daforerog's humgen [more than 800 articles] Export

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

	Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. [My Copy] Nature genetics, Vol. advance online publication (15 November 2009) by Wataru Satake, Yuko Nakabayashi, Ikuko Mizuta, et al.Yushi Hirota, Chiyomi Ito, Michiaki Kubo, Takahisa Kawaguchi, Tatsuhiko Tsunoda, Masahiko Watanabe, Atsushi Takeda, Hiroyuki Tomiyama, Kenji Nakashima, Kazuko Hasegawa, Fumiya Obata, Takeo Yoshikawa, Hideshi Kawakami, Saburo Sakoda, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho Murata, Yusuke Nakamura, Tatsushi Toda posted to parkinson neurogen humgen gwasneuro adpdgenrev by daforerog on 2009-11-20 11:04:39 as along with 2 people psique vplagnol
	Genome-wide association study reveals genetic risk underlying Parkinson's disease. [My Copy] Nature genetics, Vol. advance online publication (15 November 2009) by Javier Simón-Sánchez, Claudia Schulte, Jose M. Bras, et al.Manu Sharma, J. Raphael Gibbs, Daniela Berg, Coro Paisan-Ruiz, Peter Lichtner, Sonja W. Scholz, Dena G. Hernandez, Rejko Krüger, Monica Federoff, Christine Klein, Alison Goate, Joel Perlmutter, Michael Bonin, Michael A. Nalls, Thomas Illig, Christian Gieger, Henry Houlden, Michael Steffens, Michael S. Okun, Brad A. Racette, Mark R. Cookson, Kelly D. Foote, Hubert H. Fernandez, Bryan J. Traynor, Stefan Schreiber, Sampath Arepalli, Ryan Zonozi, Katrina Gwinn, Marcel van der Brug, Grisel Lopez, Stephen J. Chanock, Arthur Schatzkin, Yikyung Park, Albert Hollenbeck, Jianjun Gao, Xuemei Huang, Nick W. Wood, Delia Lorenz, Günther Deuschl, Honglei Chen, Olaf Riess, John A. Hardy, Andrew B. Singleton, Thomas Gasser posted to parkinson neurogen humgen gwasneuro gwas adpdgenrev by daforerog on 2009-11-20 10:59:18 as along with 2 people psique vplagnol
	A streamlined mutation detection system: multicolor post-PCR fluorescence labeling and single-strand conformational polymorphism analysis by capillary electrophoresis. [My Copy] Genome research, Vol. 7, No. 11. (November 1997), pp. 1094-1103. by M. Inazuka, H. M. Wenz, M. Sakabe, T. Tahira, K. Hayashi posted to humgen genotyping by daforerog on 2009-11-18 17:04:49 as
	Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening. [My Copy] Human mutation, Vol. 21, No. 5. (May 2003), pp. 455-465. by Paal Skytt S. Andersen, Cathrine Jespersgaard, Jens Vuust, Michael Christiansen, Lars Allan A. Larsen posted to humgen genotyping by daforerog on 2009-11-18 17:04:07 as along with 2 people Barrytheb ashishyeri
	Mutational scanning of large genes by extensive PCR multiplexing and two-dimensional electrophoresis: application to the RB1 gene. [My Copy] Human molecular genetics, Vol. 5, No. 6. (June 1996), pp. 755-761. by N. J. Van Orsouw, D. Li, P. van der Vlies, et al.H. Scheffer, C. Eng, C. H. Buys, F. P. Li, J. Vijg posted to humgen genotyping by daforerog on 2009-11-18 16:37:45 as
	Rapid design of denaturing gradient-based two-dimensional electrophoretic gene mutational scanning tests. [My Copy] Nucleic acids research, Vol. 26, No. 10. (15 May 1998), pp. 2398-2406. by N. J. van Orsouw, R. K. Dhanda, R. D. Rines, et al.W. M. Smith, I. Sigalas, C. Eng, J. Vijg posted to silico humgen genotyping by daforerog on 2009-11-18 16:21:21 as
	Enzymatic mutation detection technologies. [My Copy] BioTechniques, Vol. 38, No. 5. (May 2005), pp. 749-758. by Anthony T. Yeung, Deepali Hattangadi, Lauryn Blakesley, Emmanuelle Nicolas posted to humgen genotyping by daforerog on 2009-11-18 16:17:39 as
	Automated fluorescent analysis procedure for enzymatic mutation detection. [My Copy] Clin Chem, Vol. 44, No. 4. (April 1998), pp. 731-739. by B. J. Del Tito, H. E. Poff, M. A. Novotny, et al.D. M. Cartledge, R. I. Walker, C. D. Earl, A. L. Bailey posted to humgen genotyping by daforerog on 2009-11-18 16:15:04 as along with 1 person davidng
