Publications

Dobricic, V, Schilling, M, Farkas, I, Gveric, DO, Ohlei, O, Schulz, J et al.. Common signatures of differential microRNA expression in Parkinson's and Alzheimer's disease brains. Brain Commun. 2022;4 (6):fcac274. doi: 10.1093/braincomms/fcac274. PubMed PMID:36382223 PubMed Central PMC9645562.

Sommerer, Y, Dobricic, V, Schilling, M, Ohlei, O, Bartrés-Faz, D, Cattaneo, G et al.. Epigenome-Wide Association Study in Peripheral Tissues Highlights DNA Methylation Profiles Associated with Episodic Memory Performance in Humans. Biomedicines. 2022;10 (11):. doi: 10.3390/biomedicines10112798. PubMed PMID:36359320 .

Sommerer, Y, Ohlei, O, Dobricic, V, Oakley, DH, Wesse, T, Sedghpour Sabet, S et al.. A correlation map of genome-wide DNA methylation patterns between paired human brain and buccal samples. Clin Epigenetics. 2022;14 (1):139. doi: 10.1186/s13148-022-01357-w. PubMed PMID:36320053 PubMed Central PMC9628033.

Nyberg, L, Andersson, M, Lundquist, A, Baaré, WFC, Bartrés-Faz, D, Bertram, L et al.. Individual differences in brain aging: heterogeneity in cortico-hippocampal but not caudate atrophy rates. Cereb Cortex. 2022; :. doi: 10.1093/cercor/bhac400. PubMed PMID:36197324 .

Vetter, VM, Drewelies, J, Sommerer, Y, Kalies, CH, Regitz-Zagrosek, V, Bertram, L et al.. Epigenetic aging and perceived psychological stress in old age. Transl Psychiatry. 2022;12 (1):410. doi: 10.1038/s41398-022-02181-9. PubMed PMID:36163242 PubMed Central PMC9513097.

Drewelies, J, Hueluer, G, Duezel, S, Vetter, VM, Pawelec, G, Steinhagen-Thiessen, E et al.. Using blood test parameters to define biological age among older adults: association with morbidity and mortality independent of chronological age validated in two separate birth cohorts. Geroscience. 2022; :. doi: 10.1007/s11357-022-00662-9. PubMed PMID:36151431 .

Jansen, IE, van der Lee, SJ, Gomez-Fonseca, D, de Rojas, I, Dalmasso, MC, Grenier-Boley, B et al.. Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Acta Neuropathol. 2022;144 (5):821-842. doi: 10.1007/s00401-022-02454-z. PubMed PMID:36066633 PubMed Central PMC9547780.

Dobricic, V, Schilling, M, Schulz, J, Zhu, LS, Zhou, CW, Fuß, J et al.. Differential microRNA expression analyses across two brain regions in Alzheimer's disease. Transl Psychiatry. 2022;12 (1):352. doi: 10.1038/s41398-022-02108-4. PubMed PMID:36038535 PubMed Central PMC9424308.

Morgan, SL, Naderi, P, Koler, K, Pita-Juarez, Y, Prokopenko, D, Vlachos, IS et al.. Most Pathways Can Be Related to the Pathogenesis of Alzheimer's Disease. Front Aging Neurosci. 2022;14 :846902. doi: 10.3389/fnagi.2022.846902. PubMed PMID:35813951 PubMed Central PMC9263183.

Delvenne, A, Gobom, J, Tijms, B, Bos, I, Reus, LM, Dobricic, V et al.. Cerebrospinal fluid proteomic profiling of individuals with mild cognitive impairment and suspected non-Alzheimer's disease pathophysiology. Alzheimers Dement. 2022; :. doi: 10.1002/alz.12713. PubMed PMID:35698882 .

Lill, CM, Bertram, L. Genome-wide analysis furthers decoding of Alzheimer disease genetics. Nat Rev Neurol. 2022;18 (7):387-388. doi: 10.1038/s41582-022-00678-x. PubMed PMID:35624172 .

Wesenhagen, KEJ, Gobom, J, Bos, I, Vos, SJB, Martinez-Lage, P, Popp, J et al.. Effects of age, amyloid, sex, and APOE ε4 on the CSF proteome in normal cognition. Alzheimers Dement (Amst). 2022;14 (1):e12286. doi: 10.1002/dad2.12286. PubMed PMID:35571963 PubMed Central PMC9074716.

Vetter, VM, Sommerer, Y, Kalies, CH, Spira, D, Bertram, L, Demuth, I et al.. Vitamin D supplementation is associated with slower epigenetic aging. Geroscience. 2022;44 (3):1847-1859. doi: 10.1007/s11357-022-00581-9. PubMed PMID:35562603 PubMed Central PMC9213628.

Visser, PJ, Reus, LM, Gobom, J, Jansen, I, Dicks, E, van der Lee, SJ et al.. Correction: Cerebrospinal fluid tau levels are associated with abnormal neuronal plasticity markers in Alzheimer's disease. Mol Neurodegener. 2022;17 (1):37. doi: 10.1186/s13024-022-00540-0. PubMed PMID:35550177 PubMed Central PMC9102351.

Youn, C, Grotzinger, AD, Lill, CM, Bertram, L, Schmiedek, F, Lövdén, M et al.. Genetic associations with learning over 100 days of practice. NPJ Sci Learn. 2022;7 (1):7. doi: 10.1038/s41539-022-00121-2. PubMed PMID:35508486 PubMed Central PMC9068685.

Homann, J, Osburg, T, Ohlei, O, Dobricic, V, Deecke, L, Bos, I et al.. Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Front Aging Neurosci. 2022;14 :840651. doi: 10.3389/fnagi.2022.840651. PubMed PMID:35386118 PubMed Central PMC8979334.

Visser, PJ, Reus, LM, Gobom, J, Jansen, I, Dicks, E, van der Lee, SJ et al.. Cerebrospinal fluid tau levels are associated with abnormal neuronal plasticity markers in Alzheimer's disease. Mol Neurodegener. 2022;17 (1):27. doi: 10.1186/s13024-022-00521-3. PubMed PMID:35346299 PubMed Central PMC8962234.

Prokopenko, D, Lee, S, Hecker, J, Mullin, K, Morgan, S, Katsumata, Y et al.. Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer's disease-associated genes: DTNB and DLG2. Mol Psychiatry. 2022;27 (4):1963-1969. doi: 10.1038/s41380-022-01475-0. PubMed PMID:35246634 PubMed Central PMC9126808.

Kusters, CDJ, Paul, KC, Duarte Folle, A, Keener, AM, Bronstein, JM, Bertram, L et al.. Erratum to "Increased Menopausal Age Reduces the Risk of Parkinson's Disease: A Mendelian Approach". Mov Disord. 2022;37 (6):1282-1283. doi: 10.1002/mds.28974. PubMed PMID:35245402 .

Neumann, A, Küçükali, F, Bos, I, Vos, SJB, Engelborghs, S, De Pooter, T et al.. Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer's disease CSF profile of neuronal injury and inflammation. Mol Psychiatry. 2022;27 (4):1990-1999. doi: 10.1038/s41380-022-01437-6. PubMed PMID:35173266 PubMed Central PMC9126805.

