daforerog's cnv [97 articles] Export

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	Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients. [My Copy] Human mutation, Vol. 27, No. 9. (September 2006), pp. 914-920. by Arvid Suls, Kristl G. Claeys, Dirk Goossens, et al.Boris Harding, Rob Van Luijk, Stefaan Scheers, Liesbet Deprez, Dominique Audenaert, Tine Van Dyck, Sabine Beeckmans, Iris Smouts, Berten Ceulemans, Lieven Lagae, Gunnar Buyse, Nina Barisic, Jean-Paul P. Misson, Jan Wauters, Jurgen Del-Favero, Peter De Jonghe, Lieve R. Claes posted to genotyping cnv by daforerog on 2009-11-20 13:20:23 as
	Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR. [My Copy] Reproduction (Cambridge, England), Vol. 126, No. 3. (September 2003), pp. 279-297. by Maj A. Hultén, Seema Dhanjal, Barbara Pertl posted to genotyping cnv by daforerog on 2009-11-19 17:13:19 as
	Gene dosage methods as diagnostic tools for the identification of chromosome abnormalities. [My Copy] Pathologie-biologie, Vol. 56, No. 6. (September 2008), pp. 345-353. by L. Gouas, C. Goumy, L. Véronèse, A. Tchirkov, P. Vago posted to humgen genotyping genomics cnv by daforerog on 2009-11-18 15:57:41 as
	A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. [My Copy] Nature genetics (8 November 2009) by Marwan Shinawi, Christian P. Schaaf, Samarth S. Bhatt, et al.Zhilian Xia, Ankita Patel, Sau Wai W. Cheung, Brendan Lanpher, Sandra Nagl, Heinrich Stephan S. Herding, Claudia Nevinny-Stickel, Ladonna L. Immken, Gayle Simpson S. Patel, Jennifer Ruth R. German, Arthur L. Beaudet, Pawel Stankiewicz posted to psychgen mr cnv by daforerog on 2009-11-12 15:49:43 as
	Microduplications of 16p11.2 are associated with schizophrenia [My Copy] Nature Genetics, Vol. 41, No. 11. (25 October 2009), pp. 1223-1227. by Shane E. McCarthy, Vladimir Makarov, George Kirov, et al.Anjene M. Addington, Jon McClellan, Seungtai Yoon, Diana O. Perkins, Diane E. Dickel, Mary Kusenda, Olga Krastoshevsky, Verena Krause, Ravinesh A. Kumar, Detelina Grozeva, Dheeraj Malhotra, Tom Walsh, Elaine H. Zackai, Paige Kaplan, Jaya Ganesh, Ian D. Krantz, Nancy B. Spinner, Patricia Roccanova, Abhishek Bhandari, Kevin Pavon, B. Lakshmi, Anthony Leotta, Jude Kendall, Yoon-ha Lee, Vladimir Vacic, Sydney Gary, Lilia M. Iakoucheva, Timothy J. Crow, Susan L. Christian, Jeffrey A. Lieberman, T. Scott Stroup, Terho Lehtimaki, Kaija Puura, Chad Haldeman-Englert, Justin Pearl, Meredith Goodell, Virginia L. Willour, Pamela DeRosse, Jo Steele, Layla Kassem, Jessica Wolff, Nisha Chitkara, Francis J. McMahon, Anil K. Malhotra, James B. Potash, Thomas G. Schulze, Markus M. Nothen, Sven Cichon, Marcella Rietschel, Ellen Leibenluft, Vlad Kustanovich, Clara M. Lajonchere, James S. Sutcliffe, David Skuse, Michael Gill, Louise Gallagher, Nancy R. Mendell, Nick Craddock, Michael J. Owen, Michael C. O'Donovan, Tamim H. Shaikh, Ezra Susser, Lynn E. DeLisi, Patrick F. Sullivan, Curtis K. Deutsch, Judith Rapoport, Deborah L. Levy, Mary-Claire King, Jonathan Sebat posted to schizophrenia psychgen cnv autism by daforerog on 2009-10-26 09:14:49 as along with 3 people n0122897 dchughes vplagnol
