psique's parkinsons [at least 200 articles] Export

Recent papers added to psique's library classified by the tag parkinsons. You can also see everyone's parkinsons.

	Variability and validity of polymorphism association studies in Parkinson's disease [My Copy] Neurology, Vol. 55, No. 4. (22 August 2000), pp. 533-538. by E. K. Tan, M. Khajavi, J. I. Thornby, S. Nagamitsu, J. Jankovic, T. Ashizawa posted to review polymorphism phd parkinsons genetics by psique on 2009-10-12 11:33:20 as along with 1 person daforerog
	Implications of Genetics on the Diagnosis and Care of Patients With Parkinson Disease [My Copy] Arch Neurol, Vol. 63, No. 3. (1 March 2006), pp. 328-334. by Christine Klein posted to review parkinsons genetics clinical by psique on 2009-10-12 11:18:23 as
	Small interfering RNA targeting the PINK1 induces apoptosis in dopaminergic cells SH-SY5Y [My Copy] Biochemical and Biophysical Research Communications, Vol. 337, No. 4. (02 December 2005), pp. 1133-1138. by H. Deng, J. Jankovic, Y. Guo, W. Xie, W. Le posted to sirna pink1 parkinsons dopamine by psique on 2009-10-12 11:16:27 as
	Prevalence of Parkinson's disease in Europe: A collaborative study of population-based cohorts. Neurologic Diseases in the Elderly Research Group. [My Copy] Neurology, Vol. 54, No. 11 Suppl 5. (2000) by M. C. de Rijk, L. J. Launer, K. Berger, et al.M. M. Breteler, J. F. Dartigues, M. Baldereschi, L. Fratiglioni, A. Lobo, J. Martinez-Lage, C. Trenkwalder, A. Hofman posted to prevalence population parkinsons by psique on 2009-10-12 11:15:23 as
	Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism [My Copy] Neurology, Vol. 64, No. 11. (14 June 2005), pp. 1955-1957. by Y. Li, H. Tomiyama, K. Sato, et al.Y. Hatano, H. Yoshino, M. Atsumi, M. Kitaguchi, S. Sasaki, S. Kawaguchi, H. Miyajima, T. Toda, Y. Mizuno, N. Hattori posted to yopd pink1 parkinsons genetics by psique on 2009-10-12 10:43:03 as
	PITX3 polymorphism is associated with early onset Parkinson's disease [My Copy] Neurobiology of Aging (16 April 2008) by Olle Bergman, Anna Håkansson, Lars Westberg, et al.Kajsa Nordenström, Andrea Carmine Belin, Olof Sydow, Lars Olson, Björn Holmberg, Elias Eriksson, Hans Nissbrandt posted to transcription_factor polymorphism pitx3 parkinsons genetics by psique on 2009-10-11 13:07:28 as
	Impaired cognitive performance in Parkinson's disease is related to caudate dopaminergic hypofunction and hippocampal atrophy [My Copy] Parkinsonism & Related Disorders, Vol. 15, No. 2. (February 2009), pp. 88-93. by P. Jokinen, A. Bruck, S. Aalto, S. Forsback, R. Parkkola, J. Rinne posted to parkinsons hippocampus dopamine dementia cognitive_impairment by psique on 2009-10-11 13:04:56 as
	Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA — A key player in the pathogenesis of Parkinson's disease [My Copy] Brain Research, Vol. 1256 (23 February 2009), pp. 19-33. by Karina Häbig, Michael Walter, Heike Stappert, Olaf Riess, Michael Bonin posted to synuclein parkinsons gene_expression dopamine by psique on 2009-10-11 12:15:30 as
	Genetics of Parkinson disease: paradigm shifts and future prospects [My Copy] Nat Rev Genet, Vol. 7, No. 4. (01 April 2006), pp. 306-318. by Matthew J. Farrer posted to review parkinsons genetics by psique on 2009-10-11 11:52:34 as
