Alison Garber

ORCID

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 11

Top Venues

American journal of medical genetics. Part A

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Alison Garber, Lisa S Weingarten, Nicolas J Abreu, Houda Zghal Elloumi, Tobias Haack, Clara Hildebrant, Núria Martínez-Gil, Jennifer Mathews, Amelie Johanna Müller, Irene Valenzuela Palafoll, Connolly Steigerwald, Wendy K Chung
Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype. American journal of medical genetics. Part A 194 (7) (2024)
Khemika K Sudnawa, Alison Garber, Ryan Cohen, Sean Calamia, Cara H Kanner, Jacqueline Montes, Jennifer M Bain, Robert J Fee, Wendy K Chung
Clinical phenotypic spectrum of CTNNB1 neurodevelopmental disorder. Clinical genetics 105 (5) (2024)
Alison Garber, Lisa S Weingarten, Nicolas J Abreu, Houda Zghal Elloumi, Tobias Haack, Clara Hildebrant, Núria Martínez-Gil, Jennifer Mathews, Amelie Johanna Müller, Irene Valenzuela Palafoll, Connolly Steigerwald, Wendy K Chung
Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype. American journal of medical genetics. Part A (2024)
Alison Garber, Lisa S Weingarten, Nicolas J Abreu, Houda Zghal Elloumi, Tobias Haack, Clara Hildebrant, Núria Martínez-Gil, Jennifer Mathews, Amelie Johanna Müller, Irene Valenzuela Palafoll, Connolly Steigerwald, Wendy K Chung
Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype. American journal of medical genetics. Part A 194 (7) (2024)
Alison Garber, Lisa S Weingarten, Nicolas J Abreu, Houda Zghal Elloumi, Tobias Haack, Clara Hildebrant, Núria Martínez-Gil, Jennifer Mathews, Amelie Johanna Müller, Irene Valenzuela Palafoll, Connolly Steigerwald, Wendy K Chung
Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype. American journal of medical genetics. Part A (2024)
Alison Garber, Lisa S Weingarten, Nicolas J Abreu, Houda Zghal Elloumi, Tobias Haack, Clara Hildebrant, Núria Martínez-Gil, Jennifer Mathews, Amelie Johanna Müller, Irene Valenzuela Palafoll, Connolly Steigerwald, Wendy K Chung
Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype. American journal of medical genetics. Part A 194 (7) (2024)
Khemika K Sudnawa, Alison Garber, Ryan Cohen, Sean Calamia, Cara H Kanner, Jacqueline Montes, Jennifer M Bain, Robert J Fee, Wendy K Chung
Clinical phenotypic spectrum of CTNNB1 neurodevelopmental disorder. Clinical genetics 105 (5) (2024)
Alison Garber, Lisa S Weingarten, Nicolas J Abreu, Houda Zghal Elloumi, Tobias Haack, Clara Hildebrant, Núria Martínez-Gil, Jennifer Mathews, Amelie Johanna Müller, Irene Valenzuela Palafoll, Connolly Steigerwald, Wendy K Chung
Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype. American journal of medical genetics. Part A 194 (7) (2024)
Khemika K Sudnawa, Alison Garber, Ryan Cohen, Sean Calamia, Cara H Kanner, Jacqueline Montes, Jennifer M Bain, Robert J Fee, Wendy K Chung
Clinical phenotypic spectrum of CTNNB1 neurodevelopmental disorder. Clinical genetics 105 (5) (2024)
Alison Garber, Lisa S Weingarten, Nicolas J Abreu, Houda Zghal Elloumi, Tobias Haack, Clara Hildebrant, Núria Martínez-Gil, Jennifer Mathews, Amelie Johanna Müller, Irene Valenzuela Palafoll, Connolly Steigerwald, Wendy K Chung
Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype. American journal of medical genetics. Part A 194 (7) (2024)
Khemika K Sudnawa, Alison Garber, Ryan Cohen, Sean Calamia, Cara H Kanner, Jacqueline Montes, Jennifer M Bain, Robert J Fee, Wendy K Chung
Clinical phenotypic spectrum of CTNNB1 neurodevelopmental disorder. Clinical genetics (2024)

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Publication Activity (10 Years)

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Alison Garber