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You searched for: Author/Creator Sanders, Stephan J.

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1. A biomedical open knowledge network harnesses the power of AI to understand deep human biology. Issue 1 (31st March 2022)

2. Assessing the utility of electronic measures as a proxy for cognitive ability. Issue 6 (12th March 2022)

4. Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis. Issue 3 (March 2021)

5. Harnessing rare variants in neuropsychiatric and neurodevelopment disorders—a Keystone Symposia report. Issue 1 (2nd August 2021)

7. Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2. Issue 3 (12th May 2014)

8. Patterns of delay in early gross motor and expressive language milestone attainment in probands with genetic conditions versus idiopathic ASD from SFARI registries. (12th August 2021)

9. Prenatal Somatic Cell Gene Therapies: Charting a Path Toward Clinical Applications (Proceedings of the CERSI‐FDA Meeting). (15th September 2022)

10. Progress in Understanding and Treating SCN2A-Mediated Disorders. Issue 7 (July 2018)