giovanni's library 1019 articles Export

	Knockdown of transactive response DNA-binding protein (TDP-43) downregulates histone deacetylase 6. [My Copy] The EMBO journal (12 November 2009) by Fabienne C. Fiesel, Aaron Voigt, Stephanie S. Weber, et al.Chris Van den Haute, Andrea Waldenmaier, Karin Görner, Michael Walter, Marlene L. Anderson, Jeannine V. Kern, Tobias M. Rasse, Thorsten Schmidt, Wolfdieter Springer, Roland Kirchner, Michael Bonin, Manuela Neumann, Veerle Baekelandt, Marianna Alunni-Fabbroni, Jörg B. Schulz, Philipp J. Kahle posted to tdp43 by giovanni on 2009-11-17 13:24:47 as
	Unexpected development of artistic talents [My Copy] Postgrad Med J, Vol. 81, No. 962. (1 December 2005), pp. 753-755. by N. Gordon posted to artistic_creativity by giovanni on 2009-11-09 14:05:03 as
	Art, alpha-1-antitrypsin polymorphisms and intense creative energy: blessing or curse? [My Copy] Neurotoxicology, Vol. 28, No. 5. (September 2007), pp. 899-914. by Donald Everett E. Schmechel posted to artistic_creativity by giovanni on 2009-11-09 13:57:25 as
	Musical aptitude is associated with AVPR1A-haplotypes. [My Copy] PloS one, Vol. 4, No. 5. (2009) by Liisa T. Ukkola, Päivi Onkamo, Pirre Raijas, Kai Karma, Irma Järvelä posted to artistic_creativity by giovanni on 2009-11-09 13:56:35 as along with 1 person Terkko
	Emergence of artistic talent in frontotemporal dementia. [My Copy] Neurology, Vol. 51, No. 4. (October 1998), pp. 978-982. by B. L. Miller, J. Cummings, F. Mishkin, et al.K. Boone, F. Prince, M. Ponton, C. Cotman posted to ftd art by giovanni on 2009-11-09 13:54:34 as
	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 ftd by giovanni on 2009-11-02 22:20:57 as along with 2 people applebyb daforerog
	Genetic diagnosis by whole exome capture and massively parallel DNA sequencing. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 106, No. 45. (10 November 2009), pp. 19096-19101. by Murim Choi, Ute I. Scholl, Weizhen Ji, et al.Tiewen Liu, Irina R. Tikhonova, Paul Zumbo, Ahmet Nayir, Ayşin Bakkaloğlu, Seza Ozen, Sami Sanjad, Carol Nelson-Williams, Anita Farhi, Shrikant Mane, Richard P. Lifton posted to sequencing exome by giovanni on 2009-10-28 12:13:25 as along with 5 people daforerog liqbbi pst Peiyong chvlyl
	Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants. [My Copy] Human molecular genetics, Vol. 16, No. 8. (15 April 2007), pp. 865-873. by Andrew Grupe, Richard Abraham, Yonghong Li, et al.Charles Rowland, Paul Hollingworth, Angharad Morgan, Luke Jehu, Ricardo Segurado, David Stone, Eric Schadt, Maha Karnoub, Petra Nowotny, Kristina Tacey, Joseph Catanese, John Sninsky, Carol Brayne, David Rubinsztein, Michael Gill, Brian Lawlor, Simon Lovestone, Peter Holmans, Michael O'Donovan, John C. Morris, Leon Thal, Alison Goate, Michael J. Owen, Julie Williams posted to gwas alzheimer by giovanni on 2009-10-25 18:39:59 as along with 1 person daforerog
	A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. [My Copy] The Journal of clinical psychiatry, Vol. 68, No. 4. (April 2007), pp. 613-618. by Keith D. Coon, Amanda J. Myers, David W. Craig, et al.Jennifer A. Webster, John V. Pearson, Diane Hu H. Lince, Victoria L. Zismann, Thomas G. Beach, Doris Leung, Leslie Bryden, Rebecca F. Halperin, Lauren Marlowe, Mona Kaleem, Douglas G. Walker, Rivka Ravid, Christopher B. Heward, Joseph Rogers, Andreas Papassotiropoulos, Eric M. Reiman, John Hardy, Dietrich A. Stephan posted to gwas alzheimer by giovanni on 2009-10-25 18:39:24 as along with 2 people daforerog jo_davies
	GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. [My Copy] Neuron, Vol. 54, No. 5. (7 June 2007), pp. 713-720. by Eric M. Reiman, Jennifer A. Webster, Amanda J. Myers, et al.John Hardy, Travis Dunckley, Victoria L. Zismann, Keta D. Joshipura, John V. Pearson, Diane Hu-Lince, Matthew J. Huentelman, David W. Craig, Keith D. Coon, Winnie S. Liang, RiLee H. Herbert, Thomas Beach, Kristen C. Rohrer, Alice S. Zhao, Doris Leung, Leslie Bryden, Lauren Marlowe, Mona Kaleem, Diego Mastroeni, Andrew Grover, Christopher B. Heward, Rivka Ravid, Joseph Rogers, Michael L. Hutton, Stacey Melquist, Ron C. Petersen, Gene E. Alexander, Richard J. Caselli, Walter Kukull, Andreas Papassotiropoulos, Dietrich A. Stephan posted to gwas alzheimer by giovanni on 2009-10-25 18:37:10 as along with 1 person daforerog
	Genome screen of late-onset Alzheimer's extended pedigrees identifies TRPC4AP by haplotype analysis. [My Copy] American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, Vol. 150B, No. 1. (5 January 2009), pp. 50-55. by S. E. Poduslo, R. Huang, J. Huang, S. Smith posted to alzheimer_association by giovanni on 2009-10-25 18:36:30 as
	A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. [My Copy] BMC medical genomics, Vol. 1 (2008) by Richard Abraham, Valentina Moskvina, Rebecca Sims, et al.Paul Hollingworth, Angharad Morgan, Lyudmila Georgieva, Kimberley Dowzell, Sven Cichon, Axel M. Hillmer, Michael C. O'Donovan, Julie Williams, Michael J. Owen, George Kirov posted to gwas alzheimer by giovanni on 2009-10-25 18:35:57 as along with 2 people psique daforerog
	Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. [My Copy] American journal of human genetics, Vol. 84, No. 1. (30 January 2009), pp. 35-43. by Gary W. Beecham, Eden R. Martin, Yi-Ju J. Li, et al.Michael A. Slifer, John R. Gilbert, Jonathan L. Haines, Margaret A. Pericak-Vance posted to gwas alzheimer by giovanni on 2009-10-25 18:34:52 as along with 1 person daforerog
	Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease [My Copy] Nature Genetics, Vol. 41, No. 2. (11 January 2009), pp. 192-198. by Minerva M. Carrasquillo, Fanggeng Zou, V. Shane Pankratz, et al.Samantha L. Wilcox, Li Ma, Louise P. Walker, Samuel G. Younkin, Curtis S. Younkin, Linda H. Younkin, Gina D. Bisceglio, Nilufer Ertekin-Taner, Julia E. Crook, Dennis W. Dickson, Ronald C. Petersen, Neill R. Graff-Radford, Steven G. Younkin posted to gwas alzheimer by giovanni on 2009-10-25 18:34:32 as along with 2 people psique daforerog
	Exon sequences at the splice junctions affect splicing fidelity and alternative splicing [My Copy] Proceedings of the National Academy of Sciences (23 October 2009) by Luciana B. Crotti, David S. Horowitz posted to splicing sequencing by giovanni on 2009-10-24 17:41:08 as
	FUS-Immunoreactive Intranuclear Inclusions in Neurodegenerative Disease. [My Copy] Brain pathology (Zurich, Switzerland) (21 September 2009) by John Woulfe, Douglas A. Gray, Ian R. Mackenzie posted to fus by giovanni on 2009-10-18 14:13:35 as
	A simple and efficient algorithm for genome-wide homozygosity analysis in disease. [My Copy] Molecular systems biology, Vol. 5 (15 September 2009) by Wei Liu, Jinhui Ding, Jesse Raphael R. Gibbs, Sue Jane J. Wang, John Hardy, Andrew Singleton posted to snp_ibd by giovanni on 2009-10-15 13:16:27 as along with 3 people psique reyez daforerog
	Disease signatures are robust across tissues and experiments [My Copy] Molecular Systems Biology, Vol. 5 (15 September 2009) by Joel T. Dudley, Robert Tibshirani, Tarangini Deshpande, Atul J. Butte posted to microarray biomarkers by giovanni on 2009-10-15 13:14:58 as along with 13 people tmmurali grahamc renatomilani ptrobajo zufar jclau klo mingzhi ngehlenborg dswan winterschlaefer daforerog brianb
