psique's genetics [at least 200 articles] Export

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

	LRRK2 and GBA mutations differentially affect the initial presentation of Parkinson disease. [My Copy] Neurogenetics (21 May 2009) by Z. Gan-Or, A. Bar-Shira, A. Mirelman, et al.T. Gurevich, M. Kedmi, N. Giladi, A. Orr-Urtreger posted to pd lrrk2 genetics gba by psique on 2009-11-07 23:22:54 as
	Gain-of-function variant in GLUD2 glutamate dehydrogenase modifies Parkinson's disease onset [My Copy] European Journal of Human Genetics, Vol. aop, No. current. (14 October 2009) by Andreas Plaitakis, Helen Latsoudis, Konstantinos Kanavouras, et al.Beate Ritz, Jeff M. Bronstein, Irene Skoula, Vasileios Mastorodemos, Spyridon Papapetropoulos, Nikolas Borompokas, Ioannis Zaganas, Georgia Xiromerisiou, George M. Hadjigeorgiou, Cleanthe Spanaki posted to yopd pd gwas glutamate_dehydrogenase genetics by psique on 2009-11-07 22:59:00 as
	Sporadic cases are the norm for complex disease [My Copy] European Journal of Human Genetics, Vol. aop, No. current. (14 October 2009) by Jian Yang, Peter M. Visscher, Naomi R. Wray posted to sporadic_cases polygenic_inheritance heterogeneity genetics complex_disease by psique on 2009-11-07 22:52:24 as
	Genetics of motor neuron disorders: new insights into pathogenic mechanisms [My Copy] Nature Reviews Genetics, Vol. 10, No. 11. (13 October 2009), pp. 769-782. by Patrick A. Dion, Hussein Daoud, Guy A. Rouleau posted to review mnd genetics als by psique on 2009-11-05 13:24:29 as along with 2 people bpcusack inbetweener
	The genetics of inbreeding depression [My Copy] Nature Reviews Genetics, Vol. 10, No. 11. (01 November 2009), pp. 783-796. by Deborah Charlesworth, John H. Willis posted to review genomics genetics evolution consanguineous by psique on 2009-11-05 13:18:39 as along with 1 person and 1 group qayub Journal picks
	Origins and functional impact of copy number variation in the human genome [My Copy] Nature, Vol. advance online publication (07 October 2009) by Donald F. Conrad, Dalila Pinto, Richard Redon, et al.Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T. Daniel Andrews, Chris Barnes, Peter Campbell, Tomas Fitzgerald, Min Hu, Chun H. Ihm, Kati Kristiansson, Daniel G. MacArthur, Jeffrey R. MacDonald, Ifejinelo Onyiah, Andy W. Pang, Sam Robson, Kathy Stirrups, Armand Valsesia, Klaudia Walter, John Wei, Chris Tyler-Smith, Nigel P. Carter, Charles Lee, Stephen W. Scherer, Matthew E. Hurles posted to methods genomics genetics cnv by psique on 2009-11-05 13:02:47 as along with 16 people and 1 group chvlyl daed daforerog zufar jessopher DrRichardBadge operon colinveal frohike sf11 sameersoi polivares dswan qayub bpcusack rdiaz Journal picks
	Spatial patterns of variation due to natural selection in humans [My Copy] Nature Reviews Genetics, Vol. 10, No. 11. (13 October 2009), pp. 745-755. by John Novembre, Anna Di Rienzo posted to population_structure population_genetics population natural_selection geography genetics by psique on 2009-11-05 12:55:24 as along with 5 people and 1 group emptyhb gjuggler qayub merpublic daforerog Journal picks
	Common disorders are quantitative traits. [My Copy] Nature reviews. Genetics, Vol. advance online publication (27 October 2009) by Robert Plomin, Claire M. Haworth, Oliver S. Davis posted to quantitative_traits gwas genetics common_disease by psique on 2009-11-03 21:30:41 as along with 1 person daforerog
	Genetic and molecular insights into the development and evolution of sexual dimorphism [My Copy] Nature Reviews Genetics, Vol. 10, No. 11. (01 November 2009), pp. 797-804. by Thomas M. Williams, Sean B. Carroll posted to sexual_dimorphism review genetics gender by psique on 2009-11-02 15:23:34 as along with 4 people and 1 group gjuggler qayub reyez bpcusack Journal picks
	From the detection of population structure to the reconstruction of population history: the historical reading of the human genome [My Copy] Heredity, Vol. 103, No. 5. (22 July 2009), pp. 362-363. by H. Laayouni, J. Bertranpetit posted to population_structure methods genomics genetics evolution by psique on 2009-10-21 22:54:28 as along with 1 person Geknitics
