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Showing 1–9 of 9 results

Advanced filters: Author: M. Reza Jabalameli Clear advanced filters

Author Correction: Rare genetic coding variants associated with human longevity and protection against age-related diseases

Jhih-Rong Lin
Patrick Sin-Chan
Zhengdong D. Zhang
Amendments and Corrections28 Aug 2024
Nature Aging

Volume: 4, P: 1328
Rare genetic coding variants associated with human longevity and protection against age-related diseases

In this whole-exome sequencing study of the largest centenarian cohort to date, Lin et al. demonstrate that conserved pathways—for example, IIS and AMPK signaling—are as relevant to human longevity and healthy aging as they are in worms, flies and mice.

Jhih-Rong Lin
Patrick Sin-Chan
Zhengdong D. Zhang
Research13 Sept 2021
Nature Aging

Volume: 1, P: 783-794
Linkage disequilibrium maps for European and African populations constructed from whole genome sequence data

Alejandra Vergara-Lope
M. Reza Jabalameli
Reuben J. Pengelly
ResearchOpen Access17 Oct 2019
Scientific Data

Volume: 6, P: 1-4
Unravelling genetic components of longevity

Many aging-related traits share a common genetic component. How to disentangle it from trait-specific effects has remained largely unexplored. A new study in Nature Aging uses an analysis framework for isolating the shared genetic component in GWAS of aging-related traits, and identifies genomic loci that contribute to longevity.

M. Reza Jabalameli
Zhengdong D. Zhang
News & Views20 Jan 2022
Nature Aging

Volume: 2, P: 5-6
Genome-wide association study of delay discounting identifies 11 loci and reveals transdiagnostic associations across mental and physical health

Hayley H. A. Thorpe
Renata B. Cupertino
Sandra Sanchez-Roige
ResearchOpen Access25 Nov 2025
Molecular Psychiatry

Volume: 31, P: 2081-2093
Polygenic prediction of human longevity on the supposition of pervasive pleiotropy

M. Reza Jabalameli
Jhih-Rong Lin
Zhengdong D. Zhang
ResearchOpen Access28 Aug 2024
Scientific Reports

Volume: 14, P: 1-19
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

Jhih-Rong Lin
Yingjie Zhao
Zhengdong D. Zhang
Research03 Mar 2023
Molecular Psychiatry

Volume: 28, P: 2071-2080
Gene-dense autosomal chromosomes show evidence for increased selection

M. Reza Jabalameli
Clare Horscroft
Andrew Collins
Research01 Oct 2019
Heredity

Volume: 123, P: 774-783
Deep post-GWAS analysis identifies potential risk genes and risk variants for Alzheimer’s disease, providing new insights into its disease mechanisms

Zhen Wang
Quanwei Zhang
Zhengdong D. Zhang
ResearchOpen Access15 Oct 2021
Scientific Reports

Volume: 11, P: 1-14