Publications

Gisatulin, M, Dobricic, V, Zühlke, C, Hellenbroich, Y, Tadic, V, Münchau, A, Isenhardt, K, Bürk, K, Bahlo, M, Lockhart, PJ, Lohmann, K, Helmchen, C, Brüggemann, N (2020) Clinical spectrum of the pentanucleotide repeat expansion in the RFC1 gene in ataxia syndromes. Neurology. :. doi: 10.1212/WNL.0000000000010744 PubMed PMID:32873692

Shi, L, Winchester, LM, Liu, BY, Killick, R, Ribe, EM, Westwood, S, Baird, AL, Buckley, NJ, Hong, S, Dobricic, V, Kilpert, F, Franke, A, Kiddle, S, Sattlecker, M, Dobson, R, Cuadrado, A, Hye, A, Ashton, NJ, Morgan, AR, Bos, I et al. (2020) Dickkopf-1 Overexpression in vitro Nominates Candidate Blood Biomarkers Relating to Alzheimer's Disease Pathology. J Alzheimers Dis. 77 (3):1353-1368. doi: 10.3233/JAD-200208 PubMed PMID:32831200

Kusters, CDJ, Paul, KC, Duarte Folle, A, Keener, AM, Bronstein, JM, Dobricic, V, Tysnes, OB, Bertram, L, Alves, G, Sinsheimer, JS, Lill, CM, Maple-Grødem, J, Ritz, BR (2020) Genetic risk scores and hallucinations in patients with Parkinson disease. Neurol Genet. 6 (5):e492. doi: 10.1212/NXG.0000000000000492 PubMed PMID:32802953

Rieck, L, Bardey, F, Grenkowitz, T, Bertram, L, Helmuth, J, Mischung, C, Spranger, J, Steinhagen-Thiessen, E, Bobbert, T, Kassner, U, Demuth, I (2020) Mutation spectrum and polygenic score in German patients with familial hypercholesterolemia. Clin Genet. 98 (5):457-467. doi: 10.1111/cge.13826 PubMed PMID:32770674

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

Röhr, F, Bucholtz, N, Toepfer, S, Norman, K, Spira, D, Steinhagen-Thiessen, E, Lill, CM, Bertram, L, Demuth, I, Buchmann, N, Düzel, S (2020) Relationship between Lipoprotein (a) and cognitive function - Results from the Berlin Aging Study II. Sci Rep. 10 (1):10636. doi: 10.1038/s41598-020-66783-3 PubMed PMID:32606300

Konijnenberg, E, Tijms, BM, Gobom, J, Dobricic, V, Bos, I, Vos, S, Tsolaki, M, Verhey, F, Popp, J, Martinez-Lage, P, Vandenberghe, R, Lleó, A, Frölich, L, Lovestone, S, Streffer, J, Bertram, L, Blennow, K, Teunissen, CE, Veerhuis, R, Smit, AB et al. (2020) APOE ε4 genotype-dependent cerebrospinal fluid proteomic signatures in Alzheimer's disease. Alzheimers Res Ther. 12 (1):65. doi: 10.1186/s13195-020-00628-z PubMed PMID:32460813

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

Engel, S, Graetz, C, Salmen, A, Muthuraman, M, Toenges, G, Ambrosius, B, Bayas, A, Berthele, A, Heesen, C, Klotz, L, Kümpfel, T, Linker, RA, Meuth, SG, Paul, F, Stangel, M, Tackenberg, B, Then Bergh, F, Tumani, H, Weber, F, Wildemann, B et al. (2020) Is APOE ε4 associated with cognitive performance in early MS? Neurol Neuroimmunol Neuroinflamm. 7 (4):. doi: 10.1212/NXI.0000000000000728 PubMed PMID:32358224

Prokopenko, D, Hecker, J, Kirchner, R, Chapman, BA, Hoffman, O, Mullin, K, Hide, W, Bertram, L, Laird, N, DeMeo, DL, Lange, C, Tanzi, RE (2020) Identification of Novel Alzheimer's Disease Loci Using Sex-Specific Family-Based Association Analysis of Whole-Genome Sequence Data. Sci Rep. 10 (1):5029. doi: 10.1038/s41598-020-61883-6 PubMed PMID:32193444