Prokopenko, D, Morgan, SL, Lange, C, Hide, W, Bertram, L, Tanzi, RE et al.. Reply to Neupane et al.: Replication study of AD-associated rare variants. Alzheimers Dement. 2022;18 (4):863-864. doi: 10.1002/alz.12584. PubMed PMID:35142036 PubMed Central PMC9302627.

Vetter, VM, Kalies, CH, Sommerer, Y, Bertram, L, Demuth, I. Seven-CpG DNA Methylation Age Determined by Single Nucleotide Primer Extension and Illumina's Infinium MethylationEPIC Array Provide Highly Comparable Results. Front Genet. 2021;12 :759357. doi: 10.3389/fgene.2021.759357. PubMed PMID:35111197 PubMed Central PMC8802213.

Vetter, VM, Kalies, CH, Sommerer, Y, Spira, D, Drewelies, J, Regitz-Zagrosek, V et al.. Relationship Between 5 Epigenetic Clocks, Telomere Length, and Functional Capacity Assessed in Older Adults: Cross-Sectional and Longitudinal Analyses. J Gerontol A Biol Sci Med Sci. 2022;77 (9):1724-1733. doi: 10.1093/gerona/glab381. PubMed PMID:35032170 .

Kresojević, N, Dobričić, V, Lukić, MJ, Tomić, A, Petrović, I, Dragašević, N et al.. Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience. J Neurol. 2022;269 (6):3167-3174. doi: 10.1007/s00415-021-10918-7. PubMed PMID:34993563 .

Wang, Y, Grydeland, H, Roe, JM, Pan, M, Magnussen, F, Amlien, IK et al.. Associations of circulating C-reactive proteins, APOE ε4, and brain markers for Alzheimer's disease in healthy samples across the lifespan. Brain Behav Immun. 2022;100 :243-253. doi: 10.1016/j.bbi.2021.12.008. PubMed PMID:34920091 .

Xu, J, Green, R, Kim, M, Lord, J, Ebshiana, A, Westwood, S et al.. Sex-Specific Metabolic Pathways Were Associated with Alzheimer's Disease (AD) Endophenotypes in the European Medical Information Framework for AD Multimodal Biomarker Discovery Cohort. Biomedicines. 2021;9 (11):. doi: 10.3390/biomedicines9111610. PubMed PMID:34829839 PubMed Central PMC8615383.

Vidal-Pineiro, D, Wang, Y, Krogsrud, SK, Amlien, IK, Baaré, WFC, Bartres-Faz, D et al.. Individual variations in 'brain age' relate to early-life factors more than to longitudinal brain change. Elife. 2021;10 :. doi: 10.7554/eLife.69995. PubMed PMID:34756163 PubMed Central PMC8580481.

Karalija, N, Köhncke, Y, Düzel, S, Bertram, L, Papenberg, G, Demuth, I et al.. A common polymorphism in the dopamine transporter gene predicts working memory performance and in vivo dopamine integrity in aging. Neuroimage. 2021;245 :118707. doi: 10.1016/j.neuroimage.2021.118707. PubMed PMID:34742942 .

Villagomez Fuentes, LE, Algharably, EA, Toepfer, S, König, M, Demuth, I, Bertram, L et al.. Effect of a common UMOD variant on kidney function, blood pressure, cognitive and physical function in a community-based cohort of older adults. J Hum Hypertens. 2022;36 (11):983-988. doi: 10.1038/s41371-021-00608-2. PubMed PMID:34593962 PubMed Central PMC9649423.

Wagner, M, Lorenz, G, Volk, AE, Brunet, T, Edbauer, D, Berutti, R et al.. Clinico-genetic findings in 509 frontotemporal dementia patients. Mol Psychiatry. 2021;26 (10):5824-5832. doi: 10.1038/s41380-021-01271-2. PubMed PMID:34561610 PubMed Central PMC8758482.

Tijms, BM, Gobom, J, Teunissen, C, Dobricic, V, Tsolaki, M, Verhey, F et al.. CSF Proteomic Alzheimer's Disease-Predictive Subtypes in Cognitively Intact Amyloid Negative Individuals. Proteomes. 2021;9 (3):. doi: 10.3390/proteomes9030036. PubMed PMID:34449748 PubMed Central PMC8396164.

Balck, A, Schaake, S, Kuhnke, NS, Domingo, A, Madoev, H, Margolesky, J et al.. Genotype-Phenotype Relations in Primary Familial Brain Calcification: Systematic MDSGene Review. Mov Disord. 2021;36 (11):2468-2480. doi: 10.1002/mds.28753. PubMed PMID:34432325 .

Kusters, CDJ, Paul, KC, Duarte Folle, A, Keener, AM, Bronstein, JM, Bertram, L et al.. Increased Menopausal Age Reduces the Risk of Parkinson's Disease: A Mendelian Randomization Approach. Mov Disord. 2021;36 (10):2264-2272. doi: 10.1002/mds.28760. PubMed PMID:34426982 PubMed Central PMC8530889.

Wittke, C, Petkovic, S, Dobricic, V, Schaake, S, MDS‐endorsed PSP Study Group, Respondek, G et al.. Genotype-Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic Review. Mov Disord. 2021;36 (7):1499-1510. doi: 10.1002/mds.28517. PubMed PMID:34396589 PubMed Central PMC9070562.

Shi, L, Buckley, NJ, Bos, I, Engelborghs, S, Sleegers, K, Frisoni, GB et al.. Plasma Proteomic Biomarkers Relating to Alzheimer's Disease: A Meta-Analysis Based on Our Own Studies. Front Aging Neurosci. 2021;13 :712545. doi: 10.3389/fnagi.2021.712545. PubMed PMID:34366831 PubMed Central PMC8335587.

Reyes, CJ, Laabs, BH, Schaake, S, Lüth, T, Ardicoglu, R, Rakovic, A et al.. Brain Regional Differences in Hexanucleotide Repeat Length in X-Linked Dystonia-Parkinsonism Using Nanopore Sequencing. Neurol Genet. 2021;7 (4):e608. doi: 10.1212/NXG.0000000000000608. PubMed PMID:34250228 PubMed Central PMC8265576.

Schilling, M, Lill, CM. MicroRNAs as Molecular Biomarkers for Parkinson's Disease Progression. Mov Disord. 2021;36 (8):1793. doi: 10.1002/mds.28700. PubMed PMID:34223665 .

Demuth, I, Banszerus, V, Drewelies, J, Düzel, S, Seeland, U, Spira, D et al.. Cohort profile: follow-up of a Berlin Aging Study II (BASE-II) subsample as part of the GendAge study. BMJ Open. 2021;11 (6):e045576. doi: 10.1136/bmjopen-2020-045576. PubMed PMID:34162642 PubMed Central PMC8230995.

Radojević, B, Dragašević-Mišković, NT, Marjanović, A, Branković, M, Dobričić, V, Milovanović, A et al.. Clinical and Genetic Analysis of Psychosis in Parkinson's Disease. J Parkinsons Dis. 2021;11 (4):1973-1980. doi: 10.3233/JPD-212716. PubMed PMID:34151861 .

