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Authors
Glessner, Joseph T. http://orcid.org/0000-0001-5131-2811
Khan, Munir E.
Chang, Xiao
Liu, Yichuan
Otieno, F. George
Lemma, Maria
Slaby, Isabella
Hain, Heather
Mentch, Frank
Li, Jin
Kao, Charlly
Sleiman, Patrick M. A.
March, Michael E.
Connolly, John
Hakonarson, Hakon
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Funding
Funding for this research was provided by:
National Human Genome Research Institute (5U01HG011175-03, U01-HG006830)
Eunice Kennedy Shriver National Institute of Child Health and Human Development (U54-HD086984)
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Article History
Received: 3 October 2022
Accepted: 6 April 2023
First Online: 29 April 2023
Declarations
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: All subjects were recruited through IRB-approved protocols. Participants enrolled in various studies and completed a broad informed consent, including consent for prospective analyses of EHRs. Confidentiality is guarded to address issues of privacy and insurability. Each subject is assigned a study number upon recruitment, using complex algorithms to remove personal identification. Encrypted patient data is integrated into the lab’s custom phenotype browser, where it can be coupled with genotyping and sequencing data.
: Not applicable.
: The authors declare that they have no competing interests.