	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 popul humgen genomics cnv by daforerog on 2009-10-23 17:05:39 as along with 20 people and 1 group Zephyrus gthorisson vplagnol biovils psique chvlyl daed zufar jessopher DrRichardBadge operon colinveal frohike sf11 sameersoi polivares dswan qayub bpcusack rdiaz Journal picks
	Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 106, No. 39. (29 September 2009), pp. 16746-16751. by Bin Xu, Abigail Woodroffe, Laura Rodriguez-Murillo, et al.J. Louw Roos, Elizabeth J. van Rensburg, Gonçalo R. Abecasis, Joseph A. Gogos, Maria Karayiorgou posted to schizophrenia linkage genomics cnv by daforerog on 2009-10-02 08:49:22 as along with 1 person rdiaz
	Copy number variations of chromosome 16p13.1 region associated with schizophrenia. [My Copy] Molecular psychiatry (29 September 2009) by A. Ingason, D. Rujescu, S. Cichon, et al.E. Sigurdsson, T. Sigmundsson, O. P. Pietiläinen, J. E. Buizer-Voskamp, E. Strengman, C. Francks, P. Muglia, A. Gylfason, O. Gustafsson, P. I. Olason, S. Steinberg, T. Hansen, K. D. Jakobsen, H. B. Rasmussen, I. Giegling, H-J J. Möller, A. Hartmann, C. Crombie, G. Fraser, N. Walker, J. Lonnqvist, J. Suvisaari, A. Tuulio-Henriksson, E. Bramon, L. A. Kiemeney, B. Franke, R. Murray, E. Vassos, T. Toulopoulou, T. W. Mühleisen, S. Tosato, M. Ruggeri, S. Djurovic, O. A. Andreassen, Z. Zhang, T. Werge, R. A. Ophoff, GROUP Investigators, M. Rietschel, M. M. Nöthen, H. Petursson, H. Stefansson, L. Peltonen, D. Collier, K. Stefansson, St M. Clair posted to schizophrenia psychgen humgen cnv by daforerog on 2009-10-01 17:23:14 as along with 1 person Terkko
	Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. [My Copy] Journal of Alzheimer's disease : JAD (11 September 2009) by Erin L. Heinzen, Anna C. Need, Kathleen M. Hayden, et al.Ornit Chiba-Falek, Allen D. Roses, Warren J. Strittmatter, James R. Burke, Christine M. Hulette, Kathleen A. Welsh-Bohmer, David B. Goldstein posted to neurogen humgen gwasneuro gwas find cnv assoc adpdgenrev ad by daforerog on 2009-09-30 21:58:02 as
	A novel technique for measuring variations in DNA copy-number: competitive genomic polymerase chain reaction. [My Copy] BMC genomics, Vol. 8 (02 July 2007), 206. by Kyoko Iwao-Koizumi, Kazunori Maekawa, Yohko Nakamura, et al.Sakae Saito, Shoko Kawamoto, Akira Nakagawara, Kikuya Kato posted to genotyping cnv by daforerog on 2009-09-14 17:14:39 as along with 1 person guhjy
	Novel microdeletion syndromes detected by chromosome microarrays. [My Copy] Human genetics, Vol. 124, No. 1. (August 2008), pp. 1-17. by Anne M. Slavotinek posted to review phenomics humgen genomics cnv by daforerog on 2009-09-14 17:10:29 as
	17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction. [My Copy] Journal of medical genetics, Vol. 46, No. 8. (August 2009), pp. 524-530. by B. Grisart, L. Willatt, A. Destrée, et al.J-P P. Fryns, K. Rack, T. de Ravel, J. Rosenfeld, J. R. Vermeesch, C. Verellen-Dumoulin, R. Sandford posted to psychgen humgen genomics cnv autism by daforerog on 2009-09-14 17:08:00 as
	Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome. [My Copy] Journal of medical genetics, Vol. 46, No. 7. (July 2009), pp. 480-489. by T. Y. Tan, S. Aftimos, L. Worgan, et al.R. Susman, M. Wilson, S. Ghedia, E. P. Kirk, D. Love, A. Ronan, A. Darmanian, A. Slavotinek, J. Hogue, J. B. Moeschler, J. Ozmore, R. Widmer, R. Savarirayan, G. Peters posted to mr humgen genomics cnv by daforerog on 2009-09-14 17:04:11 as