Laabs, BH, Klein, C, Pozojevic, J, Domingo, A, Brüggemann, N, Grütz, K et al.. Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism. Nat Commun. 2021;12 (1):3216. doi: 10.1038/s41467-021-23491-4. PubMed PMID:34050153 PubMed Central PMC8163740.

Hong, S, Dobricic, V, Ohlei, O, Bos, I, Vos, SJB, Prokopenko, D et al.. TMEM106B and CPOX are genetic determinants of cerebrospinal fluid Alzheimer's disease biomarker levels. Alzheimers Dement. 2021;17 (10):1628-1640. doi: 10.1002/alz.12330. PubMed PMID:33991015 .

Grydeland, H, Sederevičius, D, Wang, Y, Bartrés-Faz, D, Bertram, L, Dobricic, V et al.. Self-reported sleep relates to microstructural hippocampal decline in ß-amyloid positive Adults beyond genetic risk. Sleep. 2021;44 (11):. doi: 10.1093/sleep/zsab110. PubMed PMID:33912975 PubMed Central PMC8598196.

Nyberg, L, Magnussen, F, Lundquist, A, Baaré, W, Bartrés-Faz, D, Bertram, L et al.. Educational attainment does not influence brain aging. Proc Natl Acad Sci U S A. 2021;118 (18):. doi: 10.1073/pnas.2101644118. PubMed PMID:33903255 PubMed Central PMC8106299.

Prokopenko, D, Morgan, SL, Mullin, K, Hofmann, O, Chapman, B, Kirchner, R et al.. Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. Alzheimers Dement. 2021;17 (9):1509-1527. doi: 10.1002/alz.12319. PubMed PMID:33797837 PubMed Central PMC8519060.

Shi, L, Winchester, LM, Westwood, S, Baird, AL, Anand, SN, Buckley, NJ et al.. Replication study of plasma proteins relating to Alzheimer's pathology. Alzheimers Dement. 2021;17 (9):1452-1464. doi: 10.1002/alz.12322. PubMed PMID:33792144 .

Lill, CM. Transcriptome-wide Association Study in Frontotemporal Dementia Identifies New Disease Loci by In Silico Analysis. Biol Psychiatry. 2021;89 (8):e37-e39. doi: 10.1016/j.biopsych.2021.02.010. PubMed PMID:33766241 .

Messerschmidt, C, Foddis, M, Blumenau, S, Müller, S, Bentele, K, Holtgrewe, M et al.. PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice. Sci Rep. 2021;11 (1):6072. doi: 10.1038/s41598-021-84919-x. PubMed PMID:33727568 PubMed Central PMC7966789.

Kronenberg, G, Gertz, K, Schöner, J, Bertram, L, Liman, T, Steinhagen-Thiessen, E et al.. BDNF serum concentrations in 2053 participants of the Berlin Aging Study II. Neurobiol Aging. 2021;101 :221-223. doi: 10.1016/j.neurobiolaging.2021.01.020. PubMed PMID:33636574 .

Jones, G, Trajanoska, K, Santanasto, AJ, Stringa, N, Kuo, CL, Atkins, JL et al.. Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women. Nat Commun. 2021;12 (1):654. doi: 10.1038/s41467-021-20918-w. PubMed PMID:33510174 PubMed Central PMC7844411.

Tijms, BM, Gobom, J, Reus, L, Jansen, I, Hong, S, Dobricic, V et al.. Pathophysiological subtypes of Alzheimer's disease based on cerebrospinal fluid proteomics. Brain. 2020;143 (12):3776-3792. doi: 10.1093/brain/awaa325. PubMed PMID:33439986 PubMed Central PMC7805814.

Pešić, M, Dragašević Mišković, N, Marjanović, A, Dobričić, V, Maksimović, N, Svetel, M et al.. Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism. Neurol Res. 2021;43 (4):321-326. doi: 10.1080/01616412.2020.1863697. PubMed PMID:33403926 .

Hong, S, Prokopenko, D, Dobricic, V, Kilpert, F, Bos, I, Vos, SJB et al.. Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Transl Psychiatry. 2020;10 (1):403. doi: 10.1038/s41398-020-01074-z. PubMed PMID:33223526 PubMed Central PMC7680793.

Visser, PJ, Reus, LM, Gobom, J, Jansen, I, Dicks, E, Tsolaki, M et al.. Cerebrospinal fluid total tau levels indicate aberrant neuronal plasticity in Alzheimer's disease. medRxiv. 2020; :. doi: 10.1101/2020.10.29.20211920. PubMed PMID:33173883 PubMed Central PMC7654872.

Walhovd, KB, Fjell, AM, Sørensen, Ø, Mowinckel, AM, Reinbold, CS, Idland, AV et al.. Genetic risk for Alzheimer disease predicts hippocampal volume through the human lifespan. Neurol Genet. 2020;6 (5):e506. doi: 10.1212/NXG.0000000000000506. PubMed PMID:33134508 PubMed Central PMC7577559.

Gisatulin, M, Dobricic, V, Zühlke, C, Hellenbroich, Y, Tadic, V, Münchau, A et al.. Clinical spectrum of the pentanucleotide repeat expansion in the RFC1 gene in ataxia syndromes. Neurology. 2020;95 (21):e2912-e2923. doi: 10.1212/WNL.0000000000010744. PubMed PMID:32873692 .

Shi, L, Winchester, LM, Liu, BY, Killick, R, Ribe, EM, Westwood, S et al.. Dickkopf-1 Overexpression in vitro Nominates Candidate Blood Biomarkers Relating to Alzheimer's Disease Pathology. J Alzheimers Dis. 2020;77 (3):1353-1368. doi: 10.3233/JAD-200208. PubMed PMID:32831200 PubMed Central PMC7683080.

Kusters, CDJ, Paul, KC, Duarte Folle, A, Keener, AM, Bronstein, JM, Dobricic, V et al.. Genetic risk scores and hallucinations in patients with Parkinson disease. Neurol Genet. 2020;6 (5):e492. doi: 10.1212/NXG.0000000000000492. PubMed PMID:32802953 PubMed Central PMC7413629.

Rieck, L, Bardey, F, Grenkowitz, T, Bertram, L, Helmuth, J, Mischung, C et al.. Mutation spectrum and polygenic score in German patients with familial hypercholesterolemia. Clin Genet. 2020;98 (5):457-467. doi: 10.1111/cge.13826. PubMed PMID:32770674 .

Bertram, L, Tanzi, RE. Genomic mechanisms in Alzheimer's disease. Brain Pathol. 2020;30 (5):966-977. doi: 10.1111/bpa.12882. PubMed PMID:32657454 PubMed Central PMC8018017.

Röhr, F, Bucholtz, N, Toepfer, S, Norman, K, Spira, D, Steinhagen-Thiessen, E et al.. Relationship between Lipoprotein (a) and cognitive function - Results from the Berlin Aging Study II. Sci Rep. 2020;10 (1):10636. doi: 10.1038/s41598-020-66783-3. PubMed PMID:32606300 PubMed Central PMC7326928.

