On Association Analysis of Rare Variants Under Population Substructure: An Approach for the Detection of Subjects That Can Cause Bias in the Analysis—T(opt): An Outlier Detection M...

Autor Qiao, Dandi, Mattheisen, Manuel, Lange, Christoph
Vydáno 2013

Response to Zhu et al.

Autor Christoforou, Andrea, Mattheisen, Manuel, Giddaluru, Sudheer, Steen, Vidar M., Le Hellard, Stéphanie
Vydáno 2012

Analyzing the Role of microRNAs in Schizophrenia in the Context of Common Genetic Risk Variants

Autor Hauberg, Mads Engel, Roussos, Panos, Grove, Jakob, Børglum, Anders Dupont, Mattheisen, Manuel
Vydáno v JAMA Psychiatry (2016)

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

Autor Habib, Rabia, Ansar, Muhammad, Mattheisen, Manuel, Shahid, Muhammad, Ali, Ghazanfar, Ahmad, Wasim, Betz, Regina C.
Vydáno v PLoS One (2015)

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

Autor Meier, Sandra M, Petersen, Liselotte, Schendel, Diana E, Mattheisen, Manuel, Mortensen, Preben B, Mors, Ole
Vydáno v PLoS One (2015)

Secondary depression in severe anxiety disorders: a population-based cohort study in Denmark

Autor Meier, Sandra M, Petersen, Liselotte, Mattheisen, Manuel, Mors, Ole, Mortensen, Preben B, Laursen, Thomas M
Vydáno v Lancet Psychiatry (2015)

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

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

Increased mortality among people with anxiety disorders: total population study

Autor Meier, Sandra M., Mattheisen, Manuel, Mors, Ole, Mortensen, Preben B., Laursen, Thomas M., Penninx, Brenda W.
Vydáno v Br J Psychiatry (2016)

Mortality Among Persons With Obsessive-Compulsive Disorder in Denmark

Autor Meier, Sandra M., Mattheisen, Manuel, Mors, Ole, Schendel, Diana E., Mortensen, Preben B., Plessen, Kerstin J.
Vydáno v JAMA Psychiatry (2016)

Chronicity and Sex Affect Genetic Risk Prediction in Schizophrenia

Autor Meier, Sandra M., Kähler, Anna K., Bergen, Sarah E., Sullivan, Patrick F., Hultman, Christina M., Mattheisen, Manuel
Vydáno v Front Psychiatry (2020)

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...

Autor Nissen, Judith Becker, Hansen, Christine Søholm, Starnawska, Anna, Mattheisen, Manuel, Børglum, Anders Dupont, Buttenschøn, Henriette Nørmølle, Hollegaard, Mads
Vydáno v Front Psychiatry (2016)

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

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

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

Autor Herold, Christine, Hooli, Basavaraj V., Mullin, Kristina, Liu, Tian, Roehr, Johannes T, Mattheisen, Manuel, Parrado, Antonio R., Bertram, Lars, Lange, Christoph, Tanzi, Rudolph E.
Vydáno v Mol Psychiatry (2016)

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

Autor Søes, Signe, Daugaard, Iben Lyster, Sørensen, Brita Singers, Carus, Andreas, Mattheisen, Manuel, Alsner, Jan, Overgaard, Jens, Hager, Henrik, Hansen, Lise Lotte, Kristensen, Lasse Sommer
Vydáno v Oncoscience (2014)

Specific anxiety disorders and subsequent risk for bipolar disorder: a nationwide study

Autor Meier, Sandra M., Uher, Rudolf, Mors, Ole, Dalsgaard, Søren, Munk‐Olsen, Trine, Laursen, Thomas M., Mattheisen, Manuel, Nordentoft, Merete, Mortensen, Preben B., Pavlova, Barbara
Vydáno v World Psychiatry (2016)

Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci

Autor 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
Vydáno v Hum Mol Genet (2017)

Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci

Autor 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
Vydáno v Hum Mol Genet (2018)

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

Autor 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.
Vydáno 2012

Beyond GWAS in COPD: Probing the landscape between gene-set associations, genome-wide associations and protein-protein interaction networks

Autor McDonald, Merry-Lynn Noelle, Mattheisen, Manuel, Cho, Michael H., Liu, Yang-Yu, Harshfield, Benjamin, Hersh, Craig P., Bakke, Per, Gulsvik, Amund, Lange, Christoph, Beaty, Terri H., Silverman, Edwin K.
Vydáno v Hum Hered (2014)

Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2

Autor Schlaweck, Annika E., Tazi-Ahnini, Rachid, Ü. Basmanav, F. Buket, Mohungoo, Javed, Pasternack-Ziach, Sandra M., Mattheisen, Manuel, Oprisoreanu, Ana-Maria, Humbatova, Aytaj, Wolf, Sabrina, Messenger, Andrew, Betz, Regina C.
Vydáno v PLoS One (2019)