• Genetic risk factors for essential tremor: A review 

      Siokas V., Aloizou A.-M., Tsouris Z., Liampas I., Aslanidou P., Dastamani M., Brotis A.G., Bogdanos D.P., Hadjigeorgiou G.M., Dardiotis E. (2020)
      Highlights In the current review, we thoroughly reviewed 74 identified articles regarding genes and genetic loci that confer susceptibility to ET. Over 50 genes/genetic loci have been examined for possible association with ...
    • Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci 

      Reppe S., Wang Y., Thompson W.K., McEvoy L.K., Schork A.J., Zuber V., LeBlanc M., Bettella F., Mills I.G., Desikan R.S., Djurovic S., Gautvik K.M., Dale A.M., Andreassen O.A., Estrada K., Styrkarsdottir U., Evangelou E., Hsu Y.-H., Duncan E.L., Ntzani E.E., Oei L., Albagha O.M.E., Amin N., Kemp J.P., Koller D.L., Li G., Liu C.-T., Minster R.L., Moayyeri A., Vandenput L., Willner D., Xiao S.-M., Yerges-Armstrong L.M., Zheng H.-F., Alonso N., Eriksson J., Kammerer C.M., Kaptoge S.K., Leo P.J., Thorleifsson G., Wilson S.G., Wilson J.F., Aalto V., Alen M., Aragaki A.K., Aspelund T., Center J.R., Dailiana Z., Duggan D.J., Garcia M., Garcia-Giralt N., Giroux S., Hallmans G., Hocking L.J., Husted L.B., Jameson K.A., Khusainova R., Kim G.S., Kooperberg C., Koromila T., Kruk M., Laaksonen M., Lacroix A.Z., Lee S.H., Leung P.C., Lewis J.R., Masi L., Mencej-Bedrac S., Nguyen T.V., Nogues X., Patel M.S., Prezelj J., Rose L.M., Scollen S., Siggeirsdottir K., Smith A.V., Svensson O., Trompet S., Trummer O., Van Schoor N.M., Woo J., Zhu K., Balcells S., Brandi M.L., Buckley B.M., Cheng S., Christiansen C., Cooper C., Dedoussis G., Ford I., Frost M., Goltzman D., González-Macías J., Kähönen M., Karlsson M., Khusnutdinova E., Koh J.-M., Kollia P., Langdahl B.L., Leslie W.D., Lips P., Ljunggren Ö., Lorenc R.S., Marc J., Mellström D., Obermayer-Pietsch B., Olmos J.M., Pettersson-Kymmer U., Reid D.M., Riancho J.A., Ridker P.M., Rousseau F., Slagboom P.E., Tang N.L.S., Urreizti R., Van Hul W., Viikari J., Zarrabeitia M.T., Aulchenko Y.S., Castano-Betancourt M., Grundberg E., Herrera L., Ingvarsson T., Johannsdottir H., Kwan T., Li R., Luben R., Medina-Gómez C., Palsson S.Th., Rotter J.I., Sigurdsson G., Van Meurs J.B.J., Verlaan D., Williams F.M.K., Wood A.R., Zhou Y., Pastinen T., Raychaudhuri S., Cauley J.A., Chasman D.I., Clark G.R., Cummings S.R., Danoy P., Dennison E.M., Eastell R., Eisman J.A., Gudnason V., Hofman A., Jackson R.D., Jones G., Jukema J.W., Khaw K.-T., Lehtimäki T., Liu Y., Lorentzon M., McCloskey E., Mitchell B.D., Nandakumar K., Nicholson G.C., Oostra B.A., Peacock M., Pols H.A.P., Prince R.L., Raitakari O., Reid I.R., Robbins J., Sambrook P.N., Sham P.C., Shuldiner A.R., Tylavsky F.A., Van Duijn C.M., Wareham N.J., Cupples L.A., Econs M.J., Evans D.M., Harris T.B., Kung A.W.C., Psaty B.M., Reeve J., Spector T.D., Streeten E.A., Zillikens M.C., Thorsteinsdottir U., Ohlsson C., Karasik D., Richards J.B., Brown M.A., Stefansson K., Uitterlinden A.G., Ralston S.H., Ioannidis J.P.A., Kiel D.P., Rivadeneira F., GEFOS Consortium (2015)
      Bone Mineral Density (BMD) is a highly heritable trait, but genome-wide association studies have identified few genetic risk factors. Epidemiological studies suggest associations between BMD and several traits and diseases, ...
    • Genetic variations in the SULF1 gene alter the risk of cervical cancer and precancerous lesions 

      Dardiotis E., Siokas V., Garas A., Paraskevaidis E., Kyrgiou M., Xiromerisiou G., Deligeoroglou E., Galazios G., Kontomanolis E.N., Spandidos D.A., Tsatsakis A., Daponte A. (2018)
      Human papillomavirus (HPV) infection alone is not sufficient to explain the development of cervical cancer. Genetic variants have been linked to the development of precancerous lesions and cervical cancer. In this study, ...
    • Genotype-Phenotype Relationships in Inheritable Idiopathic Pulmonary Fibrosis: A Greek National Cohort Study 