	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
	An update on conformation sensitive gel electrophoresis. [My Copy] Human mutation, Vol. 19, No. 4. (April 2002), pp. 334-342. by Arupa Ganguly posted to humgen genotyping by daforerog on 2009-11-18 15:16:48 as
	High-speed, multicolor fluorescent two-dimensional gene scanning. [My Copy] Genomics, Vol. 78, No. 1-2. (November 2001), pp. 83-90. by S. B. McGrath, M. Bounpheng, L. Torres, et al.M. Calavetta, C. B. Scott, Y. Suh, D. Rines, N. van Orsouw, J. Vijg posted to humgen genotyping by daforerog on 2009-11-18 14:29:21 as
	Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1. [My Copy] Journal of medical genetics, Vol. 38, No. 12. (December 2001), pp. 824-833. by C. Eng, L. C. Brody, T. M. Wagner, et al.P. Devilee, J. Vijg, C. Szabo, S. V. Tavtigian, K. L. Nathanson, E. Ostrander, T. S. Frank, Steering Committee of the Breast Cancer Information Core (BIC) Consortium posted to lab humgen highly genotyping comparison by daforerog on 2009-11-18 14:28:08 as
	A highly accurate, low cost test for BRCA1 mutations. [My Copy] Journal of medical genetics, Vol. 36, No. 10. (October 1999), pp. 747-753. by N. J. van Orsouw, R. K. Dhanda, Y. Elhaji, et al.S. A. Narod, F. P. Li, C. Eng, J. Vijg posted to humgen genotyping by daforerog on 2009-11-18 12:56:01 as
	The sensitivity of denaturing gradient gel electrophoresis: a blinded analysis. [My Copy] Mutation research, Vol. 382, No. 3-4. (May 1998), pp. 109-114. by P. V. Gejman, Q. Cao, F. Guedj, S. Sommer posted to humgen genotyping by daforerog on 2009-11-18 12:54:42 as
	Rapid, inexpensive scanning for all possible BRCA1 and BRCA2 gene sequence variants in a single assay: implications for genetic testing. [My Copy] Journal of medical genetics, Vol. 40, No. 4. (April 2003) by M. Bounpheng, S. McGrath, D. Macias, et al.N. van Orsouw, Y. Suh, D. Rines, J. Vijg posted to humgen genotyping by daforerog on 2009-11-18 11:35:16 as
	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
	Interaction map and selection of microRNA targets in Parkinson's disease-related genes. [My Copy] Journal of biomedicine & biotechnology, Vol. 2009 (2009) by Shinde Santosh P, Neelima Arora, Pranjal Sarma, Manika Pal-Bhadra, Utpal Bhadra posted to parkinson mirna humgen by daforerog on 2009-11-18 08:26:07 as
	Patrocles: a database of polymorphic miRNA-mediated gene regulation in vertebrates. [My Copy] Nucleic acids research (11 November 2009) by Samuel Hiard, Carole Charlier, Wouter Coppieters, Michel Georges, Denis Baurain posted to silico ncrna mirna mining humgen by daforerog on 2009-11-13 10:30:06 as
	Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients. [My Copy] Movement disorders : official journal of the Movement Disorder Society, Vol. 23, No. 9. (15 July 2008), pp. 1228-1233. by Patricia de Carvalho d. e. . C. Aguiar, Patricia Silva S. Lessa, Clecio Godeiro, et al.Orlando Barsottini, Andre Carvalho C. Felício, Vanderci Borges, Sonia Maria de Azevedo M. Silva, Roberta Arb A. Saba, Henrique Ballalai B. Ferraz, Carlos A. Moreira-Filho, Luiz Augusto A. Andrade posted to parkinson neurola humgen by daforerog on 2009-11-12 17:23:08 as
	A functional polymorphism in Pre-miR-146a gene is associated with prostate cancer risk and mature miR-146a expression in vivo. [My Copy] The Prostate (9 November 2009) by Bin Xu, Ning-Han H. Feng, Peng-Chao C. Li, et al.Jun Tao, Deyao Wu, Zheng-Dong D. Zhang, Na Tong, Jin-Feng F. Wang, Ning-Hong H. Song, Wei Zhang, Li-Xin X. Hua, Hong-Fei F. Wu posted to mirna humgen assoc by daforerog on 2009-11-12 15:49:17 as
