Quick, “Imputation-free” meta-analysis with proxy-SNPs

by Meesters, Christian, Leber, Markus, Herold, Christine, Angisch, Marina, Mattheisen, Manuel, Drichel, Dmitriy, Lacour, André, Becker, Tim
Published 2012

A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31

by Habib, Rabia, Ansar, Muhammad, Mattheisen, Manuel, Shahid, Muhammad, Ali, Ghazanfar, Ahmad, Wasim, Betz, Regina C.
Published 2015

Obsessive-Compulsive Disorder and Autism Spectrum Disorders: Longitudinal and Offspring Risk

by Meier, Sandra M, Petersen, Liselotte, Schendel, Diana E, Mattheisen, Manuel, Mortensen, Preben B, Mors, Ole
Published 2015

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 M...

by Nissen, Judith Becker, Hansen, Christine Søholm, Starnawska, Anna, Mattheisen, Manuel, Børglum, Anders Dupont, Buttenschøn, Henriette Nørmølle, Hollegaard, Mads
Published 2016

Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults

by Schreiner, Felix, El-Maarri, Osman, Gohlke, Bettina, Stutte, Sonja, Nuesgen, Nicole, Mattheisen, Manuel, Fimmers, Rolf, Bartmann, Peter, Oldenburg, Johannes, Woelfle, Joachim
Published 2011

Family-based Association Analyses of Imputed Genotypes Reveal Genome-Wide Significant Association of Alzheimer’s disease with OSBPL6, PTPRG and PDCL3

by Herold, Christine, Hooli, Basavaraj V., Mullin, Kristina, Liu, Tian, Roehr, Johannes T, Mattheisen, Manuel, Parrado, Antonio R., Bertram, Lars, Lange, Christoph, Tanzi, Rudolph E.
Published 2016

Hypomethylation and increased expression of the putative oncogene ELMO3 are associated with lung cancer development and metastases formation

by Søes, Signe, Daugaard, Iben Lyster, Sørensen, Brita Singers, Carus, Andreas, Mattheisen, Manuel, Alsner, Jan, Overgaard, Jens, Hager, Henrik, Hansen, Lise Lotte, Kristensen, Lasse Sommer
Published 2014

Segment-Wise Genome-Wide Association Analysis Identifies a Candidate Region Associated with Schizophrenia in Three Independent Samples

by Gladwin, Thomas E., Derks, Eske M., Rietschel, Marcella, Mattheisen, Manuel, Breuer, René, Schulze, Thomas G., Nöthen, Markus M., Levinson, Douglas, Shi, Jianxin, Gejman, Pablo V., Cichon, Sven, Ophoff, Roel A.
Published 2012

Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease

by Yildiz, Yildiz, Hoffmann, Per, vom Dahl, Stefan, Breiden, Bernadette, Sandhoff, Roger, Niederau, Claus, Horwitz, Mia, Karlsson, Stefan, Filocamo, Mirella, Elstein, Deborah, Beck, Michael, Sandhoff, Konrad, Mengel, Eugen, Gonzalez, Maria C, Nöthen, Markus M, Sidransky, Ellen, Zimran, Ari, Mattheisen, Manuel
Published 2013

Gene-Based Analysis of Regionally Enriched Cortical Genes in GWAS Data Sets of Cognitive Traits and Psychiatric Disorders

by Ersland, Kari M., Christoforou, Andrea, Stansberg, Christine, Espeseth, Thomas, Mattheisen, Manuel, Mattingsdal, Morten, Hardarson, Gudmundur A., Hansen, Thomas, Fernandes, Carla P. D., Giddaluru, Sudheer, Breuer, René, Strohmaier, Jana, Djurovic, Srdjan, Nöthen, Markus M., Rietschel, Marcella, Lundervold, Astri J., Werge, Thomas, Cichon, Sven, Andreassen, Ole A., Reinvang, Ivar, Steen, Vidar M., Le Hellard, Stephanie
Published 2012

Copy Number Variants in German Patients with Schizophrenia

by 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
Published 2013

A Genetic Deconstruction of Neurocognitive Traits in Schizophrenia and Bipolar Disorder

by Fernandes, Carla P. D., Christoforou, Andrea, Giddaluru, Sudheer, Ersland, Kari M., Djurovic, Srdjan, Mattheisen, Manuel, Lundervold, Astri J., Reinvang, Ivar, Nöthen, Markus M., Rietschel, Marcella, Ophoff, Roel A., Hofman, Albert, Uitterlinden, André G., Werge, Thomas, Cichon, Sven, Espeseth, Thomas, Andreassen, Ole A., Steen, Vidar M., Le Hellard, Stephanie
Published 2013

Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia

by Juraeva, Dilafruz, Haenisch, Britta, Zapatka, Marc, Frank, Josef, Witt, Stephanie H., Mühleisen, Thomas W., Treutlein, Jens, Strohmaier, Jana, Meier, Sandra, Degenhardt, Franziska, Giegling, Ina, Ripke, Stephan, Leber, Markus, Lange, Christoph, Schulze, Thomas G., Mössner, Rainald, Nenadic, Igor, Sauer, Heinrich, Rujescu, Dan, Maier, Wolfgang, Børglum, Anders, Ophoff, Roel, Cichon, Sven, Nöthen, Markus M., Rietschel, Marcella, Mattheisen, Manuel, Brors, Benedikt
Published 2014

Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS data

by Dunkhase, Eva, Ludwig, Kerstin U., Knapp, Michael, Skibola, Christine F., Figueiredo, Jane C., Hosking, Fay Julie, Ellinghaus, Eva, Landi, Maria Teresa, Ma, Hongxia, Nakagawa, Hidewaki, Kim, Jong-Won, Han, Jiali, Yang, Ping, Böhmer, Anne C., Mattheisen, Manuel, Nöthen, Markus M., Mangold, Elisabeth
Published 2016

Identification of the BRD1 interaction network and its impact on mental disorder risk

by Fryland, Tue, Christensen, Jane H., Pallesen, Jonatan, Mattheisen, Manuel, Palmfeldt, Johan, Bak, Mads, Grove, Jakob, Demontis, Ditte, Blechingberg, Jenny, Ooi, Hong Sain, Nyegaard, Mette, Hauberg, Mads E., Tommerup, Niels, Gregersen, Niels, Mors, Ole, Corydon, Thomas J., Nielsen, Anders L., Børglum, Anders D.
Published 2016

Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy

by Draaken, Markus, Knapp, Michael, Pennimpede, Tracie, Schmidt, Johanna M., Ebert, Anne-Karolin, Rösch, Wolfgang, Stein, Raimund, Utsch, Boris, Hirsch, Karin, Boemers, Thomas M., Mangold, Elisabeth, Heilmann, Stefanie, Ludwig, Kerstin U., Jenetzky, Ekkehart, Zwink, Nadine, Moebus, Susanne, Herrmann, Bernhard G., Mattheisen, Manuel, Nöthen, Markus M., Ludwig, Michael, Reutter, Heiko
Published 2015

DCLK1 Variants Are Associated across Schizophrenia and Attention Deficit/Hyperactivity Disorder

by 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
Published 2012

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

by Johnson, Emma C., Bjelland, Douglas W., Howrigan, Daniel P., Abdellaoui, Abdel, Breen, Gerome, Borglum, Anders, Cichon, Sven, Degenhardt, Franziska, Forstner, Andreas J., Frank, Josef, Genovese, Giulio, Heilmann-Heimbach, Stefanie, Herms, Stefan, Hoffman, Per, Maier, Wolfgang, Mattheisen, Manuel, Morris, Derek, Mowry, Bryan, Müller-Mhysok, Betram, Neale, Benjamin, Nenadic, Igor, Nöthen, Markus M., O’Dushlaine, Colm, Rietschel, Marcella, Ruderfer, Douglas M., Rujescu, Dan, Schulze, Thomas G., Simonson, Matthew A., Stahl, Eli, Strohmaier, Jana, Witt, Stephanie H., Sullivan, Patrick F., Keller, Matthew C.
Published 2016

A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry

by Lutz, Sharon M., Cho, Michael H., Young, Kendra, Hersh, Craig P., Castaldi, Peter J., McDonald, Merry-Lynn, Regan, Elizabeth, Mattheisen, Manuel, DeMeo, Dawn L., Parker, Margaret, Foreman, Marilyn, Make, Barry J., Jensen, Robert L., Casaburi, Richard, Lomas, David A., Bhatt, Surya P., Bakke, Per, Gulsvik, Amund, Crapo, James D., Beaty, Terri H., Laird, Nan M., Lange, Christoph, Hokanson, John E., Silverman, Edwin K.
Published 2015

Genome-Wide Association Study in Obsessive-Compulsive Disorder: Results from the OCGAS

by Mattheisen, Manuel, Samuels, Jack F., Wang, Ying, Greenberg, Benjamin D., Fyer, Abby J., McCracken, James T., Geller, Daniel A., Murphy, Dennis L., Knowles, James A., Grados, Marco A., Riddle, Mark A., Rasmussen, Steven A., McLaughlin, Nicole C., Nurmi, Erica, Askland, Kathleen D., Qin, Hai-De, Cullen, Bernadette A., Piacentini, John, Pauls, David L., Bienvenu, O. Joseph, Stewart, S. Evelyn, Liang, Kung-Yee, Goes, Fernando S., Maher, Brion, Pulver, Ann E., Shugart, Yin-Yao, Valle, David, Lange, Cristoph, Nestadt, Gerald
Published 2014