Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants

Yazar: MacArthur, Jacqueline A. L., Morales, Joannella, Tully, Ray E., Astashyn, Alex, Gil, Laurent, Bruford, Elspeth A., Larsson, Pontus, Flicek, Paul, Dalgleish, Raymond, Maglott, Donna R., Cunningham, Fiona
Baskı/Yayın Bilgisi 2014

ClinVar: public archive of interpretations of clinically relevant variants

Yazar: Landrum, Melissa J., Lee, Jennifer M., Benson, Mark, Brown, Garth, Chao, Chen, Chitipiralla, Shanmuga, Gu, Baoshan, Hart, Jennifer, Hoffman, Douglas, Hoover, Jeffrey, Jang, Wonhee, Katz, Kenneth, Ovetsky, Michael, Riley, George, Sethi, Amanjeev, Tully, Ray, Villamarin-Salomon, Ricardo, Rubinstein, Wendy, Maglott, Donna R.
Yayımlandı Nucleic Acids Res (2016)

Systematic documentation and analysis of human genetic variation using the microattribution approach

Yazar: Giardine, Belinda, Borg, Joseph, Higgs, Douglas R., Peterson, Kenneth R., Maglott, Donna, Basak, A. Nazli, Clark, Barnaby, Faustino, Paula, Felice, Alex E., Francina, Alain, Gallivan, Monica V. E., Georgitsi, Marianthi, Gibbons, Richard J., Giordano, Piero C., Harteveld, Cornelis L., Joly, Philippe, Kanavakis, Emmanuel, Kollia, Panagoula, Menzel, Stephan, Miller, Webb, Moradkhani, Kamran, Old, John, Papachatzopoulou, Adamantia, Papadakis, Manoussos N., Papadopoulos, Petros, Pavlovic, Sonja, Philipsen, Sjaak, Radmilovic, Milena, Riemer, Cathy, Schrijver, Iris, Stojiljkovic, Maja, Thein, Swee Lay, Traeger-Synodinos, Jan, Tully, Ray, Wada, Takahito, Waye, John, Wiemann, Claudia, Zukic, Branka, Chui, David H. K., Wajcman, Henri, Hardison, Ross C., Patrinos, George P.
Baskı/Yayın Bilgisi 2011