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Anzahl der Publikationen: 7
Zeitschriftenartikel
Wang, Hui 
ORCID: https://orcid.org/0000-0003-4043-5060; Chang, Timothy S. ORCID: https://orcid.org/0000-0002-9225-9874; Dombroski, Beth A. ORCID: https://orcid.org/0000-0002-5334-1306; Cheng, Po‐Liang ORCID: https://orcid.org/0009-0007-0046-0313; Si, Ya‐Qin ORCID: https://orcid.org/0000-0002-9968-9754; Tucci, Albert ORCID: https://orcid.org/0000-0001-5703-7208; Patil, Vishakha; Valiente‐Banuet, Leopoldo; Li, Chong ORCID: https://orcid.org/0000-0003-1949-4074; Farrell, Kurt ORCID: https://orcid.org/0000-0001-6955-7278; Mclean, Catriona ORCID: https://orcid.org/0000-0002-0302-5727; Molina‐Porcel, Laura ORCID: https://orcid.org/0000-0003-4068-8578; Rajput, Alex ORCID: https://orcid.org/0000-0001-9656-318X; De Deyn, Peter Paul ORCID: https://orcid.org/0000-0002-2228-2964; Le Bastard, Nathalie ORCID: https://orcid.org/0000-0002-7981-2866; Gearing, Marla ORCID: https://orcid.org/0000-0002-1959-7412; Donker Kaat, Laura ORCID: https://orcid.org/0009-0007-2436-0931; Swieten, John C. Van ORCID: https://orcid.org/0000-0001-6278-6844; Dopper, Elise; Ghetti, Bernardino F. ORCID: https://orcid.org/0000-0002-1842-8019; Newell, Kathy L.; Troakes, Claire ORCID: https://orcid.org/0000-0002-1790-7376; Yébenes, Justo G. de ORCID: https://orcid.org/0000-0003-0452-3223; Rábano‐Gutierrez, Alberto; Meller, Tina ORCID: https://orcid.org/0000-0002-0239-6585; Oertel, Wolfgang H. ORCID: https://orcid.org/0000-0002-7582-8166; Respondek, Gesine ORCID: https://orcid.org/0000-0002-6851-6164; Stamelou, Maria; Arzberger, Thomas; Roeber, Sigrun; Müller, Ulrich; Hopfner, Franziska ORCID: https://orcid.org/0000-0001-6524-0281; Pastor, Pau ORCID: https://orcid.org/0000-0002-7493-8777; Brice, Alexis ORCID: https://orcid.org/0000-0002-0941-3990; Durr, Alexandra ORCID: https://orcid.org/0000-0002-8921-7104; Le Ber, Isabelle; Beach, Thomas G. ORCID: https://orcid.org/0000-0003-3296-6128; Serrano, Geidy E. ORCID: https://orcid.org/0000-0002-9527-2011; Hazrati, Lili‐Naz ORCID: https://orcid.org/0000-0003-2715-1485; Litvan, Irene ORCID: https://orcid.org/0000-0002-3485-3445; Rademakers, Rosa; Ross, Owen A. ORCID: https://orcid.org/0000-0003-4813-756X; Galasko, Douglas ORCID: https://orcid.org/0000-0001-6195-3241; Boxer, Adam L. ORCID: https://orcid.org/0000-0002-1215-5064; Miller, Bruce L. ORCID: https://orcid.org/0000-0002-2152-4220; Seeley, Willian W.; Deerlin, Vivianna M. Van ORCID: https://orcid.org/0000-0002-7400-9097; Lee, Edward B. ORCID: https://orcid.org/0000-0002-4589-1180; White, Charles L. ORCID: https://orcid.org/0000-0002-3870-2804; Morris, Huw R. ORCID: https://orcid.org/0000-0002-5473-3774; Silva, Rohan de; Crary, John F. ORCID: https://orcid.org/0000-0002-0556-293X; Goate, Alison M. ORCID: https://orcid.org/0000-0002-0576-2472; Friedman, Jeffrey S.; Compta, Yaroslau; Leung, Yuk Yee ORCID: https://orcid.org/0000-0002-3047-5440; Coppola, Giovanni; Naj, Adam C.; Wang, Li‐San ORCID: https://orcid.org/0000-0002-3684-0031; Dalgard, Clifton; Dickson, Dennis W. ORCID: https://orcid.org/0000-0001-7189-7917; Höglinger, Günter U. ORCID: https://orcid.org/0000-0001-7587-6187; Tzeng, Jung‐Ying ORCID: https://orcid.org/0000-0002-5505-1775; Geschwind, Daniel H.; Schellenberg, Gerard D. ORCID: https://orcid.org/0000-0003-1115-2475 und Lee, Wan‐Ping ORCID: https://orcid.org/0000-0002-5305-1181
(2025):
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells.
