Meghan R Mulligan

4PUBLICATIONS
17CO-AUTHORS
Medical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)Molecular targetsGenome structure and regulation
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Publications (4)

|Oct 22, 2026
Meier-GORLIN Syndrome Caused by Compound Heterozygous CDC6 Variants.

|Jul 18, 2026
Strømme syndrome: the clinical and molecular spectrum associated with variants in CENPF.

|Mar 21, 2025
XRCC4-related microcephalic primordial dwarfism: description of a clinical series of 7 cases, phenotype expansion and new diagnostic approaches.

Silvestre Cuinat, Nicolas Chatron, Florence Petit

|Sep 11, 2023
The molecular genetics of nELAVL in brain development and disease.

Meghan R Mulligan, Louise S Bicknell

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Frequent Collaborators

4 joint publications

Louise S Bicknell

1 joint publications

Silvestre Cuinat

1 joint publications

Nicolas Chatron

1 joint publications

Perrine Brunelle