RaeLynn Forsyth

5PUBLICATIONS
29CO-AUTHORS
Developmental genetics (incl. sex determination)NeurogeneticsClinical midwiferyNeonatologyWork integrated learning (incl. internships)
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Publications (5)

|Aug 13, 2026
Conundrum resolved by optical genome mapping in a 46,XY girl with difference in sex development and skeletal anomalies.

|Aug 06, 2026
Equivalent gain-of-function variants in KCNK3 and KCNK9 and their contribution to distinct TASK K2P channelopathies.

|May 08, 2023
The remarkable journey of one female individual with ornithine transcarbamylase deficiency diagnosed post-mortem.

RaeLynn Forsyth, Ryan H Peretz, Angela Dempsey

|Mar 21, 2022
Systematic analysis of physical examination characteristics of 94 individuals with Joubert syndrome: Keys to suspecting the diagnosis.

RaeLynn Forsyth, Melissa A Parisi, Burak Altintas

|Dec 14, 2019
A structured genetics rotation for pediatric residents: an important educational opportunity.

RaeLynn Forsyth, Weiyi Mu, Laura Gibson

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Frequent Collaborators

1 joint publications

Melissa A Parisi

1 joint publications

Jasmine Knoll

1 joint publications

Ryan H Peretz

1 joint publications

Kate M Crowther