Augustine Kong


Ontology type: schema:Person     


Person Info

NAME

Augustine

SURNAME

Kong

Publications in SciGraph latest 50 shown

  • 2018-11-05 Multiple transmissions of de novo mutations in families in NATURE GENETICS
  • 2018-11 Author Correction: The rate of meiotic gene conversion varies by sex and age in NATURE GENETICS
  • 2018-09 Relatedness disequilibrium regression estimates heritability without environmental bias in NATURE GENETICS
  • 2018-02 Reconstructing an African haploid genome from the 18th century in NATURE GENETICS
  • 2017-09-21 Whole genome characterization of sequence diversity of 15,220 Icelanders in SCIENTIFIC DATA
  • 2017-09 Parental influence on human germline de novo mutations in 1,548 trios from Iceland in NATURE
  • 2017-08 Truncating mutations in RBM12 are associated with psychosis in NATURE GENETICS
  • 2017-06-13 Reproductive fitness and genetic risk of psychiatric disorders in the general population in NATURE COMMUNICATIONS
  • 2017-05 Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis in NATURE GENETICS
  • 2017-02-22 Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation in NATURE COMMUNICATIONS
  • 2016-12 A sequence variant associating with educational attainment also affects childhood cognition in SCIENTIFIC REPORTS
  • 2016-12 Genome-wide analysis identifies 12 loci influencing human reproductive behavior in NATURE GENETICS
  • 2016-11-16 Epigenetic and genetic components of height regulation in NATURE COMMUNICATIONS
  • 2016-11 The rate of meiotic gene conversion varies by sex and age in NATURE GENETICS
  • 2016-06 Physical and neurobehavioral determinants of reproductive onset and success in NATURE GENETICS
  • 2016-03 Weighting sequence variants based on their annotation increases power of whole-genome association studies in NATURE GENETICS
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function in NATURE COMMUNICATIONS
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-05 Large-scale whole-genome sequencing of the Icelandic population in NATURE GENETICS
  • 2015-05 Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease in NATURE GENETICS
  • 2015-05 Identification of a large set of rare complete human knockouts in NATURE GENETICS
  • 2015-05 The Y-chromosome point mutation rate in humans in NATURE GENETICS
  • 2015-03-25 Sequence variants from whole genome sequencing a large group of Icelanders in SCIENTIFIC DATA
  • 2014-06 The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms in LEUKEMIA
  • 2014-05 Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31 in NATURE GENETICS
  • 2014-04 Loss-of-function mutations in SLC30A8 protect against type 2 diabetes in NATURE GENETICS
  • 2014-03 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility in NATURE GENETICS
  • 2014-03 Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes in NATURE GENETICS
  • 2014-01 Common and low-frequency variants associated with genome-wide recombination rate in NATURE GENETICS
  • 2014-01 Common variant at 16p11.2 conferring risk of psychosis in MOLECULAR PSYCHIATRY
  • 2013-12 A common variant at 8q24.21 is associated with renal cell cancer in NATURE COMMUNICATIONS
  • 2013-11 A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration in NATURE GENETICS
  • 2012-12 A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer in NATURE GENETICS
  • 2012-10 Mapping cis- and trans-regulatory effects across multiple tissues in twins in NATURE GENETICS
  • 2012-10 A direct characterization of human mutation based on microsatellites in NATURE GENETICS
  • 2012-09 Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways in NATURE GENETICS
  • 2012-09 Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes in NATURE GENETICS
  • 2012-08 Rate of de novo mutations and the importance of father’s age to disease risk in NATURE
  • 2012-08 A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline in NATURE
  • 2012-03 Discovery of common variants associated with low TSH levels and thyroid cancer risk in NATURE GENETICS
  • 2011-11 Mutations in BRIP1 confer high risk of ovarian cancer in NATURE GENETICS
  • 2011-11 Identification of low-frequency variants associated with gout and serum uric acid levels in NATURE GENETICS
  • 2011-11 A germline variant in the TP53 polyadenylation signal confers cancer susceptibility in NATURE GENETICS
  • 2011-10 Corrigendum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes in NATURE GENETICS
  • 2011-06 Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes in NATURE GENETICS
  • 2011-03-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease in NATURE GENETICS
  • 2011-03-06 A rare variant in MYH6 is associated with high risk of sick sinus syndrome in NATURE GENETICS
  • 2011-01 Expanding the range of ZNF804A variants conferring risk of psychosis in MOLECULAR PSYCHIATRY
  • 2010-10-28 Fine-scale recombination rate differences between sexes, populations and individuals in NATURE
  • 2010-10 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in NATURE GENETICS
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