Evidence map›Paper›PMID 42486869›Full record

ArticlePediatric research2026

Rationale and Methods for the Prospective Genetic Risk Evaluation and Assessment (PROGRESS) in Autism Center at Columbia University.

Nicolò Pini, Lauren C Shuffrey, Kally C O'Reilly Sparks, Andrew T Marin, Celia L D'Amato, Renald Dambreville, Yunzhe Hu, Rebecca N Siegel, Hallie R Brown, Gazi F Azad and 11 more

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Article in Pediatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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.

2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

21 authors.

Nicolò Pini *Department of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Lauren C Shuffrey *Department of Child and Adolescent Psychiatry, New York University Grossman School of Medicine, New York, NY, USA.
Kally C O'Reilly Sparks *Department of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Andrew T MarinDepartment of Psychology, Columbia University, New York, NY, USA.
Celia L D'AmatoDepartment of Psychology, Columbia University, New York, NY, USA.
Renald DambrevilleDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Yunzhe HuDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Rebecca N SiegelDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Hallie R BrownCenter for Autism and the Developing Brain, Weill Cornell Medicine, White Plains, NY, USA.
Gazi F AzadDepartment of Population and Family Health, Columbia University Irving Medical Center, New York, NY, USA.
Rebecca A MuhleDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Carrie L Koval-BurtDepartment of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Yufeng ShenDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.
Melanie M WallDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Stephen M KanneDepartment of Health Psychology, University of Missouri, Columbia, MO, USA.
Matthew S LebowitzDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
William P FiferDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Paul S AppelbaumDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Dima AmsoDepartment of Psychology, Columbia University, New York, NY, USA.
Wendy K ChungDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Jeremy Veenstra-VanderWeeleDepartment of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA. Jeremy.Veenstra-VanderWeele@nyspi.columbia.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutism is most often diagnosed after the age of 3, despite evidence that neurodevelopmental differences emerge within the first 2 years of life and that genetic and familial risk can be identified at birth.

methodsEstablished in September 2022 (anticipated duration of 5-7 years), the Prospective Genetic Risk Evaluation and Assessment (PROGRESS) in Autism Center is an ongoing longitudinal cohort study designed to characterize early developmental trajectories associated with autism and evaluate the impact of providing genetic information to families.

resultsInfants who undergo genomic newborn screening and enroll in PROGRESS are followed from 3 to 24 months of age and categorized into three groups: identified genetic probability (IGP), familial likelihood without identified genetic probability (Baby Siblings), and no identified genetic probability (NGP). Assessments include electroencephalography, electrocardiography, auditory, eye tracking, developmental testing, caregiver-infant interaction, and caregiver-reported measures. Autism screening is conducted at 18 months, with comprehensive diagnostic evaluation at 24 months. Caregiver psychosocial experiences of receiving early genetic information are assessed through surveys and interviews.

conclusionBy integrating genomic probability with early neurobehavioral development and family experiences, PROGRESS provides a framework to inform ethical genomic screening, developmental monitoring, and timely access to early intervention supported by a family navigator. IMPACT: This study presents the rationale and methods of the ongoing Prospective Genetic Risk Evaluation and Assessment (PROGRESS) in Autism Center at Columbia University, which began in September 2022 (anticipated duration of 5-7 years). PROGRESS is a prospective longitudinal cohort assessing infants with identified genetic probability, familial likelihood, or no identified genetic probability for autism from 3 to 24 months of age. By linking early genetic probability with brain-behavioral trajectories, PROGRESS advances understanding of autism-related differences before clinical diagnosis and provides an empirically grounded foundation for ethical genomic newborn screening and optimized early developmental monitoring and intervention.

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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.