Jennifer M. Lee

According to our database, Jennifer M. Lee authored at least 5 papers between 2009 and 2018.

Collaborative distances:

• Dijkstra number of five.
• Erdős number of four.

2018

ClinVar: improving access to variant interpretations and supporting evidence.

Melissa J. Landrum, Jennifer M. Lee, Mark Benson, Garth R. Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang, Karen Karapetyan, Kenneth S. Katz, Chunlei Liu, Zenith Maddipatla, Adriana J. Malheiro, Kurt McDaniel, Michael Ovetsky, George R. Riley, George Zhou, J. Bradley Holmes, Brandi L. Kattman, Donna R. Maglott

Nucleic Acids Res., 2018

2016

ClinVar: public archive of interpretations of clinically relevant variants.

Melissa J. Landrum, Jennifer M. Lee, Mark Benson, Garth R. Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Jeffrey Hoover, Wonhee Jang, Kenneth S. Katz, Michael Ovetsky, George R. Riley, Amanjeev Sethi, Ray E. Tully, Ricardo Villamarín-Salomón, Wendy S. Rubinstein, Donna R. Maglott

Nucleic Acids Res., 2016

2014

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

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

Nucleic Acids Res., 2014

2013

The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency.

Wendy S. Rubinstein, Donna R. Maglott, Jennifer M. Lee, Brandi L. Kattman, Adriana J. Malheiro, Michael Ovetsky, Vichet Hem, Vyatcheslav Gorelenkov, Guangfeng Song, Craig Wallin, Nora Husain, Shanmuga Chitipiralla, Kenneth S. Katz, Douglas Hoffman, Wonhee Jang, Mark Johnson, Fedor Karmanov, Alexander Ukrainchik, Mikhail Denisenko, Cathy Fomous, Kathy Hudson, James Ostell

Nucleic Acids Res., 2013

2009

PineSAP - sequence alignment and SNP identification pipeline.

Jill L. Wegrzyn, Jennifer M. Lee, John Liechty, David B. Neale

Bioinform., 2009