Evidence map›Paper›PMID 36150388›Full record

ArticleAmerican journal of human genetics2022

KnockoffTrio: A knockoff framework for the identification of putative causal variants in genome-wide association studies with trio design.

Yi Yang, Chen Wang, Linxi Liu, Joseph Buxbaum, Zihuai He, Iuliana Ionita-Laza

Open access · greenAbstract read
In one paragraph

Article in American journal of human genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. The dual role of PCDH9 in tumors, neurological and developmental diseases.Medical oncology (Northwood, London, England) · 2025
    Review
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Yi YangDepartment of Biostatistics, Columbia University, New York, NY 10032, USA; Department of Biostatistics, City University of Hong Kong, Hong Kong SAR, China; School of Data Science, City University of Hong Kong, Hong Kong SAR, China.
Chen WangDepartment of Biostatistics, Columbia University, New York, NY 10032, USA.
Linxi LiuDepartment of Statistics, University of Pittsburgh, Pittsburgh, PA 15260, USA.
Joseph BuxbaumDepartments of Psychiatry, Neuroscience, and Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Zihuai HeQuantitative Sciences Unit, Department of Medicine, Stanford University, Stanford, CA 94305, USA; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA 94305, USA.
Iuliana Ionita-LazaDepartment of Biostatistics, Columbia University, New York, NY 10032, USA. Electronic address: ii2135@columbia.edu.
Columbia University · USIcahn School of Medicine at Mount Sinai · USUniversity of Pittsburgh · US

Funding

Novel Statistical methods for DNA Sequencing Data, and applications to Autism.R01MH095797 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IONITA, IULIANA · 2012 to 2022
$3.1M
Integrative methods for the identification of causal variants in mental disorderR01MH106910 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IONITA, IULIANA, XU, BIN · 2016 to 2018
$1.2M
NIMH NIH HHS R01 MH095797NIMH NIH HHS R01 MH106910
6 · The paper itself

Abstract

Family-based designs can eliminate confounding due to population substructure and can distinguish direct from indirect genetic effects, but these designs are underpowered due to limited sample sizes. Here, we propose KnockoffTrio, a statistical method to identify putative causal genetic variants for father-mother-child trio design built upon a recently developed knockoff framework in statistics. KnockoffTrio controls the false discovery rate (FDR) in the presence of arbitrary correlations among tests and is less conservative and thus more powerful than the conventional methods that control the family-wise error rate via Bonferroni correction. Furthermore, KnockoffTrio is not restricted to family-based association tests and can be used in conjunction with more powerful, potentially nonlinear models to improve the power of standard family-based tests. We show, using empirical simulations, that KnockoffTrio can prioritize causal variants over associations due to linkage disequilibrium and can provide protection against confounding due to population stratification. In applications to 14,200 trios from three study cohorts for autism spectrum disorders (ASDs), including AGP, SPARK, and SSC, we show that KnockoffTrio can identify multiple significant associations that are missed by conventional tests applied to the same data. In particular, we replicate known ASD association signals with variants in several genes such as MACROD2, NRXN1, PRKAR1B, CADM2, PCDH9, and DOCK4 and identify additional associations with variants in other genes including ARHGEF10, SLC28A1, ZNF589, and HINT1 at FDR 10%.

Indexed as

Autism Spectrum DisorderGenome-Wide Association StudyCausalityHumansLinkage DisequilibriumNerve Tissue ProteinsHINT1 protein, humanNerve Tissue Proteinscausal variant identificationfamily-based designGWASknockoff framework

Identifiers

PMID36150388
PMCPMC9606389
OpenAlexW4296663355

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.