Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Szabolics Szelinger"'
Autor:
Erin N. Smith, Cinnamon S. Bloss, Tatiana Foroud, Howard J. Edenberg, Paul D. Shilling, David Craig, Sebastian Zöllner, William A. Scheftner, Elliot S. Gershon, John I. Nurnberger, James B. Potash, William Coryell, Peng Zhang, Nicholas J. Schork, Szabolics Szelinger, Melvin G. McInnis, Sherri Liang, Judith A. Badner, Evaristus A. Nwulia, John P. Rice, Thomas B. Barrett, Maria Hipolito, Pamela B. Mahon, William Lawson, Chunyu Liu, Daniel L. Koller, William Byerley, Francis J. McMahon, Wade H. Berrettini, Peter P. Zandi, John R. Kelsoe, Caroline M. Nievergelt, Tiffany A. Greenwood, Thomas G. Schulze, Stephanie Nissen, Rebecca McKinney, Tatyana Shehktman
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :941-950
We have previously reported genome-wide significant linkage of bipolar disorder to a region on 22q12.3 near the marker D22S278. Towards identifying the susceptibility gene, we have conducted a fine-mapping association study of the region in two indep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d3a892193e10733f090edbc641fee0b
https://doi.org/10.1002/ajmg.b.32099
https://doi.org/10.1002/ajmg.b.32099
Autor:
William Lawson, John R. Kelsoe, Sebastian Zöllner, William A. Scheftner, John I. Nurnberger, Eric R. Gamazon, Rebecca McKinney, Thomas B. Barrett, Maria Hipolito, Szabolics Szelinger, Chunling Zhang, Erin N. Smith, Nancy J. Cox, William Byerley, Howard J. Edenberg, Dandan Zhang, Judith A. Badner, Caroline M. Nievergelt, Francis J. McMahon, Thomas G. Schulze, William Coryell, Daniel L. Koller, Nicholas J. Schork, T. Foroud, Melvin G. McInnis, Cinnamon S. Bloss, James B. Potash, Tiffany A. Greenwood, Peng Zhang, Wade H. Berrettini, Peter P. Zandi, Elliot S. Gershon, Lijun Cheng, Chunyu Liu, Paul D. Shilling, David Craig, Evaristus A. Nwulia, Chao Chen, John P. Rice, Pamela B. Mahon
Publikováno v:
Molecular psychiatry
We conducted a systematic study of top susceptibility variants from a genome-wide association (GWA) study of bipolar disorder to gain insight into the functional consequences of genetic variation influencing disease risk. We report here the results o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc7024a106be8832dc62d3049f3f7c14
https://doi.org/10.1038/mp.2011.174
https://doi.org/10.1038/mp.2011.174
Autor:
William Lawson, Sebastian Zöllner, Peter P. Zandi, Rebecca McKinney, Evaritus A. Nwulia, Tiffany A. Greenwood, Wade H. Berrettini, John I. Nurnberger, William Byerley, Thomas G. Schulze, Maria Hipolito, Elliot S. Gershon, Francis J. McMahon, Ney Alliey-Rodriguez, Erin N. Smith, James B. Potash, Caroline M. Nievergelt, Susan L. Christian, Tatiana Foroud, Szabolics Szelinger, William Sheftner, John P. Rice, Nicholas J. Schork, Dandan Zhang, Pamela L. Belmonte, Melvin G. McInnis, Howard J. Edenberg, David Craig, William Coryell, Cinnamon S. Bloss, Lijun Cheng, Chunyu Liu, Thomas B. Barrett, Daniel L. Koller, John R. Kelsoe, Yudong Qian
Publikováno v:
Molecular Psychiatry. 14:376-380
An overall burden of rare structural genomic variants has not been reported in bipolar disorder (BD), although there have been reports of cases with microduplication and microdeletion. Here, we present a genome-wide copy number variant (CNV) survey o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d34dc6749737a0269b29b398c698cd9
https://doi.org/10.1038/mp.2008.144
https://doi.org/10.1038/mp.2008.144
Autor:
