Zobrazeno 1 - 10
of 69
pro vyhledávání: '"I. Strom"'
Burr hole craniostomy versus minicraniotomy in chronic subdural hematoma: a comparative cohort study
Autor:
S. Zolfaghari, J. Bartek, Jr., I. Strom, F. Djärf, S.-S. Wong, N. Ståhl, A.S. Jakola, H. Nittby Redebrandt
Publikováno v:
Brain and Spine, Vol 1, Iss , Pp 100640- (2021)
Externí odkaz:
https://doaj.org/article/bf1438caf401452099c1b8da66b3b5bd
Autor:
Ibrahim Muddasser, Anh H. M. Nguyen, Aaron I. Strom, Aaron M. Hardee, Bryan G. Pluid, David T. Anderson
Publikováno v:
The Journal of Physical Chemistry A. 127:2751-2764
Autor:
Hannah K, Wayment-Steele, Wipapat, Kladwang, Alexandra I, Strom, Jeehyung, Lee, Adrien, Treuille, Alex, Becka, Rhiju, Das
Publikováno v:
Nat Methods
Despite the popularity of computer-aided study and design of RNA molecules, little is known about the accuracy of commonly used structure modeling packages in tasks sensitive to ensemble properties of RNA. Here, we demonstrate that the EternaBench da
Autor:
Nora I. Strom, Christie L. Burton, Conrad Iyegbe, Talisa Silzer, Lilit Antonyan, René Pool, Mathieu Lemire, James J. Crowley, Jouke-Jan Hottenga, Volen Z. Ivanov, Henrik Larsson, Paul Lichtenstein, Patrik Magnusson, Christian Rück, Russell Schachar, Hei Man Wu, Danielle Cath, Jennifer Crosbie, David Mataix-Cols, Dorret I. Boomsma, Manuel Mattheisen, Sandra M. Meier, Dirk J.A. Smit, Paul D. Arnold
While 1-2% of individuals meet the criteria for a clinical diagnosis of obsessive-compulsive disorder (OCD), many more (∼15-40%) experience subclinical obsessive-compulsive symptoms (OCS) during their life. To characterize the genetic underpinnings
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9c54b882a94b86076c15a3bea67f55d
https://doi.org/10.1101/2022.11.30.22282898
https://doi.org/10.1101/2022.11.30.22282898
Autor:
Nora I. Strom, Dirk J. A. Smit, Talisa Silzer, Conrad Iyegbe, Christie L. Burton, René Pool, Mathieu Lemire, James J. Crowley, Jouke-Jan Hottenga, Volen Z. Ivanov, Henrik Larsson, Paul Lichtenstein, Patrik Magnusson, Christian Rück, Russell J. Schachar, Hei Man Wu, Sandra M. Meier, Jennifer Crosbie, Paul D. Arnold, Manuel Mattheisen, Dorret I. Boomsma, David Mataix-Cols, Danielle Cath
Hoarding Disorder (HD) is a mental disorder characterized by persistent difficulties discarding or parting with possessions, often resulting in cluttered living spaces, distress, and impairment. Its etiology is largely unknown, but twin studies sugge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95a7b56d2bfb30ef21800dbbe638058a
http://edoc.hu-berlin.de/18452/26955
http://edoc.hu-berlin.de/18452/26955
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-11 (2021)
Translational Psychiatry
Strom, N I, Soda, T, Mathews, C A & Davis, L K 2021, ' A dimensional perspective on the genetics of obsessive-compulsive disorder ', Translational Psychiatry, vol. 11, 401 . https://doi.org/10.1038/s41398-021-01519-z
Translational Psychiatry
Strom, N I, Soda, T, Mathews, C A & Davis, L K 2021, ' A dimensional perspective on the genetics of obsessive-compulsive disorder ', Translational Psychiatry, vol. 11, 401 . https://doi.org/10.1038/s41398-021-01519-z
This review covers recent findings in the genomics of obsessive-compulsive disorder (OCD), obsessive-compulsive symptoms, and related traits from a dimensional perspective. We focus on discoveries stemming from technical and methodological advances o
Autor:
Nora I. Strom, Dirk J.A. Smit, Talisa Silzer, Conrad Iyegbe, Christie L. Burton, René Pool, Mathieu Lemire, James J. Crowley, Jouke-Jan Hottenga, Volen Z. Ivanov, Henrik Larsson, Paul Lichtenstein, Patrik Magnusson, Christian Rück, Russell Schachar, Hei Man Wu, Sandra M. Meier, Jennifer Crosbie, Paul D. Arnold, Manuel Mattheisen, Dorret I. Boomsma, David Mataix-Cols, Danielle Cath
