Evidence map›Paper›PMID 38184653›Full record

ArticleNature communications2024

High-dimensional phenotyping to define the genetic basis of cellular morphology.

Matthew Tegtmeyer, Jatin Arora, Samira Asgari, Beth A Cimini, Ajay Nadig, Emily Peirent, Dhara Liyanage, Gregory P Way, Erin Weisbart, Aparna Nathan and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
31.8field-weighted citation impact, top 1% 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

28 citing papers in PubMed, 51 citations in OpenAlex.

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  17. Systematic data analysis pipeline for quantitative morphological cell phenotyping.Computational and structural biotechnology journal · 2024
    Review
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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

19 authors at 2 institutions in 2 countries.

Matthew Tegtmeyer *Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0002-9032-8207
Jatin Arora *Center for Data Sciences, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Samira Asgari *Center for Data Sciences, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-2347-8985
Beth A CiminiImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0001-9640-9318
Ajay NadigStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Emily PeirentStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Dhara LiyanageStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Gregory P WayImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0002-0503-9348
Erin WeisbartImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0002-6437-2458
Aparna NathanCenter for Data Sciences, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-5975-2851
Tiffany AmariutaDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Kevin EgganStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0003-4436-8467
Marzieh HaghighiImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0002-0867-8364
Steven A McCarrollStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0002-6954-8184
Luke O'ConnorProgram in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0003-2730-9668
Anne E CarpenterImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0003-1555-8261
Shantanu SinghImaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA. shsingh@broadinstitute.org.ORCID 0000-0003-3150-3025
Ralda NehmeStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA. rnehme@broadinstitute.org.ORCID 0000-0001-7215-3311
Soumya RaychaudhuriCenter for Data Sciences, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA. soumya@broadinstitute.org.ORCID 0000-0002-1901-8265
Broad Institute · USHarvard University · US

Funding

Genetic neuroscience: How human genes and alleles shape neuronal phenotypesU01MH115727 · NIMH · BROAD INSTITUTE, INC. · PI ARLOTTA, PAOLA, BABADI, MEHRTASH · 2017 to 2021
$20.8M
Role of fibroblastic stromal cells and notch signaling in tissue inflammation in RA and SLEP01AI148102 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Michael B. Brenner, Nir Hacohen · 2021 to 2026
$17.3M
Training Program in Bioinformatics and Integrative GenomicsT32HG002295 · NHGRI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Peter J Park · 2001 to 2026
$15.8M
Medical Scientist Training ProgramT32GM144273 · NIGMS · HARVARD MEDICAL SCHOOL · PI David Shumway Jones, Jacqueline A. Lees · 2022 to 2026
$14.7M
Extracting rich information from biological imagesR35GM122547 · NIGMS · BROAD INSTITUTE, INC. · PI Anne E. Carpenter · 2017 to 2026
$6.2M
Discovery and Functional Impact of Common and Rare Variants in RAR01AR063759 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Soumya Raychaudhuri · 2013 to 2026
$5.4M
RA-SLE Molecular Deconstruction Leadership CenterUH2AR067677 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI BRENNER, MICHAEL B., RAYCHAUDHURI, SOUMYA · 2014 to 2020
$4.3M
Opera Phenix high-throughput microplate confocal imager for high-content screeningS10OD026839 · OD · BROAD INSTITUTE, INC. · PI WAGNER, BRIDGET K · 2019 to 2019
$1.0M
NHGRI NIH HHS T32 HG002295NIAID NIH HHS P01 AI148102NIAMS NIH HHS R01 AR063759NIAMS NIH HHS UH2 AR067677NIGMS NIH HHS R35 GM122547NIGMS NIH HHS T32 GM144273NIH HHS S10 OD026839NIMH NIH HHS U01 MH115727
6 · The paper itself

Abstract

The morphology of cells is dynamic and mediated by genetic and environmental factors. Characterizing how genetic variation impacts cell morphology can provide an important link between disease association and cellular function. Here, we combine genomic sequencing and high-content imaging approaches on iPSCs from 297 unique donors to investigate the relationship between genetic variants and cellular morphology to map what we term cell morphological quantitative trait loci (cmQTLs). We identify novel associations between rare protein altering variants in WASF2, TSPAN15, and PRLR with several morphological traits related to cell shape, nucleic granularity, and mitochondrial distribution. Knockdown of these genes by CRISPRi confirms their role in cell morphology. Analysis of common variants yields one significant association and nominate over 300 variants with suggestive evidence (P < 10

Indexed as

Induced Pluripotent Stem CellsQuantitative Trait LociCell NucleusCell ShapeChromosome MappingMutant ProteinsMutant Proteins

Identifiers

PMID38184653
PMCPMC10771466
OpenAlexW4390636599

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.