Fjell, AM, Sederevicius, D, Sneve, MH, de Lange, AG, Bråthen, AC, Idland, AV, Watne, LO, Wang, Y, Reinbold, C, Dobricic, V, Kilpert, F, Blennow, K, Zetterbergj, H, Hong, S, Bertram, L, Walhovd, KB, Alzheimer’s Disease Neuroimaging Initiative (2020) Self-reported Sleep Problems Related to Amyloid Deposition in Cortical Regions with High HOMER1 Gene Expression. Cereb Cortex. 30 (4):2144-2156. doi: 10.1093/cercor/bhz228 PubMed PMID:32142100

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

Westwood, S, Baird, AL, Anand, SN, Nevado-Holgado, AJ, Kormilitzin, A, Shi, L, Hye, A, Ashton, NJ, Morgan, AR, Bos, I, Vos, SJB, Baker, S, Buckley, NJ, Ten Kate, M, Scheltens, P, Teunissen, CE, Vandenberghe, R, Gabel, S, Meersmans, K, Engelborghs, S et al. (2020) Validation of Plasma Proteomic Biomarkers Relating to Brain Amyloid Burden in the EMIF-Alzheimer's Disease Multimodal Biomarker Discovery Cohort. J Alzheimers Dis. 74 (1):213-225. doi: 10.3233/JAD-190434 PubMed PMID:31985466

Gómez-Fernández, P, Lopez de Lapuente Portilla, A, Astobiza, I, Mena, J, Urtasun, A, Altmann, V, Matesanz, F, Otaegui, D, Urcelay, E, Antigüedad, A, Malhotra, S, Montalban, X, Castillo-Triviño, T, Espino-Paisán, L, Aktas, O, Buttmann, M, Chan, A, Fontaine, B, Gourraud, PA, Hecker, M et al. (2020) 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. 9 (1):. doi: 10.3390/cells9010175 PubMed PMID:31936765

Stamate, D, Kim, M, Proitsi, P, Westwood, S, Baird, A, Nevado-Holgado, A, Hye, A, Bos, I, Vos, SJB, Vandenberghe, R, Teunissen, CE, Kate, MT, Scheltens, P, Gabel, S, Meersmans, K, Blin, O, Richardson, J, De Roeck, E, Engelborghs, S, Sleegers, K et al. (2019) 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). 5 :933-938. doi: 10.1016/j.trci.2019.11.001 PubMed PMID:31890857

Prokopenko, I, Miyakawa, G, Zheng, B, Heikkinen, J, Petrova Quayle, D, Udeh-Momoh, C, Claringbould, A, Neumann, J, Haytural, H, Kaakinen, MA, Loizidou, E, Meissner, E, Bertram, L, BIOS consortium, Gveric, DO, Gentleman, SM, Attems, J, Perneczky, R, Arzberger, T, Muglia, P et al. (2019) 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). 5 :814-824. doi: 10.1016/j.trci.2019.08.005 PubMed PMID:31788537

Trinh, J, Imhoff, S, Dulovic-Mahlow, M, Kandaswamy, KK, Tadic, V, Schäfer, J, Dobricic, V, Nolte, A, Werber, M, Rolfs, A, Münchau, A, Klein, C, Lohmann, K, Brüggemann, N (2020) Novel NAXE variants as a cause for neurometabolic disorder: implications for treatment. J Neurol. 267 (3):770-782. doi: 10.1007/s00415-019-09640-2 PubMed PMID:31745726

Wohlers, I, Schulz, C, Kilpert, F, Bertram, L (2020) Alzheimer's disease risk SNPs show no strong effect on miRNA expression in human lymphoblastoid cell lines. Neurobiol Aging. 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, Faraway, R, Finan, C, Valentine, D, Fairhurst-Hunter, Z, Hartwig, FP, Horta, BL, Hypponen, E, Power, C, Moldovan, M, van Iperen, E, Hovingh, K, Demuth, I, Norman, K, Steinhagen-Thiessen, E et al. (2019) Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9. BMC Cardiovasc Disord. 19 (1):240. doi: 10.1186/s12872-019-1187-z PubMed PMID:31664920

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

Takousis, P, Sadlon, A, Schulz, J, Wohlers, I, Dobricic, V, Middleton, L, Lill, CM, Perneczky, R, Bertram, L (2019) Differential expression of microRNAs in Alzheimer's disease brain, blood, and cerebrospinal fluid. Alzheimers Dement. 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, Hong, S, Franke, A, Hye, A, Ashton, NJ, Morgan, AR, Bos, I, Vos, SJB, Buckley, NJ, Kate, MT, Scheltens, P, Vandenberghe, R, Gabel, S, Meersmans, K, Engelborghs, S et al. (2019) Discovery and validation of plasma proteomic biomarkers relating to brain amyloid burden by SOMAscan assay. Alzheimers Dement. 15 (11):1478-1488. doi: 10.1016/j.jalz.2019.06.4951 PubMed PMID:31495601

