daforerog's brainmut [at least 200 articles] Export

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

	SM2PH-db: an interactive system for the integrated analysis of phenotypic consequences of missense mutations in proteins involved in human genetic diseases. [My Copy] Human mutation (17 November 2009) by Anne Friedrich, Nicolas Garnier, Nicolas Gagnière, et al.Hoan Nguyen, Laurent-Philippe P. Albou, Valérie Biancalana, Emmanuel Bettler, Gilbert Deléage, Odile Lecompte, Jean Muller, Dino Moras, Jean-Louis L. Mandel, Thierry Toursel, Luc Moulinier, Olivier Poch posted to silico nssnps mining genomics find brainmut by daforerog on 2009-11-20 17:28:54 as
	Mutation of the Variant alpha-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia. [My Copy] American journal of human genetics (4 November 2009) by Mohammad R. Abdollahi, Ewan Morrison, Tamara Sirey, et al.Zoltan Molnar, Bruce E. Hayward, Ian M. Carr, Kelly Springell, C. Geoff Woods, Mushtaq Ahmed, Louise Hattingh, Peter Corry, Daniela T. Pilz, Neil Stoodley, Yanick Crow, Graham R. Taylor, David T. Bonthron, Eamonn Sheridan posted to find brainmut by daforerog on 2009-11-12 17:30:35 as
	TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness. [My Copy] American journal of human genetics (4 November 2009) by Isabelle Audo, Susanne Kohl, Bart P. Leroy, et al.Francis L. Munier, Xavier Guillonneau, Saddek Mohand-Saïd, Kinga Bujakowska, Emeline F. Nandrot, Birgit Lorenz, Markus Preising, Ulrich Kellner, Agnes B. Renner, Antje Bernd, Aline Antonio, Veselina Moskova-Doumanova, Marie-Elise E. Lancelot, Charlotte M. Poloschek, Isabelle Drumare, Sabine Defoort-Dhellemmes, Bernd Wissinger, Thierry Léveillard, Christian P. Hamel, Daniel F. Schorderet, Elfride De Baere, Wolfgang Berger, Samuel G. Jacobson, Eberhart Zrenner, José-Alain A. Sahel, Shomi S. Bhattacharya, Christina Zeitz posted to find brainmut by daforerog on 2009-11-12 17:27:21 as
	CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila. [My Copy] American journal of human genetics (4 November 2009) by Christiane Zweier, Eiko K. de Jong, Markus Zweier, et al.Alfredo Orrico, Lilian B. Ousager, Amanda L. Collins, Emilia K. Bijlsma, Merel A. Oortveld, Arif B. Ekici, André Reis, Annette Schenck, Anita Rauch posted to synaptic mr brainmut by daforerog on 2009-11-12 09:13:08 as
	Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies. [My Copy] Nature genetics, Vol. 41, No. 9. (September 2009), pp. 1043-1043. by Karsten Haug, Maike Warnstedt, Alexi K. Alekov, et al.Thomas Sander, Alfredo Ramírez, Barbara Poser, Snezana Maljevic, Simon Hebeisen, Christian Kubisch, Johannes Rebstock, Steve Horvath, Kerstin Hallmann, Joern S. Dullinger, Birgit Rau, Fritz Haverkamp, Stefan Beyenburg, Herbert Schulz, Dieter Janz, Bernd Giese, Gerhard Müller-Newen, Peter Propping, Christian E. Elger, Christoph Fahlke, Holger Lerche posted to brainmut by daforerog on 2009-10-29 12:54:02 as
	Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy. [My Copy] Human mutation, Vol. 30, No. 3. (March 2009), pp. 397-405. by Cécile Saint-Martin, Grégory Gauvain, Georgeta Teodorescu, et al.Isabelle Gourfinkel-An, Estelle Fedirko, Yvonne G. Weber, Snezana Maljevic, Jan-Peter P. Ernst, Jennie Garcia-Olivares, Christoph Fahlke, Rima Nabbout, Eric LeGuern, Holger Lerche, Jean Christophe C. Poncer, Christel Depienne posted to brainmut by daforerog on 2009-10-29 12:51:38 as
	Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsy. [My Copy] American journal of human genetics, Vol. 85, No. 1. (July 2009), pp. 40-52. by Annemieke J. Verkerk, Rachel Schot, Belinda Dumee, et al.Karlijn Schellekens, Sigrid Swagemakers, Aida M. Bertoli-Avella, Maarten H. Lequin, Jeroen Dudink, Paul Govaert, A. L. van Zwol, Jennifer Hirst, Marja W. Wessels, Coriene Catsman-Berrevoets, Frans W. Verheijen, Esther de Graaff, Irenaeus F. de Coo, Johan M. Kros, Rob Willemsen, Patrick J. Willems, Peter J. van der Spek, Grazia M. Mancini posted to brainmut by daforerog on 2009-10-28 16:13:38 as
	Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II. [My Copy] The Journal of clinical investigation, Vol. 118, No. 7. (July 2008), pp. 2496-2505. by Masoud Shekarabi, Nathalie Girard, Jean-Baptiste B. Rivière, et al.Patrick Dion, Martin Houle, André Toulouse, Ronald G. Lafrenière, Freya Vercauteren, Pascale Hince, Janet Laganiere, Daniel Rochefort, Laurence Faivre, Mark Samuels, Guy A. Rouleau posted to brainmut by daforerog on 2009-09-14 17:20:27 as
	Mutations in the calcium-related gene IL1RAPL1 are associated with autism. [My Copy] Human molecular genetics, Vol. 17, No. 24. (15 December 2008), pp. 3965-3974. by Amélie Piton, Jacques L. Michaud, Huashan Peng, et al.Swaroop Aradhya, Julie Gauthier, Laurent Mottron, Nathalie Champagne, Ronald G. Lafrenière, Fadi F. Hamdan, S2D team, Ridha Joober, Eric Fombonne, Claude Marineau, Patrick Cossette, Marie-Pierre P. Dubé, Pejmun Haghighi, Pierre Drapeau, Philip A. Barker, Salvatore Carbonetto, Guy A. Rouleau posted to synaptic psychgen nssnps humgen brainmut autism by daforerog on 2009-09-14 16:52:50 as along with 1 person dchughes
	De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy. [My Copy] Annals of neurology, Vol. 65, No. 6. (June 2009), pp. 748-753. by Fadi F. Hamdan, Amélie Piton, Julie Gauthier, et al.Anne Lortie, François Dubeau, Sylvia Dobrzeniecka, Dan Spiegelman, Anne Noreau, Stéphanie Pellerin, Mélanie Côté, Edouard Henrion, Eric Fombonne, Laurent Mottron, Claude Marineau, Pierre Drapeau, Ronald G. Lafrenière, Jean Claude C. Lacaille, Guy A. Rouleau, Jacques L. Michaud posted to synaptic neurogen mr humgen epilep brainmut by daforerog on 2009-09-14 15:58:39 as
	Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation. [My Copy] The New England journal of medicine, Vol. 360, No. 6. (5 February 2009), pp. 599-605. by Fadi F. Hamdan, Julie Gauthier, Dan Spiegelman, et al.Anne Noreau, Yan Yang, Stéphanie Pellerin, Sylvia Dobrzeniecka, Mélanie Côté, Elizabeth Perreault-Linck, Lionel Carmant, Guy D'Anjou, Eric Fombonne, Anjene M. Addington, Judith L. Rapoport, Lynn E. Delisi, Marie-Odile O. Krebs, Faycal Mouaffak, Ridha Joober, Laurent Mottron, Pierre Drapeau, Claude Marineau, Ronald G. Lafrenière, Jean Claude C. Lacaille, Guy A. Rouleau, Jacques L. Michaud, Synapse to Disease Group posted to synaptic nssnps mr humgen brainmut by daforerog on 2009-09-14 15:38:31 as
	Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene. [My Copy] Molecular psychiatry, Vol. 8, No. 11. (November 2003), pp. 916-924. by E. Bacchelli, F. Blasi, M. Biondolillo, et al.J. A. Lamb, E. Bonora, G. Barnby, J. Parr, K. S. Beyer, S. M. Klauck, A. Poustka, A. J. Bailey, A. P. Monaco, E. Maestrini, International Molecular Genetic Study of Autism Consortium (IMGSAC) posted to synaptic psychgen nssnps brainmut autism assoc by daforerog on 2009-09-09 11:03:41 as
	Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy [My Copy] (27 August 2009) by Lucie Gueneau, Anne T. Bertrand, Jean-Philippe Jais, et al.Mustafa A. Salih, Tanya Stojkovic, Manfred Wehnert, Maria Hoeltzenbein, Simone Spuler, Shinji Saitoh, Annie Verschueren, Christine Tranchant, Maud Beuvin, Emmanuelle Lacene, Norma B. Romero, Simon Heath, Diana Zelenika, Thomas Voit, Bruno Eymard, Rabah Ben Yaou, Gisèle Bonne posted to brainmut by daforerog on 2009-08-31 08:36:05 as
	Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker. [My Copy] Human mutation, Vol. 29, No. 1. (January 2008), pp. 6-13. by Martin Wildeman, Ernest van Ophuizen, Johan T. den Dunnen, Peter E. Taschner posted to brainmut humgen mining silico systems by daforerog on 2009-08-10 13:08:30 as
	LOVD: easy creation of a locus-specific sequence variation database using an "LSDB-in-a-box" approach. [My Copy] Human mutation, Vol. 26, No. 2. (August 2005), pp. 63-68. by Ivo F. Fokkema, Johan T. den Dunnen, Peter E. Taschner posted to brainmut humgen mining silico synaptic systems by daforerog on 2009-08-10 13:07:50 as along with 1 person Nilza
	Mutation within <I>TARDBP</I> leads to Frontotemporal Dementia without motor neuron disease [My Copy] Human Mutation, Vol. 9999, No. 9999. (2009), n/a. by B. Borroni, C. Bonvicini, A. Alberici, et al.E. Buratti, C. Agosti, S. Archetti, A. Papetti, C. Stuani, M. Di Luca, M. Gennarelli, A. Padovani posted to assoc brainmut ftd humgen by daforerog on 2009-08-05 09:02:34 as
	Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene [My Copy] (30 July 2009) by Paul Renbaum, Efrat Kellerman, Ranit Jaron, et al.Dan Geiger, Reeval Segel, Ming Lee, Mary C. King, Ephrat Levy-Lahad posted to brainmut humgen linkage by daforerog on 2009-08-03 09:51:06 as
	Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome [My Copy] (30 July 2009) by Saima Riazuddin, Saima Anwar, Martin Fischer, et al.Zubair M. Ahmed, Shahid Y. Khan, Audrey G. H. Janssen, Ahmad U. Zafar, Ute Scholl, Tayyab Husnain, Inna A. Belyantseva, Penelope L. Friedman, Sheikh Riazuddin, Thomas B. Friedman, Christoph Fahlke posted to brainmut humgen by daforerog on 2009-08-03 09:47:35 as
	Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling. [My Copy] Nature genetics, Vol. 40, No. 2. (23 February 2008), pp. 232-236. by E. Griffith, S. Walker, C. A. Martin, et al.P. Vagnarelli, T. Stiff, B. Vernay, N. Al Sanna, A. Saggar, B. Hamel, W. C. Earnshaw, P. A. Jeggo, A. P. Jackson, M. O'Driscoll posted to brainmut humgen by daforerog on 2009-07-29 12:06:45 as
	Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function [My Copy] The American Journal of Human Genetics (23 July 2009) by Caroline Huzé, Stéphanie Bauché, Pascale Richard, et al.Frédéric Chevessier, Evelyne Goillot, Karen Gaudon, Asma Ben Ammar, Annie Chaboud, Isabelle Grosjean, Heba-Aude Lecuyer posted to brainmut synaptic by daforerog on 2009-07-27 09:02:56 as
	CACNA1H mutations in autism spectrum disorders. [My Copy] The Journal of biological chemistry, Vol. 281, No. 31. (4 August 2006), pp. 22085-22091. by I. Splawski, D. S. Yoo, S. C. Stotz, A. Cherry, D. E. Clapham, M. T. Keating posted to autism brainmut humgen nssnps synaptic by daforerog on 2009-07-24 13:58:10 as along with 1 person kochhan
	Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism. [My Copy] Cell, Vol. 119, No. 1. (1 October 2004), pp. 19-31. by I. Splawski, K. W. Timothy, L. M. Sharpe, et al.N. Decher, P. Kumar, R. Bloise, C. Napolitano, P. J. Schwartz, R. M. Joseph, K. Condouris, H. Tager-Flusberg, S. G. Priori, M. C. Sanguinetti, M. T. Keating posted to autism brainmut humgen nssnps psychgen synaptic by daforerog on 2009-07-24 13:11:01 as
	MDPD: an integrated genetic information resource for Parkinson's disease. [My Copy] Nucleic acids research, Vol. 37, No. Database issue. (23 January 2009), pp. gkn770-862. by S. Tang, Z. Zhang, G. Kavitha, E. K. Tan, S. K. Ng posted to assoc brainmut humgen neurogen nssnps parkinson prevalence silico by daforerog on 2009-07-22 13:21:26 as along with 2 people psique Scis0000002
	Mutations in the human Sonic Hedgehog gene cause holoprosencephaly. [My Copy] Nature genetics, Vol. 14, No. 3. (November 1996), pp. 357-360. by E. Roessler, E. Belloni, K. Gaudenz, et al.P. Jay, P. Berta, S. W. Scherer, L. C. Tsui, M. Muenke posted to brain brainmut humgen by daforerog on 2009-07-16 08:02:38 as
	X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment. [My Copy] Nature genetics, Vol. 40, No. 6. (11 June 2008), pp. 776-781. by L. M. Dibbens, P. S. Tarpey, K. Hynes, et al.M. A. Bayly, I. E. Scheffer, R. Smith, J. Bomar, E. Sutton, L. Vandeleur, C. Shoubridge, S. Edkins, S. J. Turner, C. Stevens, S. O'Meara, C. Tofts, S. Barthorpe, G. Buck, J. Cole, K. Halliday, D. Jones, R. Lee, M. Madison, T. Mironenko, J. Varian, S. West, S. Widaa, P. Wray, J. Teague, E. Dicks, A. Butler, A. Menzies, A. Jenkinson, R. Shepherd, J. F. Gusella, Z. Afawi, A. Mazarib, M. Y. Neufeld, S. Kivity, D. Lev, T. Lerman-Sagie, A. D. Korczyn, C. P. Derry, G. R. Sutherland, K. Friend, M. Shaw, M. Corbett, H. G. Kim, D. H. Geschwind, P. Thomas, E. Haan, S. Ryan, S. McKee, S. F. Berkovic, P. A. Futreal, M. R. Stratton, J. C. Mulley, J. Gécz posted to brainmut epilep humgen mr nssnps synaptic by daforerog on 2009-07-15 15:56:29 as
	A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome. [My Copy] American journal of human genetics, Vol. 83, No. 5. (November 2008), pp. 572-581. by A. G. Bassuk, R. H. Wallace, A. Buhr, et al.A. R. Buller, Z. Afawi, M. Shimojo, S. Miyata, S. Chen, P. Gonzalez-Alegre, H. L. Griesbach, S. Wu, M. Nashelsky, E. K. Vladar, D. Antic, P. J. Ferguson, S. Cirak, T. Voit, M. P. Scott, J. D. Axelrod, C. Gurnett, A. S. Daoud, S. Kivity, M. Y. Neufeld, A. Mazarib, R. Straussberg, S. Walid, A. D. Korczyn, D. C. Slusarski, S. F. Berkovic, H. I. El-Shanti posted to brainmut epilep humgen neurogen nssnps by daforerog on 2009-07-08 16:25:29 as
	Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease. [My Copy] American journal of human genetics, Vol. 76, No. 4. (April 2005), pp. 572-580. by J. H. Roelfsema, S. J. White, Y. Ariyürek, et al.D. Bartholdi, D. Niedrist, F. Papadia, C. A. Bacino, J. T. den Dunnen, G. J. van Ommen, M. H. Breuning, R. C. Hennekam, D. J. Peters posted to brainmut humgen mr synaptic by daforerog on 2009-07-06 15:17:45 as
	Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. [My Copy] Nature genetics, Vol. 40, No. 11. (26 November 2008), pp. 1335-1340. by Z. M. Ahmed, S. Masmoudi, E. Kalay, et al.I. A. Belyantseva, M. A. Mosrati, R. W. Collin, S. Riazuddin, M. Hmani-Aifa, H. Venselaar, M. N. Kawar, A. Tlili, B. van der Zwaag, S. Y. Khan, L. Ayadi, S. A. Riazuddin, R. J. Morell, A. J. Griffith, I. Charfedine, R. Caylan, J. Oostrik, A. Karaguzel, A. Ghorbel, S. Riazuddin, T. B. Friedman, H. Ayadi, H. Kremer posted to brainmut humgen by daforerog on 2009-07-06 12:22:30 as
	Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39 [My Copy] (2 July 2009) by Julie M. Schultz, Shaheen N. Khan, Zubair M. Ahmed, et al.Saima Riazuddin, Ali M. Waryah, Dhananjay Chhatre, Matthew F. Starost, Barbara Ploplis, Stephanie Buckley, David Velásquez, Madhulika Kabra, Kwanghyuk Lee, Muhammad J. Hassan, Ghazanfar Ali, Muhammad Ansar, Manju Ghosh, Edward R. Wilcox, Wasim Ahmad, Glenn Merlino, Suzanne M. Leal, Sheikh Riazuddin, Thomas B. Friedman, Robert J. Morell posted to brainmut humgen ncrna by daforerog on 2009-07-06 12:21:23 as
	CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait [My Copy] PLoS Genet, Vol. 5, No. 5. (22 May 2009), e1000487. by Seval Türkmen, Gao Guo, Masoud Garshasbi, et al.Katrin Hoffmann, Amjad J. Alshalah, Claudia Mischung, Andreas Kuss, Nicholas Humphrey, Stefan Mundlos, Peter N. Robinson posted to brainmut humgen mr neurogen nssnps by daforerog on 2009-06-25 11:28:25 as along with 2 people darian Schmidtc
	Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, No. 46. (13 November 2007), pp. 18163-18168. by Y. Wu, A. C. Arai, G. Rumbaugh, et al.A. K. Srivastava, G. Turner, T. Hayashi, E. Suzuki, Y. Jiang, L. Zhang, J. Rodriguez, J. Boyle, P. Tarpey, F. L. Raymond, J. Nevelsteen, G. Froyen, M. Stratton, A. Futreal, J. Gecz, R. Stevenson, C. E. Schwartz, D. Valle, R. L. Huganir, T. Wang posted to assoc brainmut humgen mr synaptic systems by daforerog on 2009-06-24 11:53:46 as
	Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia [My Copy] Journal of Clinical Investigation (26 May 2009) by Manju A. Kurian, Juan Zhen, Shu-Yuan Cheng, et al.Yan Li, Santosh R. Mordekar, Philip Jardine, Neil V. Morgan, Esther Meyer, Louise Tee, Shanaz Pasha, Evangeline Wassmer, Simon J. Heales, Paul Gissen, Maarten E. Reith, Eamonn R. Maher posted to brainmut humgen neurogen nssnps parkinson synaptic by daforerog on 2009-06-23 15:09:30 as along with 1 person psique
	Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome. [My Copy] American journal of human genetics, Vol. 84, No. 6. (June 2009), pp. 728-739. by J. Armistead, S. Khatkar, B. Meyer, et al.B. L. Mark, N. Patel, G. Coghlan, R. E. Lamont, S. Liu, J. Wiechert, P. A. Cattini, P. Koetter, K. Wrogemann, C. R. Greenberg, K. D. Entian, T. Zelinski, B. Triggs-Raine posted to brainmut humgen mr neurogen by daforerog on 2009-06-19 14:59:50 as
	LRRK2 gene variation and its contribution to Parkinson disease. [My Copy] Human mutation (21 April 2009) by Coro Paisán-Ruiz posted to brainmut humgen lab neurogen nssnps parkinson by daforerog on 2009-06-19 12:53:39 as along with 1 person fazels2
	A de novo mutation affecting human TrkB associated with severe obesity and developmental delay. [My Copy] Nature neuroscience, Vol. 7, No. 11. (November 2004), pp. 1187-1189. by G. S. Yeo, C. C. Connie Hung, J. Rochford, et al.J. Keogh, J. Gray, S. Sivaramakrishnan, S. O'Rahilly, I. S. Farooqi posted to brainmut humgen psychgen synaptic by daforerog on 2009-06-05 21:24:55 as