      Manali E.D., Kannengiesser C., Borie R., Ba I., Bouros D., Markopoulou A., Antoniou K., Kolilekas L., Papaioannou A.I., Tzilas V., Tzouvelekis A., Daniil Z., Fouka E., Papakosta D., Xyfteri A., Karakatsani A., Loukides S., Korbila I., Tomos I.P., Konstantinidis A.K., Gogali A., Steiropoulos P., Papanikolaou I.C., Bazaka C., Haritou A., Vassilakopoulos T., Maniati M., Kagouridis K., Markozannes E., Bouros E., Rampiadou C., Kounti G., Trachalaki A., Dimeas I., Karampitsakos T., Lyberopoulos P., Malamadakis N., Spyropoulou S., Revy P., Lainey E., Dieudé P., Rebah K., Ménard C., Oudin C., Masson C., Plessier A., Legendre M., Nathan N., Coulomb-L'hermine A., Clement A., Amselem S., Boileau C., Crestani B., Papiris S. (2022)
      Background: Monogenic and polygenic inheritances are evidenced for idiopathic pulmonary fibrosis (IPF). Pathogenic variations in surfactant protein-related genes, telomere-related genes (TRGs), and a single-nucleotide ...
    • Haplotype structure defines effects of common DPYD variants c.85T > C (rs1801265) and c.496A > G (rs2297595) on dihydropyrimidine dehydrogenase activity: Implication for 5-fluorouracil toxicity 

      Hamzic S., Schärer D., Offer S.M., Meulendijks D., Nakas C., Diasio R.B., Fontana S., Wehrli M., Schürch S., Amstutz U., Largiadèr C.R. (2021)
      Aims: The aim of this study was to identify risk variants and haplotypes that impair dihydropyrimidine dehydrogenase (DPD) activity and are, therefore, candidate risk variants for severe toxicity to 5-fluorouracil (5-FU) ...
    • Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis 

      Schormair B., Zhao C., Bell S., Tilch E., Salminen A.V., Pütz B., Dauvilliers Y., Stefani A., Högl B., Poewe W., Kemlink D., Sonka K., Bachmann C.G., Paulus W., Trenkwalder C., Oertel W.H., Hornyak M., Teder-Laving M., Metspalu A., Hadjigeorgiou G.M., Polo O., Fietze I., Ross O.A., Wszolek Z., Butterworth A.S., Soranzo N., Ouwehand W.H., Roberts D.J., Danesh J., Allen R.P., Earley C.J., Ondo W.G., Xiong L., Montplaisir J., Gan-Or Z., Perola M., Vodicka P., Dina C., Franke A., Tittmann L., Stewart A.F.R., Shah S.H., Gieger C., Peters A., Rouleau G.A., Berger K., Oexle K., Di Angelantonio E., Hinds D.A., Müller-Myhsok B., Winkelmann J., Balkau B., Ducimetière P., Eschwège E., Rancière F., Alhenc-Gelas F., Gallois Y., Girault A., Fumeron F., Marre M., Roussel R., Bonnet F., Bonnefond A., Cauchi S., Froguel P., Cogneau J., Born C., Caces E., Cailleau M., Lantieri O., Moreau J.G., Rakotozafy F., Tichet J., Vol S., Agee M., Alipanahi B., Auton A., Bell R.K., Bryc K., Elson S.L., Fontanillas P., Furlotte N.A., Hinds D.A., Hromatka B.S., Huber K.E., Kleinman A., Litterman N.K., McIntyre M.H., Mountain J.L., Northover C.A., Pitts S.J., Sathirapongsasuti J.F., Sazonova O.V., Shelton J.F., Shringarpure S., Tian C., Tung J.Y., Vacic V., Wilson C.H., 23andMe Research Team, DESIR study group, 23andMe Research Team, DESIR study group, DESIR study group, DESIR study group (2017)
      Background Restless legs syndrome is a prevalent chronic neurological disorder with potentially severe mental and physical health consequences. Clearer understanding of the underlying pathophysiology is needed to improve ...
    • Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology 

      Jun, G.; Nicolaou, M.; Morrison, M. A.; Buros, J.; Morgan, D. J.; Radeke, M. J.; Yonekawa, Y.; Tsironi, E. E.; Kotoula, M. G.; Zacharaki, F.; Mollema, N.; Yuan, Y.; Miller, J. W.; Haider, N. B.; Hageman, G. S.; Kim, I. K.; Schaumberg, D. A.; Farrer, L. A.; DeAngelis, M. M. (2011)
      ROBO1 is a strong candidate gene for age-related macular degeneration (AMD) based upon its location under a linkage peak on chromosome 3p12, its expression pattern, and its purported function in a pathway that includes ...
    • Integrins AV and B8 Gene Polymorphisms and Risk for Intracerebral Hemorrhage in Greek and Polish Populations 

      Dardiotis E., Siokas V., Zafeiridis T., Paterakis K., Tsivgoulis G., Dardioti M., Grigoriadis S., Simeonidou C., Deretzi G., Zintzaras E., Jagiella J., Hadjigeorgiou G.M. (2017)
      Α limited number of genetic variants have been linked to the development of intracerebral hemorrhage (ICH). Ιntegrin AV and/or B8-deficient mice were found to develop ICH. The present candidate gene association study was ...
    • Investigating the genetic characteristics of CAD: Is there a role for myocardial perfusion imaging techniques? 

