M
Margaret R. Karagas
Researcher at Dartmouth College
Publications - 528
Citations - 28181
Margaret R. Karagas is an academic researcher from Dartmouth College. The author has contributed to research in topics: Population & Medicine. The author has an hindex of 84, co-authored 430 publications receiving 24195 citations. Previous affiliations of Margaret R. Karagas include Dartmouth–Hitchcock Medical Center.
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Journal ArticleDOI
Life-Long Implications of Developmental Exposure to Environmental Stressors: New Perspectives
Philippe Grandjean,Robert Barouki,David C. Bellinger,Ludwine Casteleyn,Lisa Helbling Chadwick,Sylvaine Cordier,Ruth A. Etzel,Kimberly Gray,Eun Hee Ha,Claudine Junien,Margaret R. Karagas,Toshihiro Kawamoto,B. Paige Lawrence,Frederica P. Perera,Gail S. Prins,Alvaro Puga,Cheryl S. Rosenfeld,David H. Sherr,Peter D. Sly,William A. Suk,Qi Sun,Jorma Toppari,Peter van den Hazel,Cheryl L. Walker,Jerrold J. Heindel +24 more
TL;DR: Vulnerable exposure windows that can occur as early as the preconception period and epigenetics as a major mechanism than can lead to disadvantageous "reprogramming" of the genome, thereby potentially resulting in transgenerational effects are highlighted.
Journal ArticleDOI
Genome-wide association study identifies multiple loci associated with bladder cancer risk
Jonine D. Figueroa,Yuanqing Ye,Afshan Siddiq,Afshan Siddiq,Montserrat Garcia-Closas,Montserrat Garcia-Closas,Nilanjan Chatterjee,Ludmila Prokunina-Olsson,Victoria K. Cortessis,Charles Kooperberg,Olivier Cussenot,Simone Benhamou,Simone Benhamou,Jennifer Prescott,Stefano Porru,Colin P.N. Dinney,Núria Malats,Dalsu Baris,Mark P. Purdue,Eric J. Jacobs,Demetrius Albanes,Zhaoming Wang,Xiang Deng,Charles C. Chung,Wei Tang,H. Bas Bueno-de-Mesquita,Dimitrios Trichopoulos,Dimitrios Trichopoulos,Börje Ljungberg,Françoise Clavel-Chapelon,Elisabete Weiderpass,Vittorio Krogh,Miren Dorronsoro,Ruth C. Travis,Anne Tjønneland,Paul Brenan,Jenny Chang-Claude,Elio Riboli,Elio Riboli,David V. Conti,Manuela Gago-Dominguez,Mariana C. Stern,Malcolm C. Pike,David Van Den Berg,Jian-Min Yuan,Chancellor Hohensee,Rebecca Rodabough,G. Cancel-Tassin,G. Cancel-Tassin,M. Rouprêt,M. Rouprêt,Eva Compérat,Eva Compérat,Constance Chen,Immaculata De Vivo,Edward Giovannucci,David J. Hunter,David J. Hunter,Peter Kraft,Sara Lindström,Angela Carta,Sofia Pavanello,Cecilia Arici,Giuseppe Mastrangelo,Ashish M. Kamat,Seth P. Lerner,H. Barton Grossman,Jie Lin,Jian Gu,Xia Pu,Amy Hutchinson,Laurie Burdette,William Wheeler,Manolis Kogevinas,Adonina Tardón,Consol Serra,Alfredo Carrato,Reina García-Closas,Josep Lloreta,Molly Schwenn,Margaret R. Karagas,Alison Johnson,Alan R. Schned,Karla R. Armenti,G. M. Hosain,Gerald L. Andriole,Robert L. Grubb,Amanda Black,W. Ryan Diver,Susan M. Gapstur,Stephanie J. Weinstein,Jarmo Virtamo,Christopher A. Haiman,Maria Teresa Landi,Neil E. Caporaso,Joseph F. Fraumeni,Paolo Vineis,Paolo Vineis,Xifeng Wu,Debra T. Silverman,Stephen J. Chanock,Nathaniel Rothman +101 more
TL;DR: This study has identified new susceptibility alleles for bladder cancer risk that require fine-mapping and laboratory investigation, which could further understanding into the biological underpinnings of bladder carcinogenesis.
Journal ArticleDOI
Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data.
Jianxin Shi,Ju-Hyun Park,Jubao Duan,Sonja T. Berndt,Winton Moy,Kai Yu,Lei Song,William Wheeler,Xing Hua,Debra T. Silverman,Montserrat Garcia-Closas,Chao A. Hsiung,Jonine D. Figueroa,Victoria K. Cortessis,Núria Malats,Margaret R. Karagas,Paolo Vineis,I-Shou Chang,Dongxin Lin,Baosen Zhou,Adeline Seow,Keitaro Matsuo,Yun-Chul Hong,Neil E. Caporaso,Brian M. Wolpin,Eric J. Jacobs,Gloria M. Petersen,Alison P. Klein,Donghui Li,Harvey A. Risch,Alan R. Sanders,Li Hsu,Robert E. Schoen,Hermann Brenner,Rachael Z. Stolzenberg-Solomon,Pablo V. Gejman,Qing Lan,Nathaniel Rothman,Laufey T. Amundadottir,Maria Teresa Landi,Douglas F. Levinson,Stephen J. Chanock,Nilanjan Chatterjee +42 more
TL;DR: Simulation studies illustrate why differential treatment of certain categories of functional SNPs, even when shown to be highly enriched for GWAS-heritability, does not lead to proportionate improvement in genetic risk-prediction because of non-uniform linkage disequilibrium structure.
