Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Roelof, Koster"'
Autor:
Jun Fang, Jinping Jia, Matthew Makowski, Mai Xu, Zhaoming Wang, Tongwu Zhang, Jason W. Hoskins, Jiyeon Choi, Younghun Han, Mingfeng Zhang, Janelle Thomas, Michael Kovacs, Irene Collins, Marta Dzyadyk, Abbey Thompson, Maura O'Neill, Sudipto Das, Qi Lan, Roelof Koster, PanScan Consortium, TRICL Consortium, GenoMEL Consortium, Rachael S. Stolzenberg-Solomon, Peter Kraft, Brian M. Wolpin, Pascal W. T. C. Jansen, Sara Olson, Katherine A. McGlynn, Peter A. Kanetsky, Nilanjan Chatterjee, Jennifer H. Barrett, Alison M. Dunning, John C. Taylor, Julia A. Newton-Bishop, D. Timothy Bishop, Thorkell Andresson, Gloria M. Petersen, Christopher I. Amos, Mark M. Iles, Katherine L. Nathanson, Maria Teresa Landi, Michiel Vermeulen, Kevin M. Brown, Laufey T. Amundadottir
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-17 (2017)
Genetic variants at multiple loci of chr5p15.33 have been associated with susceptibility to numerous cancers. Here the authors show that the association of one of these loci may be explained by a variant, rs36115365, influencing telomerase reverse tr
Externí odkaz:
https://doaj.org/article/6d29a2104a5544a480a010afb3a1a202
Autor:
Sharon A. Savage, Stephen J. Chanock, Robert N. Hoover, Meredith Yeager, Laurie Burdett, Aurelie Vogt, Belynda D. Hicks, Joseph F. Boland, Neil E. Caporaso, Joseph F. Fraumeni, Sholom Wacholder, Margaret Tucker, Madison T. Weg, Natalie K. Wolf, Kelsie L. Becklin, George M. Otto, Lee Helman, Neyssa Marina, Donald A. Barkauskas, Sean Davis, David M. Thomas, Mandy L. Ballinger, Dina Halai, Maria Fernanda Amary, Roberto Tirabosco, Adrienne M. Flanagan, Katia Scotlandi, Piero Picci, Claudia Hattinger, Massimo Serra, Nalan Gokgoz, Jay S. Wunder, Irene L. Andrulis, Fernando Lecanda, Luis Sierrasesúmaga, Ana Patiño-Garcia, Antonio S. Petrilli, Silvia Regina Caminada de Toledo, Chand Khanna, Richard Gorlick, Julie M. Gastier-Foster, Zhaoming Wang, David Largaespada, Orestis A. Panagiotou, Nathan Pankratz, Mitchell J. Machiela, Joy Gary, Paul S. Meltzer, Logan G. Spector, Branden S. Moriarity, Roelof Koster, Lisa Mirabello
Top 30 loci associated with metastasis at diagnosis in the discovery set of 541 European osteosarcoma cases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09f795faca595e27bc4b967075eb3a07
https://doi.org/10.1158/2159-8290.22531533
https://doi.org/10.1158/2159-8290.22531533
Autor:
Sharon A. Savage, Stephen J. Chanock, Robert N. Hoover, Meredith Yeager, Laurie Burdett, Aurelie Vogt, Belynda D. Hicks, Joseph F. Boland, Neil E. Caporaso, Joseph F. Fraumeni, Sholom Wacholder, Margaret Tucker, Madison T. Weg, Natalie K. Wolf, Kelsie L. Becklin, George M. Otto, Lee Helman, Neyssa Marina, Donald A. Barkauskas, Sean Davis, David M. Thomas, Mandy L. Ballinger, Dina Halai, Maria Fernanda Amary, Roberto Tirabosco, Adrienne M. Flanagan, Katia Scotlandi, Piero Picci, Claudia Hattinger, Massimo Serra, Nalan Gokgoz, Jay S. Wunder, Irene L. Andrulis, Fernando Lecanda, Luis Sierrasesúmaga, Ana Patiño-Garcia, Antonio S. Petrilli, Silvia Regina Caminada de Toledo, Chand Khanna, Richard Gorlick, Julie M. Gastier-Foster, Zhaoming Wang, David Largaespada, Orestis A. Panagiotou, Nathan Pankratz, Mitchell J. Machiela, Joy Gary, Paul S. Meltzer, Logan G. Spector, Branden S. Moriarity, Roelof Koster, Lisa Mirabello
