Tag neurogen [121 articles] Export

Recent papers classified by the tag neurogen.

	MicroRNA-206 Delays ALS Progression and Promotes Regeneration of Neuromuscular Synapses in Mice [My Copy] Science, Vol. 326, No. 5959. (11 December 2009), pp. 1549-1554. by Andrew H. Williams, Gregorio Valdez, Viviana Moresi, et al.Xiaoxia Qi, John McAnally, Jeffrey L. Elliott, Rhonda Bassel-Duby, Joshua R. Sanes, Eric N. Olson posted to neurogen mirna by daforerog on 2009-12-11 16:43:39 as along with 1 person and 1 group heliopais microRNA
	The collection and processing of human brain tissue for research. [My Copy] Cell and tissue banking, Vol. 9, No. 3. (September 2008), pp. 169-179. by H. J. Waldvogel, J. Y. Bullock, B. J. Synek, M. A. Curtis, W. M. van Roon-Mom, R. L. Faull posted to review parkinson neurogen brain ad by daforerog on 2009-11-20 17:24:40 as
	Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. [My Copy] Nature genetics, Vol. advance online publication (15 November 2009) by Wataru Satake, Yuko Nakabayashi, Ikuko Mizuta, et al.Yushi Hirota, Chiyomi Ito, Michiaki Kubo, Takahisa Kawaguchi, Tatsuhiko Tsunoda, Masahiko Watanabe, Atsushi Takeda, Hiroyuki Tomiyama, Kenji Nakashima, Kazuko Hasegawa, Fumiya Obata, Takeo Yoshikawa, Hideshi Kawakami, Saburo Sakoda, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho Murata, Yusuke Nakamura, Tatsushi Toda posted to parkinson neurogen humgen gwasneuro adpdgenrev by daforerog on 2009-11-20 11:04:39 as along with 2 people psique vplagnol
	Genome-wide association study reveals genetic risk underlying Parkinson's disease. [My Copy] Nature genetics, Vol. 41, No. 12. (15 December 2009), pp. 1308-1312. by Javier Simón-Sánchez, Claudia Schulte, Jose M. Bras, et al.Manu Sharma, J. Raphael Gibbs, Daniela Berg, Coro Paisan-Ruiz, Peter Lichtner, Sonja W. Scholz, Dena G. Hernandez, Rejko Krüger, Monica Federoff, Christine Klein, Alison Goate, Joel Perlmutter, Michael Bonin, Michael A. Nalls, Thomas Illig, Christian Gieger, Henry Houlden, Michael Steffens, Michael S. Okun, Brad A. Racette, Mark R. Cookson, Kelly D. Foote, Hubert H. Fernandez, Bryan J. Traynor, Stefan Schreiber, Sampath Arepalli, Ryan Zonozi, Katrina Gwinn, Marcel van der Brug, Grisel Lopez, Stephen J. Chanock, Arthur Schatzkin, Yikyung Park, Albert Hollenbeck, Jianjun Gao, Xuemei Huang, Nick W. Wood, Delia Lorenz, Günther Deuschl, Honglei Chen, Olaf Riess, John A. Hardy, Andrew B. Singleton, Thomas Gasser posted to parkinson neurogen humgen gwasneuro gwas adpdgenrev by daforerog on 2009-11-20 10:59:18 as along with 3 people ahollenbeck psique vplagnol
	The heritability and genetics of frontotemporal lobar degeneration. [My Copy] Neurology, Vol. 73, No. 18. (3 November 2009), pp. 1451-1456. by J. D. Rohrer, R. Guerreiro, J. Vandrovcova, et al.J. Uphill, D. Reiman, J. Beck, A. M. Isaacs, A. Authier, R. Ferrari, N. C. Fox, I. R. Mackenzie, J. D. Warren, R. de Silva, J. Holton, T. Revesz, J. Hardy, S. Mead, M. N. Rossor posted to neurogen humgen heritability ftd by daforerog on 2009-11-03 11:34:00 as along with 2 people applebyb giovanni
	Alzheimer's disease. [My Copy] Lancet, Vol. 368, No. 9533. (29 July 2006), pp. 387-403. by Kaj Blennow, Mony J. de Leon, Henrik Zetterberg posted to review neuropsygen neurogen ad by daforerog on 2009-10-27 14:07:59 as along with 2 people and 1 group aip giovanni GeschwindLab
