Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Daniel, Schaid"'
Autor:
Tian Ge, Marguerite R. Irvin, Amit Patki, Vinodh Srinivasasainagendra, Yen-Feng Lin, Hemant K. Tiwari, Nicole D. Armstrong, Barbara Benoit, Chia-Yen Chen, Karmel W. Choi, James J. Cimino, Brittney H. Davis, Ozan Dikilitas, Bethany Etheridge, Yen-Chen Anne Feng, Vivian Gainer, Hailiang Huang, Gail P. Jarvik, Christopher Kachulis, Eimear E. Kenny, Atlas Khan, Krzysztof Kiryluk, Leah Kottyan, Iftikhar J. Kullo, Christoph Lange, Niall Lennon, Aaron Leong, Edyta Malolepsza, Ayme D. Miles, Shawn Murphy, Bahram Namjou, Renuka Narayan, Mark J. O’Connor, Jennifer A. Pacheco, Emma Perez, Laura J. Rasmussen-Torvik, Elisabeth A. Rosenthal, Daniel Schaid, Maria Stamou, Miriam S. Udler, Wei-Qi Wei, Scott T. Weiss, Maggie C. Y. Ng, Jordan W. Smoller, Matthew S. Lebo, James B. Meigs, Nita A. Limdi, Elizabeth W. Karlson
Publikováno v:
Genome Medicine, Vol 14, Iss 1, Pp 1-16 (2022)
Abstract Background Type 2 diabetes (T2D) is a worldwide scourge caused by both genetic and environmental risk factors that disproportionately afflicts communities of color. Leveraging existing large-scale genome-wide association studies (GWAS), poly
Externí odkaz:
https://doaj.org/article/e049f828882147afa27dd2a692f0bc18
Autor:
Richard M. Weinshilboum, Alex A. Adjei, Eric D. Wieben, Daniel Schaid, Bruce W. Eckloff, Liewei Wang, Linda Pelleymounter, Josefa Coronel, Oreste E. Salavaggione, Araba A. Adjei, Cynthia X. Ma
Supplementary Materials from Human Aromatase: Gene Resequencing and Functional Genomics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b9bbc36d8b563d8b70e8b2aac944731
https://doi.org/10.1158/0008-5472.22365213
https://doi.org/10.1158/0008-5472.22365213
Autor:
Richard Weinshilboum, Daniel Schaid, Shan Wang-Gohrke, Jenny Chang-Claude, Thomas Brüning, Yon Ko, Ute Hamann, Christina Justenhoven, Michel Eichelbaum, Hiltrud Brauch, J. Michael Dixon, William Miller, Thomas Sellers, Zachary Fredericksen, James Ingle, Liewei Wang, Michelle Hildebrandt, Jianping Zhang, Janet Olson, Yuan Ji
Supplementary Table 1 from Breast Cancer Risk Reduction and Membrane-Bound Catechol O-Methyltransferase Genetic Polymorphisms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d12bf9b3cf25ba6600de0b833425abc
https://doi.org/10.1158/0008-5472.22374554.v1
https://doi.org/10.1158/0008-5472.22374554.v1
Autor:
Liewei Wang, Daniel Schaid, Matthew Ames, Michelle Hildebrandt, Stephanie Safgren, Anthony Batzler, Gregory Jenkins, Krishna Kalari, Brooke Fridley, Liang Li
Two cytidine analogues, gemcitabine (dFdC) and 1-β-d-arabinofuranosylcytosine (AraC), show significant therapeutic effect in a variety of cancers. However, response to these drugs varies widely. Evidence from tumor biopsy samples shows that expressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f685898dfcdc9887a499df1e36c07152
https://doi.org/10.1158/0008-5472.c.6497606
https://doi.org/10.1158/0008-5472.c.6497606
Autor:
Liewei Wang, Daniel Schaid, Matthew Ames, Michelle Hildebrandt, Stephanie Safgren, Anthony Batzler, Gregory Jenkins, Krishna Kalari, Brooke Fridley, Liang Li