Relationship of variables to metastasis at diagnosis in the discovery set.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a9a1b2ef77bb095791c86b743966fc3
https://doi.org/10.1158/2159-8290.22531536.v1
https://doi.org/10.1158/2159-8290.22531536.v1
Autor:
Sharon A. Savage, Stephen J. Chanock, Robert N. Hoover, Meredith Yeager, Laurie Burdett, Aurelie Vogt, Belynda D. Hicks, Joseph F. Boland, Neil E. Caporaso, Joseph F. Fraumeni, Sholom Wacholder, Margaret Tucker, Madison T. Weg, Natalie K. Wolf, Kelsie L. Becklin, George M. Otto, Lee Helman, Neyssa Marina, Donald A. Barkauskas, Sean Davis, David M. Thomas, Mandy L. Ballinger, Dina Halai, Maria Fernanda Amary, Roberto Tirabosco, Adrienne M. Flanagan, Katia Scotlandi, Piero Picci, Claudia Hattinger, Massimo Serra, Nalan Gokgoz, Jay S. Wunder, Irene L. Andrulis, Fernando Lecanda, Luis Sierrasesúmaga, Ana Patiño-Garcia, Antonio S. Petrilli, Silvia Regina Caminada de Toledo, Chand Khanna, Richard Gorlick, Julie M. Gastier-Foster, Zhaoming Wang, David Largaespada, Orestis A. Panagiotou, Nathan Pankratz, Mitchell J. Machiela, Joy Gary, Paul S. Meltzer, Logan G. Spector, Branden S. Moriarity, Roelof Koster, Lisa Mirabello
SNPs in the NFIB locus associated with metastasis at diagnosis with P{less than or equal to}1x10-5 in the discovery stage, and functionally annotated with information from the ENCODE and 1000 Genomes Project data.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0868cac5acb5964b729f531efe2c4eec
https://doi.org/10.1158/2159-8290.22531524.v1
https://doi.org/10.1158/2159-8290.22531524.v1
Autor:
Sharon A. Savage, Stephen J. Chanock, Robert N. Hoover, Meredith Yeager, Laurie Burdett, Aurelie Vogt, Belynda D. Hicks, Joseph F. Boland, Neil E. Caporaso, Joseph F. Fraumeni, Sholom Wacholder, Margaret Tucker, Madison T. Weg, Natalie K. Wolf, Kelsie L. Becklin, George M. Otto, Lee Helman, Neyssa Marina, Donald A. Barkauskas, Sean Davis, David M. Thomas, Mandy L. Ballinger, Dina Halai, Maria Fernanda Amary, Roberto Tirabosco, Adrienne M. Flanagan, Katia Scotlandi, Piero Picci, Claudia Hattinger, Massimo Serra, Nalan Gokgoz, Jay S. Wunder, Irene L. Andrulis, Fernando Lecanda, Luis Sierrasesúmaga, Ana Patiño-Garcia, Antonio S. Petrilli, Silvia Regina Caminada de Toledo, Chand Khanna, Richard Gorlick, Julie M. Gastier-Foster, Zhaoming Wang, David Largaespada, Orestis A. Panagiotou, Nathan Pankratz, Mitchell J. Machiela, Joy Gary, Paul S. Meltzer, Logan G. Spector, Branden S. Moriarity, Roelof Koster, Lisa Mirabello
Associations of the top GWAS and imputed SNP with metastasis at diagnosis in the discovery stage (European ancestry) by inheritance model.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6779d6b6c24726370fbd3daeba6bcc3d
https://doi.org/10.1158/2159-8290.22531530
https://doi.org/10.1158/2159-8290.22531530
