Manuel Mattheisen

  1. Published

    Explorative two-locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures-related photosensitivity loci. / Pinto, Dalila; Kasteleijn-Nolst Trenité, Dorothée G A; Cordell, Heather J; Mattheisen, Manuel; Strauch, Konstantin; Lindhout, Dick; Koeleman, Bobby P C.

    In: Genetic Epidemiology, Vol. 31, No. 1, 01.2007, p. 42-50.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  2. Published

    Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder. / Yilmaz, Zeynep; Halvorsen, Matthew; Bryois, Julien; Yu, Dongmei; Thornton, Laura M.; Zerwas, Stephanie; Micali, Nadia; Moessner, Rainald; Burton, Christie L.; Zai, Gwyneth; Erdman, Lauren; Kas, Martien J.; Arnold, Paul D.; Davis, Lea K.; Knowles, James A.; Breen, Gerome; Scharf, Jeremiah M.; Nestadt, Gerald; Mathews, Carol A.; Bulik, Cynthia M.; Mattheisen, Manuel; Crowley, James J.; Eating Disorders Working Group of the Psychiatric Genomics Consortium, Tourette Syndrome/Obsessive–Compulsive Disorder Working Group of the Psychiatric Genomics Consortium.

    In: Molecular Psychiatry, Vol. 25, No. 9, 09.2020, p. 2036-2046.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  3. Published

    Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. / Reutter, Heiko; Rüschendorf, Franz; Mattheisen, Manuel; Draaken, Markus; Bartels, Enrika; Hübner, Norbert; Hoffmann, Per; Payabvash, Seyedmedhi; Saar, Kathrin; Nöthen, Markus M; Kajbafzadeh, Abdol-Mohammad; Ludwig, Michael.

    In: Birth Defects Research. Part A: Clinical and Molecular Teratology, Vol. 88, No. 9, 09.2010, p. 757-61.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  4. Published

    Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. / Foo, Jerome C.; Streit, Fabian; Frank, Josef; Treutlein, Jens; Baune, Bernhard T.; Moebus, Susanne; Joeckel, Karl-Heinz; Forstner, Andreas J.; Noethen, Markus M.; Rietschel, Marcella; Sartorius, Alexander; Kranaster, Laura; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (Jakob Grove, member of -).

    In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, Vol. 180, No. 1, 01.2019, p. 35-45.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  5. Published

    Erratum : Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci (Human Molecular Genetics (2017) 26:10 (1942-1951) DOI: 10.1093/hmg/ddx103). / Fullard, John F.; Giambartolomei, Claudia; Hauberg, Mads E.; Xu, Ke; Voloudakis, Georgios; Shao, Zhiping; Bare, Christopher; Dudley, Joel T.; Mattheisen, Manuel; Robakis, Nikolaos K.; Haroutunian, Vahram; Roussos, Panos.

    In: Human Molecular Genetics, Vol. 29, No. 16, 08.2020, p. 2812.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperComment/debate/letter to the editorResearchpeer-review

  6. Published

    Epidemiology, genetics, and subtyping of preserved ratio impaired spirometry (PRISm) in COPDGene. / Wan, Emily S; Castaldi, Peter J; Cho, Michael H; Hokanson, John E; Regan, Elizabeth A; Make, Barry J; Beaty, Terri H; Han, MeiLan K; Curtis, Jeffrey L; Curran-Everett, Douglas; Lynch, David A; DeMeo, Dawn L; Crapo, James D; Silverman, Edwin K; COPDGene Investigators ; Mattheisen, Manuel.

    In: Respiratory Research Review, Vol. 15, 2014, p. 89.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  7. Published

    Enrichment Analysis of Genomic features to Identify Genome-Wide Patterns of Insertions/Deletions in Cases of Psychiatric Disorders from the Faroe Islands. / Eickhardt, Esben Ahlburg; Als, Thomas Damm; Mattheisen, Manuel; Nyegaard, Mette; Demontis, Ditte; Grove, Jakob; Andorsdottir, Gudrid; Biskopstø, Marjun; Wang, August; Mors, Ole; Bolund, Lars; Wang, Jun; Børglum, Anders; Lescai, Francesco.

    2014. Poster session presented at XXII World Congress of Psychiatric Genetics, København, Danmark, Denmark.

    Research output: Contribution to conferencePosterResearchpeer-review

  8. Published

    Efficient Strategy for Detecting Gene × Gene Joint Action and Its Application in Schizophrenia. / Won, Sungho; Kwon, Min-Seok; Mattheisen, Manuel; Park, Suyeon; Park, Changsoon; Kihara, Daisuke; Cichon, Sven; Ophoff, Roel; Nöthen, Markus M; Rietschel, Marcella; Baur, Max; Uitterlinden, Andre G; Hofmann, A; Lange, Christoph; GROUP Investigators.

