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Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register
Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register
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Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register

Hilker, Rikke ; Helenius, Dorte ; Fagerlund, Birgitte ; Skytthe, Axel ; Christensen, Kaare ; Werge, Thomas M. ; Nordentoft, Merete ; Glenthøj, Birte

Biological psychiatry (1969), 2018-03, Vol.83 (6), p.492-498 [Periódico revisado por pares]

United States: Elsevier Inc

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2
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants
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Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

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 ; Bo Mortensen, Preben ; Neale, Benjamin M ; Børglum, Anders D ; Daly, Mark J

Nature neuroscience, 2019-12, Vol.22 (12), p.1961-1965 [Periódico revisado por pares]

United States: Nature Publishing Group

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3
Analysis of genes within the schizophrenia-linked 22q11.2 deletion identifies interaction of night owl/LZTR1 and NF1 in GABAergic sleep control
Analysis of genes within the schizophrenia-linked 22q11.2 deletion identifies interaction of night owl/LZTR1 and NF1 in GABAergic sleep control
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Analysis of genes within the schizophrenia-linked 22q11.2 deletion identifies interaction of night owl/LZTR1 and NF1 in GABAergic sleep control

Maurer, Gianna W ; Malita, Alina ; Nagy, Stanislav ; Koyama, Takashi ; Werge, Thomas M ; Halberg, Kenneth A ; Texada, Michael J ; Rewitz, Kim Wegener, Christian

PLoS genetics, 2020-04, Vol.16 (4), p.e1008727-e1008727 [Periódico revisado por pares]

United States: Public Library of Science

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4
Exploring Comorbidity Within Mental Disorders Among a Danish National Population
Exploring Comorbidity Within Mental Disorders Among a Danish National Population
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Exploring Comorbidity Within Mental Disorders Among a Danish National Population

Plana-Ripoll, Oleguer ; Pedersen, Carsten Bøcker ; Holtz, Yan ; Benros, Michael E ; Dalsgaard, Søren ; de Jonge, Peter ; Fan, Chun Chieh ; Degenhardt, Louisa ; Ganna, Andrea ; Greve, Aja Neergaard ; Gunn, Jane ; Iburg, Kim Moesgaard ; Kessing, Lars Vedel ; Lee, Brian K ; Lim, Carmen C. W ; Mors, Ole ; Nordentoft, Merete ; Prior, Anders ; Roest, Annelieke M ; Saha, Sukanta ; Schork, Andrew ; Scott, James G ; Scott, Kate M ; Stedman, Terry ; Sørensen, Holger J ; Werge, Thomas ; Whiteford, Harvey A ; Laursen, Thomas Munk ; Agerbo, Esben ; Kessler, Ronald C ; Mortensen, Preben Bo ; McGrath, John J

JAMA psychiatry (Chicago, Ill.), 2019-03, Vol.76 (3), p.259-270 [Periódico revisado por pares]

United States: American Medical Association

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5
AMPK signaling linked to the schizophrenia-associated 1q21.1 deletion is required for neuronal and sleep maintenance
AMPK signaling linked to the schizophrenia-associated 1q21.1 deletion is required for neuronal and sleep maintenance
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AMPK signaling linked to the schizophrenia-associated 1q21.1 deletion is required for neuronal and sleep maintenance

Nagy, Stanislav ; Maurer, Gianna W ; Hentze, Julie L ; Rose, Morten ; Werge, Thomas M ; Rewitz, Kim Gandal, Michael

PLoS genetics, 2018-12, Vol.14 (12), p.e1007623-e1007623 [Periódico revisado por pares]

United States: Public Library of Science

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6
An epigenetic clock for gestational age at birth based on blood methylation data
An epigenetic clock for gestational age at birth based on blood methylation data
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An epigenetic clock for gestational age at birth based on blood methylation data

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

Genome Biology, 2016-10, Vol.17 (1), p.206, Article 206 [Periódico revisado por pares]