Konijnenberg, E, Tijms, BM, Gobom, J, Dobricic, V, Bos, I, Vos, S et al.. APOE ε4 genotype-dependent cerebrospinal fluid proteomic signatures in Alzheimer's disease. Alzheimers Res Ther. 2020;12 (1):65. doi: 10.1186/s13195-020-00628-z. PubMed PMID:32460813 PubMed Central PMC7254647.

Lill, CM. Corrigendum to "Genetics of Parkinson's disease" [Mol. Cell. Probes (2016) 386-396]. Mol Cell Probes. 2020;52 :101537. doi: 10.1016/j.mcp.2020.101537. PubMed PMID:32386924 .

Engel, S, Graetz, C, Salmen, A, Muthuraman, M, Toenges, G, Ambrosius, B et al.. Is APOE ε4 associated with cognitive performance in early MS?. Neurol Neuroimmunol Neuroinflamm. 2020;7 (4):. doi: 10.1212/NXI.0000000000000728. PubMed PMID:32358224 PubMed Central PMC7217661.

Prokopenko, D, Hecker, J, Kirchner, R, Chapman, BA, Hoffman, O, Mullin, K et al.. Identification of Novel Alzheimer's Disease Loci Using Sex-Specific Family-Based Association Analysis of Whole-Genome Sequence Data. Sci Rep. 2020;10 (1):5029. doi: 10.1038/s41598-020-61883-6. PubMed PMID:32193444 PubMed Central PMC7081222.

Fjell, AM, Sederevicius, D, Sneve, MH, de Lange, AG, Bråthen, AC, Idland, AV et al.. Self-reported Sleep Problems Related to Amyloid Deposition in Cortical Regions with High HOMER1 Gene Expression. Cereb Cortex. 2020;30 (4):2144-2156. doi: 10.1093/cercor/bhz228. PubMed PMID:32142100 PubMed Central PMC7174994.

Kresojević, N, Mandić-Stojmenović, G, Dobričić, V, Petrović, I, Brajković, L, Stefanova, E et al.. Very Late-Onset Niemann Pick Type C Disease: Example of Progressive Supranuclear Palsy Look-Alike Disorder. Mov Disord Clin Pract. 2020;7 (2):211-214. doi: 10.1002/mdc3.12892. PubMed PMID:32071943 PubMed Central PMC7011656.

Westwood, S, Baird, AL, Anand, SN, Nevado-Holgado, AJ, Kormilitzin, A, Shi, L et al.. Validation of Plasma Proteomic Biomarkers Relating to Brain Amyloid Burden in the EMIF-Alzheimer's Disease Multimodal Biomarker Discovery Cohort. J Alzheimers Dis. 2020;74 (1):213-225. doi: 10.3233/JAD-190434. PubMed PMID:31985466 PubMed Central PMC7175945.

Lill, CM. WITHDRAWN: Genetics of Parkinson's disease. Mol Cell Probes. 2020; :101471. doi: 10.1016/j.mcp.2019.101471. PubMed PMID:31978549 .

Gómez-Fernández, P, Lopez de Lapuente Portilla, A, Astobiza, I, Mena, J, Urtasun, A, Altmann, V et al.. The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple Sclerosis. Cells. 2020;9 (1):. doi: 10.3390/cells9010175. PubMed PMID:31936765 PubMed Central PMC7017210.

Stamate, D, Kim, M, Proitsi, P, Westwood, S, Baird, A, Nevado-Holgado, A et al.. A metabolite-based machine learning approach to diagnose Alzheimer-type dementia in blood: Results from the European Medical Information Framework for Alzheimer disease biomarker discovery cohort. Alzheimers Dement (N Y). 2019;5 :933-938. doi: 10.1016/j.trci.2019.11.001. PubMed PMID:31890857 PubMed Central PMC6928349.

Prokopenko, I, Miyakawa, G, Zheng, B, Heikkinen, J, Petrova Quayle, D, Udeh-Momoh, C et al.. Alzheimer's disease pathology explains association between dementia with Lewy bodies and APOE-ε4/TOMM40 long poly-T repeat allele variants. Alzheimers Dement (N Y). 2019;5 :814-824. doi: 10.1016/j.trci.2019.08.005. PubMed PMID:31788537 PubMed Central PMC6880091.

Trinh, J, Imhoff, S, Dulovic-Mahlow, M, Kandaswamy, KK, Tadic, V, Schäfer, J et al.. Novel NAXE variants as a cause for neurometabolic disorder: implications for treatment. J Neurol. 2020;267 (3):770-782. doi: 10.1007/s00415-019-09640-2. PubMed PMID:31745726 .

Wohlers, I, Schulz, C, Kilpert, F, Bertram, L. Alzheimer's disease risk SNPs show no strong effect on miRNA expression in human lymphoblastoid cell lines. Neurobiol Aging. 2020;86 :202.e1-202.e3. doi: 10.1016/j.neurobiolaging.2019.08.013. PubMed PMID:31685236 .

Schmidt, AF, Holmes, MV, Preiss, D, Swerdlow, DI, Denaxas, S, Fatemifar, G et al.. Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9. BMC Cardiovasc Disord. 2019;19 (1):240. doi: 10.1186/s12872-019-1187-z. PubMed PMID:31664920 PubMed Central PMC6820948.

Grover, S, Lill, CM, Kasten, M, Klein, C, Del Greco M, F, König, IR et al.. Risky behaviors and Parkinson disease: A mendelian randomization study. Neurology. 2019;93 (15):e1412-e1424. doi: 10.1212/WNL.0000000000008245. PubMed PMID:31527283 PubMed Central PMC7010323.

Takousis, P, Sadlon, A, Schulz, J, Wohlers, I, Dobricic, V, Middleton, L et al.. Differential expression of microRNAs in Alzheimer's disease brain, blood, and cerebrospinal fluid. Alzheimers Dement. 2019;15 (11):1468-1477. doi: 10.1016/j.jalz.2019.06.4952. PubMed PMID:31495604 .

Shi, L, Westwood, S, Baird, AL, Winchester, L, Dobricic, V, Kilpert, F et al.. Discovery and validation of plasma proteomic biomarkers relating to brain amyloid burden by SOMAscan assay. Alzheimers Dement. 2019;15 (11):1478-1488. doi: 10.1016/j.jalz.2019.06.4951. PubMed PMID:31495601 PubMed Central PMC6880298.

Krause, C, Sievert, H, Geißler, C, Grohs, M, El Gammal, AT, Wolter, S et al.. Critical evaluation of the DNA-methylation markers ABCG1 and SREBF1 for Type 2 diabetes stratification. Epigenomics. 2019;11 (8):885-897. doi: 10.2217/epi-2018-0159. PubMed PMID:31169416 .

Kim, M, Snowden, S, Suvitaival, T, Ali, A, Merkler, DJ, Ahmad, T et al.. Primary fatty amides in plasma associated with brain amyloid burden, hippocampal volume, and memory in the European Medical Information Framework for Alzheimer's Disease biomarker discovery cohort. Alzheimers Dement. 2019;15 (6):817-827. doi: 10.1016/j.jalz.2019.03.004. PubMed PMID:31078433 PubMed Central PMC6849698.

