| Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1 E Jaeger, S Leedham, A Lewis, S Segditsas, M Becker, PR Cuadrado, ... Nature genetics 44 (6), 699-703, 2012 | 290 | 2012 |
| A polymorphic enhancer near GREM1 influences bowel cancer risk through differential CDX2 and TCF7L2 binding A Lewis, L Freeman-Mills, E de la Calle-Mustienes, RM Giráldez-Pérez, ... Cell reports 8 (4), 983-990, 2014 | 54 | 2014 |
| Presynaptic dysfunction in CASK-related neurodevelopmental disorders M Becker, F Mastropasqua, JP Reising, S Maier, ML Ho, I Rabkina, D Li, ... Translational psychiatry 10 (1), 312, 2020 | 33 | 2020 |
| Mapping of Human FOXP2 Enhancers Reveals Complex Regulation M Becker, P Devanna, SE Fisher, SC Vernes Frontiers in molecular neuroscience 11, 47, 2018 | 25 | 2018 |
| Enrichment of rare copy number variation in children with developmental language disorder N Kalnak, S Stamouli, M Peyrard‐Janvid, I Rabkina, M Becker, ... Clinical Genetics 94 (3-4), 313-320, 2018 | 24 | 2018 |
| Association between copy number variation and response to social skills training in autism spectrum disorder K Tammimies, D Li, I Rabkina, S Stamouli, M Becker, V Nicolaou, ... Scientific reports 9 (1), 9810, 2019 | 22 | 2019 |
| A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer M Becker, P Devanna, SE Fisher, SC Vernes Molecular cytogenetics 8, 1-3, 2015 | 17 | 2015 |
| Spermatogonia loss correlates with LAMA 1 expression in human prepubertal testes stored for fertility preservation M Kurek, E Åkesson, M Yoshihara, E Oliver, Y Cui, M Becker, ... Cells 10 (2), 241, 2021 | 15 | 2021 |
| Early developmental gene enhancers affect subcortical volumes in the adult human brain M Becker, T Guadalupe, B Franke, DP Hibar, ME Renteria, JL Stein, ... Human brain mapping 37 (5), 1788-1800, 2016 | 10 | 2016 |
| Rare variants in the outcome of social skills group training for autism D Li, N Choque Olsson, M Becker, A Arora, H Jiao, N Norgren, U Jonsson, ... Autism Research 15 (3), 434-446, 2022 | 7 | 2022 |
| East J, Taylor J, Thomas H, Tomlinson I. Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP … E Jaeger, S Leedham, A Lewis, S Segditsas, M Becker, PR Cuadrado, ... Nat Genet 44 (6), 699-703, 2012 | 7 | 2012 |
| Deficiency of the Heterogeneous Nuclear Ribonucleoprotein U locus leads to delayed hindbrain neurogenesis F Mastropasqua, M Oksanen, C Soldini, S Alatar, A Arora, R Ballarino, ... Biology open 12 (10), 2023 | 4 | 2023 |
| Screening autism-associated environmental factors in differentiating human neural progenitors with fractional factorial design-based transcriptomics A Arora, M Becker, C Marques, M Oksanen, D Li, F Mastropasqua, ... Scientific Reports 13 (1), 10519, 2023 | 3 | 2023 |
| Transcriptomic and functional mapping of autism associated environmental factors in developing human neurons A Arora, M Becker, C Marques, M Oksanen, D Li, F Mastropasqua, ... bioRxiv, 2022 | 1 | 2022 |
| On the identification of FOXP2 gene enhancers and their role in brain development M Becker [Sl]:[Sn], 2016 | 1 | 2016 |
| Hnrnpu Expression Affects Transcriptional Programs and Chromatin Organization during Neuronal Maturation F Mastropasqua, M Oksanen, C Soldini, S Alatar, A Arora, R Ballarino, ... INSAR 2023, 2023 | | 2023 |
| Transcriptomic and functional mapping of autism associated environmental factors in differentiating human neural progenitors A Arora, M Becker, C Marques, M Oksanen, D Li, F Mastropasqua, ... bioRxiv, 2022.06. 27.497311, 2022 | | 2022 |
| Genetic determinants for social skill training outcomes in autism spectrum disorder D Li, I Rabkina, S Stamouli, H Jiao, M Becker, U Jonsson, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1421-1422, 2019 | | 2019 |
| Resolving effects of CASK mutations in children with neurodevelopmental disorders M Becker, F Mastropasqua, JP Reising, I Rabkina, L Ballenberger, M Kele, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1423-1423, 2019 | | 2019 |
| Understanding the role of HNRNPU in brain development and neurodevelopmental disorders F Mastropasqua, I Rabkina, M Becker, B Anderlid, S Bolte, A Falk, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1437-1437, 2019 | | 2019 |
Kristiina TammimiesCentre of Neurodevelopmental Disorders at Karolinska InstitutetVerified email at ki.se
