| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Estimating carrier frequencies of newborn screening disorders using a whole-genome reference panel of 3552 Japanese individuals
|
Yamaguchi-Kabata, Yumi
|
|
2019
|
138 |
4 |
p. 389-409
|
artikel
|
| 2 |
Genetic kinship and admixture in Iron Age Scytho-Siberians
|
Mary, Laura
|
|
2019
|
138 |
4 |
p. 411-423
|
artikel
|
| 3 |
Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer
|
Bien, Stephanie A.
|
|
2019
|
138 |
4 |
p. 307-326
|
artikel
|
| 4 |
Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33
|
Musolf, Anthony M.
|
|
2019
|
138 |
4 |
p. 339-354
|
artikel
|
| 5 |
How to increase our belief in discovered statistical interactions via large-scale association studies?
|
Van Steen, K.
|
|
2019
|
138 |
4 |
p. 293-305
|
artikel
|
| 6 |
Molybdenum cofactor deficiency type B knock-in mouse models carrying patient-identical mutations and their rescue by singular AAV injections
|
Reiss, Jochen
|
|
2019
|
138 |
4 |
p. 355-361
|
artikel
|
| 7 |
Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation
|
Zhou, Zhou
|
|
2019
|
138 |
4 |
p. 327-337
|
artikel
|
| 8 |
On the relationship between the heritability and the attributable fraction
|
Dahlqwist, Elisabeth
|
|
2019
|
138 |
4 |
p. 425-435
|
artikel
|
| 9 |
Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders
|
Beaumont, Marie
|
|
2019
|
138 |
4 |
p. 363-374
|
artikel
|
| 10 |
The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus
|
Schlicht, Kristina
|
|
2019
|
138 |
4 |
p. 375-388
|
artikel
|
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