    In: Genetic Epidemiology, 23.11.2013.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  9. Published

    Effects of BDNF Val 66 Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans. / Schweiger, J. I.; Bilek, E.; Schäfer, A.; Braun, U.; Moessnang, C.; Harneit, A.; Post, P.; Otto, K.; Romanczuk-Seiferth, N.; Erk, S.; Wackerhagen, C.; Mattheisen, M.; Mühleisen, T. W.; Cichon, S.; Nöthen, M. M.; Frank, J.; Witt, S. H.; Rietschel, M.; Heinz, A.; Walter, H.; Meyer-Lindenberg, A.; Tost, H.

    In: Neuropsychopharmacology, Vol. 44, No. 3, 02.2019, p. 590-597.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  10. Published

    Dysregulation of miRNA-9 in a Subset of Schizophrenia Patient-Derived Neural Progenitor Cells. / Topol, Aaron; Zhu, Shijia; Hartley, Brigham J; English, Jane; Hauberg, Mads E; Tran, Ngoc; Rittenhouse, Chelsea Ann; Simone, Anthony; Ruderfer, Douglas M; Johnson, Jessica; Readhead, Ben; Hadas, Yoav; Gochman, Peter A; Wang, Ying-Chih; Shah, Hardik; Cagney, Gerard; Rapoport, Judith; Gage, Fred H; Dudley, Joel T; Sklar, Pamela; Mattheisen, Manuel; Cotter, David; Fang, Gang; Brennand, Kristen J.

    In: Cell Reports, Vol. 15, No. 5, 03.05.2016, p. 1024-36.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  11. Published

    Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter. / Treutlein, Jens; Mühleisen, Thomas W; Frank, Josef; Mattheisen, Manuel; Herms, Stefan; Ludwig, Kerstin U; Treutlein, Tsendsesmee; Schmael, Christine; Strohmaier, Jana; Bösshenz, Katja Veronika; Breuer, René; Paul, Torsten; Witt, Stephanie H; Schulze, Thomas G; Schlösser, Ralf G M; Nenadic, Igor; Sauer, Heinrich; Becker, Tim; Maier, Wolfgang; Cichon, Sven; Nöthen, Markus M; Rietschel, Marcella.

    In: Schizophrenia research, Vol. 111, No. 1-3, 06.2009, p. 123-30.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  12. Published

    Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. / Demontis, Ditte; Walters, Raymond K.; Martin, Joanna; Mattheisen, Manuel; Als, Thomas D.; Agerbo, Esben; Baldursson, Gísli; Belliveau, Rich; Bybjerg-Grauholm, Jonas; Bækvad-Hansen, Marie; Cerrato, Felecia; Chambert, Kimberly; Churchhouse, Claire; Dumont, Ashley; Eriksson, Nicholas; Gandal, Michael; Goldstein, Jacqueline I.; Grasby, Katrina L.; Grove, Jakob; Gudmundsson, Olafur O.; Hansen, Christine S.; Hauberg, Mads Engel; Hollegaard, Mads V.; Howrigan, Daniel P.; Huang, Hailiang; Maller, Julian B.; Martin, Alicia R.; Martin, Nicholas G.; Moran, Jennifer; Pallesen, Jonatan; Palmer, Duncan S.; Pedersen, Carsten Bøcker; Pedersen, Marianne Giørtz; Poterba, Timothy; Poulsen, Jesper Buchhave; Ripke, Stephan; Robinson, Elise B.; Satterstrom, F. Kyle; Stefansson, Hreinn; Stevens, Christine; Turley, Patrick; Walters, G. Bragi; Won, Hyejung; Wright, Margaret J.; ADHD Working Group of the Psychiatric Genomics Consortium (PGC); Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium; 23andMe Research Team ; Dalsgaard, Søren; Mors, Ole; Mortensen, Preben Bo; Børglum, Anders D.

    In: Nature Genetics, Vol. 51, 2019, p. 63–75.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  13. Published

    Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls. / Hauberg, Mads E.; Fullard, John F.; Zhu, Lingxue; Cohain, Ariella T.; Giambartolomei, Claudia; Misir, Ruth; Reach, Sarah; Johnson, Jessica S.; Wang, Minghui; Mattheisen, Manuel; Børglum, Anders Dupont; Zhang, Bin; Sieberts, Solveig K.; Peters, Mette A.; Domenici, Enrico; Schadt, Eric E.; Devlin, Bernie; Sklar, Pamela; Roeder, Kathryn; Roussos, Panos; the CommonMind Consortium.