	Distinct genetic forms of frontotemporal dementia. [My Copy] Neurology, Vol. 71, No. 16. (14 October 2008), pp. 1220-1226. by H. Seelaar, W. Kamphorst, S. M. Rosso, et al.A. Azmani, R. Masdjedi, I. de Koning, J. A. Maat-Kievit, B. Anar, L. Donker Kaat, G. J. Breedveld, D. Dooijes, J. M. Rozemuller, I. F. Bronner, P. Rizzu, J. C. van Swieten posted to neurogen heritability ftd assoc by daforerog on 2009-10-23 16:51:18 as along with 2 people giovanni applebyb
	Prevalence of dementia and major dementia subtypes in Spanish populations: A reanalysis of dementia prevalence surveys, 1990-2008. [My Copy] BMC Neurology, Vol. 9, No. 1. (2009), 55. by Jesus de Pedro Cuesta, Javier V. Ortega, Saturio Vega, et al.Manuel S. Martinez, Pedro Saz, Fernanda Rodriguez, Angel R. Laso, Ramon Rene, Susana Perez de las Heras, Raimundo Mateos, Pablo M. Martin, Jose M. Manubens, Ignacio M. Fernandez, Secundino L. Pousa, Antonio Lobo, Jordi L. Regla, Jordi Gascon, Francisco J. Garcia, Manuel F. Martinez, Raquel Boix, Felix B. Pareja, Alberto Bergareche, Julian Benito, Ana de Arce, Jose Luis del Barrio posted to prevalence popul neurogen ad by daforerog on 2009-10-20 11:05:42 as
	The Pain Genes Database: An interactive web browser of pain-related transgenic knockout studies. [My Copy] Pain, Vol. 131, No. 1-2. (September 2007), pp. 3.e1-3.e4. by Michael L. Lacroix-Fralish, Jean B. Ledoux, Jeffrey S. Mogil posted to silico phenomics neurogen mining by daforerog on 2009-10-19 16:28:06 as
	Four Decades of Neurodegenerative Disease Research: How Far We Have Come! [My Copy] J. Neurosci., Vol. 29, No. 41. (14 October 2009), pp. 12722-12728. by Anne B. Young posted to synaptic review neurogen brain ad by daforerog on 2009-10-15 17:25:07 as
	A genome-wide linkage and association scan reveals novel loci for autism. [My Copy] Nature, Vol. 461, No. 7265. (8 October 2009), pp. 802-808. by Lauren A. Weiss, Dan E. Arking, Gene Discovery Project of Johns Hopkins & the Autism Consortium, Mark J. Daly, Aravinda Chakravarti posted to synaptic neuropsygen neurogen humgen gwasneuro gwas autism by daforerog on 2009-10-09 10:47:15 as along with 4 people and 1 group wangngu ns6 Terkko fenghezi Journal picks
	Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease. [My Copy] PloS one, Vol. 3, No. 7. (2008) by Yonghong Li, Charles Rowland, Georgia Xiromerisiou, et al.Robert J. Lagier, Steven J. Schrodi, Efthimios Dradiotis, David Ross, Nam Bui, Joseph Catanese, Konstantinos Aggelakis, Andrew Grupe, Georgios Hadjigeorgiou posted to synaptic parkinson neurogen humgen assoc adpdgenrev by daforerog on 2009-10-02 10:58:37 as
	Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. [My Copy] Journal of Alzheimer's disease : JAD (11 September 2009) by Erin L. Heinzen, Anna C. Need, Kathleen M. Hayden, et al.Ornit Chiba-Falek, Allen D. Roses, Warren J. Strittmatter, James R. Burke, Christine M. Hulette, Kathleen A. Welsh-Bohmer, David B. Goldstein posted to neurogen humgen gwasneuro gwas find cnv assoc adpdgenrev ad by daforerog on 2009-09-30 21:58:02 as
	Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate alpha-secretase activity. [My Copy] Human molecular genetics (15 July 2009) by Minji Kim, Jaehong Suh, Donna Romano, et al.Mimy H. Truong, Kristina Mullin, Basavaraj Hooli, David Norton, Giuseppina Tesco, Kathy Elliott, Steven L. Wagner, Robert D. Moir, K. David Becker, Rudolph E. Tanzi posted to nssnps neurogen humgen assoc ad by daforerog on 2009-09-23 15:57:51 as
	Genomewide Association Study for Onset Age in Parkinson Disease. [My Copy] BMC medical genetics, Vol. 10, No. 1. (22 September 2009), 98. by Jeanne C. Latourelle, Nathan Pankratz, Alexandra Dumitriu, et al.Jemma B. Wilk, Stefano Goldwurm, Gianni Pezzoli, Claudio B. Mariani, Anita L. Destefano, Cheryl Halter, James F. Gusella, William C. Nichols, Richard H. Myers, Tatiana Foroud, Psg-Progeni Investigators And P. Coordinators, Psg-Progeni Molecular Genetic P. Laboratory, Genepd Investigators And I. Coordinators, Genepd Molecular Genetics M. Laboratories posted to parkinson neurogen humgen gwasneuro gwas adpdgenrev by daforerog on 2009-09-23 14:54:11 as along with 1 person psique
	The LRRK2 G2019S mutation as the cause of Parkinson's disease in Ashkenazi Jews. [My Copy] Journal of neural transmission (Vienna, Austria : 1996) (15 September 2009) by Avner Thaler, Elissa Ash, Ziv Gan-Or, Avi Orr-Urtreger, Nir Giladi posted to review parkinson neurogen humgen by daforerog on 2009-09-21 13:21:11 as
	LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay. [My Copy] Parkinsonism & related disorders, Vol. 15, No. 5. (June 2009), pp. 370-373. by Ignacio F. Mata, Carlos Cosentino, Victoria Marca, et al.Luis Torres, Pilar Mazzetti, Olimpio Ortega, Victor Raggio, Ruth Aljanati, Ricardo Buzó, Dora Yearout, Elena Dieguez, Cyrus P. Zabetian posted to parkinson nssnps neurola neurogen humgen by daforerog on 2009-09-21 12:19:02 as
	Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. [My Copy] Journal of medical genetics, Vol. 45, No. 11. (November 2008), pp. 710-720. by D. A. Koolen, A. J. Sharp, J. A. Hurst, et al.H. V. Firth, S. J. Knight, A. Goldenberg, P. Saugier-Veber, R. Pfundt, L. E. Vissers, A. Destrée, B. Grisart, L. Rooms, N. Van der Aa, M. Field, A. Hackett, K. Bell, M. J. Nowaczyk, G. M. Mancini, P. J. Poddighe, C. E. Schwartz, E. Rossi, M. De Gregori, L. L. Antonacci-Fulton, M. D. McLellan, J. M. Garrett, M. A. Wiechert, T. L. Miner, S. Crosby, R. Ciccone, L. Willatt, A. Rauch, M. Zenker, S. Aradhya, M. A. Manning, T. M. Strom, J. Wagenstaller, A. C. Krepischi-Santos, A. M. Vianna-Morgante, C. Rosenberg, S. M. Price, H. Stewart, C. Shaw-Smith, H. G. Brunner, A. O. Wilkie, J. A. Veltman, O. Zuffardi, E. E. Eichler, B. B. de Vries posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:59:40 as
	A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. [My Copy] Nature genetics, Vol. 38, No. 9. (13 September 2006), pp. 999-1001. by David A. Koolen, Lisenka E. Vissers, Rolph Pfundt, et al.Nicole de Leeuw, Samantha J. Knight, Regina Regan, R. Frank Kooy, Edwin Reyniers, Corrado Romano, Marco Fichera, Albert Schinzel, Alessandra Baumer, Britt-Marie M. Anderlid, Jacqueline Schoumans, Nine V. Knoers, Ad Geurts G. van Kessel, Erik A. Sistermans, Joris A. Veltman, Han G. Brunner, Bert B. de Vries posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:56:36 as
	Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. [My Copy] Nature genetics, Vol. 38, No. 9. (13 September 2006), pp. 1038-1042. by Andrew J. Sharp, Sierra Hansen, Rebecca R. Selzer, et al.Ze Cheng, Regina Regan, Jane A. Hurst, Helen Stewart, Sue M. Price, Edward Blair, Raoul C. Hennekam, Carrie A. Fitzpatrick, Rick Segraves, Todd A. Richmond, Cheryl Guiver, Donna G. Albertson, Daniel Pinkel, Peggy S. Eis, Stuart Schwartz, Samantha J. Knight, Evan E. Eichler posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:53:42 as along with 1 person waszak
	Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2. [My Copy] Nature genetics, Vol. 39, No. 9. (19 September 2007), pp. 1071-1073. by Blake C. Ballif, Sara A. Hornor, Elizabeth Jenkins, et al.Suneeta Madan-Khetarpal, Urvashi Surti, Kelly E. Jackson, Alexander Asamoah, Pamela L. Brock, Gordon C. Gowans, Robert L. Conway, John M. Graham, Livija Medne, Elaine H. Zackai, Tamim H. Shaikh, Joel Geoghegan, Rebecca R. Selzer, Peggy S. Eis, Bassem A. Bejjani, Lisa G. Shaffer posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:37:01 as
	De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy. [My Copy] Annals of neurology, Vol. 65, No. 6. (June 2009), pp. 748-753. by Fadi F. Hamdan, Amélie Piton, Julie Gauthier, et al.Anne Lortie, François Dubeau, Sylvia Dobrzeniecka, Dan Spiegelman, Anne Noreau, Stéphanie Pellerin, Mélanie Côté, Edouard Henrion, Eric Fombonne, Laurent Mottron, Claude Marineau, Pierre Drapeau, Ronald G. Lafrenière, Jean Claude C. Lacaille, Guy A. Rouleau, Jacques L. Michaud posted to synaptic neurogen mr humgen epilep brainmut by daforerog on 2009-09-14 15:58:39 as
	Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. [My Copy] Journal of medical genetics, Vol. 46, No. 8. (21 August 2009), pp. 511-523. by B. W. van Bon, H. C. Mefford, B. Menten, et al.D. A. Koolen, A. J. Sharp, W. M. Nillesen, J. W. Innis, T. J. de Ravel, C. L. Mercer, M. Fichera, H. Stewart, L. E. Connell, K. Ounap, K. Lachlan, B. Castle, N. Van der Aa, C. van Ravenswaaij, M. A. Nobrega, C. Serra-Juhé, I. Simonic, N. de Leeuw, R. Pfundt, E. M. Bongers, C. Baker, P. Finnemore, S. Huang, V. K. Maloney, J. A. Crolla, M. van Kalmthout, M. Elia, G. Vandeweyer, J. P. Fryns, S. Janssens, N. Foulds, S. Reitano, K. Smith, S. Parkel, B. Loeys, C. G. Woods, A. Oostra, F. Speleman, A. C. Pereira, A. Kurg, L. Willatt, S. J. Knight, J. R. Vermeesch, C. Romano, J. C. Barber, G. Mortier, L. A. Pérez-Jurado, F. Kooy, H. G. Brunner, E. E. Eichler, T. Kleefstra, B. B. de Vries posted to neurogen mr humgen cnv by daforerog on 2009-09-14 14:01:28 as along with 1 person bmenten
	A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. [My Copy] Nature genetics, Vol. 40, No. 3. (17 March 2008), pp. 322-328. by Andrew J. Sharp, Heather C. Mefford, Kelly Li, et al.Carl Baker, Cindy Skinner, Roger E. Stevenson, Richard J. Schroer, Francesca Novara, Manuela De Gregori, Roberto Ciccone, Adam Broomer, Iris Casuga, Yu Wang, Chunlin Xiao, Catalin Barbacioru, Giorgio Gimelli, Bernardo Dalla D. Bernardina, Claudia Torniero, Roberto Giorda, Regina Regan, Victoria Murday, Sahar Mansour, Marco Fichera, Lucia Castiglia, Pinella Failla, Mario Ventura, Zhaoshi Jiang, Gregory M. Cooper, Samantha J. Knight, Corrado Romano, Orsetta Zuffardi, Caifu Chen, Charles E. Schwartz, Evan E. Eichler posted to neuropsygen neurogen mr humgen epilep cnv by daforerog on 2009-09-14 13:57:07 as