	Visualization of <I>MAPT</I> inversion on stretched chromosomes of tau-negative frontotemporal dementia patients [My Copy] Human Mutation, Vol. 27, No. 10. (2006), pp. 1057-1059. by Ilse Gijselinck, Veerle Bogaerts, Rosa Rademakers, Julie van der Zee, Christine Van Broeckhoven, Marc Cruts posted to mapt_haplotype by giovanni on 2009-10-14 14:32:19 as
	Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region [My Copy] Hum. Mol. Genet., Vol. 14, No. 13. (1 July 2005), pp. 1753-1762. by Marc Cruts, Rosa Rademakers, Ilse Gijselinck, et al.Julie van der Zee, Bart Dermaut, Tim de Pooter, Peter de Rijk, Jurgen Del-Favero, Christine van Broeckhoven posted to mapt_haplotype by giovanni on 2009-10-14 14:29:26 as
	A common inversion under selection in Europeans. [My Copy] Nature genetics, Vol. 37, No. 2. (16 February 2005), pp. 129-137. by Hreinn Stefansson, Agnar Helgason, Gudmar Thorleifsson, et al.Valgerdur Steinthorsdottir, Gisli Masson, John Barnard, Adam Baker, Aslaug Jonasdottir, Andres Ingason, Vala G. Gudnadottir, Natasa Desnica, Andrew Hicks, Arnaldur Gylfason, Daniel F. Gudbjartsson, Gudrun M. Jonsdottir, Jesus Sainz, Kari Agnarsson, Birgitta Birgisdottir, Shyamali Ghosh, Adalheidur Olafsdottir, Jean-Baptiste B. Cazier, Kristleifur Kristjansson, Michael L. Frigge, Thorgeir E. Thorgeirsson, Jeffrey R. Gulcher, Augustine Kong, Kari Stefansson posted to mapt_haplotype by giovanni on 2009-10-14 14:26:39 as along with 4 people vplagnol daforerog APRegier kndiaye
	The architecture of the tau haplotype block in different ethnicities [My Copy] Neuroscience Letters, Vol. 377, No. 2. (29 March 2005), pp. 81-84. by H. Fung, J. Evans, W. Evans, et al.J. Duckworth, A. Pittman, R. DeSilva, A. Myers, J. Hardy posted to mapt_haplotype by giovanni on 2009-10-14 14:22:50 as
	High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy [My Copy] Hum. Mol. Genet., Vol. 14, No. 21. (1 November 2005), pp. 3281-3292. by Rosa Rademakers, Stacey Melquist, Marc Cruts, et al.Jessie Theuns, Jurgen Del-Favero, Parvoneh Poorkaj, Matt Baker, Kristel Sleegers, Richard Crook, Tim De Pooter, Samira B. Kacem, Jennifer Adamson, Dirk Van den Bossche, Marleen Van den Broeck, Jennifer Gass, Ellen Corsmit, Peter De Rijk, Natalie Thomas, Sebastiaan Engelborghs, Michael Heckman, Irene Litvan, Julia Crook, Peter P. De Deyn, Dennis Dickson, Gerard D. Schellenberg, Christine Van Broeckhoven, Michael L. Hutton posted to mapt_haplotype by giovanni on 2009-10-14 14:20:15 as
	Evolutionary toggling of the MAPT 17q21.31 inversion region. [My Copy] Nature genetics, Vol. 40, No. 9. (September 2008), pp. 1076-1083. by Michael C. Zody, Zhaoshi Jiang, Hon-Chung C. Fung, et al.Francesca Antonacci, LaDeana W. Hillier, Maria Francesca F. Cardone, Tina A. Graves, Jeffrey M. Kidd, Ze Cheng, Amr Abouelleil, Lin Chen, John Wallis, Jarret Glasscock, Richard K. Wilson, Amy Denise D. Reily, Jaime Duckworth, Mario Ventura, John Hardy, Wesley C. Warren, Evan E. Eichler posted to mapt_haplotype by giovanni on 2009-10-14 13:56:14 as along with 2 people daforerog fenghezi
	From 1997 to 2007: a decade journey through the H1 haplotype on 17q21 chromosome. [My Copy] Parkinsonism & related disorders, Vol. 15, No. 1. (January 2009), pp. 2-5. by Kallirhoe Kalinderi, Liana Fidani, Sevasti Bostantjopoulou posted to mapt_haplotype by giovanni on 2009-10-14 13:53:43 as