In: Movement Disorders [Forthcoming]
ORCID: https://orcid.org/0000-0003-4043-5060; Chang, Timothy S. ORCID: https://orcid.org/0000-0002-9225-9874; Dombroski, Beth A. ORCID: https://orcid.org/0000-0002-5334-1306; Cheng, Po‐Liang ORCID: https://orcid.org/0009-0007-0046-0313; Si, Ya‐Qin ORCID: https://orcid.org/0000-0002-9968-9754; Tucci, Albert ORCID: https://orcid.org/0000-0001-5703-7208; Patil, Vishakha; Valiente‐Banuet, Leopoldo; Li, Chong ORCID: https://orcid.org/0000-0003-1949-4074; Farrell, Kurt ORCID: https://orcid.org/0000-0001-6955-7278; Mclean, Catriona ORCID: https://orcid.org/0000-0002-0302-5727; Molina‐Porcel, Laura ORCID: https://orcid.org/0000-0003-4068-8578; Rajput, Alex ORCID: https://orcid.org/0000-0001-9656-318X; De Deyn, Peter Paul ORCID: https://orcid.org/0000-0002-2228-2964; Le Bastard, Nathalie ORCID: https://orcid.org/0000-0002-7981-2866; Gearing, Marla ORCID: https://orcid.org/0000-0002-1959-7412; Donker Kaat, Laura ORCID: https://orcid.org/0009-0007-2436-0931; Swieten, John C. Van ORCID: https://orcid.org/0000-0001-6278-6844; Dopper, Elise; Ghetti, Bernardino F. ORCID: https://orcid.org/0000-0002-1842-8019; Newell, Kathy L.; Troakes, Claire ORCID: https://orcid.org/0000-0002-1790-7376; Yébenes, Justo G. de ORCID: https://orcid.org/0000-0003-0452-3223; Rábano‐Gutierrez, Alberto; Meller, Tina ORCID: https://orcid.org/0000-0002-0239-6585; Oertel, Wolfgang H. ORCID: https://orcid.org/0000-0002-7582-8166; Respondek, Gesine ORCID: https://orcid.org/0000-0002-6851-6164; Stamelou, Maria; Arzberger, Thomas; Roeber, Sigrun; Müller, Ulrich; Hopfner, Franziska ORCID: https://orcid.org/0000-0001-6524-0281; Pastor, Pau ORCID: https://orcid.org/0000-0002-7493-8777; Brice, Alexis ORCID: https://orcid.org/0000-0002-0941-3990; Durr, Alexandra ORCID: https://orcid.org/0000-0002-8921-7104; Le Ber, Isabelle; Beach, Thomas G. ORCID: https://orcid.org/0000-0003-3296-6128; Serrano, Geidy E. ORCID: https://orcid.org/0000-0002-9527-2011; Hazrati, Lili‐Naz ORCID: https://orcid.org/0000-0003-2715-1485; Litvan, Irene ORCID: https://orcid.org/0000-0002-3485-3445; Rademakers, Rosa; Ross, Owen A. ORCID: https://orcid.org/0000-0003-4813-756X; Galasko, Douglas ORCID: https://orcid.org/0000-0001-6195-3241; Boxer, Adam L. ORCID: https://orcid.org/0000-0002-1215-5064; Miller, Bruce L. ORCID: https://orcid.org/0000-0002-2152-4220; Seeley, Willian W.; Deerlin, Vivianna M. Van ORCID: https://orcid.org/0000-0002-7400-9097; Lee, Edward B. ORCID: https://orcid.org/0000-0002-4589-1180; White, Charles L. ORCID: https://orcid.org/0000-0002-3870-2804; Morris, Huw R. ORCID: https://orcid.org/0000-0002-5473-3774; Silva, Rohan de; Crary, John F. ORCID: https://orcid.org/0000-0002-0556-293X; Goate, Alison M. ORCID: https://orcid.org/0000-0002-0576-2472; Friedman, Jeffrey S.; Compta, Yaroslau; Leung, Yuk Yee ORCID: https://orcid.org/0000-0002-3047-5440; Coppola, Giovanni; Naj, Adam C.; Wang, Li‐San ORCID: https://orcid.org/0000-0002-3684-0031; Dalgard, Clifton; Dickson, Dennis W. ORCID: https://orcid.org/0000-0001-7189-7917; Höglinger, Günter U. ORCID: https://orcid.org/0000-0001-7587-6187; Tzeng, Jung‐Ying ORCID: https://orcid.org/0000-0002-5505-1775; Geschwind, Daniel H.; Schellenberg, Gerard D. ORCID: https://orcid.org/0000-0003-1115-2475 und Lee, Wan‐Ping ORCID: https://orcid.org/0000-0002-5305-1181
(2025):
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells.
In: Movement Disorders [Forthcoming]
Hopfner, Franziska; Tietz, Anja K.; Ruf, Viktoria C.; Ross, Owen A.; Koga, Shunsuke; Dickson, Dennis; Aguzzi, Adriano; Attems, Johannes; Beach, Thomas; Beller, Allison; Cheshire, William P.; Deerlin, Vivianna van; Desplats, Paula; Deuschl, Guenther; Duyckaerts, Charles; Ellinghaus, David; Evsyukov, Valentin; Flanagan, Margaret Ellen; Franke, Andre; Frosch, Matthew P.; Gearing, Marla; Gelpi, Ellen; Gerpen, Jay A. van; Ghetti, Bernardino; Glass, Jonathan D.; Grinberg, Lea T.; Halliday, Glenda; Helbig, Ingo; Hollerhage, Matthias; Huitinga, Inge; Irwin, David John; Keene, Dirk C.; Kovacs, Gabor G.; Lee, Edward B.; Levin, Johannes; Marti, Maria J.; Mackenzie, Ian; McKeith, Ian; Mclean, Catriona; Mollenhauer, Brit; Neumann, Manuela; Newell, Kathy L.; Pantelyat, Alex; Pendziwiat, Manuela; Peters, Annette; Porcel, Laura Molina; Rabano, Alberto; Matej, Radoslav; Rajput, Alex; Rajput, Ali; Reimann, Regina; Scott, William K.; Seeley, William; Selvackadunco, Sashika; Simuni, Tanya; Stadelmann, Christine; Svenningsson, Per; Thomas, Alan; Trenkwalder, Claudia; Troakes, Claire; Trojanowski, John Q.; Uitti, Ryan J.; White, Charles L.; Wszolek, Zbigniew K.; Xie, Tao; Ximelis, Teresa; Yebenes, Justo; Mueller, Ulrich; Schellenberg, Gerard D.; Herms, Jochen; Kuhlenbaumer, Gregor und Hoeglinger, Gunter
(2022):
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy.
In: Movement Disorders, Bd. 37, Nr. 10: S. 2110-2121
[PDF, 2MB]
Cali, Christopher P.; Patino, Maribel; Tai, Yee Kit; Ho, Wan Yun; McLean, Catriona A.; Morris, Christopher M.; Seeley, William W.; Miller, Bruce L.; Gaig, Carles; Vonsattel, Jean Paul G.; White, Charles L.; Roeber, Sigrun; Kretzschmar, Hans; Troncoso, Juan C.; Troakes, Claire; Gearing, Marla; Ghetti, Bernardino; Deerlin, Vivianna M. van; Lee, Virginia M-Y; Trojanowski, John Q.; Mok, Kin Y.; Ling, Helen; Dickson, Dennis W.; Schellenberg, Gerard D.; Ling, Shuo-Chien und Lee, Edward B.