Morgan, AR, Touchard, S, Leckey, C, O'Hagan, C, Nevado-Holgado, AJ, NIMA Consortium et al.. Inflammatory biomarkers in Alzheimer's disease plasma. Alzheimers Dement. 2019;15 (6):776-787. doi: 10.1016/j.jalz.2019.03.007. PubMed PMID:31047856 PubMed Central PMC6565806.

Davies, G, Lam, M, Harris, SE, Trampush, JW, Luciano, M, Hill, WD et al.. Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nat Commun. 2019;10 (1):2068. doi: 10.1038/s41467-019-10160-w. PubMed PMID:31043617 PubMed Central PMC6494826.

Schulz, J, Takousis, P, Wohlers, I, Itua, IOG, Dobricic, V, Rücker, G et al.. Meta-analyses identify differentially expressed micrornas in Parkinson's disease. Ann Neurol. 2019;85 (6):835-851. doi: 10.1002/ana.25490. PubMed PMID:30990912 .

Westenberger, A, Reyes, CJ, Saranza, G, Dobricic, V, Hanssen, H, Domingo, A et al.. A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism. Ann Neurol. 2019;85 (6):812-822. doi: 10.1002/ana.25488. PubMed PMID:30973967 .

Bos, I, Vos, S, Verhey, F, Scheltens, P, Teunissen, C, Engelborghs, S et al.. Cerebrospinal fluid biomarkers of neurodegeneration, synaptic integrity, and astroglial activation across the clinical Alzheimer's disease spectrum. Alzheimers Dement. 2019;15 (5):644-654. doi: 10.1016/j.jalz.2019.01.004. PubMed PMID:30853464 .

Bertram, L, Tanzi, RE. Alzheimer disease risk genes: 29 and counting. Nat Rev Neurol. 2019;15 (4):191-192. doi: 10.1038/s41582-019-0158-4. PubMed PMID:30833695 .

Karasik, D, Zillikens, MC, Hsu, YH, Aghdassi, A, Akesson, K, Amin, N et al.. Disentangling the genetics of lean mass. Am J Clin Nutr. 2019;109 (2):276-287. doi: 10.1093/ajcn/nqy272. PubMed PMID:30721968 PubMed Central PMC6500901.

Karlsson Linnér, R, Biroli, P, Kong, E, Meddens, SFW, Wedow, R, Fontana, MA et al.. Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Nat Genet. 2019;51 (2):245-257. doi: 10.1038/s41588-018-0309-3. PubMed PMID:30643258 PubMed Central PMC6713272.

Kresojević, N, Petrović, I, Dobričić, V, Tomić, A, Branković, V, Milić Rašić, V et al.. Phenotype of PLP1-related Disorder Caused by Novel Mutation: A Case Report. Mov Disord Clin Pract. 2018;5 (5):548-550. doi: 10.1002/mdc3.12644. PubMed PMID:30637272 PubMed Central PMC6207126.

Trinh, J, Lohmann, K, Baumann, H, Balck, A, Borsche, M, Brüggemann, N et al.. Utility and implications of exome sequencing in early-onset Parkinson's disease. Mov Disord. 2019;34 (1):133-137. doi: 10.1002/mds.27559. PubMed PMID:30537300 PubMed Central PMC8950081.

Reinthaler, EM, Graf, E, Zrzavy, T, Wieland, T, Hotzy, C, Kopecky, C et al.. TPP2 mutation associated with sterile brain inflammation mimicking MS. Neurol Genet. 2018;4 (6):e285. doi: 10.1212/NXG.0000000000000285. PubMed PMID:30533531 PubMed Central PMC6244017.

Trinh, J, Zeldenrust, FMJ, Huang, J, Kasten, M, Schaake, S, Petkovic, S et al.. Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review. Mov Disord. 2018;33 (12):1857-1870. doi: 10.1002/mds.27527. PubMed PMID:30357936 .

Herwest, S, Albers, C, Schmiester, M, Salewsky, B, Hopfenmüller, W, Meyer, A et al.. The hSNM1B/Apollo variant rs11552449 is associated with cellular sensitivity towards mitomycin C and ionizing radiation. DNA Repair (Amst). 2018;72 :93-98. doi: 10.1016/j.dnarep.2018.09.004. PubMed PMID:30262195 .

Ten Kate, M, Redolfi, A, Peira, E, Bos, I, Vos, SJ, Vandenberghe, R et al.. MRI predictors of amyloid pathology: results from the EMIF-AD Multimodal Biomarker Discovery study. Alzheimers Res Ther. 2018;10 (1):100. doi: 10.1186/s13195-018-0428-1. PubMed PMID:30261928 PubMed Central PMC6161396.

Wohlers, I, Bertram, L. Taking genomics research to the next level: The Genotype-Tissue expression project. Mov Disord. 2018;33 (7):1097. doi: 10.1002/mds.27445. PubMed PMID:30153387 .

Wohlers, I, Bertram, L, Lill, CM. Evidence for a potential role of miR-1908-5p and miR-3614-5p in autoimmune disease risk using integrative bioinformatics. J Autoimmun. 2018;94 :83-89. doi: 10.1016/j.jaut.2018.07.010. PubMed PMID:30143393 .

Ohlei, O, Dobricic, V, Lohmann, K, Klein, C, Lill, CM, Bertram, L et al.. Field synopsis and systematic meta-analyses of genetic association studies in isolated dystonia. Parkinsonism Relat Disord. 2018;57 :50-57. doi: 10.1016/j.parkreldis.2018.07.018. PubMed PMID:30100364 .

Weppner, G, Ohlei, O, Hammers, CM, Holl-Ulrich, K, Voswinkel, J, Bischof, J et al.. In situ detection of PR3-ANCA+ B cells and alterations in the variable region of immunoglobulin genes support a role of inflamed tissue in the emergence of auto-reactivity in granulomatosis with polyangiitis. J Autoimmun. 2018;93 :89-103. doi: 10.1016/j.jaut.2018.07.004. PubMed PMID:30054207 .

Bos, I, Vos, S, Vandenberghe, R, Scheltens, P, Engelborghs, S, Frisoni, G et al.. The EMIF-AD Multimodal Biomarker Discovery study: design, methods and cohort characteristics. Alzheimers Res Ther. 2018;10 (1):64. doi: 10.1186/s13195-018-0396-5. PubMed PMID:29980228 PubMed Central PMC6035398.

Davies, G, Lam, M, Harris, SE, Trampush, JW, Luciano, M, Hill, WD et al.. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nat Commun. 2018;9 (1):2098. doi: 10.1038/s41467-018-04362-x. PubMed PMID:29844566 PubMed Central PMC5974083.

Kasten, M, Hartmann, C, Hampf, J, Schaake, S, Westenberger, A, Vollstedt, EJ et al.. Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic Review. Mov Disord. 2018;33 (5):730-741. doi: 10.1002/mds.27352. PubMed PMID:29644727 .

