psique's cnv [47 articles] Export

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

	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 20 people and 1 group Zephyrus gthorisson vplagnol biovils chvlyl daed daforerog zufar jessopher DrRichardBadge operon colinveal frohike sf11 sameersoi polivares dswan qayub bpcusack rdiaz Journal picks
	Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen [My Copy] The Lancet Neurology, Vol. 7, No. 4. (April 2008), pp. 319-326. by Hylke M. Blauw, Jan H. Veldink, Michael A. van Es, et al.Paul W. van Vught, Christiaan G. J. Saris, Bert van der Zwaag, Lude Franke, Burbach, John H. Wokke, Roel A. Ophoff posted to gwas genomics cnv als by psique on 2009-10-12 11:02:59 as
	DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources [My Copy] Vol. 84, No. 4. (10 April 2009), pp. 524-533. by Helen V. Firth, Shola M. Richards, A. Paul Bevan, et al.Stephen Clayton, Manuel Corpas, Diana Rajan, Steven V. Vooren, Yves Moreau, Roger M. Pettett, Nigel P. Carter posted to genomics database cnv bioinformatics by psique on 2009-10-12 10:49:26 as along with 2 people bmenten pkonings
	Common variants conferring risk of schizophrenia [My Copy] Nature, Vol. 460, No. 7256. (01 July 2009), pp. 744-747. by Hreinn Stefansson, Roel A. Ophoff, Stacy Steinberg, et al.Ole A. Andreassen, Sven Cichon, Dan Rujescu, Thomas Werge, Olli P. H. Pietilainen, Ole Mors, Preben B. Mortensen, Engilbert Sigurdsson, Omar Gustafsson, Mette Nyegaard, Annamari Tuulio-Henriksson, Andres Ingason, Thomas Hansen, Jaana Suvisaari, Jouko Lonnqvist, Tiina Paunio, Anders D. Borglum, Annette Hartmann, Anders Fink-Jensen, Merete Nordentoft, David Hougaard, Bent Norgaard-Pedersen, Yvonne Bottcher, Jes Olesen, Rene Breuer, Hans-Jurgen Moller, Ina Giegling, Henrik B. Rasmussen, Sally Timm, Manuel Mattheisen, Istvan Bitter, Janos M. Rethelyi, Brynja B. Magnusdottir, Thordur Sigmundsson, Pall Olason, MassonGisli, Jeffrey R. Gulcher, Magnus Haraldsson, Ragnheidur Fossdal, Thorgeir E. Thorgeirsson, Unnur Thorsteinsdottir, Mirella Ruggeri, Sarah Tosato, Barbara Franke, Eric Strengman, Lambertus A. Kiemeney, Ingrid Melle, Srdjan Djurovic, Lilia Abramova, Vasily Kaleda, Julio Sanjuan, Rosa de Frutos, Elvira Bramon, Evangelos Vassos, Gillian Fraser, Ulrich Ettinger, Marco Picchioni, Nicholas Walker, Timi Toulopoulou, Anna C. Need, Dongliang Ge, Joeng Lim Yoon, Kevin V. Shianna, Nelson B. Freimer, Rita M. Cantor, Robin Murray, Augustine Kong, Vera Golimbet, Angel Carracedo, Celso Arango, Javier Costas, Erik G. Jonsson, Lars Terenius, Ingrid Agartz, Hannes Petursson, Markus M. Nothen, Marcella Rietschel, Paul M. Matthews, Pierandrea Muglia, Leena Peltonen, David St Clair, David B. Goldstein, Kari Stefansson, David A. Collier posted to schizo gwas genomics cnv by psique on 2009-10-11 11:54:20 as along with 5 people and 1 group pkonings djkt jbhiatt Terkko daforerog Journal picks
	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
	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
	Genomic copy number variation, human health, and disease. [My Copy] Lancet, Vol. 374, No. 9686. (25 July 2009), pp. 340-350. by Louise V. Wain, John A. Armour, Martin D. Tobin posted to review genomics genetics cnv by psique on 2009-09-06 09:31:57 as along with 5 people jandot daforerog guhjy rdiaz pkonings
