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

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

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

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

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

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

Chronicity and Sex Affect Genetic Risk Prediction in Schizophrenia

por Meier, Sandra M., Kähler, Anna K., Bergen, Sarah E., Sullivan, Patrick F., Hultman, Christina M., Mattheisen, Manuel
Publicado 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...

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

Antipsychotics in routine treatment are minor contributors to QT prolongation compared to genetics and age

por Hommers, Leif, Scherf-Clavel, Maike, Stempel, Roberta, Roth, Julian, Falter, Matthias, Deckert, Jürgen, Mattheisen, Manuel, Unterecker, Stefan, Gawlik, Micha
Publicado 2021

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

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

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

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

A Mobile Sensing App to Monitor Youth Mental Health: Observational Pilot Study

por MacLeod, Lucy, Suruliraj, Banuchitra, Gall, Dominik, Bessenyei, Kitti, Hamm, Sara, Romkey, Isaac, Bagnell, Alexa, Mattheisen, Manuel, Muthukumaraswamy, Viswanath, Orji, Rita, Meier, Sandra
Publicado 2021

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

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

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

por 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.
Publicado 2012

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

por 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.
Publicado 2019

Predicting eating disorder and anxiety symptoms using disorder-specific and transdiagnostic polygenic scores for anorexia nervosa and obsessive-compulsive disorder

por Yilmaz, Zeynep, Schaumberg, Katherine, Halvorsen, Matthew, Goodman, Erica L., Brosof, Leigh C., Crowley, James J., Mathews, Carol A., Mattheisen, Manuel, Breen, Gerome, Bulik, Cynthia M., Micali, Nadia, Zerwas, Stephanie C.
Publicado 2023

Elevated Common Variant Genetic Risk for Tourette Syndrome in a Densely Affected Pedigree

por Halvorsen, Matthew, Szatkiewicz, Jin, Mudgal, Poorva, Yu, Dongmei, Nordsletten, Ashley E., Mataix-Cols, David, Mathews, Carol A., Scharf, Jeremiah M., Mattheisen, Manuel, Robertson, Mary M., McQuillin, Andrew, Crowley, James J.
Publicado 2021

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

por 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
Publicado 2013

1,25-Dihydroxyvitamin D modulates L-type voltage-gated calcium channels in a subset of neurons in the developing mouse prefrontal cortex

por Gooch, Helen, Cui, Xiaoying, Anggono, Victor, Trzaskowski, Maciej, Tan, Men Chee, Eyles, Darryl W., Burne, Thomas H. J., Jang, Se Eun, Mattheisen, Manuel, Hougaard, David M., Pedersen, Bent Nørgaard, Cohen, Arieh, Mortensen, Preben B., Sah, Pankaj, McGrath, John J.
Publicado 2019

Copy Number Variants in German Patients with Schizophrenia

por 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
Publicado 2013

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

por 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.
Publicado 2016

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

por 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
Publicado 2016

Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis

por Strom, Nora I., Grove, Jakob, Meier, Sandra M., Bækvad-Hansen, Marie, Becker Nissen, Judith, Damm Als, Thomas, Halvorsen, Matthew, Nordentoft, Merete, Mortensen, Preben B., Hougaard, David M., Werge, Thomas, Mors, Ole, Børglum, Anders D., Crowley, James J., Bybjerg-Grauholm, Jonas, Mattheisen, Manuel
Publicado 2021