Kaya K. Jacobsen, Caroline M. Nievergelt, Tetyana Zayats, Tiffany A. Greenwood, Verneri Anttila, Hagop S. Akiskal, Jan Haavik, Ole Bernt Fasmer, John R. Kelsoe, Stefan Johansson, Ketil J. Oedegaard, Rebecca McKinney, Paul D. Shilling, Erin N. Smith, Nicholas J. Schork, Cinnamon S. Bloss, John I. Nurnberger, Howard J. Edenberg, Tatiana Foroud, Daniel L. Koller, Elliot S. Gershon, Judith A. Badner, Chunyu Liu, William A. Scheftner, William B. Lawson, Evaristus A. Nwulia, Maria Hipolito, James Potash, William Coryell, John Rice, William Byerley, Francis J. McMahon, Wade H. Berrettini, Peter P. Zandi, Pamela B. Mahon, Melvin G. McInnis, Sebastian Zöllner, Peng Zhang, David W. Craig, Szabolics Szelinger, Thomas B. Barrett, Thomas G. Schulze, Juho Wedenoja, Mari A. Kaunisto, Kauko Heikkilä, Jaakko Kaprio, Maija Wessman, Mikko Kallela, Markus Färkkilä, Ville Artto, Arpo Aromaa, Johan G. Eriksson, Bendik S. Winsvold, John-Anker Zwart, Padhraig Gormley, Aarno Palotie, Tobias Kurth, Lynda M. Rose, Julie E. Buring, Paul M. Ridker, Daniel I. Chasman, Francesco Bettella, Stacy Steinberg, Hreinn Stefansson, Kari Stefansson, George McMahon, George Davey-Smith, Rainer Malik, Tobias Freilinger, Heinz Erich Wichmann, Martin Dichgans, Bertram Muller-Myhsok, Thomas Meitinger, Boukje de Vries, Gisela Terwindt, Anine H. Stam, Rune R. Frants, Nadine Pelzer, Claudia M. Weller, Ronald Zielman, Michel D. Ferrari, Arn M.J.M. van den Maagdenberg, Sarah E. Medland, Grant W. Montgomery, Nicholas G. Martin, Dale R. Nyholt, Unda Todt, Guntram Borck, Christian Kubisch, Lydia Quaye, Frances M.K. Williams, Lynn Cherkas, Markku Koiranen, Anna-Liisa Hartikainen, Anneli Pouta, Marjo-Riitta Jarvelin, M. Arfan Ikram, Joyce van den Ende, Andre G. Uitterlinden, Albert Hofman, Najaf Amin, Cornelia van Duijn, Terho Lehtimäki, Lannie Ligthart, Jouke-Jan Hottenga, Jacqueline M. Vink, Brenda W. Penninx, Dorret I. Boomsma, Markus Schürks, Finnbogi Jakobsson, Jean Schoenen, Andrew C. Heath, Pamela A.F. Madden, Hartmut Göbel, Axel Heinze, Katja Heinze-Kuhn, Stefan Schreiber, Mark J. Daly, Michael Alexander, Olli Raitakari, David P. Strachan
Publikováno v:
Jacobsen, K K, Nievergelt, C M, Zayats, T, Greenwood, T A, Anttila, V, Akiskal, H S, Ligthart, R S L, Hottenga, J J, Vink, J M, Penninx, B W J H, Boomsma, D I, Haavik, J, Fasmer, O B, Kelsoe, J R, Johansson, S & Oedegaard, K J 2015, ' Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder ', Journal of Affective Disorders, vol. 172, pp. 453-461 . https://doi.org/10.1016/j.jad.2014.10.004
Journal of Affective Disorders, 172, 453-461. Elsevier
Jacobsen, K K, Nievergelt, C M, Zayats, T, Greenwood, T A, Anttila, V, Akiskal, H S, Ligthart, L, Hottenga, J J, Vink, J M, Penninx, B W J H, Boomsma, D I, Haavik, J, Fasmer, O B, Kelsoe, J R, Johansson, S & Oedegaard, K J 2015, ' Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder ', Journal of Affective Disorders, vol. 172, pp. 453-461 . https://doi.org/10.1016/j.jad.2014.10.004
Journal of Affective Disorders, 172, 453-461. Elsevier
Jacobsen, K K, Nievergelt, C M, Zayats, T, Greenwood, T A, Anttila, V, Akiskal, H S, Ligthart, L, Hottenga, J J, Vink, J M, Penninx, B W J H, Boomsma, D I, Haavik, J, Fasmer, O B, Kelsoe, J R, Johansson, S & Oedegaard, K J 2015, ' Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder ', Journal of Affective Disorders, vol. 172, pp. 453-461 . https://doi.org/10.1016/j.jad.2014.10.004
Background Migraine is a common comorbidity among individuals with bipolar disorder, but the underlying mechanisms for this co-occurrence are poorly understood. The aim of this study was to investigate the genetic background of bipolar patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f60f6bf6631a01a769965c7db4360e86
https://research.vumc.nl/en/publications/c0b993d5-332a-4e34-b94d-ce3910bc8e93
https://research.vumc.nl/en/publications/c0b993d5-332a-4e34-b94d-ce3910bc8e93
Autor:
Keith D. Coon, Jon Valla, Richard J. Caselli, Rebecca F. Halperin, Andreas Papassotiropoulos, Lonnie Schneider, Tracy L. Niedzielko, Travis Dunckley, John V. Pearson, Dietrich A. Stephan, Szabolics Szelinger, Eric M. Reiman, Kevin M. Brown
Publikováno v:
Mitochondrion. 6:194-210
The role of mitochondrial dysfunction in the pathogenesis of Alzheimer's disease (AD) has been well documented. Though evidence for the role of mitochondria in AD seems incontrovertible, the impact of mitochondrial DNA (mtDNA) mutations in AD etiolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17fc2ffb14deae5998ec1b696f50c382
https://doi.org/10.1016/j.mito.2006.07.002
https://doi.org/10.1016/j.mito.2006.07.002
Autor:
Keith D. Coon, Jon Valla, Szabolics Szelinger, Lonnie E. Schneider, Tracy L. Niedzielko, Kevin M. Brown, John V. Pearson, Rebecca Halperin, Phillip Stafford, Andreas Papassotiropoulos, Richard J. Casseli, Eric M. Reiman, Dietrich A. Stephan
Publikováno v:
Mitochondrion. 6:266-267
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c518819df327a6c0bf05b3dac7268f7a
https://doi.org/10.1016/j.mito.2006.08.010
https://doi.org/10.1016/j.mito.2006.08.010
Autor:
Ashley N. Sigafoos, Salima El Chehadeh, Marcia C. Willing, Ela Akay, Florian Cherik, Anne-Marie E. Goyette, Vinodh Narayanan, Diane Masser-Frye, Catherine Karimov, Rhonda E. Schnur, Rebekah Bressi, Rhys H. Thomas, Gary D. Clark, Tina Barbaro-Dieber, Jill A. Rosenfeld, Carlos A. Bacino, Maria J. Guillen Sacoto, Laura Russell, Kristin Lindstrom, Caroline Schluth-Bolard, Xia Wang, Yvonne Hilhorst-Hofstee, Marcelo Vargas, Zehua Zhu, Ash Zawerton, Boris Keren, Mariëtte J.V. Hoffer, Isabelle Marey, Alice Poisson, Daphné Lehalle, Maries Joseph, Gaetan Lesca, Simon Zwolinski, Laurence Perrin, Rhoda Akilapa, Emilia K. Bijlsma, Christel Depienne, Amélie Piton, Claire G. Salter, Lucie Dupuis, Daryl A. Scott, Jolien S. Klein Wassink-Ruiter, Benjamin Cogné, Mathilde Nizon, Richard Chang, Kirsty McWalter, Myriam Srour, Perrine Charles, Anne-Claude Tabet, Natalie Canham, Sylvie Odent, Caroline Nava, Karl J. Clark, Elizabeth J. Bhoj, Jonathan Levy, Keri Ramsey, Yves Alembik, Lucia Ortega, Sophie Dupuis-Girod, Shoji Ichikawa, Christine Francannet, Marta Bertoli, Christèle Dubourg, Eric W. Klee, Ange-Line Bruel, Sebastien Moutton, Emily Fassi, Anthony Vandersteen, Abdul Haseeb, Antonina Wojcik, Patrick R. Blackburn, Lynne M. Bird, Patrick Rump, Véronique Lefebvre, Alma Kuechler, Sophie Nambot, Keren Machol, Cyril Mignot, Andreas Hartmann, Rossana Sanchez Russo, Erica H. Gerkes, Sylvie Jaillard, Roberto Mendoza-Londono, Trevor Cole, Pauline Monin
Publikováno v:
Genetics in Medicine
Genetics in Medicine, Nature Publishing Group, 2020, 22 (3), pp.524-537. ⟨10.1038/s41436-019-0657-0⟩
Genetics in medicine : official journal of the American College of Medical Genetics, vol 22, iss 3
Genetics in Medicine, 22(3), 524-537. Nature Publishing Group
Genet Med
Genetics in Medicine, 22(3), 524-537. NATURE PUBLISHING GROUP
Genetics in Medicine, Nature Publishing Group, 2020, 22 (3), pp.524-537. ⟨10.1038/s41436-019-0657-0⟩
Genetics in medicine : official journal of the American College of Medical Genetics, vol 22, iss 3
Genetics in Medicine, 22(3), 524-537. Nature Publishing Group
Genet Med
Genetics in Medicine, 22(3), 524-537. NATURE PUBLISHING GROUP
International audience; PURPOSE: Lamb-Shaffer syndrome (LAMSHF) is a neurodevelopmental disorder described in just over two dozen patients with heterozygous genetic alterations involving SOX5, a gene encoding a transcription factor regulating cell fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e572914cd3ed1c6195ff6874c9228a5a
https://doi.org/10.1038/s41436-019-0657-0
https://doi.org/10.1038/s41436-019-0657-0