Publications

Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history

Emadeldin Hassanin, Patrick May, Rana Aldisi, Isabel Spier, Andreas J Forstner, Markus M Nöthen, Stefan Aretz, Peter Krawitz, Dheeraj Reddy Bobbili, Carlo Maj
Genet Med. 2022 Mar;24(3):576-585. doi: 10.1016/j.gim.2021.11.009. Epub 2021 Nov 18.
https://pubmed.ncbi.nlm.nih.gov/34906469/

Genotype-Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic Review

Wittke C, Petkovic S, Dobricic V, Schaake S, MDS‐endorsed PSP Study Group, Respondek G, Weissbach A,Madoev H, Trinh J, Vollstedt E-J, Kuhnke N, Lohmann K, Dulovic Mahlow M, Marras C, König IR, Stamelou M, Bonifati V, Lill CM, Kasten M, Hupp HJ, Klein C
Mov Disord. 2021 Jul;36(7):1499-1510. doi: 10.1002/mds.28517. Epub 2021 Mar 19.
https://pubmed.ncbi.nlm.nih.gov/34396589/

The Importance of Drosophila melanogaster Research to UnCover Cellular Pathways Underlying Parkinson’s Disease

Vos M, Klein C.
Cells. 2021 Mar 6;10(3):579. doi: 10.3390/cells10030579.
https://pubmed.ncbi.nlm.nih.gov/33800736/

First Case of Parkinsonian-Pyramidal Syndrome Associated with a TBK1 Mutation

Santos-García D, Pozojevic J, de Deus Fonticoba T, Kurtis M, Gamez J, Klein C, Monje MHG, Westenberger A
Mov Disord. 2021 Feb;36(2):523-525. doi: 10.1002/mds.28405. Epub 2020 Nov 27.
https://pubmed.ncbi.nlm.nih.gov/33245169/

Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson’s disease: mutational spectrum and clinical features

Lim JL, Lohmann K, Tan AH, Tay YW, Ibrahim KA, Abdul Aziz Z, Mawardi AS, Puvanarajah SD, Lim TT, Looi I, Ooi JCE, Chia YK, Muthusamy KA, Bauer P, Rolfs A, Klein C, Ahmad-Annuar A, Lim SY.
J Neural Transm (Vienna). 2022 Jan;129(1):37-48. doi: 10.1007/s00702-021-02421-0. Epub 2021 Nov 15.
https://pubmed.ncbi.nlm.nih.gov/34779914/

Monogenic Causes of Dystonic Syndromes: Common in Dystonic Cerebral Palsy, Rare in Isolated Dystonia

Lara Mariah Lange, Christine Klein
Mov Disord. 2021 Jan;36(1):84. doi: 10.1002/mds.28420. Epub 2020 Dec 7.
https://pubmed.ncbi.nlm.nih.gov/33284469/

Genetic Risk of Alzheimer’s Disease – Sleepless with the Enemy

Alastair J Noyce, Christine Klein
Ann Neurol. 2021 Jan;89(1):27-29. doi: 10.1002/ana.25938. Epub 2020 Oct 29.
https://pubmed.ncbi.nlm.nih.gov/33070350/

Discordant Monozygotic Parkinson Disease Twins: Role of Mitochondrial Integrity

Dulovic-Mahlow M , König IR , Trinh J , Diaw SH , Urban PP, Knappe E, Kuhnke N , Ingwersen LC , Hinrichs F, Weber J, Kupnicka P, Balck A, Delcambre S, Vollbrandt T, Grünewald A, Klein C, Seibler P, Lohmann K
Ann Neurol. 2021 Jan;89(1):158-164. doi: 10.1002/ana.25942. Epub 2020 Nov 4.
https://pubmed.ncbi.nlm.nih.gov/33094862/

Parkin Deficiency Appears Not to Be Associated with Cardiac Damage in Parkinson’s Disease

Trilck-Winkler M, Borsche M, König IR, Balck A, Lenz I, Kasten M, Lohmann K, Brockmann K, Valente EM, Klein C, Brüggemann N, Seibler P
Mov Disord. 2021 Jan;36(1):271-273. doi: 10.1002/mds.28422.
https://pubmed.ncbi.nlm.nih.gov/33492791/

A mixed-ethnicity myoclonus-dystonia patient with a novel SGCE nonsense mutation: a case report

Meliza Angelica J de Leon, Raymond L Rosales, Christine Klein, Ana Westenberger
BMC Neurol. 2022 Jan 5;22(1):11. doi: 10.1186/s12883-021-02530-z.
https://pubmed.ncbi.nlm.nih.gov/34986800/

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