| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Accommodating Linkage Disequilibrium in Genetic-Association Analyses via Ridge Regression
|
Malo, Nathalie
|
|
2008
|
82 |
2 |
p. 375-385
11 p.
|
artikel
|
| 2 |
Acetylcholine Receptor Pathway Mutations Explain Various Fetal Akinesia Deformation Sequence Disorders
|
Michalk, Anne
|
|
2008
|
82 |
2 |
p. 464-476
13 p.
|
artikel
|
| 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.
|
artikel
|
| 4 |
A Powerful and Flexible Multilocus Association Test for Quantitative Traits
|
Kwee, Lydia Coulter
|
|
2008
|
82 |
2 |
p. 386-397
12 p.
|
artikel
|
| 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.
|
artikel
|
| 6 |
A Unified Association Analysis Approach for Family and Unrelated Samples Correcting for Stratification
|
Zhu, Xiaofeng
|
|
2008
|
82 |
2 |
p. 352-365
14 p.
|
artikel
|
| 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.
|
artikel
|
| 8 |
Comment on a Simple and Improved Correction for Population Stratification
|
Lee, Seunggeun
|
|
2008
|
82 |
2 |
p. 524-526
3 p.
|
artikel
|
| 9 |
Course and Employment Opportunities
|
|
|
2008
|
82 |
2 |
p. 533-534
2 p.
|
artikel
|
| 10 |
Estimating Local Ancestry in Admixed Populations
|
Sankararaman, Sriram
|
|
2008
|
82 |
2 |
p. 290-303
14 p.
|
artikel
|
| 11 |
FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta
|
Kim, Jung-Wook
|
|
2008
|
82 |
2 |
p. 489-494
6 p.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 16 |
Neocentromeres: New Insights into Centromere Structure, Disease Development, and Karyotype Evolution
|
Marshall, Owen J.
|
|
2008
|
82 |
2 |
p. 261-282
22 p.
|
artikel
|
| 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.
|
artikel
|
| 18 |
Renal Aplasia in Humans Is Associated with RET Mutations
|
Skinner, Michael A.
|
|
2008
|
82 |
2 |
p. 344-351
8 p.
|
artikel
|
| 19 |
Response to Ding and Lin
|
Chung, Ren-Hua
|
|
2008
|
82 |
2 |
p. 530-531
2 p.
|
artikel
|
| 20 |
Response to Lee et al.
|
Epstein, Michael P.
|
|
2008
|
82 |
2 |
p. 526-528
3 p.
|
artikel
|
| 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.
|
artikel
|
| 22 |
Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration
|
Tsaousidou, Maria K.
|
|
2008
|
82 |
2 |
p. 510-515
6 p.
|
artikel
|
| 23 |
Simple and Efficient Analysis of Disease Association with Missing Genotype Data
|
Lin, D.Y.
|
|
2008
|
82 |
2 |
p. 444-452
9 p.
|
artikel
|
| 24 |
Structural Variation of Chromosomes in Autism Spectrum Disorder
|
Marshall, Christian R.
|
|
2008
|
82 |
2 |
p. 477-488
12 p.
|
artikel
|
| 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.
|
artikel
|
| 26 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2008
|
82 |
2 |
p. 259-260
2 p.
|
artikel
|
| 27 |
This Month in the Journal
|
Williamson, Robin E.
|
|
2008
|
82 |
2 |
p. 257-258
2 p.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 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.
|
artikel
|
| 32 |
XMCPDT Does Have Correct Type I Error Rates
|
Ding, Jie
|
|
2008
|
82 |
2 |
p. 528-530
3 p.
|
artikel
|
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