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Katie Ayers

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Group Leader

Murdoch Childrens Research Institute

Australia

Research Interests

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Professors in Australia Professors in Biochemistry Biochemistry professors in Australia

Recent Grants

Grant: Close

Discovering new drugs for epilepsy using personalised medicine.

Open Date: 2020-01-01

Close Date: 2021-01-01

Grant: Close

A novel role for spliceosome dysfunction in gonadal dysgenesis and intellectual disability.

Open Date: 2019-01-01

Close Date: 2021-01-01

Grant: Close

Stem cell models for DSD

Open Date: 2019-01-01

Close Date: 2020-01-01

Articles (18)

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2025

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2025

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2023

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2023

Collaborators (8)

David Arthur Stroud

Associate Professor

University of Melbourne

AUSTRALIA

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Hedi L. Claahsen - van der Grinten

Professor, MD, PhD

Radboud University Medical Center

NETHERLANDS

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Sumudu Amarasekera

University of Melbourne

AUSTRALIA

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Rachel Conyers

Group Leader

Murdoch Childrens Research Institute

AUSTRALIA

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David Elliott

Group Leader

Murdoch Childrens Research Institute

AUSTRALIA

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Andrea Simpson

Monash Health

AUSTRALIA

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Elena Tucker

Murdoch Childrens Research Institute

AUSTRALIA

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Michael Assis

Murdoch Childrens Research Institute

AUSTRALIA

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Katie Ayers

Research Interests

Make your next move.

Explore related searches

Recent Grants

Articles (18)

Challenges in Care Provision for Children and Adolescents With Differences of Sex Development.

Functional analysis of SRY variants in individuals with 46,XY differences of sex development.

Functional characterization of human recessive DIS3 variants in premature ovarian insufficiency†.

A Human Homozygous <i>HELQ</i> Missense Variant Does Not Cause Premature Ovarian Insufficiency in a Mouse Model

Pharmacogenomic studies of fertility outcomes in pediatric cancer survivors – A systematic review

Biallelic RXFP2 variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesis

Generation of a homozygous (MCRIi031-A-3) WT1 knockout human iPSC line

Generation of heterozygous (MCRIi031-A-1) and homozygous (MCRIi031-A-2) SOX9 knockout human iPSC lines

Genomic testing for differences of sex development: Practices and perceptions of clinicians.

Consider CUX1 variants in children with a variation of sex development: a case report and review of the literature.

Genomic technologies and the diagnosis of 46, XY differences of sex development

Diverse genetic causes of amenorrhea in an ethnically homogeneous cohort and an evolving approach to diagnosis

Biallelic FANCA variants detected in sisters with isolated premature ovarian insufficiency.

Generation of heterozygous (MCRIi030-A-1) and homozygous (MCRIi030-A-2) NR2F2/COUP-TFII knockout human iPSC lines.

COUP-TFII regulates early bipotential gonad signaling and commitment to ovarian progenitors

Genetic control of fetal sex development

Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiency

Lessons Learned from 17 Years of Multidisciplinary Care for Differences of Sex Development Patients at a Single Indonesian Center

Collaborators (8)

David Arthur Stroud

Hedi L. Claahsen - van der Grinten

Sumudu Amarasekera

Rachel Conyers

David Elliott

Andrea Simpson

Elena Tucker

Michael Assis

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