Katie L Ayers

14PUBLICATIONS
31CO-AUTHORS
Foetal development and medicineHaematological tumoursCancer geneticsCell and nuclear divisionNeurology and neuromuscular diseases
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Publications (14)

|Jul 23, 2026
Post-translational modification of proteins in the human testis development pathway.

|Sep 02, 2024
Biallelic RXFP2 variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesis.

Hannes Syryn, Julie Van de Velde, Griet De Clercq

|Jun 26, 2024
Pharmacogenomic studies of fertility outcomes in pediatric cancer survivors - A systematic review.

Tayla Stenta, Michael Assis, Katie Ayers

|Mar 28, 2024
A Human Homozygous HELQ Missense Variant Does Not Cause Premature Ovarian Insufficiency in a Mouse Model.

Shabnam Bakhshalizadeh, Anthony D Bird, Rajini Sreenivasan

|Jun 15, 2023
Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects.

Katie L Ayers, Stefanie Eggers, Ben N Rollo

|Jun 09, 2023
Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects.

Katie L Ayers, Stefanie Eggers, Ben N Rollo

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Frequent Collaborators

4 joint publications

Elena J Tucker

4 joint publications

Andrew H Sinclair

3 joint publications

Sylvie Jaillard

2 joint publications

Ralf B Schittenhelm