psique's parkin [39 articles] Export

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

	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
	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
	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
	Parkin mutations and susceptibility alleles in late-onset Parkinson's disease. [My Copy] Annals of neurology, Vol. 53, No. 5. (May 2003), pp. 624-629. by Sofia A. Oliveira, William K. Scott, Eden R. Martin, et al.Martha A. Nance, Ray L. Watts, Jean P. Hubble, William C. Koller, Rajesh Pahwa, Matthew B. Stern, Bradley C. Hiner, William G. Ondo, Fred H. Allen, Burton L. Scott, Christopher G. Goetz, Gary W. Small, Frank Mastaglia, Jeffrey M. Stajich, Fengyu Zhang, Michael W. Booze, Michelle P. Winn, Lefkos T. Middleton, Jonathan L. Haines, Margaret A. Pericak-Vance, Jeffery M. Vance posted to parkin mutation_frequency lopd genetics by psique on 2009-10-01 12:21:55 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
	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
	Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations [My Copy] Neurology, Vol. 73, No. 4. (28 July 2009), pp. 279-286. by N. Pankratz, D. K. Kissell, M. W. Pauciulo, et al.C. A. Halter, A. Rudolph, R. F. Pfeiffer, K. S. Marder, T. Foroud, W. C. Nichols, For the Parkinson Study Group-PROGENI Investigators posted to parkinsons parkin genetics by psique on 2009-09-10 16:34:32 as
	Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations [My Copy] Movement Disorders, Vol. 24, No. 5. (2009), pp. 662-666. by Sarah T. Camargos, Leonardo O. Dornas, Parastoo Momeni, et al.Andrew Lees, John Hardy, Andrew Singleton, Francisco Cardoso posted to genetics lrrk2 parkin pink1 synuclein yopd parkinsons by psique on 2009-07-06 11:53:04 as
	Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism [My Copy] BMC Neurology, Vol. 8, No. 1. (16 December 2008), 47. by Ronny Myhre, Stina Steinkjer, Alice Stormyr, et al.Gina Nilsen, Hiba Zayyad, Khalid Horany, Mohamad Nusier, Helge Klungland posted to genetics parkin pink1 yopd parkinsons by psique on 2009-07-06 11:22:04 as
	Detection of <I>Parkin</I> (<I>PARK2</I>) and <I>DJ1</I> (<I>PARK7</I>) mutations in early-onset Parkinson disease: <I>Parkin</I> mutation frequency depends on ethnic origin of patients [My Copy] Human Mutation, Vol. 23, No. 5. (2004), 525. by Ana Djarmati, Katja Hedrich, Marina Svetel, et al.Nora Schäfer, Vladislava Juric, Slobodanka Vukosavic, Robert Hering, Olaf Riess, Stanka Romac, Christine Klein, Vladimir Kostic posted to dj-1 genetics parkin parkinsons by psique on 2009-07-05 15:59:25 as
	The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism [My Copy] Hum. Mol. Genet., Vol. 10, No. 16. (1 August 2001), pp. 1649-1656. by Katja Hedrich, Martin Kann, Andrea J. Lanthaler, et al.Andreas Dalski, Cordula Eskelson, Olfert Landt, Eberhard Schwinger, Peter Vieregge, Anthony E. Lang, Xandra O. Breakefield, Laurie J. Ozelius, Peter P. Pramstaller, Christine Klein posted to genetics parkin parkinsons by psique on 2009-07-05 15:56:48 as
	Parkinson's disease in Ireland: clinical presentation and genetic heterogeneity in patients with parkin mutations. [My Copy] Movement disorders : official journal of the Movement Disorder Society, Vol. 19, No. 6. (June 2004), pp. 677-681. by J. Wiley, T. Lynch, S. Lincoln, et al.L. Skipper, M. Hulihan, D. Gosal, G. Bisceglio, J. Kachergus, J. Hardy, M. J. Farrer posted to genetics parkin parkinsons by psique on 2009-07-05 15:01:16 as
	Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control [My Copy] J Med Genet, Vol. 46, No. 6. (1 June 2009), pp. 375-381. by J. Brooks, J. Ding, J. Simon-Sanchez, C. Paisan-Ruiz, A. B. Singleton, S. W. Scholz posted to genetics parkin pink1 parkinsons by psique on 2009-07-02 15:27:05 as along with 1 person fazels2
	Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene [My Copy] N Engl J Med, Vol. 342, No. 21. (25 May 2000), pp. 1560-1567. by Christoph B. Lücking, Alexandra Durr, Vincenzo Bonifati, et al.Jenny Vaughan, Giuseppe De Michele, Thomas Gasser, Biswadjiet S. Harhangi, Giuseppe Meco, Patrice Denefle, Nicholas W. Wood, Yves Agid, Alexis Brice, The European Consortium on Genetic Susceptibility in Parkinson posted to genetics parkin parkinsons by psique on 2009-07-02 15:20:45 as