	Evolutionary toggling of the MAPT 17q21.31 inversion region. [My Copy] Nature genetics, Vol. 40, No. 9. (September 2008), pp. 1076-1083. by Michael C. Zody, Zhaoshi Jiang, Hon-Chung C. Fung, et al.Francesca Antonacci, LaDeana W. Hillier, Maria Francesca F. Cardone, Tina A. Graves, Jeffrey M. Kidd, Ze Cheng, Amr Abouelleil, Lin Chen, John Wallis, Jarret Glasscock, Richard K. Wilson, Amy Denise D. Reily, Jaime Duckworth, Mario Ventura, John Hardy, Wesley C. Warren, Evan E. Eichler posted to popul humgen genomics cnv by daforerog on 2009-09-14 17:02:47 as along with 2 people giovanni fenghezi
	Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. [My Copy] Journal of medical genetics, Vol. 45, No. 11. (November 2008), pp. 710-720. by D. A. Koolen, A. J. Sharp, J. A. Hurst, et al.H. V. Firth, S. J. Knight, A. Goldenberg, P. Saugier-Veber, R. Pfundt, L. E. Vissers, A. Destrée, B. Grisart, L. Rooms, N. Van der Aa, M. Field, A. Hackett, K. Bell, M. J. Nowaczyk, G. M. Mancini, P. J. Poddighe, C. E. Schwartz, E. Rossi, M. De Gregori, L. L. Antonacci-Fulton, M. D. McLellan, J. M. Garrett, M. A. Wiechert, T. L. Miner, S. Crosby, R. Ciccone, L. Willatt, A. Rauch, M. Zenker, S. Aradhya, M. A. Manning, T. M. Strom, J. Wagenstaller, A. C. Krepischi-Santos, A. M. Vianna-Morgante, C. Rosenberg, S. M. Price, H. Stewart, C. Shaw-Smith, H. G. Brunner, A. O. Wilkie, J. A. Veltman, O. Zuffardi, E. E. Eichler, B. B. de Vries posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:59:40 as
	A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. [My Copy] Nature genetics, Vol. 38, No. 9. (13 September 2006), pp. 999-1001. by David A. Koolen, Lisenka E. Vissers, Rolph Pfundt, et al.Nicole de Leeuw, Samantha J. Knight, Regina Regan, R. Frank Kooy, Edwin Reyniers, Corrado Romano, Marco Fichera, Albert Schinzel, Alessandra Baumer, Britt-Marie M. Anderlid, Jacqueline Schoumans, Nine V. Knoers, Ad Geurts G. van Kessel, Erik A. Sistermans, Joris A. Veltman, Han G. Brunner, Bert B. de Vries posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:56:36 as
	A common inversion under selection in Europeans. [My Copy] Nature genetics, Vol. 37, No. 2. (16 February 2005), pp. 129-137. by Hreinn Stefansson, Agnar Helgason, Gudmar Thorleifsson, et al.Valgerdur Steinthorsdottir, Gisli Masson, John Barnard, Adam Baker, Aslaug Jonasdottir, Andres Ingason, Vala G. Gudnadottir, Natasa Desnica, Andrew Hicks, Arnaldur Gylfason, Daniel F. Gudbjartsson, Gudrun M. Jonsdottir, Jesus Sainz, Kari Agnarsson, Birgitta Birgisdottir, Shyamali Ghosh, Adalheidur Olafsdottir, Jean-Baptiste B. Cazier, Kristleifur Kristjansson, Michael L. Frigge, Thorgeir E. Thorgeirsson, Jeffrey R. Gulcher, Augustine Kong, Kari Stefansson posted to popul humgen highly genomics cnv by daforerog on 2009-09-14 16:55:58 as along with 4 people vplagnol giovanni APRegier kndiaye
	Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. [My Copy] Nature genetics, Vol. 38, No. 9. (13 September 2006), pp. 1038-1042. by Andrew J. Sharp, Sierra Hansen, Rebecca R. Selzer, et al.Ze Cheng, Regina Regan, Jane A. Hurst, Helen Stewart, Sue M. Price, Edward Blair, Raoul C. Hennekam, Carrie A. Fitzpatrick, Rick Segraves, Todd A. Richmond, Cheryl Guiver, Donna G. Albertson, Daniel Pinkel, Peggy S. Eis, Stuart Schwartz, Samantha J. Knight, Evan E. Eichler posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:53:42 as along with 1 person waszak
