no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
Accommodating Linkage Disequilibrium in Genetic-Association Analyses via Ridge Regression
|
Malo, Nathalie |
|
2008 |
82 |
2 |
p. 375-385 11 p. |
article |
2 |
Acetylcholine Receptor Pathway Mutations Explain Various Fetal Akinesia Deformation Sequence Disorders
|
Michalk, Anne |
|
2008 |
82 |
2 |
p. 464-476 13 p. |
article |
3 |
Admixture Mapping of White Cell Count: Genetic Locus Responsible for Lower White Blood Cell Count in the Health ABC and Jackson Heart Studies
|
Nalls, Michael A. |
|
2008 |
82 |
2 |
p. 532- 1 p. |
article |
4 |
A Powerful and Flexible Multilocus Association Test for Quantitative Traits
|
Kwee, Lydia Coulter |
|
2008 |
82 |
2 |
p. 386-397 12 p. |
article |
5 |
A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color
|
Sturm, Richard A. |
|
2008 |
82 |
2 |
p. 424-431 8 p. |
article |
6 |
A Unified Association Analysis Approach for Family and Unrelated Samples Correcting for Stratification
|
Zhu, Xiaofeng |
|
2008 |
82 |
2 |
p. 352-365 14 p. |
article |
7 |
Basal Laminar Drusen Caused by Compound Heterozygous Variants in the CFH Gene
|
Boon, Camiel J.F. |
|
2008 |
82 |
2 |
p. 516-523 8 p. |
article |
8 |
Comment on a Simple and Improved Correction for Population Stratification
|
Lee, Seunggeun |
|
2008 |
82 |
2 |
p. 524-526 3 p. |
article |
9 |
Course and Employment Opportunities
|
|
|
2008 |
82 |
2 |
p. 533-534 2 p. |
article |
10 |
Estimating Local Ancestry in Admixed Populations
|
Sankararaman, Sriram |
|
2008 |
82 |
2 |
p. 290-303 14 p. |
article |
11 |
FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta
|
Kim, Jung-Wook |
|
2008 |
82 |
2 |
p. 489-494 6 p. |
article |
12 |
Gross Deletions Involving IGHM, BTK, or Artemis: A Model for Genomic Lesions Mediated by Transposable Elements
|
van Zelm, Menno C. |
|
2008 |
82 |
2 |
p. 320-332 13 p. |
article |
13 |
Identification of Somatic Chromosomal Abnormalities in Hypothalamic Hamartoma Tissue at the GLI3 Locus
|
Craig, David W. |
|
2008 |
82 |
2 |
p. 366-374 9 p. |
article |
14 |
Mechanisms and Consequences of Small Supernumerary Marker Chromosomes: From Barbara McClintock to Modern Genetic-Counseling Issues
|
Baldwin, Erin L. |
|
2008 |
82 |
2 |
p. 398-410 13 p. |
article |
15 |
Mutations in BMP4 Cause Eye, Brain, and Digit Developmental Anomalies: Overlap between the BMP4 and Hedgehog Signaling Pathways
|
Bakrania, Preeti |
|
2008 |
82 |
2 |
p. 304-319 16 p. |
article |
16 |
Neocentromeres: New Insights into Centromere Structure, Disease Development, and Karyotype Evolution
|
Marshall, Owen J. |
|
2008 |
82 |
2 |
p. 261-282 22 p. |
article |
17 |
On the Use of General Control Samples for Genome-wide Association Studies: Genetic Matching Highlights Causal Variants
|
Luca, Diana |
|
2008 |
82 |
2 |
p. 453-463 11 p. |
article |
18 |
Renal Aplasia in Humans Is Associated with RET Mutations
|
Skinner, Michael A. |
|
2008 |
82 |
2 |
p. 344-351 8 p. |
article |
19 |
Response to Ding and Lin
|
Chung, Ren-Hua |
|
2008 |
82 |
2 |
p. 530-531 2 p. |
article |
20 |
Response to Lee et al.
|
Epstein, Michael P. |
|
2008 |
82 |
2 |
p. 526-528 3 p. |
article |
21 |
Selection against Pathogenic mtDNA Mutations in a Stem Cell Population Leads to the Loss of the 3243A→G Mutation in Blood
|
Rajasimha, Harsha Karur |
|
2008 |
82 |
2 |
p. 333-343 11 p. |
article |
22 |
Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration
|
Tsaousidou, Maria K. |
|
2008 |
82 |
2 |
p. 510-515 6 p. |
article |
23 |
Simple and Efficient Analysis of Disease Association with Missing Genotype Data
|
Lin, D.Y. |
|
2008 |
82 |
2 |
p. 444-452 9 p. |
article |
24 |
Structural Variation of Chromosomes in Autism Spectrum Disorder
|
Marshall, Christian R. |
|
2008 |
82 |
2 |
p. 477-488 12 p. |
article |
25 |
Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation
|
Froyen, Guy |
|
2008 |
82 |
2 |
p. 432-443 12 p. |
article |
26 |
This Month in Genetics
|
Garber, Kathryn B. |
|
2008 |
82 |
2 |
p. 259-260 2 p. |
article |
27 |
This Month in the Journal
|
Williamson, Robin E. |
|
2008 |
82 |
2 |
p. 257-258 2 p. |
article |
28 |
Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color Gene
|
Kayser, Manfred |
|
2008 |
82 |
2 |
p. 411-423 13 p. |
article |
29 |
TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita
|
Savage, Sharon A. |
|
2008 |
82 |
2 |
p. 501-509 9 p. |
article |
30 |
Variation in the miRNA-433 Binding Site of FGF20 Confers Risk for Parkinson Disease by Overexpression of α-Synuclein
|
Wang, Gaofeng |
|
2008 |
82 |
2 |
p. 283-289 7 p. |
article |
31 |
Warfarin Pharmacogenetics: CYP2C9 and VKORC1 Genotypes Predict Different Sensitivity and Resistance Frequencies in the Ashkenazi and Sephardi Jewish Populations
|
Scott, Stuart A. |
|
2008 |
82 |
2 |
p. 495-500 6 p. |
article |
32 |
XMCPDT Does Have Correct Type I Error Rates
|
Ding, Jie |
|
2008 |
82 |
2 |
p. 528-530 3 p. |
article |