ArticleScience advances2019
Data-driven phenotype discovery of
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In one paragraph
Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.
0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
What it found
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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.
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Who cites it
24 citing papers in PubMed.
- Cerebellar GABA and executive function among adult female carriers of the fragile X messenger ribonucleoprotein 1 premutation: a pilot study to examine neural underpinnings of the clinical phenotype.Neurobiology of disease · 2026Article
- Use of Machine Learning to Identify Markers of Risk for Fragile X-Associated Tremor/Ataxia Syndrome: A Preliminary Analysis.Annals of neurology · 2026Article
- Social Communication Delay in an Unbiased Sample of Preschoolers With theJournal of speech, language, and hearing research : JSLHR · 2024Article
- Review
- Article
- Social and physical predictors of mental health impact in adult women who have anGenetics in medicine open · 2023Article
- FMR1 CGG Repeats and Stress Influence Self-Reported Cognitive Functioning in Mothers.American journal on intellectual and developmental disabilities · 2023Article
- Change in Maladaptive Behavior Affects Intergenerational Relationships in Fragile X Syndrome.American journal on intellectual and developmental disabilities · 2022Article
- Maternal Pragmatic Language Difficulties in the FMR1 Premutation and the Broad Autism Phenotype: Associations with Individual and Family Outcomes.Journal of autism and developmental disorders · 2022Article
- Family history of FXTAS is associated with age-related cognitive-linguistic decline among mothers with the FMR1 premutation.Journal of neurodevelopmental disorders · 2022Article
- Health profiles of adults with autism spectrum disorder: Differences between women and men.Autism research : official journal of the International Society for Autism Research · 2021Article
- Artificial intelligence-assisted phenotype discovery of fragile X syndrome in a population-based sample.Genetics in medicine : official journal of the American College of Medical Genetics · 2021Article
- Stress and genetics influence hair cortisol in FMR1 premutation carrier mothers of children with fragile X syndrome.Psychoneuroendocrinology · 2021Article
- Response Inhibition Deficits in Women with the FMR1 Premutation are Associated with Age and Fall Risk.Brain and cognition · 2021Article
- IsFrontiers in psychiatry · 2021Article
- Predictors of Comorbid Conditions in Women Who Carry anFrontiers in psychiatry · 2021Article
- Fragile X associated neuropsychiatric disorders in a male without FXTAS.Intractable & rare diseases research · 2020Article
- Molecular analysis ofExpert review of molecular diagnostics · 2020Article
- Inhibition deficits are modulated by age and CGG repeat length in carriers of the FMR1 premutation allele who are mothers of children with fragile X syndrome.Brain and cognition · 2020Article
- Article
Corrections and comments
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Authors and funding
12 authors.
Arezoo MovagharWaisman Center, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0002-2156-3991
David PageDepartment of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0003-0576-2912
Murray BrilliantMarshfield Clinic Research Institute, Marshfield, WI, USA.
Mei Wang BakerWisconsin State Laboratory of Hygiene, Madison, WI, USA.
Jan GreenbergWaisman Center, University of Wisconsin-Madison, Madison, WI, USA.
Jinkuk HongWaisman Center, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0002-6789-2571
Leann Smith DaWaltWaisman Center, University of Wisconsin-Madison, Madison, WI, USA.
Krishanu SahaWaisman Center, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0003-2837-0858
Finn KuusistoMorgridge Institute for Research, Madison, WI, USA.ORCID 0000-0001-6487-4397
Ron StewartMorgridge Institute for Research, Madison, WI, USA.
Elizabeth Berry-KravisRush University Medical Center, Chicago, IL, USA.ORCID 0000-0001-7099-1522
Marsha R MailickWaisman Center, University of Wisconsin-Madison, Madison, WI, USA.ORCID 0000-0001-6548-2096
Funding
University of Wisconsin Institute for Clinical and Translational ResearchUL1TR002373 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI ELIZABETH S BURNSIDE, Allan R. Brasier · 2017 to 2026
$75.9MInstitutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2MCooperative Agreement for a Nat'l Research & Training Org for People with DevelopU01DD000231 · DD · ASSN OF UNIVERSITY CENTERS/ DISABILITIES · PI JESIEN, GEORGE S. · 2007 to 2012
$16.8MThe Electronic Medical Records and Genomics (eMERGE) Network Phase III Coordinating Center (U01)U01HG008701 · NHGRI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PETERSON, JOSEPH F. · 2015 to 2019
$7.1MWaisman Intellectual and Developmental Disabilities Research Center Down Syndrome RegistryU54HD090256 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI MESSING, ALBEE · 2016 to 2020
$6.0MFMR1 Premutation Phenotypes in Population-Based & Clinically-Ascertained SamplesR01HD082110 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI Leann Smith DaWalt, MARSHA RUTH MAILICK · 2015 to 2026
$5.1MNCATS NIH HHS UL1 TR000427NCATS NIH HHS UL1 TR002373NCBDD CDC HHS U01 DD000231NHGRI NIH HHS U01 HG008701NICHD NIH HHS R01 HD082110NICHD NIH HHS U54 HD090256
Abstract
The impact of the
Indexed as
HeterozygoteMutationPhenotypeDatabases, GeneticFemaleFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeGenetic Association StudiesGenetic Predisposition to DiseaseHumansMalePopulation SurveillanceROC CurveWorkflowFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1
Identifiers
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Read underepoch 390
Registered trials
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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.