Kulikovskaja, L, Sarajlija, A, Savic-Pavicevic, D, Dobricic, V, Klein, C, Westenberger, A et al.. WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype. Neurol Genet. 2018;4 (2):e227. doi: 10.1212/NXG.0000000000000227. PubMed PMID:29600274 PubMed Central PMC5873728.

Graetz, C, Gröger, A, Luessi, F, Salmen, A, Zöller, D, Schultz, J et al.. Association of smoking but not HLA-DRB1*15:01, APOE or body mass index with brain atrophy in early multiple sclerosis. Mult Scler. 2019;25 (5):661-668. doi: 10.1177/1352458518763541. PubMed PMID:29532745 .

Walhovd, KB, Fjell, AM, Westerhausen, R, Nyberg, L, Ebmeier, KP, Lindenberger, U et al.. Healthy minds 0-100 years: Optimising the use of European brain imaging cohorts ("Lifebrain"). Eur Psychiatry. 2018;50 :47-56. doi: 10.1016/j.eurpsy.2017.12.006. PubMed PMID:29449073 .

Paul, KC, Schulz, J, Bronstein, JM, Lill, CM, Ritz, BR. Association of Polygenic Risk Score With Cognitive Decline and Motor Progression in Parkinson Disease. JAMA Neurol. 2018;75 (3):360-366. doi: 10.1001/jamaneurol.2017.4206. PubMed PMID:29340614 PubMed Central PMC5885856.

Mitropoulos, K, Merkouri Papadima, E, Xiromerisiou, G, Balasopoulou, A, Charalampidou, K, Galani, V et al.. Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients. Hum Genomics. 2017;11 (1):30. doi: 10.1186/s40246-017-0126-2. PubMed PMID:29216901 PubMed Central PMC5721583.

Walhovd, KB, Fjell, AM, Westerhausen, R, Nyberg, L, Ebmeier, KP, Lindenberger, U et al.. Healthy minds from 0-100 years: Optimising the use of European brain imaging cohorts ("Lifebrain"). Eur Psychiatry. 2018;47 :76-87. doi: 10.1016/j.eurpsy.2017.10.005. PubMed PMID:29127911 .

Zillikens, MC, Demissie, S, Hsu, YH, Yerges-Armstrong, LM, Chou, WC, Stolk, L et al.. Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nat Commun. 2017;8 (1):1414. doi: 10.1038/s41467-017-01008-2. PubMed PMID:29116125 PubMed Central PMC5676783.

Schuck, NW, Petok, JR, Meeter, M, Schjeide, BM, Schröder, J, Bertram, L et al.. Aging and a genetic KIBRA polymorphism interactively affect feedback- and observation-based probabilistic classification learning. Neurobiol Aging. 2018;61 :36-43. doi: 10.1016/j.neurobiolaging.2017.08.026. PubMed PMID:29032191 PubMed Central PMC5705462.

Joshi, PK, Pirastu, N, Kentistou, KA, Fischer, K, Hofer, E, Schraut, KE et al.. Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nat Commun. 2017;8 (1):910. doi: 10.1038/s41467-017-00934-5. PubMed PMID:29030599 PubMed Central PMC5715013.

Chuang, YH, Lee, PC, Vlaar, T, Mulot, C, Loriot, MA, Hansen, J et al.. Pooled analysis of the HLA-DRB1 by smoking interaction in Parkinson disease. Ann Neurol. 2017;82 (5):655-664. doi: 10.1002/ana.25065. PubMed PMID:28981958 PubMed Central PMC5798887.

Dobričić, V, Tomić, A, Branković, V, Kresojević, N, Janković, M, Westenberger, A et al.. GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia. Parkinsonism Relat Disord. 2017;45 :81-84. doi: 10.1016/j.parkreldis.2017.09.017. PubMed PMID:28958832 .

Buchmann, N, Scholz, M, Lill, CM, Burkhardt, R, Eckardt, R, Norman, K et al.. Association between lipoprotein(a) level and type 2 diabetes: no evidence for a causal role of lipoprotein(a) and insulin. Acta Diabetol. 2017;54 (11):1031-1038. doi: 10.1007/s00592-017-1036-4. PubMed PMID:28866807 .

Lill, CM, Klein, C. What would Dr. James Parkinson think today? The role of genetics in Parkinson's disease. Mov Disord. 2017;32 (8):1115-1116. doi: 10.1002/mds.27141. PubMed PMID:28836355 .

Zillikens, MC, Demissie, S, Hsu, YH, Yerges-Armstrong, LM, Chou, WC, Stolk, L et al.. Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nat Commun. 2017;8 (1):80. doi: 10.1038/s41467-017-00031-7. PubMed PMID:28724990 PubMed Central PMC5517526.

Chuang, YH, Lill, CM, Lee, PC, Hansen, J, Lassen, CF, Bertram, L et al.. Gene-Environment Interaction in Parkinson's Disease: Coffee, ADORA2A, and CYP1A2. Neuroepidemiology. 2016;47 (3-4):192-200. doi: 10.1159/000450855. PubMed PMID:28135712 PubMed Central PMC5465963.

Lohmann, K, Masuho, I, Patil, DN, Baumann, H, Hebert, E, Steinrücke, S et al.. Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans. Hum Mol Genet. 2017;26 (6):1078-1086. doi: 10.1093/hmg/ddx018. PubMed PMID:28087732 PubMed Central PMC6075543.

Schmidt, AF, Swerdlow, DI, Holmes, MV, Patel, RS, Fairhurst-Hunter, Z, Lyall, DM et al.. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study. Lancet Diabetes Endocrinol. 2017;5 (2):97-105. doi: 10.1016/S2213-8587(16)30396-5. PubMed PMID:27908689 PubMed Central PMC5266795.

Kostić, M, Munjiza, A, Pesic, D, Peljto, A, Novakovic, I, Dobricic, V et al.. A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorder. J Affect Disord. 2017;209 :66-70. doi: 10.1016/j.jad.2016.11.034. PubMed PMID:27888722 .

Lill, CM. Genetics of Parkinson's disease. Mol Cell Probes. 2016;30 (6):386-396. doi: 10.1016/j.mcp.2016.11.001. PubMed PMID:27818248 .

Biernacka, JM, Chung, SJ, Armasu, SM, Anderson, KS, Lill, CM, Bertram, L et al.. Genome-wide gene-environment interaction analysis of pesticide exposure and risk of Parkinson's disease. Parkinsonism Relat Disord. 2016;32 :25-30. doi: 10.1016/j.parkreldis.2016.08.002. PubMed PMID:27545685 PubMed Central PMC5125780.

Barban, N, Jansen, R, de Vlaming, R, Vaez, A, Mandemakers, JJ, Tropf, FC et al.. Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat Genet. 2016;48 (12):1462-1472. doi: 10.1038/ng.3698. PubMed PMID:27798627 PubMed Central PMC5695684.

Mišković, ND, Domingo, A, Dobričić, V, Max, C, Braenne, I, Petrović, I et al.. Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia. Mov Disord. 2016;31 (12):1929-1931. doi: 10.1002/mds.26816. PubMed PMID:27787937 .