	Genomic disorders ten years on. [My Copy] Genome medicine, Vol. 1, No. 4. (2009) by James R. Lupski posted to review humgen genomics cnv by daforerog on 2009-09-14 16:41:38 as
	Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2. [My Copy] Nature genetics, Vol. 39, No. 9. (19 September 2007), pp. 1071-1073. by Blake C. Ballif, Sara A. Hornor, Elizabeth Jenkins, et al.Suneeta Madan-Khetarpal, Urvashi Surti, Kelly E. Jackson, Alexander Asamoah, Pamela L. Brock, Gordon C. Gowans, Robert L. Conway, John M. Graham, Livija Medne, Elaine H. Zackai, Tamim H. Shaikh, Joel Geoghegan, Rebecca R. Selzer, Peggy S. Eis, Bassem A. Bejjani, Lisa G. Shaffer posted to neurogen mr humgen genomics cnv by daforerog on 2009-09-14 16:37:01 as
	Genetic compensation in a human genomic disorder. [My Copy] The New England journal of medicine, Vol. 360, No. 12. (19 March 2009), pp. 1211-1216. by Nadège Carelle-Calmels, Pascale Saugier-Veber, Françoise Girard-Lemaire, et al.Gabrielle Rudolf, Bérénice Doray, Eric Guérin, Pierre Kuhn, Mathilde Arrivé, Catherine Gilch, Evelyne Schmitt, Séverine Fehrenbach, Albert Schnebelen, Thierry Frébourg, Elisabeth Flori posted to humgen highly genomics cnv by daforerog on 2009-09-14 16:29:21 as along with 3 people Amazoness absterga jbhiatt
	MLGA--a rapid and cost-efficient assay for gene copy-number analysis. [My Copy] Nucleic acids research, Vol. 35, No. 17. (27 September 2007), e115. by Magnus Isaksson, Johan Stenberg, Fredrik Dahl, Ann-Charlotte C. Thuresson, Marie-Louise L. Bondeson, Mats Nilsson posted to humgen genotyping cnv by daforerog on 2009-09-14 16:19:42 as along with 2 people guhjy rdiaz
	Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder. [My Copy] Human molecular genetics, Vol. 18, No. 10. (15 May 2009), pp. 1795-1804. by Ivon Cuscó, Andrés Medrano, Blanca Gener, et al.Mireia Vilardell, Fátima Gallastegui, Olaya Villa, Eva González, Benjamín Rodríguez-Santiago, Elisabet Vilella, Miguel Del Campo, Luis A. Pérez-Jurado posted to psychgen humgen genomics cnv autism by daforerog on 2009-09-14 15:48:41 as
	Universal multiplex PCR and CE for quantification of SMN1/SMN2 genes in spinal muscular atrophy. [My Copy] Electrophoresis, Vol. 30, No. 7. (April 2009), pp. 1102-1110. by Chun-Chi C. Wang, Jan-Gowth G. Chang, Yuh-Jyh J. Jong, Shou-Mei M. Wu posted to humgen genotyping cnv by daforerog on 2009-09-14 15:34:19 as
	A 15q13.3 microdeletion segregating with autism. [My Copy] European journal of human genetics : EJHG, Vol. 17, No. 5. (May 2009), pp. 687-692. by Alistair T. Pagnamenta, Kirsty Wing, Elham Sadighi S. Akha, et al.Samantha J. Knight, Sven Bölte, Gabriele Schmötzer, Eftichia Duketis, Fritz Poustka, Sabine M. Klauck, Annemarie Poustka, Jiannis Ragoussis, Anthony J. Bailey, Anthony P. Monaco, International Molecular Genetic Study of Autism Consortium posted to psychgen humgen cnv autism by daforerog on 2009-09-14 14:28:28 as
	Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. [My Copy] Journal of medical genetics, Vol. 46, No. 4. (April 2009), pp. 242-248. by D. T. Miller, Y. Shen, L. A. Weiss, et al.J. Korn, I. Anselm, C. Bridgemohan, G. F. Cox, H. Dickinson, J. Gentile, D. J. Harris, V. Hegde, R. Hundley, O. Khwaja, S. Kothare, C. Luedke, R. Nasir, A. Poduri, K. Prasad, P. Raffalli, A. Reinhard, S. E. Smith, M. M. Sobeih, J. S. Soul, J. Stoler, M. Takeoka, W-H H. Tan, J. Thakuria, R. Wolff, R. Yusupov, J. F. Gusella, M. J. Daly, B-L L. Wu posted to psychgen humgen cnv autism by daforerog on 2009-09-14 14:25:47 as
	Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. [My Copy] Journal of medical genetics, Vol. 46, No. 8. (21 August 2009), pp. 511-523. by B. W. van Bon, H. C. Mefford, B. Menten, et al.D. A. Koolen, A. J. Sharp, W. M. Nillesen, J. W. Innis, T. J. de Ravel, C. L. Mercer, M. Fichera, H. Stewart, L. E. Connell, K. Ounap, K. Lachlan, B. Castle, N. Van der Aa, C. van Ravenswaaij, M. A. Nobrega, C. Serra-Juhé, I. Simonic, N. de Leeuw, R. Pfundt, E. M. Bongers, C. Baker, P. Finnemore, S. Huang, V. K. Maloney, J. A. Crolla, M. van Kalmthout, M. Elia, G. Vandeweyer, J. P. Fryns, S. Janssens, N. Foulds, S. Reitano, K. Smith, S. Parkel, B. Loeys, C. G. Woods, A. Oostra, F. Speleman, A. C. Pereira, A. Kurg, L. Willatt, S. J. Knight, J. R. Vermeesch, C. Romano, J. C. Barber, G. Mortier, L. A. Pérez-Jurado, F. Kooy, H. G. Brunner, E. E. Eichler, T. Kleefstra, B. B. de Vries posted to neurogen mr humgen cnv by daforerog on 2009-09-14 14:01:28 as along with 1 person bmenten
	A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. [My Copy] Nature genetics, Vol. 40, No. 3. (17 March 2008), pp. 322-328. by Andrew J. Sharp, Heather C. Mefford, Kelly Li, et al.Carl Baker, Cindy Skinner, Roger E. Stevenson, Richard J. Schroer, Francesca Novara, Manuela De Gregori, Roberto Ciccone, Adam Broomer, Iris Casuga, Yu Wang, Chunlin Xiao, Catalin Barbacioru, Giorgio Gimelli, Bernardo Dalla D. Bernardina, Claudia Torniero, Roberto Giorda, Regina Regan, Victoria Murday, Sahar Mansour, Marco Fichera, Lucia Castiglia, Pinella Failla, Mario Ventura, Zhaoshi Jiang, Gregory M. Cooper, Samantha J. Knight, Corrado Romano, Orsetta Zuffardi, Caifu Chen, Charles E. Schwartz, Evan E. Eichler posted to neuropsygen neurogen mr humgen epilep cnv by daforerog on 2009-09-14 13:57:07 as
	15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. [My Copy] Nature genetics, Vol. 41, No. 2. (11 February 2009), pp. 160-162. by Ingo Helbig, Heather C. Mefford, Andrew J. Sharp, et al.Michel Guipponi, Marco Fichera, Andre Franke, Hiltrud Muhle, Carolien de Kovel, Carl Baker, Sarah von Spiczak, Katherine L. Kron, Ines Steinich, Ailing A. Kleefuss-Lie, Costin Leu, Verena Gaus, Bettina Schmitz, Karl M. Klein, Philipp S. Reif, Felix Rosenow, Yvonne Weber, Holger Lerche, Fritz Zimprich, Lydia Urak, Karoline Fuchs, Martha Feucht, Pierre Genton, Pierre Thomas, Frank Visscher, Gerrit-Jan J. de Haan, Rikke S. Møller, Helle Hjalgrim, Daniela Luciano, Michael Wittig, Michael Nothnagel, Christian E. Elger, Peter Nürnberg, Corrado Romano, Alain Malafosse, Bobby P. Koeleman, Dick Lindhout, Ulrich Stephani, Stefan Schreiber, Evan E. Eichler, Thomas Sander posted to neurogen humgen epilep cnv assoc by daforerog on 2009-09-14 13:30:12 as
