RefSeq and LocusLink: NCBI gene-centered resources

od Pruitt, Kim D., Maglott, Donna R.
Wydane 2001

NCBI Reference Sequence Project: update and current status

od Pruitt, Kim D., Tatusova, Tatiana, Maglott, Donna R.
Wydane 2003

NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

od Pruitt, Kim D., Tatusova, Tatiana, Maglott, Donna R.
Wydane 2005

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

od Pruitt, Kim D., Tatusova, Tatiana, Maglott, Donna R.
Wydane 2007

NCBI’s LocusLink and RefSeq

od Maglott, Donna R., Katz, Kenneth S., Sicotte, Hugues, Pruitt, Kim D.
Wydane 2000

NCBI Reference Sequences: current status, policy and new initiatives

od Pruitt, Kim D., Tatusova, Tatiana, Klimke, William, Maglott, Donna R.
Wydane 2009

NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy

od Pruitt, Kim D., Tatusova, Tatiana, Brown, Garth R., Maglott, Donna R.
Wydane 2012

Human immunodeficiency virus type 1, human protein interaction database at NCBI

od Fu, William, Sanders-Beer, Brigitte E., Katz, Kenneth S., Maglott, Donna R., Pruitt, Kim D., Ptak, Roger G.
Wydane 2009

Human Variome Project Quality Assessment Criteria for Variation Databases

od Vihinen, Mauno, Hancock, John M., Maglott, Donna R., Landrum, Melissa J., Schaafsma, Gerard C. P., Taschner, Peter
Wydane w Hum Mutat (2016)

ClinVar: public archive of relationships among sequence variation and human phenotype

od Landrum, Melissa J., Lee, Jennifer M., Riley, George R., Jang, Wonhee, Rubinstein, Wendy S., Church, Deanna M., Maglott, Donna R.
Wydane 2014

Clone DB: an integrated NCBI resource for clone-associated data

od Schneider, Valerie A., Chen, Hsiu-Chuan, Clausen, Cliff, Meric, Peter A., Zhou, Zhigang, Bouk, Nathan, Husain, Nora, Maglott, Donna R., Church, Deanna M.
Wydane 2013

Gene: a gene-centered information resource at NCBI

od Brown, Garth R., Hem, Vichet, Katz, Kenneth S., Ovetsky, Michael, Wallin, Craig, Ermolaeva, Olga, Tolstoy, Igor, Tatusova, Tatiana, Pruitt, Kim D., Maglott, Donna R., Murphy, Terence D.
Wydane w Nucleic Acids Res (2014)

The chicken gene nomenclature committee report

od Burt, David W, Carrë, Wilfrid, Fell, Mark, Law, Andy S, Antin, Parker B, Maglott, Donna R, Weber, Janet A, Schmidt, Carl J, Burgess, Shane C, McCarthy, Fiona M
Wydane 2009

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

od 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
Wydane 2014

Using ClinVar as a Resource to Support Variant Interpretations

od Harrison, Steven M., Riggs, Erin R., Maglott, Donna R., Lee, Jennifer M., Azzariti, Danielle R., Niehaus, Annie, Ramos, Erin M., Martin, Christa L., Landrum, Melissa J., Rehm, Heidi L.
Wydane w Curr Protoc Hum Genet (2016)

Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard

od Heale, Bret S.E., Overby, Casey Lynnette, Del Fiol, Guilherme, Rubinstein, Wendy S., Maglott, Donna R., Nelson, Tristan H., Milosavljevic, Aleksandar, Martin, Christa L., Goehringer, Scott R., Freimuth, Robert R., Williams, Marc S.
Wydane w Appl Clin Inform (2016)

Short Communication: Cataloguing the HIV Type 1 Human Protein Interaction Network

od Ptak, Roger G., Fu, William, Sanders-Beer, Brigitte E., Dickerson, Jonathan E., Pinney, John W., Robertson, David L., Rozanov, Mikhail N., Katz, Kenneth S., Maglott, Donna R., Pruitt, Kim D., Dieffenbach, Carl W.
Wydane 2008

ClinGen — The Clinical Genome Resource

od Rehm, Heidi L., Berg, Jonathan S., Brooks, Lisa D., Bustamante, Carlos D., Evans, James P., Landrum, Melissa J., Ledbetter, David H., Maglott, Donna R., Martin, Christa Lese, Nussbaum, Robert L., Plon, Sharon E., Ramos, Erin M., Sherry, Stephen T., Watson, Michael S.
Wydane w N Engl J Med (2015)

ClinVar: public archive of interpretations of clinically relevant variants

od 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.
Wydane w Nucleic Acids Res (2016)

Locus Reference Genomic sequences: an improved basis for describing human DNA variants

od Dalgleish, Raymond, Flicek, Paul, Cunningham, Fiona, Astashyn, Alex, Tully, Raymond E, Proctor, Glenn, Chen, Yuan, McLaren, William M, Larsson, Pontus, Vaughan, Brendan W, Béroud, Christophe, Dobson, Glen, Lehväslaiho, Heikki, Taschner, Peter EM, den Dunnen, Johan T, Devereau, Andrew, Birney, Ewan, Brookes, Anthony J, Maglott, Donna R
Wydane 2010