    In: Molecular Psychiatry, Vol. 24, No. 11, 11.2019, p. 1685-1695.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  14. Published

    Diagnosed Anxiety Disorders and the Risk of Subsequent Anorexia Nervosa : A Danish Population Register Study. / Meier, Sandra M; Bulik, Cynthia M; Thornton, Laura M; Mattheisen, Manuel; Mortensen, Preben B; Petersen, Liselotte.

    In: European Eating Disorders Review, Vol. 23, No. 6, 08.09.2015, p. 524-530.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  15. Published

    Detecting significant genotype–phenotype association rules in bipolar disorder : market research meets complex genetics. / Breuer, René; Mattheisen, Manuel; Frank, Josef; Krumm, Bertram; Treutlein, Jens; Kassem, Layla; Strohmaier, Jana; Herms, Stefan; Mühleisen, Thomas W.; Degenhardt, Franziska; Cichon, Sven; Nöthen, Markus M.; Karypis, George; Kelsoe, John; Greenwood, Tiffany; Nievergelt, Caroline; Shilling, Paul; Shekhtman, Tatyana; Edenberg, Howard; Craig, David; Szelinger, Szabolcs; Nurnberger, John; Gershon, Elliot; Alliey-Rodriguez, Ney; Zandi, Peter; Goes, Fernando; Schork, Nicholas; Smith, Erin; Koller, Daniel; Zhang, Peng; Badner, Judith; Berrettini, Wade; Bloss, Cinnamon; Byerley, William; Coryell, William; Foroud, Tatiana; Guo, Yirin; Hipolito, Maria; Keating, Brendan; Lawson, William; Liu, Chunyu; Mahon, Pamela; McInnis, Melvin; Murray, Sarah; Nwulia, Evaristus; Potash, James; Rice, John; Scheftner, William; Zöllner, Sebastian; McMahon, Francis J.; Rietschel, Marcella; Schulze, Thomas G.

    In: International Journal of Bipolar Disorders, Vol. 6, No. 1, 24, 01.12.2018.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  16. Published

    DNAH5 is associated with total lung capacity in chronic obstructive pulmonary disease. / Lee, Jin Hwa; McDonald, Merry-Lynn N; Cho, Michael H; Wan, Emily S; Castaldi, Peter J; Hunninghake, Gary M; Marchetti, Nathaniel; Lynch, David A; Crapo, James D; Lomas, David A; Coxson, Harvey O; Bakke, Per S; Silverman, Edwin K; Hersh, Craig P; COPDGene and ECLIPSE Investigators ; Mattheisen, Manuel.

    In: Respiratory Research Review, Vol. 15, 2014, p. 97.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  17. Published

    DNA Methylation at the Neonatal State and at the Time of Diagnosis: Preliminary Support for an Association with the Estrogen Receptor 1, Gamma-Aminobutyric Acid B Receptor 1, and Myelin Oligodendrocyte Glycoprotein in Female Adolescent Patients with OCD. / Nissen, Judith Becker; Søholm Hansen, Christine; Starnawska, Anna; Mattheisen, Manuel; Børglum, Anders; Buttenschøn, Henriette Nørmølle; Hollegård, Mads.

    In: Frontiers in Psychiatry, Vol. 7, No. 35, 2016.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  18. Published

    DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. / Håvik, Bjarte; Degenhardt, Franziska A; Johansson, Stefan; Fernandes, Carla P D; Hinney, Anke; Scherag, André; Lybæk, Helle; Djurovic, Srdjan; Christoforou, Andrea; Ersland, Kari M; Giddaluru, Sudheer; O'Donovan, Michael C; Owen, Michael J; Craddock, Nick; Mühleisen, Thomas W; Mattheisen, Manuel; Schimmelmann, Benno G; Renner, Tobias; Warnke, Andreas; Herpertz-Dahlmann, Beate; Sinzig, Judith; Albayrak, Özgür; Rietschel, Marcella; Nöthen, Markus M; Bramham, Clive R; Werge, Thomas; Hebebrand, Johannes; Haavik, Jan; Andreassen, Ole A; Cichon, Sven; Steen, Vidar M; Le Hellard, Stéphanie.