	15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. [My Copy] Nature genetics, Vol. 41, No. 2. (11 February 2009), pp. 160-162. by Ingo Helbig, Heather C. Mefford, Andrew J. Sharp, et al.Michel Guipponi, Marco Fichera, Andre Franke, Hiltrud Muhle, Carolien de Kovel, Carl Baker, Sarah von Spiczak, Katherine L. Kron, Ines Steinich, Ailing A. Kleefuss-Lie, Costin Leu, Verena Gaus, Bettina Schmitz, Karl M. Klein, Philipp S. Reif, Felix Rosenow, Yvonne Weber, Holger Lerche, Fritz Zimprich, Lydia Urak, Karoline Fuchs, Martha Feucht, Pierre Genton, Pierre Thomas, Frank Visscher, Gerrit-Jan J. de Haan, Rikke S. Møller, Helle Hjalgrim, Daniela Luciano, Michael Wittig, Michael Nothnagel, Christian E. Elger, Peter Nürnberg, Corrado Romano, Alain Malafosse, Bobby P. Koeleman, Dick Lindhout, Ulrich Stephani, Stefan Schreiber, Evan E. Eichler, Thomas Sander posted to neurogen humgen epilep cnv assoc by daforerog on 2009-09-14 13:30:12 as
	Familial and sporadic 15q13.3 microdeletions in Idiopathic Generalized Epilepsy: Precedent for Disorders with Complex Inheritance. [My Copy] Human molecular genetics (10 July 2009) by Leanne M. Dibbens, Saul Mullen, Ingo Helbig, et al.Heather C. Mefford, Marta A. Bayly, Susannah Bellows, Costin Leu, Holger Trucks, Tanja Obermeier, Michael Wittig, Andre Franke, Hande Caglayan, Zuhal Yapici, EPICURE Consortium, Thomas Sander, Evan E. Eichler, Ingrid E. Scheffer, John C. Mulley, Samuel F. Berkovic posted to neurogen humgen genomics epilep cnv by daforerog on 2009-09-14 12:41:09 as
	Identification of novel susceptibility loci for Guam neurodegenerative disease: Challenges of genome scans in genetic isolates. [My Copy] Human molecular genetics (30 June 2009) by Weiva Sieh, Yoonha Choi, Nicola H. Chapman, et al.Ulla-Katrina K. Craig, Ellen J. Steinbart, Joseph H. Rothstein, Kiyomitsu Oyanagi, Ralph M. Garruto, Thomas D. Bird, Douglas R. Galasko, Gerard D. Schellenberg, Ellen M. Wijsman posted to parkinson neurogen linkage humgen ad by daforerog on 2009-09-14 12:25:46 as
	Molecular cytogenetics and cytogenomics of brain diseases. [My Copy] Current genomics, Vol. 9, No. 7. (November 2008), pp. 452-465. by I. Y. Iourov, S. G. Vorsanova, Y. B. Yurov posted to review psychgen neuropsygen neurogen humgen genomics cnv brain by daforerog on 2009-09-14 09:49:01 as
	EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias. [My Copy] European journal of neurology : the official journal of the European Federation of Neurological Societies, Vol. 16, No. 7. (July 2009), pp. 777-785. by H. F. Harbo, J. Finsterer, J. Baets, et al.C. Van Broeckhoven, S. Di Donato, B. Fontaine, P. De Jonghe, A. Lossos, T. Lynch, C. Mariotti, L. Schöls, A. Spinazzola, Z. Szolnoki, S. J. Tabrizi, C. Tallaksen, M. Zeviani, J-M M. Burgunder, T. Gasser, EFNS posted to parkinson neurogen motordis humgen highly genotyping genomics by daforerog on 2009-09-11 16:53:42 as
	Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His. [My Copy] Neurology, Vol. 73, No. 8. (25 August 2009), pp. 626-632. by J. van der Zee, D. Pirici, T. Van Langenhove, et al.S. Engelborghs, R. Vandenberghe, M. Hoffmann, G. Pusswald, M. Van den Broeck, K. Peeters, M. Mattheijssens, J-J J. Martin, P. P. De Deyn, M. Cruts, D. Haubenberger, S. Kumar-Singh, A. Zimprich, C. Van Broeckhoven posted to neurogen humgen ftd by daforerog on 2009-09-08 12:46:16 as
	Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. [My Copy] Nature genetics, Vol. 41, No. 10. (06 October 2009), pp. 1088-1093. by Denise Harold, Richard Abraham, Paul Hollingworth, et al.Rebecca Sims, Amy Gerrish, Marian L. Hamshere, Jaspreet Singh S. Pahwa, Valentina Moskvina, Kimberley Dowzell, Amy Williams, Nicola Jones, Charlene Thomas, Alexandra Stretton, Angharad R. Morgan, Simon Lovestone, John Powell, Petroula Proitsi, Michelle K. Lupton, Carol Brayne, David C. Rubinsztein, Michael Gill, Brian Lawlor, Aoibhinn Lynch, Kevin Morgan, Kristelle S. Brown, Peter A. Passmore, David Craig, Bernadette McGuinness, Stephen Todd, Clive Holmes, David Mann, A. David Smith, Seth Love, Patrick G. Kehoe, John Hardy, Simon Mead, Nick Fox, Martin Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Britta Schürmann, Hendrik van den Bussche, Isabella Heuser, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frölich, Harald Hampel, Michael Hüll, Dan Rujescu, Alison M. Goate, John S. Kauwe, Carlos Cruchaga, Petra Nowotny, John C. Morris, Kevin Mayo, Kristel Sleegers, Karolien Bettens, Sebastiaan Engelborghs, Peter P. De Deyn, Christine Van Broeckhoven, Gill Livingston, Nicholas J. Bass, Hugh Gurling, Andrew McQuillin, Rhian Gwilliam, Panagiotis Deloukas, Ammar Al-Chalabi, Christopher E. Shaw, Magda Tsolaki, Andrew B. Singleton, Rita Guerreiro, Thomas W. Mühleisen, Markus M. Nöthen, Susanne Moebus, Karl-Heinz H. Jöckel, Norman Klopp, H-Erich E. Wichmann, Minerva M. Carrasquillo, V. Shane Pankratz, Steven G. Younkin, Peter A. Holmans, Michael O'Donovan, Michael J. Owen, Julie Williams posted to neuropsygen neurogen humgen gwasneuro assoc apoe adpdgenrev ad by daforerog on 2009-09-06 22:01:31 as along with 4 people jeremymiller vplagnol psique giovanni
	Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. [My Copy] Nature genetics, Vol. 41, No. 10. (06 October 2009), pp. 1094-1099. by Jean-Charles C. Lambert, Simon Heath, Gael Even, et al.Dominique Campion, Kristel Sleegers, Mikko Hiltunen, Onofre Combarros, Diana Zelenika, Maria J. Bullido, Béatrice Tavernier, Luc Letenneur, Karolien Bettens, Claudine Berr, Florence Pasquier, Nathalie Fiévet, Pascale Barberger-Gateau, Sebastiaan Engelborghs, Peter De Deyn, Ignacio Mateo, Ana Franck, Seppo Helisalmi, Elisa Porcellini, Olivier Hanon, European Alzheimer's Disease Initiative Investigators, Marian M. de Pancorbo, Corinne Lendon, Carole Dufouil, Céline Jaillard, Thierry Leveillard, Victoria Alvarez, Paolo Bosco, Michelangelo Mancuso, Francesco Panza, Benedetta Nacmias, Paola Bossù, Paola Piccardi, Giorgio Annoni, Davide Seripa, Daniela Galimberti, Didier Hannequin, Federico Licastro, Hilkka Soininen, Karen Ritchie, Hélène Blanché, Jean-François F. Dartigues, Christophe Tzourio, Ivo Gut, Christine Van Broeckhoven, Annick Alpérovitch, Mark Lathrop, Philippe Amouyel posted to neuropsygen neurogen humgen gwasneuro assoc apoe adpdgenrev ad by daforerog on 2009-09-06 22:00:27 as along with 3 people jeremymiller vplagnol giovanni