	Familial and sporadic 15q13.3 microdeletions in Idiopathic Generalized Epilepsy: Precedent for Disorders with Complex Inheritance. [My Copy] Human molecular genetics (10 July 2009) by Leanne M. Dibbens, Saul Mullen, Ingo Helbig, et al.Heather C. Mefford, Marta A. Bayly, Susannah Bellows, Costin Leu, Holger Trucks, Tanja Obermeier, Michael Wittig, Andre Franke, Hande Caglayan, Zuhal Yapici, EPICURE Consortium, Thomas Sander, Evan E. Eichler, Ingrid E. Scheffer, John C. Mulley, Samuel F. Berkovic posted to neurogen humgen genomics epilep cnv by daforerog on 2009-09-14 12:41:09 as
	Gene copy number variation in schizophrenia. [My Copy] American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, Vol. 147B, No. 5. (5 July 2008), pp. 606-611. by Smitha R. Sutrala, Nadine Norton, Nigel M. Williams, Paul R. Buckland posted to schizophrenia psychgen humgen genotyping cnv by daforerog on 2009-09-14 10:50:36 as
	Gene copy number variation in schizophrenia. [My Copy] Schizophrenia research, Vol. 96, No. 1-3. (November 2007), pp. 93-99. by Smitha R. Sutrala, Dirk Goossens, Nigel M. Williams, et al.Lien Heyrman, Rolf Adolfsson, Nadine Norton, Paul R. Buckland, Jurgen Del-Favero posted to schizophrenia psychgen humgen cnv by daforerog on 2009-09-14 10:39:25 as along with 1 person tuannn
	Molecular cytogenetics and cytogenomics of brain diseases. [My Copy] Current genomics, Vol. 9, No. 7. (November 2008), pp. 452-465. by I. Y. Iourov, S. G. Vorsanova, Y. B. Yurov posted to review psychgen neuropsygen neurogen humgen genomics cnv brain by daforerog on 2009-09-14 09:49:01 as
	The role of DNA copy number variation in schizophrenia. [My Copy] Biological psychiatry, Vol. 66, No. 11. (1 December 2009), pp. 1005-1012. by Gloria W. Tam, Richard Redon, Nigel P. Carter, Seth G. Grant posted to schizophrenia review psychgen humgen genomics cnv by daforerog on 2009-09-14 09:04:31 as along with 2 people Leaflet vplagnol
	Designing a simple multiplex ligation-dependent probe amplification (MLPA) assay for rapid detection of copy number variants in the genome. [My Copy] Journal of genetics and genomics = Yi chuan xue bao, Vol. 36, No. 4. (April 2009), pp. 257-265. by Yiping Shen, Bai-Lin L. Wu posted to review humgen genotyping cnv by daforerog on 2009-09-08 17:32:40 as along with 1 person jdbowes
	Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia. [My Copy] Molecular psychiatry, Vol. aop, No. current. (16 June 2009) by B. Rodríguez-Santiago, A. Brunet, B. Sobrino, et al.C. Serra-Juhé, R. Flores, Ll Armengol, E. Vilella, E. Gabau, M. Guitart, R. Guillamat, L. Martorell, J. Valero, A. Gutiérrez-Zotes, A. Labad, A. Carracedo, X. Estivill, L. A. Pérez-Jurado posted to schizophrenia cnv assoc by daforerog on 2009-09-08 17:31:31 as
	New applications and developments in the use of multiplex ligation-dependent probe amplification. [My Copy] Electrophoresis, Vol. 29, No. 23. (December 2008), pp. 4627-4636. by Piotr Kozlowski, Anna J. Jasinska, David J. Kwiatkowski posted to review humgen genotyping cnv by daforerog on 2009-09-08 15:45:43 as along with 1 person jbhiatt
	Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. [My Copy] The New England journal of medicine, Vol. 359, No. 16. (16 October 2008), pp. 1685-1699. by Heather C. Mefford, Andrew J. Sharp, Carl Baker, et al.Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K. Maloney, John A. Crolla, Diana Baralle, Amanda Collins, Catherine Mercer, Koen Norga, Thomy de Ravel, Koen Devriendt, Ernie M. Bongers, Nicole de Leeuw, William Reardon, Stefania Gimelli, Frederique Bena, Raoul C. Hennekam, Alison Male, Lorraine Gaunt, Jill Clayton-Smith, Ingrid Simonic, Soo Mi M. Park, Sarju G. Mehta, Serena Nik-Zainal, C. Geoffrey Woods, Helen V. Firth, Georgina Parkin, Marco Fichera, Santina Reitano, Mariangela Lo Giudice, Kelly E. Li, Iris Casuga, Adam Broomer, Bernard Conrad, Markus Schwerzmann, Lorenz Räber, Sabina Gallati, Pasquale Striano, Antonietta Coppola, John L. Tolmie, Edward S. Tobias, Chris Lilley, Lluis Armengol, Yves Spysschaert, Patrick Verloo, Anja De Coene, Linde Goossens, Geert Mortier, Frank Speleman, Ellen van Binsbergen, Marcel R. Nelen, Ron Hochstenbach, Martin Poot, Louise Gallagher, Michael Gill, Jon McClellan, Mary-Claire C. King, Regina Regan, Cindy Skinner, Roger E. Stevenson, Stylianos E. Antonarakis, Caifu Chen, Xavier Estivill, Björn Menten, Giorgio Gimelli, Susan Gribble, Stuart Schwartz, James S. Sutcliffe, Tom Walsh, Samantha J. Knight, Jonathan Sebat, Corrado Romano, Charles E. Schwartz, Joris A. Veltman, Bert B. de Vries, Joris R. Vermeesch, John C. Barber, Lionel Willatt, May Tassabehji, Evan E. Eichler posted to psychgen mr humgen cnv assoc by daforerog on 2009-09-08 15:44:17 as along with 2 people jbhiatt bmenten
	Candidate gene copy number analysis by PCR and multicapillary electrophoresis. [My Copy] Electrophoresis, Vol. 30, No. 7. (April 2009), pp. 1098-1101. by Eszter Szantai, Zsuzsanna Elek, András Guttman, Maria Sasvari-Szekely posted to humgen genotyping cnv by daforerog on 2009-09-08 15:26:16 as along with 1 person guhjy
	Extending genome-wide association studies to copy-number variation. [My Copy] Human molecular genetics, Vol. 17, No. R2. (15 October 2008) by Steven A. McCarroll posted to humgen highly gwas genomics cnv by daforerog on 2009-09-08 13:42:03 as along with 3 people daed guhjy cheyloveday
	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. [My Copy] Human molecular genetics, Vol. 18, No. 23. (1 December 2009), pp. 4650-4661. by Anna C. Need, Deborah K. Attix, Jill M. McEvoy, et al.Elizabeth T. Cirulli, Kristen L. Linney, Priscilla Hunt, Dongliang Ge, Erin L. Heinzen, Jessica M. Maia, Kevin V. Shianna, Michael E. Weale, Lynn F. Cherkas, Gail Clement, Tim D. Spector, Greg Gibson, David B. Goldstein posted to qtl gwasneuro cognition cnv by daforerog on 2009-09-08 13:03:25 as along with 1 person rdiaz
	Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation [My Copy] Archives of General Psychiatry, Vol. 66, No. 9. (2009), pp. 947-956. by PhD; C. Audrey Guilmatre posted to tf synaptic schizophrenia psychgen network mr cnv autism by daforerog on 2009-09-08 10:59:30 as
	Rapid detection of novel BRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments. [My Copy] Human mutation, Vol. 20, No. 3. (September 2002), pp. 218-226. by Federica Casilli, Zorika Christiana C. Di Rocco, Sophie Gad, et al.Isabelle Tournier, Dominique Stoppa-Lyonnet, Thierry Frebourg, Mario Tosi posted to humgen genotyping cnv by daforerog on 2009-09-08 10:16:04 as
	Strong association of de novo copy number mutations with sporadic schizophrenia. [My Copy] Nature genetics, Vol. 40, No. 7. (30 July 2008), pp. 880-885. by Bin Xu, J. Louw Roos, Shawn Levy, E. J. van Rensburg, Joseph A. Gogos, Maria Karayiorgou posted to schizophrenia humgen cnv by daforerog on 2009-09-02 17:49:47 as along with 4 people noushin jo_davies slevy03 vmsr
