daforerog's nssnps [178 articles] Export

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	Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. [My Copy] Human mutation, Vol. 15, No. 1. (2000), pp. 7-12. by J. T. den Dunnen, S. E. Antonarakis posted to nssnps humgen highly genotyping find by daforerog on 2009-11-23 10:00:49 as along with 1 person and 1 group caporaso biomedical-nlp
	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
	Lessons learnt from large-scale exon re-sequencing of the X chromosome. [My Copy] Human molecular genetics, Vol. 18, No. R1. (15 April 2009) by F. Lucy Raymond, Annabel Whibley, Michael R. Stratton, Jozef Gecz posted to synaptic nssnps mr genomics by daforerog on 2009-11-18 17:10:57 as along with 1 person jdbowes
	Genetic diagnosis by whole exome capture and massively parallel DNA sequencing. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 106, No. 45. (10 November 2009), pp. 19096-19101. by Murim Choi, Ute I. Scholl, Weizhen Ji, et al.Tiewen Liu, Irina R. Tikhonova, Paul Zumbo, Ahmet Nayir, Ayşin Bakkaloğlu, Seza Ozen, Sami Sanjad, Carol Nelson-Williams, Anita Farhi, Shrikant Mane, Richard P. Lifton posted to nssnps linkage humgen genotyping genomics by daforerog on 2009-11-18 10:29:25 as along with 5 people liqbbi pst Peiyong chvlyl giovanni
	Exome sequencing identifies the cause of a mendelian disorder [My Copy] Nature Genetics, Vol. advance online publication (13 November 2009) by Sarah B. Ng, Kati J. Buckingham, Choli Lee, et al.Abigail W. Bigham, Holly K. Tabor, Karin M. Dent, Chad D. Huff, Paul T. Shannon, Ethylin W. Jabs, Deborah A. Nickerson, Jay Shendure, Michael J. Bamshad posted to nssnps linkage humgen highly genotyping genomics by daforerog on 2009-11-18 10:26:46 as along with 5 people cajunsushi pst seb1 Peiyong psique
	Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation. [My Copy] Molecular psychiatry (10 November 2009) by T. C. Bates, P. A. Lind, M. Luciano, G. W. Montgomery, N. G. Martin, M. J. Wright posted to psychgen nssnps by daforerog on 2009-11-12 17:37:11 as
	A survey of proteins encoded by non-synonymous single nucleotide polymorphisms reveals a significant fraction with altered stability and activity. [My Copy] The Biochemical journal, Vol. 424, No. 1. (15 November 2009), pp. 15-26. by Abdellah Allali-Hassani, Gregory A. Wasney, Irene Chau, et al.Bum Soo S. Hong, Guillermo Senisterra, Peter Loppnau, Zhen Shi, John Moult, Aled M. Edwards, Cheryl H. Arrowsmith, Hee Won W. Park, Matthieu Schapira, Masoud Vedadi posted to nssnps mining by daforerog on 2009-11-12 17:24:06 as
	The VNTR polymorphism of the human dopamine transporter (DAT1) gene affects gene expression. [My Copy] The pharmacogenomics journal, Vol. 1, No. 2. (2001), pp. 152-156. by S. Fuke, S. Suo, N. Takahashi, H. Koike, N. Sasagawa, S. Ishiura posted to synaptic parkinson nssnps humgen brain by daforerog on 2009-10-30 14:23:42 as
	Mutation screening of the <I>DTNBP1</I> exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis [My Copy] American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Vol. 9999, No. 9999. (2009), n/a. by S. Dwyer, L. Carroll, K. K. Mantripragada, M. J. Owen, M. C. O'Donovan, N. M. Williams posted to synaptic schizophrenia nssnps humgen find by daforerog on 2009-10-27 09:42:49 as
	Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. [My Copy] The New England journal of medicine, Vol. 361, No. 17. (22 October 2009), pp. 1651-1661. by E. Sidransky, M. A. Nalls, J. O. Aasly, et al.J. Aharon-Peretz, G. Annesi, E. R. Barbosa, A. Bar-Shira, D. Berg, J. Bras, A. Brice, C-M M. Chen, L. N. Clark, C. Condroyer, E. V. De Marco, A. Dürr, M. J. Eblan, S. Fahn, M. J. Farrer, H-C C. Fung, Z. Gan-Or, T. Gasser, R. Gershoni-Baruch, N. Giladi, A. Griffith, T. Gurevich, C. Januario, P. Kropp, A. E. Lang, G-J J. Lee-Chen, S. Lesage, K. Marder, I. F. Mata, A. Mirelman, J. Mitsui, I. Mizuta, G. Nicoletti, C. Oliveira, R. Ottman, A. Orr-Urtreger, L. V. Pereira, A. Quattrone, E. Rogaeva, A. Rolfs, H. Rosenbaum, R. Rozenberg, A. Samii, T. Samaddar, C. Schulte, M. Sharma, A. Singleton, M. Spitz, E-K K. Tan, N. Tayebi, T. Toda, A. R. Troiano, S. Tsuji, M. Wittstock, T. G. Wolfsberg, Y-R R. Wu, C. P. Zabetian, Y. Zhao, S. G. Ziegler posted to parkinson nssnps humgen by daforerog on 2009-10-23 16:05:12 as
	Identification and characterization of missense alterations in the BRCA1 associated RING domain (BARD1) gene in breast and ovarian cancer. [My Copy] Journal of medical genetics, Vol. 42, No. 8. (August 2005), pp. 633-638. by M. K. Sauer, I. L. Andrulis posted to nssnps by daforerog on 2009-10-21 16:51:08 as
	Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan. [My Copy] Gastroenterology, Vol. 124, No. 1. (January 2003), pp. 140-146. by Denise K. Bonen, Yasunori Ogura, Dan L. Nicolae, et al.Naohiro Inohara, Lisa Saab, Tsuyoshi Tanabe, Felicia F. Chen, Simon J. Foster, Richard H. Duerr, Steven R. Brant, Judy H. Cho, Gabriel Nuñez posted to nssnps by daforerog on 2009-10-21 16:51:01 as
	Sequence variations of ABCB1, SLC6A2, SLC6A3, SLC6A4, CREB1, CRHR1 and NTRK2: association with major depression and antidepressant response in Mexican-Americans [My Copy] Molecular Psychiatry, Vol. aop, No. current. (20 October 2009) by C. Dong, M. L. Wong, J. Licinio posted to synaptic psychgen nssnps humgen depression by daforerog on 2009-10-21 16:45:03 as
	Identification of a novel functional deletion variant in the 5'-UTR of the DJ-1 gene [My Copy] BMC Medical Genetics, Vol. 10, No. 1. (13 October 2009), 105. by Rowena Keyser, Lize van der Merwe, Mauritz Venter, et al.Craig Kinnear, Louise Warnich, Jonathan Carr, Soraya Bardien posted to parkinson nssnps humgen find by daforerog on 2009-10-21 15:41:01 as
	Evaluation of in silico splice tools for decision-making in molecular diagnosis. [My Copy] Human mutation, Vol. 29, No. 7. (July 2008), pp. 975-982. by Claude Houdayer, Catherine Dehainault, Christophe Mattler, et al.Dorothée Michaux, Virginie Caux-Moncoutier, Sabine Pagès-Berhouet, Catherine Dubois D. d'Enghien, Anthony Laugé, Laurent Castera, Marion Gauthier-Villars, Dominique Stoppa-Lyonnet posted to silico nssnps mining humgen genotyping genomics find assoc by daforerog on 2009-10-20 18:15:01 as along with 1 person guhjy
	Rare plus common SERT variants in obsessive-compulsive disorder [My Copy] Molecular Psychiatry, Vol. 12, No. 5. (01 May 2007), pp. 422-423. by M. A. Grados, J. Samuels, Y. Y. Shugart, et al.V. L. Willour, Y. Wang, B. Cullen, O. J. Bienvenu, R. Hoehn-Saric, D. Valle, K. Y. Liang, M. A. Riddle, J. R. Wendland, D. L. Murphy, G. Nestadt, S. Detera-Wadleigh posted to psychgen ocd nssnps humgen htt by daforerog on 2009-10-20 11:23:05 as
	Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder [My Copy] Molecular Psychiatry, Vol. 10, No. 12. (09 August 2005), pp. 1059-1061. by R. Delorme, C. Betancur, M. Wagner, et al.M. O. Krebs, P. Gorwood, P. Pearl, G. Nygren, C. M. Durand, F. Buhtz, P. Pickering, J. Melke, S. Ruhrmann, H. Anckarsater, N. Chabane, A. Kipman, C. Reck, B. Millet, I. Roy, M. C. Mouren-Simeoni, W. Maier, M. Rastam, C. Gillberg, M. Leboyer, T. Bourgeron posted to ocd nssnps humgen htt by daforerog on 2009-10-20 11:22:17 as
	SERT Ileu425Val in autism, Asperger syndrome and obsessive-compulsive disorder. [My Copy] Psychiatric genetics, Vol. 18, No. 1. (February 2008), pp. 31-39. by Jens R. Wendland, Theresa B. DeGuzman, Francis McMahon, Gary Rudnick, Sevilla D. Detera-Wadleigh, Dennis L. Murphy posted to psychgen ocd nssnps htt autism by daforerog on 2009-10-20 11:21:24 as
	Candidate nsSNPs that can affect the functions and interactions of cell cycle proteins. [My Copy] Proteins, Vol. 58, No. 3. (15 February 2005), pp. 697-705. by Sevtap Savas, M. Farhan Ahmad, Mehjabeen Shariff, David Y. Kim, Hilmi Ozcelik posted to nssnps humgen by daforerog on 2009-10-16 16:45:28 as
	PicSNP: a browsable catalog of nonsynonymous single nucleotide polymorphisms in the human genome. [My Copy] Biochemical and biophysical research communications, Vol. 287, No. 1. (14 September 2001), pp. 288-291. by H. Chang, T. Fujita posted to silico nssnps mining by daforerog on 2009-10-16 12:16:08 as
	Prediction of deleterious non-synonymous single nucleotide polymorphisms of genes related to ethanol-induced toxicity. [My Copy] Toxicology letters, Vol. 187, No. 2. (1 June 2009), pp. 99-114. by Lin-Lin L. Wang, Yong Li, Shu-Feng F. Zhou posted to silico nssnps neuropsygen mining humgen by daforerog on 2009-10-16 10:58:43 as along with 1 person orzenil
	Association of Ala72Ser polymorphism with COMT enzyme activity and the risk of schizophrenia in Koreans [My Copy] Human Genetics, Vol. 116, No. 4. (17 March 2005), pp. 319-328. by Seong-Gene Lee, Yeonho Joo, Byungsu Kim, et al.Seockhoon Chung, Hie-Lim Kim, Inchul Lee, Boyoul Choi, Changyoon Kim, Kyuyoung Song posted to synaptic psychgen nssnps humgen by daforerog on 2009-10-16 10:42:55 as
	Impact of the DISC1 Ser704Cys polymorphism on risk for major depression, brain morphology and ERK signaling. [My Copy] Human molecular genetics, Vol. 15, No. 20. (15 October 2006), pp. 3024-3033. by Ryota Hashimoto, Tadahiro Numakawa, Takashi Ohnishi, et al.Emi Kumamaru, Yuki Yagasaki, Tetsuya Ishimoto, Takeyuki Mori, Kiyotaka Nemoto, Naoki Adachi, Aiko Izumi, Sachie Chiba, Hiroko Noguchi, Tatsuyo Suzuki, Nakao Iwata, Norio Ozaki, Takahisa Taguchi, Atsushi Kamiya, Asako Kosuga, Masahiko Tatsumi, Kunitoshi Kamijima, Daniel R. Weinberger, Akira Sawa, Hiroshi Kunugi posted to synaptic psychgen nssnps humgen by daforerog on 2009-10-16 10:41:10 as along with 2 people and 1 group mgaldzic AdamWysokinski CHIP
	Joint reanalysis of 29 correlated SNPs supports the role of PCLO\|[sol]\|Piccolo as a causal risk factor for major depressive disorder [My Copy] Molecular Psychiatry, Vol. 14, No. 7. (01 July 2009), pp. 650-652. by Z. Bochdanovits, M. Verhage, A. B. Smit, et al.E. J. C. De Geus, D. Posthuma, D. I. Boomsma, B. W. J. H. Penninx, W. J. Hoogendijk, P. Heutink posted to synaptic nssnps humgen gwas depression assoc by daforerog on 2009-10-15 17:10:24 as
