Evidence map›Paper›PMID 38978643›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing.

Cyril Pottier, Fahri Küçükali, Matt Baker, Anthony Batzler, Gregory D Jenkins, Marka van Blitterswijk, Cristina T Vicente, Wouter De Coster, Sarah Wynants, Pieter Van de Walle and 108 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. 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

5 · Who and what money

Authors and funding

118 authors.

Cyril Pottier
Fahri KüçükaliORCID 0000-0002-3835-9639
Matt Baker
Anthony Batzler
Gregory D Jenkins
Marka van Blitterswijk
Cristina T Vicente
Wouter De Coster
Sarah Wynants
Pieter Van de Walle
Owen A Ross
Júlia Faura
Stephen J Haggarty
Jeroen Gj van Rooij
Ging-Yuek R HsiungORCID 0000-0002-8017-0856
Linn Öijerstedt
Manuela Neumann
Yan Asmann
Shannon K McDonnell
Saurabh Baheti
Keith A Josephs
Jennifer L Whitwell
Kevin F Bieniek
Leah Forsberg
Hilary Heuer
Argentina Lario Lago
Ethan G Geier
Jennifer S YokoyamaORCID 0000-0001-7274-2634
Alexis P Oddi
Margaret Flanagan
Qinwen Mao
John R Hodges
John B Kwok
Kimiko Domoto-Reilly
Bradford C DickersonORCID 0000-0002-5958-3445
Bret M Evers
Brittany N DuggerORCID 0000-0003-2141-8855
David G Munoz
Julia Keith
Lorne Zinman
Ekaterina Rogaeva
EunRan Suh
Tamar Gefen
Changiz Geula
Sandra Weintraub
Janine Diehl-Schmid
Martin R Farlow
Dieter Edbauer
Bryan K Woodruff
Richard J Caselli
Laura L Donker Kaat
Edward D Huey
Simon Mead
Andrew King
Sigrun Roeber
Alissa L Nana
Nilufer Ertekin-Taner
David S Knopman
Ronald C Petersen
Leonard Petrucelli
Ryan J Uitti
Zbigniew K Wszolek
Eliana Marisa Ramos
Lea T Grinberg
Maria Luisa Gorno Tempini
Howard J Rosen
Salvatore Spina
Murray Grossman
John Q Trojanowski
Dirk C Keene
Jin Lee-Way
Johannes Prudlo
Daniel H Geschwind
Robert A Rissman
Bernardino Ghetti
Glenda M HallidayORCID 0000-0003-0422-8398
Thomas G Beach
Thomas Arzberger
Jochen Herms
Adam L Boxer
Jean P Vonsattel
Oscar L Lopez
Julia Kofler
Marla Gearing
Jonathan Glass
Jonathan D Rohrer
David J Irwin
Vivianna Van Deerlin
Rudolph Castellani
Marsel M Mesulam
Maria C Tartaglia
Elizabeth C Finger
Claire Troakes
Safa Al-Sarraj
Bruce L Miller
Neill R Graff-Radford
Ian Ra Mackenzie
John C van Swieten
William W Seeley
Kristel Sleegers
Joanna M Biernacka

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
Research Education ComponentP30AG062422 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Katherine P Rankin · 2019 to 2026
$36.9M
UCSD Shiley-Marcos Alzheimer's Disease Research Center P30P30AG062429 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DOUGLAS R GALASKO · 2019 to 2026
$34.9M
Neuropathology CoreP30AG013854 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI VASSAR, ROBERT J · 1996 to 2020
$28.9M
Research Education Core FP30AG072977 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ROBERT J VASSAR · 2021 to 2026
$26.3M
Research Education ComponentP30AG072979 · NIA · UNIVERSITY OF PENNSYLVANIA · PI DAVID A WOLK · 2021 to 2026
$24.8M
Progressive Aphasia Cognition Anatomy and ProgressionR01NS050915 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARIA LUISA GORNO TEMPINI · 2004 to 2026
$11.0M
Primary Progressive Aphasia: Cognition, Anatomy and ProgressionRF1NS050915 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GORNO TEMPINI, MARIA LUISA · 2022 to 2022
$4.7M
Whole genome sequencing consortium on Frontotemporal dementia with underlying TDP-43 pathologyUH3NS103870 · NINDS · MAYO CLINIC JACKSONVILLE · PI RADEMAKERS, ROSA · 2019 to 2021
$3.7M
Whole genome sequencing consortium on Frontotemporal dementia with underlying TDP-43 pathologyUG3NS103870 · NINDS · MAYO CLINIC JACKSONVILLE · PI RADEMAKERS, ROSA · 2017 to 2018
$1.9M
Training program in the neurology of language and neurodegenerative aphasiasK24DC015544 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GORNO TEMPINI, MARIA LUISA · 2016 to 2025
$1.9M
Medical Research Council MC_U123160651Medical Research Council MC_UU_00024/1Medical Research Council MC_UU_00037/1NIA NIH HHS P01 AG019724NIA NIH HHS P30 AG013854NIA NIH HHS P30 AG062422NIA NIH HHS P30 AG062429NIA NIH HHS P30 AG072977NIA NIH HHS P30 AG072979NIDCD NIH HHS K24 DC015544NINDS NIH HHS R01 NS050915NINDS NIH HHS RF1 NS050915NINDS NIH HHS UG3 NS103870NINDS NIH HHS UH3 NS103870
6 · The paper itself

Abstract

Frontotemporal lobar degeneration with neuronal inclusions of the TAR DNA-binding protein 43 (FTLD-TDP) is a fatal neurodegenerative disorder with only a limited number of risk loci identified. We report our comprehensive genome-wide association study as part of the International FTLD-TDP Whole-Genome Sequencing Consortium, including 985 cases and 3,153 controls, and meta-analysis with the Dementia-seq cohort, compiled from 26 institutions/brain banks in the United States, Europe and Australia. We confirm

Identifiers

PMID38978643
PMCPMC11230325

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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.