Autor:
Sharon A. Savage, Stephen J. Chanock, Robert N. Hoover, Meredith Yeager, Laurie Burdett, Aurelie Vogt, Belynda D. Hicks, Joseph F. Boland, Neil E. Caporaso, Joseph F. Fraumeni, Sholom Wacholder, Margaret Tucker, Madison T. Weg, Natalie K. Wolf, Kelsie L. Becklin, George M. Otto, Lee Helman, Neyssa Marina, Donald A. Barkauskas, Sean Davis, David M. Thomas, Mandy L. Ballinger, Dina Halai, Maria Fernanda Amary, Roberto Tirabosco, Adrienne M. Flanagan, Katia Scotlandi, Piero Picci, Claudia Hattinger, Massimo Serra, Nalan Gokgoz, Jay S. Wunder, Irene L. Andrulis, Fernando Lecanda, Luis Sierrasesúmaga, Ana Patiño-Garcia, Antonio S. Petrilli, Silvia Regina Caminada de Toledo, Chand Khanna, Richard Gorlick, Julie M. Gastier-Foster, Zhaoming Wang, David Largaespada, Orestis A. Panagiotou, Nathan Pankratz, Mitchell J. Machiela, Joy Gary, Paul S. Meltzer, Logan G. Spector, Branden S. Moriarity, Roelof Koster, Lisa Mirabello
Top genotyped SNP associations with metastasis at diagnosis in the discovery and all replication studies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d70fb538e43a27b7e78138d56990fe0
https://doi.org/10.1158/2159-8290.22531527
https://doi.org/10.1158/2159-8290.22531527
Autor:
Sharon A. Savage, Stephen J. Chanock, Robert N. Hoover, Meredith Yeager, Laurie Burdett, Aurelie Vogt, Belynda D. Hicks, Joseph F. Boland, Neil E. Caporaso, Joseph F. Fraumeni, Sholom Wacholder, Margaret Tucker, Madison T. Weg, Natalie K. Wolf, Kelsie L. Becklin, George M. Otto, Lee Helman, Neyssa Marina, Donald A. Barkauskas, Sean Davis, David M. Thomas, Mandy L. Ballinger, Dina Halai, Maria Fernanda Amary, Roberto Tirabosco, Adrienne M. Flanagan, Katia Scotlandi, Piero Picci, Claudia Hattinger, Massimo Serra, Nalan Gokgoz, Jay S. Wunder, Irene L. Andrulis, Fernando Lecanda, Luis Sierrasesúmaga, Ana Patiño-Garcia, Antonio S. Petrilli, Silvia Regina Caminada de Toledo, Chand Khanna, Richard Gorlick, Julie M. Gastier-Foster, Zhaoming Wang, David Largaespada, Orestis A. Panagiotou, Nathan Pankratz, Mitchell J. Machiela, Joy Gary, Paul S. Meltzer, Logan G. Spector, Branden S. Moriarity, Roelof Koster, Lisa Mirabello
Supplementary Figure 1. Manhattan plot of the Discovery stage. SNPs in the NFIB risk locus are highlighted in green. Supplementary Figure 2. LD structure of the NFIB risk locus. Plot was made using the CEU population of the 1000 Genomes Project data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54e5173b5aa9967e1aca5796a6cb988e
https://doi.org/10.1158/2159-8290.22531542.v1
https://doi.org/10.1158/2159-8290.22531542.v1
Autor:
Sharon A. Savage, Stephen J. Chanock, Robert N. Hoover, Meredith Yeager, Laurie Burdett, Aurelie Vogt, Belynda D. Hicks, Joseph F. Boland, Neil E. Caporaso, Joseph F. Fraumeni, Sholom Wacholder, Margaret Tucker, Madison T. Weg, Natalie K. Wolf, Kelsie L. Becklin, George M. Otto, Lee Helman, Neyssa Marina, Donald A. Barkauskas, Sean Davis, David M. Thomas, Mandy L. Ballinger, Dina Halai, Maria Fernanda Amary, Roberto Tirabosco, Adrienne M. Flanagan, Katia Scotlandi, Piero Picci, Claudia Hattinger, Massimo Serra, Nalan Gokgoz, Jay S. Wunder, Irene L. Andrulis, Fernando Lecanda, Luis Sierrasesúmaga, Ana Patiño-Garcia, Antonio S. Petrilli, Silvia Regina Caminada de Toledo, Chand Khanna, Richard Gorlick, Julie M. Gastier-Foster, Zhaoming Wang, David Largaespada, Orestis A. Panagiotou, Nathan Pankratz, Mitchell J. Machiela, Joy Gary, Paul S. Meltzer, Logan G. Spector, Branden S. Moriarity, Roelof Koster, Lisa Mirabello