	Large-scale characterization of public database SNPs causing non-synonymous changes in three ethnic groups. [My Copy] Human genetics, Vol. 119, No. 1-2. (March 2006), pp. 75-83. by James Ireland, Victoria E. Carlton, Matthew Falkowski, et al.Martin Moorhead, Karen Tran, Francisco Useche, Paul Hardenbol, Ayca Erbilgin, Ron Fitzgerald, Thomas D. Willis, Malek Faham posted to silico popul nssnps mining humgen genomics assoc by daforerog on 2009-10-15 16:56:21 as along with 1 person ashandanj
	A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation [My Copy] neurogenetics by Ginevra Zanni, Hilde van Esch, Anissa Bensalem, et al.Yoann Saillour, Karine Poirier, Laetitia Castelnau, Hans Ropers, Arjan de Brouwer, Fréderic Laumonnier, Jean-Pierre Fryns, Jamel Chelly posted to synaptic nssnps mr humgen by daforerog on 2009-10-02 11:52:28 as
	Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast Cancer [My Copy] (24 September 2009) by Sean V. Tavtigian, Peter J. Oefner, Davit Babikyan, et al.Anne Hartmann, Sue Healey, Florence Le Calvez-Kelm, Fabienne Lesueur, Graham B. Byrnes, Shu-Chun Chuang, Nathalie Forey, Corinna Feuchtinger, Lydie Gioia, Janet Hall, Mia Hashibe, Barbara Herte, Sandrine McKay-Chopin, Alun Thomas, Maxime P. Vallée, Catherine Voegele, Penelope M. Webb, David C. Whiteman, Suleeporn Sangrajrang, John L. Hopper, Melissa C. Southey, Irene L. Andrulis, Esther M. John, Georgia Chenevix-Trench posted to nssnps find by daforerog on 2009-09-29 16:51:53 as
	Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate alpha-secretase activity. [My Copy] Human molecular genetics (15 July 2009) by Minji Kim, Jaehong Suh, Donna Romano, et al.Mimy H. Truong, Kristina Mullin, Basavaraj Hooli, David Norton, Giuseppina Tesco, Kathy Elliott, Steven L. Wagner, Robert D. Moir, K. David Becker, Rudolph E. Tanzi posted to nssnps neurogen humgen assoc ad by daforerog on 2009-09-23 15:57:51 as
	LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay. [My Copy] Parkinsonism & related disorders, Vol. 15, No. 5. (June 2009), pp. 370-373. by Ignacio F. Mata, Carlos Cosentino, Victoria Marca, et al.Luis Torres, Pilar Mazzetti, Olimpio Ortega, Victor Raggio, Ruth Aljanati, Ricardo Buzó, Dora Yearout, Elena Dieguez, Cyrus P. Zabetian posted to parkinson nssnps neurola neurogen humgen by daforerog on 2009-09-21 12:19:02 as
	The proportion of mutations predicted to have a deleterious effect differs between gain and loss of function genes in neurodegenerative disease. [My Copy] Human mutation, Vol. 30, No. 3. (March 2009) by Paul N. Valdmanis, Dominique J. Verlaan, Guy A. Rouleau posted to silico nssnps mining humgen by daforerog on 2009-09-14 17:24:22 as
	Novel de novo SHANK3 mutation in autistic patients. [My Copy] American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, Vol. 150B, No. 3. (5 April 2009), pp. 421-424. by Julie Gauthier, Dan Spiegelman, Amélie Piton, et al.Ronald G. Lafrenière, Sandra Laurent, Judith St-Onge, Line Lapointe, Fadi F. Hamdan, Patrick Cossette, Laurent Mottron, Eric Fombonne, Ridha Joober, Claude Marineau, Pierre Drapeau, Guy A. Rouleau posted to synaptic psychgen nssnps autism by daforerog on 2009-09-14 17:11:20 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
	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