	016 A POPULATION BASED STUDY OF YOUNG ONSET PARKINSON'S DISEASE IN SOUTH WALES. [My Copy] Journal of Neurology, Neurosurgery & Psychiatry, Vol. 77, No. 1. (January 2006), 129. by M. M. Wickremaratchi, A. Jones, N. P. Robertson, Y. Ben-Shlomo, H. R. Morris posted to population parkinsons cardiff by psique on 2009-10-11 11:48:36 as
	Parkin variants in North American Parkinson's disease: cases and controls. [My Copy] Movement disorders : official journal of the Movement Disorder Society, Vol. 18, No. 11. (November 2003), pp. 1306-1311. by Sarah J. Lincoln, Demetrius M. Maraganore, Timothy G. Lesnick, et al.Rebecca Bounds, Mariza de Andrade, James H. Bower, John A. Hardy, Matthew J. Farrer posted to parkinsons parkin genetics by psique on 2009-10-09 18:28:45 as
	Nigrostriatal Dopaminergic Deficits and Hypokinesia Caused by Inactivation of the Familial Parkinsonism-Linked Gene DJ-1. [My Copy] Neuron., Vol. 45, No. 4. (17 February 2005), pp. 489-496. by Matthew S. Goldberg, Antonio Pisani, Marian Haburcak, et al.Timothy A. Vortherms, Tohru Kitada, Cinzia Costa, Youren Tong, Giuseppina Martella, Anne Tscherter, Andrea Martins, Giorgio Bernardi, Bryan L. Roth, Emmanuel N. Pothos, Paolo Calabresi, Jie Shen posted to parkinsons mouse ko dj-1 by psique on 2009-10-07 16:25:15 as along with 1 person brian
	Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons. [My Copy] The Journal of biological chemistry, Vol. 278, No. 44. (31 October 2003), pp. 43628-43635. by Matthew S. Goldberg, Sheila M. Fleming, James J. Palacino, et al.Carlos Cepeda, Hoa A. Lam, Anushree Bhatnagar, Edward G. Meloni, Nanping Wu, Larry C. Ackerson, Gloria J. Klapstein, Mahadevan Gajendiran, Bryan L. Roth, Marie-Francoise F. Chesselet, Nigel T. Maidment, Michael S. Levine, Jie Shen posted to parkinsons parkin mouse ko by psique on 2009-10-07 16:22:34 as
	Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase [My Copy] Nat Genet, Vol. 38, No. 10. (10 September 2006), pp. 1184-1191. by Alfredo Ramirez, Andre Heimbach, Jan Grundemann, et al.Barbara Stiller, Dan Hampshire, L. Pablo Cid, Ingrid Goebel, Ammar F. Mubaidin, Abdul-Latif Wriekat, Jochen Roeper, Amir Al-Din, Axel M. Hillmer, Meliha Karsak, Birgit Liss, C. Geoffrey Woods, Maria I. Behrens, Christian Kubisch posted to yopd parkinsons genetics atp13a2 by psique on 2009-10-07 15:17:01 as along with 1 person daforerog
	Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36. [My Copy] American journal of human genetics, Vol. 69, No. 3. (September 2001), pp. 629-634. by C. M. van Duijn, M. C. Dekker, V. Bonifati, et al.R. J. Galjaard, J. J. Houwing-Duistermaat, P. J. Snijders, L. Testers, G. J. Breedveld, M. Horstink, L. A. Sandkuijl, J. C. van Swieten, B. A. Oostra, P. Heutink posted to yopd parkinsons park7 genetics dj-1 by psique on 2009-10-07 14:12:00 as
	Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (<I>PARK7</I>) in an independent dataset [My Copy] Annals of Neurology, Vol. 51, No. 2. (2002), pp. 253-256. by Vincenzo Bonifati, Guido J. Breedveld, Ferdinando Squitieri, et al.Nicola Vanacore, Pierluigi Brustenghi, Biswadjiet S. Harhangi, Pasquale Montagna, Milena Cannella, Giovanni Fabbrini, Patrizia Rizzu, Cornelia M. van Duijn, Ben A. Oostra, Giuseppe Meco, Peter Heutink posted to yopd parkinsons park7 genetics dj-1 by psique on 2009-10-07 14:10:21 as
	Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. [My Copy] Nature, Vol. 392, No. 6676. (9 April 1998), pp. 605-608. by T. Kitada, S. Asakawa, N. Hattori, et al.H. Matsumine, Y. Yamamura, S. Minoshima, M. Yokochi, Y. Mizuno, N. Shimizu posted to parkinsons parkin genetics by psique on 2009-10-07 12:59:16 as along with 1 person daforerog
	Population genetic approaches to neurological disease: Parkinson's disease as an example. [My Copy] Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 360, No. 1460. (29 August 2005), pp. 1573-1578. by S. Gandhi, P. M. Abou-Sleiman, D. G. Healy, et al.M. Weale, W. Gilks, K. Ahmadi, D. B. Goldstein, N. W. Wood posted to review population parkinsons genetics by psique on 2009-10-07 12:21:59 as
	Parkinson Disease in Twins: An Etiologic Study [My Copy] JAMA, Vol. 281, No. 4. (27 January 1999), pp. 341-346. by Caroline M. Tanner, Ruth Ottman, Samuel M. Goldman, et al.Jonas Ellenberg, Piu Chan, Richard Mayeux, J. William Langston posted to twin_pairs phd parkinsons heritability aetiology by psique on 2009-10-07 11:40:17 as along with 1 person daforerog
	Increased risk of Parkinson's disease in parents and siblings of patients [My Copy] Annals of Neurology, Vol. 36, No. 4. (1994), pp. 659-661. by Haydeh Payami, Kimberly Larsen, Steven Bernard, John Nutt posted to population parkinsons heritability by psique on 2009-10-07 11:30:23 as
	Incidence of Parkinson's disease: variation by age, gender, and race/ethnicity. [My Copy] American journal of epidemiology, Vol. 157, No. 11. (1 June 2003), pp. 1015-1022. by Stephen K. Van Den Eeden, Caroline M. Tanner, Allan L. Bernstein, et al.Robin D. Fross, Amethyst Leimpeter, Daniel A. Bloch, Lorene M. Nelson posted to population parkinsons by psique on 2009-10-07 11:14:53 as
	Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease. [My Copy] The FEBS journal, Vol. 275, No. 23. (December 2008), pp. 5767-5773. by Jose Bras, Andrew Singleton, Mark R. Cookson, John Hardy posted to review parkinsons genetics ceramide by psique on 2009-10-06 18:13:09 as
	The genetics of Parkinson's syndromes: a critical review. [My Copy] Current opinion in genetics & development, Vol. 19, No. 3. (June 2009), pp. 254-265. by John Hardy, Patrick Lewis, Tamas Revesz, Andrew Lees, Coro Paisan-Ruiz posted to review parkinsons genetics by psique on 2009-10-06 18:09:44 as
	Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations. [My Copy] Neurology, Vol. 58, No. 8. (23 April 2002), pp. 1239-1246. by K. Hedrich, K. Marder, J. Harris, et al.M. Kann, T. Lynch, H. Meija-Santana, P. P. Pramstaller, E. Schwinger, S. B. Bressman, S. Fahn, C. Klein posted to yopd parkinsons parkin mutation_frequency genetics by psique on 2009-10-01 12:17:42 as
	Case-control study of the parkin gene in early-onset Parkinson disease. [My Copy] Archives of neurology, Vol. 63, No. 4. (April 2006), pp. 548-552. by Lorraine N. Clark, Shehla Afridi, Eric Karlins, et al.Yuanjia Wang, Helen Mejia-Santana, Juliette Harris, Elan D. Louis, Lucien J. Cote, Howard Andrews, Stanley Fahn, Cheryl Waters, Blair Ford, Steven Frucht, Ruth Ottman, Karen Marder posted to parkinsons parkin genetics by psique on 2009-10-01 12:08:18 as
