Lyndon Gallacher

9PUBLICATIONS
122CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Medical biotechnology diagnostics (incl. biosensors)Epigenetics (incl. genome methylation and epigenomics)
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Publications (9)

|Jul 26, 2024
Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.

Dana E Layo-Carris, Emily E Lubin, Annabel K Sangree

|Jul 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.

Yuyang Chen, Ruebena Dawes, Hyung Chul Kim

|Apr 27, 2024
Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.

Dana E Layo-Carris, Emily E Lubin, Annabel K Sangree

|Apr 22, 2024
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders.

Yuyang Chen, Ruebena Dawes, Hyung Chul Kim

|Apr 18, 2024
"Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance.

Cassandra Muller, Lyndon Gallacher, Louise Keogh

|Feb 08, 2024
Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis.

Monica H Wojcik, Gabrielle Lemire, Maha S Zaki

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Frequent Collaborators

3 joint publications

Zornitza Stark

3 joint publications

Tiong Yang Tan

2 joint publications

Samantha Ayres

2 joint publications

Alison G Compton