| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Case-Control Association Study of the 12 Single-Nucleotide Polymorphisms Implicated in Parkinson Disease by a Recent Genome Scan
|
Li, Yonghong
|
|
2006
|
78 |
6 |
p. 1090-1092
3 p.
|
artikel
|
| 2 |
A Mutation of β-Actin That Alters Depolymerization Dynamics Is Associated with Autosomal Dominant Developmental Malformations, Deafness, and Dystonia
|
Procaccio, Vincent
|
|
2006
|
78 |
6 |
p. 947-960
14 p.
|
artikel
|
| 3 |
Announcements 1 1 Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please e-mail announcements to ajhg@ajhg.net. Submission must be received at least 7 weeks before the month of issue in which publication is requested. They must be double spaced with a 1½-inch margin on all sides. The maximum length is 250 words, excluding the address for correspondence. Please include a cover letter indicating the name of the sponsoring ASHG member.
|
|
|
2006
|
78 |
6 |
p. 1101-1106
6 p.
|
artikel
|
| 4 |
A Note on Permutation Tests in Multistage Association Scans
|
Dudbridge, Frank
|
|
2006
|
78 |
6 |
p. 1094-1095
2 p.
|
artikel
|
| 5 |
Cathepsin D Deficiency Is Associated with a Human Neurodegenerative Disorder
|
Steinfeld, Robert
|
|
2006
|
78 |
6 |
p. 988-998
11 p.
|
artikel
|
| 6 |
Conflicting Results Regarding the Semaphorin Gene (SEMA5A) and the Risk for Parkinson Disease
|
Clarimon, Jordi
|
|
2006
|
78 |
6 |
p. 1082-1083
2 p.
|
artikel
|
| 7 |
Considerations for Genomewide Association Studies in Parkinson Disease
|
Myers, Dr. Richard H.
|
|
2006
|
78 |
6 |
p. 1081-1082
2 p.
|
artikel
|
| 8 |
Contiguous Gene Deletion within Chromosome Arm 10q Is Associated with Juvenile Polyposis of Infancy, Reflecting Cooperation between the BMPR1A and PTEN Tumor-Suppressor Genes
|
Delnatte, Capucine
|
|
2006
|
78 |
6 |
p. 1066-1074
9 p.
|
artikel
|
| 9 |
Diplotype Trend Regression Analysis of the ADH Gene Cluster and the ALDH2 Gene: Multiple Significant Associations with Alcohol Dependence
|
Luo, Xingguang
|
|
2006
|
78 |
6 |
p. 973-987
15 p.
|
artikel
|
| 10 |
Elevated Expression and Genetic Association Links the SOCS3 Gene to Atopic Dermatitis
|
Ekelund, E.
|
|
2006
|
78 |
6 |
p. 1060-1065
6 p.
|
artikel
|
| 11 |
Errata
|
|
|
2006
|
78 |
6 |
p. 1097-
1 p.
|
artikel
|
| 12 |
Errata
|
|
|
2006
|
78 |
6 |
p. 1097-1098
2 p.
|
artikel
|
| 13 |
Fibulin-4: A Novel Gene for an Autosomal Recessive Cutis Laxa Syndrome
|
Hucthagowder, Vishwanathan
|
|
2006
|
78 |
6 |
p. 1075-1080
6 p.
|
artikel
|
| 14 |
Genomewide Association, Parkinson Disease, and PARK10
|
Farrer, Matthew J.
|
|
2006
|
78 |
6 |
p. 1084-1088
5 p.
|
artikel
|
| 15 |
Haplotype Homozygosity and Derived Alleles in the Human Genome
|
Fry, Andrew E.
|
|
2006
|
78 |
6 |
p. 1053-1059
7 p.
|
artikel
|
| 16 |
Multilocus Association Mapping Using Variable-Length Markov Chains
|
Browning, Sharon R.
|
|
2006
|
78 |
6 |
p. 903-913
11 p.
|
artikel
|
| 17 |
Mutant POLG2 Disrupts DNA Polymerase γ Subunits and Causes Progressive External Ophthalmoplegia
|
Longley, Matthew J.
|
|
2006
|
78 |
6 |
p. 1026-1034
9 p.
|
artikel
|
| 18 |
Mutations in the Gene Encoding Peroxisomal Sterol Carrier Protein X (SCPx) Cause Leukencephalopathy with Dystonia and Motor Neuropathy
|
Ferdinandusse, S.
|
|
2006
|
78 |
6 |
p. 1046-1052
7 p.
|
artikel
|
| 19 |
No Evidence for Association with Parkinson Disease for 13 Single-Nucleotide Polymorphisms Identified by Whole-Genome Association Screening
|
Goris, A.
|
|
2006
|
78 |
6 |
p. 1088-1090
3 p.
|
artikel
|
| 20 |
Online System for Faster Multipoint Linkage Analysis via Parallel Execution on Thousands of Personal Computers
|
Silberstein, M.
|
|
2006
|
78 |
6 |
p. 922-935
14 p.
|
artikel
|
| 21 |
Ordered Genotypes: An Extended ITO Method and a General Formula for Genetic Covariance
|
Dai, Feng
|
|
2006
|
78 |
6 |
p. 1035-1045
11 p.
|
artikel
|
| 22 |
Promoter Mutations That Increase Amyloid Precursor-Protein Expression Are Associated with Alzheimer Disease
|
Theuns, Jessie
|
|
2006
|
78 |
6 |
p. 936-946
11 p.
|
artikel
|
| 23 |
Reconstruction of a Functional Human Gene Network, with an Application for Prioritizing Positional Candidate Genes
|
Franke, Lude
|
|
2006
|
78 |
6 |
p. 1011-1025
15 p.
|
artikel
|
| 24 |
Reply to Dudbridge
|
Lin, D.Y.
|
|
2006
|
78 |
6 |
p. 1096-
1 p.
|
artikel
|
| 25 |
Response from Maraganore et al.
|
Maraganore, Demetrius M.
|
|
2006
|
78 |
6 |
p. 1092-1094
3 p.
|
artikel
|
| 26 |
Society News
|
Boughman, Joann A.
|
|
2006
|
78 |
6 |
p. 1099-1100
2 p.
|
artikel
|
| 27 |
The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males
|
Twigg, Stephen R.F.
|
|
2006
|
78 |
6 |
p. 999-1010
12 p.
|
artikel
|
| 28 |
This Month in the Journal
|
Williamson, Robin E.
|
|
2006
|
78 |
6 |
p. i-ii
nvt p.
|
artikel
|
| 29 |
Total-Genome Analysis of BRCA1/2-Related Invasive Carcinomas of the Breast Identifies Tumor Stroma as Potential Landscaper for Neoplastic Initiation
|
Weber, Frank
|
|
2006
|
78 |
6 |
p. 961-972
12 p.
|
artikel
|
| 30 |
Variance Calculations for Identity-by-Descent Estimation
|
McQueen, Matthew B.
|
|
2006
|
78 |
6 |
p. 914-921
8 p.
|
artikel
|
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