	Genome-wide Association Studies and Human Disease: From Trickle to Flood [My Copy] JAMA, Vol. 302, No. 18. (11 November 2009), pp. 2028-2029. by Peter M. Visscher, Grant W. Montgomery posted to humgen gwas by daforerog on 2009-11-12 14:52:11 as
	Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays [My Copy] Science (5 November 2009), 1181498. by Radoje Drmanac, Andrew B. Sparks, Matthew J. Callow, et al.Aaron L. Halpern, Norman L. Burns, Bahram G. Kermani, Paolo Carnevali, Igor Nazarenko, Geoffrey B. Nilsen, George Yeung, Fredrik Dahl, Andres Fernandez, Bryan Staker, Krishna P. Pant, Jonathan Baccash, Adam P. Borcherding, Anushka Brownley, Ryan Cedeno, Linsu Chen, Dan Chernikoff, Alex Cheung, Razvan Chirita, Benjamin Curson, Jessica C. Ebert, Coleen R. Hacker, Robert Hartlage, Brian Hauser, Steve Huang, Yuan Jiang, Vitali Karpinchyk, Mark Koenig, Calvin Kong, Tom Landers, Catherine Le, Jia Liu, Celeste E. McBride, Matt Morenzoni, Robert E. Morey, Karl Mutch, Helena Perazich, Kimberly Perry, Brock A. Peters, Joe Peterson, Charit L. Pethiyagoda, Kaliprasad Pothuraju, Claudia Richter, Abraham M. Rosenbaum, Shaunak Roy, Jay Shafto, Uladzislau Sharanhovich, Karen W. Shannon, Conrad G. Sheppy, Michel Sun, Joseph V. Thakuria, Anne Tran, Dylan Vu, Alexander W. Zaranek, Xiaodi Wu, Snezana Drmanac, Arnold R. Oliphant, William C. Banyai, Bruce Martin, Dennis G. Ballinger, George M. Church, Clifford A. Reid posted to humgen highly genotyping genomics find by daforerog on 2009-11-12 11:03:18 as along with 12 people and 1 group JonD qayub sandfire Peiyong chvlyl JamesBarger natstreet heliopais rwst orzenil zufar frohike Journal picks
	Common disorders are quantitative traits [My Copy] Nat Rev Genet, Vol. 10, No. 12. (27 October 2009), pp. 872-878. by Robert Plomin, Claire M. A. Haworth, Oliver S. P. Davis posted to qtl humgen highly gwas genomics assoc by daforerog on 2009-11-04 22:47:51 as along with 3 people and 1 group qayub misonneh psique Journal picks
	International web-based survey of informed consent procedures in genetic epidemiological studies: towards the establishment of a research coordinator accreditation system. [My Copy] Journal of human genetics (30 October 2009) by Midori Yamamoto, Makiko Funamizu, Kaori Muto, Akira Hata posted to humgen find ethics by daforerog on 2009-11-04 20:45:16 as
	The heritability and genetics of frontotemporal lobar degeneration. [My Copy] Neurology, Vol. 73, No. 18. (3 November 2009), pp. 1451-1456. by J. D. Rohrer, R. Guerreiro, J. Vandrovcova, et al.J. Uphill, D. Reiman, J. Beck, A. M. Isaacs, A. Authier, R. Ferrari, N. C. Fox, I. R. Mackenzie, J. D. Warren, R. de Silva, J. Holton, T. Revesz, J. Hardy, S. Mead, M. N. Rossor posted to neurogen humgen heritability ftd by daforerog on 2009-11-03 11:34:00 as along with 2 people applebyb giovanni
	Singapore Genome Variation Project: A haplotype map of three Southeast Asian populations. [My Copy] Genome research, Vol. 19, No. 11. (29 September 2009), pp. 2154-2162. by Yik-Ying Y. Teo, Xueling Sim, Rick T. Ong, et al.Adrian K. Tan, Jieming Chen, Erwin Tantoso, Kerrin S. Small, Chee-Seng S. Ku, Edmund J. Lee, Mark Seielstad, Kee-Seng S. Chia posted to silico popul mining humgen genomics by daforerog on 2009-11-03 11:33:40 as along with 4 people jasontsai djkt misonneh pkonings
	Rapid inexpensive genome-wide association using pooled whole blood. [My Copy] Genome research, Vol. 19, No. 11. (3 October 2009), pp. 2075-2080. by Jamie E. Craig, Alex W. Hewitt, Amy E. McMellon, et al.Anjali K. Henders, Lingjun Ma, Leanne Wallace, Shiwani Sharma, Kathryn P. Burdon, Peter M. Visscher, Grant W. Montgomery, Stuart Macgregor posted to humgen gwas genotyping genomics by daforerog on 2009-11-03 11:33:17 as along with 5 people neils giovanni rdiaz natstreet merpublic
