A. Morris

发表

Assessing Rare Variation in Complex Traits

Eleftheria Zeggini, E. Zeggini, Andrew Morris, 2015, Springer: New York.

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Kyle J. Gaulton, Yoonjung Yoonie Joo, Cassandra N. Spracklen, 2020, Nature Genetics.

A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries

Aaron F. McDaid, Yan V. Sun, Cassandra N. Spracklen, 2022 .

Rare Variant Association Testing for Next-Generation Sequencing Data via Hierarchical Clustering

E. Zeggini, I. Tachmazidou, Andrew Morris, 2013, Human Heredity.

Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations

R. Mägi, C. Wijmenga, Z. Kutalik, 2022, bioRxiv.

Genetic variation at RAB3GAP2 and its role in exercise-related adaptation and recovery

C. Lindgren, K. Eriksson, L. Groop, 2021 .

Underlying genetic models of inheritance in established type 2 diabetes associations.

M. McCarthy, E. Zeggini, F. Hu, 2009, American journal of epidemiology.

A saturated map of common genetic variants associated with human height

Aaron F. McDaid, M. P. Concas, Cassandra N. Spracklen, 2022, Nature.

Regulatory variants at KLF14 influence type 2 diabetes risk via a female- 1 specific effect on adipocyte size and body composition 2

J. Bell, U. Thorsteinsdóttir, M. Laakso, 2018 .

Underlying genetic models of inheritance in established type 2 diabetes associations.

E. Zeggini, D. Altshuler, N. Grarup, 2009, American Journal of Epidemiology.