	Recent progress in Frontotemporal lobar degeneration. [My Copy] Neuropathology and applied neurobiology (10 October 2009) by Stuart M. Pickering-Brown posted to ftd_review by giovanni on 2009-10-14 13:51:51 as
	The resolution of the genetics of gene expression [My Copy] Hum. Mol. Genet., Vol. 18, No. R2. (15 October 2009), pp. R211-215. by Stephen B. Montgomery, Emmanouil T. Dermitzakis posted to genetics_genomics by giovanni on 2009-10-13 14:00:35 as along with 3 people and 1 group rcr1991 lp2 sbmontgomery Journal picks
	Genome-wide association studies in Alzheimer's disease [My Copy] Hum. Mol. Genet., Vol. 18, No. R2. (15 October 2009), pp. R137-145. by Lars Bertram, Rudolph E. Tanzi posted to review gwas alzheimer_association by giovanni on 2009-10-13 13:59:59 as along with 2 people daforerog mwilcox
	Predicting functional regulatory polymorphisms [My Copy] Bioinformatics, Vol. 24, No. 16. (15 August 2008), pp. 1787-1792. by Ali Torkamani, Nicholas J. Schork posted to snp by giovanni on 2009-10-13 13:55:35 as along with 4 people greg guhjy ramensky djkt
	Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb). [My Copy] Human mutation (6 October 2009) by Ivy Jennes, Elena Pedrini, Monia Zuntini, et al.Marina Mordenti, Sahila Balkassmi, Carla G. Asteggiano, Brett Casey, Bert Bakker, Luca Sangiorgi, Wim Wuyts posted to ext2 by giovanni on 2009-10-10 13:51:29 as
	Rapid inexpensive genome-wide association using pooled whole blood. [My Copy] Genome research, Vol. 19, No. 11. (3 October 2009), pp. 2075-2080. by Jamie E. Craig, Alex W. Hewitt, Amy E. McMellon, et al.Anjali K. Henders, Lingjun Ma, Leanne Wallace, Shiwani Sharma, Kathryn P. Burdon, Peter M. Visscher, Grant W. Montgomery, Stuart Macgregor posted to snp_pool snp by giovanni on 2009-10-07 13:57:02 as along with 5 people daforerog neils rdiaz natstreet merpublic
	Genetic variants in AVPR1A linked to autism predict amygdala activation and personality traits in healthy humans [My Copy] Molecular Psychiatry, Vol. 14, No. 10. (20 May 2008), pp. 968-975. by A. Meyer-Lindenberg, B. Kolachana, B. Gold, et al.A. Olsh, K. K. Nicodemus, V. Mattay, M. Dean, D. R. Weinberger posted to avpr1a by giovanni on 2009-09-29 17:35:58 as
	Genetic Variants of the α-Synuclein Gene SNCA Are Associated with Multiple System Atrophy [My Copy] PLoS ONE, Vol. 4, No. 9. (22 September 2009), e7114. by Ammar Al-Chalabi, Alexandra Dürr, Nicholas W. Wood, et al.Michael H. Parkinson, Agnes Camuzat, Jean-Sébastien Hulot, Karen E. Morrison, Alan Renton, Sigurd D. Sussmuth, Bernhard G. Landwehrmeyer, Albert Ludolph, Yves Agid, Alexis Brice, P. Nigel Leigh, Gilbert Bensimon, for the NNIPPS Genetic Study Group posted to snp snca msa by giovanni on 2009-09-23 23:34:26 as
	Transcriptional Profiling of the Dose Response: A More Powerful Approach for Characterizing Drug Activities [My Copy] PLoS Comput Biol, Vol. 5, No. 9. (18 September 2009), e1000512. by Rui-Ru Ji, Heshani de Silva, Yisheng Jin, et al.Robert E. Bruccoleri, Jian Cao, Aiqing He, Wenjun Huang, Paul S. Kayne, Isaac M. Neuhaus, Karl-Heinz Ott, Becky Penhallow, Mark I. Cockett, Michael G. Neubauer, Nathan O. Siemers, Petra Ross-Macdonald posted to methods dose_response by giovanni on 2009-09-18 17:34:38 as along with 3 people klexa mingzhi kshameer
	Automated multidimensional phenotypic profiling using large public microarray repositories. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 106, No. 30. (28 July 2009), pp. 12323-12328. by Min Xu, Wenyuan Li, Gareth M. James, Michael R. Mehan, Xianghong Jasmine J. Zhou posted to classifier by giovanni on 2009-09-12 01:50:34 as along with 8 people zufar tmmurali Borelli rdiaz guhjy TRHvidsten yaredo ptrobajo
