ArticleMolecular psychiatry2014
Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'.
Abstract readLetterComment
In one paragraph
Article in Molecular psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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.
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.
Who cites it
12 citing papers in PubMed.
- Navigating the pitfalls of applying machine learning in genomics.Nature reviews. Genetics · 2022Review
- Polygenic Risk Scores in Clinical Psychology: Bridging Genomic Risk to Individual Differences.Annual review of clinical psychology · 2018Review
- Bio-collections in autism research.Molecular autism · 2017Review
- Advancing the understanding of autism disease mechanisms through genetics.Nature medicine · 2016Review
- Response to Robinson et al.Molecular psychiatry · 2015Article
- RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.Science (New York, N.Y.) · 2015Article
- High-Dimensional Statistical Learning: Roots, Justifications, and Potential Machineries.Cancer informatics · 2015Review
- Psychiatrists' views of the genetic bases of mental disorders and behavioral traits and their use of genetic tests.The Journal of nervous and mental disease · 2014Article
- A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism.Translational psychiatry · 2014Article
- γ-band abnormalities as markers of autism spectrum disorders.Biomarkers in medicine · 2014Review
- A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism.Frontiers in genetics · 2014Article
- Genetic testing and autism: Tutorial for communication sciences and disorders.Journal of communication disordersArticle
Corrections and comments
- Commented on by
- Comment on
Authors and funding
18 authors.
E B Robinson1] Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA [2] Department of Medicine, Harvard Medical School, Boston, MA, USA [3] Medical and Population Genetics Program, Broad Institute for Harvard and MIT, Cambridge, MA, USA.
D Howrigan1] Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA [2] Department of Medicine, Harvard Medical School, Boston, MA, USA [3] Medical and Population Genetics Program, Broad Institute for Harvard and MIT, Cambridge, MA, USA.
J Yang1] The University of Queensland, Queensland Brain Institute, Brisbane, QLD, Australia [2] The Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.
S Ripke1] Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA [2] Department of Medicine, Harvard Medical School, Boston, MA, USA [3] Medical and Population Genetics Program, Broad Institute for Harvard and MIT, Cambridge, MA, USA [4] Stanley Center for Psychiatric Research, Broad Institute for Harvard and MIT, Cambridge, MA, USA.
V Anttila1] Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA [2] Department of Medicine, Harvard Medical School, Boston, MA, USA [3] Medical and Population Genetics Program, Broad Institute for Harvard and MIT, Cambridge, MA, USA [4] Stanley Center for Psychiatric Research, Broad Institute for Harvard and MIT, Cambridge, MA, USA.
L E Duncan1] Medical and Population Genetics Program, Broad Institute for Harvard and MIT, Cambridge, MA, USA [2] Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA [3] Psychiatric and Neurodevelopmental Genetics Unit, Massachusetts, General Hospital, Boston, MA, USA [4] Department of Psychiatry, Harvard Medical School, Boston, MA, USA.
L JostinsWellcome Trust Sanger Institute, Cambridge, UK.
J C BarrettWellcome Trust Sanger Institute, Cambridge, UK.
S E MedlandQueensland Institute of Medical Research, Brisbane, QLD, Australia.
D G MacArthur1] Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA [2] Department of Medicine, Harvard Medical School, Boston, MA, USA [3] Medical and Population Genetics Program, Broad Institute for Harvard and MIT, Cambridge, MA, USA.
G BreenSocial Genetic and Developmental Psychiatry Center, Institute of Psychiatry, King's College London, London, UK.
M C O'DonovanMRC Centre for Neuropsychiatric Genetics & Genomics, Cardiff University School of Medicine, Cardiff, UK.
N R Wray1] The University of Queensland, Queensland Brain Institute, Brisbane, QLD, Australia [2] The Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.
B DevlinDepartment of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
M J Daly1] Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA [2] Department of Medicine, Harvard Medical School, Boston, MA, USA [3] Medical and Population Genetics Program, Broad Institute for Harvard and MIT, Cambridge, MA, USA [4] Stanley Center for Psychiatric Research, Broad Institute for Harvard and MIT, Cambridge, MA, USA.
P M Visscher1] The University of Queensland, Queensland Brain Institute, Brisbane, QLD, Australia [2] The Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.
P F SullivanDepartment of Genetics, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC, USA.
B M Neale1] Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA [2] Department of Medicine, Harvard Medical School, Boston, MA, USA [3] Medical and Population Genetics Program, Broad Institute for Harvard and MIT, Cambridge, MA, USA [4] Stanley Center for Psychiatric Research, Broad Institute for Harvard and MIT, Cambridge, MA, USA.
Funding
Institute for Clinical and Translational Research (UL1)UL1RR025005 · NCRR · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2007 to 2011
$75.8MInstitute for Clinical and Translational ResearchUL1TR001079 · NCATS · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2013 to 2017
$60.1MGenome-Wide Association Analysis in Essential Hypertension (FEHGAS study)R01HL086694 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ARAVINDA CHAKRAVARTI · 2007 to 2026
$21.2MGenome-Wide Association for Loci Influencing CHD and Other Heart, Lung and BloodR01HL087641 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BOERWINKLE, ERIC A. · 2006 to 2008
$3.7MGWA for Gene-Environment Interaction Effects Influencing CHDU01HG004402 · NHGRI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BOERWINKLE, ERIC A. · 2007 to 2009
$1.6MMedical Research Council G0800509Medical Research Council G0801418Medical Research Council MR/L010305/1NCATS NIH HHS UL1 TR001079NCRR NIH HHS UL1 RR025005NHGRI NIH HHS U01 HG004402NHLBI NIH HHS HHSN268201100005CNHLBI NIH HHS HHSN268201100006CNHLBI NIH HHS HHSN268201100007CNHLBI NIH HHS HHSN268201100008CNHLBI NIH HHS HHSN268201100009CNHLBI NIH HHS HHSN268201100010CNHLBI NIH HHS HHSN268201100011CNHLBI NIH HHS HHSN268201100012CNHLBI NIH HHS R01 HL086694NHLBI NIH HHS R01 HL087641
Abstract
PubMed holds no abstract for this paper.
Indexed as
Child Development Disorders, PervasiveFemaleGene Regulatory NetworksGenetic Predisposition to DiseaseHumansMalePolymorphism, Single Nucleotide
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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.