| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A cis-eQTL genetic variant of the cancer–testis gene CCDC116 is associated with risk of multiple cancers
|
Qin, Na
|
|
2017
|
136 |
8 |
p. 987-997
|
artikel
|
| 2 |
A genetic risk score is differentially associated with migraine with and without aura
|
Pisanu, Claudia
|
|
2017
|
136 |
8 |
p. 999-1008
|
artikel
|
| 3 |
Analysis of case-parent trios for imprinting effect using a loglinear model with adjustment for sex-of-parent-specific transmission ratio distortion
|
Huang, Lam Opal
|
|
2017
|
136 |
8 |
p. 951-961
|
artikel
|
| 4 |
Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma
|
Kabra, Meha
|
|
2017
|
136 |
8 |
p. 941-949
|
artikel
|
| 5 |
Dosage effects of ZP2 and ZP3 heterozygous mutations cause human infertility
|
Liu, Wenqiang
|
|
2017
|
136 |
8 |
p. 975-985
|
artikel
|
| 6 |
Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features
|
Zhang, Jing
|
|
2017
|
136 |
8 |
p. 1009-1011
|
artikel
|
| 7 |
Regulatory element-based prediction identifies new susceptibility regulatory variants for osteoporosis
|
Yao, Shi
|
|
2017
|
136 |
8 |
p. 963-974
|
artikel
|
| 8 |
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes
|
Monies, Dorota
|
|
2017
|
136 |
8 |
p. 921-939
|
artikel
|
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