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Previous Next 		Contents: Volume 18, Number 8, 15 April 2009   [Index by Author] 

Down ARTICLES
Down ASSOCIATION STUDIES ARTICLES
Down CORRIGENDUM
Down ERRATUM
Down FRONT-MATTER/BACK-MATTER


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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

Justine Coppinger, Donna McDonald-McGinn, Elaine Zackai, Kate Shane, Joan F. Atkin, Alexander Asamoah, Robert Leland, David D. Weaver, Susan Lansky-Shafer, Karen Schmidt, Heidi Feldman, William Cohen, Judy Phalin, Berkley Powell, Blake C. Ballif, Aaron Theisen, Elizabeth Geiger, Chad Haldeman-Englert, Tamim H. Shaikh, Sulagna Saitta, Bassem A. Bejjani, and Lisa G. Shaffer
Identification of familial and de novo microduplications of 22q11.21–q11.23 distal to the 22q11.21 microdeletion syndrome region
Human Molecular Genetics Advance Access published on February 3, 2009
Hum. Mol. Genet. 2009 18: 1377-1383; doi:10.1093/hmg/ddp042 [Abstract] [Full Text] [PDF] [Request Permissions]  

Don W. Cleveland, Koji Yamanaka, and Pascale Bomont
Gigaxonin controls vimentin organization through a tubulin chaperone-independent pathway
Human Molecular Genetics Advance Access published on January 24, 2009
Hum. Mol. Genet. 2009 18: 1384-1394; doi:10.1093/hmg/ddp044 [Abstract] [Full Text] [PDF] [Request Permissions]  

Jason D. Heaney, Megan V. Michelson, Kirsten K. Youngren, Man-Yee J. Lam, and Joseph H. Nadeau
Deletion of eIF2beta suppresses testicular cancer incidence and causes recessive lethality in agouti-yellow mice
Human Molecular Genetics Advance Access published on January 23, 2009
Hum. Mol. Genet. 2009 18: 1395-1404; doi:10.1093/hmg/ddp045 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Aude-Marie Lepagnol-Bestel, Agnes Zvara, Gilles Maussion, Frédérique Quignon, Bedel Ngimbous, Nicolas Ramoz, Sandrine Imbeaud, Yann Loe-Mie, Karim Benihoud, Nicolas Agier, Paul A. Salin, Ana Cardona, Suonavy Khung-Savatovsky, Pekka Kallunki, Jean-Maurice Delabar, Laszlo G. Puskas, Hervé Delacroix, Lawrence Aggerbeck, Anne-Lise Delezoide, Olivier Delattre, Philip Gorwood, Jean-Marie Moalic, and Michel Simonneau
DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome
Human Molecular Genetics Advance Access published on February 12, 2009
Hum. Mol. Genet. 2009 18: 1405-1414; doi:10.1093/hmg/ddp047 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Liron Abuhatzira, Ruth Shemer, and Aharon Razin
MeCP2 involvement in the regulation of neuronal {alpha}-tubulin production
Human Molecular Genetics Advance Access published on January 27, 2009
Hum. Mol. Genet. 2009 18: 1415-1423; doi:10.1093/hmg/ddp048 [Abstract] [Full Text] [PDF] [Request Permissions]  

Hirosuke Shiura, Kenji Nakamura, Takafusa Hikichi, Toshiaki Hino, Kanako Oda, Rika Suzuki-Migishima, Takashi Kohda, Tomoko Kaneko-Ishino, and Fumitoshi Ishino
Paternal deletion of Meg1/Grb10 DMR causes maternalization of the Meg1/Grb10 cluster in mouse proximal Chromosome 11 leading to severe pre- and postnatal growth retardation
Human Molecular Genetics Advance Access published on January 27, 2009
Hum. Mol. Genet. 2009 18: 1424-1438; doi:10.1093/hmg/ddp049 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Michael Zeschnigk, Marcel Martin, Gisela Betzl, Andreas Kalbe, Caroline Sirsch, Karin Buiting, Stephanie Gross, Epameinondas Fritzilas, Bruno Frey, Sven Rahmann, and Bernhard Horsthemke
Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete
Human Molecular Genetics Advance Access published on February 17, 2009
Hum. Mol. Genet. 2009 18: 1439-1448; doi:10.1093/hmg/ddp054 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Micaela Galante, Harsha Jani, Lesley Vanes, Hervé Daniel, Elizabeth M.C. Fisher, Victor L.J. Tybulewicz, Timothy V.P. Bliss, and Elise Morice
Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome
Human Molecular Genetics Advance Access published on January 29, 2009
Hum. Mol. Genet. 2009 18: 1449-1463; doi:10.1093/hmg/ddp055 [Abstract] [FREE Full Text] [PDF]   Creative Commons License OPEN ACCESS  