	'The quicksand of forgetfulness': semantic dementia in One Hundred Years of Solitude. [My Copy] Brain : a journal of neurology (15 May 2009) by Katya Rascovsky, Matthew E. Growdon, Isela R. Pardo, Scott Grossman, Bruce L. Miller posted to phenomics neurogen ftd by daforerog on 2009-08-27 12:20:36 as
	Schizophrenia. [My Copy] Lancet, Vol. 374, No. 9690. (22 August 2009), pp. 635-645. by Jim van Os, Shitij Kapur posted to review phenomics neuropsygen neurogen by daforerog on 2009-08-26 12:12:33 as
	Global prevalence of dementia: a Delphi consensus study. [My Copy] Lancet, Vol. 366, No. 9503. (17 December 2005), pp. 2112-2117. by Cleusa P. Ferri, Martin Prince, Carol Brayne, et al.Henry Brodaty, Laura Fratiglioni, Mary Ganguli, Kathleen Hall, Kazuo Hasegawa, Hugh Hendrie, Yueqin Huang, Anthony Jorm, Colin Mathers, Paulo R. Menezes, Elizabeth Rimmer, Marcia Scazufca, Alzheimer's Disease International posted to prevalence neuropsygen neurogen lab adpdgenrev ad by daforerog on 2009-08-24 14:16:19 as along with 1 person kerri3278
	Age at onset in two common neurodegenerative diseases is genetically controlled. [My Copy] American journal of human genetics, Vol. 70, No. 4. (April 2002), pp. 985-993. by Yi-Ju J. Li, William K. Scott, Dale J. Hedges, et al.Fengyu Zhang, P. Craig Gaskell, Martha A. Nance, Ray L. Watts, Jean P. Hubble, William C. Koller, Rajesh Pahwa, Matthew B. Stern, Bradley C. Hiner, Joseph Jankovic, Fred A. Allen, Christopher G. Goetz, Frank Mastaglia, Jeffrey M. Stajich, Rachel A. Gibson, Lefkos T. Middleton, Ann M. Saunders, Burton L. Scott, Gary W. Small, Kristin K. Nicodemus, Allison D. Reed, Donald E. Schmechel, Kathleen A. Welsh-Bohmer, P. Michael Conneally, Allen D. Roses, John R. Gilbert, Jeffery M. Vance, Jonathan L. Haines, Margaret A. Pericak-Vance posted to qtl parkinson neuropsygen neurogen humgen assoc ad by daforerog on 2009-08-11 21:07:51 as
	Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis. [My Copy] American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, Vol. 144B, No. 7. (5 October 2007), pp. 841-848. by P. Hollingworth, M. L. Hamshere, P. A. Holmans, et al.M. C. O'Donovan, Rebecca Sims, J. Powell, S. Lovestone, A. Myers, F. W. DeVrieze, J. Hardy, A. Goate, M. Owen, J. Williams posted to qtl neuropsygen neurogen ad by daforerog on 2009-08-11 21:01:15 as
	Functional brain abnormalities in young adults at genetic risk for late-onset Alzheimer's dementia. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 101, No. 1. (6 January 2004), pp. 284-289. by Eric M. Reiman, Kewei Chen, Gene E. Alexander, et al.Richard J. Caselli, Daniel Bandy, David Osborne, Ann M. Saunders, John Hardy posted to ad apoe behavior brain early neurogen neuropsygen qtl by daforerog on 2009-08-10 13:33:55 as
	Molecular Pathways of Neurodegeneration in Parkinson's Disease [My Copy] Science, Vol. 302, No. 5646. (31 October 2003), pp. 819-822. by Ted M. Dawson, Valina L. Dawson posted to review parkinson neuropsygen neurogen brain by daforerog on 2009-08-09 21:51:03 as along with 2 people jirak chemnerd1
