PineSAP - sequence alignment and SNP identification pipeline. - Jill L. Wegrzyn; Jennifer M. Lee; John Liechty; David B. Neale (Bioinform., 2009)

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; et al. (Nucleic Acids Res., 2013)

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)

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; et al. (Nucleic Acids Res., 2016)

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; et al. (Nucleic Acids Res., 2018)