	Complex disease: Schizophrenia: missing heritability found? [My Copy] Nat Rev Genet, Vol. 10, No. 8. (August 2009), pp. 509-509. by Chris Gunter posted to schizophrenia polygenic_score genetics cnv by psique on 2009-08-15 23:38:37 as along with 1 person fenghezi
	Mechanisms of change in gene copy number [My Copy] Nature Reviews Genetics, Vol. 10, No. 8. (01 August 2009), pp. 551-564. by P. J. Hastings, James R. Lupski, Susan M. Rosenberg, Grzegorz Ira posted to cnv genetics genomics review by psique on 2009-07-17 08:16:31 as along with 13 people and 1 group biovils Zephyrus sameersoi xingxu qayub nicolesoranzo pkonings jandot rdiaz misonneh fenghezi daforerog ppgardne Journal picks
	Complex human chromosomal and genomic rearrangements. [My Copy] Trends in genetics : TIG, Vol. 25, No. 7. (25 July 2009), pp. 298-307. by Feng Zhang, Claudia M. Carvalho, James R. Lupski posted to cnv genomics review by psique on 2009-07-11 14:33:52 as along with 1 person sameersoi
	Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. [My Copy] Nature, Vol. 459, No. 7246. (28 May 2009), pp. 569-573. by Joseph T. Glessner, Kai Wang, Guiqing Cai, et al.Olena Korvatska, Cecilia E. Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W. Brune, Jonathan P. Bradfield, Marcin Imielinski, Edward C. Frackelton, Jennifer Reichert, Emily L. Crawford, Jeffrey Munson, Patrick M. Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James Flory, Frederick Otieno, Maria Garris, Latha Soorya, Lambertus Klei, Joseph Piven, Kacie J. Meyer, Evdokia Anagnostou, Takeshi Sakurai, Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, Christopher J. McDougle, Lea K. Davis, Judith Miller, David J. Posey, Shana Michaels, Alexander Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, Robert T. Schultz, Geraldine Dawson, Thomas Owley, William M. McMahon, Thomas H. Wassink, John A. Sweeney, John I. Nurnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F. Grant, Maja Bucan, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Gerard D. Schellenberg, Hakon Hakonarson posted to autism cnv genomics gwas by psique on 2009-05-08 14:27:34 as along with 8 people rdiaz daforerog pkonings fenghezi scjparker dswan neils jbhiatt
	The evolutionary relationship between gene duplication and alternative splicing [My Copy] Gene, Vol. 427, No. 1-2. (31 December 2008), pp. 19-31. by L. Jin, K. Kryukov, J. Clemente, et al.T. Komiyama, Y. Suzuki, T. Imanishi, K. Ikeo, T. Gojobori posted to cnv dna evolution genetics splicing by psique on 2009-05-03 02:16:18 as
	Emerging microdeletion and microduplication syndromes; the counseling paradigm [My Copy] European Journal of Medical Genetics (24 March 2009) by Conny M. van Ravenswaaij-Arts, Tjitske Kleefstra posted to genetics cnv by psique on 2009-05-02 11:11:38 as
	DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources [My Copy] The American Journal of Human Genetics, Vol. 84, No. 4. (10 April 2009), pp. 524-533. by Helen V. Firth, Shola M. Richards, Paul A. Bevan, et al.Stephen Clayton, Manuel Corpas, Diana Rajan, Steven V. Vooren, Yves Moreau, Roger M. Pettett, Nigel P. Carter posted to database genomics cnv by psique on 2009-04-21 18:24:23 as along with 1 person guhjy
	The impact of copy number variation on local gene expression in mouse hematopoietic stem and progenitor cells. [My Copy] Nature genetics (8 March 2009) by Patrick Cahan, Yedda Li, Masayo Izumi, Timothy A A. Graubert posted to cnv gene_expression genetics by psique on 2009-04-15 12:40:35 as along with 5 people rdiaz shikin fenghezi djkt jdbowes