Description of participating case studies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::153801629bcf0fee71ff6efeb9967b1a
https://doi.org/10.1158/2159-8290.22531539.v1
https://doi.org/10.1158/2159-8290.22531539.v1
Autor:
Jun Fang, Jinping Jia, Matthew Makowski, Mai Xu, Zhaoming Wang, Tongwu Zhang, Jason W. Hoskins, Jiyeon Choi, Younghun Han, Mingfeng Zhang, Janelle Thomas, Michael Kovacs, Irene Collins, Marta Dzyadyk, Abbey Thompson, Maura O'Neill, Sudipto Das, Qi Lan, Roelof Koster, Rachael S. Stolzenberg-Solomon, Peter Kraft, Brian M. Wolpin, Pascal W. T. C. Jansen, Sara Olson, Katherine A. McGlynn, Peter A. Kanetsky, Nilanjan Chatterjee, Jennifer H. Barrett, Alison M. Dunning, John C. Taylor, Julia A. Newton-Bishop, D Timothy Bishop, Thorkell Andresson, Gloria M. Petersen, Christopher I. Amos, Mark M. Iles, Katherine L. Nathanson, Maria Teresa Landi, Michiel Vermeulen, Kevin M. Brown, Laufey T. Amundadottir
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-2 (2018)
Nature Communications 8: Article number: 15034 (2017); Published: 27 May 2017; Updated: 5 March 2018 The original version of this Article contained an error in the spelling of two members of the GenoMEL Consortium, Joan Anton Puig-Butille and Pol Gim
Externí odkaz:
https://doaj.org/article/147c64a9878c4dcc95df20ed5c41cdd3
Autor:
Danielle M. Karyadi, Michael Dean, Piero Picci, Roberto Tirabosco, Adrienne M. Flanagan, Meredith Yeager, Claudia Maria Hattinger, Ana Patiño-García, Antonio Sergio Petrilli, Leslie L. Robison, Miriam Gutiérrez-Jimeno, Donald A. Barkauskas, Lisa Mirabello, Amy Hutchinson, Smita Bhatia, Sharon A. Savage, Silvia Regina Caminada de Toledo, Nathan Pankratz, Brian D. Carter, Neal D. Freedman, Julie M. Gastier-Foster, Massimo Serra, Stephen J. Chanock, Patricia Valverde, Inci Ergurhan Ilhan, Gregory T. Armstrong, Mandy L. Ballinger, Richard Gorlick, Maria Fernanda Amary, Maisa Pinheiro, Katia Scotlandi, Joshua N. Sampson, Lindsay M. Morton, Robert N. Hoover, Gerardo Mejia-Baltodano, Margaret A. Tucker, David Thomas, Mingyi Wang, Lei Song, Nilgun Kurucu, Logan G. Spector, Fernando Lecanda, Maria Teresa Landi, Susan M. Gapstur, Bin Zhu, Eric Karlins, Roelof Koster, Matthew Gianferante, Belynda Hicks
Publikováno v:
JAMA Oncol
IMPORTANCE: Osteosarcoma, the most common malignant bone tumor in children and adolescents, occurs in a high number of cancer predisposition syndromes that are defined by highly penetrant germline mutations. The germline genetic susceptibility to ost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4369d687decacc760cba945a2f3c9d37
https://europepmc.org/articles/PMC7082769/
https://europepmc.org/articles/PMC7082769/