Carolyn Raski

9PUBLICATIONS
18CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cellular nervous systemMultimorbidityNeurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)
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Publications (9)

|Sep 03, 2026
The Evaluation of Molecular Genetics and Clinical Manifestations in Patients With LZTR1-Associated Noonan Syndrome: A Retrospective Chart Review and Review of Literature.

|Aug 12, 2026
Harmonizing Multi-Institutional Clinical Documentation Using Natural Language Processing in Neurofibromatosis Type 1.

|Nov 11, 2025
Syndrome of the Month: An Update on Smith-Kingsmore Syndrome: Characterization of Developmental Milestones and a Review of the Literature.

Carolyn R Raski, Carlos E Prada

|Aug 29, 2025
Sacroiliac Joint Involvement: An Underreported Complication of NF1.

Jenny P Garzon, Eva Dombi, Jonathan Samet

|Sep 11, 2024
Further Delineation of the Proximal 16p11.2 Microdeletion Syndrome: Novel Findings Among 22 New Individuals.

Anne M McRae, Jaime Duncan, Andy Drackley

|Jul 18, 2024
Expanding the phenotype of neurofibromatosis type 1 microdeletion syndrome.

Jenny P Garzon, Andrea Patete, Lindsey Aschbacher-Smith

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Frequent Collaborators

4 joint publications

Carlos E Prada

3 joint publications

Jenny P Garzon

2 joint publications

Maria P Silva

2 joint publications

Andy Drackley