OMIA (Online Mendelian Inheritance in Animals): an enhanced platform and integration into the Entrez search interface at NCBI

Por Lenffer, Johann, Nicholas, Frank W., Castle, Kao, Rao, Arjun, Gregory, Stefan, Poidinger, Michael, Mailman, Matthew D., Ranganathan, Shoba
Publicado em 2006

PlasmoDB: the Plasmodium genome resource. A database integrating experimental and computational data

Por Bahl, Amit, Brunk, Brian, Crabtree, Jonathan, Fraunholz, Martin J., Gajria, Bindu, Grant, Gregory R., Ginsburg, Hagai, Gupta, Dinesh, Kissinger, Jessica C., Labo, Philip, Li, Li, Mailman, Matthew D., Milgram, Arthur J., Pearson, David S., Roos, David S., Schug, Jonathan, Stoeckert, Christian J., Whetzel, Patricia
Publicado em 2003

The NCBI dbGaP database of genotypes and phenotypes

Por Mailman, Matthew D., Feolo, Michael, Jin, Yumi, Kimura, Masato, Tryka, Kimberly, Bagoutdinov, Rinat, Hao, Luning, Kiang, Anne, Paschall, Justin, Phan, Lon, Popova, Natalia, Pretel, Stephanie, Ziyabari, Lora, Shao, Yu, Wang, Zhen Y., Sirotkin, Karl, Ward, Minghong, Kholodov, Michael, Zbicz, Kerry, Beck, Jeffrey, Kimelman, Michael, Shevelev, Sergey, Preuss, Don, Yaschenko, Eugene, Graeff, Alan, Ostell, James, Sherry, Stephen T.
Publicado em 2007

Amyotrophic Lateral Sclerosis: An Emerging Era of Collaborative Gene Discovery

Por Gwinn, Katrina, Corriveau, Roderick A., Mitsumoto, Hiroshi, Bednarz, Kate, Brown, Robert H., Cudkowicz, Merit, Gordon, Paul H., Hardy, John, Kasarskis, Edward J., Kaufmann, Petra, Miller, Robert, Sorenson, Eric, Tandan, Rup, Traynor, Bryan J., Nash, Josefina, Sherman, Alex, Mailman, Matthew D., Ostell, James, Bruijn, Lucie, Cwik, Valerie, Rich, Stephen S., Singleton, Andrew, Refolo, Larry, Andrews, Jaime, Zhang, Ran, Conwit, Robin, Keller, Margaret A.
Publicado em 2007

Identifying amyloid pathology–related cerebrospinal fluid biomarkers for Alzheimer's disease in a multicohort study

Por Leung, Yuk Yee, Toledo, Jon B., Nefedov, Alexey, Polikar, Robi, Raghavan, Nandini, Xie, Sharon X., Farnum, Michael, Schultz, Tim, Baek, Young, Van Deerlin, Vivianna M., Hu, William T., Holtzman, David M., Fagan, Anne M., Perrin, Richard J., Grossman, Murray, Soares, Holly D., Kling, Mitchel A., Mailman, Matthew, Arnold, Steven E., Narayan, Vaibhav A., Lee, Virginia M-Y., Shaw, Leslie M., Baker, David, Wittenberg, Gayle M., Trojanowski, John Q., Wang, Li-San
Publicado no Alzheimers Dement (Amst) (2015)

The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports

Por Cupples, L Adrienne, Arruda, Heather T, Benjamin, Emelia J, D'Agostino, Ralph B, Demissie, Serkalem, DeStefano, Anita L, Dupuis, Josée, Falls, Kathleen M, Fox, Caroline S, Gottlieb, Daniel J, Govindaraju, Diddahally R, Guo, Chao-Yu, Heard-Costa, Nancy L, Hwang, Shih-Jen, Kathiresan, Sekar, Kiel, Douglas P, Laramie, Jason M, Larson, Martin G, Levy, Daniel, Liu, Chun-Yu, Lunetta, Kathryn L, Mailman, Matthew D, Manning, Alisa K, Meigs, James B, Murabito, Joanne M, Newton-Cheh, Christopher, O'Connor, George T, O'Donnell, Christopher J, Pandey, Mona, Seshadri, Sudha, Vasan, Ramachandran S, Wang, Zhen Y, Wilk, Jemma B, Wolf, Philip A, Yang, Qiong, Atwood, Larry D
Publicado em 2007