	New mutation (R42P) of the parkin gene in the ubiquitinlike domain associated with parkinsonism [My Copy] Neurology, Vol. 56, No. 4. (27 February 2001), pp. 463-466. by L. Terreni, E. Calabrese, A. M. Calella, G. Forloni, C. Mariani posted to parkinsons parkin genetics by psique on 2009-10-01 12:02:44 as
	Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease [My Copy] J Neurol Neurosurg Psychiatry, Vol. 76, No. 11. (1 November 2005), pp. 1588-1590. by R. H. Madegowda, A. Kishore, A. Anand posted to parkinsons parkin mutation_frequency genetics by psique on 2009-10-01 11:48:57 as
	Heterozygous <I>parkin</I> point mutations are as common in control subjects as in Parkinson's patients [My Copy] Annals of Neurology, Vol. 61, No. 1. (2007), pp. 47-54. by Denise M. Kay, Dawn Moran, Lina Moses, et al.Parvoneh Poorkaj, Cyrus P. Zabetian, John Nutt, Stewart A. Factor, Chang-En Yu, Jennifer S. Montimurro, Robert G. Keefe, Gerard D. Schellenberg, Haydeh Payami posted to parkinsons parkin mutation_frequency genetics by psique on 2009-10-01 11:48:07 as
	A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease. [My Copy] Human molecular genetics, Vol. 8, No. 4. (April 1999), pp. 567-574. by N. Abbas, C. B. Lücking, S. Ricard, et al.A. Dürr, V. Bonifati, G. De Michele, S. Bouley, J. R. Vaughan, T. Gasser, R. Marconi, E. Broussolle, C. Brefel-Courbon, B. S. Harhangi, B. A. Oostra, E. Fabrizio, G. A. Böhme, L. Pradier, N. W. Wood, A. Filla, G. Meco, P. Denefle, Y. Agid, A. Brice posted to parkinsons parkin genetics by psique on 2009-10-01 10:47:03 as
	A common A340T variant in PINK1 gene associated with late-onset Parkinson's disease in Chinese. [My Copy] Neuroscience letters, Vol. 410, No. 2. (20 December 2006), pp. 121-125. by Feng Wang, Xiuli Feng, Jinhong Ma, Haiqiang Zou, Piu Chan posted to pink1 parkinsons genetics by psique on 2009-09-30 17:31:27 as
	Genetic association study of PINK1 coding polymorphisms in Parkinson's disease. [My Copy] Neuroscience letters, Vol. 372, No. 3. (6 December 2004), pp. 226-229. by Justus L. Groen, Toshitaka Kawarai, Anna Toulina, et al.Chiara Rivoiro, Shabnam Salehi-Rad, Christine Sato, Angharad Morgan, Yan Liang, Ronald B. Postuma, Peter St George-Hyslop, Anthony E. Lang, Ekaterina Rogaeva posted to pink1 parkinsons genetics by psique on 2009-09-30 17:29:36 as
	Genomewide SNP assay reveals mutations underlying Parkinson disease [My Copy] Human Mutation, Vol. 29, No. 2. (February 2008), pp. 315-322. by Javier Simon-Sanchez, Sonja Scholz, Maria del Mar Matarin, et al.Hon-Chung Fung, Dena Hernandez, J. Raphael Gibbs, Angela Britton, John Hardy, Andrew Singleton posted to parkinsons methods genotyping gene_dosage cnv by psique on 2009-09-30 11:33:26 as
	Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease. [My Copy] Annals of neurology, Vol. 64, No. 1. (July 2008), pp. 88-92. by Owen A. Ross, Yih-Ru R. Wu, Mei-Ching C. Lee, et al.Manabu Funayama, Meng-Ling L. Chen, Alexandra I. Soto, Ignacio F. Mata, Guey-Jen J. Lee-Chen, Chiung Mei M. Chen, Michelle Tang, Yi Zhao, Nobutaka Hattori, Matthew J. Farrer, Eng-King K. Tan, Ruey-Meei M. Wu posted to snp parkinsons lrrk2 genetics by psique on 2009-09-29 17:32:15 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 parkinsons gwas genomics genetics by psique on 2009-09-24 19:45:56 as along with 1 person daforerog