    In: P L o S One, Vol. 7, No. 4, 2012, p. e35424.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  19. Published

    Copy number variants in german patients with schizophrenia. / Priebe, Lutz; Degenhardt, Franziska; Strohmaier, Jana; Breuer, René; Herms, Stefan; Witt, Stephanie H; Hoffmann, Per; Kulbida, Rebecca; Mattheisen, Manuel; Moebus, Susanne; Meyer-Lindenberg, Andreas; Walter, Henrik; Mössner, Rainald; Nenadic, Igor; Sauer, Heinrich; Rujescu, Dan; Maier, Wolfgang; Rietschel, Marcella; Nöthen, Markus M; Cichon, Sven.

    In: P L o S One, Vol. 8, No. 7, 2013, p. e64035.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  20. Published

    Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene. / Luo, X-J; Li, Menxing; Huang, Liping; Steinberg, S; Mattheisen, Manuel; Liang, G; Donohoe, G; Shi, Y; Chen, Andrew C. N.; Yue, Wei; Alkelai, A; Lerer, B; Li, Z; Yi, Q; Rietschel, M; Cichon, S; Collier, D A; Tosato, S; Suvisaari, J; Rujescu, Dan; Golimbet, V; Silagadze, T; Durmishi, N; Milovancevic, M P; Stefansson, H; Schulze, T G; Nöthen, M M; Chen, Andrew C. N.; Lyne, R; Morris, D W; Gill, M; Corvin, A; Zhang, D; Dong, Q; Moyzis, R K; Stefansson, K; Sigurdsson, Eythor; Hu, F; Su, B; Gan, L; MooDS SCZ Consortium.

    In: Molecular Psychiatry, 20.08.2013.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  21. Published

    Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia. / Gockel, Ines; Becker, Jessica; Wouters, Mira M; Niebisch, Stefan; Gockel, Henning R; Hess, Timo; Ramonet, David; Zimmermann, Julian; Vigo, Ana González; Trynka, Gosia; de León, Antonio Ruiz; de la Serna, Julio Pérez; Urcelay, Elena; Kumar, Vinod; Franke, Lude; Westra, Harm-Jan; Drescher, Daniel; Kneist, Werner; Marquardt, Jens U; Galle, Peter R; Mattheisen, Manuel; Annese, Vito; Latiano, Anna; Fumagalli, Uberto; Laghi, Luigi; Cuomo, Rosario; Sarnelli, Giovanni; Müller, Michaela; Eckardt, Alexander J; Tack, Jan; Hoffmann, Per; Herms, Stefan; Mangold, Elisabeth; Heilmann, Stefanie; Kiesslich, Ralf; von Rahden, Burkhard H A; Allescher, Hans-Dieter; Schulz, Henning G; Wijmenga, Cisca; Heneka, Michael T; Lang, Hauke; Hopfner, Karl-Peter; Nöthen, Markus M; Boeckxstaens, Guy E; de Bakker, Paul I W; Knapp, Michael; Schumacher, Johannes.

    In: Nature Genetics, 06.07.2014.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  22. Published

    Common variants conferring risk of schizophrenia. / Stefansson, Hreinn; Ophoff, Roel A.; Steinberg, Stacy; Andreassen, Ole A.; Cichon, Sven; Rujescu, Dan; Werge, Thomas; Pietiläinen, Olli P. H.; Mors, Ole; Mortensen, Preben B.; Sigurdsson, Engilbert; Gustafsson, Omar; Nyegaard, Mette; Tuulio-Henriksson, Annamari; Ingason, Andres; Hansen, Thomas; Suvisaari, Jaana; Lonnqvist, Jouko; Paunio, Tiina; Børglum, Anders D.; Hartmann, Annette; Fink-Jensen, Anders; Nordentoft, Merete; Hougaard, David; Norgaard-Pedersen, Bent; Böttcher, Yvonne; Olesen, Jes; Breuer, René; Möller, Hans-Jürgen; Giegling, Ina; Rasmussen, Henrik B.; Timm, Sally; Mattheisen, Manuel; Bitter, István; Réthelyi, János M.; Magnusdottir, Brynja B.; Sigmundsson, Thordur; Olason, Pall; Masson, Gisli; Gulcher, Jeffrey R.; Haraldsson, Magnus; Fossdal, Ragnheidur; Thorgeirsson, Thorgeir E.; Thorsteinsdottir, Unnur; Ruggeri, Mirella; Tosato, Sarah; Franke, Barbara; Strengman, Eric; Kiemeney, Lambertus A.; Kahn, René S.; Linszen, Don H.; van Os, Jim; Wiersma, Durk; Bruggeman, Richard; Cahn, Wiepke; de Haan, Lieuwe; Krabbendam, Lydia; Myin-Germeys, Inez; Melle, Ingrid; Djurovic, Srdjan; Abramova, Lilia; Kaleda, Vasily; Sanjuan, Julio; de Frutos, Rosa; Bramon, Elvira; Vassos, Evangelos; Fraser, Gillian; Ettinger, Ulrich; Picchioni, Marco; Walker, Nicholas; Toulopoulou, Timi; Need, Anna C.; Ge, Dongliang; Lim Yoon, Joeng; Shianna, Kevin V.; Freimer, Nelson B.; Cantor, Rita M.; Murray, Robin; Kong, Augustine; Golimbet, Vera; Carracedo, Angel; Arango, Celso; Costas, Javier; Jönsson, Erik G.; Terenius, Lars; Agartz, Ingrid; Petursson, Hannes; Nöthen, Markus M.; Rietschel, Marcella; Matthews, Paul M.; Muglia, Pierandrea; Peltonen, Leena; St Clair, David; Goldstein, David B.; Stefansson, Kari; Collier, David A.