Kim, M, Snowden, S, Suvitaival, T, Ali, A, Merkler, DJ, Ahmad, T, Westwood, S, Baird, A, Proitsi, P, Nevado-Holgado, A, Hye, A, Bos, I, Vos, S, Vandenberghe, R, Teunissen, C, Ten Kate, M, Scheltens, P, Gabel, S, Meersmans, K, Blin, O et al. (2019) 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. 15 (6):817-827. doi: 10.1016/j.jalz.2019.03.004 PubMed PMID:31078433

Morgan, AR, Touchard, S, Leckey, C, O'Hagan, C, Nevado-Holgado, AJ, NIMA Consortium, Barkhof, F, Bertram, L, Blin, O, Bos, I, Dobricic, V, Engelborghs, S, Frisoni, G, Frölich, L, Gabel, S, Johannsen, P, Kettunen, P, Kłoszewska, I, Legido-Quigley, C, Lleó, A et al. (2019) Inflammatory biomarkers in Alzheimer's disease plasma. Alzheimers Dement. 15 (6):776-787. doi: 10.1016/j.jalz.2019.03.007 PubMed PMID:31047856

Davies, G, Lam, M, Harris, SE, Trampush, JW, Luciano, M, Hill, WD, Hagenaars, SP, Ritchie, SJ, Marioni, RE, Fawns-Ritchie, C, Liewald, DCM, Okely, JA, Ahola-Olli, AV, Barnes, CLK, Bertram, L, Bis, JC, Burdick, KE, Christoforou, A, DeRosse, P, Djurovic, S et al. (2019) Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nat Commun. 10 (1):2068. doi: 10.1038/s41467-019-10160-w PubMed PMID:31043617

Schulz, J, Takousis, P, Wohlers, I, Itua, IOG, Dobricic, V, Rücker, G, Binder, H, Middleton, L, Ioannidis, JPA, Perneczky, R, Bertram, L, Lill, CM (2019) Meta-analyses identify differentially expressed micrornas in Parkinson's disease. Ann Neurol. 85 (6):835-851. doi: 10.1002/ana.25490 PubMed PMID:30990912

Westenberger, A, Reyes, CJ, Saranza, G, Dobricic, V, Hanssen, H, Domingo, A, Laabs, BH, Schaake, S, Pozojevic, J, Rakovic, A, Grütz, K, Begemann, K, Walter, U, Dressler, D, Bauer, P, Rolfs, A, Münchau, A, Kaiser, FJ, Ozelius, LJ, Jamora, RD et al. (2019) A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism. Ann Neurol. 85 (6):812-822. doi: 10.1002/ana.25488 PubMed PMID:30973967

Bos, I, Vos, S, Verhey, F, Scheltens, P, Teunissen, C, Engelborghs, S, Sleegers, K, Frisoni, G, Blin, O, Richardson, JC, Bordet, R, Tsolaki, M, Popp, J, Peyratout, G, Martinez-Lage, P, Tainta, M, Lleó, A, Johannsen, P, Freund-Levi, Y, Frölich, L et al. (2019) Cerebrospinal fluid biomarkers of neurodegeneration, synaptic integrity, and astroglial activation across the clinical Alzheimer's disease spectrum. Alzheimers Dement. 15 (5):644-654. doi: 10.1016/j.jalz.2019.01.004 PubMed PMID:30853464

Bertram, L, Tanzi, RE (2019) Alzheimer disease risk genes: 29 and counting. Nat Rev Neurol. 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, Barroso, I, Bennett, DA, Bertram, L, Bochud, M, Borecki, IB, Broer, L, Buchman, AS, Byberg, L, Campbell, H, Campos-Obando, N, Cauley, JA, Cawthon, PM, Chambers, JC, Chen, Z et al. (2019) Disentangling the genetics of lean mass. Am J Clin Nutr. 109 (2):276-287. doi: 10.1093/ajcn/nqy272 PubMed PMID:30721968

Karlsson Linnér, R, Biroli, P, Kong, E, Meddens, SFW, Wedow, R, Fontana, MA, Lebreton, M, Tino, SP, Abdellaoui, A, Hammerschlag, AR, Nivard, MG, Okbay, A, Rietveld, CA, Timshel, PN, Trzaskowski, M, Vlaming, R, Zünd, CL, Bao, Y, Buzdugan, L, Caplin, AH et al. (2019) 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. 51 (2):245-257. doi: 10.1038/s41588-018-0309-3 PubMed PMID:30643258