	PINK1 Protects against Oxidative Stress by Phosphorylating Mitochondrial Chaperone TRAP1 [My Copy] PLoS Biol, Vol. 5, No. 7. (19 June 2007), e172. by Julia W. Pridgeon, James A. Olzmann, Lih-Shen Chin, Lian Li posted to pink1 parkinsons oxidative_stress mitochondria by psique on 2009-09-23 08:24:15 as
	PINK1 defect causes mitochondrial dysfunction, proteasomal deficit and alpha-synuclein aggregation in cell culture models of Parkinson's disease. [My Copy] PloS one, Vol. 4, No. 2. (2009) by Wencheng Liu, Cristofol Vives-Bauza, Rebeca Acín-Peréz-, et al.Ai Yamamoto, Yingcai Tan, Yanping Li, Jordi Magrané, Mihaela A. Stavarache, Sebastian Shaffer, Simon Chang, Michael G. Kaplitt, Xin-Yun Y. Huang, M. Flint Beal, Giovanni Manfredi, Chenjian Li posted to ups synuclein pink1 parkinsons mitochondria by psique on 2009-09-23 08:21:46 as
	Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function [My Copy] EMBO Molecular Medicine, Vol. 1, No. 2. (2009), pp. 99-111. by Vanessa A. Morais, Patrik Verstreken, Anne Roethig, et al.Joél Smet, An Snellinx, Mieke Vanbrabant, Dominik Haddad, Christian Frezza, Wim Mandemakers, Daniela Vogt-Weisenhorn, Rudy Van Coster, Wolfgang Wurst, Luca Scorrano, Bart De Strooper posted to pink1 parkinsons mitochondria by psique on 2009-09-23 08:20:53 as
	Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 102, No. 16. (19 April 2005), pp. 5703-5708. by Alexandra Beilina, Marcel Van Der Brug, Rili Ahmad, et al.Sashi Kesavapany, David W. Miller, Gregory A. Petsko, Mark R. Cookson posted to parkinsons pink1 l347p by psique on 2009-09-23 08:13:32 as
	Novel features in a patient homozygous for the L347P mutation in the PINK1 gene [My Copy] Parkinsonism & Related Disorders, Vol. 13, No. 6. (August 2007), pp. 359-361. by J. Doostzadeh, J. Tetrud, M. Allenauerbach, J. Langston, B. Schule posted to parkinsons pink1 l347p genetics by psique on 2009-09-22 18:53:21 as
	C-terminal truncation and Parkinson's disease-associated mutations down-regulate the protein serine/threonine kinase activity of PTEN-induced kinase-1 [My Copy] Hum. Mol. Genet., Vol. 15, No. 21. (1 November 2006), pp. 3251-3262. by Chou H. Sim, Daisy S. Lio, Su S. Mok, et al.Colin L. Masters, Andrew F. Hill, Janetta G. Culvenor, Heung-Chin Cheng posted to parkinsons pink1 by psique on 2009-09-22 18:22:19 as
	Mitochondrial Cell Death Control in Familial Parkinson Disease [My Copy] PLoS Biol, Vol. 5, No. 7. (17 July 2007), e206. by Guido Kroemer, Klas Blomgren posted to parkinsons pink1 mitochondria by psique on 2009-09-22 17:09:11 as
	Molecular interaction between parkin and PINK1 in mammalian neuronal cells. [My Copy] Molecular and cellular neurosciences, Vol. 40, No. 4. (April 2009), pp. 421-432. by Ji Won W. Um, Christine Stichel-Gunkel, Hermann Lübbert, Gwang Lee, Kwang Chul C. Chung posted to parkinsons pink1 parkin by psique on 2009-09-22 16:31:31 as
	Homozygous and heterozygous PINK1 mutations: considerations for diagnosis and care of Parkinson's disease patients. [My Copy] Movement disorders : official journal of the Movement Disorder Society, Vol. 21, No. 6. (June 2006), pp. 875-879. by Cindy Zadikoff, Ekaterina Rogaeva, Ana Djarmati, et al.Christine Sato, Shabnam Salehi-Rad, Peter St George-Hyslop, Christine Klein, Anthony E. Lang posted to parkinsons pink1 genetics by psique on 2009-09-22 16:28:15 as
