Brandon Colby (English Wikipedia)

Guerrini, Christi J.; Lewellyn, Meaganne; Majumder, Mary A.; Trejo, Meredith; Canfield, Isabel; McGuire, Amy L. (2019). "Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?". BMC Medical Ethics. 20 (1): 84. doi:10.1186/s12910-019-0419-1. ISSN 1472-6939. PMC 6868686. PMID 31752834.
Shady, Amr A.; Colby, Brandon R.; Cunha, Luis F.; Astrin, Kenneth H.; Bishop, David F.; Desnick, Robert J. (2002). "Congenital erythropoietic porphyria: identification and expression of eight novel mutations in the uroporphyrinogen III synthase gene". British Journal of Haematology. 117 (4): 980–987. doi:10.1046/j.1365-2141.2002.03558.x. ISSN 0007-1048. PMID 12060141.

gale.com

Andrea Hoffmann and Panagiotis A Tsonis. Book Review: Outsmart Your Genes Human Genomics 2011, 5:516-517

Guerrini, Christi J.; Lewellyn, Meaganne; Majumder, Mary A.; Trejo, Meredith; Canfield, Isabel; McGuire, Amy L. (2019). "Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?". BMC Medical Ethics. 20 (1): 84. doi:10.1186/s12910-019-0419-1. ISSN 1472-6939. PMC 6868686. PMID 31752834.
Shady, Amr A.; Colby, Brandon R.; Cunha, Luis F.; Astrin, Kenneth H.; Bishop, David F.; Desnick, Robert J. (2002). "Congenital erythropoietic porphyria: identification and expression of eight novel mutations in the uroporphyrinogen III synthase gene". British Journal of Haematology. 117 (4): 980–987. doi:10.1046/j.1365-2141.2002.03558.x. ISSN 0007-1048. PMID 12060141.

Guerrini, Christi J.; Lewellyn, Meaganne; Majumder, Mary A.; Trejo, Meredith; Canfield, Isabel; McGuire, Amy L. (2019). "Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?". BMC Medical Ethics. 20 (1): 84. doi:10.1186/s12910-019-0419-1. ISSN 1472-6939. PMC 6868686. PMID 31752834.

Rabbitt, Meghan (February 24, 2021). "Tips to Outsmart Genetic Health Risks". Prevention. Retrieved July 17, 2024.

DNA Can Guide the Way: Genome Mapping Offers Look Into Medical Future. Corpus Christi Caller - Times, July 07, 2016. https://www.proquest.com/newspapers/dna-can-guide-way/docview/2581329790/se-2 (accessed July 19, 2024).
"Sequencing.com launches genetic data platform". ProQuest. ProQuest 1847407330. Retrieved 2024-07-19.
"VC Health Pulse: Expected Gridlock in Washington Shifts Healthcare VCs' Attention to States; Biotech Startup Juvena Therapeutics Grabs $41 Million." Dow Jones Institutional News, November 10, 2022, https://www.proquest.com/wire-feeds/vc-health-pulse-expected-gridlock-washington/docview/2734893339/se-2 (accessed July 19, 2024).
Kelly, Megyn. A look at the story of Taylor Muhl. Today (Feb 23, 2018), https://www.proquest.com/other-sources/look-at-story-taylor-muhl/docview/2008176519/se-2 (accessed July 19, 2024).

Richards, Sarah Elizabeth (February 5, 2018). "Now You Can Genetically Test Your Child For Disease Risks. Should You?". Smithsonian Magazine. Retrieved July 17, 2024.

Mauriello, Dana (November 2, 2017). "Brandon Colby, MBA '07: Charting the Course for a Predictive Medicine Venture". Stanford Graduate School of Business. Retrieved July 17, 2024.

"Show Synopsis". Thedoctorstv.com. Archived from the original on 2011-04-26. Retrieved 2011-06-01.

"Sequencing.com Raises $5M In Venture Capital". VC News Daily. Massinvestor. November 9, 2022. Retrieved July 18, 2024.

"Show Synopsis". Thedoctorstv.com. Archived from the original on 2011-04-26. Retrieved 2011-06-01.

Guerrini, Christi J.; Lewellyn, Meaganne; Majumder, Mary A.; Trejo, Meredith; Canfield, Isabel; McGuire, Amy L. (2019). "Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?". BMC Medical Ethics. 20 (1): 84. doi:10.1186/s12910-019-0419-1. ISSN 1472-6939. PMC 6868686. PMID 31752834.
Shady, Amr A.; Colby, Brandon R.; Cunha, Luis F.; Astrin, Kenneth H.; Bishop, David F.; Desnick, Robert J. (2002). "Congenital erythropoietic porphyria: identification and expression of eight novel mutations in the uroporphyrinogen III synthase gene". British Journal of Haematology. 117 (4): 980–987. doi:10.1046/j.1365-2141.2002.03558.x. ISSN 0007-1048. PMID 12060141.