RefSeq and LocusLink: NCBI gene-centered resources

Por Pruitt, Kim D., Maglott, Donna R.
Publicado em 2001

NCBI Reference Sequence Project: update and current status

Por Pruitt, Kim D., Tatusova, Tatiana, Maglott, Donna R.
Publicado em 2003

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

Por Pruitt, Kim D., Tatusova, Tatiana, Maglott, Donna R.
Publicado em 2005

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

Por Pruitt, Kim D., Tatusova, Tatiana, Maglott, Donna R.
Publicado em 2007

NCBI’s LocusLink and RefSeq

Por Maglott, Donna R., Katz, Kenneth S., Sicotte, Hugues, Pruitt, Kim D.
Publicado em 2000

NCBI Reference Sequences: current status, policy and new initiatives

Por Pruitt, Kim D., Tatusova, Tatiana, Klimke, William, Maglott, Donna R.
Publicado em 2009

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

Por Pruitt, Kim D., Tatusova, Tatiana, Brown, Garth R., Maglott, Donna R.
Publicado em 2012

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

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

Human Variome Project Quality Assessment Criteria for Variation Databases

Por Vihinen, Mauno, Hancock, John M., Maglott, Donna R., Landrum, Melissa J., Schaafsma, Gerard C. P., Taschner, Peter
Publicado no Hum Mutat (2016)

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

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

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

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

Gene: a gene-centered information resource at NCBI

Por 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.
Publicado no Nucleic Acids Res (2014)

The chicken gene nomenclature committee report

Por 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
Publicado em 2009

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

Por 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
Publicado em 2014

Using ClinVar as a Resource to Support Variant Interpretations

Por 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.
Publicado no Curr Protoc Hum Genet (2016)

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

Por 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.
Publicado no Appl Clin Inform (2016)

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

Por 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.
Publicado em 2008

ClinGen — The Clinical Genome Resource

Por 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.
Publicado no N Engl J Med (2015)

ClinVar: public archive of interpretations of clinically relevant variants

Por 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.
Publicado no Nucleic Acids Res (2016)

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

Por 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
Publicado em 2010