Lesley Trinker

Dr. Lesley Trinker


Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 September 2014 in Nature Genetics
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Journal Article
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JCJames Cerhan
James Cerhan
SBSonja I Berndt
Sonja I Berndt
VJVijai Joseph
Vijai Joseph
HGHervé Ghesquières
Hervé Ghesquières
JMJames McKay
James McKay
SCStephen J Chanock
Stephen J Chanock
James Cerhan and colleagues report genome-wide association and meta-analysis studies to identify genetic susceptibility loci for diffuse large B cell lymphoma. They identify four loci that influence genetic susceptibility to this B cell malignancy. Diffuse large B cell lymphoma (DLBCL) is the most common lymphoma subtype and is clinically aggressive. To identify genetic susceptibility loci for DLBCL, we conducted a meta-analysis of 3 new genome-wide association studies (GWAS) and 1 previous scan, totaling 3,857 cases and 7,666 controls of European ancestry, with additional genotyping of 9 promising SNPs in 1,359 cases and 4,557 controls. In our multi-stage analysis, five independent SNPs in four loci achieved genome-wide significance marked by rs116446171 at 6p25.3 (EXOC2; P = 2.33 × 10−21), rs2523607 at 6p21.33 (HLA-B; P = 2.40 × 10−10), rs79480871 at 2p23.3 (NCOA1; P = 4.23 × 10−8) and two independent SNPs, rs13255292 and rs4733601, at 8q24.21 (PVT1; P = 9.98 × 10−13 and 3.63 × 10−11, respectively). These data provide substantial new evidence for genetic susceptibility to this B cell malignancy and point to pathways involved in immune recognition and immune function in the pathogenesis of DLBCL.

28 July 2008 in Archives of internal medicine (1960)
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Journal Article
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LTLesley Trinker
Lesley Trinker
DBDenise E. Bonds
Denise E. Bonds
KMKaren L. Margolis
Karen L. Margolis
JMJoAnn E. Manson
JoAnn E. Manson
BHBarbara V. Howard
Barbara V. Howard
LPLinda M. Parker
Linda M. Parker
The incidence and burden of diabetes continue to rise, particularly in developed countries. The prevalence among US adults 20 years and older is expected to increase to 11.2% by the year 2030.1 In women, the prevalence of diabetes rises sharply with each decade of age after menopause and surpasses that in men after the seventh decade of life.2,3 Women with diabetes who are 50 years and older live fewer years than women without diabetes,4 and comorbidity with cardiovascular disease is common.4,5 A further toll is extracted in health care costs6 and decreased work productivity.7

1 December 2011 in The American Journal of Clinical Nutrition
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Journal Article
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LTLesley Trinker
Lesley Trinker
GSGloria E Sarto
Gloria E Sarto
BHBarbara V Howard
Barbara V Howard
YHYing Huang
Ying Huang
MNMarian L Neuhouser
Marian L Neuhouser
RPRoss L Prentice
Ross L Prentice
Background: Self-report of dietary energy and protein intakes has been shown to be systematically and differentially underreported.Objective: We asse

1 January 2019 in Gastroenterology
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Journal Article
Closed access
JBJulia Butt
Julia Butt
MVMatthew Varga
Matthew Varga
WBWilliam J. Blot
William J. Blot
LTLauren Teras
Lauren Teras
KVKala Visvanathan
Kala Visvanathan
MEMeira Epplein
Meira Epplein

1 June 2023 in Nature Communications
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Journal Article
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T(The Lung Cancer Cohort Consortium (LC3)
The Lung Cancer Cohort Consortium (LC3)
DADemetrius Albanes
Demetrius Albanes
KAKarine Alcala
Karine Alcala
NANicolas Alcala
Nicolas Alcala
CAChristopher I. Amos
Christopher I. Amos
WZWei Zheng
Wei Zheng
Identification of risk biomarkers may enhance early detection of smoking-related lung cancer. We measured between 392 and 1,162 proteins in blood samples drawn at most three years before diagnosis in 731 smoking-matched case-control sets nested within six prospective cohorts from the US, Europe, Singapore, and Australia. We identify 36 proteins with independently reproducible associations with risk of imminent lung cancer diagnosis (all p < 4 × 10−5). These include a few markers (e.g. CA-125/MUC-16 and CEACAM5/CEA) that have previously been reported in studies using pre-diagnostic blood samples for lung cancer. The 36 proteins include several growth factors (e.g. HGF, IGFBP-1, IGFP-2), tumor necrosis factor-receptors (e.g. TNFRSF6B, TNFRSF13B), and chemokines and cytokines (e.g. CXL17, GDF-15, SCF). The odds ratio per standard deviation range from 1.31 for IGFBP-1 (95% CI: 1.17–1.47) to 2.43 for CEACAM5 (95% CI: 2.04–2.89). We map the 36 proteins to the hallmarks of cancer and find that activation of invasion and metastasis, proliferative signaling, tumor-promoting inflammation, and angiogenesis are most frequently implicated.

14 February 2017 in BMC Public Health
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Journal Article
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ALAndrea Z. LaCroix
Andrea Z. LaCroix
EREileen Rillamas-Sun
Eileen Rillamas-Sun
DBDavid Buchner
David Buchner
KEKelly Evenson
Kelly Evenson
CDChongzhi Di
Chongzhi Di
AHAmy H. Herring
Amy H. Herring
Limited evidence exists to inform physical activity (PA) and sedentary behavior guidelines for older people, especially women. Rigorous evidence on the amounts, intensities, and movement patterns associated with better health in later life is needed. The Objective PA and Cardiovascular Health (OPACH) Study is an ancillary study to the Women’s Health Initiative (WHI) Program that examines associations of accelerometer-assessed PA and sedentary behavior with cardiovascular and fall events. Between 2012 and 2014, 7048 women aged 63–99 were provided with an ActiGraph GT3X+ (Pensacola, Florida) triaxial accelerometer, a sleep log, and an OPACH PA Questionnaire; 6489 have accelerometer data. Most women were in their 70s (40%) or 80s (46%), while approximately 10% were in their 60s and 4% were age 90 years or older. Non-Hispanic Black or Hispanic/Latina women comprise half of the cohort. Follow-up includes 1-year of falls surveillance with monthly calendars and telephone interviews of fallers, and annual follow-up for outcomes with adjudication of incident cardiovascular disease (CVD) events through 2020. Over 63,600 months of calendar pages were returned by 5,776 women, who reported 5,980 falls. Telephone interviews were completed for 1,492 women to ascertain the circumstances, injuries and medical care associated with falling. The dataset contains extensive information on phenotypes related to healthy aging, including inflammatory and CVD biomarkers, breast and colon cancer, hip and other fractures, diabetes, and physical disability. This paper describes the study design, methods, and baseline data for a diverse cohort of postmenopausal women who wore accelerometers under free-living conditions as part of the OPACH Study. By using accelerometers to collect more precise and complete data on PA and sedentary behavior in a large cohort of older women, this study will contribute crucial new evidence about how much, how vigorous, and what patterns of PA are necessary to maintain optimal cardiovascular health and to avoid falls in later life. ClinicalTrials.gov identifier NCT00000611 . Registered 27 October 1999.