Evidence map›Paper›PMID 23599027›Full record

SynthesisHuman molecular genetics2013

Genome-wide association study of age at menarche in African-American women.

Ellen W Demerath, Ching-Ti Liu, Nora Franceschini, Gary Chen, Julie R Palmer, Erin N Smith, Christina T L Chen, Christine B Ambrosone, Alice M Arnold, Elisa V Bandera and 46 more

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Human molecular genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 5 pooled it
4.7field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 5 syntheses or guidelines pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Review
  7. Article
  8. Maternal Age at Menarche Genes Determines Fetal Growth Restriction Risk.International journal of molecular sciences · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Genetics of pubertal timing.Current opinion in pediatrics · 2018
    Review
  19. Article
  20. Article
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

56 authors at 20 institutions in 3 countries.

Ellen W DemerathDivision of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, MN, USA. ewd@umn.edu
Ching-Ti Liu
Nora Franceschini
Gary Chen
Julie R Palmer
Erin N Smith
Christina T L Chen
Christine B Ambrosone
Alice M Arnold
Elisa V Bandera
Gerald S Berenson
Leslie Bernstein
Angela Britton
Anne R Cappola
Christopher S Carlson
Stephen J Chanock
Wei Chen
Zhao Chen
Sandra L Deming
Cathy E Elks
Michelle K Evans
Zofia Gajdos
Brian E Henderson
Jennifer J Hu
Sue Ingles
Esther M John
Kathleen F Kerr
Laurence N Kolonel
Loic Le Marchand
Xiaoning Lu
Robert C Millikan
Solomon K Musani
Nora L Nock
Kari North
Sarah Nyante
Michael F Press
Jorge L Rodriquez-Gil
Edward A Ruiz-Narvaez
Nicholas J Schork
Sathanur R Srinivasan
Nancy F Woods
Wei Zheng
Regina G Ziegler
Alan Zonderman
Gerardo Heiss
B Gwen Windham
Melissa Wellons
Sarah S Murray
Michael Nalls
Tomi Pastinen
Aleksandar Rajkovic
Joel Hirschhorn
L Adrienne Cupples
Charles Kooperberg
Joanne M Murabito
Christopher A Haiman
National Institutes of Health · USBoston University · USFred Hutch Cancer Center · USTulane University · USFramingham Heart Study · USJackson Memorial Hospital · USNational Institute on Aging · USUniversity of Miami · USBeckman Research InstituteBeth Israel Deaconess Medical Center · USBoston Children's Hospital · USCancer Institute of Florida · USCancer Prevention Institute of California · USHarvard University · USHuman Genome Sciences (United States) · USMcGill University and Génome Québec Innovation Centre · CAMedical Research Council · GBNational Cancer Institute · USRoswell Park Comprehensive Cancer Center · USScripps Research Institute · US