Lee, PC, Raaschou-Nielsen, O, Lill, CM, Bertram, L, Sinsheimer, JS, Hansen, J et al.. Gene-environment interactions linking air pollution and inflammation in Parkinson's disease. Environ Res. 2016;151 :713-720. doi: 10.1016/j.envres.2016.09.006. PubMed PMID:27640071 .

Herold, C, Hooli, BV, Mullin, K, Liu, T, Roehr, JT, Mattheisen, M et al.. Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. Mol Psychiatry. 2016;21 (11):1608-1612. doi: 10.1038/mp.2015.218. PubMed PMID:26830138 PubMed Central PMC4970971.

Klein, C, Lang, A, van de Warrenburg, BP, Sue, CM, Tabrizi, SJ, Bertram, L et al.. Reply letter to Jinnah "Locus pocus" and Albanese "Complex dystonia is not a category in the new 2013 consensus classification": Necessary evolution, no magic!. Mov Disord. 2016;31 (11):1760-1762. doi: 10.1002/mds.26763. PubMed PMID:27619077 .

Andlauer, TF, Buck, D, Antony, G, Bayas, A, Bechmann, L, Berthele, A et al.. Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. Sci Adv. 2016;2 (6):e1501678. doi: 10.1126/sciadv.1501678. PubMed PMID:27386562 PubMed Central PMC4928990.

Vuletic, V, Chudy, D, Almahariq, F, Dobricic, V, Kostic, V, Bogdanovic, N et al.. Excellent outcome of pallidal deep brain stimulation in DYT6 dystonia: A case report. J Neurol Sci. 2016;366 :18-19. doi: 10.1016/j.jns.2016.04.032. PubMed PMID:27288769 .

Okbay, A, Beauchamp, JP, Fontana, MA, Lee, JJ, Pers, TH, Rietveld, CA et al.. Genome-wide association study identifies 74 loci associated with educational attainment. Nature. 2016;533 (7604):539-42. doi: 10.1038/nature17671. PubMed PMID:27225129 PubMed Central PMC4883595.

Peric, M, Peric, S, Rapajic, N, Dobricic, V, Savic-Pavicevic, D, Nesic, I et al.. Multidimensional aspects of pain in myotonic dystrophies. Acta Myol. 2015;34 (2-3):126-32. . PubMed PMID:27199540 PubMed Central PMC4859081.

Sadovnick, AD, Traboulsee, AL, Bernales, CQ, Ross, JP, Forwell, AL, Yee, IM et al.. Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients. G3 (Bethesda). 2016;6 (7):2073-9. doi: 10.1534/g3.116.030841. PubMed PMID:27194806 PubMed Central PMC4938660.

Lill, CM, Mashychev, A, Hartmann, C, Lohmann, K, Marras, C, Lang, AE et al.. Launching the movement disorders society genetic mutation database (MDSGene). Mov Disord. 2016;31 (5):607-9. doi: 10.1002/mds.26651. PubMed PMID:27156390 .

Dobričić, V, Kresojević, N, Marjanović, A, Tomić, A, Svetel, M, Novaković, I et al.. HPCA-related dystonia: Too rare to be found?. Mov Disord. 2016;31 (7):1071. doi: 10.1002/mds.26634. PubMed PMID:27145302 .

Okbay, A, Baselmans, BM, De Neve, JE, Turley, P, Nivard, MG, Fontana, MA et al.. Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat Genet. 2016;48 (6):624-33. doi: 10.1038/ng.3552. PubMed PMID:27089181 PubMed Central PMC4884152.

Marras, C, Lang, A, van de Warrenburg, BP, Sue, CM, Tabrizi, SJ, Bertram, L et al.. Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force. Mov Disord. 2016;31 (4):436-57. doi: 10.1002/mds.26527. PubMed PMID:27079681 .

Kypreou, KP, Stefanaki, I, Antonopoulou, K, Karagianni, F, Ntritsos, G, Zaras, A et al.. Prediction of Melanoma Risk in a Southern European Population Based on a Weighted Genetic Risk Score. J Invest Dermatol. 2016;136 (3):690-695. doi: 10.1016/j.jid.2015.12.007. PubMed PMID:27015455 .

Dubois, B, Hampel, H, Feldman, HH, Scheltens, P, Aisen, P, Andrieu, S et al.. Preclinical Alzheimer's disease: Definition, natural history, and diagnostic criteria. Alzheimers Dement. 2016;12 (3):292-323. doi: 10.1016/j.jalz.2016.02.002. PubMed PMID:27012484 PubMed Central PMC6417794.

Kostic, M, Canu, E, Agosta, F, Munjiza, A, Novakovic, I, Dobricic, V et al.. The cumulative effect of genetic polymorphisms on depression and brain structural integrity. Hum Brain Mapp. 2016;37 (6):2173-84. doi: 10.1002/hbm.23165. PubMed PMID:26956059 PubMed Central PMC6867528.

Lu, Y, Day, FR, Gustafsson, S, Buchkovich, ML, Na, J, Bataille, V et al.. New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk. Nat Commun. 2016;7 :10495. doi: 10.1038/ncomms10495. PubMed PMID:26833246 PubMed Central PMC4740398.

Lill, CM, Liu, T, Norman, K, Meyer, A, Steinhagen-Thiessen, E, Demuth, I et al.. Genetic Burden Analyses of Phenotypes Relevant to Aging in the Berlin Aging Study II (BASE-II). Gerontology. 2016;62 (3):316-22. doi: 10.1159/000438900. PubMed PMID:26821332 .

Gerstorf, D, Bertram, L, Lindenberger, U, Pawelec, G, Demuth, I, Steinhagen-Thiessen, E et al.. Editorial. Gerontology. 2016;62 (3):311-5. doi: 10.1159/000441495. PubMed PMID:26820471 .

Damnjanovic, T, Cuturilo, G, Maksimovic, N, Dimitrijevic, N, Mitic, V, Jekic, B et al.. Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities. Turk J Pediatr. 2015;57 (2):154-60. . PubMed PMID:26690596 .

Schrewe, L, Lill, CM, Liu, T, Salmen, A, Gerdes, LA, Guillot-Noel, L et al.. Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS. J Neuroinflammation. 2015;12 :234. doi: 10.1186/s12974-015-0429-y. PubMed PMID:26669675 PubMed Central PMC4681148.

Dankowski, T, Buck, D, Andlauer, TF, Antony, G, Bayas, A, Bechmann, L et al.. Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array. Genet Epidemiol. 2015;39 (8):601-8. doi: 10.1002/gepi.21933. PubMed PMID:26497834 .

Lill, CM, Luessi, F, Alcina, A, Sokolova, EA, Ugidos, N, de la Hera, B et al.. Genome-wide significant association with seven novel multiple sclerosis risk loci. J Med Genet. 2015;52 (12):848-55. doi: 10.1136/jmedgenet-2015-103442. PubMed PMID:26475045 .

Mandic-Stojmenovic, G, Stefanova, E, Dobricic, V, Novakovic, I, Stojkovic, T, Jesic, A et al.. Screening for C9orf72 Expansion Mutation in Serbian Patients with Early-Onset Dementia. Dement Geriatr Cogn Disord. 2015;40 (5-6):358-65. doi: 10.1159/000438748. PubMed PMID:26401819 .

