| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An Efficient Multiple-Testing Adjustment for eQTL Studies that Accounts for Linkage Disequilibrium between Variants
|
Davis, Joe R.
|
|
2016
|
98 |
1 |
p. 216-224
9 p.
|
artikel
|
| 2 |
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2
|
Davidson, Alice E.
|
|
2016
|
98 |
1 |
p. 75-89
15 p.
|
artikel
|
| 3 |
Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability
|
Stray-Pedersen, Asbjørg
|
|
2016
|
98 |
1 |
p. 202-209
8 p.
|
artikel
|
| 4 |
Correlations between Synaptic Initiation and Meiotic Recombination: A Study of Humans and Mice
|
Gruhn, Jennifer R.
|
|
2016
|
98 |
1 |
p. 102-115
14 p.
|
artikel
|
| 5 |
Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos
|
Conomos, Matthew P.
|
|
2016
|
98 |
1 |
p. 165-184
20 p.
|
artikel
|
| 6 |
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA
|
Turner, Tychele N.
|
|
2016
|
98 |
1 |
p. 58-74
17 p.
|
artikel
|
| 7 |
Genomic Signatures of Selective Pressures and Introgression from Archaic Hominins at Human Innate Immunity Genes
|
Deschamps, Matthieu
|
|
2016
|
98 |
1 |
p. 5-21
17 p.
|
artikel
|
| 8 |
Genotype Imputation with Millions of Reference Samples
|
Browning, Brian L.
|
|
2016
|
98 |
1 |
p. 116-126
11 p.
|
artikel
|
| 9 |
Introgression of Neandertal- and Denisovan-like Haplotypes Contributes to Adaptive Variation in Human Toll-like Receptors
|
Dannemann, Michael
|
|
2016
|
98 |
1 |
p. 22-33
12 p.
|
artikel
|
| 10 |
Invariant TAD Boundaries Constrain Cell-Type-Specific Looping Interactions between Promoters and Distal Elements around the CFTR Locus
|
Smith, Emily M.
|
|
2016
|
98 |
1 |
p. 185-201
17 p.
|
artikel
|
| 11 |
Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities
|
Lo, Kitty K.
|
|
2016
|
98 |
1 |
p. 34-44
11 p.
|
artikel
|
| 12 |
Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV
|
Duyzend, Michael H.
|
|
2016
|
98 |
1 |
p. 45-57
13 p.
|
artikel
|
| 13 |
Model-free Estimation of Recent Genetic Relatedness
|
Conomos, Matthew P.
|
|
2016
|
98 |
1 |
p. 127-148
22 p.
|
artikel
|
| 14 |
Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy
|
Shamseldin, Hanan E.
|
|
2016
|
98 |
1 |
p. 210-215
6 p.
|
artikel
|
| 15 |
Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders
|
Wojtal, Daria
|
|
2016
|
98 |
1 |
p. 90-101
12 p.
|
artikel
|
| 16 |
Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules
|
Kochinke, Korinna
|
|
2016
|
98 |
1 |
p. 149-164
16 p.
|
artikel
|
| 17 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2016
|
98 |
1 |
p. 3-4
2 p.
|
artikel
|
| 18 |
This Month in The Journal
|
Ratzel, Sarah
|
|
2016
|
98 |
1 |
p. 1-2
2 p.
|
artikel
|
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