Volume 18; Issue 8

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Human Molecular Genetics
Volume 18; Issue 8

Human Molecular Genetics

Volume 18; Issue 8

1

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

Chio, A., Schymick, J. C., Restagno, G., Scholz, S. W., Lombardo, F., Lai, S.-L., Mora, G., Fung, H.-C., Britton, A., Arepalli, S., Gibbs, J. R., Nalls, M., Berger, S., Kwee, L. C., Oddone, E. Z., Din

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 287 KB

english, 2009

2

Contents Page

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 39 KB

english, 2009

3

Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete

Zeschnigk, M., Martin, M., Betzl, G., Kalbe, A., Sirsch, C., Buiting, K., Gross, S., Fritzilas, E., Frey, B., Rahmann, S., Horsthemke, B.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 416 KB

english, 2009

4

Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder

Cohen-Woods, S., Gaysina, D., Craddock, N., Farmer, A., Gray, J., Gunasinghe, C., Hoda, F., Jones, L., Knight, J., Korszun, A., Owen, M. J., Sterne, A., Craig, I. W., McGuffin, P.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 82 KB

english, 2009

5

Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region

Coppinger, J., McDonald-McGinn, D., Zackai, E., Shane, K., Atkin, J. F., Asamoah, A., Leland, R., Weaver, D. D., Lansky-Shafer, S., Schmidt, K., Feldman, H., Cohen, W., Phalin, J., Powell, B., Ballif,

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 198 KB

english, 2009

6

Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6

Little, H. J., Rorick, N. K., Su, L.-I, Baldock, C., Malhotra, S., Jowitt, T., Gakhar, L., Subramanian, R., Schutte, B. C., Dixon, M. J., Shore, P.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 21 KB

english, 2009

7

Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome

Galante, M., Jani, H., Vanes, L., Daniel, H., Fisher, E. M.C., Tybulewicz, V. L.J., Bliss, T. V.P., Morice, E.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 346 KB

english, 2009

8

Common variants in the region around Osterix are associated with bone mineral density and growth in childhood

Timpson, N. J., Tobias, J. H., Richards, J. B., Soranzo, N., Duncan, E. L., Sims, A.-M., Whittaker, P., Kumanduri, V., Zhai, G., Glaser, B., Eisman, J., Jones, G., Nicholson, G., Prince, R., Seeman, E

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 163 KB

english, 2009

9

MeCP2 involvement in the regulation of neuronal -tubulin production

Abuhatzira, L., Shemer, R., Razin, A.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 292 KB

english, 2009

10

Notch signaling contributes to the pathogenesis of human osteosarcomas

Engin, F., Bertin, T., Ma, O., Jiang, M. M., Wang, L., Sutton, R. E., Donehower, L. A., Lee, B.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 362 KB

english, 2009

11

Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease

Stayner, C., Iglesias, D. M., Goodyer, P. R., Ellis, L., Germino, G., Zhou, J., Eccles, M. R.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 27 KB

english, 2009

12

No evidence for activation of the unfolded protein response in neuronopathic models of Gaucher disease

Farfel-Becker, T., Vitner, E., Dekel, H., Leshem, N., Enquist, I. B., Karlsson, S., Futerman, A. H.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 166 KB

english, 2009

13

Transcriptional and post-transcriptional impact of toxic RNA in myotonic dystrophy

Osborne, R. J., Lin, X., Welle, S., Sobczak, K., O'Rourke, J. R., Swanson, M. S., Thornton, C. A.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 174 KB

english, 2009

14

ADH single nucleotide polymorphism associations with alcohol metabolism in vivo

Birley, A. J., James, M. R., Dickson, P. A., Montgomery, G. W., Heath, A. C., Martin, N. G., Whitfield, J. B.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 153 KB

english, 2009

15

Subscription Page

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 32 KB

english, 2009

16

Cover Page

Journal:

Human Molecular Genetics

Year:

2009

File:

PDF, 512 KB

2009

17

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

Shiura, H., Nakamura, K., Hikichi, T., Hino, T., Oda, K., Suzuki-Migishima, R., Kohda, T., Kaneko-Ishino, T., Ishino, F.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 772 KB

english, 2009

18

Deletion of eIF2beta suppresses testicular cancer incidence and causes recessive lethality in agouti-yellow mice

Heaney, J. D., Michelson, M. V., Youngren, K. K., Lam, M.-Y. J., Nadeau, J. H.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 265 KB

english, 2009

19

Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden

Renstrom, F., Payne, F., Nordstrom, A., Brito, E. C., Rolandsson, O., Hallmans, G., Barroso, I., Nordstrom, P., Franks, P. W.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 236 KB

english, 2009

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