	Clinical diagnostics in human genetics with semantic similarity searches in ontologies. [My Copy] American journal of human genetics, Vol. 85, No. 4. (October 2009), pp. 457-464. by Sebastian Köhler, Marcel H. Schulz, Peter Krawitz, et al.Sebastian Bauer, Sandra Dölken, Claus E. Ott, Christine Mundlos, Denise Horn, Stefan Mundlos, Peter N. Robinson posted to silico phenomics mining humgen genomics by daforerog on 2009-11-02 12:36:48 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
	Developing a set of ancestry-sensitive DNA markers reflecting continental origins of humans. [My Copy] BMC Genetics, Vol. 10, No. 1. (27 October 2009), 69. by Paula Kersbergen, Kate van Duijn, Ate Kloosterman, Johan den Dunnen, Manfred Kayser, Peter de Knijff posted to popul mining humgen genomics find by daforerog on 2009-10-29 16:13:09 as along with 3 people and 1 group qayub jsatkosk Geknitics Journal picks
	External oligonucleotide standards enable cross laboratory comparison and exchange of real-time quantitative PCR data. [My Copy] Nucleic acids research (4 September 2009) by Joëlle Vermeulen, Filip Pattyn, Katleen De Preter, et al.Liesbeth Vercruysse, Stefaan Derveaux, Pieter Mestdagh, Steve Lefever, Jan Hellemans, Frank Speleman, Jo Vandesompele posted to silico metaadpd humgen genomics expression by daforerog on 2009-10-27 09:43:32 as along with 1 person guhjy
	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
	Multiplex primer prediction software for divergent targets. [My Copy] Nucleic acids research (16 September 2009), gkp659. by Shea N. Gardner, Amy L. Hiddessen, Peter L. Williams, Christine Hara, Mark C. Wagner, Bill W. Colston posted to humgen genotyping genomics by daforerog on 2009-10-27 09:39:05 as along with 1 group Journal picks
	Genetic research on stored tissue samples from minors: A systematic review of the ethical literature [My Copy] American Journal of Medical Genetics Part A, Vol. 149A, No. 10. (October 2009), pp. 2346-2358. by Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx posted to phenomics humgen ethics by daforerog on 2009-10-26 16:25:11 as along with 2 people ErinC plosmedicine
	Recommendations for standardized human pedigree nomenclature. Pedigree Standardization Task Force of the National Society of Genetic Counselors. [My Copy] American journal of human genetics, Vol. 56, No. 3. (March 1995), pp. 745-752. by R. L. Bennett, K. A. Steinhaus, S. B. Uhrich, et al.C. K. O'Sullivan, R. G. Resta, D. Lochner-Doyle, D. S. Markel, V. Vincent, J. Hamanishi posted to phenomics humgen heritability by daforerog on 2009-10-26 10:36:32 as along with 1 person pedrohorna
	Recommendations for standardized human pedigree nomenclature [My Copy] Journal of Genetic Counseling, Vol. 4, No. 4. (1 December 1995), pp. 267-279. by Robin L. Bennett, Kathryn A. Steinhaus, Stefanie B. Uhrich, et al.Corrine K. O'Sullivan, Robert G. Resta, Debra Lochner-Doyle, Dorene S. Markel, Victoria Vincent, Jan Hamanishi posted to phenomics humgen heritability by daforerog on 2009-10-26 10:36:14 as
	Standardized human pedigree nomenclature: update and assessment of the recommendations of the National Society of Genetic Counselors. [My Copy] Journal of genetic counseling, Vol. 17, No. 5. (1 October 2008), pp. 424-433. by Robin L. Bennett, Kathryn Steinhaus S. French, Robert G. Resta, Debra Lochner L. Doyle posted to teaching phenomics humgen highly heritability by daforerog on 2009-10-26 10:27:15 as