	Genomic landscape of positive natural selection in Northern European populations. [My Copy] European journal of human genetics : EJHG (21 October 2009) by Tuuli Lappalainen, Elina Salmela, Peter M. Andersen, et al.Karin Dahlman-Wright, Pertti Sistonen, Marja-Liisa L. Savontaus, Stefan Schreiber, Päivi Lahermo, Juha Kere posted to population_structure genomics genetics evolution by psique on 2009-10-21 22:51:06 as along with 1 person Terkko
	Global patterns of cis variation in human cells revealed by high-density allelic expression analysis [My Copy] Nature Genetics, Vol. 41, No. 11. (18 October 2009), pp. 1216-1222. by Bing Ge, Dmitry K. Pokholok, Tony Kwan, et al.Elin Grundberg, Lisanne Morcos, Dominique J. Verlaan, Jennie Le, Vonda Koka, Kevin C. L. Lam, Vincent Gagne, Joana Dias, Rose Hoberman, Alexandre Montpetit, Marie-Michele Joly, Edward J. Harvey, Daniel Sinnett, Patrick Beaulieu, Robert Hamon, Alexandru Graziani, Ken Dewar, Eef Harmsen, Jacek Majewski, Harald H. H. Goring, Anna K. Naumova, Mathieu Blanchette, Kevin L. Gunderson, Tomi Pastinen posted to methods genetics bioinformatics allelic_expression by psique on 2009-10-20 20:48:36 as along with 9 people and 1 group fenghezi songpku gderwin djkt qayub dill2009 zufar daforerog vplagnol Journal picks
	Recent de novo origin of human protein-coding genes. [My Copy] Genome research, Vol. 19, No. 10. (2 October 2009), pp. 1752-1759. by David G. Knowles, Aoife McLysaght posted to human_evolution genetics evolution by psique on 2009-10-20 12:40:51 as along with 8 people and 2 groups xianjun gjuggler biomcgary megraw fenghezi avilella bpcusack djkt Journal picks Ensembl Compara citations
	Differential contribution of genetic variation in multiple brain nicotinic cholinergic receptors to nicotine dependence: recent progress and emerging open questions [My Copy] Molecular Psychiatry, Vol. 14, No. 10. (30 June 2009), pp. 912-945. by L. Greenbaum, B. Lerer posted to nicotine genetics addiction by psique on 2009-10-19 19:52:45 as
	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
	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
	Worldwide Human Relationships Inferred from Genome-Wide Patterns of Variation [My Copy] Science, Vol. 319, No. 5866. (22 February 2008), pp. 1100-1104. by Jun Z. Li, Devin M. Absher, Hua Tang, et al.Audrey M. Southwick, Amanda M. Casto, Sohini Ramachandran, Howard M. Cann, Gregory S. Barsh, Marcus Feldman, Luigi L. Cavalli-Sforza, Richard M. Myers posted to population_structure population gwas genomics genetics by psique on 2009-10-12 10:39:01 as along with 14 people and 1 group ilyashl daforerog Zephyrus cgravlee echinotrix EsepBib ramensky zwang qwermish xingxu mailund Dorkins adacier Archaeogenetics Roswell Cancer Crosstalk
	How to interpret a genome-wide association study. [My Copy] JAMA : the journal of the American Medical Association, Vol. 299, No. 11. (19 March 2008), pp. 1335-1344. by Thomas A. Pearson, Teri A. Manolio posted to review gwas genomics genetics by psique on 2009-10-11 22:06:52 as along with 11 people and 1 group operon daforerog kshameer Zephyrus ptrobajo qfwills cheyloveday misonneh guhjy BrianTomasik xingxu Roswell Cancer Crosstalk
	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
	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
	Comparing population structure as inferred from genealogical versus genetic information [My Copy] European Journal of Human Genetics, Vol. aop, No. current. (24 June 2009) by Vincenza Colonna, Teresa Nutile, Ronald R. Ferrucci, et al.Giulio Fardella, Mario Aversano, Guido Barbujani, Marina Ciullo posted to population_structure population genomics genetics by psique on 2009-10-11 11:36:47 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
	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
	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
