Point mutation increases a form of the NK(1) receptor with high affinity for neurokinin A and B and septide

door Ciucci, Alessandra, Palma, Carla, Manzini, Stefano, Werge, Thomas M
Gepubliceerd in 1998

Interactive effects between hemizygous 15q13.3 microdeletion and peripubertal stress on adult behavioral functions

door Giovanoli, Sandra, Werge, Thomas M., Mortensen, Preben B., Didriksen, Michael, Meyer, Urs
Gepubliceerd in Neuropsychopharmacology (2018)

AMPK signaling linked to the schizophrenia-associated 1q21.1 deletion is required for neuronal and sleep maintenance

door Nagy, Stanislav, Maurer, Gianna W., Hentze, Julie L., Rose, Morten, Werge, Thomas M., Rewitz, Kim
Gepubliceerd in PLoS Genet (2018)

Is an Early Age at Illness Onset in Schizophrenia Associated With Increased Genetic Susceptibility? Analysis of Data From the Nationwide Danish Twin Register

door Hilker, Rikke, Helenius, Dorte, Fagerlund, Birgitte, Skytthe, Axel, Christensen, Kaare, Werge, Thomas M., Nordentoft, Merete, Glenthøj, Birte
Gepubliceerd in EBioMedicine (2017)

Analysis of genes within the schizophrenia-linked 22q11.2 deletion identifies interaction of night owl/LZTR1 and NF1 in GABAergic sleep control

door Maurer, Gianna W., Malita, Alina, Nagy, Stanislav, Koyama, Takashi, Werge, Thomas M., Halberg, Kenneth A., Texada, Michael J., Rewitz, Kim
Gepubliceerd in PLoS Genet (2020)

Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort

door Padmanabhuni, Shanmukha S., Houssari, Rayan, Esserlind, Ann-Louise, Olesen, Jes, Werge, Thomas M., Hansen, Thomas F., Bertelsen, Birgitte, Tsetsos, Fotis, Paschou, Peristera, Tümer, Zeynep
Gepubliceerd in Front Neurosci (2016)

Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic Overlap

door Gandal, Michael J., Haney, Jillian R., Parikshak, Neelroop N., Leppa, Virpi, Ramaswami, Gokul, Hartl, Chris, Schork, Andrew J., Appadurai, Vivek, Buil, Alfonso, Werge, Thomas M., Liu, Chunyu, White, Kevin P., Geschwind, Daniel H.
Gepubliceerd in Focus (Am Psychiatr Publ) (2019)

A mouse model of the schizophrenia-associated 1q21.1 microdeletion syndrome exhibits altered mesolimbic dopamine transmission

door Nielsen, Jacob, Fejgin, Kim, Sotty, Florence, Nielsen, Vibeke, Mørk, Arne, Christoffersen, Claus T., Yavich, Leonid, Lauridsen, Jes B., Clausen, Dorte, Larsen, Peter H., Egebjerg, Jan, Werge, Thomas M., Kallunki, Pekka, Christensen, Kenneth V., Didriksen, Michael
Gepubliceerd in Transl Psychiatry (2017)

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

door Gandal, Michael J., Haney, Jillian R., Parikshak, Neelroop N., Leppa, Virpi, Ramaswami, Gokul, Hartl, Chris, Schork, Andrew J., Appadurai, Vivek, Buil, Alfonso, Werge, Thomas M., Liu, Chunyu, White, Kevin P., Horvath, Steve, Geschwind, Daniel H.
Gepubliceerd in Science (2018)

Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease

door Hagen, Christian M., Gonçalves, Vanessa F., Hedley, Paula L., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Hansen, Christine S., Kanters, Jørgen K., Nielsen, Jimmi, Mors, Ole, Demur, Alfonso B., Als, Thomas D., Nordentoft, Merete, Børglum, Anders, Mortensen, Preben B., Kennedy, James, Werge, Thomas M., Hougaard, David M., Christiansen, Michael
Gepubliceerd in PLoS One (2018)

Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice

door Didriksen, Michael, Fejgin, Kim, Nilsson, Simon R.O., Birknow, Michelle R., Grayton, Hannah M., Larsen, Peter H., Lauridsen, Jes B., Nielsen, Vibeke, Celada, Pau, Santana, Noemi, Kallunki, Pekka, Christensen, Kenneth V., Werge, Thomas M., Stensbøl, Tine B., Egebjerg, Jan, Gastambide, Francois, Artigas, Francesc, Bastlund, Jesper F., Nielsen, Jacob
Gepubliceerd in J Psychiatry Neurosci (2017)

Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes

door Bybjerg-Grauholm, Jonas, Hagen, Christian M., Gonçalves, Vanessa F., Bækvad-Hansen, Marie, Hansen, Christine S., Hedley, Paula L., Kanters, Jørgen K., Nielsen, Jimmi, Theisen, Michael, Mors, Ole, Kennedy, James, Als, Thomas D., Demur, Alfonso B., Nordentoft, Merete, Børglum, Anders, Mortensen, Preben B., Werge, Thomas M., Hougaard, David M., Christiansen, Michael
Gepubliceerd in PLoS One (2018)

Autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD) have a similar burden of rare protein-truncating variants

door Satterstrom, F. Kyle, Walters, Raymond K., Singh, Tarjinder, Wigdor, Emilie M., Lescai, Francesco, Demontis, Ditte, Kosmicki, Jack A., Grove, Jakob, Stevens, Christine, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Palmer, Duncan S., Maller, Julian B., Nordentoft, Merete, Mors, Ole, Robinson, Elise B., Hougaard, David M., Werge, Thomas M., Mortensen, Preben Bo, Neale, Benjamin M., Børglum, Anders D., Daly, Mark J.
Gepubliceerd in Nat Neurosci (2019)

Quetiapine versus aripiprazole in children and adolescents with psychosis - protocol for the randomised, blinded clinical Tolerability and Efficacy of Antipsychotics (TEA) trial

door Pagsberg, Anne Katrine, Jeppesen, Pia, Klauber, Dea Gowers, Jensen, Karsten Gjessing, Rudå, Ditte, Stentebjerg-Olesen, Marie, Jantzen, Peter, Rasmussen, Simone, Saldeen, Eva Ann-Sofie, Lauritsen, Maj-Britt Glenn, Bilenberg, Niels, Stenstrøm, Anne Dorte, Pedersen, Jesper, Nyvang, Louise, Madsen, Sarah, Lauritsen, Marlene B, Vernal, Ditte Lammers, Thomsen, Per Hove, Paludan, Jakob, Werge, Thomas M, Winge, Kristian, Juul, Klaus, Gluud, Christian, Skoog, Maria, Wetterslev, Jørn, Jepsen, Jens Richardt M, Correll, Christoph U, Fink-Jensen, Anders, Fagerlund, Birgitte
Gepubliceerd in BMC Psychiatry (2014)

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders

door Isles, Anthony R., Ingason, Andrés, Lowther, Chelsea, Walters, James, Gawlick, Micha, Stöber, Gerald, Rees, Elliott, Martin, Joanna, Little, Rosie B., Potter, Harry, Georgieva, Lyudmila, Pizzo, Lucilla, Ozaki, Norio, Aleksic, Branko, Kushima, Itaru, Ikeda, Masashi, Iwata, Nakao, Levinson, Douglas F., Gejman, Pablo V., Shi, Jianxin, Sanders, Alan R., Duan, Jubao, Willis, Joseph, Sisodiya, Sanjay, Costain, Gregory, Werge, Thomas M., Degenhardt, Franziska, Giegling, Ina, Rujescu, Dan, Hreidarsson, Stefan J., Saemundsen, Evald, Ahn, Joo Wook, Ogilvie, Caroline, Girirajan, Santhosh D., Stefansson, Hreinn, Stefansson, Kari, O’Donovan, Michael C., Owen, Michael J., Bassett, Anne, Kirov, George
Gepubliceerd in PLoS Genet (2016)

Population genetic differentiation of height and body mass index across Europe

door Robinson, Matthew R., Hemani, Gibran, Medina-Gomez, Carolina, Mezzavilla, Massimo, Esko, Tonu, Shakhbazov, Konstantin, Powell, Joseph E., Vinkhuyzen, Anna, Berndt, Sonja I., Gustafsson, Stefan, Justice, Anne E., Kahali, Bratati, Locke, Adam E., Pers, Tune H., Vedantam, Sailaja, Wood, Andrew R., van Rheenen, Wouter, Andreassen, Ole A., Gasparini, Paolo, Metspalu, Andres, van den Berg, Leonard H., Veldink, Jan H., Rivadeneira, Fernando, Werge, Thomas M., Abecasis, Goncalo R., Boomsma, Dorret I., Chasman, Daniel I., de Geus, Eco J.C., Frayling, Timothy M., Hirschhorn, Joel N., Hottenga, Jouke Jan, Ingelsson, Erik, Loos, Ruth J.F., Magnusson, Patrik K. E., Martin, Nicholas G., Montgomery, Grant W., North, Kari E., Pedersen, Nancy L., Spector, Timothy D., Speliotes, Elizabeth K., Goddard, Michael E., Yang, Jian, Visscher, Peter M.
Gepubliceerd in Nat Genet (2015)

The Anorexia Nervosa Genetics Initiative (ANGI): Overview and Methods

door Thornton, Laura M, Munn-Chernoff, Melissa A, Baker, Jessica H, Juréus, Anders, Parker, Richard, Henders, Anjali K, Larsen, Janne T, Petersen, Liselotte, Watson, Hunna J, Yilmaz, Zeynep, Kirk, Katherine M, Gordon, Scott, Leppä, Virpi M, Martin, Felicity C, Whiteman, David C, Olsen, Catherine M, Werge, Thomas M, Pedersen, Nancy L, Kaye, Walter, Bergen, Andrew W, Halmi, Katherine A, Strober, Michael, Kaplan, Allan S, Woodside, D. Blake, Mitchell, James, Johnson, Craig L, Brandt, Harry, Crawford, Steven, Horwood, L. John, Boden, Joseph M, Pearson, John F, Duncan, Laramie E, Grove, Jakob, Mattheisen, Manuel, Jordan, Jennifer, Kennedy, Martin A, Birgegård, Andreas, Lichtenstein, Paul, Norring, Claes, Wade, Tracey D, Montgomery, Grant W, Martin, Nicholas G, Landén, Mikael, Bo Mortensen, Preben, Sullivan, Patrick F, Bulik, Cynthia M
Gepubliceerd in Contemp Clin Trials (2018)

Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes

door Delio, Maria, Guo, Tingwei, McDonald-McGinn, Donna M., Zackai, Elaine, Herman, Sean, Kaminetzky, Mark, Higgins, Anne Marie, Coleman, Karlene, Chow, Carolyn, Jarlbrzkowski, Maria, Bearden, Carrie E., Bailey, Alice, Vangkilde, Anders, Olsen, Line, Olesen, Charlotte, Skovby, Flemming, Werge, Thomas M., Templin, Ludivine, Busa, Tiffany, Philip, Nicole, Swillen, Ann, Vermeesch, Joris R., Devriendt, Koen, Schneider, Maude, Dahoun, Sophie, Eliez, Stephan, Schoch, Kelly, Hooper, Stephen R., Shashi, Vandana, Samanich, Joy, Marion, Robert, van Amelsvoort, Therese, Boot, Erik, Klaassen, Petra, Duijff, Sasja N., Vorstman, Jacob, Yuen, Tracy, Silversides, Candice, Chow, Eva, Bassett, Anne, Frisch, Amos, Weizman, Abraham, Gothelf, Doron, Niarchou, Maria, van den Bree, Marianne, Owen, Michael J., Suñer, Damian Heine, Andreo, Jordi Rosell, Armando, Marco, Vicari, Stefano, Digilio, Maria Cristina, Auton, Adam, Kates, Wendy R., Wang, Tao, Shprintzen, Robert J., Emanuel, Beverly S., Morrow, Bernice E.
Gepubliceerd in 2013

Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes

door Delio, Maria, Guo, Tingwei, McDonald-McGinn, Donna M., Zackai, Elaine, Herman, Sean, Kaminetzky, Mark, Higgins, Anne Marie, Coleman, Karlene, Chow, Carolyn, Jalbrzikowski, Maria, Bearden, Carrie E., Bailey, Alice, Vangkilde, Anders, Olsen, Line, Olesen, Charlotte, Skovby, Flemming, Werge, Thomas M., Templin, Ludivine, Busa, Tiffany, Philip, Nicole, Swillen, Ann, Vermeesch, Joris R., Devriendt, Koen, Schneider, Maude, Dahoun, Sophie, Eliez, Stephan, Schoch, Kelly, Hooper, Stephen R., Shashi, Vandana, Samanich, Joy, Marion, Robert, van Amelsvoort, Therese, Boot, Erik, Klaassen, Petra, Duijff, Sasja N., Vorstman, Jacob, Yuen, Tracy, Silversides, Candice, Chow, Eva, Bassett, Anne, Frisch, Amos, Weizman, Abraham, Gothelf, Doron, Niarchou, Maria, van den Bree, Marianne, Owen, Michael J., Suñer, Damian Heine, Andreo, Jordi Rosell, Armando, Marco, Vicari, Stefano, Digilio, Maria Cristina, Auton, Adam, Kates, Wendy R., Wang, Tao, Shprintzen, Robert J., Emanuel, Beverly S., Morrow, Bernice E.
Gepubliceerd in 2013

An epigenetic clock for gestational age at birth based on blood methylation data

door Knight, Anna K., Craig, Jeffrey M., Theda, Christiane, Bækvad-Hansen, Marie, Bybjerg-Grauholm, Jonas, Hansen, Christine S., Hollegaard, Mads V., Hougaard, David M., Mortensen, Preben B., Weinsheimer, Shantel M., Werge, Thomas M., Brennan, Patricia A., Cubells, Joseph F., Newport, D. Jeffrey, Stowe, Zachary N., Cheong, Jeanie L. Y., Dalach, Philippa, Doyle, Lex W., Loke, Yuk J., Baccarelli, Andrea A., Just, Allan C., Wright, Robert O., Téllez-Rojo, Mara M., Svensson, Katherine, Trevisi, Letizia, Kennedy, Elizabeth M., Binder, Elisabeth B., Iurato, Stella, Czamara, Darina, Räikkönen, Katri, Lahti, Jari M. T., Pesonen, Anu-Katriina, Kajantie, Eero, Villa, Pia M., Laivuori, Hannele, Hämäläinen, Esa, Park, Hea Jin, Bailey, Lynn B., Parets, Sasha E., Kilaru, Varun, Menon, Ramkumar, Horvath, Steve, Bush, Nicole R., LeWinn, Kaja Z., Tylavsky, Frances A., Conneely, Karen N., Smith, Alicia K.
Gepubliceerd in Genome Biol (2016)