Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Esther D. A. van Duin"'
Autor:
Maude Schneider, Thomas Vaessen, Esther D. A. van Duin, Zuzana Kasanova, Wolfgang Viechtbauer, Ulrich Reininghaus, Claudia Vingerhoets, Jan Booij, Ann Swillen, Jacob A. S. Vorstman, Thérèse van Amelsvoort, Inez Myin-Germeys
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-11 (2020)
Abstract Background 22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with an increased risk of psychiatric disorders. Vulnerability for psychopathology has been related to an increased reactivity to stress. Here, we examined affec
Externí odkaz:
https://doaj.org/article/e5c9717a88ca4f39bcb6f0b689677f25
Autor:
Zuzana Kasanova, Jacob A. S. Vorstman, Wolfgang Viechtbauer, Ann Swillen, Therese van Amelsvoort, Claudia Vingerhoets, Esther D. A. van Duin, Thomas Vaessen, Inez Myin-Germeys, Jan Booij, Ulrich Reininghaus, Maude Schneider
Publikováno v:
Journal of Neurodevelopmental Disorders, 12(1):30. Springer Verlag
Journal of Neurodevelopmental Disorders
Journal of neurodevelopmental disorders, 12(1):30. Springer New York
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-11 (2020)
Journal of Neurodevelopmental Disorders
Journal of neurodevelopmental disorders, 12(1):30. Springer New York
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-11 (2020)
Background 22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with an increased risk of psychiatric disorders. Vulnerability for psychopathology has been related to an increased reactivity to stress. Here, we examined affective stat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::116fa0907c9cf2229332dcbb88a28fd5
https://cris.maastrichtuniversity.nl/en/publications/f9b540d9-1f3b-4012-aaf5-a583762c9e74
https://cris.maastrichtuniversity.nl/en/publications/f9b540d9-1f3b-4012-aaf5-a583762c9e74
Autor:
Claudia Ornstein, Anne S. Bassett, Matthew S. Hestand, Bruno Marino, Kelly Schoch, Tony J. Simon, Therese van Amelsvoort, Doron Gothelf, Carrie E. Bearden, Elemi J. Breetvelt, Michael P. Epstein, Tiffany Busa, Robert J. Shprintzen, David Cutler, Tao Wang, Leila Kushan-Wells, Donna M. McDonald-McGinn, Raquel E. Gur, Hayley Moss, Esther D. A. van Duin, B Dallapiccola, Joris Vermeesch, Clodagh M. Murphy, Yingjie Zhao, Rens Evers, María Angeles de la Fuente Sanches, Ann Swillen, H. Richard Johnston, Maria Pontillo, Steve Warren, Guido Lattanzi, Michael E. Zwick, Jacob A. S. Vorstman, Jeroen Breckpot, Oanh Tran, Stylianos E. Antonarakis, Stefano Vicari, Andrea Jin, Alexander Diacou, Miri Carmel, Christian R. Marshall, Abraham Weizman, Bernice E. Morrow, Fadi I Musfee, Wendy R. Kates, Michael John Owen, Fabio Di Fabio, Marco Armando, Erik Boot, Claudia Vingerhoets, Elizabeth Goldmuntz, Massimo Biondi, Kieran C. Murphy, Nancy Butcher, Declan G. Murphy, Candice K. Silversides, Isabelle Cleynen, T. Blaine Crowley, Vandana Shashi, Linda E. Campbell, Elaine H. Zackai, Ronnie Weinberger, Sixto García-Miñaur, Marianne Bernadette van den Bree, Fernando García Algas, Damian Heine-Suñer, Tracy Heung, Daniel E. McGinn, Maude Schneider, Stephan Eliez, Marta Unolt, Stephen R. Hooper, Kathryn McCabe, A. J. Agopian, Tingwei Guo, Zhengdong Zhang, Rosemarie Fritsch, Luis Fernández, Beverly S. Emanuel, Elfi Vergaelen, Alejandra Laorden-Nieto, Flora Tassone, Gabriela M. Repetto, Laura E. Mitchell, Antonino Buzzanca, Elena Michaelovsky, M. Cristina Digilio, Nicole Philip
Publikováno v:
American Journal of Human Genetics, 106(1), 26-40. Cell Press
Am J Hum Genet
American Journal of Human Genetics, Vol. 106, No 1 (2020) pp. 26-40
American journal of human genetics, vol 106, iss 1
Am J Hum Genet
American Journal of Human Genetics, Vol. 106, No 1 (2020) pp. 26-40
American journal of human genetics, vol 106, iss 1
The 22q11.2 deletion syndrome (22q11.2DS) results from non-allelic homologous recombination between low-copy repeats termed LCR22. About 60%-70% of individuals with the typical 3 megabase (Mb) deletion from LCR22A-D have congenital heart disease, mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8700304c185800fa1b2e56de201d2874
https://cris.maastrichtuniversity.nl/en/publications/fcebc151-7a92-4dbe-8f36-bd15cb7462bb