England: BioMed Central

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7
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Gormley, Padhraig ; Anttila, Verneri ; Winsvold, Bendik S ; Palta, Priit ; Esko, Tonu ; Pers, Tune H ; Farh, Kai-How ; Cuenca-Leon, Ester ; Muona, Mikko ; Furlotte, Nicholas A ; Kurth, Tobias ; Ingason, Andres ; McMahon, George ; Terwindt, Gisela M ; Kallela, Mikko ; Freilinger, Tobias M ; Ran, Caroline ; Gordon, Scott G ; Stam, Anine H ; Borck, Guntram ; Koiranen, Markku ; Quaye, Lydia ; Adams, Hieab H H ; Lehtimäki, Terho ; Sarin, Antti-Pekka ; Wedenoja, Juho ; Hinds, David A ; Schürks, Markus ; Ridker, Paul M ; Hrafnsdottir, Maria Gudlaug ; Stefansson, Hreinn ; Ring, Susan M ; Hottenga, Jouke-Jan ; Penninx, Brenda W J H ; Färkkilä, Markus ; Artto, Ville ; Kaunisto, Mari ; Vepsäläinen, Salli ; Malik, Rainer ; Heath, Andrew C ; Madden, Pamela A F ; Martin, Nicholas G ; Montgomery, Grant W ; Kurki, Mitja I ; Kals, Mart ; Mägi, Reedik ; Pärn, Kalle ; Hämäläinen, Eija ; Huang, Hailiang ; Byrnes, Andrea E ; Franke, Lude ; Huang, Jie ; Stergiakouli, Evie ; Lee, Phil H ; Sandor, Cynthia ; Webber, Caleb ; Cader, Zameel ; Muller-Myhsok, Bertram ; Schreiber, Stefan ; Meitinger, Thomas ; Eriksson, Johan G ; Salomaa, Veikko ; Heikkilä, Kauko ; Loehrer, Elizabeth ; Uitterlinden, Andre G ; Hofman, Albert ; Cherkas, Lynn ; Pedersen, Linda M ; Stubhaug, Audun ; Männikkö, Minna ; Milani, Lili ; Göbel, Hartmut ; Esserlind, Ann-Louise ; Christensen, Anne Francke ; Hansen, Thomas Folkmann ; Werge, Thomas ; Kaprio, Jaakko ; Aromaa, Arpo J ; Ikram, M Arfan ; Spector, Tim ; Järvelin, Marjo-Riitta ; Metspalu, Andres ; Kubisch, Christian ; Strachan, David P ; Ferrari, Michel D ; Belin, Andrea C ; Dichgans, Martin ; Wessman, Maija ; van den Maagdenberg, Arn M J M ; Zwart, John-Anker ; Boomsma, Dorret I ; Smith, George Davey ; Stefansson, Kari ; Eriksson, Nicholas ; Daly, Mark J ; Neale, Benjamin M ; Olesen, Jes ; Chasman, Daniel I ; Nyholt, Dale R ; Palotie, Aarno

Nature genetics, 2016-08, Vol.48 (8), p.856-866 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease
Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease
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Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease

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 Arking, Dan E.

PloS one, 2018-12, Vol.13 (12), p.e0208828-e0208828 [Periódico revisado por pares]

United States: Public Library of Science

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9
Structural basis of organic cation transporter-3 inhibition
Structural basis of organic cation transporter-3 inhibition
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Structural basis of organic cation transporter-3 inhibition

Khanppnavar, Basavraj ; Maier, Julian ; Herborg, Freja ; Gradisch, Ralph ; Lazzarin, Erika ; Luethi, Dino ; Yang, Jae-Won ; Qi, Chao ; Holy, Marion ; Jäntsch, Kathrin ; Kudlacek, Oliver ; Schicker, Klaus ; Werge, Thomas ; Gether, Ulrik ; Stockner, Thomas ; Korkhov, Volodymyr M ; Sitte, Harald H

Nature communications, 2022-11, Vol.13 (1), p.6714-6714, Article 6714 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders
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Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders

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 Bartolomei, Marisa S

PLoS genetics, 2016-05, Vol.12 (5), p.e1005993 [Periódico revisado por pares]

United States: Public Library of Science

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