	A Systems Genetics Approach Implicates USF1, FADS3, and Other Causal Candidate Genes for Familial Combined Hyperlipidemia [My Copy] PLoS Genet, Vol. 5, No. 9. (11 September 2009), e1000642. by Christopher L. Plaisier, Steve Horvath, Adriana Huertas-Vazquez, et al.Ivette Cruz-Bautista, Miguel F. Herrera, Teresa Tusie-Luna, Carlos Aguilar-Salinas, Päivi Pajukanta posted to wgcna snp by giovanni on 2009-09-11 18:49:16 as
	Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients [My Copy] BMC Genomics, Vol. 10, No. 1. (2009), 405. by Christiaan Saris, Steve Horvath, Paul van Vught, et al.Michael van Es, Hylke Blauw, Tova Fuller, Peter Langfelder, Joseph DeYoung, John Wokke, Jan Veldink, Leonard van den Berg, Roel Ophoff posted to blood_classifier als by giovanni on 2009-09-07 13:40:52 as along with 1 person druvus
	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 gwas alzheimer_association alzheimer by giovanni on 2009-09-07 13:29:32 as along with 2 people vplagnol daforerog
	Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease [My Copy] Nature Genetics, Vol. 41, No. 10. (06 September 2009), pp. 1088-1093. by Denise Harold, Richard Abraham, Paul Hollingworth, et al.Rebecca Sims, Amy Gerrish, Marian L. Hamshere, Jaspreet 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 Schurmann, Hendrik van den Bussche, Isabella Heuser, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frolich, Harald Hampel, Michael Hull, Dan Rujescu, Alison M. Goate, John S. K. 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. Muhleisen, Markus M. Nothen, Susanne Moebus, Karl-Heinz Jockel, Norman Klopp, H-Erich Wichmann, Minerva M. Carrasquillo, V. Shane Pankratz, Steven G. Younkin, Peter A. Holmans, Michael O'Donovan, Michael J. Owen, Julie Williams posted to gwas alzheimer_association alzheimer by giovanni on 2009-09-07 13:20:15 as along with 3 people vplagnol psique daforerog
	Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathways. [My Copy] PloS one, Vol. 4, No. 8. (2009) by Iraad F. Bronner, Zoltán Bochdanovits, Patrizia Rizzu, et al.Wouter Kamphorst, Rivka Ravid, John C. van Swieten, Peter Heutink posted to ftd by giovanni on 2009-08-29 13:13:42 as
	Human Y Chromosome Base-Substitution Mutation Rate Measured by Direct Sequencing in a Deep-Rooting Pedigree [My Copy] Vol. 19, No. 17. (15 September 2009), pp. 1453-1457. by Yali Xue, Qiuju Wang, Quan Long, et al.Bee L. Ng, Harold Swerdlow, John Burton, Carl Skuce, Ruth Taylor, Zahra Abdellah, Yali Zhao, Daniel G. MacArthur, Michael A. Quail, Nigel P. Carter, Huanming Yang, Chris Tyler-Smith posted to sequencing by giovanni on 2009-08-28 20:51:19 as along with 1 person vtraag
	Limitations in a frataxin knockdown cell model for Friedreich ataxia in a high-throughput drug screen [My Copy] BMC Neurology, Vol. 9, No. 1. (24 August 2009), 46. by Nadege Calmels, Herve Seznec, Pascal Villa, et al.Laurence Reutenauer, Marcel Hibert, Jacques Haiech, Pierre Rustin, Michel Koenig, Helene Puccio posted to frda by giovanni on 2009-08-26 20:31:54 as
	Biomarkers to predict and track diseases [My Copy] The Lancet Neurology, Vol. 8, No. 9. (29 September 2009), pp. 776-777. by Jane S. Paulsen posted to biomarkers by giovanni on 2009-08-24 20:50:49 as along with 1 person Amazoness
	Genetics of human gene expression: mapping DNA variants that influence gene expression. [My Copy] Nature reviews. Genetics, Vol. 10, No. 9. (28 September 2009), pp. 595-604. by Vivian G. Cheung, Richard S. Spielman posted to qtl by giovanni on 2009-08-24 14:40:31 as along with 17 people and 1 group rcr1991 PaulaBO Zephyrus greg frohike psique PabloMarin TRHvidsten misonneh sameersoi rdiaz ericrpaquet engelhardt ilyashl jbhiatt pkonings guhjy Journal picks
