Skip Navigation

Receive this page by email each issue: [Sign up for eTOCs]

Cover Image
[Cover Caption] 
Other Issues:
Previous Next 		Contents: Volume 17, Number 5, 1 March 2008   [Index by Author] 

Down ARTICLES


[Search ALL Issues]

Front Matter (PDF) | Table of Contents (PDF)

To see an article, click its [Full Text] or [PDF] link. To review many abstracts, check the boxes to the left of the titles you want, and click the 'Get All Checked Abstract(s)' button. To see one abstract at a time, click its [Abstract] link.

ARTICLES Back

Claire Farrington-Rock, Veneta Kirilova, Lisa Dillard-Telm, Alexander D. Borowsky, Sara Chalk, Matthew J. Rock, Daniel H. Cohn, and Deborah Krakow
Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome
Human Molecular Genetics Advance Access published on July 17, 2007
Hum. Mol. Genet. 2008 17: 631-641; doi:10.1093/hmg/ddm188 [Abstract] [Full Text] [PDF] [Request Permissions]  

Damon S. Perez, Tiffany R. Hoage, Jay R. Pritchett, Allison L. Ducharme-Smith, Meredith L. Halling, Sree C. Ganapathiraju, Paul S. Streng, and David I. Smith
Long, abundantly expressed non-coding transcripts are altered in cancer
Human Molecular Genetics Advance Access published on November 15, 2007
Hum. Mol. Genet. 2008 17: 642-655; doi:10.1093/hmg/ddm336 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Eranga N. Vithana, Patricio E. Morgan, Vedam Ramprasad, Donald T.H. Tan, Victor H.K Yong, Divya Venkataraman, Anandalakshmi Venkatraman, Gary H.F. Yam, Soumittra Nagasamy, Ricky W.K. Law, Rama Rajagopal, Chi P. Pang, Govindsamy Kumaramanickevel, Joseph R. Casey, and Tin Aung
SLC4A11 mutations in Fuchs endothelial corneal dystrophy
Human Molecular Genetics Advance Access published on November 16, 2007
Hum. Mol. Genet. 2008 17: 656-666; doi:10.1093/hmg/ddm337 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Maria Carmen Solaz-Fuster, José Vicente Gimeno-Alcañiz, Susana Ros, Maria Elena Fernandez-Sanchez, Belen Garcia-Fojeda, Olga Criado Garcia, David Vilchez, Jorge Dominguez, Mar Garcia-Rocha, Maribel Sanchez-Piris, Carmen Aguado, Erwin Knecht, Jose Serratosa, Joan Josep Guinovart, Pascual Sanz, and Santiago Rodriguez de Córdoba
Regulation of glycogen synthesis by the laforin–malin complex is modulated by the AMP-activated protein kinase pathway
Human Molecular Genetics Advance Access published on November 20, 2007
Hum. Mol. Genet. 2008 17: 667-678; doi:10.1093/hmg/ddm339 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Jean-Hugues Guervilly, Gaëtane Macé-Aimé, and Filippo Rosselli
Loss of CHK1 function impedes DNA damage-induced FANCD2 monoubiquitination but normalizes the abnormal G2 arrest in Fanconi anemia
Human Molecular Genetics Advance Access published on November 20, 2007
Hum. Mol. Genet. 2008 17: 679-689; doi:10.1093/hmg/ddm340 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Bilian Jin, Qian Tao, Jinrong Peng, Hui Meng Soo, Wei Wu, Jianming Ying, C. Robert Fields, Amber L. Delmas, Xuefeng Liu, Jingxin Qiu, and Keith D. Robertson
DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function
Human Molecular Genetics Advance Access published on November 20, 2007
Hum. Mol. Genet. 2008 17: 690-709; doi:10.1093/hmg/ddm341 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Alex W. Hewitt, Shiwani Sharma, Kathryn P. Burdon, Jie Jin Wang, Paul N. Baird, David P. Dimasi, David A. Mackey, Paul Mitchell, and Jamie E. Craig
Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people
Human Molecular Genetics Advance Access published on November 23, 2007
Hum. Mol. Genet. 2008 17: 710-716; doi:10.1093/hmg/ddm342 [Abstract] [Full Text] [PDF] [Request Permissions]  

