L. A. Lansdon

Genotype–phenotype correlation in GNB1‐related neurodevelopmental disorder: Potential association of p.Leu95Pro with cleft palate

C. Saunders, L. A. Lansdon, L. Lansdon, 2021, American journal of medical genetics. Part A.

Genome-wide analysis of copy number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes.

Lisa A. Lansdon, K. Mohlke, S. Girirajan, 2022, American journal of human genetics.

The Use of Variant Maps to Explore Domain-Specific Mutations of FGFR1

Lisa A. Lansdon, M. Schnieders, N. Nidey, 2017, Journal of dental research.

Second patient with GNB2-related neurodevelopmental disease: further evidence for a gene-disease association.

Lisa A. Lansdon, C. Saunders, F. del Viso, 2021, European journal of medical genetics.

Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disorders

Lisa A. Lansdon, J. Murray, B. Darbro, 2020, Genesis.