D. Alankarage

Dataset of differentially expressed genes in mouse P12 testes in response to the loss of ATRX in Sertoli cells

V. Harley, S. Bagheri-Fam, D. Alankarage, 2022, Data in brief.

Disorders of Sex Development Loci

V. Harley, R. Sreenivasan, D. Alankarage, 2016 .

Functional genomics and gene-environment interaction highlight the complexity of Congenital Heart Disease caused by Notch pathway variants.

S. Grieve, E. Giannoulatou, S. Dunwoodie, 2019, Human molecular genetics.

Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease

E. Giannoulatou, S. Dunwoodie, N. Pachter, 2020 .

Functional characterisation of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease.

E. Giannoulatou, S. Dunwoodie, N. Pachter, 2019, Human molecular genetics.

Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factors.

D. Humphreys, P. Giampietro, S. Dunwoodie, 2022, Differentiation; research in biological diversity.

Identification of clinically actionable variants from genome sequencing of families with congenital heart disease

Jacob T. Munro, D. Humphreys, E. Giannoulatou, 2018, Genetics in Medicine.

SOX9 regulates expression of the male fertility gene Ets variant factor 5 (ETV5) during mammalian sex development.

P. Koopman, T. Svingen, V. Harley, 2016, The international journal of biochemistry & cell biology.

Identification of clinically actionable variants from genome sequencing of families with congenital heart disease

Jacob T. Munro, D. Humphreys, E. Giannoulatou, 2018, Genetics in Medicine.