	Segmental copy number variation shapes tissue transcriptomes. [My Copy] Nature genetics (8 March 2009) by Charlotte N N. Henrichsen, Nicolas Vinckenbosch, Sebastian Zöllner, et al.Evelyne Chaignat, Sylvain Pradervand, Frédéric Schütz, Manuel Ruedi, Henrik Kaessmann, Alexandre Reymond posted to cnv gene_expression transcription by psique on 2009-04-03 14:44:32 as along with 11 people leemachado stubrown absterga lwaldron bertrandservin fenghezi megraw djkt rdiaz daforerog buyske
	Detection of large-scale variation in the human genome. [My Copy] Nature genetics, Vol. 36, No. 9. (September 2004), pp. 949-951. by A. John Iafrate, Lars Feuk, Miguel N. Rivera, et al.Marc L. Listewnik, Patricia K. Donahoe, Ying Qi, Stephen W. Scherer, Charles Lee posted to cnv genomics by psique on 2009-04-01 19:58:10 as along with 7 people and 2 groups daforerog daed pcahan1 dchughes ealloza bioguru2000 Ema G4ID Genetics-of-Gambling
	Large-Scale Copy Number Polymorphism in the Human Genome [My Copy] Science, Vol. 305, No. 5683. (23 July 2004), pp. 525-528. by Jonathan Sebat, B. Lakshmi, Jennifer Troge, et al.Joan Alexander, Janet Young, Par Lundin, Susanne Maner, Hillary Massa, Megan Walker, Maoyen Chi, Nicholas Navin, Robert Lucito, John Healy, James Hicks, Kenny Ye, Andrew Reiner, T. Conrad Gilliam, Barbara Trask, Nick Patterson, Anders Zetterberg, Michael Wigler posted to cnv genomics by psique on 2009-04-01 19:45:04 as along with 11 people and 2 groups stharward krokicki waszak mercaptan pcahan1 mrkrause rdiaz jeremymiller massivemayhem jpdemuth Ema Bioinformatics GeschwindLab
	A burst of segmental duplications in the genome of the African great ape ancestor [My Copy] Nature, Vol. 457, No. 7231. (12 February 2009), pp. 877-881. by Tomas Marques-Bonet, Jeffrey M. Kidd, Mario Ventura, et al.Tina A. Graves, Ze Cheng, Ladeana W. Hillier, Zhaoshi Jiang, Carl Baker, Ray Malfavon-Borja, Lucinda A. Fulton, Can Alkan, Gozde Aksay, Santhosh Girirajan, Priscillia Siswara, Lin Chen, Maria F. Cardone, Arcadi Navarro, Elaine R. Mardis, Richard K. Wilson, Evan E. Eichler posted to cnv evolution genomics by psique on 2009-03-25 17:09:08 as along with 8 people dakelley provero shoshin anphony pkonings treangen djkt jbhiatt
	New handles on genomic structural variation. [My Copy] Nature genetics, Vol. 40, No. 10. (October 2008) posted to cnv genetics methods snp by psique on 2009-03-24 17:57:01 as along with 3 people slevy03 cheyloveday Zephyrus
	Rare chromosomal deletions and duplications increase risk of schizophrenia. [My Copy] Nature, Vol. 455, No. 7210. (11 September 2008), pp. 237-241. by International Schizophrenia Consortium posted to cnv genetics genomics schizophrenia by psique on 2009-03-24 17:40:02 as along with 2 people daed daforerog
	Structural variation in the human genome [My Copy] Nature Reviews Genetics, Vol. 7, No. 2. (01 February 2006), pp. 85-97. by Lars Feuk, Andrew R. Carson, Stephen W. Scherer posted to cnv genetics genomics review by psique on 2009-03-24 16:26:26 as along with 25 people and 11 groups ajbattle bertelsen baizhang APRegier Neeperando xingxu daforerog Zephyrus dlobo jandot cgreal balajis bala balicea dchughes tabu darcyduke adepace AaronDarling rdiaz massivemayhem cat_worth jmrivort ccr Lip GEB CGREL structural_bioinformatics Bioinformatics EisenLab SFX-Verde-team-MITLibraries G4ID G-quadruplex Supramolecular DictyosteliumGroup Genetics-of-Gambling