	Genetics in geographically structured populations: defining, estimating and interpreting FST [My Copy] Nature Reviews Genetics, Vol. 10, No. 9. (01 September 2009), pp. 639-650. by Kent E. Holsinger, Bruce S. Weir posted to stats review population_structure population_stratification genetics by psique on 2009-10-02 07:44:04 as along with 7 people and 1 group Geknitics songpku theodorejmorgan echinotrix misonneh sameersoi ilyashl Morgan Lab-KSU
	Gene-Environment-Wide Interaction Studies in Psychiatry [My Copy] Am J Psychiatry, Vol. 166, No. 9. (1 September 2009), pp. 964-966. by Jim van Os, Bart P. F. Rutten posted to psychiatry genetics environmental_factors by psique on 2009-10-01 15:40:34 as
	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
	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
	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
	A comprehensive analysis of common copy-number variations in the human genome. [My Copy] American journal of human genetics, Vol. 80, No. 1. (January 2007), pp. 91-104. by Kendy K. Wong, Ronald J. deLeeuw, Nirpjit S. Dosanjh, et al.Lindsey R. Kimm, Ze Cheng, Douglas E. Horsman, Calum MacAulay, Raymond T. Ng, Carolyn J. Brown, Evan E. Eichler, Wan L. Lam posted to methods genomics genetics cnv by psique on 2009-09-29 16:21:01 as along with 2 people and 1 group daforerog jlangdon Bioinformatics
	American Founder Mutation for Attenuated Familial Adenomatous Polyposis [My Copy] Clinical Gastroenterology and Hepatology, Vol. 6, No. 1. (January 2008), pp. 46-52. by Deborah W. Neklason, Jeffery Stevens, Kenneth M. Boucher, et al.Richard A. Kerber, Nori Matsunami, Jahn Barlow, Geraldine Mineau, Mark F. Leppert, Randall W. Burt posted to genetics founder_mutation cancer by psique on 2009-09-29 11:05:00 as
	Human population structure, genome autozygosity and human health [My Copy] Genome Medicine, Vol. 1, No. 9. (28 September 2009), 91. by Harry Campbell, Igor Rudan, Alan H. Bittles, Alan F. Wright posted to population_structure population homozygosity genetics by psique on 2009-09-28 18:42:54 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
	The genetic aetiology of late-onset chronic progressive cerebellar ataxia. A population-based study. [My Copy] Journal of neurology, Vol. 256, No. 3. (March 2009), pp. 343-348. by Mark Wardle, Elisa Majounie, Mustapha B. Muzaimi, Nigel M. Williams, Huw R. Morris, Neil P. Robertson posted to population genetics cerebellar_ataxia cardiff by psique on 2009-09-24 18:59:10 as
	Principal components analysis corrects for stratification in genome-wide association studies. [My Copy] Nature genetics, Vol. 38, No. 8. (23 August 2006), pp. 904-909. by Alkes L. Price, Nick J. Patterson, Robert M. Plenge, Michael E. Weinblatt, Nancy A. Shadick, David Reich posted to stats population_stratification methods genomics genetics bioinformatics by psique on 2009-09-23 12:27:25 as along with 11 people Zephyrus engelhardt floatingpoint guhjy sriram_s vplagnol qmwwallace ryanraaum dalexander caseybrown StatAnika
	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
	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

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genetics	276
parkinsons	224
genomics	162
methods	98
gwas	88
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
cognition	29
gene_expression	29
mitochondria	29
addiction	27
basal_ganglia	27
stats	27
pharmacology	26
neurogenesis	24
alzheimers	22
population	21
dj-1	20
psychiatry	20
reward	19
sequencing	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
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
schizo	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
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
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
pd	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
exome	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

psique's genetics [at least 200 articles] Export

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