      Angelidis G., Valotassiou V., Satra M., Psimadas D., Koutsikos J., Skoularigis J., Kollia P., Georgoulias P. (2022)
      Several environmental and genetic factors have been found to influence the development and progression of coronary artery disease (CAD). Although the effects of the environmental hazards on CAD pathophysiology are well ...
    • Lack of Association of the rs11655081 ARSG Gene with Blepharospasm 

      Siokas V., Kardaras D., Aloizou A.-M., Asproudis I., Boboridis K.G., Papageorgiou E., Spandidos D.A., Tsatsakis A., Tsironi E.E., Dardiotis E. (2019)
      Blepharospasm (BSP) is a sub-phenotype of focal dystonia. A few genetic risk factors are considered to be implicated in the risk of developing BSP. There is recent evidence, based on results from GWAS and meta-analyses, ...
    • Large replication study and meta-analyses of DVWA as an osteoarthritis susceptibility locus in European and Asian populations 

      Meulenbelt, I.; Chapman, K.; Dieguez-Gonzalez, R.; Shi, D.; Tsezou, A.; Dai, J.; Malizos, K. N.; Kloppenburg, M.; Carr, A.; Nakajima, M.; van der Breggen, R.; Lakenberg, N.; Gomez-Reino, J. J.; Jiang, Q.; Ikegawa, S.; Gonzalez, A.; Loughlin, J.; Slagboom, E. P. (2009)
      Recently, through a genome wide association study in Japanese knee osteoarthritis (OA) cases, a previously unknown gene, DVWA, was identified. The non-synonymous single nucleotide polymorphism (SNP) rs7639618 was subsequently ...
    • Large-scale assessment of polyglutamine repeat expansions in Parkinson disease 

      Wang L., Aasly J.O., Annesi G., Bardien S., Bozi M., Brice A., Carr J., Chung S.J., Clarke C., Crosiers D., Deutschländer A., Eckstein G., Farrer M.J., Goldwurm S., Garraux G., Hadjigeorgiou G.M., Hicks A.A., Hattori N., Klein C., Jeon B., Kim Y.J., Lesage S., Lin J.-J., Lynch T., Lichtner P., Lang A.E., Mok V., Jasinska-Myga B., Mellick G.D., Morrison K.E., Opala G., PihlstrØm L., Pramstaller P.P., Park S.S., Quattrone A., Rogaeva E., Ross O.A., Stefanis L., Stockton J.D., Silburn P.A., Theuns J., Tan E.K., Tomiyama H., Toft M., Van Broeckhoven C., Uitti R.J., Wirdefeldt K., Wszolek Z., Xiromerisiou G., Yueh K.-C., Zhao Y., Gasser T., Maraganore D.M., Krüger R., Sharma M. (2015)
      Objectives: We aim to clarify the pathogenic role of intermediate size repeat expansions of SCA2, SCA3, SCA6, and SCA17 as risk factors for idiopathic Parkinson disease (PD). Methods: We invited researchers from the Genetic ...
    • Large-scale replication and heterogeneity in Parkinson disease genetic loci 

      Sharma, M.; Ioannidis, J. P. A.; Aasly, J. O.; Annesi, G.; Brice, A.; Van Broeckhoven, C.; Bertram, L.; Bozi, M.; Crosiers, D.; Clarke, C.; Facheris, M.; Farrer, M.; Garraux, G.; Gispert, S.; Auburger, G.; Vilariño-Güell, C.; Hadjigeorgiou, G. M.; Hicks, A. A.; Hattori, N.; Jeon, B.; Lesage, S.; Lill, C. M.; Lin, J. J.; Lynch, T.; Lichtner, P.; Lang, A. E.; Mok, V.; Jasinska-Myga, B.; Mellick, G. D.; Morrison, K. E.; Opala, G.; Pramstaller, P. P.; Pichler, I.; Park, S. S.; Quattrone, A.; Rogaeva, E.; Ross, O. A.; Stefanis, L.; Stockton, J. D.; Satake, W.; Silburn, P. A.; Theuns, J.; Tan, E. K.; Toda, T.; Tomiyama, H.; Uitti, R. J.; Wirdefeldt, K.; Wszolek, Z.; Xiromerisiou, G.; Yueh, K. C.; Zhao, Y.; Gasser, T.; Maraganore, D.; Krüger, R. (2012)
      Objective: Eleven genetic loci have reached genome-wide significance in a recent meta-analysis of genome-wide association studies in Parkinson disease (PD) based on populations of Caucasian descent. The extent to which ...
    • A meta-analysis of FZD3 gene polymorphisms and their association with schizophrenia 

      Pantavou K.G., Braliou G.G., Kontou P.I., Dimou N.L., Bagos P.G. (2016)
      Objective The aim of this study was to investigate the potential association of FZD3 polymorphisms with schizophrenia. Methods A systematic review and a meta-analysis were carried out comprising of nine genetic association ...
    • Motor and Nonmotor Features of Carriers of the p.A53T Alpha-Synuclein Mutation: A Longitudinal Study 

