| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos
|
Feofanova, Elena V.
|
|
|
107 |
5 |
p. 849-863
|
artikel
|
| 2 |
Analogies in Genomics Policymaking: Debates and Drawbacks
|
Lynch, John A.
|
|
|
107 |
5 |
p. 797-801
|
artikel
|
| 3 |
Analysis of Trans-Ancestral SLE Risk Loci Identifies Unique Biologic Networks and Drug Targets in African and European Ancestries
|
Owen, Katherine A.
|
|
|
107 |
5 |
p. 864-881
|
artikel
|
| 4 |
An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm
|
Dimmock, David P.
|
|
|
107 |
5 |
p. 942-952
|
artikel
|
| 5 |
Apigenin as a Candidate Prenatal Treatment for Trisomy 21: Effects in Human Amniocytes and the Ts1Cje Mouse Model
|
Guedj, Faycal
|
|
|
107 |
5 |
p. 911-931
|
artikel
|
| 6 |
A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants
|
Cakici, Julie A.
|
|
|
107 |
5 |
p. 953-962
|
artikel
|
| 7 |
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk
|
Kramer, Iris
|
|
|
107 |
5 |
p. 837-848
|
artikel
|
| 8 |
Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks
|
Fritsche, Lars G.
|
|
|
107 |
5 |
p. 815-836
|
artikel
|
| 9 |
Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome
|
Palencia-Campos, Adrian
|
|
|
107 |
5 |
p. 977-988
|
artikel
|
| 10 |
Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2
|
van Dijk, Fleur S.
|
|
|
107 |
5 |
p. 989-999
|
artikel
|
| 11 |
NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism
|
Guo, Hui
|
|
|
107 |
5 |
p. 963-976
|
artikel
|
| 12 |
Not All Autism Genes Are Created Equal: A Response to Myers et al.
|
Buxbaum, Joseph D.
|
|
|
107 |
5 |
p. 1000-1003
|
artikel
|
| 13 |
Plasma DNA Profile Associated with DNASE1L3 Gene Mutations: Clinical Observations, Relationships to Nuclease Substrate Preference, and In Vivo Correction
|
Chan, Rebecca W.Y.
|
|
|
107 |
5 |
p. 882-894
|
artikel
|
| 14 |
Probabilistic Estimation of Identity by Descent Segment Endpoints and Detection of Recent Selection
|
Browning, Sharon R.
|
|
|
107 |
5 |
p. 895-910
|
artikel
|
| 15 |
Response to Buxbaum et al.
|
Myers, Scott M.
|
|
|
107 |
5 |
p. 1004
|
artikel
|
| 16 |
Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa
|
de Bruijn, Suzanne E.
|
|
|
107 |
5 |
p. 802-814
|
artikel
|
| 17 |
The Practice of Anti-racist Science Requires an Internationalist Perspective
|
Cooper, Richard S.
|
|
|
107 |
5 |
p. 793-796
|
artikel
|
| 18 |
This Month in The Journal
|
Ratzel, Sarah
|
|
|
107 |
5 |
p. 791-792
|
artikel
|
| 19 |
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies
|
Amendola, Laura M.
|
|
|
107 |
5 |
p. 932-941
|
artikel
|
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