PMC Links for Nucleotide (Select 1677530411) - PMC

Select item 38123241.

Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans

J L Del-Aguila, A L Beitelshees, R M Cooper-DeHoff, A B Chapman, J G Gums, K Bailey, Y Gong, S T Turner, J A Johnson, E Boerwinkle

Pharmacogenomics J. 2014 Feb; 14(1): 35–40. Published online 2013 Feb 12. doi: 10.1038/tpj.2013.3

PMCID:: PMC3812324

Abstract Article PDF–662K

Select item 37912652.

Mutations in AGBL1 Cause Dominant Late-Onset Fuchs Corneal Dystrophy and Alter Protein-Protein Interaction with TCF4

S. Amer Riazuddin, Shivakumar Vasanth, Nicholas Katsanis, John D. Gottsch

Am J Hum Genet. 2013 Oct 3; 93(4): 758–764. doi: 10.1016/j.ajhg.2013.08.010

PMCID:: PMC3791265

Abstract Article PDF–1003K

Select item 37467033.

Evidence for Shared Genetic Risk Between Methamphetamine-Induced Psychosis and Schizophrenia

Masashi Ikeda, Yuko Okahisa, Branko Aleksic, Mujun Won, Naoki Kondo, Nobuya Naruse, Kumi Aoyama-Uehara, Ichiro Sora, Masaomi Iyo, Ryota Hashimoto, Yoshiya Kawamura, Nao Nishida, Taku Miyagawa, Masatoshi Takeda, Tsukasa Sasaki, Katsushi Tokunaga, Norio Ozaki, Hiroshi Ujike, Nakao Iwata

Neuropsychopharmacology. 2013 Sep; 38(10): 1864–1870. Prepublished online 2013 Apr 12. Published online 2013 Jun 12. doi: 10.1038/npp.2013.94

PMCID:: PMC3746703

Abstract Article PDF–381K

Select item 36275034.

Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D

S. L. Clark, D. E. Adkins, K. Aberg, J. M. Hettema, J. L. McClay, R. P. Souza, E. J. C. G. van den Oord

Psychol Med. Author manuscript; available in PMC 2013 Jun 1.

Published in final edited form as: Psychol Med. 2012 Jun; 42(6): 1151–1162. Published online 2011 Nov 1. doi: 10.1017/S003329171100239X

PMCID:: PMC3627503

Abstract Article PDF–834K

Select item 33972735.

Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease

Weihong Tang, Christine Schwienbacher, Lorna M. Lopez, Yoav Ben-Shlomo, Tiphaine Oudot-Mellakh, Andrew D. Johnson, Nilesh J. Samani, Saonli Basu, Martin Gögele, Gail Davies, Gordon D.O. Lowe, David-Alexandre Tregouet, Adrian Tan, James S. Pankow, Albert Tenesa, Daniel Levy, Claudia B. Volpato, Ann Rumley, Alan J. Gow, Cosetta Minelli, John W.G. Yarnell, David J. Porteous, John M. Starr, John Gallacher, Eric Boerwinkle, Peter M. Visscher, Peter P. Pramstaller, Mary Cushman, Valur Emilsson, Andrew S. Plump, Nena Matijevic, Pierre-Emmanuel Morange, Ian J. Deary, Andrew A. Hicks, Aaron R. Folsom

Am J Hum Genet. 2012 Jul 13; 91(1): 152–162. doi: 10.1016/j.ajhg.2012.05.009

PMCID:: PMC3397273

Abstract Article PDF–367K

Select item 67267416.

Novel Mutations Associated With Various Types of Corneal Dystrophies in a Han Chinese Population

Jing Zhang, Dan Wu, Yue Li, Yidan Fan, Huiyu Chen, Jiaxu Hong, Jianjiang Xu

Front Genet. 2019; 10: 881. Published online 2019 Aug 29. doi: 10.3389/fgene.2019.00881

PMCID:: PMC6726741

Abstract Article PDF–3.0M

Select item 44084287.

Differential DNA methylation profiles of coding and non-coding genes define hippocampal sclerosis in human temporal lobe epilepsy

Suzanne F.C. Miller-Delaney, Kenneth Bryan, Sudipto Das, Ross C. McKiernan, Isabella M. Bray, James P. Reynolds, Ryder Gwinn, Raymond L. Stallings, David C. Henshall

Brain. 2015 Mar; 138(3): 616–631. Published online 2014 Dec 31. doi: 10.1093/brain/awu373

PMCID:: PMC4408428

Abstract Article PDF–1.3M

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