https://cris.maastrichtuniversity.nl/en/publications/fcebc151-7a92-4dbe-8f36-bd15cb7462bb
Autor:
Therese van Amelsvoort, Claudia Vingerhoets, Jenny Ceccarini, Jan Booij, Esther D. A. van Duin, Desmond H. Y. Tse
Publikováno v:
Biological Psychiatry. 89:S162
Autor:
Esther D A, van Duin, Jenny, Ceccarini, Jan, Booij, Zuzana, Kasanova, Claudia, Vingerhoets, Jytte, van Huijstee, Alexander, Heinzel, Siamak, Mohammadkhani-Shali, Oliver, Winz, Felix, Mottaghy, Inez, Myin-Germeys, Thérèse, van Amelsvoort
Publikováno v:
Psychological Medicine
Background The 22q11.2 deletion syndrome (22q11DS) is caused by a deletion on chromosome 22 locus q11.2. This copy number variant results in haplo-insufficiency of the catechol-O-methyltransferase (COMT) gene, and is associated with a significant inc
Autor:
J.G. Ramaekers, Desmond H. Y. Tse, Claudia Vingerhoets, Mathilde van Oudenaren, Oswald J.N. Bloemen, Jaap Janssen, Therese van Amelsvoort, Dennis Hernaus, Esther D. A. van Duin, Grainne M. McAlonan
Publikováno v:
Biological Psychiatry. 83:S198-S199
Autor:
Therese van Amelsvoort, Mariken B. de Koning, Oswald J.N. Bloemen, Kathryn M. Abel, Jaap A. Bakker, Erik Boot, Esther D. A. van Duin
Publikováno v:
Psychopharmacology, 232(17), 3111-3122. Springer
Psychopharmacology, 232(17), 3111-3122. Springer Verlag
Psychopharmacology, 232(17), 3111-3122. Springer Verlag
22q11 deletion syndrome (22q11DS) is associated with an increased risk for psychotic disorders, suggesting a relationship between genotypes and the pathophysiology of psychotic disorders. Two genes in the deleted region, catechol-O-methyl-transferase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ea522a4d161f870304e7279b384142d
https://cris.maastrichtuniversity.nl/en/publications/e74b2b87-ab2e-4491-a7a3-be39fdbb7af5
https://cris.maastrichtuniversity.nl/en/publications/e74b2b87-ab2e-4491-a7a3-be39fdbb7af5
Autor:
Mariken B, de Koning, Esther D A, van Duin, Erik, Boot, Oswald J N, Bloemen, Jaap A, Bakker, Kathryn M, Abel, Thérèse A M J, van Amelsvoort
Publikováno v:
Psychopharmacology. 232(17)
22q11 deletion syndrome (22q11DS) is associated with an increased risk for psychotic disorders, suggesting a relationship between genotypes and the pathophysiology of psychotic disorders. Two genes in the deleted region, catechol-O-methyl-transferase
Autor:
Joris Vermeesch, M. Cristina Digilio, Nicole Philip, Doron Gothelf, Anne S. Bassett, Anna Blonska, Elizabeth Goldmuntz, H. Richard Johnston, Tao Wang, Leila Kushan-Wells, Carrie E. Bearden, B Dallapiccola, Therese van Amelsvoort, Wanda Hawuła, Elaine H. Zackai, Elisabeth E. Mlynarski, S Eliez, Gabriela M. Repetto, Amy E. Roberts, Elena Michaelovsky, Aoy Tomita-Mitchell, Tony J. Simon, Esther D. A. van Duin, Michael E. Mitchell, Donna M. McDonald McGinn, Eva W.C. Chow, Stylianos E. Antonarakis, Ann Swillen, Hiroko Nomaru, Flora Tassone, Małgorzata Piotrowicz, Laura E. Mitchell, David J. Cutler, Maude Schneider, Bruno Marino, A. J. Agopian, Tiffany Busa, Wendy R. Kates, Beverly S. Emanuel, Tingwei Guo, Bernice E. Morrow, Miri Carmel, Christopher L. Campbell, Karlene Coleman, Jonathan H. Chung, K Devriendt
Publikováno v:
Circulation. Cardiovascular Genetics
Circulation: Cardiovascular Genetics, Vol. 10, No 5 (2017)
Circulation : Cardiovascular Genetics, 10(5):e001690. LIPPINCOTT WILLIAMS & WILKINS
Circulation: Cardiovascular Genetics, Vol. 10, No 5 (2017)
Circulation : Cardiovascular Genetics, 10(5):e001690. LIPPINCOTT WILLIAMS & WILKINS
Supplemental Digital Content is available in the text.
Background— The 22q11.2 deletion syndrome (22q11.2DS; DiGeorge syndrome/velocardiofacial syndrome) occurs in 1 of 4000 live births, and 60% to 70% of affected individuals have congenital h
Background— The 22q11.2 deletion syndrome (22q11.2DS; DiGeorge syndrome/velocardiofacial syndrome) occurs in 1 of 4000 live births, and 60% to 70% of affected individuals have congenital h
Autor:
Esther D. A. van Duin, Thomas Vaessen, Felix M. Mottaghy, T. van Amelsvoort, Henrietta Steinhart, Michael J. Frank, I. Myin-Germeys, Jan Booij, Zuzana Kasanova, Jenny Ceccarini
Publikováno v:
European Neuropsychopharmacology. 27:S896