      Papadimitriou D., Antonelou R., Miligkos M., Maniati M., Papagiannakis N., Bostantjopoulou S., Leonardos A., Koros C., Simitsi A., Papageorgiou S.G., Kapaki E., Alcalay R.N., Papadimitriou A., Athanassiadou A., Stamelou M., Stefanis L. (2016)
      Background: G209A SNCA mutation carriers represent an important group of genetic PD. We describe motor and nonmotor features of G209A SNCA mutation carriers. Methods: Longitudinal clinical assessments over 2 years were ...
    • Multiple sclerosis: Shall we target cd33? 

      Siokas V., Tsouris Z., Aloizou A.-M., Bakirtzis C., Liampas I., Koutsis G., Anagnostouli M., Bogdanos D.P., Grigoriadis N., Hadjigeorgiou G.M., Dardiotis E. (2020)
      Background: Multiple sclerosis (MS) is a chronic disease of the central nervous system (CNS). Myeloid lineage cells (microglia and macrophages) may participate in the pathogenic mechanisms leading to MS. CD33 is a transmembrane ...
    • Myelin-associated oligodendrocyte basic protein rs616147 polymorphism as a risk factor for Parkinson's disease 

      Siokas V., Aloizou A.-M., Liampas I., Bakirtzis C., Tsouris Z., Sgantzos M., Liakos P., Bogdanos D.P., Hadjigeorgiou G.M., Dardiotis E. (2022)
      BACKGROUND: The rs616147 polymorphism of the myelin-associated oligodendrocyte basic protein (MOBP) gene locus has been associated with amyotrophic lateral sclerosis (ALS). ALS and Parkinson's disease (PD) are two common ...
    • Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease 

      Li, Y.; Rowland, C.; Xiromerisiou, G.; Lagier, R. J.; Schrodi, S. J.; Dradiotis, E.; Ross, D.; Bui, N.; Catanese, J.; Aggelakis, K.; Grupe, A.; Hadjigeorgiou, G. (2008)
      Susceptibility to sporadic Parkinson's diseases (PD) is thought to be influence by both genetic and environmental factors and thier interaction with each other. Statistical models including multiples variants in axon ...
    • New insights into the genetic etiology of Alzheimer’s disease and related dementias 