	L347P PINK1 mutant that fails to bind to Hsp90/Cdc37 chaperones is rapidly degraded in a proteasome-dependent manner. [My Copy] Neuroscience research, Vol. 61, No. 1. (May 2008), pp. 43-48. by Yasuhiro Moriwaki, Yeon-Jeong J. Kim, Yukari Ido, et al.Hidemi Misawa, Koichiro Kawashima, Shogo Endo, Ryosuke Takahashi posted to parkinsons pink1 l347p by psique on 2009-09-22 16:01:10 as
	Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional study. [My Copy] Movement disorders : official journal of the Movement Disorder Society, Vol. 23, No. 6. (30 April 2008), pp. 881-885. by Vania Gelmetti, Alessandro Ferraris, Livia Brusa, et al.Francesca Romano, Federica Lombardi, Chiara Barzaghi, Paolo Stanzione, Barbara Garavaglia, Bruno Dallapiccola, Enza Maria M. Valente posted to parkinsons pink1 lopd by psique on 2009-09-22 15:49:32 as
	Expanding insights of mitochondrial dysfunction in Parkinson's disease [My Copy] Nature Reviews Neuroscience, Vol. 7, No. 3. (01 March 2006), pp. 207-219. by Patrick M. Abou-Sleiman, Miratul M. K. Muqit, Nicholas W. Wood posted to parkinsons review pink1 mitochondria dj-1 by psique on 2009-09-22 15:45:25 as
	Tickled PINK1: Mitochondrial homeostasis and autophagy in recessive Parkinsonism [My Copy] Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (09 July 2009) by Charleen T. Chu posted to parkinsons pink1 mitochondria autophagy by psique on 2009-09-22 15:43:46 as
	Mitochondrial dysfunction in Parkinson's disease [My Copy] Cell Death & Differentiation, Vol. 14, No. 7. (27 April 2007), pp. 1261-1266. by A. H. V. Schapira posted to parkinsons review mitochondria by psique on 2009-09-16 17:14:09 as
	PINK1 mutants associated with recessive Parkinson's disease are defective in inhibiting mitochondrial release of cytochrome c. [My Copy] Neurobiology of disease, Vol. 28, No. 2. (November 2007), pp. 216-226. by Hung-Li L. Wang, An-Hsun H. Chou, Tu-Hsueh H. Yeh, et al.Allen H. Li, Ying-Ling L. Chen, Yu-Li L. Kuo, Shu-Ru R. Tsai, Szu-Tzu T. Yu posted to parkinsons protein pink1 l347p by psique on 2009-09-16 17:08:02 as
	The second brain and Parkinson's disease. [My Copy] The European journal of neuroscience, Vol. 30, No. 5. (September 2009), pp. 735-741. by Thibaud Lebouvier, Tanguy Chaumette, Sébastien Paillusson, et al.Charles Duyckaerts, Stanislas Bruley des Varannes, Michel Neunlist, Pascal Derkinderen posted to parkinsons enteric_nervous_system by psique on 2009-09-13 22:32:10 as

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genetics	279
parkinsons	224
genomics	162
methods	98
gwas	90
pink1	74
dopamine	69
snp	60
depression	57
synuclein	55
review	52
cnv	47
parkin	39
serotonin	39
bioinformatics	36
neurodegeneration	33
aging	32
evolution	30
gene_expression	30
cognition	29
mitochondria	29
addiction	27
basal_ganglia	27
stats	27
pharmacology	26
neurogenesis	24
alzheimers	22
population	21
dj-1	20
psychiatry	20
sequencing	20
reward	19
stress	19
drug_discovery	18
hippocampus	18
stem_cells	18
cardiff	17
homozygosity	15
structure	15
lrrk2	14
pharmacogenomics	14
plasticity	14
corticoids	13
rna	13
schizophrenia	13
yopd	13
bdnf	12
imaging	12
transcription	12
database	11
genotyping	11
memory	11
neurotrophic	11
noradrenaline	11
pfc	11
psychosis	11
anxiety	10
career	10
computational	10
oxidative_stress	10
brain_implant	9
development	9
learning	9
protein	9
biochem	8
decision_making	8
dementia	8
enhancement	8
epistasis	8
pathway	8
