Scientists

Vollstedt EJ, Schaake S, Lohmann K, Padmanabhan S, Brice A, Lesage S, Tesson C, Vidailhet M, Wurster I, Hentati F, Mirelman A, Giladi N, Marder K, Waters C, Fahn S, Kasten M, Brüggemann N, Borsche M, Foroud T, Tolosa E, Garrido A, Annesi G, Gagliardi M, Bozi M, Stefanis L et al. (2023)
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Mov Disord (in press)
DOI 10.1002/mds.29288, PubMed 36692014

Yousaf H, Fatima A, Ali Z, Baig SM, Toft M, Iqbal Z (2022)
A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family
Genes (Basel), 13 (9)
DOI 10.3390/genes13091667, PubMed 36140834

Pihlstrøm L, Shireby G, Geut H, Henriksen SP, Rozemuller AJM, Tunold JA, Hannon E, Francis P, Thomas AJ, Love S, Mill J, van de Berg WDJ, Toft M (2022)
Epigenome-wide association study of human frontal cortex identifies differential methylation in Lewy body pathology
Nat Commun, 13 (1), 4932
DOI 10.1038/s41467-022-32619-z, PubMed 35995800