| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Integrative genomic analysis predicts novel functional enhancer-SNPs for bone mineral density
|
Qiu, Chuan
|
|
2019
|
138 |
2 |
p. 167-185
|
artikel
|
| 2 |
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
|
He, Karen Y.
|
|
2019
|
138 |
2 |
p. 199-210
|
artikel
|
| 3 |
LncRNA ZBTB40-IT1 modulated by osteoporosis GWAS risk SNPs suppresses osteogenesis
|
Mei, Bing
|
|
2019
|
138 |
2 |
p. 151-166
|
artikel
|
| 4 |
Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy
|
Fichera, Marco
|
|
2019
|
138 |
2 |
p. 187-198
|
artikel
|
| 5 |
New insights into the genetics of spermatogenic failure: a review of the literature
|
Cannarella, Rossella
|
|
2019
|
138 |
2 |
p. 125-140
|
artikel
|
| 6 |
Translating cancer genomics into precision medicine with artificial intelligence: applications, challenges and future perspectives
|
Xu, Jia
|
|
2019
|
138 |
2 |
p. 109-124
|
artikel
|
| 7 |
Whole-genome sequencing identifies complex contributions to genetic risk by variants in genes causing monogenic systemic lupus erythematosus
|
Almlöf, Jonas Carlsson
|
|
2019
|
138 |
2 |
p. 141-150
|
artikel
|
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