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Works by DaWalt, L.

Results: 3

1

Expansion of the Genotypic and Phenotypic Spectrum of SETD5 Disorder Using Data From the National Brain Gene Registry.

Published in:

Clinical Genetics, 2025, v. 108, n. 3, p. 279, doi. 10.1111/cge.14746

By:

Callahan, Nora C.;
Mahida, Sonal;
Sveden, Abigail;
Quinn, Meg;
Chopra, Maya;
Srivastava, Siddharth;
Wasserstein, M.;
Chopra, M.;
Sahin, M.;
Wangler, M.;
Schultz, B.;
Izumi, K.;
Gropman, A.;
Smith‐Hicks, C.;
Abbeduto, L.;
Hazlett, H.;
German, K.;
DaWalt, L.;
Neul, J.;
Constantino, J.

Publication type:

Article

2

Medication use by adolescents and adults with fragile X syndrome.

Published in:

Journal of Intellectual Disability Research, 2018, v. 62, n. 2, p. 94, doi. 10.1111/jir.12433

By:

Laxman, D. J.;
Greenberg, J. S.;
DaWalt, L. S.;
Hong, J.;
Aman, M. G.;
Mailick, M.

Publication type:

Article

3

Automated extraction of functional biomarkers of verbal and ambulatory ability from multi-institutional clinical notes using large language models.

Published in:

Journal of Neurodevelopmental Disorders, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s11689-025-09612-w

By:

Kaster, Levi;
Hillis, Ethan;
Oh, Inez Y.;
Aravamuthan, Bhooma R.;
Lanzotti, Virginia C.;
Vickstrom, Casey R.;
Wasserstein, M;
Chopra, M;
Sahin, M;
Wangler, M;
Schultz, B;
Izumi, K;
Bergner, S;
Gropman, A;
Smith-Hicks, C;
Abbeduto, L;
Hazlett, H;
Doherty, D;
German, K;
DaWalt, L

Publication type:

Article