Publications: Ms Alice Williamson
Smith K, Deutsch AJ, McGrail C, Kim H, Hsu S, Mandla R, Schroeder PH, Westerman KE et al.
(
2023
)
.
Multi-ancestry Polygenic Mechanisms of Type 2 Diabetes Elucidate Disease Processes and Clinical Heterogeneity
.
vol.
4
,
(
10-06
)
Alwan H, Luan J, Williamson A, Steward I, Wareham N, Langenberg C, Pietzner M
(
2023
)
.
Testing for a causal role of thyroid hormone measurements within the normal range: a systematic mendelian randomization study
.
Endocrine Abstracts
Duckett K, Williamson A, Kincaid JWR, Rainbow K, Corbin LJ, Martin HC, Eberhardt RY, Huang QQ et al.
(
2023
)
.
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and Puberty
.
The Journal of Clinical Endocrinology & Metabolism
vol.
108
,
(
12
)
e1580
-
e1587
.
Williamson A, Norris DM, Yin X, Broadaway KA, Moxley AH, Vadlamudi S, Wilson EP, Jackson AU et al.
(
2023
)
.
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
.
Nature Genetics
vol.
55
,
(
6
)
973
-
983
.
Broadaway KA, Yin X, Williamson A, Parsons VA, Wilson EP, Moxley AH, Vadlamudi S, Varshney A et al.
(
2023
)
.
Loci for insulin processing and secretion provide insight into type 2 diabetes risk
.
American Journal of Human Genetics
vol.
110
,
(
2
)
284
-
299
.
Lam BYH, Williamson A, Finer S, Day FR, Tadross JA, Gonçalves Soares A, Wade K, Sweeney P et al.
(
2021
)
.
MC3R links nutritional state to childhood growth and the timing of puberty
.
Nature
vol.
599
,
(
7885
)
436
-
441
.
Wade KH, Lam BYH, Melvin A, Pan W, Corbin LJ, Hughes DA, Rainbow K, Chen J-H et al.
(
2021
)
.
Loss-of-function mutations in the melanocortin 4 receptor in a UK birth cohort
.
Nature Medicine
vol.
27
,
(
6
)
1088
-
1096
.