Trinh, J, Lohmann, K, Baumann, H, Balck, A, Borsche, M, Brüggemann, N, Dure, L, Dean, M, Volkmann, J, Tunc, S, Prasuhn, J, Pawlack, H, Imhoff, S, Lill, CM, Kasten, M, Bauer, P, Rolfs, A, International Parkinson's Disease Genomics Consortium (IPDGC), Klein, C (2019) Utility and implications of exome sequencing in early-onset Parkinson's disease. Mov Disord. 34 (1):133-137. doi: 10.1002/mds.27559 PubMed PMID:30537300

Reinthaler, EM, Graf, E, Zrzavy, T, Wieland, T, Hotzy, C, Kopecky, C, Pferschy, S, Schmied, C, Leutmezer, F, Keilani, M, Lill, CM, Hoffjan, S, Epplen, JT, Zettl, UK, Hecker, M, Deutschländer, A, Meuth, SG, Ahram, M, Mustafa, B, El-Khateeb, M et al. (2018) TPP2 mutation associated with sterile brain inflammation mimicking MS. Neurol Genet. 4 (6):e285. doi: 10.1212/NXG.0000000000000285 PubMed PMID:30533531

Trinh, J, Zeldenrust, FMJ, Huang, J, Kasten, M, Schaake, S, Petkovic, S, Madoev, H, Grünewald, A, Almuammar, S, König, IR, Lill, CM, Lohmann, K, Klein, C, Marras, C (2018) Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review. Mov Disord. 33 (12):1857-1870. doi: 10.1002/mds.27527 PubMed PMID:30357936

Herwest, S, Albers, C, Schmiester, M, Salewsky, B, Hopfenmüller, W, Meyer, A, Bertram, L, Demuth, I (2018) The hSNM1B/Apollo variant rs11552449 is associated with cellular sensitivity towards mitomycin C and ionizing radiation. DNA Repair (Amst). 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, Gabel, S, Schaeverbeke, J, Scheltens, P, Blin, O, Richardson, JC, Bordet, R, Wallin, A, Eckerstrom, C, Molinuevo, JL, Engelborghs, S, Van Broeckhoven, C, Martinez-Lage, P, Popp, J, Tsolaki, M et al. (2018) MRI predictors of amyloid pathology: results from the EMIF-AD Multimodal Biomarker Discovery study. Alzheimers Res Ther. 10 (1):100. doi: 10.1186/s13195-018-0428-1 PubMed PMID:30261928

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

Wohlers, I, Bertram, L, Lill, CM (2018) Evidence for a potential role of miR-1908-5p and miR-3614-5p in autoimmune disease risk using integrative bioinformatics. J Autoimmun. 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 (2018) Field synopsis and systematic meta-analyses of genetic association studies in isolated dystonia. Parkinsonism Relat Disord. 57 :50-57. doi: 10.1016/j.parkreldis.2018.07.018 PubMed PMID:30100364

Bos, I, Vos, S, Vandenberghe, R, Scheltens, P, Engelborghs, S, Frisoni, G, Molinuevo, JL, Wallin, A, Lleó, A, Popp, J, Martinez-Lage, P, Baird, A, Dobson, R, Legido-Quigley, C, Sleegers, K, Van Broeckhoven, C, Bertram, L, Ten Kate, M, Barkhof, F, Zetterberg, H et al. (2018) The EMIF-AD Multimodal Biomarker Discovery study: design, methods and cohort characteristics. Alzheimers Res Ther. 10 (1):64. doi: 10.1186/s13195-018-0396-5 PubMed PMID:29980228

Davies, G, Lam, M, Harris, SE, Trampush, JW, Luciano, M, Hill, WD, Hagenaars, SP, Ritchie, SJ, Marioni, RE, Fawns-Ritchie, C, Liewald, DCM, Okely, JA, Ahola-Olli, AV, Barnes, CLK, Bertram, L, Bis, JC, Burdick, KE, Christoforou, A, DeRosse, P, Djurovic, S et al. (2018) Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nat Commun. 9 (1):2098. doi: 10.1038/s41467-018-04362-x PubMed PMID:29844566