      Bellenguez C., Küçükali F., Jansen I.E., Kleineidam L., Moreno-Grau S., Amin N., Naj A.C., Campos-Martin R., Grenier-Boley B., Andrade V., Holmans P.A., Boland A., Damotte V., van der Lee S.J., Costa M.R., Kuulasmaa T., Yang Q., de Rojas I., Bis J.C., Yaqub A., Prokic I., Chapuis J., Ahmad S., Giedraitis V., Aarsland D., Garcia-Gonzalez P., Abdelnour C., Alarcón-Martín E., Alcolea D., Alegret M., Alvarez I., Álvarez V., Armstrong N.J., Tsolaki A., Antúnez C., Appollonio I., Arcaro M., Archetti S., Pastor A.A., Arosio B., Athanasiu L., Bailly H., Banaj N., Baquero M., Barral S., Beiser A., Pastor A.B., Below J.E., Benchek P., Benussi L., Berr C., Besse C., Bessi V., Binetti G., Bizarro A., Blesa R., Boada M., Boerwinkle E., Borroni B., Boschi S., Bossù P., Bråthen G., Bressler J., Bresner C., Brodaty H., Brookes K.J., Brusco L.I., Buiza-Rueda D., Bûrger K., Burholt V., Bush W.S., Calero M., Cantwell L.B., Chene G., Chung J., Cuccaro M.L., Carracedo Á., Cecchetti R., Cervera-Carles L., Charbonnier C., Chen H.-H., Chillotti C., Ciccone S., Claassen J.A.H.R., Clark C., Conti E., Corma-Gómez A., Costantini E., Custodero C., Daian D., Dalmasso M.C., Daniele A., Dardiotis E., Dartigues J.-F., de Deyn P.P., de Paiva Lopes K., de Witte L.D., Debette S., Deckert J., del Ser T., Denning N., DeStefano A., Dichgans M., Diehl-Schmid J., Diez-Fairen M., Rossi P.D., Djurovic S., Duron E., Düzel E., Dufouil C., Eiriksdottir G., Engelborghs S., Escott-Price V., Espinosa A., Ewers M., Faber K.M., Fabrizio T., Nielsen S.F., Fardo D.W., Farotti L., Fenoglio C., Fernández-Fuertes M., Ferrari R., Ferreira C.B., Ferri E., Fin B., Fischer P., Fladby T., Fließbach K., Fongang B., Fornage M., Fortea J., Foroud T.M., Fostinelli S., Fox N.C., Franco-Macías E., Bullido M.J., Frank-García A., Froelich L., Fulton-Howard B., Galimberti D., García-Alberca J.M., García-González P., Garcia-Madrona S., Garcia-Ribas G., Ghidoni R., Giegling I., Giorgio G., Goate A.M., Goldhardt O., Gomez-Fonseca D., González-Pérez A., Graff C., Grande G., Green E., Grimmer T., Grünblatt E., Grunin M., Gudnason V., Guetta-Baranes T., Haapasalo A., Hadjigeorgiou G., Haines J.L., Hamilton-Nelson K.L., Hampel H., Hanon O., Hardy J., Hartmann A.M., Hausner L., Harwood J., Heilmann-Heimbach S., Helisalmi S., Heneka M.T., Hernández I., Herrmann M.J., Hoffmann P., Holmes C., Holstege H., Vilas R.H., Hulsman M., Humphrey J., Biessels G.J., Jian X., Johansson C., Jun G.R., Kastumata Y., Kauwe J., Kehoe P.G., Kilander L., Ståhlbom A.K., Kivipelto M., Koivisto A., Kornhuber J., Kosmidis M.H., Kukull W.A., Kuksa P.P., Kunkle B.W., Kuzma A.B., Lage C., Laukka E.J., Launer L., Lauria A., Lee C.-Y., Lehtisalo J., Lerch O., Lleó A., Longstreth W., Jr, Lopez O., de Munain A.L., Love S., Löwemark M., Luckcuck L., Lunetta K.L., Ma Y., Macías J., MacLeod C.A., Maier W., Mangialasche F., Spallazzi M., Marquié M., Marshall R., Martin E.R., Montes A.M., Rodríguez C.M., Masullo C., Mayeux R., Mead S., Mecocci P., Medina M., Meggy A., Mehrabian S., Mendoza S., Menéndez-González M., Mir P., Moebus S., Mol M., Molina-Porcel L., Montrreal L., Morelli L., Moreno F., Morgan K., Mosley T., Nöthen M.M., Muchnik C., Mukherjee S., Nacmias B., Ngandu T., Nicolas G., Nordestgaard B.G., Olaso R., Orellana A., Orsini M., Ortega G., Padovani A., Paolo C., Papenberg G., Parnetti L., Pasquier F., Pastor P., Peloso G., Pérez-Cordón A., Pérez-Tur J., Pericard P., Peters O., Pijnenburg Y.A.L., Pineda J.A., Piñol-Ripoll G., Pisanu C., Polak T., Popp J., Posthuma D., Priller J., Puerta R., Quenez O., Quintela I., Thomassen J.Q., Rábano A., Rainero I., Rajabli F., Ramakers I., Real L.M., Reinders M.J.T., Reitz C., Reyes-Dumeyer D., Ridge P., Riedel-Heller S., Riederer P., Roberto N., Rodriguez-Rodriguez E., Rongve A., Allende I.R., Rosende-Roca M., Royo J.L., Rubino E., Rujescu D., Sáez M.E., Sakka P., Saltvedt I., Sanabria Á., Sánchez-Arjona M.B., Sanchez-Garcia F., Juan P.S., Sánchez-Valle R., Sando S.B., Sarnowski C., Satizabal C.L., Scamosci M., Scarmeas N., Scarpini E., Scheltens P., Scherbaum N., Scherer M., Schmid M., Schneider A., Schott J.M., Selbæk G., Seripa D., Serrano M., Sha J., Shadrin A.A., Skrobot O., Slifer S., Snijders G.J.L., Soininen H., Solfrizzi V., Solomon A., Song Y., Sorbi S., Sotolongo-Grau O., Spalletta G., Spottke A., Squassina A., Stordal E., Tartan J.P., Tárraga L., Tesí N., Thalamuthu A., Thomas T., Tosto G., Traykov L., Tremolizzo L., Tybjærg-Hansen A., Uitterlinden A., Ullgren A., Ulstein I., Valero S., Valladares O., Broeckhoven C.V., Vance J., Vardarajan B.N., van der Lugt A., Dongen J.V., van Rooij J., van Swieten J., Vandenberghe R., Verhey F., Vidal J.