(2019):
C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy.
In: Acta Neuropathologica, Bd. 138, Nr. 5: S. 795-811
Pottier, Cyril; Ren, Yingxue; Perkerson, Ralph B.; Baker, Matt; Jenkins, Gregory D.; Blitterswijk, Marka van; DeJesus-Hernandez, Mariely; van Rooij, Jeroen G. J.; Murray, Melissa E.; Christopher, Elizabeth; McDonnell, Shannon K.; Fogarty, Zachary; Batzler, Anthony; Tian, Shulan; Vicente, Cristina T.; Matchett, Billie; Karydas, Anna M.; Hsiung, Ging-Yuek Robin; Seelaar, Harro; Mol, Merel O.; Finger, Elizabeth C.; Graff, Caroline; Oijerstedt, Linn; Neumann, Manuela; Heutink, Peter; Synofzik, Matthis; Wilke, Carlo; Prudlo, Johannes; Rizzu, Patrizia; Simon-Sanchez, Javier; Edbauer, Dieter; Roeber, Sigrun; Diehl-Schmid, Janine; Evers, Bret M.; King, Andrew; Mesulam, M. Marsel; Weintraub, Sandra; Geula, Changiz; Bieniek, Kevin F.; Petrucelli, Leonard; Ahern, Geoffrey L.; Reiman, Eric M.; Woodruff, Bryan K.; Caselli, Richard J.; Huey, Edward D.; Farlow, Martin R.; Grafman, Jordan; Mead, Simon; Grinberg, Lea T.; Spina, Salvatore; Grossman, Murray; Irwin, David J.; Lee, Edward B.; Suh, EunRan; Snowden, Julie; Mann, David; Ertekin-Taner, Nilufer; Uitti, Ryan J.; Wszolek, Zbigniew K.; Josephs, Keith A.; Parisi, Joseph E.; Knopman, David S.; Petersen, Ronald C.; Hodges, John R.; Piguet, Olivier; Geier, Ethan G.; Yokoyama, Jennifer S.; Rissman, Robert A.; Rogaeva, Ekaterina; Keith, Julia; Zinman, Lorne; Tartaglia, Maria Carmela; Cairns, Nigel J.; Cruchaga, Carlos; Ghetti, Bernardino; Kofler, Julia; Lopez, Oscar L.; Beach, Thomas G.; Arzberger, Thomas; Herms, Jochen; Honig, Lawrence S.; Vonsattel, Jean Paul; Halliday, Glenda M.; Kwok, John B.; White, Charles L.; Gearing, Marla; Glass, Jonathan; Rollinson, Sara; Pickering-Brown, Stuart; Rohrer, Jonathan D.; Trojanowski, John Q.; Van Deerlin, Vivianna; Bigio, Eileen H.; Troakes, Claire; Al-Sarraj, Safa; Asmann, Yan; Miller, Bruce L.; Graff-Radford, Neill R.; Boeve, Bradley F.; Seeley, William W.; Mackenzie, Ian R. A.; van Swieten, John C.; Dickson, Dennis W.; Biernacka, Joanna M. und Rademakers, Rosa
(2019):
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.
