Publicacións en colaboración con investigadores/as de Duke NUS Graduate Medical School (13)

2020

  1. Complement genes contribute sex-biased vulnerability in diverse disorders

    Nature, Vol. 582, Núm. 7813, pp. 577-581

2019

  1. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

    Nature Genetics, Vol. 51, Núm. 4, pp. 659-674

  2. Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (Nature Genetics, (2019), 51, 4, (659-674), 10.1038/s41588-019-0364-4)

    Nature Genetics

2018

  1. Age at first birth in women is genetically associated with increased risk of schizophrenia

    Scientific Reports, Vol. 8, Núm. 1

2017

  1. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

    Nature Communications, Vol. 8

2016

  1. A century of trends in adult human height

    eLife, Vol. 5

  2. Trends in adult body-mass index in 200 countries from 1975 to 2014: A pooled analysis of 1698 population-based measurement studies with 19.2 million participants

    The Lancet, Vol. 387, Núm. 10026, pp. 1377-1396

  3. Worldwide trends in diabetes since 1980: A pooled analysis of 751 population-based studies with 4.4 million participants

    The Lancet, Vol. 387, Núm. 10027

  4. Worldwide trends in diabetes since 1980: A pooled analysis of 751 population-based studies with 4.4 million participants

    The Lancet, Vol. 387, Núm. 10027, pp. 1513-1530

2015

  1. Effects of diabetes definition on global surveillance of diabetes prevalence and diagnosis: A pooled analysis of 96 population-based studies with 331 288 participants

    The Lancet Diabetes and Endocrinology, Vol. 3, Núm. 8, pp. 624-637

  2. LD score regression distinguishes confounding from polygenicity in genome-wide association studies

    Nature Genetics, Vol. 47, Núm. 3, pp. 291-295

2014

  1. Biological insights from 108 schizophrenia-associated genetic loci

    Nature, Vol. 511, Núm. 7510, pp. 421-427

  2. Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33

    Human Molecular Genetics, Vol. 23, Núm. 24, pp. 6616-6633