Supplementary Table 1 from Gemcitabine and Cytosine Arabinoside Cytotoxicity: Association with Lymphoblastoid Cell Expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23adabd27aadb530bf03d132be2099fa
https://doi.org/10.1158/0008-5472.22374845
https://doi.org/10.1158/0008-5472.22374845
Autor:
Richard Weinshilboum, Daniel Schaid, Shan Wang-Gohrke, Jenny Chang-Claude, Thomas Brüning, Yon Ko, Ute Hamann, Christina Justenhoven, Michel Eichelbaum, Hiltrud Brauch, J. Michael Dixon, William Miller, Thomas Sellers, Zachary Fredericksen, James Ingle, Liewei Wang, Michelle Hildebrandt, Jianping Zhang, Janet Olson, Yuan Ji
Catechol O-methyltransferase (COMT)-catalyzed methylation of catecholestrogens has been proposed to play a protective role in estrogen-induced genotoxic carcinogenesis. We have taken a comprehensive approach to test the hypothesis that genetic variat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9837c88ec97a97bac3f17620a4dd9199
https://doi.org/10.1158/0008-5472.c.6497492
https://doi.org/10.1158/0008-5472.c.6497492
Autor:
Richard Weinshilboum, Daniel Schaid, Shan Wang-Gohrke, Jenny Chang-Claude, Thomas Brüning, Yon Ko, Ute Hamann, Christina Justenhoven, Michel Eichelbaum, Hiltrud Brauch, J. Michael Dixon, William Miller, Thomas Sellers, Zachary Fredericksen, James Ingle, Liewei Wang, Michelle Hildebrandt, Jianping Zhang, Janet Olson, Yuan Ji
Supplementary Table 2 from Breast Cancer Risk Reduction and Membrane-Bound Catechol O-Methyltransferase Genetic Polymorphisms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0be945122ccff08961ec3e2f8e3f4edd
https://doi.org/10.1158/0008-5472.22374551
https://doi.org/10.1158/0008-5472.22374551
Autor:
Richard Weinshilboum, Daniel Schaid, Shan Wang-Gohrke, Jenny Chang-Claude, Thomas Brüning, Yon Ko, Ute Hamann, Christina Justenhoven, Michel Eichelbaum, Hiltrud Brauch, J. Michael Dixon, William Miller, Thomas Sellers, Zachary Fredericksen, James Ingle, Liewei Wang, Michelle Hildebrandt, Jianping Zhang, Janet Olson, Yuan Ji
Supplementary Table 3 from Breast Cancer Risk Reduction and Membrane-Bound Catechol O-Methyltransferase Genetic Polymorphisms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6292cb9b3457424193335e24b79f15e4
https://doi.org/10.1158/0008-5472.22374548.v1
https://doi.org/10.1158/0008-5472.22374548.v1
Autor:
Daniel Hui, Brenda Xiao, Ozan Dikilitas, Robert R. Freimuth, Marguerite R. Irvin, Gail P. Jarvik, Leah Kottyan, Iftikhar Kullo, Nita A. Limdi, Cong Liu, Yuan Luo, Bahram Namjou, Megan J. Puckelwartz, Daniel Schaid, Hemant Tiwari, Wei-Qi Wei, Shefali Verma, Dokyoon Kim, Marylyn D. Ritchie
Publikováno v:
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing. 28
Polygenic risk scores (PRS) have led to enthusiasm for precision medicine. However, it is well documented that PRS do not generalize across groups differing in ancestry or sample characteristics e.g., age. Quantifying performance of PRS across differ
Autor:
Jodell E. Linder, Aimee Allworth, Sarah T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton, David R. Crosslin, Ozan Dikilitas, Alanna DiVietro, Edward D. Esplin, Sophie Forman, Robert R. Freimuth, Adam S. Gordon, Richard Green, Maegan V. Harden, Ingrid A. Holm, Gail P. Jarvik, Elizabeth W. Karlson, Sofia Labrecque, Niall J. Lennon, Nita A. Limdi, Kathleen F. Mittendorf, Shawn N. Murphy, Lori Orlando, Cynthia A. Prows, Luke V. Rasmussen, Laura Rasmussen-Torvik, Robb Rowley, Konrad Teodor Sawicki, Tara Schmidlen, Shannon Terek, David Veenstra, Digna R. Velez Edwards, Devin Absher, Noura S. Abul-Husn, Jorge Alsip, Hana Bangash, Mark Beasley, Jennifer E. Below, Eta S. Berner, James Booth, Wendy K. Chung, James J. Cimino, John Connolly, Patrick Davis, Beth Devine, Stephanie M. Fullerton, Candace Guiducci, Melissa L. Habrat, Heather Hain, Hakon Hakonarson, Margaret Harr, Eden Haverfield, Valentina Hernandez, Christin Hoell, Martha Horike-Pyne, George Hripcsak, Marguerite R. Irvin, Christopher Kachulis, Dean Karavite, Eimear E. Kenny, Atlas Khan, Krzysztof Kiryluk, Bruce Korf, Leah Kottyan, Iftikhar J. Kullo, Katie Larkin, Cong Liu, Edyta Malolepsza, Teri A. Manolio, Thomas May, Elizabeth M. McNally, Frank Mentch, Alexandra Miller, Sean D. Mooney, Priyanka Murali, Brenda Mutai, Naveen Muthu, Bahram Namjou, Emma F. Perez, Megan J. Puckelwartz, Tejinder Rakhra-Burris, Dan M. Roden, Elisabeth A. Rosenthal, Seyedmohammad Saadatagah, Maya Sabatello, Dan J. Schaid, Baergen Schultz, Lynn Seabolt, Gabriel Q. Shaibi, Richard R. Sharp, Brian Shirts, Maureen E. Smith, Jordan W. Smoller, Rene Sterling, Sabrina A. Suckiel, Jeritt Thayer, Hemant K. Tiwari, Susan B. Trinidad, Theresa Walunas, Wei-Qi Wei, Quinn S. Wells, Chunhua Weng, Georgia L. Wiesner, Ken Wiley, Josh F. Peterson, Adam Gordon, Agboade Sobowale, Akshar Patel, Alanna Strong, Alborz Sherafati, Alborz Sherfati, Alex Bick, Alka Chandel, Alyssa Rosenthal, Amit Khera, Amy Kontorovich, Andrew Beck, Andy Beck, Angelica Espinoza, Anna Lewis, Anya Prince, Ayuko Iverson, Bahram Namjou Khales, Barbara Benoit, Becca Hernan, Ben Kallman, Ben Kerman, Ben Shoemaker, Benjamin Satterfield, Bethany Etheridge, Blake Goff, Bob Freimuth, Bob Grundmeier, Brenae Collier, Brett Harnett, Brian Chang, Brian Piening, Brittney Davis, Candace Patterson, Carmen Demetriou, Casey Ta, Catherine Hammack, Catrina Nelson, Caytie Gascoigne, Chad Dorn, Chad Moretz, Chris Kachulis, Christie Hoell, Christine Cowles, Christoph Lange, Cindy Prows, Cole Brokamp, Courtney Scherr, Crystal Gonzalez, Cynthia Ramirez, Daichi Shimbo, Dan Roden, Daniel Schaid, Dave Kaufman, David Crosslin, David Kochan, Davinder Singh, Debbie Abrams, Digna Velez Edwards, Eduardo Morales, Edward Esplin, Ehsan Alipour, Eimear Kenny, Elisabeth Rosenthal, Eliza Duvall, Elizabeth McNally, Elizabeth Bhoj, Elizabeth Cohn, Elizabeth Hibler, Elizabeth Karlson, Ellen Clayton, Emily Chesnut, Emily DeFranco, Emily Gallagher, Emily Soper, Emma Perez, Erin Cash, Eta Berner, Fei Wang, Firas Wehbe, Francisco Ricci, Gabriel Shaibi, Gail Jarvik, George Hahn, Georgia Wiesner, Gillian