The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic Variants

The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic Variants

<div><p>Approximately 0.5–1.4% of natal males and 0.2–0.3% of natal females meet DSM-5 criteria for gender dysphoria, with many of these individuals self-describing as transgender men or women. Despite recent improvements both in social acceptance of transgender individuals as well as ac...

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Bibliographic Details
Main Author: J. Graham Theisen (18618646) (author)
Other Authors: Viji Sundaram (18618649) (author), Mary S. Filchak (18618652) (author), Lynn P. Chorich (14776984) (author), Megan E. Sullivan (15016457) (author), James Knight (3664885) (author), Hyung-Goo Kim (728597) (author), Lawrence C. Layman (13913559) (author)
Published: 2019
Subjects:
Biological sciences
Genetics
Gender Dysphoria
Transgender
DSM-5
Social Acceptance
Gender Affirming Therapy
Etiology
Genetic Contribution
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