	Strong association of de novo copy number mutations with autism. [My Copy] Science (New York, N.Y.), Vol. 316, No. 5823. (20 April 2007), pp. 445-449. by Jonathan Sebat, B. Lakshmi, Dheeraj Malhotra, et al.Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall, Anthony Leotta, Deepa Pai, Ray Zhang, Yoon-Ha H. Lee, James Hicks, Sarah J. Spence, Annette T. Lee, Kaija Puura, Terho Lehtimäki, David Ledbetter, Peter K. Gregersen, Joel Bregman, James S. Sutcliffe, Vaidehi Jobanputra, Wendy Chung, Dorothy Warburton, Mary-Claire C. King, David Skuse, Daniel H. Geschwind, T. Conrad Gilliam, Kenny Ye, Michael Wigler posted to autism cnv genomics by psique on 2009-03-24 16:18:34 as along with 7 people and 2 groups fenghezi jbhiatt daforerog noushin jo_davies sekulerlab mrkrause Bioinformatics VisionLab
	Copy number variation showers in schizophrenia: an emerging hypothesis [My Copy] Molecular Psychiatry, Vol. aop, No. current. by S. M. Singh, C. A. Castellani, R. L. O'Reilly posted to cnv genomics schizophrenia by psique on 2009-03-24 16:14:22 as along with 1 person hkl128
	The fine-scale and complex architecture of human copy-number variation. [My Copy] American journal of human genetics, Vol. 82, No. 3. (24 March 2008), pp. 685-695. by George H. Perry, Amir Ben-Dor, Anya Tsalenko, et al.Nick Sampas, Laia Rodriguez-Revenga, Charles W. Tran, Alicia Scheffer, Israel Steinfeld, Peter Tsang, N. Alice Yamada, Han Soo S. Park, Jong-Il I. Kim, Jeong-Sun S. Seo, Zohar Yakhini, Stephen Laderman, Laurakay Bruhn, Charles Lee posted to cnv genomics methods by psique on 2009-03-19 17:21:51 as along with 4 people daforerog vplagnol daed guhjy
	Copy-number variation and association studies of human disease. [My Copy] Nature genetics, Vol. 39, No. 7 Suppl. (July 2007) by Steven A. McCarroll, David M. Altshuler posted to cnv genomics methods by psique on 2009-03-19 17:11:21 as along with 9 people and 1 group daforerog waszak jo_davies vplagnol guhjy mrkrause balicea rdiaz jasonflannick Bioinformatics
	Common deletion polymorphisms in the human genome [My Copy] Nature Genetics, Vol. 38, No. 1. (04 December 2005), pp. 86-92. by Steven A. Mccarroll, Tracy N. Hadnott, George H. Perry, et al.Pardis C. Sabeti, Michael C. Zody, Jeffrey C. Barrett, Stephanie Dallaire, Stacey B. Gabriel, Charles Lee, Mark J. Daly, David M. Altshuler, The posted to cnv genomics by psique on 2009-03-19 17:08:45 as along with 1 person bpb
	Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. [My Copy] Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1253-1260. by Joshua M. Korn, Finny G. Kuruvilla, Steven A. McCarroll, et al.Alec Wysoker, James Nemesh, Simon Cawley, Earl Hubbell, Jim Veitch, Patrick J. Collins, Katayoon Darvishi, Charles Lee, Marcia M. Nizzari, Stacey B. Gabriel, Shaun Purcell, Mark J. Daly, David Altshuler posted to bioinformatics cnv methods snp by psique on 2009-03-19 17:05:59 as along with 14 people shikin sameersoi fenghezi buyske maren guhjy pdexheimer pengchy caseybrown dakelley djkt daed rdiaz vplagnol
	Hidden copy number variation in the HapMap population. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 105, No. 29. (22 July 2008), pp. 10067-10072. by J. C. Marioni, M. White, S. Tavaré, A. G. Lynch posted to bioinformatics cnv genomics hapmap methods by psique on 2009-03-19 16:55:55 as along with 5 people and 1 group Zephyrus jfr waszak guhjy Stew Roswell Cancer Crosstalk
