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Nature Genetics|December 23, 2018
The copy number variation landscape of congenital anomalies of the kidney and urinary tractMiguel Verbitsky, Rik Westland, Alejandra Perez, et al.Nature Genetics|March 1, 2019
Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tractMiguel Verbitsky, Rik Westland, Alejandra Perez, et al.American Journal of Human Genetics|September 6, 2020
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract MalformationsDervla M Connaughton, Rufeng Dai, Danielle J Owen, et al.Nature Communications|August 7, 2025
Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.Nature|June 6, 2020
Identification of type 2 diabetes loci in 433,540 East Asian individualsCassandra N Spracklen, Momoko Horikoshi, Young Jin Kim, et al.British Journal of Cancer|February 20, 2014
FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association ConsortiumD Agarwal, S Pineda, K Michailidou, et al.The Lancet. Diabetes & Endocrinology|May 1, 2023
Effect of the COVID-19 pandemic on surgery for indeterminate thyroid nodules (THYCOVID): a retrospective, international, multicentre, cross-sectional studyFabio Medas, Chiara Dobrinja, Ebtesam Abdullah Al-Suhaimi, et al.Nature Genetics|May 13, 2022
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translationAnubha Mahajan, Cassandra N Spracklen, Weihua Zhang, et al.Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complicationsKen Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, et al.Nature|February 19, 2024
Genetic drivers of heterogeneity in type 2 diabetes pathophysiologyKen Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, et al.Pageof 125