	Epac2 induces synapse remodeling and depression and its disease-associated forms alter spines [My Copy] Nature Neuroscience, Vol. advance online publication (06 September 2009) by Kevin M. Woolfrey, Deepak P. Srivastava, Huzefa Photowala, et al.Megumi Yamashita, Maria V. Barbolina, Michael E. Cahill, Zhong Xie, Kelly A. Jones, Lawrence A. Quilliam, Murali Prakriya, Peter Penzes posted to synaptic nssnps autism by daforerog on 2009-09-09 13:33:40 as along with 1 person wangngu
	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
	Pharmacological analysis of human D1 AND D2 dopamine receptor missense variants. [My Copy] Journal of molecular neuroscience : MN, Vol. 34, No. 3. (March 2008), pp. 211-223. by Munya A. Al-Fulaij, Yong Ren, Martin Beinborn, Alan S. Kopin posted to nssnps humgen find assoc by daforerog on 2009-09-07 15:38:50 as
	FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization. [My Copy] Nucleic acids research, Vol. 34, No. Web Server issue. (1 July 2006) by Hsiang-Yu Y. Yuan, Jen-Jie J. Chiou, Wen-Hsien H. Tseng, et al.Chia-Hung H. Liu, Chuan-Kun K. Liu, Yi-Jung J. Lin, Hui-Hung H. Wang, Adam Yao, Yuan-Tsong T. Chen, Chun-Nan N. Hsu posted to silico nssnps mining humgen by daforerog on 2009-09-03 18:17:41 as along with 1 person misonneh
	Applications of computational algorithm tools to identify functional SNPs. [My Copy] Functional & integrative genomics, Vol. 8, No. 4. (1 November 2008), pp. 309-316. by C. George Priya Doss, C. Sudandiradoss, R. Rajasekaran, et al.Parikshit Choudhury, Priyanka Sinha, Pragnya Hota, Udit Prakash P. Batra, Sethumadhavan Rao posted to silico nssnps mining humgen by daforerog on 2009-09-03 18:16:48 as
	Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. [My Copy] Nature protocols, Vol. 4, No. 7. (2009), pp. 1073-1081. by Prateek Kumar, Steven Henikoff, Pauline C. Ng posted to silico review nssnps mining by daforerog on 2009-09-03 09:54:31 as
	Genetic Variation in Healthy Oldest-Old [My Copy] PLoS ONE, Vol. 4, No. 8. (14 August 2009), e6641. by Julius Halaschek-Wiener, Mahsa Amirabbasi-Beik, Nasim Monfared, et al.Markus Pieczyk, Christian Sailer, Anita Kollar, Ruth Thomas, Georgios Agalaridis, So Yamada, Lisa Oliveira, Jennifer A. Collins, Graydon Meneilly, Marco A. Marra, Kenneth M. Madden, Nhu D. Le, Joseph M. Connors, Angela R. Brooks-Wilson posted to nssnps humgen genomics assoc aging by daforerog on 2009-08-31 14:25:20 as along with 2 people ejbaldon greg
	To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies? [My Copy] European journal of human genetics : EJHG, Vol. 16, No. 6. (June 2008), pp. 718-723. by David M. Evans, Jeffrey C. Barrett, Lon R. Cardon posted to nssnps mining humgen gwas genotyping genomics assoc by daforerog on 2009-08-28 17:24:53 as along with 1 person guhjy
	Targeted capture and massively parallel sequencing of 12 human exomes. [My Copy] Nature, Vol. 461, No. 7261. (10 September 2009), pp. 272-276. by Sarah B. Ng, Emily H. Turner, Peggy D. Robertson, et al.Steven D. Flygare, Abigail W. Bigham, Choli Lee, Tristan Shaffer, Michelle Wong, Arindam Bhattacharjee, Evan E. Eichler, Michael Bamshad, Deborah A. Nickerson, Jay Shendure posted to nssnps humgen highly genotyping genomics assoc by daforerog on 2009-08-28 15:27:43 as along with 23 people and 1 group seb1 hzoltan liqbbi chvlyl ongenetics psique fenghezi n00c dswan jmanning2k torfinnnome GeeSharpMinor pkonings neils djkt PabloMarin stubrown danmaclean xingxu vplagnol druvus jandot frohike Journal picks