	Copy-number variation in control population cohorts. [My Copy] Hum Mol Genet, Vol. 16 Spec No. 2 (15 October 2007) by D. Pinto, C. Marshall, L. Feuk, S. W. Scherer posted to cnv genomics methods population by psique on 2009-03-19 16:29:31 as along with 1 person giovanni
	Copy Number Variation Detection via High-Density SNP Genotyping [My Copy] Cold Spring Harbor Protocols, Vol. 2008, No. 7. (1 June 2008), pdb.top46. by Kai Wang, Maja Bucan posted to cnv genetics methods penncnv by psique on 2009-03-19 16:28:23 as along with 1 person waszak
	On the frequency of copy number variants [My Copy] Bioinformatics, Vol. 24, No. 20. (15 October 2008), pp. 2350-2355. by Iuliana Ionita-Laza, Nan M. Laird, Benjamin A. Raby, Scott T. Weiss, Christoph Lange posted to cnv genomics by psique on 2009-03-19 15:26:16 as along with 2 people rdiaz djkt
	Genotype, haplotype and copy-number variation in worldwide human populations. [My Copy] Nature, Vol. 451, No. 7181. (21 February 2008), pp. 998-1003. by Mattias Jakobsson, Sonja W. Scholz, Paul Scheet, et al.J. Raphael Gibbs, Jenna M. VanLiere, Hon-Chung C. Fung, Zachary A. Szpiech, James H. Degnan, Kai Wang, Rita Guerreiro, Jose M. Bras, Jennifer C. Schymick, Dena G. Hernandez, Bryan J. Traynor, Javier Simon-Sanchez, Mar Matarin, Angela Britton, Joyce van de Leemput, Ian Rafferty, Maja Bucan, Howard M. Cann, John A. Hardy, Noah A. Rosenberg, Andrew B. Singleton posted to cnv genomics penncnv population by psique on 2009-03-19 14:51:59 as along with 15 people and 2 groups misonneh vplagnol turnersd daforerog sameersoi ilyashl Zephyrus djkt ramensky mailund thomaskelder Archaeogenetics jo_davies guhjy frohike Roswell Cancer Crosstalk Fasting, food and evolution
	Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles [My Copy] Vol. 82, No. 3. (3 March 2008), pp. 763-771. by Carl E. Bruder, Arkadiusz Piotrowski, Antoinet A. Gijsbers, et al.Robin Andersson, Stephen Erickson, Diaz, Uwe Menzel, Johanna Sandgren, Desiree von Tell, Andrzej Poplawski, Michael Crowley, Chiquito Crasto, Christopher E. Partridge, Hemant Tiwari, David B. Allison, Jan Komorowski, Gert-Jan B. van Ommen, Dorret I. Boomsma, Nancy L. Pedersen, Johan T. den Dunnen, Karin Wirdefeldt, Jan P. Dumanski posted to cnv genetics by psique on 2009-03-13 06:31:52 as
	ALOHOMORA: a tool for linkage analysis using 10K SNP array data [My Copy] Bioinformatics, Vol. 21, No. 9. (1 May 2005), pp. 2123-2125. by Franz Ruschendorf, Peter Nurnberg posted to bioinformatics cnv methods by psique on 2009-03-11 10:59:59 as along with 1 person darian
	DNA variations in human and medical genetics: 25 years of my experience [My Copy] J Hum Genet, Vol. 54, No. 1. (January 2009), pp. 1-8. by Yusuke Nakamura posted to cnv genetics snp by psique on 2009-02-12 13:58:42 as along with 2 people guhjy pkonings
	A genome-wide investigation of SNPs and CNVs in schizophrenia. [My Copy] PLoS genetics, Vol. 5, No. 2. (6 February 2009), e1000373. by Anna C. Need, Dongliang Ge, Michael E. Weale, et al.Jessica Maia, Sheng Feng, Erin L. Heinzen, Kevin V. Shianna, Woohyun Yoon, Dalia Kasperaviciūte, Massimo Gennarelli, Warren J. Strittmatter, Cristian Bonvicini, Giuseppe Rossi, Karu Jayathilake, Philip A. Cola, Joseph P. McEvoy, Richard S. Keefe, Elizabeth M. Fisher, Pamela L. St Jean, Ina Giegling, Annette M. Hartmann, Hans-Jürgen J. Möller, Andreas Ruppert, Gillian Fraser, Caroline Crombie, Lefkos T. Middleton, David St Clair, Allen D. Roses, Pierandrea Muglia, Clyde Francks, Dan Rujescu, Herbert Y. Meltzer, David B. Goldstein posted to cnv genomics gwas schizophrenia snp by psique on 2009-02-07 02:16:11 as along with 7 people fenghezi xingxu rdiaz skembel pkonings daforerog djkt
	PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data [My Copy] Genome Research, Vol. 17 (5 October 2007), pp. 1665-1674. by Kai Wang, Mingyao Li, Dexter Hadley, et al.Rui Liu, Joseph Glessner, Struan F. A. Grant, Hakon Hakonarson, Maja Bucan posted to bioinformatics cnv genomics methods by psique on 2009-02-02 16:21:59 as
	Modeling genetic inheritance of copy number variations [My Copy] Nucl. Acids Res., Vol. 36, No. 21. (1 December 2008), e138. by Kai Wang, Zhen Chen, Mahlet G. Tadesse, et al.Joseph Glessner, Struan F. A. Grant, Hakon Hakonarson, Maja Bucan, Mingyao Li posted to bioinformatics cnv genomics methods penncnv by psique on 2009-02-02 16:18:55 as along with 3 people sameersoi noushin rdiaz
	Population analysis of large copy number variants and hotspots of human genetic disease. [My Copy] American journal of human genetics, Vol. 84, No. 2. (22 February 2009), pp. 148-161. by Andy Itsara, Gregory M. Cooper, Carl Baker, et al.Santhosh Girirajan, Jun Li, Devin Absher, Ronald M. Krauss, Richard M. Myers, Paul M. Ridker, Daniel I. Chasman, Heather Mefford, Phyllis Ying, Deborah A. Nickerson, Evan E. Eichler posted to cnv genetics population by psique on 2009-01-23 17:23:37 as along with 8 people and 1 group daforerog jsatkosk turnersd sameersoi guhjy Zephyrus pkonings jdbowes Roswell Cancer Crosstalk
	Analysis of copy number variation using quantitative interspecies competitive PCR. [My Copy] Nucleic acids research, Vol. 36, No. 17. (1 October 2008), e112. by Nigel M. Williams, Hywel Williams, Elisa Majounie, et al.Nadine Norton, Beate Glaser, Huw R. Morris, Michael J. Owen, Michael C. O'Donovan posted to cnv methods by psique on 2008-10-29 07:29:34 as along with 2 people daforerog rdiaz
	Copy-number variations associated with neuropsychiatric conditions. [My Copy] Nature, Vol. 455, No. 7215. (16 October 2008), pp. 919-923. by Edwin H. Cook, Stephen W. Scherer posted to autism cnv development psychiatry schizophrenia by psique on 2008-10-17 14:55:55 as along with 3 people daforerog waszak jdbowes
	Integrated detection and population-genetic analysis of SNPs and copy number variation. [My Copy] Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1166-1174. by Steven A. McCarroll, Finny G. Kuruvilla, Joshua M. Korn, et al.Simon Cawley, James Nemesh, Alec Wysoker, Michael H. Shapero, Paul I. de Bakker, Julian B. Maller, Andrew Kirby, Amanda L. Elliott, Melissa Parkin, Earl Hubbell, Teresa Webster, Rui Mei, James Veitch, Patrick J. Collins, Robert Handsaker, Steve Lincoln, Marcia Nizzari, John Blume, Keith W. Jones, Rich Rava, Mark J. Daly, Stacey B. Gabriel, David Altshuler posted to cnv genomics genotyping snp by psique on 2008-10-02 13:51:49 as along with 20 people and 1 group shikin vplagnol buyske turnersd sameersoi gruberjd Hans45 pdexheimer madreach waszak caseybrown rsantana Zephyrus jbsaltz Ema misonneh djkt daed rdiaz guhjy Roswell Cancer Crosstalk
