Publications by authors named "S Baer"

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GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy.
Johannes R Lemke, Andrea Eoli, Ilona Krey, Bernt Popp, Vincent Strehlow, Sarah Baer

Mol Psychiatry· January 2026

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Genome region aware CADD thresholds for noncoding variant prioritization.
Jude-Félix Tenywa, Jean-Baptiste Lamouche, Sarah Baer, Samuel Nicaise, Antony Le Béchec

NAR Genom Bioinform· December 2025

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Ictal Asystole in a Patient With DEE due to an FGF12 Pathogenic Variant: A Reminder to Monitor Cardiac Function.
Johanne Piotrowski, Élise Schaefer, Michael Kuntz, Virginie Bois, Franz Schieffer, Sarah Baer

Clin Genet· October 2025

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Preoperative Onyx embolization of a large facial intraosseous cavernous venous malformation.
Nicole B Duncan, Makayla McCoskey, Kendall Goodyear, Susan C Baer, Karen Brown

Orbit· October 2025

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Systematic analysis of snRNA genes reveals frequent variants in dominant and recessive developmental and epileptic encephalopathies.
Elsa Leitão, Amandine Santini, Benjamin Cogne, Myriam Essid, Maria Athanasiadou, Sarah Baer

medRxiv· September 2025

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