25 results on '"Ryan, Niamh M"'
Search Results
2. Investigating copy number variants in schizophrenia pedigrees using a new consensus pipeline called PECAN
3. Investigating the dark-side of the genome: a barrier to human disease variant discovery?
4. Evidence for parent-of-origin effects in autism spectrum disorder: a narrative review
5. Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With Schizophrenia
6. Schizophrenia genomics
7. List of contributors
8. DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders
9. Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disorders
10. Ultra-rare missense variants implicated in Utah pedigrees multiply affected with schizophrenia
11. Altered DNA methylation associated with a translocation linked to major mental illness
12. Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank
13. TU74. A CO-SEGREGATION ANALYSIS OF ULTRA-RARE VARIANTS IN FAMILIES MULTIPLY AFFECTED BY SCHIZOPHRENIA USING WHOLE GENOME SEQUENCING
14. Converting single nucleotide variants between genome builds: from cautionary tale to solution
15. Methyl-CpG2-binding protein 2 mediates overlapping mechanisms across brain disorders
16. Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density
17. Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density
18. Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density
19. Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank
20. Balanced translocation linked to psychiatric disorder, glutamate, and cortical structure/function
21. SuRFing the genomics wave: an R package for prioritising SNPs by functionality
22. BRD7, a Subunit of SWI/SNF Complexes, Binds Directly to BRCA1 and Regulates BRCA1-Dependent Transcription
23. Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density
24. Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density
25. Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density.
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