Alan N. Wilton

UNSW Sydney

Papers

1

Total Citations

176

H-Index

1

About

Alan N. Wilton is a geneticist whose work has significantly advanced the understanding of the genetic underpinnings of pre-eclampsia, a dangerous pregnancy complication. His research centers on the genetic epidemiology of complex disorders, with a particular focus on maternal susceptibility loci. Wilton’s landmark contribution came from a genome-wide scan of families from Australia and New Zealand, which confirmed the presence of a maternal susceptibility locus for pre-eclampsia on chromosome 2. This 2000 study, which has garnered 176 citations, was pivotal in shifting the field toward identifying specific genetic risk factors for the condition. By demonstrating that pre-eclampsia has a heritable component linked to a defined chromosomal region, Wilton’s work laid the foundation for subsequent candidate gene studies and has influenced how researchers approach the genetics of pregnancy-related disorders. His findings remain a cornerstone for those investigating the molecular mechanisms of pre-eclampsia, highlighting his lasting impact on reproductive genetics.

Research Focus

Key Achievements

1
H-Index
1
Papers
176
Total Citations
176
Avg Citations/Paper
🏆 Most Cited Paper
A Genome Scan in Families from Australia and New Zealand Confirms the Presence of a Maternal Susceptibility Locus for Pre-Eclampsia, on Chromosome 2
176 citations · 2000
📈 Most Prolific Year: 2000 (1 Papers)
🤝 Key Collaborators: 10
🏛 Institutions: UNSW Sydney

Top Papers

  1. 1

Key Collaborators

Contact & Links

Available for collaboration
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