| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
AFA: Ancestry-specific allele frequency estimation in admixed populations: The Hispanic Community Health Study/Study of Latinos
|
Granot-Hershkovitz, Einat
|
|
|
3 |
2 |
p.
|
artikel
|
| 2 |
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium
|
Fernández-Rhodes, Lindsay
|
|
|
3 |
2 |
p.
|
artikel
|
| 3 |
A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors
|
Thibord, Florian
|
|
|
3 |
2 |
p.
|
artikel
|
| 4 |
Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease
|
Thompson, Kyle
|
|
|
3 |
2 |
p.
|
artikel
|
| 5 |
Clinical validation of genomic functional screen data: Analysis of observed BRCA1 variants in an unselected population cohort
|
Schiabor Barrett, Kelly M.
|
|
|
3 |
2 |
p.
|
artikel
|
| 6 |
CRISPR/Cas9-induced gene conversion between ATAD3 paralogs
|
Yanovsky-Dagan, Shira
|
|
|
3 |
2 |
p.
|
artikel
|
| 7 |
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B
|
Gehlen, Jan
|
|
|
3 |
2 |
p.
|
artikel
|
| 8 |
From pharmacogenetics to pharmaco-omics: Milestones and future directions
|
Auwerx, Chiara
|
|
|
3 |
2 |
p.
|
artikel
|
| 9 |
Hereditary alpha-tryptasemia modifies clinical phenotypes among individuals with congenital hypermobility disorders
|
Vazquez, Maribel
|
|
|
3 |
2 |
p.
|
artikel
|
| 10 |
HLA-A∗03:01 is associated with increased risk of fever, chills, and stronger side effects from Pfizer-BioNTech COVID-19 vaccination
|
Bolze, Alexandre
|
|
|
3 |
2 |
p.
|
artikel
|
| 11 |
Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients
|
Sun, Quan
|
|
|
3 |
2 |
p.
|
artikel
|
| 12 |
Maternal effect genes as risk factors for congenital heart defects
|
Musfee, Fadi I.
|
|
|
3 |
2 |
p.
|
artikel
|
| 13 |
Prediction of breast cancer risk based on flow variant analysis of circulating peripheral blood mononuclear cells
|
Loke, Johnny
|
|
|
3 |
2 |
p.
|
artikel
|
| 14 |
Rare coding variants in DNA damage repair genes associated with timing of natural menopause
|
Ward, Lucas D.
|
|
|
3 |
2 |
p.
|
artikel
|
| 15 |
Somatic activating BRAF variants cause isolated lymphatic malformations
|
Zenner, Kaitlyn
|
|
|
3 |
2 |
p.
|
artikel
|
| 16 |
Stability of polygenic scores across discovery genome-wide association studies
|
Schultz, Laura M.
|
|
|
3 |
2 |
p.
|
artikel
|
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