	Personalized copy number and segmental duplication maps using next-generation sequencing. [My Copy] Nature genetics, Vol. 41, No. 10. (30 October 2009), pp. 1061-1067. by Can Alkan, Jeffrey M. Kidd, Tomas Marques-Bonet, et al.Gozde Aksay, Francesca Antonacci, Fereydoun Hormozdiari, Jacob O. Kitzman, Carl Baker, Maika Malig, Onur Mutlu, S. Cenk Sahinalp, Richard A. Gibbs, Evan E. Eichler posted to humgen genomics cnv by daforerog on 2009-08-31 13:02:20 as along with 30 people and 1 group ongenetics chvlyl leemachado daed gbenson n00c bozdagd dakelley sbmontgomery eshirdel merpublic shyamsg scmelton qayub natstreet fenghezi Annab djkt nuin xingxu jamesmorris rdiaz brant torfinnnome jandot pkonings danmaclean frohike rschulz gangcai Journal picks
	Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals [My Copy] Hum. Mol. Genet., Vol. 16, No. 1. (1 January 2007), pp. 1-14. by Javier Simon-Sanchez, Sonja Scholz, Hon-Chung Fung, et al.Mar Matarin, Dena Hernandez, J. Raphael Gibbs, Angela Britton, Fabienne W. de Vrieze, Elizabeth Peckham, Katrina Gwinn-Hardy, Anthony Crawley, Judith C. Keen, Josefina Nash, Digamber Borgaonkar, John Hardy, Andrew Singleton posted to popul linkage lab humgen genomics cnv assoc by daforerog on 2009-08-31 12:48:50 as along with 2 people and 2 groups psique dchughes G4ID Genetics-of-Gambling
	Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex. [My Copy] European journal of human genetics : EJHG, Vol. aop, No. current. (22 July 2009) by Martin Poot, Marc J. Eleveld, Ruben van 't Slot, Hans Kristian K. Ploos van Amstel, Ron Hochstenbach posted to synaptic mr humgen genomics cnv assoc by daforerog on 2009-08-27 13:42:42 as
	"GenotypeColour": colour visualisation of SNPs and CNVs. [My Copy] BMC bioinformatics, Vol. 10, No. 1. (2009) by Sergio Barlati, Sergio Chiesa, Chiara Magri posted to silico mining lab humgen gwas cnv assoc by daforerog on 2009-08-19 00:37:41 as along with 4 people guhjy pkonings skap nuin
	Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism [My Copy] PLoS ONE, Vol. 4, No. 5. (28 May 2009), e5324. by Bert van der Zwaag, Lude Franke, Martin Poot, et al.Ron Hochstenbach, Henk A. Spierenburg, Jacob A. S. Vorstman, Emma van Daalen, Maretha V. de Jonge, Nienke E. Verbeek, Eva H. Brilstra, Ruben van 't Slot, Roel A. Ophoff, Michael A. van Es, Hylke M. Blauw, Jan H. Veldink, Jacobine E. Buizer-Voskamp, Frits A. Beemer, Leonard H. van den Berg, Cisca Wijmenga, Hans K. van Amstel, Herman van Engeland, Burbach, Wouter G. Staal posted to systems mining humgen grad cnv autism assoc by daforerog on 2009-08-17 19:59:09 as along with 2 people rdiaz daed
	Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data. [My Copy] BMC bioinformatics, Vol. 8, No. 1. (2007) by Agnes Baross, Allen D. Delaney, H. Irene Li, et al.Tarun Nayar, Stephane Flibotte, Hong Qian, Susanna Y. Chan, Jennifer Asano, Adrian Ally, Manqiu Cao, Patricia Birch, Mabel Brown-John, Nicole Fernandes, Anne Go, Giulia Kennedy, Sylvie Langlois, Patrice Eydoux, J. M. Friedman, Marco A. Marra posted to silico mining lab humgen highly gwas genomics comparison cnv by daforerog on 2009-08-17 19:38:36 as along with 2 people jfr niallhaslam

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