Jens R. Wendland, Pablo R. Moya, Matthew R. Kruse, Renee F. Ren-Patterson, Catherine L. Jensen, Kiara R. Timpano, and Dennis L. Murphy
A novel, putative gain-of-function haplotype at SLC6A4 associates with obsessive-compulsive disorder
Human Molecular Genetics Advance Access published on November 30, 2007
Hum. Mol. Genet. 2008 17: 717-723; doi:10.1093/hmg/ddm343 [Abstract] [Full Text] [PDF] [Request Permissions]  

Joanna S. Zeiger, Brett C. Haberstick, Isabel Schlaepfer, Allan C. Collins, Robin P. Corley, Thomas J. Crowley, John K. Hewitt, Christian J. Hopfer, Jeffrey Lessem, Matthew B. McQueen, Soo Hyun Rhee, and Marissa A. Ehringer
The neuronal nicotinic receptor subunit genes (CHRNA6 and CHRNB3) are associated with subjective responses to tobacco
Human Molecular Genetics Advance Access published on November 30, 2007
Hum. Mol. Genet. 2008 17: 724-734; doi:10.1093/hmg/ddm344 [Abstract] [Full Text] [PDF] [Request Permissions]  

Sahar Al-Mahdawi, Ricardo Mouro Pinto, Ozama Ismail, Dhaval Varshney, Stefania Lymperi, Chiranjeevi Sandi, Daniah Trabzuni, and Mark Pook
The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues
Human Molecular Genetics Advance Access published on November 27, 2007
Hum. Mol. Genet. 2008 17: 735-746; doi:10.1093/hmg/ddm346 [Abstract] [Full Text] [PDF] [Request Permissions]  

Michael E. Talkowski, George Kirov, Mikhil Bamne, Lyudmila Georgieva, Gonzalo Torres, Hader Mansour, Kodavali V. Chowdari, Vihra Milanova, Joel Wood, Lora McClain, Konasale Prasad, Brian Shirts, Jianping Zhang, Michael C. O’Donovan, Michael J. Owen, Bernie Devlin, and Vishwajit L. Nimgaonkar
A network of dopaminergic gene variations implicated as risk factors for schizophrenia
Human Molecular Genetics Advance Access published on November 27, 2007
Hum. Mol. Genet. 2008 17: 747-758; doi:10.1093/hmg/ddm347 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Yonghong Li, Andrew Grupe, Charles Rowland, Peter Holmans, Ricardo Segurado, Richard Abraham, Lesley Jones, Joseph Catanese, David Ross, Kevin Mayo, Maribel Martinez, Paul Hollingworth, Alison Goate, Nigel J. Cairns, Brad A. Racette, Joel S. Perlmutter, Michael C. O'Donovan, John C. Morris, Carol Brayne, David C. Rubinsztein, Simon Lovestone, Leon J. Thal, Michael J. Owen, and Julie Williams
Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease
Human Molecular Genetics Advance Access published on December 6, 2007
Hum. Mol. Genet. 2008 17: 759-767; doi:10.1093/hmg/ddm348 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

Simon Cronin, Stephen Berger, Jinhui Ding, Jennifer C Schymick, Nicole Washecka, Dena G. Hernandez, Matthew J. Greenway, Daniel G. Bradley, Bryan J. Traynor, and Orla Hardiman
A genome-wide association study of sporadic ALS in a homogenous Irish population
Human Molecular Genetics Advance Access published on December 5, 2007
Hum. Mol. Genet. 2008 17: 768-774; doi:10.1093/hmg/ddm361 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

To see an article, click its [Full Text] or [PDF] link. To review many abstracts, check the boxes to the left of the titles you want, and click the 'Get All Checked Abstract(s)' button. To see one abstract at a time, click its [Abstract] link.