    In: Nature, Volume 460, Issue 7256, pp. 744-747 (2009)., Vol. 460, 01.08.2009, p. 744-747.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  23. Published

    Common variants at 12q14 and 12q24 are associated with hippocampal volume. / Bis, Joshua C; DeCarli, Charles; Smith, Albert Vernon; van der Lijn, Fedde; Crivello, Fabrice; Fornage, Myriam; Debette, Stephanie; Shulman, Joshua M; Schmidt, Helena; Srikanth, Velandai; Schuur, Maaike; Yu, Lei; Choi, Seung-Hoan; Sigurdsson, Sigurdur; Verhaaren, Benjamin F J; DeStefano, Anita L; Lambert, Jean-Charles; Jack, Clifford R; Struchalin, Maksim; Stankovich, Jim; Ibrahim-Verbaas, Carla A; Fleischman, Debra; Zijdenbos, Alex; den Heijer, Tom; Mazoyer, Bernard; Coker, Laura H; Enzinger, Christian; Danoy, Patrick; Amin, Najaf; Arfanakis, Konstantinos; van Buchem, Mark A; de Bruijn, Renée F A G; Beiser, Alexa; Dufouil, Carole; Huang, Juebin; Cavalieri, Margherita; Thomson, Russell; Niessen, Wiro; Chibnik, Lori B; Gislason, Gauti K; Hofman, Albert; Pikula, Aleksandra; Amouyel, Philippe; Freeman, Kevin B; Phan, Thanh G; Oostra, Ben A; Stein, Jason L; Medland, Sarah E; Vasquez, Alejandro Arias; Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium ; Mattheisen, Manuel.

    In: Nature Genetics, Vol. 44, No. 5, 05.2012, p. 545-51.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  24. Published

    Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. / GERAD1 Consortium:.

    In: Nature Genetics, Vol. 50, No. 3, 03.2018, p. 381-389.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  25. Published

    Common genetic variants influence human subcortical brain structures. / Hibar, Derrek P; Stein, Jason L; Renteria, Miguel E; Arias-Vasquez, Alejandro; Desrivières, Sylvane; Jahanshad, Neda; Toro, Roberto; Wittfeld, Katharina; Abramovic, Lucija; Andersson, Micael; Aribisala, Benjamin S; Armstrong, Nicola J; Bernard, Manon; Bohlken, Marc M; Boks, Marco P; Bralten, Janita; Brown, Andrew A; Mallar Chakravarty, M; Chen, Qiang; Ching, Christopher R K; Cuellar-Partida, Gabriel; den Braber, Anouk; Giddaluru, Sudheer; Goldman, Aaron L; Grimm, Oliver; Guadalupe, Tulio; Hass, Johanna; Woldehawariat, Girma; Holmes, Avram J; Hoogman, Martine; Janowitz, Deborah; Jia, Tianye; Kim, Sungeun; Klein, Marieke; Kraemer, Bernd; Lee, Phil H; Olde Loohuis, Loes M; Luciano, Michelle; Macare, Christine; Mather, Karen A; Mattheisen, Manuel; Milaneschi, Yuri; Nho, Kwangsik; Papmeyer, Martina; Ramasamy, Adaikalavan; Risacher, Shannon L; Roiz-Santiañez, Roberto; Rose, Emma J; Salami, Alireza; Sämann, Philipp G; The Alzheimer’s Disease Neuroimaging Initiative.

    In: Nature, 21.01.2015.

    Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

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