	Screening PARK genes for mutations in early-onset Parkinson's disease patients from Queensland, Australia [My Copy] Parkinsonism & Related Disorders, Vol. 15, No. 2. (February 2009), pp. 105-109. by G. Mellick, G. Siebert, M. Funayama, et al.D. Buchanan, Y. Li, Y. Imamichi, H. Yoshino, P. Silburn, N. Hattori posted to dj-1 genetics lrrk2 parkin pink1 parkinsons by psique on 2009-02-12 14:21:37 as
	Loss-of-Function Analysis Suggests That Omi/HtrA2 Is Not an Essential Component of the pink1/parkin Pathway In Vivo [My Copy] J. Neurosci., Vol. 28, No. 53. (31 December 2008), pp. 14500-14510. by Jina Yun, Joseph H. Cao, Mark W. Dodson, et al.Ira E. Clark, Pankaj Kapahi, Ruhena B. Chowdhury, Ming Guo posted to mitochondria parkin pink1 parkinsons by psique on 2009-01-07 16:35:43 as
	Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin [My Copy] Nature, Vol. 441, No. 7097. (03 May 2006), pp. 1162-1166. by Ira E. Clark, Mark W. Dodson, Changan Jiang, et al.Joseph H. Cao, Jun R. Huh, Jae H. Seol, Soon J. Yoo, Bruce A. Hay, Ming Guo posted to mitochondria parkin pink1 parkinsons by psique on 2009-01-07 14:29:53 as
	PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism [My Copy] Eur J Hum Genet, Vol. 13, No. 9. (22 June 2005), pp. 1086-1093. by Christine Klein, Ana Djarmati, Katja Hedrich, et al.Nora Schafer, Cesa Scaglione, Roberta Marchese, Norman Kock, Birgitt Schule, Anja Hiller, Thora Lohnau, Susen Winkler, Karin Wiegers, Robert Hering, Peter Bauer, Olaf Riess, Giovanni Abbruzzese, Paolo Martinelli, Peter P. Pramstaller posted to dj-1 parkin pink1 parkinsons by psique on 2008-09-18 13:26:37 as
	Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin [My Copy] Nature, Vol. 441, No. 7097. (03 May 2006), pp. 1157-1161. by Jeehye Park, Sung B. Lee, Sungkyu Lee, et al.Yongsung Kim, Saera Song, Sunhong Kim, Eunkyung Bae, Jaeseob Kim, Minho Shong, Jin-Man Kim, Jongkyeong Chung posted to mitochondria parkin pink1 parkinsons by psique on 2008-09-18 13:23:57 as along with 1 group parkinson's disease references
	Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2 [My Copy] BMC Neurology, Vol. 8 (22 January 2008), 1. by Jose Bras, Rita Guerreiro, Maria Ribeiro, et al.Ana Morgadinho, Cristina Januario, Margarida Dias, Ana Calado, Cristina Semedo, Catarina Oliveira, John Hardy, Andrew Singleton posted to lrrk2 parkin pink1 synuclein parkinsons by psique on 2008-09-18 13:13:31 as along with 1 group parkinson's disease references
	Pink1 Parkinson mutations, the Cdc37/Hsp90 chaperones and Parkin all influence the maturation or subcellular distribution of Pink1. [My Copy] Hum Mol Genet (14 November 2007) by Andreas Weihofen, Beth Ostaszewski, Yasufumi Minami, Dennis J J. Selkoe posted to parkin pink1 parkinsons by psique on 2008-09-18 12:59:40 as along with 1 person and 1 group lenov parkinson's disease references
	Loss-of-function of human PINK1 results in mitochondrial pathology and can be rescued by parkin. [My Copy] J Neurosci, Vol. 27, No. 45. (7 November 2007), pp. 12413-12418. by N. Exner, B. Treske, D. Paquet, et al.K. Holmström, C. Schiesling, S. Gispert, I. Carballo-Carbajal, D. Berg, H. H. Hoepken, T. Gasser, R. Krüger, K. F. Winklhofer, F. Vogel, A. S. Reichert, G. Auburger, P. J. Kahle, B. Schmid, C. Haass posted to mitochondria parkin pink1 parkinsons by psique on 2008-09-18 12:58:55 as along with 1 person and 1 group lenov parkinson's disease references
	Programmed cell death and new discoveries in the genetics of parkinsonism [My Copy] Journal of Neurochemistry, Vol. 104, No. 4. (February 2008), pp. 875-890. by Burke, E. Robert posted to dj-1 genetics parkin pink1 parkinsons by psique on 2008-06-12 18:47:09 as along with 1 group parkinson's disease references
	Expression of alpha-synuclein, parkin, and ubiquitin carboxy-terminal hydrolase L1 mRNA in human brain: Genes associated with familial Parkinson's disease [My Copy] Annals of Neurology, Vol. 47, No. 2. (26 April 2001), pp. 201-210. by Solano, Miller, Augood, Young, Penney posted to uchl1 synuclein phd parkinsons parkin gene_expression by psique on 2008-06-03 19:05:11 as along with 1 group parkinson's disease references
