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

מאת Ciucci, Alessandra, Palma, Carla, Manzini, Stefano, Werge, Thomas M
יצא לאור 1998

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

מאת Giovanoli, Sandra, Werge, Thomas M., Mortensen, Preben B., Didriksen, Michael, Meyer, Urs
הוצא לאור ב Neuropsychopharmacology (2018)

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

מאת Nagy, Stanislav, Maurer, Gianna W., Hentze, Julie L., Rose, Morten, Werge, Thomas M., Rewitz, Kim
הוצא לאור ב 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

מאת Hilker, Rikke, Helenius, Dorte, Fagerlund, Birgitte, Skytthe, Axel, Christensen, Kaare, Werge, Thomas M., Nordentoft, Merete, Glenthøj, Birte
הוצא לאור ב EBioMedicine (2017)

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

מאת Maurer, Gianna W., Malita, Alina, Nagy, Stanislav, Koyama, Takashi, Werge, Thomas M., Halberg, Kenneth A., Texada, Michael J., Rewitz, Kim
הוצא לאור ב PLoS Genet (2020)

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

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

Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic Overlap

מאת 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.
הוצא לאור ב Focus (Am Psychiatr Publ) (2019)

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

מאת 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
הוצא לאור ב Transl Psychiatry (2017)

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

מאת 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.
הוצא לאור ב 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

מאת 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
הוצא לאור ב 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

מאת 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
הוצא לאור ב J Psychiatry Neurosci (2017)

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

מאת 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
הוצא לאור ב PLoS One (2018)

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

מאת 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.
הוצא לאור ב 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

מאת 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
הוצא לאור ב BMC Psychiatry (2014)

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

מאת 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
הוצא לאור ב PLoS Genet (2016)

Population genetic differentiation of height and body mass index across Europe

מאת 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.
הוצא לאור ב Nat Genet (2015)

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

מאת 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
הוצא לאור ב Contemp Clin Trials (2018)

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

מאת 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.
יצא לאור 2013

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

מאת 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.
יצא לאור 2013

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

מאת 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.
הוצא לאור ב Genome Biol (2016)