	Friedreich ataxia. [My Copy] Archives of neurology, Vol. 65, No. 10. (October 2008), pp. 1296-1303. by Massimo Pandolfo posted to frda_review by giovanni on 2009-08-24 14:28:44 as
	Cerebrospinal fluid biomarkers and rate of cognitive decline in very mild dementia of the Alzheimer type. [My Copy] Archives of neurology, Vol. 66, No. 5. (May 2009), pp. 638-645. by Barbara J. Snider, Anne M. Fagan, Catherine Roe, et al.Aarti R. Shah, Elizabeth A. Grant, Chengjie Xiong, John C. Morris, David M. Holtzman posted to alzheimer by giovanni on 2009-08-24 14:18:22 as along with 1 person jeremymiller
	Recombinant human erythropoietin: effects on frataxin expression in vitro. [My Copy] European journal of clinical investigation, Vol. 35, No. 11. (November 2005), pp. 711-717. by B. Sturm, D. Stupphann, C. Kaun, et al.S. Boesch, M. Schranzhofer, J. Wojta, H. Goldenberg, B. Scheiber-Mojdehkar posted to frda epo by giovanni on 2009-08-24 14:06:58 as along with 1 person cchand
	Breaking the silence in Friedreich's ataxia. [My Copy] Nature chemical biology, Vol. 2, No. 10. (October 2006), pp. 512-513. by Richard Festenstein posted to frda by giovanni on 2009-08-24 14:02:48 as
	HIF prolyl hydroxylase inhibitors prevent neuronal death induced by mitochondrial toxins: therapeutic implications for Huntington's disease and Alzheimer's disease. [My Copy] Antioxidants & redox signaling (6 August 2009) by Zoya Niatsetskaya, Manuela Basso, Rachel Speer, et al.Stephen McConoughey, Giovanni Coppola, Thong Chi C. Ma, Rajiv Ratan posted to no-tag by giovanni on 2009-08-24 13:55:05 as along with 1 person rcr1991
	Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study. [My Copy] Journal of neurology, Vol. 256, No. 8. (August 2009), pp. 1252-1257. by Chiara Criscuolo, Alessandro Filla, Giovanni Coppola, et al.Carlo Rinaldi, Rosa Carbone, Stefano Pinto, Qing Wang, Maria Fulvia F. de Leva, Elena Salvatore, Sandro Banfi, Arturo Brunetti, Mario Quarantelli, Daniel H. Geschwind, Sabina Pappatà, Giuseppe De Michele posted to no-tag by giovanni on 2009-08-24 13:54:29 as

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endnote	327
tau	231
frda	146
drg	66
microarray	59
diabetes	49
alzheimer	38
pgc1-alpha	31
ftd	30
bibtex-import	29
review	26
snp	26
biomarkers	22
ox_stress	22
progranulin	22
pgc	19
classifier	18
huntington	18
insulin_r	18
association	17
bdnf	16
blood_classifier	16
heart	15
mitochondria	15
tdp43	11
gwas	10
copy_number	9
resequencing	9
frataxin	8
frda_model	8
muscle	8
mapt_haplotype	7
ppar	7
qtl	7
sequencing	7
alzheimer_association	6
blood	6
fahr	6
parkinson	6
sirt1	6
worm	6
als	5
amyloid	5
cardiomyopathy	5
diagnostic_criteria	5
fiber_switch	5
genetics_genomics	5
ibd	5
neurodegeneration	5
resveratrol	5
toprint	5
hif	4
insulin	4
mirna	4
network	4
polyglutamine	4
presenilin	4
rnaseq	4
snp_pool	4
transcription_factors	4
yeast	4
affy	3
aluminum	3
alzheimer_model	3
apoe	3
artistic_creativity	3
cgh	3
frda_review	3
hdaci	3
iron	3
nurr77	3
regulatory	3
snp_ibd	3
srebp	3
vasopressin	3
vcp	3
wgcna	3
aging	2
app	2
ataxia_review	2
autism	2
aved	2
brain	2
chmp2b	2
epo	2
exome	2
frda_muscle	2
geschwindlab	2
granulin	2
heme	2
inflammation	2
kiko_muscle	2
lcm	2
lipogenesis	2
methods	2
model	2
ms	2
nextgenseq	2
nurr1	2
oxphos	2
phred	2
pink1	2
sca	2
solexa	2
sox11	2
stroke	2
synuclein	2
taup	2
tau_review	2
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