	A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan. [My Copy] Neurogenetics, Vol. 7, No. 3. (July 2006), pp. 133-138. by Alessio Di Fonzo, Yah-Huei H. Wu-Chou, Chin-Song S. Lu, et al.Marina van Doeselaar, Erik J. Simons, Christan F. Rohé, Hsiu-Chen C. Chang, Rou-Shayn S. Chen, Yi-Hsin H. Weng, Nicola Vanacore, Guido J. Breedveld, Ben A. Oostra, Vincenzo Bonifati posted to parkinson nssnps humgen assoc by daforerog on 2009-08-11 19:08:01 as
	A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism. [My Copy] Journal of medical genetics (21 June 2009) by Ravinesh A. Kumar, Jyotsna Sudi, Timothy D. Babatz, et al.Camille W. Brune, Donald Oswald, Mayon Yen, Norma J. Nowak, Edwin H. Cook, Susan L. Christian, William B. Dobyns posted to autism brain find nssnps psychgen synaptic by daforerog on 2009-08-05 17:33:04 as
	Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 102, No. 24. (14 June 2005), pp. 8627-8632. by Joseph H. Callicott, Richard E. Straub, Lukas Pezawas, et al.Michael F. Egan, Venkata S. Mattay, Ahmad R. Hariri, Beth A. Verchinski, Andreas Meyer-Lindenberg, Rishi Balkissoon, Bhaskar Kolachana, Terry E. Goldberg, Daniel R. Weinberger posted to assoc humgen neuropsygen nssnps psychgen qtl schizophrenia synaptic by daforerog on 2009-08-05 12:36:20 as along with 2 people yanhaomouse AdamWysokinski
	SLITRK1 mutations in trichotillomania. [My Copy] Molecular psychiatry, Vol. 11, No. 10. (October 2006), pp. 887-889. by S. Zuchner, M. L. Cuccaro, K. N. Tran-Viet, et al.H. Cope, R. R. Krishnan, M. A. Pericak-Vance, H. H. Wright, A. Ashley-Koch posted to assoc humgen nssnps synaptic psychgen by daforerog on 2009-08-04 09:59:50 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
	An integrative scoring system for ranking SNPs by their potential deleterious effects. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 8. (15 April 2009), pp. 1048-1055. by Phil Hyoun H. Lee, Hagit Shatkay posted to assoc gamma-sec humgen mining nssnps silico by daforerog on 2009-07-23 16:28:07 as along with 6 people and 1 group jandot george_g rdiaz djkt Zephyrus pkonings Roswell Cancer Crosstalk
	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

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humgen	1052
silico	838
mining	749
mirna	469
assoc	457
genomics	431
highly	352
genotyping	349
synaptic	279
psychgen	240
microarray	233
metaadpd	211
lab	204
brainmut	200
meta-analysis	181
brain	180
sci	180
nssnps	178
mirrev	176
systems	175
gwas	174
ad	156
review	156
expression	137
neuropsygen	134
find	131
neurogen	120
schizophrenia	114
cnv	97
popul	95
apoe	85
qtl	83
phenomics	78
stat	77
parkinson	76
adpdgenrev	75
gwasneuro	75
linkage	75
histor	68
neurola	67
ncrna	61
teaching	55
snp	54
autism	51
network	45
prevalence	44
adhd	42
bipolar	42
aging	40
gamma-sec	40
heritability	37
behavior	30
mr	29
neuroarray	29
htt	27
depression	25
citations	24
papers	19
drosophila	18
tf	18
cognition	14
ocd	14
adhdmeta	12
comparison	12
gnun	11
anxiety	10
epilep	10
ftd	10
genetics	10
bdnf	9
ethics	9
cell	7
comt	6
early	5
longevity	4
candidates	3
motordis	3
biology	2
epigenet	2
grad	2
processing	2
video	2
gene	1
let-7	1
mir-124	1
mir-137	1
mir-214	1
reviewed	1
stroke	1

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