Hoarding Disorder (HD) is a mental disorder characterized by persistent difficulties discarding or parting with possessions, often resulting in cluttered living spaces, distress, and impairment. Its etiology is largely unknown, but twin studies sugge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9851d128aa0794943f8f498b2bd1fda2
https://doi.org/10.1101/2022.06.19.22276077
https://doi.org/10.1101/2022.06.19.22276077
Autor:
Manuel Mattheisen, Jakob Grove, Thomas D. Als, Joanna Martin, Georgios Voloudakis, Sandra Meier, Ditte Demontis, Jaroslav Bendl, Raymond Walters, Caitlin E. Carey, Anders Rosengren, Nora I. Strom, Mads Engel Hauberg, Biao Zeng, Gabriel Hoffman, Wen Zhang, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen, Esben Agerbo, Bru Cormand, Merete Nordentoft, Thomas Werge, Ole Mors, David M. Hougaard, Joseph D. Buxbaum, Stephen V. Faraone, Barbara Franke, Søren Dalsgaard, Preben B. Mortensen, Elise B. Robinson, Panos Roussos, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum
Publikováno v:
Nat Genet
Nature Genetics, 54, 1470-1478
Mattheisen, M, Grove, J, Als, T D, Martin, J, Voloudakis, G, Meier, S, Demontis, D, Bendl, J, Walters, R, Carey, C E, Rosengren, A, Strom, N I, Hauberg, M E, Zeng, B, Hoffman, G, Zhang, W, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Agerbo, E, Cormand, B, Nordentoft, M, Werge, T, Mors, O, Hougaard, D M, Buxbaum, J D, Faraone, S V, Franke, B, Dalsgaard, S, Mortensen, P B, Robinson, E B, Roussos, P, Neale, B M, Daly, M J & Børglum, A D 2022, ' Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups ', Nature Genetics, vol. 54, no. 10, pp. 1470-1478 . https://doi.org/10.1038/s41588-022-01171-3
Nature Genetics, 54, 10, pp. 1470-1478
Nature Genetics, 54, 1470-1478
Mattheisen, M, Grove, J, Als, T D, Martin, J, Voloudakis, G, Meier, S, Demontis, D, Bendl, J, Walters, R, Carey, C E, Rosengren, A, Strom, N I, Hauberg, M E, Zeng, B, Hoffman, G, Zhang, W, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Agerbo, E, Cormand, B, Nordentoft, M, Werge, T, Mors, O, Hougaard, D M, Buxbaum, J D, Faraone, S V, Franke, B, Dalsgaard, S, Mortensen, P B, Robinson, E B, Roussos, P, Neale, B M, Daly, M J & Børglum, A D 2022, ' Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups ', Nature Genetics, vol. 54, no. 10, pp. 1470-1478 . https://doi.org/10.1038/s41588-022-01171-3
Nature Genetics, 54, 10, pp. 1470-1478
Contains fulltext : 287469.pdf (Publisher’s version ) (Open Access) Attention-deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) are highly heritable neurodevelopmental conditions, with considerable overlap in their genetic et
Autor:
Danielle Posthuma, Bernie Devlin, Edna Grünblatt, Ying Wang, Daniele Cusi, Stephan Ruhrmann, Steven A. Rasmussen, Michael S. Breen, Julia Klawohn, Ana Gabriela Hounie, Aline S. Sampaio, Cristina Barlassina, Marta Ribasés, Jackson G. Thorp, Cynthia M. Bulik, Marco A. Grados, Dan J. Stein, Abby Fyer, Vladimir Coric, Martha J. Falkenstein, Stephanie Le Hellard, Behrang Mahjani, Nathaniel McGregor, Homero Vallada, Miguel Casas, Laurent F. Thomas, Janice Krasnow, Abraham Reichenberg, Donald W. Black, Gwyneth Zai, Norbert Kathmann, Manuel Mattheisen, Nicholas G. Martin, Jason W. Krompinger, Josep Antoni Ramos-Quiroga, Judith Becker Nissen, Helga Ask, Damiaan Denys, Carolina Cappi, Euripedes Constantino Miguel, O. Joseph Bienvenu, Bengt T. Fundin, Lisa Osiecki, Karin J. H. Verweij, Paul Sandor, Jeremy Veenstra-VanderWeele, Maureen Mulhern, Sarah E. Medland, David M. Hougaard, Lauren Erdman, Jan Haavik, James L. Kennedy, Christopher P. Walker, Jurjen J. Luykx, Tim B. Bigdeli, Ian M. Hickie, Nienke Vulink, Maurizio Turiel, Peter Falkai, Enda M. Byrne, Valentina Ciullo, Daniel A. Geller, Liang