Oriane Trouillard

Paris, France

Last Updated: 09/26/2026

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Found 25 publications

Distinct Brain Drivers and Shared Cerebello-Cortical Input in ADCY5 and SGCE Hyperkinetic Movements.

Distinct Brain Drivers and Shared Cerebello-Cortical Input in ADCY5 and SGCE Hyperkinetic Movements.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: February 09, 2026

Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5).

Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5).

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 10, 2025

Deep brain stimulation in patients with mixed movement disorders linked to ADCY5.

Deep brain stimulation in patients with mixed movement disorders linked to ADCY5.

Journal: Revue neurologique

Published: July 02, 2025

Comment on Schwarz et al. "EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder".

Comment on Schwarz et al. "EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder".

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: June 24, 2025

ADCY5-Mosaic Variants: A Diagnosis Not to Be Missed.

ADCY5-Mosaic Variants: A Diagnosis Not to Be Missed.

Journal: Movement disorders clinical practice

Published: March 13, 2025

Comment on "Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals".

Comment on "Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals".

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: February 15, 2024

Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia.

Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 18, 2023

Mirror Movements Due To a TUBB3 Variant.

Mirror Movements Due To a TUBB3 Variant.

Journal: Pediatric neurology

Published: July 09, 2023

Correction: Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome.

Correction: Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome.

Journal: Tremor and other hyperkinetic movements (New York, N.Y.)

Published: June 24, 2023

Congenital mirror movements are associated with defective polymerisation of RAD51.

Congenital mirror movements are associated with defective polymerisation of RAD51.

Journal: Journal of medical genetics

Published: January 27, 2023

SCN1A-related epilepsy with recessive inheritance: Two further families.

SCN1A-related epilepsy with recessive inheritance: Two further families.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: December 02, 2020

Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome.

Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome.

Journal: Tremor and other hyperkinetic movements (New York, N.Y.)

Published: June 25, 2019

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Last Updated: 09/26/2026