, Sveinbjornsson, Gardar, Eiriksdottir, Valgerdur K., Agustsdottir, Arna B., Jonsdottir, Gudrun A., Steinberg, Stacy, Gunnarsson, Arni F., Magnusson, Magnus I., Unnsteinsdottir, Unnur, Lee, Amy L., Jonasdottir, Adalbjorg, Sigurdsson, Asgeir, Jonasdottir, Aslaug, Skuladottir, Astros, Jonsson, Lina, Nawaz, Muhammad S., Sulem, Patrick, Frigge, Mike, Ingason, Andres, Love, Askell, Norddhal, Gudmundur L., Zervas, Mark, Gudbjartsson, Daniel F., Ulfarsson, Magnus O., Saemundsen, Evald, Stefansson, Hreinn, Stefansson, Kari

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Polygenic risk scores of lithium response and treatment resistance in major depressive disorder von Xiong, Ying, Karlsson, Robert, Song, Jie, Kowalec, Kaarina, Rück, Christian, Sigström, Robert, Jonsson, Lina, Clements, Caitlin C., Andersson, Evelyn, Boberg, Julia, Lewis, Cathryn M., Sullivan, Patrick F., Landén, Mikael, Lu, Yi

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Therapeutic Effect of Nicotinamide Mononucleotide for Hypoxic–Ischemic Brain Injury in Neonatal Mice von Kawamura, Takuya, Singh Mallah, Gagandeep, Ardalan, Maryam, Chumak, Tetyana, Svedin, Pernilla, Jonsson, Lina, Jabbari Shiadeh, Seyedeh Marziyeh, Goretta, Fanny, Ikeda, Tomoaki, Hagberg, Henrik, Sandberg, Mats, Mallard, Carina

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Associations between polymorphisms in sex steroid related genes and autistic-like traits von Zettergren, Anna, Jonsson, Lina, Johansson, Daniel, Melke, Jonas, Lundström, Sebastian, Anckarsäter, Henrik, Lichtenstein, Paul, Westberg, Lars

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Examining neurodevelopmental problems in 15q11.2 (BP1‐BP2) copy number variation carriers at ages 9/12 and 18 in a Swedish twin sample von Jonsson, Lina, Martin, Joanna, Lichtenstein, Paul, Magnusson, Patrik K. E., Lundström, Sebastian, Westberg, Lars, Tammimies, Kristiina

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Associations between oxytocin-related genes and autistic-like traits von Johansson, Daniel, Zettergren, Anna, Jonsson, Lina, Melke, Jonas, Anckarsäter, Henrik, Lichtenstein, Paul, Westberg, Lars

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Genomic applications in horse breeding von Stock, Kathrin F., Jönsson, Lina, Ricard, Anne, Mark, Thomas

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Mutation screening of melatonin-related genes in patients with autism spectrum disorders von Jonsson, Lina, Ljunggren, Elin, Bremer, Anna, Pedersen, Christin, Landén, Mikael, Thuresson, Kent, Giacobini, Maibritt, Melke, Jonas

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Possible association between the androgen receptor gene and autism spectrum disorder von Henningsson, Susanne, Jonsson, Lina, Ljunggren, Elin, Westberg, Lars, Gillberg, Carina, Råstam, Maria, Anckarsäter, Henrik, Nygren, Gudrun, Landén, Mikael, Thuresson, Kent, Betancur, Catalina, Leboyer, Marion, Gillberg, Christopher, Eriksson, Elias, Melke, Jonas

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Prevalence of clinical findings at examinations of young Swedish warmblood riding horses von Jönsson, Lina, Roepstorff, Lars, Egenvall, Agneta, Näsholm, Anna, Dalin, Göran, Philipsson, Jan

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Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder von Gudmundsson, Ólafur Ó, Walters, Gudmundur Bragi, Ingason, Andrés, Johansson, Stefan, Zayats, Tetyana, Athanasiu, Lavinia, Sønderby, Ida Elken, Gustafsson, Omar, Nawaz, Muhammad Sulaman, Jónsson, Gudbjörn F, Jónsson, Lina, Knappskog, Per, Ingvarsdóttir, Ester, Davidsdóttir, Katrin, Djurovic, Srdjan, Knudsen, Gun Peggy Strømstad, Askeland, Ragna Bugge, Haraldsdóttir, Gyda S, Baldursson, Gísli, Magnússon, Páll, Sigurdsson, Engilbert, Gudbjartsson, Daníel Fannar, Stéfansson, Hreinn, Andreassen, Ole Andreas, Haavik, Jan, Reichborn-Kjennerud, Ted, Stefánsson, Kári

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The unexpected “yes”: Explanatory factors behind the positive attitudes to congestion charges in Stockholm von Eliasson, Jonas, Jonsson, Lina

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