Kasten, M, Hartmann, C, Hampf, J, Schaake, S, Westenberger, A, Vollstedt, EJ, Balck, A, Domingo, A, Vulinovic, F, Dulovic, M, Zorn, I, Madoev, H, Zehnle, H, Lembeck, CM, Schawe, L, Reginold, J, Huang, J, König, IR, Bertram, L, Marras, C et al. (2018) Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic Review. Mov Disord. 33 (5):730-741. doi: 10.1002/mds.27352 PubMed PMID:29644727

Graetz, C, Gröger, A, Luessi, F, Salmen, A, Zöller, D, Schultz, J, Siller, N, Fleischer, V, Bellenberg, B, Berthele, A, Biberacher, V, Havla, J, Hecker, M, Hohlfeld, R, Infante-Duarte, C, Kirschke, JS, Kümpfel, T, Linker, R, Paul, F, Pfeuffer, S et al. (2019) Association of smoking but not HLA-DRB1*15:01, APOE or body mass index with brain atrophy in early multiple sclerosis. Mult Scler. 25 (5):661-668. doi: 10.1177/1352458518763541 PubMed PMID:29532745

Walhovd, KB, Fjell, AM, Westerhausen, R, Nyberg, L, Ebmeier, KP, Lindenberger, U, Bartrés-Faz, D, Baaré, WFC, Siebner, HR, Henson, R, Drevon, CA, Strømstad Knudsen, GP, Ljøsne, IB, Penninx, BWJH, Ghisletta, P, Rogeberg, O, Tyler, L, Bertram, L, Lifebrain Consortium (2018) Healthy minds 0-100 years: Optimising the use of European brain imaging cohorts ("Lifebrain"). Eur Psychiatry. 50 :47-56. doi: 10.1016/j.eurpsy.2017.12.006 PubMed PMID:29449073

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

Walhovd, KB, Fjell, AM, Westerhausen, R, Nyberg, L, Ebmeier, KP, Lindenberger, U, Bartrés-Faz, D, Baaré, WFC, Siebner, HR, Henson, R, Drevon, CA, Knudsen, GP, Budin-Ljøsne, I, Penninx, BWJH, Ghisletta, P, Rogeberg, O, Tyler, L, Bertram, L, for Lifebrain Consortium (2018) Healthy minds from 0-100 years: Optimising the use of European brain imaging cohorts ("Lifebrain"). Eur Psychiatry. 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, Livshits, G, Broer, L, Johnson, T, Koller, DL, Kutalik, Z, Luan, J, Malkin, I, Ried, JS, Smith, AV, Thorleifsson, G, Vandenput, L, Hua Zhao, J, Zhang, W, Aghdassi, A et al. (2017) Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nat Commun. 8 (1):1414. doi: 10.1038/s41467-017-01008-2 PubMed PMID:29116125

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

Joshi, PK, Pirastu, N, Kentistou, KA, Fischer, K, Hofer, E, Schraut, KE, Clark, DW, Nutile, T, Barnes, CLK, Timmers, PRHJ, Shen, X, Gandin, I, McDaid, AF, Hansen, TF, Gordon, SD, Giulianini, F, Boutin, TS, Abdellaoui, A, Zhao, W, Medina-Gomez, C et al. (2017) Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nat Commun. 8 (1):910. doi: 10.1038/s41467-017-00934-5 PubMed PMID:29030599

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

Buchmann, N, Scholz, M, Lill, CM, Burkhardt, R, Eckardt, R, Norman, K, Loeffler, M, Bertram, L, Thiery, J, Steinhagen-Thiessen, E, Demuth, I (2017) Association between lipoprotein(a) level and type 2 diabetes: no evidence for a causal role of lipoprotein(a) and insulin. Acta Diabetol. 54 (11):1031-1038. doi: 10.1007/s00592-017-1036-4 PubMed PMID:28866807

Lill, CM, Klein, C (2017) What would Dr. James Parkinson think today? The role of genetics in Parkinson's disease. Mov Disord. 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, Livshits, G, Broer, L, Johnson, T, Koller, DL, Kutalik, Z, Luan, J, Malkin, I, Ried, JS, Smith, AV, Thorleifsson, G, Vandenput, L, Hua Zhao, J, Zhang, W, Aghdassi, A et al. (2017) Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nat Commun. 8 (1):80. doi: 10.1038/s41467-017-00031-7 PubMed PMID:28724990

Marras, C, Lang, A, van de Warrenburg, BP, Sue, CM, Tabrizi, SJ, Bertram, L, Mercimek-Mahmutoglu, S, Ebrahimi-Fakhari, D, Warner, TT, Durr, A, Assmann, B, Lohmann, K, Kostic, V, Klein, C (2017) Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force. Mov Disord. 32 (5):724-725. doi: 10.1002/mds.27045 PubMed PMID:28513081

