Search

Your search keyword '"MacDonald, Jeffrey R."' showing total 42 results

Search Constraints

Start Over You searched for: Author "MacDonald, Jeffrey R." Remove constraint Author: "MacDonald, Jeffrey R." Database Unpaywall Remove constraint Database: Unpaywall
42 results on '"MacDonald, Jeffrey R."'

Search Results

1. Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy

2. Genetic variants inDDX53contribute to Autism Spectrum Disorder associated with the Xp22.11 locus

3. 70. GENE-BASED ANALYSIS OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IDENTIFIES COMMON BIOLOGICAL COMPONENTS BUT DISTINCTLY DIFFERENT GENETIC EFFECTS IN AUTISM AND SCHIZOPHRENIA

4. Gene copy number variation and pediatric mental health/neurodevelopment in a general population

5. Genomic architecture of autism from comprehensive whole-genome sequence annotation

6. Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder

7. Gene copy number variation in pediatric mental illness in a general population

8. Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

9. Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder

10. A large data resource of genomic copy number variation across neurodevelopmental disorders

11. The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants

12. De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy

13. A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data

15. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

16. Genome-wide characteristics of de novo mutations in autism

17. A high-resolution copy-number variation resource for clinical and population genetics

23. Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

26. Towards a comprehensive structural variation map of an individual human genome

27. The Diploid Genome Sequence of an Individual Human

29. Genome assembly comparison identifies structural variants in the human genome

30. Global variation in copy number in the human genome

32. Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy

35. Human Chromosome 7: DNA Sequence and Biology

Catalog

Books, media, physical & digital resources