-S., Vogelgsang J., Vyhnalek M., Wagner M., Wallon D., Wang L.-S., Wang R., Weinhold L., Wiltfang J., Windle G., Woods B., Yannakoulia M., Zare H., Zhao Y., Zhang X., Zhu C., Zulaica M., Laczo J., Matoska V., Serpente M., Assogna F., Piras F., Piras F., Ciullo V., Shofany J., Ferrarese C., Andreoni S., Sala G., Zoia C.P., Zompo M.D., Benussi A., Bastiani P., Takalo M., Natunen T., Laatikainen T., Tuomilehto J., Antikainen R., Strandberg T., Lindström J., Peltonen M., Abraham R., Al-Chalabi A., Bass N.J., Brayne C., Brown K.S., Collinge J., Craig D., Deloukas P., Fox N., Gerrish A., Gill M., Gwilliam R., Harold D., Hollingworth P., Johnston J.A., Jones L., Lawlor B., Livingston G., Lovestone S., Lupton M., Lynch A., Mann D., McGuinness B., McQuillin A., O’Donovan M.C., Owen M.J., Passmore P., Powell J.F., Proitsi P., Rossor M., Shaw C.E., Smith A.D., Gurling H., Todd S., Mummery C., Ryan N., Lacidogna G., Adarmes-Gómez A., Mauleón A., Pancho A., Gailhajenet A., Lafuente A., Macias-García D., Martín E., Pelejà E., Carrillo F., Merlín I.S., Garrote-Espina L., Vargas L., Carrion-Claro M., Marín M., Labrador M., Buendia M., Alonso M.D., Guitart M., Moreno M., Ibarria M., Periñán M., Aguilera N., Gómez-Garre P., Cañabate P., Escuela R., Pineda-Sánchez R., Vigo-Ortega R., Jesús S., Preckler S., Rodrigo-Herrero S., Diego S., Vacca A., Roveta F., Salvadori N., Chipi E., Boecker H., Laske C., Perneczky R., Anastasiou C., Janowitz D., Malik R., Anastasiou A., Parveen K., Lage C., López-García S., Antonell A., Mihova K.Y., Belezhanska D., Weber H., Kochen S., Solis P., Medel N., Lisso J., Sevillano Z., Politis D.G., Cores V., Cuesta C., Ortiz C., Bacha J.I., Rios M., Saenz A., Abalos M.S., Kohler E., Palacio D.L., Etchepareborda I., Kohler M., Novack G., Prestia F.A., Galeano P., Castaño E.M., Germani S., Toso C.R., Rojo M., Ingino C., Mangone C., Rubinsztein D.C., Teipel S., Fievet N., Deramerourt V., Forsell C., Thonberg H., Bjerke M., Roeck E.D., Martínez-Larrad M.T., Olivar N., Aguilera N., Cano A., Cañabate P., Macias J., Maroñas O., Nuñez-Llaves R., Olivé C., Pelejá E., Adarmes-Gómez A.D., Alonso M.D., Amer-Ferrer G., Antequera M., Burguera J.A., Carrillo F., Carrión-Claro M., Casajeros M.J., Martinez de Pancorbo M., Escuela R., Garrote-Espina L., Gómez-Garre P., Hevilla S., Jesús S., Espinosa M.A.L., Legaz A., López-García S., Macias-García D., Manzanares S., Marín M., Marín-Muñoz J., Marín T., Martínez B., Martínez V., Martínez-Lage Álvarez P., Iriarte M.M., Periñán-Tocino M.T., Pineda-Sánchez R., Real de Asúa D., Rodrigo S., Sastre I., Vicente M.P., Vigo-Ortega R., Vivancos L., Epelbaum J., Hannequin D., campion D., Deramecourt V., Tzourio C., Brice A., Dubois B., Williams A., Thomas C., Davies C., Nash W., Dowzell K., Morales A.C., Bernardo-Harrington M., Turton J., Lord J., Brown K., Vardy E., Fisher E., Warren J.D., Rossor M., Ryan N.S., Guerreiro R., Uphill J., Bass N., Heun R., Kölsch H., Schürmann B., Lacour A., Herold C., Johnston J.A., Passmore P., Powell J., Patel Y., Hodges A., Becker T., Warden D., Wilcock G., Clarke R., Deloukas P., Ben-Shlomo Y., Hooper N.M., Pickering-Brown S., Sussams R., Warner N., Bayer A., Heuser I., Drichel D., Klopp N., Mayhaus M., Riemenschneider M., Pinchler S., Feulner T., Gu W., van den Bussche H., Hüll M., Frölich L., Wichmann H.-E., Jöckel K.-H., O’Donovan M., Owen M., Bahrami S., Bosnes I., Selnes P., Bergh S., Palotie A., Daly M., Jacob H., Matakidou A., Runz H., John S., Plenge R., McCarthy M., Hunkapiller J., Ehm M., Waterworth D., Fox C., Malarstig A., Klinger K., Call K., Behrens T., Loerch P., Mäkelä T., Kaprio J., Virolainen P., Pulkki K., Kilpi T., Perola M., Partanen J., Pitkäranta A., Kaarteenaho R., Vainio S., Turpeinen M., Serpi R., Laitinen T., Mäkelä J., Kosma V.