Moutsianas, L, Jostins, L, Beecham, AH, Dilthey, AT, Xifara, DK, Ban, M et al.. Class II HLA interactions modulate genetic risk for multiple sclerosis. Nat Genet. 2015;47 (10):1107-1113. doi: 10.1038/ng.3395. PubMed PMID:26343388 PubMed Central PMC4874245.

Nikpay, M, Goel, A, Won, HH, Hall, LM, Willenborg, C, Kanoni, S et al.. A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nat Genet. 2015;47 (10):1121-1130. doi: 10.1038/ng.3396. PubMed PMID:26343387 PubMed Central PMC4589895.

Dobričić, V, Kresojević, N, Žarković, M, Tomić, A, Marjanović, A, Westenberger, A et al.. Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited. Parkinsonism Relat Disord. 2015;21 (10):1256-9. doi: 10.1016/j.parkreldis.2015.08.001. PubMed PMID:26297380 .

Park, S, Lee, S, Lee, Y, Herold, C, Hooli, B, Mullin, K et al.. Adjusting heterogeneous ascertainment bias for genetic association analysis with extended families. BMC Med Genet. 2015;16 :62. doi: 10.1186/s12881-015-0198-6. PubMed PMID:26286599 PubMed Central PMC4593209.

Bertram, L. Next Generation Sequencing in Alzheimer's Disease. Methods Mol Biol. 2016;1303 :281-97. doi: 10.1007/978-1-4939-2627-5_17. PubMed PMID:26235074 .

Rakocevic-Stojanovic, V, Peric, S, Basta, I, Dobricic, V, Ralic, V, Kacar, A et al.. Variability of multisystemic features in myotonic dystrophy type 1--lessons from Serbian registry. Neurol Res. 2015;37 (11):939-44. doi: 10.1179/1743132815Y.0000000068. PubMed PMID:26184384 .

Joshi, PK, Esko, T, Mattsson, H, Eklund, N, Gandin, I, Nutile, T et al.. Directional dominance on stature and cognition in diverse human populations. Nature. 2015;523 (7561):459-462. doi: 10.1038/nature14618. PubMed PMID:26131930 PubMed Central PMC4516141.

Kresojević, N, Janković, M, Petrović, I, Kumar, KR, Dragašević, N, Dobričić, V et al.. Presenting symptoms of GBA-related Parkinson's disease. Parkinsonism Relat Disord. 2015;21 (7):804-7. doi: 10.1016/j.parkreldis.2015.04.028. PubMed PMID:25957717 .

Lill, CM, Rengmark, A, Pihlstrøm, L, Fogh, I, Shatunov, A, Sleiman, PM et al.. The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease. Alzheimers Dement. 2015;11 (12):1407-1416. doi: 10.1016/j.jalz.2014.12.009. PubMed PMID:25936935 PubMed Central PMC4627856.

Lill, CM, Hansen, J, Olsen, JH, Binder, H, Ritz, B, Bertram, L et al.. Impact of Parkinson's disease risk loci on age at onset. Mov Disord. 2015;30 (6):847-50. doi: 10.1002/mds.26237. PubMed PMID:25914293 .

Janković, MZ, Kresojević, ND, Dobričić, VS, Marković, VV, Petrović, IN, Novaković, IV et al.. Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population. J Neurol Sci. 2015;353 (1-2):59-62. doi: 10.1016/j.jns.2015.04.002. PubMed PMID:25899316 .

Hooli, BV, Lill, CM, Mullin, K, Qiao, D, Lange, C, Bertram, L et al.. PLD3 gene variants and Alzheimer's disease. Nature. 2015;520 (7545):E7-8. doi: 10.1038/nature14040. PubMed PMID:25832413 .

Tomić, A, Petrović, I, Svetel, M, Dobričić, V, Dragašević Mišković, N, Kostić, VS et al.. Pattern of disease progression in atypical form of pantothenate-kinase-associated neurodegeneration (PKAN) - Prospective study. Parkinsonism Relat Disord. 2015;21 (5):521-4. doi: 10.1016/j.parkreldis.2015.02.006. PubMed PMID:25724846 .

Bertram, L, Klein, C. Probing the exome in Alzheimer disease and other neurodegenerative disorders. JAMA Neurol. 2015;72 (4):389-91. doi: 10.1001/jamaneurol.2014.4495. PubMed PMID:25706056 .

Hoppmann, N, Graetz, C, Paterka, M, Poisa-Beiro, L, Larochelle, C, Hasan, M et al.. New candidates for CD4 T cell pathogenicity in experimental neuroinflammation and multiple sclerosis. Brain. 2015;138 (Pt 4):902-17. doi: 10.1093/brain/awu408. PubMed PMID:25665584 .

Lill, CM, Bertram, L. Probing the epigenome by EWAS: a new era in brain disease research. Mov Disord. 2015;30 (2):197. doi: 10.1002/mds.26143. PubMed PMID:25639491 .

Domingo, A, Westenberger, A, Lee, LV, Brænne, I, Liu, T, Vater, I et al.. New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3). Eur J Hum Genet. 2015;23 (10):1334-40. doi: 10.1038/ejhg.2014.292. PubMed PMID:25604858 PubMed Central PMC4592086.

Vujnic, M, Peric, S, Popovic, S, Raseta, N, Ralic, V, Dobricic, V et al.. Metabolic syndrome in patients with myotonic dystrophy type 1. Muscle Nerve. 2015;52 (2):273-7. doi: 10.1002/mus.24540. PubMed PMID:25487787 .

Nalls, MA, Bras, J, Hernandez, DG, Keller, MF, Majounie, E, Renton, AE et al.. NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases. Neurobiol Aging. 2015;36 (3):1605.e7-12. doi: 10.1016/j.neurobiolaging.2014.07.028. PubMed PMID:25444595 PubMed Central PMC4317375.

Antonopoulou, K, Stefanaki, I, Lill, CM, Chatzinasiou, F, Kypreou, KP, Karagianni, F et al.. Updated field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma: the MelGene database. J Invest Dermatol. 2015;135 (4):1074-1079. doi: 10.1038/jid.2014.491. PubMed PMID:25407435 .

Ziegan, J, Wittstock, M, Westenberger, A, Dobričić, V, Wolters, A, Benecke, R et al.. Novel GNAL mutations in two German patients with sporadic dystonia. Mov Disord. 2014;29 (14):1833-4. doi: 10.1002/mds.26066. PubMed PMID:25382112 .

Wilcox, R, Brænne, I, Brüggemann, N, Winkler, S, Wiegers, K, Bertram, L et al.. Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only. J Neurol. 2015;262 (1):187-93. doi: 10.1007/s00415-014-7547-9. PubMed PMID:25359261 .

Peric, S, Mandic-Stojmenovic, G, Stefanova, E, Savic-Pavicevic, D, Pesovic, J, Ilic, V et al.. Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2. J Neurol. 2015;262 (1):142-8. doi: 10.1007/s00415-014-7545-y. PubMed PMID:25346064 .