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You searched for: Author/Creator Swertz, Morris A.

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1. A pipeline‐friendly software tool for genome diagnostics to prioritize genes by matching patient symptoms to literature. Issue 1 (10th August 2020)

2. A pipeline‐friendly software tool for genome diagnostics to prioritize genes by matching patient symptoms to literature. Issue 1 (10th August 2020)

3. Advancing tools for human early lifecourse exposome research and translation (ATHLETE): Project overview. Issue 5 (1st October 2021)

4. An Overview and Online Registry of Microvillus Inclusion Disease Patients and their MYO5B Mutations. Issue 12 (16th October 2013)

5. CoNVaDING: Single Exon Variation Detection in Targeted NGS Data. Issue 5 (24th February 2016)

6. Evaluation of CADD Scores in Curated Mismatch Repair Gene Variants Yields a Model for Clinical Validation and Prioritization. Issue 7 (20th May 2015)

7. Life course of retrospective harmonization initiatives: key elements to consider. (12th April 2023)

8. Metabolic Age Based on the BBMRI-NL 1H-NMR Metabolomics Repository as Biomarker of Age-related Disease. (October 2020)

9. MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Issue 3 (17th January 2018)

10. Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs. (April 2016)