Zobrazeno 1 - 10
of 126
pro vyhledávání: '"Christensen Jane H"'
Autor:
Qvist, Per, Rajkumar, Anto P., Redrobe, John P., Nyegaard, Mette, Christensen, Jane H., Mors, Ole, Wegener, Gregers, Didriksen, Michael, Børglum, Anders D.
Publikováno v:
In Neurobiology of Learning and Memory May 2017 141:44-52
Autor:
Christensen, Jane H., Nielsen, Marit N., Hansen, Jakob, Füchtbauer, Annette, Füchtbauer, Ernst-Martin, West, Mark, Corydon, Thomas J., Gregersen, Niels, Bross, Peter
Publikováno v:
Cell Stress & Chaperones, 2010 Nov 01. 15(6), 851-863.
Externí odkaz:
https://www.jstor.org/stable/20799980
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Christensen, Jane H., Rittig, Søren
Publikováno v:
In Seminars in Nephrology 2006 26(3):209-223
Autor:
Leduc-Galindo, Desiree, Qvist, Per, Tóth, Andrea E., Fryland, Tue, Nielsen, Morten S., Børglum, Anders D., Christensen, Jane H.
Publikováno v:
In Microvascular Research March 2019 122:131-135
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Grove, Jakob, Ripke, Stephan, Als, Thomas D, Mattheisen, Manuel, Walters, Raymond K, Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A, Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H, Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L, Goldstein, Jacqueline I, Hansen, Christine S, Hauberg, Mads Engel, Hollegaard, Mads V, Hope, Sigrun, Howrigan, Daniel P, Huang, Hailiang, Hultman, Christina M, Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R, Moran, Jennifer L, Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S, Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B, Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R, Sullivan, Patrick F, Turley, Patrick, Walters, G Bragi, Xu, Xinyi, Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium, BUPGEN, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 23andMe Research Team, Stefansson, Kari, Geschwind, Daniel H, Nordentoft, Merete, Hougaard, David M, Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M, Daly, Mark J, Børglum, Anders D
Publikováno v:
Nature genetics, vol 51, iss 3
Autism spectrum disorder (ASD) is a highly heritable and heterogeneous group of neurodevelopmental phenotypes diagnosed in more than 1% of children. Common genetic variants contribute substantially to ASD susceptibility, but to date no individual var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::691eb1d7680f90e341d947bf0ecb819a
https://escholarship.org/uc/item/4k2655gb
https://escholarship.org/uc/item/4k2655gb
Autor:
Fryland, Tue1,2,3, Christensen, Jane H.1,2,3, Pallesen, Jonatan1,2,3, Mattheisen, Manuel1,2,3, Palmfeldt, Johan4, Bak, Mads5, Grove, Jakob1,2,3,6, Demontis, Ditte1,2,3, Blechingberg, Jenny1, Hong Sain Ooi1,2,3, Nyegaard, Mette1,2,3, Hauberg, Mads E.1,2,3, Tommerup, Niels5, Gregersen, Niels4, Mors, Ole2,3,7, Corydon, Thomas J.1,2,3, Nielsen, Anders L.1,2,3, Børglum, Anders D.1,2,3,7 anders@biomed.au.dk
Publikováno v:
Genome Medicine. 5/3/2016, Vol. 8, p1-20. 20p.
Autor:
Rajkumar, Anto P1,2,3,4, Christensen, Jane H1,3,4, Mattheisen, Manuel1,3,4, Jacobsen, Iben2, Bache, Iben5, Pallesen, Jonatan1,3,4, Grove, Jakob1,3,4,6, Qvist, Per1,3,4, McQuillin, Andrew7, Gurling, Hugh M7, Tümer, Zeynep8, Mors, Ole3,4,9, Børglum, Anders D1,2,3,4,9
Publikováno v:
Bipolar Disorders. Mar2015, Vol. 17 Issue 2, p205-211. 7p. 1 Diagram, 1 Graph.
Autor:
Kvistgaard, Helene, Christensen, Jane H, Johansson, Jan-Ove, Gregersen, Niels, Siggaard Rittig, Charlotte, Rittig, Søren, Corydon, Thomas J
Publikováno v:
Kvistgaard, H, Christensen, J H, Johansson, J-O, Gregersen, N, Siggaard Rittig, C, Rittig, S & Corydon, T J 2018, ' A Novel Synonymous Variant in the AVP Gene Associated with Autosomal Dominant Familial Neurohypophyseal Diabetes Insipidus Causes Partial RNA Missplicing ', Neuroendocrinology, vol. 107, no. 2, pp. 167-180 . https://doi.org/10.1159/000491579
OBJECTIVE: Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI) is characterized by severe polyuria and polydipsia and is caused by variations in the gene encoding the AVP prohormone. This study aimed to ascertain a correct diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::7b328cae3f1b883fbe288dc5121fbca1
https://pure.au.dk/portal/da/publications/a-novel-synonymous-variant-in-the-avp-gene-associated-with-autosomal-dominant-familial-neurohypophyseal-diabetes-insipidus-causes-partial-rna-missplicing(2005355f-eb38-4aff-94e8-db66cf1888c6).html
https://pure.au.dk/portal/da/publications/a-novel-synonymous-variant-in-the-avp-gene-associated-with-autosomal-dominant-familial-neurohypophyseal-diabetes-insipidus-causes-partial-rna-missplicing(2005355f-eb38-4aff-94e8-db66cf1888c6).html