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Number of items: 9.


van Dam, Sipko, Vosa, Urmo, van der Graaf, Adriaan, Franke, Lude and de Magalhaes, Joao Pedro ORCID: 0000-0002-6363-2465
(2018) Gene co-expression analysis for functional classification and gene-disease predictions. BRIEFINGS IN BIOINFORMATICS, 19 (4). pp. 575-592.


Huckins, Laura M, Dobbyn, Amanda, Ruderfer, Douglas M, Hoffman, Gabriel, Wang, Weiqing, Pardinas, Antonio F, Rajagopal, Veera M, Als, Thomas D, Nguyen, Hoang T, Girdhar, Kiran
et al (show 346 more authors) (2019) Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. NATURE GENETICS, 51 (4). 659-+.


Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tonu, van Mill, Josine G, Mbarek, Hamdi
et al (show 64 more authors) (2016) Genetic variants in <i>RBFOX3</i> are associated with sleep latency. EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (10). pp. 1488-1495.


Ligthart, Symen, Vaez, Ahmad, Vosa, Urmo, Stathopoulou, Maria G, de Vries, Paul S, Prins, Bram P, Van der Most, Peter J, Tanaka, Toshiko, Naderi, Elnaz, Rose, Lynda M
et al (show 276 more authors) (2018) Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. AMERICAN JOURNAL OF HUMAN GENETICS, 103 (5). pp. 691-706.


Coffee and Caffeine Genetics Consortium, , Cornelis, Marilyn C, Byrne, Enda M ORCID: 0000-0002-9491-7797, Esko, Tõnu ORCID: 0000-0003-1982-6569, Nalls, Michael A, Ganna, Andrea ORCID: 0000-0002-8147-240X, Paynter, Nina, Monda, Keri L, Amin, Najaf ORCID: 0000-0002-8944-1771, Fischer, Krista
et al (show 148 more authors) (2015) Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Molecular psychiatry, 20 (5). pp. 647-656.


Ruderfer, Douglas M, Ripke, Stephan, McQuillin, Andrew, Boocock, James, Stahl, Eli A, Pavlides, Jennifer M Whitehead, Mullins, Niamh, Charney, Alexander W, Ori, Anil PS, Loohuis, Loes M Olde
et al (show 534 more authors) (2018) Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes. CELL, 173 (7). pp. 1705-1715.


Wild, Philipp S, Felix, Janine F, Schillert, Arne, Teumer, Alexander, Chen, Ming-Huei, Leening, Maarten JG, Voelker, Uwe, Grossmann, Vera, Brody, Jennifer A, Irvin, Marguerite R
et al (show 113 more authors) (2017) Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. JOURNAL OF CLINICAL INVESTIGATION, 127 (5). pp. 1798-1812.


Niemi, Mari EK, Karjalainen, Juha, Daly, Mark, Ganna, Andrea, Mehtonen, Juha, Cordioli, Mattia, Kaunisto, Mari, Pigazzini, Sara, Donner, Kati, Kivinen, Katja
et al (show 3481 more authors) (2021) Mapping the human genetic architecture of COVID-19. NATURE, 600 (7889). 472-+.


Harold, Denise, Connolly, Siobhan, Riley, Brien P, Kendler, Kenneth S, McCarthy, Shane E, McCombie, William R, Richards, Alex, Owen, Michael J, O'Donovan, Michael C, Walters, James
et al (show 350 more authors) (2019) Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 180 (3). pp. 223-231.

This list was generated on Sat Mar 23 19:59:28 2024 GMT.