Funding

Institute for Clinical and Translational Research (UL1)UL1RR025005 · NCRR · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2007 to 2011
$75.8M
Healthy Aging In Neighborhoods of Diversity Across the Life Span (HANDLS)ZIAAG000513 · NIA · NATIONAL INSTITUTE ON AGING · PI EVANS, MICHELE K · 2009 to 2025
$70.9M
Tissue Procurement & PathologyP50CA058223 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHARLES M PEROU · 1992 to 2026
$59.3M
UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Stephanie Engel · 2001 to 2026
$36.3M
GENETIC SUSCEPTIBILITY TO CANCER IN MULTIETHNIC COHORTSR01CA063464 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HENDERSON, BRIAN E · 2001 to 2005
$23.2M
Multiethnic Cohort Study of Diet and CancerR37CA054281 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI KOLONEL, LAURENCE N. · 2003 to 2012
$23.2M
Northern California Cooperative Family Registry for Breast CancerU01CA069417 · NCI · NORTHERN CALIFORNIA CANCER CENTER · PI JOHN, ESTHER M. · 1995 to 2010
$22.4M
Zosuquidar trihydrochloride for acute myeloid leukemia &refractory anemiaM01RR000080 · NCRR · UNIVERSITY HOSPITALS OF CLEVELAND · PI DEARBORN, DORR GELLATLY · 1985 to 2007
$22.2M
Genome-Wide Association Analysis in Essential Hypertension (FEHGAS study)R01HL086694 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ARAVINDA CHAKRAVARTI · 2007 to 2026
$21.2M
FOLLOW-UP STUDY FOR CAUSES OF ILLNESS IN BLACK WOMENR01CA058420 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ROSENBERG, LYNN · 1999 to 2013
$20.7M
SCRIPPS TRANSLATIONAL SCIENCE INSTITUTE (UL1)UL1RR025774 · NCRR · SCRIPPS RESEARCH INSTITUTE, THE · PI TOPOL, ERIC JEFFREY · 2008 to 2011
$16.3M
A Follow-up Study for Causes of Cancer in Black WomenUM1CA164974 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ROSENBERG, LYNN · 2012 to 2017
$13.7M
Intramural NIH HHS Z01 AG000513NCI NIH HHS P50 CA058223NCI NIH HHS P50-CA58223NCI NIH HHS R01 CA058420NCI NIH HHS R01 CA063464NCI NIH HHS R01 CA073629NCI NIH HHS R01 CA098663NCI NIH HHS R01 CA100374NCI NIH HHS R01-CA100374NCI NIH HHS R01 CA100598NCI NIH HHS R01-CA100598NCI NIH HHS R01-CA63464NCI NIH HHS R01-CA73629NCI NIH HHS R01-CA77305NCI NIH HHS R37 CA054281NCI NIH HHS R37-CA54281NCI NIH HHS RFA CA-95-011NCI NIH HHS U01 CA069417NCI NIH HHS U01-CA69417NCI NIH HHS UM1 CA164920NCI NIH HHS UM1 CA164974NCRR NIH HHS 1U54RR025204-01NCRR NIH HHS M01 RR000080NCRR NIH HHS M01-RR-00080NCRR NIH HHS UL1 RR025005NCRR NIH HHS UL1RR025005NCRR NIH HHS UL1 RR025774NCRR NIH HHS UL1RR025774NHGRI NIH HHS U01 HG004402NHGRI NIH HHS U01HG004402NHLBI NIH HHS HHSN268200900055CNHLBI NIH HHS HHSN268201100001INHLBI NIH HHS HHSN268201100002INHLBI NIH HHS HHSN268201100003INHLBI NIH HHS HHSN268201100004INHLBI NIH HHS HHSN268201100005CNHLBI NIH HHS HHSN268201100005GNHLBI NIH HHS HHSN268201100005INHLBI NIH HHS HHSN268201100006CNHLBI NIH HHS HHSN268201100007CNHLBI NIH HHS HHSN268201100007INHLBI NIH HHS HHSN268201100008CNHLBI NIH HHS HHSN268201100008INHLBI NIH HHS HHSN268201100009CNHLBI NIH HHS HHSN268201100009INHLBI NIH HHS HHSN268201100010CNHLBI NIH HHS HHSN268201100011CNHLBI NIH HHS HHSN268201100011INHLBI NIH HHS HHSN268201100012CNHLBI NIH HHS HHSN268201100046CNHLBI NIH HHS K23 HL087114NHLBI NIH HHS K23-HL-87114NHLBI NIH HHS N01 HC005187NHLBI NIH HHS N01 HC045134NHLBI NIH HHS N01 HC045204NHLBI NIH HHS N01 HC045205NHLBI NIH HHS N01 HC048047NHLBI NIH HHS N01 HC048048NHLBI NIH HHS N01 HC048049NHLBI NIH HHS N01 HC048050NHLBI NIH HHS N01-HC-05187NHLBI NIH HHS N01 HC065226NHLBI NIH HHS N01 HC095095NHLBI NIH HHS N01 HC095170NHLBI NIH HHS N01 HC095171NHLBI NIH HHS N01 HC095172NHLBI NIH HHS N01-HC-45134NHLBI NIH HHS N01-HC-45204NHLBI NIH HHS N01-HC-45205NHLBI NIH HHS N01-HC-48047NHLBI NIH HHS N01-HC-48048NHLBI NIH HHS N01-HC-48049NHLBI NIH HHS N01-HC-48050NHLBI NIH HHS N01-HC-65226NHLBI NIH HHS N01-HC-95095NHLBI NIH HHS N01-HC-95100NHLBI NIH HHS N01-HC-95170NHLBI NIH HHS N01-HC-95171NHLBI NIH HHS N01-HC-95172NHLBI NIH HHS N02 HL064278NHLBI NIH HHS N02-HL-64278NHLBI NIH HHS R01 HL046380NHLBI NIH HHS R01 HL059367NHLBI NIH HHS R01 HL086694NHLBI NIH HHS R01HL086694NHLBI NIH HHS R01 HL087641NHLBI NIH HHS R01HL087641NHLBI NIH HHS R01 HL105756NHLBI NIH HHS R01-HL4638NHLBI NIH HHS R01HL59367NIA NIH HHS AG-16592NIA NIH HHS HHSN271201100004CNIA NIH HHS R01 AG016592NIA NIH HHS R21 AG032598NIA NIH HHS R21AG032598NIA NIH HHS Z01-AG000513NICHD NIH HHS HD-061437NICHD NIH HHS HD-062783NICHD NIH HHS N01-HD-3-3175NICHD NIH HHS R03 HD061437NICHD NIH HHS R03 HD062783NIEHS NIH HHS P30 ES010126NIEHS NIH HHS P30-ES10126NIEHS NIH HHS R01 ES021724PHS HHS 5215810-550000234PHS HHS DAMD17-96-6071PHS HHS HHSN268200625226CPHS HHS HHSN 268201100002CWHI NIH HHS HHSN268201100001CWHI NIH HHS HHSN268201100002CWHI NIH HHS HHSN268201100003CWHI NIH HHS HHSN268201100004C
6 · The paper itself

