Suchergebnisse - "Hawkes, Gareth"

PubPharm (29)

1

Clustering of predicted loss-of-function variants in genes linked with monogenic disease can explain incomplete penetrance

enthalten in: Genome medicine | 2024

von Beaumont, R. | Hawkes, G. | Gunning, A. | +1

2

Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling

enthalten in: bioRxiv.org | 2024

von Kentistou, K. | Lim, B. | Kaisinger, L. | +19

3

Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling

enthalten in: medRxiv : the preprint server for health sciences | 2024

von Kentistou, K. | Lim, B. | Kaisinger, L. | +19

4

Penetrance and expressivity of mitochondrial variants in a large clinically unselected population

enthalten in: Human molecular genetics | 2024

von Cannon, S. | Hall, T. | Hawkes, G. | +7

5

A Federated Database for Obesity Research : An IMI-SOPHIA Study

enthalten in: Life (Basel, Switzerland) | 2024

von Delfin, C. | Dragan, I. | Kuznetsov, D. | +45

6

Whole genome association testing in 333,100 individuals across three biobanks identifies rare non-coding single variant and genomic aggregate associations with height

enthalten in: bioRxiv.org | 2023

von Hawkes, G. | Beaumont, R. | Li, Z. | +52

7

Whole genome sequencing analysis identifies rare, large-effect non-coding variants and regions associated with circulating protein levels

enthalten in: bioRxiv.org | 2023

von Hawkes, G. | Chundru, K. | Jackson, L. | +7

8

The Role of ONECUT1 Variants in Monogenic and Type 2 Diabetes Mellitus

enthalten in: Diabetes | 2023

von Russ-Silsby, J. | Patel, K. | Laver, T. | +8

9

Effects of childhood and adult height on later life cardiovascular disease risk estimated through Mendelian randomization

enthalten in: bioRxiv.org | 2023

von Richardson, T. | Urquijo, H. | Howe, L. | +3

10

Clustering of predicted loss-of-function variants in genes linked with monogenic disease can explain incomplete penetrance

enthalten in: bioRxiv.org | 2023

von Beaumont, R. | Hawkes, G. | Gunning, A. | +1