Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Eric Gamazon"'
Publikováno v:
PLoS Genetics, Vol 6, Iss 4, p e1000888 (2010)
Although genome-wide association studies (GWAS) of complex traits have yielded more reproducible associations than had been discovered using any other approach, the loci characterized to date do not account for much of the heritability to such traits
Externí odkaz:
https://doaj.org/article/fc3aca6fd6ec4a9aabd90395e72c946d
Autor:
Alice S. Whittemore, Nancy J. Cox, Douglas F. Easton, Dan Nicolae, Fernando Rivadeneira, Andre G. Uitterlinden, Hanne Meijers-Heijboer, Quinten Waisfisz, Paul Pharoah, Alison M. Dunning, Clare Turnbull, Nazneen Rahman, Jianjun Liu, Astrid Irwanto, Kamila Czene, Per Hall, Carl Blomqvist, Kristiina Aittomäki, Heli Nevanlinna, Norbert Dahmen, Dieter Flesch-Janys, Jennifer Stone, Quang Minh Bui, Daniel F. Schmidt, Enes Makalic, Rebecca Hein, Lars Beckmann, Magdalena Lochmann, Bertram Müller-Myhsok, Rita K. Schmutzler, Alfons Meindl, Stephen J. Chanock, David J. Hunter, Mark Lathrop, Isabel dos Santos Silva, Olivia Fletcher, Julian Peto, Daniel J. Park, Carmel Apicella, Kyriaki Michailidou, Polly Newcomb, Noralane M. Lindor, Mark Jenkins, Robert Haile, Steve Gallinger, David Duggan, David Conti, Eunjung Lee, Regina M. Santella, Graham G. Giles, Melissa C. Southey, Julia A. Knight, Graham Casey, Daniela Seminara, Duncan C. Thomas, Marilie D. Gammon, Giske Ursin, Kathi Malone, Esther M. John, John L. Hopper, Irene Andrulis, Jenny Chang-Claude, Stephanie Melkonian, Maria Argos, Rachelle Brutus, Shantanu Roy, Farzana Jasmine, Jianxin Shi, Anna Felberg, Valerie McGuire, Eric Gamazon, Lin Tong, Brandon L. Pierce, Muhammad G. Kibriya, Jerry Halpern, Habibul Ahsan
Early-onset breast cancer (EOBC) causes substantial loss of life and productivity, creating a major burden among women worldwide. We analyzed 1,265,548 Hapmap3 single-nucleotide polymorphisms (SNP) among a discovery set of 3,523 EOBC incident cases a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::447201ac529828c2509e3c7b7268d0a9
https://doi.org/10.1158/1055-9965.c.6515769
https://doi.org/10.1158/1055-9965.c.6515769
Autor:
Alice S. Whittemore, Nancy J. Cox, Douglas F. Easton, Dan Nicolae, Fernando Rivadeneira, Andre G. Uitterlinden, Hanne Meijers-Heijboer, Quinten Waisfisz, Paul Pharoah, Alison M. Dunning, Clare Turnbull, Nazneen Rahman, Jianjun Liu, Astrid Irwanto, Kamila Czene, Per Hall, Carl Blomqvist, Kristiina Aittomäki, Heli Nevanlinna, Norbert Dahmen, Dieter Flesch-Janys, Jennifer Stone, Quang Minh Bui, Daniel F. Schmidt, Enes Makalic, Rebecca Hein, Lars Beckmann, Magdalena Lochmann, Bertram Müller-Myhsok, Rita K. Schmutzler, Alfons Meindl, Stephen J. Chanock, David J. Hunter, Mark Lathrop, Isabel dos Santos Silva, Olivia Fletcher, Julian Peto, Daniel J. Park, Carmel Apicella, Kyriaki Michailidou, Polly Newcomb, Noralane M. Lindor, Mark Jenkins, Robert Haile, Steve Gallinger, David Duggan, David Conti, Eunjung Lee, Regina M. Santella, Graham G. Giles, Melissa C. Southey, Julia A. Knight, Graham Casey, Daniela Seminara, Duncan C. Thomas, Marilie D. Gammon, Giske Ursin, Kathi Malone, Esther M. John, John L. Hopper, Irene Andrulis, Jenny Chang-Claude, Stephanie Melkonian, Maria Argos, Rachelle Brutus, Shantanu Roy, Farzana Jasmine, Jianxin Shi, Anna Felberg, Valerie McGuire, Eric Gamazon, Lin Tong, Brandon L. Pierce, Muhammad G. Kibriya, Jerry Halpern, Habibul Ahsan
PDF file - 197K, Table S1. Discovery set study populations. Table S2. Distribution of discovery set subjects by site, case-control status and chip. Table S3. Discovery set quality control summary. Table S4. SNPs with score-based P-values < 4 X 10-8 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59da784c5c7f4419931b160e781ad99a
