PMC Links for Nucleotide (Select 1527146897) - PMC

Select item 69272061.

Genome-Wide Association Study of Multiplex Schizophrenia Pedigrees

Douglas F. Levinson, Jianxin Shi, Kai Wang, Sang Oh, Brien Riley, Ann E. Pulver, Dieter B. Wildenauer, Claudine Laurent, Bryan J. Mowry, Pablo V. Gejman, Michael J. Owen, Kenneth S. Kendler, Gerald Nestadt, Sibylle G. Schwab, Jacques Mallet, Deborah Nertney, Alan R. Sanders, Nigel M. Williams, Brandon Wormley, Virginia K. Lasseter, Margot Albus, Stephanie Godard-Bauché, Madeline Alexander, Jubao Duan, Michael C. O’Donovan, Dermot Walsh, Anthony O’Neill, George N. Papadimitriou, Dimitris Dikeos, Wolfgang Maier, Bernard Lerer, Dominique Campion, David Cohen, Maurice Jay, Ayman Fanous, Peter Eichhammer, Jeremy M. Silverman, Nadine Norton, Nancy Zhang, Hakon Hakonarson, Cynthia Gao, Ami Citri, Mark Hansen, Stephan Ripke, The Schizophrenia Psychiatric GWAS Consortium, Frank Dudbridge, Peter A. Holmans

Am J Psychiatry. Author manuscript; available in PMC 2019 Dec 23.

Published in final edited form as: Am J Psychiatry. 2012 Sep; 169(9): 963–973. doi: 10.1176/appi.ajp.2012.11091423

PMCID:: PMC6927206

Abstract Article PDF–975K

Select item 49824822.

Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease

Jonathan M. Schott, Sebastian J. Crutch, Minerva M. Carrasquillo, James Uphill, Tim J. Shakespeare, Natalie S. Ryan, Keir X. Yong, Manja Lehmann, Nilufer Ertekin-Taner, Neill R. Graff-Radford, Bradley F. Boeve, Melissa E. Murray, Qurat ul Ain Khan, Ronald C. Petersen, Dennis W. Dickson, David S. Knopman, Gil D. Rabinovici, Bruce L. Miller, Aida Suárez González, Eulogio Gil-Néciga, Julie S. Snowden, Jenny Harris, Stuart M. Pickering-Brown, Eva Louwersheimer, Wiesje M. van der Flier, Philip Scheltens, Yolande A. Pijnenburg, Douglas Galasko, Marie Sarazin, Bruno Dubois, Eloi Magnin, Daniela Galimberti, Elio Scarpini, Stefano F. Cappa, John R. Hodges, Glenda M. Halliday, Lauren Bartley, Maria C. Carrillo, Jose T. Bras, John Hardy, Martin N. Rossor, John Collinge, Nick C. Fox, Simon Mead

Alzheimers Dement. 2016 Aug; 12(8): 862–871. doi: 10.1016/j.jalz.2016.01.010

PMCID:: PMC4982482

Abstract Article

Select item 29410173.

Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia

Alistair T. Pagnamenta, Elena Bacchelli, Maretha V. de Jonge, Ghazala Mirza, Thomas S. Scerri, Fiorella Minopoli, Andreas Chiocchetti, Kerstin U. Ludwig, Per Hoffmann, Silvia Paracchini, Ernesto Lowy, Denise H. Harold, Jade A. Chapman, Sabine M. Klauck, Fritz Poustka, Renske H. Houben, Wouter G. Staal, Roel A. Ophoff, Michael C. O'Donovan, Julie Williams, Markus M. Nöthen, Gerd Schulte-Körne, Panos Deloukas, Jiannis Ragoussis, Anthony J. Bailey, Elena Maestrini, Anthony P. Monaco, International Molecular Genetic Study Of Autism Consortium

Biol Psychiatry. 2010 Aug 15; 68(4): 320–328. doi: 10.1016/j.biopsych.2010.02.002

PMCID:: PMC2941017

Abstract Article

Select item 28888954.

Genomewide Pharmacogenomic Analysis of Response to Treatment with Antipsychotics

Joseph L. McClay, Daniel E. Adkins, Karolina Åberg, Scott Stroup, Diana O. Perkins, Vladimir I. Vladimirov, Jeffrey A. Lieberman, Patrick F. Sullivan, Edwin J.C.G. van den Oord

Mol Psychiatry. Author manuscript; available in PMC 2011 Jul 1.

Published in final edited form as: Mol Psychiatry. 2011 Jan; 16(1): 76–85. Published online 2009 Sep 1. doi: 10.1038/mp.2009.89

PMCID:: PMC2888895

Abstract Article PDF–257K

Select item 28422985.

Genome-Wide Association of Lipid-Lowering Response to Statins in Combined Study Populations

Mathew J. Barber, Lara M. Mangravite, Craig L. Hyde, Daniel I. Chasman, Joshua D. Smith, Catherine A. McCarty, Xiaohui Li, Russell A. Wilke, Mark J. Rieder, Paul T. Williams, Paul M. Ridker, Aurobindo Chatterjee, Jerome I. Rotter, Deborah A. Nickerson, Matthew Stephens, Ronald M. Krauss

PLoS One. 2010; 5(3): e9763. Published online 2010 Mar 22. doi: 10.1371/journal.pone.0009763

PMCID:: PMC2842298

Abstract Article PDF–162K

Select item 19956216.

Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness

Daniel Levy, Martin G Larson, Emelia J Benjamin, Christopher Newton-Cheh, Thomas J Wang, Shih-Jen Hwang, Ramachandran S Vasan, Gary F Mitchell

BMC Med Genet. 2007; 8(Suppl 1): S3. Published online 2007 Sep 19. doi: 10.1186/1471-2350-8-S1-S3

PMCID:: PMC1995621

Abstract Article PDF–283K

Select item 66117327.

Abstracts of the 12^th European Cytogenomics Conference 2019: Salzburg, Austria. 6-9 July 2019

Mol Cytogenet. 2019; 12(Suppl 1): 30. Published online 2019 Jul 5. doi: 10.1186/s13039-019-0439-z

PMCID:: PMC6611732

Article PDF–1.4M

Select item 54043308.

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

Xiaowei Sylvia Chen, Rose H. Reader, Alexander Hoischen, Joris A. Veltman, Nuala H. Simpson, Clyde Francks, Dianne F. Newbury, Simon E. Fisher

Sci Rep. 2017; 7: 46105. Published online 2017 Apr 25. doi: 10.1038/srep46105

PMCID:: PMC5404330

Abstract Article PDF–1.2M

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