Journal ArticleDOI
Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight
Leanne K. Küpers,Claire Monnereau,Gemma C Sharp,Paul Yousefi,Paul Yousefi,Lucas A. Salas,Akram Ghantous,Christian M. Page,Christian M. Page,Sarah E. Reese,Allen J. Wilcox,Darina Czamara,Anne P. Starling,Alexei Novoloaca,Samantha Lent,Ritu Roy,Cathrine Hoyo,Carrie V. Breton,Catherine Allard,Allan C. Just,Kelly M. Bakulski,John W. Holloway,John W. Holloway,Todd M. Everson,Cheng-Jian Xu,Rae-Chi Huang,Diana A van der Plaat,Matthias Wielscher,Simon Kebede Merid,Vilhelmina Ullemar,Faisal I. Rezwan,Jari Lahti,Jenny van Dongen,Sabine A. S. Langie,Tom G. Richardson,Maria C. Magnus,Maria C. Magnus,Ellen A. Nohr,Zongli Xu,Liesbeth Duijts,Liesbeth Duijts,Shanshan Zhao,Weiming Zhang,Michelle Plusquin,Michelle Plusquin,Dawn L. DeMeo,Olivia Solomon,Joosje H. Heimovaara,Dereje D. Jima,Lu Gao,Mariona Bustamante,Patrice Perron,Robert O. Wright,Irva Hertz-Picciotto,Hongmei Zhang,Margaret R. Karagas,Ulrike Gehring,Carmen J. Marsit,Lawrence J. Beilin,Judith M. Vonk,Marjo-Riitta Järvelin,Anna Bergström,Anna Bergström,Anne K. Örtqvist,Susan Ewart,Pia M. Villa,Sophie E. Moore,Sophie E. Moore,Gonneke Willemsen,Arnout Standaert,Siri E. Håberg,Thorkild I. A. Sørensen,Thorkild I. A. Sørensen,Jack A. Taylor,Katri Räikkönen,Ivana V. Yang,Katerina Kechris,Tim S. Nawrot,Tim S. Nawrot,Matt J. Silver,Yun Yun Gong,Lorenzo Richiardi,Manolis Kogevinas,Augusto A. Litonjua,Brenda Eskenazi,Karen Huen,Hamdi Mbarek,Rachel L. Maguire,Rachel L. Maguire,Terence Dwyer,Martine Vrijheid,Luigi Bouchard,Andrea A. Baccarelli,Lisa A. Croen,Wilfried Karmaus,Denise Anderson,Maaike de Vries,Sylvain Sebert,Sylvain Sebert,Juha Kere,Juha Kere,Juha Kere,Robert Karlsson,Syed Hasan Arshad,Esa Hämäläinen,Michael N. Routledge,Dorret I. Boomsma,Andrew P. Feinberg,Craig J. Newschaffer,Eva Govarts,Matthieu Moisse,M. Daniele Fallin,Erik Melén,Erik Melén,Andrew M. Prentice,Eero Kajantie,Eero Kajantie,Eero Kajantie,Catarina Almqvist,Catarina Almqvist,Emily Oken,Dana Dabelea,Dana Dabelea,H. Marike Boezen,Philip E. Melton,Philip E. Melton,Rosalind J. Wright,Gerard H. Koppelman,Letizia Trevisi,Marie-France Hivert,Marie-France Hivert,Marie-France Hivert,Jordi Sunyer,Monica Cheng Munthe-Kaas,Monica Cheng Munthe-Kaas,Susan K. Murphy,Eva Corpeleijn,Joseph L. Wiemels,Nina Holland,Zdenko Herceg,Elisabeth B. Binder,Elisabeth B. Binder,George Davey Smith,Vincent V. W. Jaddoe,Rolv T. Lie,Rolv T. Lie,Wenche Nystad,Stephanie J. London,Debbie A Lawlor,Caroline L Relton,Harold Snieder,Janine F. Felix +151 more
TL;DR: In this article, a meta-analysis of epigenome-wide association studies of 8,825 neonates from 24 birth cohorts in the Pregnancy And Childhood Epigenetics Consortium was conducted, and the authors found that DNA methylation in neonatal blood is associated with birthweight at 914 sites, with a difference in birthweight ranging from -183 to 178 grams per 10% increase in methylation.
Journal ArticleDOI
Drinking Water Arsenic Contamination, Skin Lesions, and Malignancies: A Systematic Review of the Global Evidence
TL;DR: Accumulating evidence suggests that arsenic may increase risk of skin lesions and skin cancers at levels not previously considered harmful, and that genetic factors may influence risk.