-M., Kujala U., Tuovila O., Hendolin M., Pakkanen R., Waring J., Riley-Gillis B., Liu J., Biswas S., Diogo D., Marshall C., Hu X., Gossel M., Graham R., Cummings B., Ripatti S., Schleutker J., Arvas M., Carpén O., Hinttala R., Kettunen J., Mannermaa A., Laukkanen J., Julkunen V., Remes A., Kälviäinen R., Peltola J., Tienari P., Rinne J., Ziemann A., Waring J., Esmaeeli S., Smaoui N., Lehtonen A., Eaton S., Lahdenperä S., van Adelsberg J., Michon J., Kerchner G., Bowers N., Teng E., Eicher J., Mehta V., Gormley P., Linden K., Whelan C., Xu F., Pulford D., Färkkilä M., Pikkarainen S., Jussila A., Blomster T., Kiviniemi M., Voutilainen M., Georgantas B., Heap G., Rahimov F., Usiskin K., Lu T., Oh D., Kalpala K., Miller M., McCarthy L., Eklund K., Palomäki A., Isomäki P., Pirilä L., Kaipiainen-Seppänen O., Huhtakangas J., Lertratanakul A., Hochfeld M., Bing N., Gordillo J.E., Mars N., Pelkonen M., Kauppi P., Kankaanranta H., Harju T., Close D., Greenberg S., Chen H., Betts J., Ghosh S., Salomaa V., Niiranen T., Juonala M., Metsärinne K., Kähönen M., Junttila J., Laakso M., Pihlajamäki J., Sinisalo J., Taskinen M.-R., Tuomi T., Challis B., Peterson A., Chu A., Parkkinen J., Muslin A., Joensuu H., Meretoja T., Aaltonen L., Mattson J., Auranen A., Karihtala P., Kauppila S., Auvinen P., Elenius K., Popovic R., Schutzman J., Loboda A., Chhibber A., Lehtonen H., McDonough S., Crohns M., Kulkarni D., Kaarniranta K., Turunen J.A., Ollila T., Seitsonen S., Uusitalo H., Aaltonen V., Uusitalo-Järvinen H., Luodonpää M., Hautala N., Loomis S., Strauss E., Chen H., Podgornaia A., Hoffman J., Tasanen K., Huilaja L., Hannula-Jouppi K., Salmi T., Peltonen S., Koulu L., Harvima I., Wu Y., Choy D., Pussinen P., Salminen A., Salo T., Rice D., Nieminen P., Palotie U., Siponen M., Suominen L., Mäntylä P., Gursoy U., Anttonen V., Sipilä K., Davis J.W., Quarless D., Petrovski S., Wigmore E., Chen C.-Y., Bronson P., Tsai E., Huang Y., Maranville J., Shaikho E., Mohammed E., Wadhawan S., Kvikstad E., Caliskan M., Chang D., Bhangale T., Pendergrass S., Holzinger E., Chen X., Hedman Å., King K.S., Wang C., Xu E., Auge F., Chatelain C., Rajpal D., Liu D., Call K., Xia T.-H., Brauer M., Kurki M., Karjalainen J., Havulinna A., Jalanko A., Palta P., della Briotta Parolo P., Zhou W., Lemmelä S., Rivas M., Harju J., Lehisto A., Ganna A., Llorens V., Laivuori H., Rüeger S., Niemi M.E., Tukiainen T., Reeve M.P., Heyne H., Palin K., Garcia-Tabuenca J., Siirtola H., Kiiskinen T., Lee J., Tsuo K., Elliott A., Kristiansson K., Hyvärinen K., Ritari J., Koskinen M., Pylkäs K., Kalaoja M., Karjalainen M., Mantere T., Kangasniemi E., Heikkinen S., Laakkonen E., Sipeky C., Heron S., Karlsson A., Jambulingam D., Rathinakannan V.S., Kajanne R., Aavikko M., Jiménez M.G., della Briotta Parola P., Lehistö A., Kanai M., Kaunisto M., Kilpeläinen E., Sipilä T.P., Brein G., Awaisa G., Shcherban A., Donner K., Loukola A., Laiho P., Sistonen T., Kaiharju E., Laukkanen M., Järvensivu E., Lähteenmäki S., Männikkö L., Wong R., Mattsson H., Hiekkalinna T., Paajanen T., Pärn K., Gracia-Tabuenca J., Abner E., Adams P.M., Aguirre A., Albert M.S., Albin R.L., Allen M., Alvarez L., Apostolova L.G., Arnold S.E., Asthana S., Atwood C.S., Ayres G., Baldwin C.T., Barber R.C., Barnes L.L., Barral S., Beach T.G., Becker J.T., Beecham G.W., Beekly D., Below J.E., Benchek P., Benitez B.A., Bennett D., Bertelson J., Margaret F.E., Bird T.D., Blacker D., Boeve B.F., Bowen J.D., Boxer A., Brewer J., Burke J.R., Burns J.M., Bush W.S., Buxbaum J.D., Cairns N.J., Cao C., Carlson C.S., Carlsson C.M., Carney R.M., Carrasquillo M.M., Chasse S., Chesselet M.