| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Allowing for population stratification in case-only studies of gene–environment interaction, using genomic control
|
Yadav, Pankaj
|
|
2015
|
134 |
10 |
p. 1117-1125
|
artikel
|
| 2 |
Common polygenic variation contributes to risk of migraine in the Norfolk Island population
|
Rodriguez-Acevedo, A. J.
|
|
2015
|
134 |
10 |
p. 1079-1087
|
artikel
|
| 3 |
Investigation of genes important in neurodevelopment disorders in adult human brain
|
Maussion, Gilles
|
|
2015
|
134 |
10 |
p. 1037-1053
|
artikel
|
| 4 |
Mutations in human IFT140 cause non-syndromic retinal degeneration
|
Xu, Mingchu
|
|
2015
|
134 |
10 |
p. 1069-1078
|
artikel
|
| 5 |
Sequencing of candidate genes in Dominican families implicates both rare exonic and common non-exonic variants for carotid intima-media thickness at bifurcation
|
Wang, Liyong
|
|
2015
|
134 |
10 |
p. 1127-1138
|
artikel
|
| 6 |
‘Splitting versus lumping’: Temple–Baraitser and Zimmermann–Laband Syndromes
|
Bramswig, Nuria C.
|
|
2015
|
134 |
10 |
p. 1089-1097
|
artikel
|
| 7 |
T (brachyury) is linked to a Mendelian form of neural tube defects in humans
|
Shaheen, Ranad
|
|
2015
|
134 |
10 |
p. 1139-1141
|
artikel
|
| 8 |
The nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulation
|
Carmona-Mora, Paulina
|
|
2015
|
134 |
10 |
p. 1099-1115
|
artikel
|
| 9 |
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes
|
Chapman, Nicola H.
|
|
2015
|
134 |
10 |
p. 1055-1068
|
artikel
|
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