Belbin, Gio Davogustto, Girish Nadkarni, Haijun Qiu, Hannah Beasley, Hao Liu, Heide Aungst, Hemant Tiwari, Hillary Duckham, Hope Thomas, Iftikhar Kullo, Ingrid Holm, Isabelle Allen, Iuliana Ionita-Laza, Jacklyn Hellwege, Jacob Petrzelka, Jacqueline Odgis, Jahnavi Narula, Jake Petrzelka, Jalpa Patel, James Cimino, James Meigs, James Snyder, Janet Olson, Janet Zahner, Jeff Pennington, Jen Pacheco, Jennifer Allen Pacheco, Jennifer Morse, Jeremy Corsmo, Jim Cimino, Jingheng Chen, Jocelyn Fournier, Jodell Jackson, Joe Glessner, Joel Pacyna, Johanna Smith, John Lynch, John Shelley, Jonathan Mosley, Jordan Nestor, Jordan Smoller, Joseph Kannry, Joseph Sutton, Josh Peterson, Joshua Smith, Julia Galasso, Julia Smith, Julia Wynn, Justin Gundelach, Justin Starren, Karmel Choi, Kate Mittendorf, Katherine Anderson, Katherine Bonini, Kathleen Leppig, Kathleen Muenzen, Kelsey Stuttgen, Kenny Nguyen, Kevin Dufendach, Kiley Atkins, Konrad Sawicki, Kristjan Norland, Laura Beskow, Li Hsu, Lifeng Tian, Lisa Mahanta, Lisa Martin, Lisa Wang, Lizbeth Gomez, Lorenzo Thompson, Lucas Richter, Luke Rasmussen, Lynn Petukhova, Madison O’Brien, Maegan Harden, Malia Fullerton, Marta Guindo, Martha Horike, Marwah Abdalla, Marwan Hamed, Mary Beth Terry, Mary Maradik, Matt Wyatt, Matthew Davis, Matthew Lebo, Maureen Smith, Maya del Rosario, Meckenzie Behr, Meg Roy-Puckelwartz, Mel Habrat, Melanie Myers, Meliha Yetisgen, Merve Iris, Michael DaSilva, Michael Preuss, Michelle McGowan, Mingjian Shi, Minoli Perera, Minta Thomas, Mitch Elkind, Mohammad Abbass, Mohammad Saadatagah, Molly Hess, Molly Maradik, Nataraja 'RJ' Vaitinadin, Nataraja Vaitinadin, Neil Netherly, Niall Lennon, Ning Shang, Nita Limdi, Noah Forrest, Noheli Romero, Nora Robinson, Noura Abul-Husn, Omar Elsekaily, Patricia Kovatch, Paul Appelbaum, Paul Francaviglia, Paul O’Reilly, Paulette Chandler, Pedro Caraballo, Peter Tarczy-Hornoch, Pierre Shum, Priya Marathe, Qiping Feng, Quinn Wells, Rachel Atchley, Radhika Narla, Rene Barton, Rex Chisholm, Richard Sharp, Riki Peters, Rita Kukafka, Robert Freimuth, Robert Green, Robert Winter, Roger Mueller, Ruth Loos, Ryan Irvin, Sabrina Suckiel, Sajjad Hussain, Samer Sharba, Sandy Aronson, Sarah Jones, Sarah Knerr, Scott Nigbur, Scott Weiss, Sean Mooney, Sharon Aufox, Sharon Nirenberg, Shawn Murphy, Sheila O’Byrne, Shing Wang (Sam) Choi, Sienna Aguilar, S.T. Bland, Stefanie Rodrigues, Stephanie Ledbetter, Stephanie Rutledge, Stuart James Booth, Su Xian, Susan Brown Trinidad, Suzanne Bakken, Teri Manolio, Tesfaye Mersha, Thevaa Chandereng, Tian Ge, Todd Edwards, Tom Kaszemacher, Valerie Willis, Vemi Desai, Vimi Desai, Virginia Lorenzi, Vivian Gainer, Wendy Chung, Wu-Chen Su, Xiao Chang, Yiqing Zhao, Yuan Luo, Yufeng Shen
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics.
Assessing the risk of common, complex diseases requires consideration of clinical risk factors as well as monogenic and polygenic risks, which in turn may be reflected in family history. Returning risks to individuals and providers may influence prev