In: Acta Neuropathologica, Bd. 137, Nr. 6: S. 879-899
[PDF, 1MB]
Kovacs, Gabor G.; Ferrer, Isidro; Grinberg, Lea T.; Alafuzoff, Irina; Attems, Johannes; Budka, Herbert; Cairns, Nigel J.; Crary, John F.; Duyckaerts, Charles; Ghetti, Bernardino; Halliday, Glenda M.; Ironside, James W.; Love, Seth; Mackenzie, Ian R.; Munoz, David G.; Murray, Melissa E.; Nelson, Peter T.; Takahashi, Hitoshi; Trojanowski, John Q.; Ansorge, Olaf; Arzberger, Thomas; Baborie, Atik; Beach, Thomas G.; Bieniek, Kevin F.; Bigio, Eileen H.; Bodi, Istvan; Dugger, Brittany N.; Feany, Mel; Gelpi, Ellen; Gentleman, Stephen M.; Giaccone, Giorgio; Hatanpaa, Kimmo J.; Heale, Richard; Hof, Patrick R.; Hofer, Monika; Hortobágyi, Tibor; Jellinger, Kurt; Jicha, Gregory A.; Ince, Paul; Kofler, Julia; Kövari, Enikö; Kril, Jillian J.; Mann, David M.; Matej, Radoslav; McKee, Ann C.; McLean, Catriona; Milenkovic, Ivan; Montine, Thomas J.; Murayama, Shigeo; Lee, Edward B.; Rahimi, Jasmin; Rodriguez, Roberta D.; Rozemüller, Annemieke; Schneider, Julie A.; Schultz, Christian; Seeley, William; Seilhean, Danielle; Smith, Colin; Tagliavini, Fabrizio; Takao, Masaki; Thal, Dietmar Rudolf; Toledo, Jon B.; Tolnay, Markus; Troncoso, Juan C.; Vinters, Harry V.; Weis, Serge; Wharton, Stephen B.; White, Charles L.; Wisniewski, Thomas; Woulfe, John M.; Yamada, Masahito und Dickson, Dennis W.
(2016):
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy.
In: Acta Neuropathologica, Bd. 131, Nr. 1: S. 87-102
Ligocki, Ann J.; Rivas, Jacqueline R.; Rounds, William H.; Guzman, Alyssa A.; Li, Min; Spadaro, Melania; Lahey, Lauren; Chen, Ding; Henson, Paul M.; Graves, Donna; Greenberg, Benjamin M.; Frohman, Elliot M.; Ward, E. Sally; Robinson, William; Meinl, Edgar; White, Charles L.; Stowe, Ann M. und Monson, Nancy L.
(2015):
A Distinct Class of Antibodies May Be an Indicator of Gray Matter Autoimmunity in Early and Established Relapsing Remitting Multiple Sclerosis Patients.
In: Asn Neuro, Bd. 7, Nr. 5
[PDF, 3MB]
Kouri, Naomi; Ross, Owen A.; Dombroski, Beth; Younkin, Curtis S.; Serie, Daniel J.; Soto-Ortolaza, Alexandra; Baker, Matthew; Finch, Ni Cole A.; Yoon, Hyejin; Kim, Jungsu; Fujioka, Shinsuke; McLean, Catriona A.; Ghetti, Bernardino; Spina, Salvatore; Cantwell, Laura B.; Farlow, Martin R.; Grafman, Jordan; Huey, Edward D.; Han, Mi Ryung; Beecher, Sherry; Geller, Evan T.; Kretzschmar, Hans A.; Roeber, Sigrun; Gearing, Marla; Juncos, Jorge L.; Vonsattel, Jean Paul G.; Deerlin, Vivianna M. van; Grossman, Murray; Hurtig, Howard I.; Gross, Rachel G.; Arnold, Steven E.; Trojanowski, John Q.; Lee, Virginia M.; Wenning, Gregor K.; White, Charles L.; Hoeglinger, Gunter U.; Mueller, Ulrich; Devlin, Bernie; Golbe, Lawrence I.; Crook, Julia; Parisi, Joseph E.; Boeve, Bradley F.; Josephs, Keith A.; Wszolek, Zbigniew K.; Uitti, Ryan J.; Graff-Radford, Neill R.; Litvan, Irene; Younkin, Steven G.; Wang, Li-San; Ertekin-Taner, Niluefer; Rademakers, Rosa; Hakonarsen, Hakon; Schellenberg, Gerard D. und Dickson, Dennis W.
(2015):
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
In: Nature Communications, Bd. 6, 7247
[PDF, 729kB]