	Evaluation of SNPs in miR-146a, miR196a2 and miR-499 as low-penetrance alleles in German and Italian familial breast cancer cases. [My Copy] Human mutation (21 October 2009) by Irene Catucci, Rongxi Yang, Paolo Verderio, et al.Sara Pizzamiglio, Ludwig Heesen, Kari Hemminki, Christian Sutter, Barbara Wappenschmidt, Michelle Dick, Norbert Arnold, Peter Bugert, Dieter Niederacher, Alfons Meindl, Rita K. Schmutzler, Claus C. Bartram, Filomena Ficarazzi, Laura Tizzoni, Daniela Zaffaroni, Siranoush Manoukian, Monica Barile, Marco A. Pierotti, Paolo Radice, Barbara Burwinkel, Paolo Peterlongo posted to mirna humgen by daforerog on 2009-10-23 17:14:54 as
	Identification of Novel Candidate Genes for Treatment Response to Risperidone and Susceptibility for Schizophrenia: Integrated Analysis Among Pharmacogenomics, Mouse Expression, and Genetic Case-Control Association Approaches [My Copy] Biological Psychiatry (2009) posted to schizophrenia psychgen mining humgen genomics by daforerog on 2009-10-23 17:12:45 as
	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
	Variation at GRN 3′-UTR rs5848 Is Not Associated with a Risk of Frontotemporal Lobar Degeneration in Dutch Population [My Copy] PLoS ONE, Vol. 4, No. 10. (22 October 2009), e7494. by Javier Simón-Sánchez, Harro Seelaar, Zoltán Bochdanovits, Dorly J. H. Deeg, John C. van Swieten, Peter Heutink posted to mirna humgen ftd assoc by daforerog on 2009-10-23 16:47:55 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
	SNPLims: a data management system for genome wide association studies. [My Copy] BMC bioinformatics, Vol. 9 Suppl 2 (2008) by Alessandro Orro, Guia Guffanti, Erika Salvi, Fabio Macciardi, Luciano Milanesi posted to silico mining humgen genomics assoc by daforerog on 2009-10-23 15:20:04 as along with 1 person guhjy
	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
	How to interpret a genome-wide association study. [My Copy] JAMA : the journal of the American Medical Association, Vol. 299, No. 11. (19 March 2008), pp. 1335-1344. by Thomas A. Pearson, Teri A. Manolio posted to teaching humgen highly gwas assoc by daforerog on 2009-10-21 14:21:28 as along with 11 people and 1 group operon kshameer Zephyrus psique ptrobajo qfwills cheyloveday misonneh guhjy BrianTomasik xingxu Roswell Cancer Crosstalk
	SPSmart: adapting population based SNP genotype databases for fast and comprehensive web access. [My Copy] BMC bioinformatics, Vol. 9 (10 October 2008), 428. by Jorge Amigo, Antonio Salas, Christopher Phillips, Angel Carracedo posted to silico popul mining humgen genomics by daforerog on 2009-10-20 21:57:34 as along with 1 person guhjy
	Online resources for SNP analysis: a review and route map. [My Copy] Molecular biotechnology, Vol. 35, No. 1. (January 2007), pp. 65-97. by Christopher Phillips posted to silico review mining humgen genomics assoc by daforerog on 2009-10-20 18:56:04 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

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humgen	1048
silico	834
mining	747
mirna	467
assoc	456
genomics	431
highly	351
genotyping	340
synaptic	279
psychgen	239
microarray	233
metaadpd	211
lab	204
brainmut	200
meta-analysis	181
brain	180
nssnps	177
mirrev	176
systems	175
gwas	171
ad	156
review	156
sci	156
expression	137
neuropsygen	134
find	122
neurogen	120
schizophrenia	114
cnv	97
popul	94
apoe	85
qtl	83
phenomics	78
parkinson	76
stat	76
adpdgenrev	75
gwasneuro	75
linkage	75
histor	68
neurola	63
ncrna	60
snp	54
autism	51
teaching	47
network	44
prevalence	43
adhd	42
bipolar	42
gamma-sec	40
aging	39
heritability	37
behavior	30
mr	29
neuroarray	29
htt	27
depression	25
citations	24
drosophila	18
papers	18
tf	18
cognition	14
ocd	14
comparison	12
adhdmeta	11
anxiety	10
epilep	10
ftd	10
genetics	10
gnun	10
bdnf	9
cell	7
comt	6
ethics	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

daforerog's humgen [more than 800 articles] Export

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