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2023
Mark Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia
Rezayee, Fatemah ; Eisfeldt, Jesper ; Skaftason, Aron ; Öfverholm, Ingegerd ; Sayyab, Shumaila ; Syvänen, Ann Christine ; Maqbool, Khurram ; Lilljebjörn, Henrik ^LU ; Johansson, Bertil ^LU and Olsson-Arvidsson, Linda ^LU , et al. (2023) In Frontiers in Oncology 13.
- Contribution to journal › Article
2022
Mark Multi-Omic Investigations of a 17-19 Translocation Links MINK1 Disruption to Autism, Epilepsy and Osteoporosis
Eisfeldt, Jesper ; Schuy, Jakob ; Stattin, Eva-Lena ; Kvarnung, Malin ; Falk, Anna ^LU ; Feuk, Lars and Lindstrand, Anna (2022) In International Journal of Molecular Sciences 23(16).
- Contribution to journal › Article
Mark Multi-omics analysis reveals multiple mechanisms causing Prader-Willi like syndrome in a family with a X;15 translocation
Eisfeldt, Jesper ; Rezayee, Fatemah ; Pettersson, Maria ^LU ; Lagerstedt, Kristina ; Malmgren, Helena ; Falk, Anna ^LU ; Grigelioniene, Giedre and Lindstrand, Anna (2022) In Human Mutation 43(11). p.1567-1575
- Contribution to journal › Article
Mark Partial Monosomy 21 Mirrors Gene Expression of Trisomy 21 in a Patient-Derived Neuroepithelial Stem Cell Model
Schuy, Jakob ; Eisfeldt, Jesper ; Pettersson, Maria ; Shahrokhshahi, Niloofar ; Moslem, Mohsen ; Nilsson, Daniel ; Dahl, Niklas ; Shahsavani, Mansoureh ; Falk, Anna ^LU and Lindstrand, Anna (2022) In Frontiers in Genetics 12.
- Contribution to journal › Article

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