	Systematic assessment of copy number variant detection via genome-wide SNP genotyping. [My Copy] Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1199-1203. by Gregory M. Cooper, Troy Zerr, Jeffrey M. Kidd, Evan E. Eichler, Deborah A. Nickerson posted to cnv genomics genotyping snp by psique on 2008-10-02 13:50:05 as along with 12 people and 1 group shikin sameersoi daforerog maren pengchy vplagnol waszak caseybrown Zephyrus misonneh rdiaz guhjy Roswell Cancer Crosstalk
	Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes [My Copy] Science, Vol. 315, No. 5813. (9 February 2007), pp. 848-853. by Barbara E. Stranger, Matthew S. Forrest, Mark Dunning, et al.Catherine E. Ingle, Claude Beazley, Natalie Thorne, Richard Redon, Christine P. Bird, Anna de Grassi, Charles Lee, Chris Tyler-Smith, Nigel Carter, Stephen W. Scherer, Simon Tavare, Panagiotis Deloukas, Matthew E. Hurles, Emmanouil T. Dermitzakis posted to cnv gene_expression genomics hapmap snp by psique on 2008-09-23 16:17:37 as along with 32 people and 5 groups biovils lp2 daveGerrard sameersoi timhubbard Zephyrus ajbattle jonilaserson ilyashl emptyhb buyske zufar koller waszak daed jo_davies srp33 guhjy jfr dpollard balicea rdiaz qfwills djkt vplagnol shigepong jlangdon xingxu cisevol caseybrown frohike jandot Roswell Cancer Crosstalk Visiting Position Bioinformatics EisenLab cis-regulatory-evolution
	alpha-Synuclein locus triplication causes Parkinson's disease. [My Copy] Science (New York, N.Y.), Vol. 302, No. 5646. (31 October 2003) by A. B. Singleton, M. Farrer, J. Johnson, et al.A. Singleton, S. Hague, J. Kachergus, M. Hulihan, T. Peuralinna, A. Dutra, R. Nussbaum, S. Lincoln, A. Crawley, M. Hanson, D. Maraganore, C. Adler, M. R. Cookson, M. Muenter, M. Baptista, D. Miller, J. Blancato, J. Hardy, K. Gwinn-Hardy posted to cnv synuclein parkinsons by psique on 2008-09-15 11:36:32 as along with 1 group parkinson's disease references
	Global variation in copy number in the human genome [My Copy] Nature, Vol. 444, No. 7118. (23 November 2006), pp. 444-454. by Richard Redon, Shumpei Ishikawa, Karen R. Fitch, et al.Lars Feuk, George H. Perry, T. Daniel Andrews, Heike Fiegler, Michael H. Shapero, Andrew R. Carson, Wenwei Chen, Eun K. Cho, Stephanie Dallaire, Jennifer L. Freeman, Juan R. Gonzalez, Monica Gratacos, Jing Huang, Dimitrios Kalaitzopoulos, Daisuke Komura, Jeffrey R. MacDonald, Christian R. Marshall, Rui Mei, Lyndal Montgomery, Kunihiro Nishimura, Kohji Okamura, Fan Shen, Martin J. Somerville, Joelle Tchinda, Armand Valsesia, Cara Woodwark, Fengtang Yang, Junjun Zhang, Tatiana Zerjal, Jane Zhang, Lluis Armengol, Donald F. Conrad, Xavier Estivill, Chris Tyler-Smith, Nigel P. Carter, Hiroyuki Aburatani, Charles Lee, Keith W. Jones, Stephen W. Scherer, Matthew E. Hurles posted to cnv genomics by psique on 2008-09-15 10:50:33 as along with 41 people and 7 groups sameersoi lp2 ilyashl ajbattle darian jonilaserson jrvalcourt turnersd guhjy daforerog noushin Glires ivanek waszak jo_davies bpb jfr balajis pradiptaray dpollard mtagaya adepace aswin rdiaz qfwills ealloza vplagnol giovanni jeremymiller frohike vpschulz raiyar ramensky ccr azazello dbgrant colinveal xingxu srp33 Ema daed parkinson's disease references Bioinformatics EisenLab BioinfoCIPF GeschwindLab steinmetzlab MBLAB

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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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