	Parkinson Disease [My Copy] Encyclopedia of Life Sciences (2006) by N. Hattori, Y. Mizuno posted to parkinsons parkin by psique on 2008-06-03 18:57:33 as along with 1 group parkinson's disease references
	The biochemistry of Parkinson's disease. [My Copy] Annu Rev Biochem, Vol. 74 (2005), pp. 29-52. by M. R. Cookson posted to dj-1 parkin pink1 synuclein dopamine parkinsons by psique on 2008-05-28 22:25:27 as along with 2 people monimonicas lenov
	Parkinson Disease : Encyclopedia of Life Sciences [My Copy] In Encyclopedia of Life Sciences (2006) by N. Hattori, Y. Mizuno posted to parkin parkinsons by psique on 2008-05-07 10:00:07 as along with 1 group parkinson's disease references
	Association study of Parkin gene polymorphisms with idiopathic Parkinson disease. [My Copy] Archives of neurology, Vol. 60, No. 7. (July 2003), pp. 975-980. by S. A. Oliveira, W. K. Scott, M. A. Nance, et al.R. L. Watts, J. P. Hubble, W. C. Koller, K. E. Lyons, R. Pahwa, M. B. Stern, B. C. Hiner, J. Jankovic, W. G. Ondo, F. H. Allen, B. L. Scott, C. G. Goetz, G. W. Small, F. L. Mastaglia, J. M. Stajich, F. Zhang, M. W. Booze, J. A. Reaves, L. T. Middleton, J. L. Haines, M. A. Pericak-Vance, J. M. Vance, E. R. Martin posted to parkin genomics snp parkinsons by psique on 2008-04-29 17:33:58 as along with 1 group parkinson's disease references
	Recessive Parkinson's disease. [My Copy] Movement disorders : official journal of the Movement Disorder Society, Vol. 21, No. 7. (July 2006), pp. 885-893. by Shin-ichiro Kubo, Nobutaka Hattori, Yoshikuni Mizuno posted to dj-1 parkin pink1 parkinsons by psique on 2008-04-29 17:22:15 as along with 1 group parkinson's disease references
	Pink1, Parkin, DJ-1 and mitochondrial dysfunction in Parkinson's disease. [My Copy] Curr Opin Neurobiol, Vol. 17, No. 3. (June 2007), pp. 331-337. by M. W. Dodson, M. Guo posted to dj-1 mitochondria parkin pink1 parkinsons by psique on 2008-04-29 17:19:08 as along with 1 person and 1 group novrain parkinson's disease references
	Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and parkin-linked Parkinson's disease. [My Copy] Mov Disord (6 October 2005) by Michele T M T. Hu, Christoph Scherfler, Naheed L L. Khan, et al.Jo V V. Hajnal, Andrew J J. Lees, Niall Quinn, Nicholas W W. Wood, David J J. Brooks posted to parkin dopamine basal_ganglia parkinsons by psique on 2008-04-29 17:12:10 as along with 1 person and 1 group brian parkinson's disease references
	Parkin polymorphisms and environmental exposure: decrease in age at onset of Parkinson's disease. [My Copy] Neurotoxicology, Vol. 28, No. 3. (May 2007), pp. 698-701. by I. Ghione, A. Di Fonzo, F. Saladino, et al.R. Del Bo, N. Bresolin, G. P. Comi, M. Rango posted to genetics parkin snp parkinsons by psique on 2008-04-29 17:10:10 as along with 1 group parkinson's disease references
	Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease. [My Copy] Parkinsonism & related disorders, Vol. 11, No. 6. (September 2005), pp. 341-347. by R. Sinha, B. Racette, J. S. Perlmutter, A. Parsian posted to genetics parkin snp parkinsons by psique on 2008-04-29 17:09:14 as along with 1 group parkinson's disease references
	Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study. [My Copy] Archives of neurology, Vol. 63, No. 6. (June 2006), pp. 826-832. by M. Sun, J. C. Latourelle, G. F. Wooten, et al.M. F. Lew, C. Klein, H. A. Shill, L. I. Golbe, M. H. Mark, B. A. Racette, J. S. Perlmutter, A. Parsian, M. Guttman, G. Nicholson, G. Xu, J. B. Wilk, M. H. Saint-Hilaire, A. L. DeStefano, R. Prakash, S. Williamson, O. Suchowersky, N. Labelle, J. H. Growdon, C. Singer, R. L. Watts, S. Goldwurm, G. Pezzoli, K. B. Baker, P. P. Pramstaller, D. J. Burn, P. F. Chinnery, S. Sherman, P. Vieregge, I. Litvan, T. Gillis, M. E. MacDonald, R. H. Myers, J. F. Gusella posted to genetics parkin parkinsons by psique on 2008-04-29 17:07:27 as along with 1 group parkinson's disease references

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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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