Kung-Yee, Miriam A. Schiele, Lambertus Klei, Götz Berberich, Thomas Werge, Brion S. Maher, Christie L. Burton, Julia M. Sealock, Sandra Meier, Bernadette Cullen, Stephan Ripke, Dorothy E. Grice, Richard Delorme, Ted Reichborn-Kjennerud, Dongmei Yu, Danielle C. Cath, Lili Milani, Abdel Abdellaoui, Andres Metspalu, María Soler Artigas, Maria Conceição do Rosário, Ole Mors, Brian P. Brennan, Barbara E. Stranger, Ann E. Pulver, Nora I. Strom, Joseph D. Buxbaum, Hans J. Grabe, Jens R. Wendland, Michael H. Bloch, Srdjan Djurovic, Raquel Rabionet, Angel Carracedo, Carlos N. Pato, Erika L. Nurmi, Janet L. Sobell, Kevin S. O’Connell, Michael Wagner, David R. Rosenberg, Jonathan R. I. Coleman, Jeremiah M. Scharf, Kerry J. Ressler, Jaakko Kaprio, Edwin H. Cook, Scott L. Rauch, Federica Piras, Merete Nordentoft, Christian Rück, Fabrizio Piras, John-Anker Zwart, Jason A. Elias, Christopher Pittenger, Lea K. Davis, Margaret A. Richter, Evonne McArthur, Bendik S. Winsvold, Yin Yao, James J. Crowley, David L. Pauls, Rosa Bosch, Xavier Estivil, Matthew Halvorsen, Adrian Camarena, Nancy L. Pedersen, Pino Alonso, Eric A. Storch, Bjarne Hansen, Helena Brentani, James T. McCracken, Jan Maerten Smit, Donald Hucks, Alexandra Havdahl, Gerome Breen, Christina M. Hultman, Benjamin M. Neale, Gregory L. Hanna, Mikael Landén, Christine Lochner, Dirk J.A. Smit, Fabio Macciardi, Carol A. Mathews, Nuria Lanzagorta, Laura G. Sloofman, Cristina Rodriguez-Fontenla, Michael A. Jenike, Michele T. Pato, Marion Leboyer, Humberto Nicolini, Anders D. Børglum, Maria Cristina Cavallini, Wei Guo, Benjamin D. Greenberg, Maiken Elvestad Gabrielsen, Magdalena Janecka, Mark A. Riddle, Paul S. Nestadt, Beatriz Camarena, Valsamma Eapen, Susanne Walitza, Jack Samuels, Fernando S. Goes, Nicole C.R. McLaughlin, S. Evelyn Stewart, Jennifer Reichert, Sven Sandin, Gerd Kvale, Katharina Domschke, Ole A. Andreassen, Elles de Schipper, Paul D. Arnold, Kristi Krebs, Zachary Gerring, Teemu Palviainen, Kathleen D. Askland, Alfredo Ramirez, James A. Knowles, Laura Bellodi, Kristen Hagen, Julia Boberg, Thomas V. Fernandez, Gerald Nestadt, John Piacentini, Jakob Grove, Eske M. Derks, Preben Bo Mortensen, Elinor K. Karlsson, Gianfranco Spalletta, David Mataix-Cols, Katharina Bey, Jonas Bybjerg-Grauholm
Obsessive-compulsive disorder (OCD) is a heritable disorder, but no definitive, replicated OCD susceptibility loci have yet been identified by any genome-wide association study (GWAS). Here, we report results from a GWAS in the largest OCD case-contr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c8180dd21a6e65014d2b62d43825d7f
https://doi.org/10.1101/2021.10.13.21261078
https://doi.org/10.1101/2021.10.13.21261078
Autor:
N. I. Strom, Jonas Bybjerg-Grauholm, Jakob Grove, Thomas Werge, P. B. Mortensen, Anders D. Børglum, T. Damm Als, Marie Bækvad-Hansen, James J. Crowley, Manuel Mattheisen, J. Becker Nissen, Matthew Halvorsen, Merete Nordentoft, Sandra Meier, David M. Hougaard, Ole Mors
Publikováno v:
Strom, N I, Grove, J, Meier, S M, Bækvad-Hansen, M, Becker Nissen, J, Damm Als, T, Halvorsen, M, Nordentoft, M, Mortensen, P B, Hougaard, D M, Werge, T, Mors, O, Børglum, A D, Crowley, J J, Bybjerg-Grauholm, J & Mattheisen, M 2021, ' Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis ', Frontiers in Genetics, vol. 12, 711624 . https://doi.org/10.3389/fgene.2021.711624
Among patients with obsessive-compulsive disorder (OCD), 65-85% manifest another psychiatric disorder concomitantly or at some other time point during their life. OCD is highly heritable, as are many of its comorbidities. A possible genetic heterogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac605308604a6d5703216727c69933ae
http://edoc.hu-berlin.de/18452/24163
http://edoc.hu-berlin.de/18452/24163