policy	8
population_structure	8
psychology	8
rna_interference	8
roh	8
ros	8
web	8
ed	7
epigenetics	7
feeding	7
microrna	7
mol_bio	7
neuroethics	7
phosphorylation	7
autism	6
behaviour	6
bipolar	6
complex_disease	6
drugs	6
ethanol	6
fmri	6
glutamate	6
ld	6
linkage_analysis	6
mdma	6
msa	6
proteomics	6
schizo	6
amygdala	5
blood_brain_barrier	5
cell_bio	5
cocaine	5
dna	5
emotion	5
heritability	5
insula	5
irritable_bowel_syndrome	5
personality	5
phd	5
proteins	5
systems_bio	5
attention	4
caloric_restriction	4
cancer	4
case-control	4
common_disease	4
comt	4
darpp-32	4
dystonia	4
hapmap	4
history_of_science	4
l347p	4
meta	4
motivation	4
mouse	4
mutation_frequency	4
nicotine	4
ocd	4
omics	4
pd	4
penncnv	4
primates	4
sirtuins	4
suicide	4
synaptic_plasticity	4
ups	4
acetylcholine	3
adhd	3
biotech	3
borderline	3
camp	3
consanguineous	3
consciousness	3
dtc	3
endophenotype	3
exercise	3
gba	3
genetic_testing	3
glia	3
haplotype	3
nanotechnology	3
neuroprotection	3
news	3
opiods	3
philosophy	3
publishing	3
qtl	3
social	3
splicing	3
tutorial	3
als	2
amino_acids	2
amphetamine	2
amyloid	2
autophagy	2
biomarker	2
camkii	2
circadian_rhythms	2
circuit_busting	2
codon	2
cortex	2
cre-lox	2
data_mining	2
education	2
endocrinology	2
environmental_factors	2
exome	2
gaba	2
gene_dosage	2
gene_ontology	2
gpcr	2
hedonism	2
histamine	2
hwe	2
igf-1	2
immunology	2
kinase	2
ko	2
lopd	2
ltp	2
maoa	2
metabolism	2
motherhood	2
neuroscience	2
neuroticism	2
park7	2
personal	2
personal_genomics	2
phenotype	2
pitx3	2
politics	2
polygenic_score	2
polymorphism	2
population_stratification	2
potassium	2
rat	2
ritalin	2
science_communication	2
sex	2
transgenic	2
yeast	2
adenosine	1
adolescence	1
aetiology	1
allelic_expression	1
archaeology	1
artificial_intelligence	1
atp13a2	1
caffeine	1
calcium	1
ceramide	1
cerebellar_ataxia	1
chaperones	1
clinical	1
clinical_trials	1
cloning	1
cognitive_impairment	1
common_variant_common_disease	1
computational_biology	1
creutzfeldt_jakob_disease	1
cryo	1
dna-pooling	1
doublecortin	1
ecology	1
economy	1
electrophysiology	1
enteric_nervous_system	1
entropy	1
ephb	1
ethics	1
exploration	1
fear	1
fluorescence	1
for:daforerog	1
founder_mutation	1
free_will	1
freud	1
ftd	1
ganglia	1
gaucher	1
gender	1
genome_sequencing	1
geography	1
ghrelin	1
glutamate_dehydrogenase	1
h2o2	1
habit	1
heat_shock_protein	1
heterogeneity	1
histology	1
hmgb1	1
human_evolution	1
imprinting	1
journalism	1
lithium	1
malaria	1
mathematics	1
mci	1
meditation	1
metabonomic	1
mnd	1
motor_cortex	1
multielectrode_array	1
myelin	1
natural_selection	1
neuroeconomics	1
nigrostriatal	1
nitrogen_oxide	1
non-coding	1
nurr1	1
nutrition	1
obesity	1
omim	1
ontology	1
open_science	1
optimism	1
orf	1
oxytocin	1
pain	1
pcr	1
penetrance	1
pesticides	1
phenomics	1
pheromones	1
pink1_origins	1
polygenic_inheritance	1
population_genetics	1
postsynaptic	1
prevalence	1
protocells	1
psoriasis	1
psychiatriy	1
psychoanalysis	1
pyy	1
quality_control	1
quantitative_traits	1
rare_variants	1
recessive	1
reinforcement_learning	1
report	1
risk_factors	1
robot	1
self-injury	1
sexual_dimorphism	1
simulation	1
sirna	1
sleep	1
smoking	1
society	1
spinal_cord	1
sporadic_cases	1
tau	1
technology	1
tms	1
transcription_factor	1
translation	1
twin_pairs	1
uchl1	1
ucsc	1
vision	1
wtccc	1

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