| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A Combinatorial Approach to Detecting Gene-Gene and Gene-Environment Interactions in Family Studies
|
Lou, Xiang-Yang
|
|
2008
|
83 |
4 |
p. 457-467
11 p.
|
article
|
| 2 |
A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene
|
Salo, Antti M.
|
|
2008
|
83 |
4 |
p. 495-503
9 p.
|
article
|
| 3 |
Civilian and Military Genetics: Nondiscrimination Policy in a Post-GINA World
|
Baruch, Susannah
|
|
2008
|
83 |
4 |
p. 435-444
10 p.
|
article
|
| 4 |
Comparing Algorithms for Genotype Imputation
|
Marchini, Jonathan
|
|
2008
|
83 |
4 |
p. 535-539
5 p.
|
article
|
| 5 |
HLA-DRB1∗0401 and HLA-DRB1∗0408 Are Strongly Associated with the Development of Antibodies against Interferon-β Therapy in Multiple Sclerosis
|
Hoffmann, Steve
|
|
2008
|
83 |
4 |
p. 541-
1 p.
|
article
|
| 6 |
Japanese Population Structure, Based on SNP Genotypes from 7003 Individuals Compared to Other Ethnic Groups: Effects on Population-Based Association Studies
|
Yamaguchi-Kabata, Yumi
|
|
2008
|
83 |
4 |
p. 445-456
12 p.
|
article
|
| 7 |
Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease
|
Sugiana, Canny
|
|
2008
|
83 |
4 |
p. 468-478
11 p.
|
article
|
| 8 |
Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
|
Kim, Hyung-Goo
|
|
2008
|
83 |
4 |
p. 511-519
9 p.
|
article
|
| 9 |
Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood
|
Zeharia, Avraham
|
|
2008
|
83 |
4 |
p. 489-494
6 p.
|
article
|
| 10 |
[No title]
|
|
|
2008
|
83 |
4 |
p. 542-
1 p.
|
article
|
| 11 |
Population-Based Genome-wide Association Studies Reveal Six Loci Influencing Plasma Levels of Liver Enzymes
|
Yuan, Xin
|
|
2008
|
83 |
4 |
p. 520-528
9 p.
|
article
|
| 12 |
Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients
|
Vrijenhoek, Terry
|
|
2008
|
83 |
4 |
p. 504-510
7 p.
|
article
|
| 13 |
Reply to Marchini and Howie
|
Lin, D.Y.
|
|
2008
|
83 |
4 |
p. 539-540
2 p.
|
article
|
| 14 |
Targeting Dyrk1A with AAVshRNA Attenuates Motor Alterations in TgDyrk1A, a Mouse Model of Down Syndrome
|
Ortiz-Abalia, Jon
|
|
2008
|
83 |
4 |
p. 479-488
10 p.
|
article
|
| 15 |
The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3
|
Molho-Pessach, Vered
|
|
2008
|
83 |
4 |
p. 529-534
6 p.
|
article
|
| 16 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2008
|
83 |
4 |
p. 433-434
2 p.
|
article
|
| 17 |
This Month in The Journal
|
Williamson, Robin E.
|
|
2008
|
83 |
4 |
p. 431-432
2 p.
|
article
|
Journal description