nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Functional Polymorphism in COL11A1, Which Encodes the α1 Chain of Type XI Collagen, Is Associated with Susceptibility to Lumbar Disc Herniation
|
Mio, Futoshi |
|
2007 |
81 |
6 |
p. 1271-1277 7 p. |
artikel |
2 |
A Genomewide Association Study of Skin Pigmentation in a South Asian Population
|
Stokowski, Renee P. |
|
2007 |
81 |
6 |
p. 1119-1132 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.
|
|
|
2007 |
81 |
6 |
p. 1321-1323 3 p. |
artikel |
4 |
Common Single-Nucleotide Polymorphisms Act in Concert to Affect Plasma Levels of High-Density Lipoprotein Cholesterol
|
Spirin, Victor |
|
2007 |
81 |
6 |
p. 1298-1303 6 p. |
artikel |
5 |
Contribution of SHANK3 Mutations to Autism Spectrum Disorder
|
Moessner, Rainald |
|
2007 |
81 |
6 |
p. 1289-1297 9 p. |
artikel |
6 |
Deletions at the SOX10 Gene Locus Cause Waardenburg Syndrome Types 2 and 4
|
Bondurand, Nadege |
|
2007 |
81 |
6 |
p. 1169-1185 17 p. |
artikel |
7 |
DNA Methylation Signatures within the Human Brain
|
Ladd-Acosta, Christine |
|
2007 |
81 |
6 |
p. 1304-1315 12 p. |
artikel |
8 |
Editorial Reviewers for 2007
|
|
|
2007 |
81 |
6 |
p. 1316-1320 5 p. |
artikel |
9 |
Genetic Basis for Correction of Very-Long-Chain Acyl–Coenzyme A Dehydrogenase Deficiency by Bezafibrate in Patient Fibroblasts: Toward a Genotype-Based Therapy
|
Gobin-Limballe, S. |
|
2007 |
81 |
6 |
p. 1133-1143 11 p. |
artikel |
10 |
High-Throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language Disorders
|
Vernes, Sonja C. |
|
2007 |
81 |
6 |
p. 1232-1250 19 p. |
artikel |
11 |
Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain
|
Spiteri, Elizabeth |
|
2007 |
81 |
6 |
p. 1144-1157 14 p. |
artikel |
12 |
Multifactor Dimensionality Reduction–Phenomics: A Novel Method to Capture Genetic Heterogeneity with Use of Phenotypic Variables
|
Mei, H. |
|
2007 |
81 |
6 |
p. 1251-1261 11 p. |
artikel |
13 |
Novel Association in Chromosome 4q27 Region with Rheumatoid Arthritis and Confirmation of Type 1 Diabetes Point to a General Risk Locus for Autoimmune Diseases
|
Zhernakova, Alexandra |
|
2007 |
81 |
6 |
p. 1284-1288 5 p. |
artikel |
14 |
Pathway-Based Approaches for Analysis of Genomewide Association Studies
|
Wang, Kai |
|
2007 |
81 |
6 |
p. 1278-1283 6 p. |
artikel |
15 |
Propionic and Methylmalonic Acidemia: Antisense Therapeutics for Intronic Variations Causing Aberrantly Spliced Messenger RNA
|
Rincón, A. |
|
2007 |
81 |
6 |
p. 1262-1270 9 p. |
artikel |
16 |
RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies
|
Antoniou, Antonis C. |
|
2007 |
81 |
6 |
p. 1186-1200 15 p. |
artikel |
17 |
So Many Correlated Tests, So Little Time! Rapid Adjustment of P Values for Multiple Correlated Tests
|
Conneely, Karen N. |
|
2007 |
81 |
6 |
p. 1158-1168 11 p. |
artikel |
18 |
The Structure of Common Genetic Variation in United States Populations
|
Guthery, Stephen L. |
|
2007 |
81 |
6 |
p. 1221-1231 11 p. |
artikel |
19 |
This Month in the Journal
|
Williamson, Robin E. |
|
2007 |
81 |
6 |
p. i-ii nvt p. |
artikel |
20 |
Type 2 NF1 Deletions Are Highly Unusual by Virtue of the Absence of Nonallelic Homologous Recombination Hotspots and an Apparent Preference for Female Mitotic Recombination
|
Steinmann, Katharina |
|
2007 |
81 |
6 |
p. 1201-1220 20 p. |
artikel |