Feyza Engin, Terry Bertin, Ou Ma, Ming Ming Jiang, Lisa Wang, Richard E. Sutton, Lawrence A. Donehower, and Brendan Lee
Notch signaling contributes to the pathogenesis of human osteosarcomas
Human Molecular Genetics Advance Access published on February 19, 2009
Hum. Mol. Genet. 2009 18: 1464-1470; doi:10.1093/hmg/ddp057 [Abstract] [Full Text] [PDF] [Request Permissions]  

Robert J. Osborne, Xiaoyan Lin, Stephen Welle, Krzysztof Sobczak, Jason R. O'Rourke, Maurice S. Swanson, and Charles A. Thornton
Transcriptional and post-transcriptional impact of toxic RNA in myotonic dystrophy
Human Molecular Genetics Advance Access published on February 17, 2009
Hum. Mol. Genet. 2009 18: 1471-1481; doi:10.1093/hmg/ddp058 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Tamar Farfel-Becker, Einat Vitner, Hani Dekel, Noa Leshem, Ida Berglin Enquist, Stefan Karlsson, and Anthony H. Futerman
No evidence for activation of the unfolded protein response in neuronopathic models of Gaucher disease
Human Molecular Genetics Advance Access published on February 3, 2009
Hum. Mol. Genet. 2009 18: 1482-1488; doi:10.1093/hmg/ddp061 [Abstract] [Full Text] [PDF] [Request Permissions]  

ASSOCIATION STUDIES ARTICLES Back

Frida Renström, Felicity Payne, Anna Nordström, Ema C. Brito, Olov Rolandsson, Göran Hallmans, Ines Barroso, Peter Nordström, Paul W. Franks, and GIANT Consortium
Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden
Human Molecular Genetics Advance Access published on January 22, 2009
Hum. Mol. Genet. 2009 18: 1489-1496; doi:10.1093/hmg/ddp041 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

George Kirov, Detelina Grozeva, Nadine Norton, Dobril Ivanov, Kiran K. Mantripragada, Peter Holmans, International Schizophrenia Consortium, the Wellcome Trust Case Control Consortium, Nick Craddock, Michael J. Owen, and Michael C. O'Donovan
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
Human Molecular Genetics Advance Access published on January 29, 2009
Hum. Mol. Genet. 2009 18: 1497-1503; doi:10.1093/hmg/ddp043 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Sarah Cohen-Woods, Daria Gaysina, Nick Craddock, Anne Farmer, Joanna Gray, Cerisse Gunasinghe, Farzana Hoda, Lisa Jones, Jo Knight, Ania Korszun, Michael J. Owen, Abram Sterne, Ian W. Craig, and Peter McGuffin
Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder
Human Molecular Genetics Advance Access published on January 30, 2009
Hum. Mol. Genet. 2009 18: 1504-1509; doi:10.1093/hmg/ddp051 [Abstract] [Full Text] [PDF] [Request Permissions]  

Nicholas J. Timpson, Jon H. Tobias, J. Brent Richards, Nicole Soranzo, Emma L. Duncan, Anne-Marie Sims, Pamela Whittaker, Vasudev Kumanduri, Guangju Zhai, Beate Glaser, John Eisman, Graeme Jones, Geoff Nicholson, Richard Prince, Ego Seeman, Tim D. Spector, Matthew A. Brown, Leena Peltonen, George Davey Smith, Panos Deloukas, and David M. Evans
Common variants in the region around Osterix are associated with bone mineral density and growth in childhood
Human Molecular Genetics Advance Access published on January 30, 2009
Hum. Mol. Genet. 2009 18: 1510-1517; doi:10.1093/hmg/ddp052 [Abstract] [FREE Full Text] [PDF] [Supplementary Data]   Creative Commons License OPEN ACCESS  