	Mutations in the ²-tubulin gene TUBB2B result in asymmetrical polymicrogyria [My Copy] Nature Genetics, Vol. 41, No. 6. (24 May 2009), pp. 746-752. by Xavier H. Jaglin, Karine Poirier, Yoann Saillour, et al.Emmanuelle Buhler, Guoling Tian, Nadia Bahi-Buisson, Catherine Fallet-Bianco, Françoise Phan-Dinh-Tuy, Xiang P. Kong, Pascale Bomont, Laëtitia Castelnau-Ptakhine, Sylvie Odent, Philippe Loget, Manoelle Kossorotoff, Irina Snoeck, Ghislaine Plessis, Philippe Parent, Cherif Beldjord, Carlos Cardoso, Alfonso Represa, Jonathan Flint, David A. Keays, Nicholas J. Cowan, Jamel Chelly posted to brainmut by daforerog on 2009-06-05 13:08:10 as
	SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy [My Copy] Nature Genetics, Vol. 41, No. 6. (24 May 2009), pp. 654-656. by Daniele Ghezzi, Paola Goffrini, Graziella Uziel, et al.Rita Horvath, Thomas Klopstock, Hanns Lochmüller, Pio D'Adamo, Paolo Gasparini, Tim M. Strom, Holger Prokisch, Federica Invernizzi, Ileana Ferrero, Massimo Zeviani posted to brainmut by daforerog on 2009-06-05 13:06:43 as
	XLMR genes: update 2007 [My Copy] European Journal of Human Genetics, Vol. aop, No. current. by Pietro Chiurazzi, Charles E. Schwartz, Jozef Gecz, Giovanni Neri posted to assoc brainmut humgen mining mr neurogen neuropsygen psychgen by daforerog on 2009-05-21 23:05:06 as along with 1 person dchughes
	Molecular basis of genetic neuropsychiatric disorders. [My Copy] Child and adolescent psychiatric clinics of North America, Vol. 16, No. 3. (July 2007), pp. 541-556. by D. V. Venkitaramani, P. J. Lombroso posted to brain brainmut find psychgen by daforerog on 2009-05-11 13:17:25 as
	Psychiatric genetics: the case of single gene disorders. [My Copy] European child & adolescent psychiatry, Vol. 11, No. 5. (October 2002), pp. 201-209. by J. Steyaert, J. P. Fryns posted to brain brainmut psychgen by daforerog on 2009-05-11 13:15:30 as
	Mutations in the gene encoding CADM1 are associated with autism spectrum disorder. [My Copy] Biochemical and biophysical research communications, Vol. 377, No. 3. (19 December 2008), pp. 926-929. by Y. Zhiling, E. Fujita, Y. Tanabe, T. Yamagata, T. Momoi, M. Y. Momoi posted to autism brainmut synaptic by daforerog on 2009-04-23 14:57:51 as
	Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. [My Copy] Science (New York, N.Y.), Vol. 323, No. 5918. (27 February 2009), pp. 1208-1211. by Caroline Vance, Boris Rogelj, Tibor Hortobágyi, et al.Kurt J. De Vos, Agnes Lumi L. Nishimura, Jemeen Sreedharan, Xun Hu, Bradley Smith, Deborah Ruddy, Paul Wright, Jeban Ganesalingam, Kelly L. Williams, Vineeta Tripathi, Safa Al-Saraj, Ammar Al-Chalabi, P. Nigel Leigh, Ian P. Blair, Garth Nicholson, Jackie de Belleroche, Jean-Marc M. Gallo, Christopher C. Miller, Christopher E. Shaw posted to brainmut by daforerog on 2009-02-27 08:41:07 as
	Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis [My Copy] Science, Vol. 323, No. 5918. (27 February 2009), pp. 1205-1208. by T. J. Kwiatkowski, D. A. Bosco, A. L. LeClerc, et al.E. Tamrazian, C. R. Vanderburg, C. Russ, A. Davis, J. Gilchrist, E. J. Kasarskis, T. Munsat, P. Valdmanis, G. A. Rouleau, B. A. Hosler, P. Cortelli, P. J. de Jong, Y. Yoshinaga, J. L. Haines, M. A. Pericak-Vance, J. Yan, N. Ticozzi, T. Siddique, D. McKenna-Yasek, P. C. Sapp, H. R. Horvitz, J. E. Landers, R. H. Brown posted to brainmut by daforerog on 2009-02-27 08:40:40 as along with 2 people StuartForrest inbetweener
	TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. [My Copy] Science (New York, N.Y.), Vol. 319, No. 5870. (21 March 2008), pp. 1668-1672. by Jemeen Sreedharan, Ian P. Blair, Vineeta B. Tripathi, et al.Xun Hu, Caroline Vance, Boris Rogelj, Steven Ackerley, Jennifer C. Durnall, Kelly L. Williams, Emanuele Buratti, Francisco Baralle, Jacqueline de Belleroche, J. Douglas Mitchell, P. Nigel Leigh, Ammar Al-Chalabi, Christopher C. Miller, Garth Nicholson, Christopher E. Shaw posted to brainmut by daforerog on 2009-02-27 08:35:19 as along with 4 people StuartForrest inbetweener giovanni davidlott
	TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. [My Copy] Nature genetics, Vol. 40, No. 5. (30 May 2008), pp. 572-574. by Edor Kabashi, Paul N. Valdmanis, Patrick Dion, et al.Dan Spiegelman, Brendan J. McConkey, Christine Vande Velde, Jean-Pierre P. Bouchard, Lucette Lacomblez, Ksenia Pochigaeva, Francois Salachas, Pierre-Francois F. Pradat, William Camu, Vincent Meininger, Nicolas Dupre, Guy A. Rouleau posted to brainmut by daforerog on 2009-02-27 08:35:11 as along with 2 people inbetweener giovanni
	Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia. [My Copy] Nature genetics (1 February 2009) by Tania Fuchs, Sophie Gavarini, Rachel Saunders-Pullman, et al.Deborah Raymond, Michelle E E. Ehrlich, Susan B B. Bressman, Laurie J J. Ozelius posted to brainmut by daforerog on 2009-02-17 13:09:41 as
	Genome-Wide Analysis of Human Disease Alleles Reveals That Their Locations Are Correlated in Paralogous Proteins [My Copy] PLoS Comput Biol, Vol. 4, No. 11. (7 November 2008), e1000218. by Mark Yandell, Barry Moore, Fidel Salas, et al.Chris Mungall, Andrew Macbride, Charles White, Martin G. Reese posted to brainmut mining by daforerog on 2009-02-16 11:47:19 as along with 9 people biomcgary druvus rsantana Zalanszabo rdiaz bpcusack cabbagesofdoom grahamc djkt
	Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. [My Copy] Nature genetics, Vol. 26, No. 1. (September 2000), pp. 93-96. by S. E. Hong, Y. Y. Shugart, D. T. Huang, et al.S. A. Shahwan, P. E. Grant, J. O. Hourihane, N. D. Martin, C. A. Walsh posted to brainmut by daforerog on 2009-02-11 15:44:38 as
	Homozygosity mapping through whole genome analysis identifies a <I>COL18A1</I> mutation in an Indian family presenting with an autosomal recessive neurological disorder [My Copy] American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Vol. 150B, No. 7. (21 January 2009), pp. 993-997. by Coro Paisán-Ruiz, Geoff Scopes, Philip Lee, Henry Houlden posted to linkage brainmut by daforerog on 2009-01-28 05:37:32 as
	Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia. [My Copy] American journal of human genetics, Vol. 83, No. 5. (November 2008), pp. 643-648. by S. Edvardson, H. Hama, A. Shaag, et al.J. M. Gomori, I. Berger, D. Soffer, S. H. Korman, I. Taustein, A. Saada, O. Elpeleg posted to brainmut by daforerog on 2009-01-21 14:59:40 as

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silico	838
mining	749
mirna	469
assoc	457
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microarray	233
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adpdgenrev	75
gwasneuro	75
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