-F., Chesi A., Chin N.A., Chui H.C., Chung J., Craft S., Crane P.K., Cribbs D.H., Crocco E.A., Cruchaga C., Cullum M., Darby E., Davis B., De Jager P.L., DeCarli C., DeToledo J., Dick M., Dickson D.W., Dombroski B.A., Doody R.S., Duara R., Ertekin-Taner N., Evans D.A., Fairchild T.J., Fallon K.B., Farlow M.R., Farrell J.J., Fernandez-Hernandez V., Ferris S., Frosch M.P., Fulton-Howard B., Galasko D.R., Gamboa A., Gearing M., Geschwind D.H., Ghetti B., Gilbert J.R., Grabowski T.J., Graff-Radford N.R., Grant S.F.A., Green R.C., Growdon J.H., Haines J.L., Hakonarson H., Hall J., Hamilton R.L., Harari O., Harrell L.E., Haut J., Head E., Henderson V.W., Hernandez M., Hohman T., Honig L.S., Huebinger R.M., Huentelman M.J., Hulette C.M., Hyman B.T., Hynan L.S., Ibanez L., Jarvik G.P., Jayadev S., Jin L.-W., Johnson K., Johnson L., Kamboh M.I., Karydas A.M., Katz M.J., Kaye J.A., Keene C.D., Khaleeq A., Kim R., Knebl J., Kowall N.W., Kramer J.H., Kuksa P.P., LaFerla F.M., Lah J.J., Larson E.B., Lee C.-Y., Lee E.B., Lerner A., Leung Y.Y., Leverenz J.B., Levey A.I., Li M., Lieberman A.P., Lipton R.B., Logue M., Lyketsos C.G., Malamon J., Mains D., Marson D.C., Martiniuk F., Mash D.C., Masliah E., Massman P., Masurkar A., McCormick W.C., McCurry S.M., McDavid A.N., McDonough S., McKee A.C., Mesulam M., Mez J., Miller B.L., Miller C.A., Miller J.W., Montine T.J., Monuki E.S., Morris J.C., Myers A.J., Nguyen T., O’Bryant S., Olichney J.M., Ory M., Palmer R., Parisi J.E., Paulson H.L., Pavlik V., Paydarfar D., Perez V., Peskind E., Petersen R.C., Phillips-Cremins J.E., Pierce A., Polk M., Poon W.W., Potter H., Qu L., Quiceno M., Quinn J.F., Raj A., Raskind M., Reiman E.M., Reisberg B., Reisch J.S., Ringman J.M., Roberson E.D., Rodriguear M., Rogaeva E., Rosen H.J., Rosenberg R.N., Royall D.R., Sager M.A., Sano M., Saykin A.J., Schneider J.A., Schneider L.S., Seeley W.W., Slifer S.H., Small S., Smith A.G., Smith J.P., Song Y.E., Sonnen J.A., Spina S., George-Hyslop P.S., Stern R.A., Stevens A.B., Strittmatter S.M., Sultzer D., Swerdlow R.H., Tanzi R.E., Tilson J.L., Trojanowski J.Q., Troncoso J.C., Tsuang D.W., Valladares O., Van Deerlin V.M., van Eldik L.J., Vassar R., Vinters H.V., Vonsattel J.-P., Weintraub S., Welsh-Bohmer K.A., Whitehead P.L., Wijsman E.M., Wilhelmsen K.C., Williams B., Williamson J., Wilms H., Wingo T.S., Wisniewski T., Woltjer R.L., Woon M., Wright C.B., Wu C.-K., Younkin S.G., Yu C.-E., Yu L., Zhang Y., Zhao Y., Zhu X., Adams H., Akinyemi R.O., Ali M., Aparicio H.J., Bahadori M., Becker J.T., Breteler M., Chasman D., Chauhan G., Comic H., Cox S., Cupples A.L., Davies G., DeCarli C.S., Duperron M.-G., Dupuis J., Evans T., Fan F., Fitzpatrick A., Fohner A.E., Ganguli M., Geerlings M., Glatt S.J., Gonzalez H.M., Goss M., Grabe H., Habes M., Heckbert S.R., Hofer E., Hong E., Hughes T., Kautz T.F., Knol M., Kremen W., Lacaze P., Lahti J., Grand Q.L., Litkowski E., Li S., Liu D., Liu X., Loitfelder M., Manning A., Maillard P., Marioni R., Mazoyer B., van Lent D.M., Mei H., Mishra A., Nyquist P., O’Connell J., Patel Y., Paus T., Pausova Z., Raikkonen-Talvitie K., Riaz M., Rich S., Rotter J., Romero J., Roshchupkin G., Saba Y., Sargurupremraj M., Schmidt H., Schmidt R., Shulman J.M., Smith J., Sekhar H., Rajula R., Shin J., Simino J., Sliz E., Teumer A., Thomas A., Tin A., Tucker-Drob E., Vojinovic D., Wang Y., Weinstein G., Williams D., Wittfeld K., Yanek L., Yang Y., Farrer L.A., Psaty B.M., Ghanbari M., Raj T., Sachdev P., Mather K., Jessen F., Ikram M.A., de Mendonça A., Hort J., Tsolaki M., Pericak-Vance M.A., Amouyel P., Williams J., Frikke-Schmidt R., Clarimon J., Deleuze J.-F., Rossi G., Seshadri S., Andreassen O.A., Ingelsson M., Hiltunen M., Sleegers K., Schellenberg G.D., van Duijn C.M., Sims R., van der Flier W.M., Ruiz A., Ramirez A., Lambert J.-C., EADB, GR@ACE, DEGESCO, EADI, GERAD, Demgene, FinnGen, ADGC, CHARGE (2022)
      Characterization of the genetic landscape of Alzheimer’s disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We performed a ...
    • Non-genetic risk and protective factors and biomarkers for neurological disorders: a meta-umbrella systematic review of umbrella reviews 

      Mentis A.-F.A., Dardiotis E., Efthymiou V., Chrousos G.P. (2021)
      Background: The etiologies of chronic neurological diseases, which heavily contribute to global disease burden, remain far from elucidated. Despite available umbrella reviews on single contributing factors or diseases, no ...