	Parkinson disease, 10 years after its genetic revolution: multiple clues to a complex disorder. [My Copy] Neurology, Vol. 69, No. 22. (27 November 2007), pp. 2093-2104. by Christine Klein, Michael G. Schlossmacher posted to heritability humgen neurogen neuropsygen parkinson review by daforerog on 2009-08-09 19:23:58 as
	Genetic aspects of Alzheimer disease. [My Copy] Genetics in medicine : official journal of the American College of Medical Genetics, Vol. 10, No. 4. (April 2008), pp. 231-239. by Thomas D. Bird posted to ad genetics heritability neurogen neuropsygen review by daforerog on 2009-08-09 19:21:05 as along with 1 person applebyb
	Alzheimer's Disease [My Copy] N Engl J Med, Vol. 351, No. 1. (1 July 2004), pp. 56-67. by Jeffrey L. Cummings posted to review prevalence phenomics neuropsygen neurogen highly ad by daforerog on 2009-08-09 18:21:49 as along with 1 person amandaalders
	Parkinson's disease. [My Copy] Lancet, Vol. 373, No. 9680. (13 June 2009), pp. 2055-2066. by Andrew J. Lees, John Hardy, Tamas Revesz posted to highly neurogen neuropsygen parkinson phenomics review by daforerog on 2009-08-09 18:15:40 as
	A review of Parkinson's disease. [My Copy] British medical bulletin, Vol. 86 (2008), pp. 109-127. by C. A. Davie posted to brain highly neurogen neuropsygen parkinson phenomics review by daforerog on 2009-08-09 18:06:16 as
	The economic impact of Parkinson's disease. [My Copy] Parkinsonism & related disorders, Vol. 13 Suppl (September 2007) by Leslie J. Findley posted to prevalence phenomics parkinson neuropsygen neurogen by daforerog on 2009-08-09 17:35:01 as
	Costs of brain disorders in Finland. [My Copy] Acta neurologica Scandinavica, Vol. 117, No. 3. (March 2008), pp. 167-172. by M. Sillanpää, P. Andlin-Sobocki, J. Lönnqvist posted to prevalence phenomics neuropsygen neurogen by daforerog on 2009-08-09 17:33:56 as
	Burden of illness in Parkinson's disease. [My Copy] Movement disorders : official journal of the Movement Disorder Society, Vol. 20, No. 11. (November 2005), pp. 1449-1454. by Daniel M. Huse, Kathy Schulman, Lucinda Orsini, Jane Castelli-Haley, Sean Kennedy, Gregory Lenhart posted to prevalence phenomics parkinson neuropsygen neurogen adpdgenrev by daforerog on 2009-08-09 17:31:56 as
	An estimate of the total worldwide societal costs of dementia in 2005. [My Copy] Alzheimer's & dementia : the journal of the Alzheimer's Association, Vol. 3, No. 2. (April 2007), pp. 81-91. by Anders Wimo, Bengt Winblad, Linus Jönsson posted to prevalence phenomics neuropsygen neurogen adpdgenrev ad by daforerog on 2009-08-09 17:15:07 as
	An estimate of the worldwide prevalence and direct costs of dementia in 2003. [My Copy] Dementia and geriatric cognitive disorders, Vol. 21, No. 3. (2006), pp. 175-181. by A. Wimo, L. Jonsson, B. Winblad posted to ad adpdgenrev neurogen neuropsygen phenomics prevalence by daforerog on 2009-08-09 17:10:28 as
	Conjugal Alzheimer disease: risk in children when both parents have Alzheimer disease. [My Copy] Archives of neurology, Vol. 65, No. 3. (March 2008), pp. 373-378. by Suman Jayadev, Ellen J. Steinbart, Yueh-Yun Y. Chi, Walter A. Kukull, Gerard D. Schellenberg, Thomas D. Bird posted to ad assoc heritability neurogen by daforerog on 2009-08-07 17:28:30 as

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