Bibliotecas PUC-SP - Busca Integrada

The Foundation of Precision Medicine: Integration of Electronic Health Records with Nenomics Through Basic, Clinical, and Translational Research

Por Mariza de Andrade, Helena Kuivaniemi, Marylyn D. Ritchie
Publicado em 2016

An Efficient Test for Gene-Environment Interaction in Generalized Linear Mixed Models with Family Data

Por Mauricio A. Mazo Lopera, Brandon J. Coombes, Mariza de Andrade
Publicado no International Journal of Environmental Research and Public Health (2017-09-01)

Quantitative trait loci influencing low density lipoprotein particle size in African Americans

Por Iftikhar J. Kullo, Keyue Ding, Eric Boerwinkle, Stephen T. Turner, Mariza de Andrade
Publicado no Journal of Lipid Research (2006-07-01)

Identification of Genetic Interaction with Risk Factors Using a Time-To-Event Model

Por Mariza de Andrade, Sebastian M. Armasu, Bryan M. McCauley, Tanya M. Petterson, John A. Heit
Publicado no International Journal of Environmental Research and Public Health (2017-10-01)

A Digital Health Weight Loss Program in 250,000 Individuals

Por Conor Senecal, Robert Jay Widmer, Beth R. Larrabee, Mariza de Andrade, Lilach O. Lerman, Amir Lerman, Francisco Lopez-Jimenez
Publicado no Journal of Obesity (2020-01-01)

A digital health weight-loss intervention in severe obesity

Por Conor Senecal, Maria Collazo-Clavell, Beth R Larrabee, Mariza de Andrade, Weihua Lin, Bing Chen, Lilach O. Lerman, Amir Lerman, Francisco Lopez-Jimenez
Publicado no Digital Health (2020-03-01)

Leukocyte DNA methylation signature differentiates pancreatic cancer patients from healthy controls.

Por Katrina S Pedersen, William R Bamlet, Ann L Oberg, Mariza de Andrade, Martha E Matsumoto, Hui Tang, Stephen N Thibodeau, Gloria M Petersen, Liang Wang
Publicado no PLoS ONE (2011-03-01)

Lung adenocarcinoma patients with ROS1-rearranged tumors by sex and smoking intensity

Por Yanmei Peng, Vinicius Ernani, Dan Liu, Qian Guo, Markay Hopps, Joseph C. Cappelleri, Ruchi Gupta, Mariza de Andrade, Jun Chen, Eunhee S. Yi, Ping Yang
Publicado no Heliyon (2024-04-01)

Sex‐Specific Genetic Variants are Associated With Coronary Endothelial Dysfunction

Por Satoshi Yoshino, Rebecca Cilluffo, Megha Prasad, Patricia J. M. Best, Elizabeth J. Atkinson, Tatsuo Aoki, Julie M. Cunningham, Mariza de Andrade, Lilach O. Lerman, Amir Lerman
Publicado no Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease (2016-04-01)

The challenge of detecting genotype-by-methylation interaction: GAW20

Por Mariza de Andrade, E. Warwick Daw, Aldi T. Kraja, Virginia Fisher, Lan Wang, Ke Hu, Jing Li, Razvan Romanescu, Jenna Veenstra, Rui Sun, Haoyi Weng, Wenda Zhou
Publicado no BMC Genetics (2018-09-01)

Clinical Correlates of Autosomal Chromosomal Abnormalities in an Electronic Medical Record–Linked Genome-Wide Association Study

Por Hayan Jouni M.D., Khader Shameer Ph.D., Yan W. Asmann Ph.D., Ribhi Hazin M.D., Mariza de Andrade Ph.D., Iftikhar J. Kullo M.D.
Publicado no Journal of Investigative Medicine High Impact Case Reports (2013-10-01)

A genomic pathway approach to a complex disease: axon guidance and Parkinson disease.

Por Timothy G Lesnick, Spiridon Papapetropoulos, Deborah C Mash, Jarlath Ffrench-Mullen, Lina Shehadeh, Mariza de Andrade, John R Henley, Walter A Rocca, J Eric Ahlskog, Demetrius M Maraganore
Publicado no PLoS Genetics (2007-06-01)

GAW20: methods and strategies for the new frontiers of epigenetics and pharmacogenomics

Por Nathan L. Tintle, David W. Fardo, Mariza de Andrade, Stella Aslibekyan, Julia N. Bailey, Justo Lorenzo Bermejo, Rita M. Cantor, Saurabh Ghosh, Philip Melton, Xuexia Wang, Jean W. MacCluer, Laura Almasy
Publicado no BMC Proceedings (2018-09-01)

Familial Lung Cancer: A Brief History from the Earliest Work to the Most Recent Studies