Ingrid Meulenbelt, Kay Chapman, Rebeca Dieguez-Gonzalez, Dongquan Shi, Aspasia Tsezou, Jin Dai, Konstantinos N. Malizos, Margreet Kloppenburg, Andrew Carr, Masahiro Nakajima, Ruud van der Breggen, Nico Lakenberg, Juan J. Gomez-Reino, Qing Jiang, Shiro Ikegawa, Antonio Gonzalez, John Loughlin, and Eline P. Slagboom
Large replication study and meta-analyses of DVWA as an osteoarthritis susceptibility locus in European and Asian populations
Human Molecular Genetics Advance Access published on January 30, 2009
Hum. Mol. Genet. 2009 18: 1518-1523; doi:10.1093/hmg/ddp053 [Abstract] [Full Text] [PDF] [Request Permissions]  

Adriano Chiò, Jennifer C. Schymick, Gabriella Restagno, Sonja W. Scholz, Federica Lombardo, Shiao-Lin Lai, Gabriele Mora, Hon-Chung Fung, Angela Britton, Sampath Arepalli, J. Raphael Gibbs, Michael Nalls, Stephen Berger, Lydia Coulter Kwee, Eugene Z. Oddone, Jinhui Ding, Cynthia Crews, Ian Rafferty, Nicole Washecka, Dena Hernandez, Luigi Ferrucci, Stefania Bandinelli, Jack Guralnik, Fabio Macciardi, Federica Torri, Sara Lupoli, Stephen J. Chanock, Gilles Thomas, David J. Hunter, Christian Gieger, H. Erich Wichmann, Andrea Calvo, Roberto Mutani, Stefania Battistini, Fabio Giannini, Claudia Caponnetto, Giovanni Luigi Mancardi, Vincenzo La Bella, Francesca Valentino, Maria Rosaria Monsurrò, Gioacchino Tedeschi, Kalliopi Marinou, Mario Sabatelli, Amelia Conte, Jessica Mandrioli, Patrizia Sola, Fabrizio Salvi, Ilaria Bartolomei, Gabriele Siciliano, Cecilia Carlesi, Richard W. Orrell, Kevin Talbot, Zachary Simmons, James Connor, Erik P. Pioro, Travis Dunkley, Dietrich A. Stephan, Dalia Kasperaviciute, Elizabeth M. Fisher, Sibylle Jabonka, Michael Sendtner, Marcus Beck, Lucie Bruijn, Jeffrey Rothstein, Silke Schmidt, Andrew Singleton, John Hardy, and Bryan J. Traynor
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis
Human Molecular Genetics Advance Access published on February 4, 2009
Hum. Mol. Genet. 2009 18: 1524-1532; doi:10.1093/hmg/ddp059 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

Andrew J. Birley, Michael R. James, Peter A. Dickson, Grant W. Montgomery, Andrew C. Heath, Nicholas G. Martin, and John B. Whitfield
ADH single nucleotide polymorphism associations with alcohol metabolism in vivo
Human Molecular Genetics Advance Access published on February 4, 2009
Hum. Mol. Genet. 2009 18: 1533-1542; doi:10.1093/hmg/ddp060 [Abstract] [Full Text] [PDF] [Supplementary Data] [Request Permissions]  

CORRIGENDUM Back

Cherie Stayner, Diana M. Iglesias, Paul R. Goodyer, Lana Ellis, Greg Germino, Jing Zhou, and Michael R. Eccles
Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease
Human Molecular Genetics Advance Access published on February 9, 2009
Hum. Mol. Genet. 2009 18: 1543; doi:10.1093/hmg/ddp050 [Extract] [Full Text] [PDF] [Request Permissions]  

ERRATUM Back

Hayley J. Little, Nicholas K. Rorick, Ling-I Su, Clair Baldock, Saimon Malhotra, Tom Jowitt, Lokesh Gakhar, Ramaswamy Subramanian, Brian C. Schutte, Michael J. Dixon, and Paul Shore
Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6
Human Molecular Genetics Advance Access published on February 9, 2009
Hum. Mol. Genet. 2009 18: 1544; doi:10.1093/hmg/ddp056 [Extract] [Full Text] [PDF] [Request Permissions]  

FRONT-MATTER/BACK-MATTER Back

Cover Page
Hum. Mol. Genet. 2009 18: NP; doi:10.1093/hmg/ddp140 [PDF] [Request Permissions]  

Editorial Board
Hum. Mol. Genet. 2009 18: NP; doi:10.1093/hmg/ddp141 [PDF] [Request Permissions]  

Subscription Page
Hum. Mol. Genet. 2009 18: NP; doi:10.1093/hmg/ddp142 [PDF] [Request Permissions]  

Contents Page
Hum. Mol. Genet. 2009 18: NP; doi:10.1093/hmg/ddp139 [PDF] [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.