Abstract

African-American (AA) women have earlier menarche on average than women of European ancestry (EA), and earlier menarche is a risk factor for obesity and type 2 diabetes among other chronic diseases. Identification of common genetic variants associated with age at menarche has a potential value in pointing to the genetic pathways underlying chronic disease risk, yet comprehensive genome-wide studies of age at menarche are lacking for AA women. In this study, we tested the genome-wide association of self-reported age at menarche with common single-nucleotide polymorphisms (SNPs) in a total of 18 089 AA women in 15 studies using an additive genetic linear regression model, adjusting for year of birth and population stratification, followed by inverse-variance weighted meta-analysis (Stage 1). Top meta-analysis results were then tested in an independent sample of 2850 women (Stage 2). First, while no SNP passed the pre-specified P < 5 × 10(-8) threshold for significance in Stage 1, suggestive associations were found for variants near FLRT2 and PIK3R1, and conditional analysis identified two independent SNPs (rs339978 and rs980000) in or near RORA, strengthening the support for this suggestive locus identified in EA women. Secondly, an investigation of SNPs in 42 previously identified menarche loci in EA women demonstrated that 25 (60%) of them contained variants significantly associated with menarche in AA women. The findings provide the first evidence of cross-ethnic generalization of menarche loci identified to date, and suggest a number of novel biological links to menarche timing in AA women.

Indexed as

Genome-Wide Association StudyAdolescentBlack or African AmericanCase-Control StudiesChildDiabetes Mellitus, Type 2FemaleGenetic LociGenetic VariationHumansLinear ModelsMembrane GlycoproteinsMembrane ProteinsMenarcheNuclear Receptor Subfamily 1, Group F, Member 1ObesityFLRT2 protein, humanMembrane GlycoproteinsMembrane ProteinsNuclear Receptor Subfamily 1, Group F, Member 1RORA protein, human

Identifiers

PMID23599027
PMCPMC3723312
OpenAlexW2163780587

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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.