Por Anthony M. Musolf, Claire L. Simpson, Mariza de Andrade, Diptasri Mandal, Colette Gaba, Ping Yang, Yafang Li, Ming You, Elena Y. Kupert, Marshall W. Anderson, Ann G. Schwartz, Susan M. Pinney, Christopher I. Amos, Joan E. Bailey-Wilson
Publicado no Genes (2017-01-01)

Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

Por Kathleen Ferar, Taryn O. Hall, Dana C. Crawford, Robb Rowley, Benjamin A. Satterfield, Rongling Li, Loren Gragert, Elizabeth W. Karlson, Mariza de Andrade, Iftikhar J. Kullo, Catherine A. McCarty, Abel Kho, M. Geoffrey Hayes, Marylyn D. Ritchie, Paul K. Crane, Daniel B. Mirel, Christopher Carlson, John J. Connolly, Hakon Hakonarson, Andrew T. Crenshaw, David Carrell, Yuan Luo, Ozan Dikilitas, Joshua C. Denny, Gail P. Jarvik, David R. Crosslin
Publicado no Scientific Reports (2023-10-01)

Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.

Por Jennifer R Malinowski, Joshua C Denny, Suzette J Bielinski, Melissa A Basford, Yuki Bradford, Peggy L Peissig, David Carrell, David R Crosslin, Jyotishman Pathak, Luke Rasmussen, Jennifer Pacheco, Abel Kho, Katherine M Newton, Rongling Li, Iftikhar J Kullo, Christopher G Chute, Rex L Chisholm, Gail P Jarvik, Eric B Larson, Catherine A McCarty, Daniel R Masys, Dan M Roden, Mariza de Andrade, Marylyn D Ritchie, Dana C Crawford
Publicado no PLoS ONE (2014-01-01)

Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

Por Kathleen Ferar, Taryn O. Hall, Dana C. Crawford, Robb Rowley, Benjamin A. Satterfield, Rongling Li, Loren Gragert, Elizabeth W. Karlson, Mariza de Andrade, Iftikhar J. Kullo, Catherine A. McCarty, Abel Kho, M. Geoffrey Hayes, Marylyn D. Ritchie, Paul K. Crane, Daniel B. Mirel, Christopher Carlson, John J. Connolly, Hakon Hakonarson, Andrew T. Crenshaw, David Carrell, Yuan Luo, Ozan Dikilitas, Joshua C. Denny, Gail P. Jarvik, David R. Crosslin
Publicado no Scientific Reports (2023-11-01)

Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.

Por Yoonjung Yoonie Joo, Jennifer A Pacheco, William K Thompson, Laura J Rasmussen-Torvik, Luke V Rasmussen, Frederick T J Lin, Mariza de Andrade, Kenneth M Borthwick, Erwin Bottinger, Andrew Cagan, David S Carrell, Joshua C Denny, Stephen B Ellis, Omri Gottesman, James G Linneman, Jyotishman Pathak, Peggy L Peissig, Ning Shang, Gerard Tromp, Annapoorani Veerappan, Maureen E Smith, Rex L Chisholm, Andrew J Gawron, M Geoffrey Hayes, Abel N Kho
Publicado no PLoS ONE (2023-01-01)

Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.

Por Andrew McDavid, Paul K Crane, Katherine M Newton, David R Crosslin, Wayne McCormick, Noah Weston, Kelly Ehrlich, Eugene Hart, Robert Harrison, Walter A Kukull, Carla Rottscheit, Peggy Peissig, Elisha Stefanski, Catherine A McCarty, Rebecca Lynn Zuvich, Marylyn D Ritchie, Jonathan L Haines, Joshua C Denny, Gerard D Schellenberg, Mariza de Andrade, Iftikhar Kullo, Rongling Li, Daniel Mirel, Andrew Crenshaw, James D Bowen, Ge Li, Debby Tsuang, Susan McCurry, Linda Teri, Eric B Larson, Gail P Jarvik, Chris S Carlson
Publicado no PLoS ONE (2013-01-01)

Genome-wide study of resistant hypertension identified from electronic health records.

Por Logan Dumitrescu, Marylyn D Ritchie, Joshua C Denny, Nihal M El Rouby, Caitrin W McDonough, Yuki Bradford, Andrea H Ramirez, Suzette J Bielinski, Melissa A Basford, High Seng Chai, Peggy Peissig, David Carrell, Jyotishman Pathak, Luke V Rasmussen, Xiaoming Wang, Jennifer A Pacheco, Abel N Kho, M Geoffrey Hayes, Martha Matsumoto, Maureen E Smith, Rongling Li, Rhonda M Cooper-DeHoff, Iftikhar J Kullo, Christopher G Chute, Rex L Chisholm, Gail P Jarvik, Eric B Larson, David Carey, Catherine A McCarty, Marc S Williams, Dan M Roden, Erwin Bottinger, Julie A Johnson, Mariza de Andrade, Dana C Crawford
Publicado no PLoS ONE (2017-01-01)