https://doi.org/10.1158/1055-9965.22437186
https://doi.org/10.1158/1055-9965.22437186
Publikováno v:
Blood. 140:10708-10709
Autor:
Dan Zhou, Eric Gamazon
Publikováno v:
npj Genomic Medicine. 7
We developed an integrative transcriptomic, evolutionary, and causal inference framework for a deep region-level analysis, which integrates several published approaches and a new summary-statistics-based methodology. To illustrate the framework, we a
Publikováno v:
European Neuropsychopharmacology. 63:e154
Autor:
Patrick Evans, Eric Gamazon
Publikováno v:
European Neuropsychopharmacology. 63:e249
Autor:
Jibril Hirbo, Francesca Pasutto, Eric Gamazon, Patrick Evans, Priyanka Pawar, Daniel Berner, Julia Sealock, Ran Tao, Peter Straub, Anuar Konkashbaev, Max Breyer, Ursula Schlötzer-Schrehardt, Andre Reis, Milam Brantley, Chiea Chuen Khor, Karen Joos, Nancy Cox
Exfoliation syndrome (XFS) is an age-related systemic disorder characterized by excessive production and progressive accumulation of abnormal extracellular material, with pathognomonic ocular manifestations. It is the most common cause of secondary g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d4e3f596dad3490dea5338afa9ae49d
https://doi.org/10.21203/rs.3.rs-53203/v1
https://doi.org/10.21203/rs.3.rs-53203/v1
Identifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis
Autor:
Eric Gamazon, Martijn Van de Bunt, Roger Little, Jemma Nelson, Thomas Juettemann, Olivier Delaneau, Fan Wu, Magali Ruffier, Halit Ongen, Daniel MacArthur, Daniel Zerbino, Peter Hickey, Yaping Liu, Esti Yeger-Lotem, Rajinder Kaul, Dan Nicolae, David Davis, Ruth Barshir, Michael Sammeth, Diego Garrido-Martín, Jiebiao Wang, Joshua Akey
Publikováno v:
Genome Research, Vol. 27, No 11 (2017) pp. 1859-1871
Genome research
Genome research, vol 27, iss 11
Genome research
Genome research, vol 27, iss 11
The impact of inherited genetic variation on gene expression in humans is well-established. The majority of known expression quantitative trait loci (eQTLs) impact expression of local genes (cis-eQTLs). More research is needed to identify effects of
Autor:
Manuel Muñoz-Aguirre, Pejman Mohammadi, Boxiang Liu, Eric Gamazon, Martijn Van de Bunt, Roger Little, Ferran Reverter, Richard Sandstrom, Jemma Nelson, Omer Basha, Thomas Juettemann, Yi-Hui Zhou, Olivier Delaneau, Robert Handsaker, Gerald Quon, Fan Wu, Panagiotis Papasaikas, Magali Ruffier, Halit Ongen, Daniel MacArthur, Daniel Zerbino, Carlos D. Bustamante, Peter Hickey, Pedro Ferreira, Sarah Kim-Hellmuth, Paul Flicek, Yaping Liu, Tuuli Lappalainen, Barbara Engelhardt, Esti Yeger-Lotem, Christine Peterson, Rajinder Kaul, Dan Nicolae, David Davis, Ruth Barshir, Michael Sammeth, Stephen Montgomery, Diego Garrido-Martín, Kasper Hansen, Andrew Brown, Taru Tukiainen, Tyler Shimko, Laure Frésard, Mark McCarthy, Joshua Akey, Brian Jo
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Nature, Vol. 550, No 7675 (2017) pp. 204-213
Nature, 550(7675), 204-213. Nature Publishing Group
Nature
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
instname
Nature, Vol. 550, No 7675 (2017) pp. 204-213
Nature, 550(7675), 204-213. Nature Publishing Group
Nature
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Characterization of the molecular function of the human genome and its variation across individuals is essential for identifying the cellular mechanisms that underlie human genetic traits and diseases. The Genotype-Tissue Expression (GTEx) project ai