Evidence map›Paper›PMID 39896631›Full record

ArticlebioRxiv : the preprint server for biology2025

Transcriptomic Convergence and the Female Protective Effect in Autism.

Rebecca E Andersen, Maya Talukdar, Tyler Sakamoto, David Exposito-Alonso, Janet H T Song, Xuyu Qian, Seungil Lee, Nila Murugan, Ryan N Delgado, Sijing Zhao and 4 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Rebecca E AndersenDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0002-0702-3120
Maya TalukdarDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0002-5997-5633
Tyler SakamotoDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0009-0001-5972-8288
David Exposito-AlonsoDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0002-4950-2744
Janet H T SongDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0002-7898-0227
Xuyu QianDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0001-5944-3816
Seungil LeeDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0003-2829-2941
Nila MuruganDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0009-0001-8805-8025
Ryan N DelgadoDepartment of Genetics, Blavatnik Institute, and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-7551-0182
Sijing ZhaoDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0003-1247-6834
Gwenyth EichfeldDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0009-0007-6618-5406
Julia HarmsDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.
David C PageWhitehead Institute, Cambridge, MA, USA.ORCID 0000-0001-9920-3411
Christopher A WalshDivision of Genetics and Genomics and Manton Center for Orphan Diseases, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0002-0156-2238

Funding

Medical Scientist Training ProgramT32GM007753 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WALENSKY, LOREN DAVID · 1985 to 2021
$50.0M
Medical Scientist Training ProgramT32GM144273 · NIGMS · HARVARD MEDICAL SCHOOL · PI David Shumway Jones, Jacqueline A. Lees · 2022 to 2026
$14.7M
TRAINING GRANT IN GENETICST32GM007748 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI Anne O'Donnell-Luria, Louise Wilkins-Haug · 1985 to 2026
$12.0M
Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Hisashi Umemori · 2021 to 2026
$9.4M
1/2-Somatic mosaicism and autism spectrum disorderU01MH106883 · NIMH · BOSTON CHILDREN'S HOSPITAL · PI PARK, PETER J, WALSH, CHRISTOPHER A. · 2015 to 2019
$9.2M
Project-002U54DK110805 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI ORKIN, STUART H, ZON, LEONARD IRA · 2016 to 2020
$5.9M
The role of lineage in the temporospatial genesis of retinal bipolar cell subtypesK99EY034603 · NEI · HARVARD MEDICAL SCHOOL · PI DELGADO, RYAN · 2023 to 2024
$247k
Genomic approaches to understand human neural specializationsK99MH136290 · NIMH · BOSTON CHILDREN'S HOSPITAL · PI SONG, JANET · 2024 to 2025
$180k
Development of Distinct Areas in the Human Cerebral CortexK99NS135123 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI QIAN, XUYU · 2024 to 2024
$127k
NEI NIH HHS K99 EY034603NICHD NIH HHS P50 HD105351NIDDK NIH HHS U54 DK110805NIGMS NIH HHS T32 GM007748NIGMS NIH HHS T32 GM007753NIGMS NIH HHS T32 GM144273NIMH NIH HHS K99 MH136290NIMH NIH HHS U01 MH106883NINDS NIH HHS K99 NS135123
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a common neurodevelopmental condition characterized by deficits in social communication as well as restricted and/or repetitive behaviors. ASD is highly heritable

Identifiers

PMID39896631
PMCPMC11785016

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.