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2024
Mark Malignant hyperthermia safety - A nationwide survey of publicly funded Swedish healthcare
Hellblom, Anna ^LU ; Pettersson Miller, William ; Soller, Maria ^LU and Samuelsson, Carolina ^LU (2024) In Acta Anaesthesiologica Scandinavica p.1-6
- Contribution to journal › Article
2022
Mark Implementing precision medicine in a regionally organized healthcare system in Sweden
Fioretos, Thoas ^LU ; Wirta, Valtteri ; Cavelier, Lucia ; Berglund, Eva ; Friedman, Mikaela ; Akhras, Michael ; Botling, Johan ; Ehrencrona, Hans ^LU ; Engstrand, Lars and Helenius, Gisela , et al. (2022) In Nature Medicine 28(10). p.1980-1982
- Contribution to journal › Letter
2020
Mark Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
Ilinca, Andreea ^LU ; Martinez-Majander, Nicolas ; Samuelsson, Sofie ^LU ; Piccinelli, Paul ^LU ; Truvé, Katarina ; Cole, John ; Kittner, Steven ; Soller, Maria ^LU ; Kristoffersson, Ulf ^LU and Tatlisumak, Turgut , et al. (2020) In Stroke 51(4). p.1056-1063
- Contribution to journal › Article
2019
Mark A stroke gene panel for whole-exome sequencing
Ilinca, Andreea ^LU ; Samuelsson, Sofie ^LU ; Piccinelli, Paul ^LU ; Soller, Maria ^LU ; Kristoffersson, Ulf ^LU and Lindgren, Arne G. ^LU (2019) In European Journal of Human Genetics 27(2). p.317-324
- Contribution to journal › Article
2017
Mark Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU
Depienne, Christel ; Nava, Caroline ; Keren, Boris ; Heide, Solveig ; Rastetter, Agnès ; Passemard, Sandrine ; Chantot-Bastaraud, Sandra ; Moutard, Marie Laure ; Agrawal, Pankaj B. and VanNoy, Grace , et al. (2017) In Human Genetics 136(4). p.463-479
- Contribution to journal › Article
Mark Respiratory chain complex III deficiency due to mutated BCS1L : A novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model
Tegelberg, Saara ^LU ; Tomašić, Nikica ^LU ; Kallijärvi, Jukka ^LU ; Purhonen, Janne ; Elmér, Eskil ^LU ; Lindberg, Eva ; Nord, David Gisselsson ^LU ; Soller, Maria ^LU ; Lesko, Nicole and Wedell, Anna , et al. (2017) In Orphanet Journal of Rare Diseases 12(1).
- Contribution to journal › Article
2016
Mark Familial aggregation of stroke amongst young patients in Lund Stroke Register.
Ilinca, Andreea ^LU ; Kristoffersson, Ulf ^LU ; Soller, Maria ^LU and Lindgren, Arne ^LU (2016) In European Journal of Neurology 23(2). p.401-407
- Contribution to journal › Article
Mark The fetal thymus has a unique genomic copy number profile resulting from physiological T cell receptor gene rearrangement
Valind, Anders ^LU ; HAIKAL, CAROLINE ^LU ; Klasson, M E K ; Johansson, M C ^LU ; Gullander, J ^LU ; Soller, M ^LU ; Baldetorp, B ^LU and Gisselsson, David ^LU (2016) In Scientific Reports 6.
- Contribution to journal › Article
Mark No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
Hollestelle, Antoinette ; Van Der Baan, Frederieke H. ; Berchuck, Andrew ; Johnatty, Sharon E. ; Aben, Katja K. ; Agnarsson, Bjarni A. ; Aittomäki, Kristiina ; Alducci, Elisa ; Andrulis, Irene L. and Anton-Culver, Hoda , et al. (2016) In Gynecologic Oncology 141(2). p.386-401
- Contribution to journal › Article
2015
Mark No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.
Schlögel, Matthieu J ; Mendola, Antonella ; Fastré, Elodie ; Vasudevan, Pradeep ; Devriendt, Koen ; de Ravel, Thomy Jl ; Van Esch, Hilde ; Casteels, Ingele ; Arroyo Carrera, Ignacio and Cristofoli, Francesca , et al. (2015) In Orphanet Journal of Rare Diseases 10(1).
- Contribution to journal › Article

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your query:: Remove author: Soller, Maria (LU); Remove department: Division of Clinical Genetics