Lill, CM, Klein, C (2017) [Epidemiology and causes of Parkinson's disease]. Nervenarzt. 88 (4):345-355. doi: 10.1007/s00115-017-0288-0 PubMed PMID:28289797

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

Schmidt, AF, Swerdlow, DI, Holmes, MV, Patel, RS, Fairhurst-Hunter, Z, Lyall, DM, Hartwig, FP, Horta, BL, Hyppönen, E, Power, C, Moldovan, M, van Iperen, E, Hovingh, GK, Demuth, I, Norman, K, Steinhagen-Thiessen, E, Demuth, J, Bertram, L, Liu, T, Coassin, S et al. (2017) PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study. Lancet Diabetes Endocrinol. 5 (2):97-105. doi: 10.1016/S2213-8587(16)30396-5 PubMed PMID:27908689

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

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

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

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

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Ahmed, I, Lee, PC, Lill, CM, Searles Nielsen, S, Artaud, F, Gallagher, LG, Loriot, MA, Mulot, C, Nacfer, M, Liu, T, Biernacka, JM, Armasu, S, Anderson, K, Farin, FM, Lassen, CF, Hansen, J, Olsen, JH, Bertram, L, Maraganore, DM, Checkoway, H et al. (2014) Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease. PLoS Genet. 10 (11):e1004788. doi: 10.1371/journal.pgen.1004788 PubMed PMID:25412286

Antonopoulou, K, Stefanaki, I, Lill, CM, Chatzinasiou, F, Kypreou, KP, Karagianni, F, Athanasiadis, E, Spyrou, GM, Ioannidis, JPA, Bertram, L, Evangelou, E, Stratigos, AJ (2015) Updated field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma: the MelGene database. J Invest Dermatol. 135 (4):1074-1079. doi: 10.1038/jid.2014.491 PubMed PMID:25407435

Athanasiadis, EI, Antonopoulou, K, Chatzinasiou, F, Lill, CM, Bourdakou, MM, Sakellariou, A, Kypreou, K, Stefanaki, I, Evangelou, E, Ioannidis, JP, Bertram, L, Stratigos, AJ, Spyrou, GM (2014) A Web-based database of genetic association studies in cutaneous melanoma enhanced with network-driven data exploration tools. Database (Oxford). 2014 :. doi: 10.1093/database/bau101 PubMed PMID:25380778

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

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Hooli, BV, Parrado, AR, Mullin, K, Yip, WK, Liu, T, Roehr, JT, Qiao, D, Jessen, F, Peters, O, Becker, T, Ramirez, A, Lange, C, Bertram, L, Tanzi, RE (2014) The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk. Neurology. 83 (15):1353-8. doi: 10.1212/WNL.0000000000000855 PubMed PMID:25186855

Lill, CM (2014) Recent advances and future challenges in the genetics of multiple sclerosis. Front Neurol. 5 :130. doi: 10.3389/fneur.2014.00130 PubMed PMID:25071715

Schröder, J, Ansaloni, S, Schilling, M, Liu, T, Radke, J, Jaedicke, M, Schjeide, BM, Mashychev, A, Tegeler, C, Radbruch, H, Papenberg, G, Düzel, S, Demuth, I, Bucholtz, N, Lindenberger, U, Li, SC, Steinhagen-Thiessen, E, Lill, CM, Bertram, L (2014) MicroRNA-138 is a potential regulator of memory performance in humans. Front Hum Neurosci. 8 :501. doi: 10.3389/fnhum.2014.00501 PubMed PMID:25071529

Nalls, MA, Pankratz, N, Lill, CM, Do, CB, Hernandez, DG, Saad, M, DeStefano, AL, Kara, E, Bras, J, Sharma, M, Schulte, C, Keller, MF, Arepalli, S, Letson, C, Edsall, C, Stefansson, H, Liu, X, Pliner, H, Lee, JH, Cheng, R et al. (2014) Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nat Genet. 46 (9):989-93. doi: 10.1038/ng.3043 PubMed PMID:25064009

Bellander, M, Bäckman, L, Liu, T, Schjeide, BM, Bertram, L, Schmiedek, F, Lindenberger, U, Lövdén, M (2015) Lower baseline performance but greater plasticity of working memory for carriers of the val allele of the COMT Val¹⁵⁸Met polymorphism. Neuropsychology. 29 (2):247-54. doi: 10.1037/neu0000088 PubMed PMID:24819065