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Browsing by Project Canadian Institutes of Health Research (CIHR)
Showing results 1 to 8 of 8
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2021 | A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants![]() | Chawner, Samuel JRA; ...; Čuturilo, Goran | Article | 21a+M21a+ |
| 2017 | Assessment of the ExAC data set for the presence of individuals with pathogenic genotypes implicated in severe Mendelian pediatric disorders | Tarailo-Graovac, Maja; Zhu, Jing Yun Alice; Matthews, Allison; van, Karnebeek Clara DM; Wasserman, Wyeth W | Article | 21a+M21a+ |
| 2025 | Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets![]() | Weisburd, Ben; ...; Perić, Stojan Z. | Article | 21aM21a |
| 2022 | Emerging Clinical Features of COVID-19 Related Pancreatitis: Case Reports and Review of the Literature![]() | Fiore, Vito; Beretta, Rosalba; De Vito, Andrea; Barać, Aleksandra M. | Article | 21aM21a |
| 2021 | Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C![]() | Pelletier, Felixe; ...; Potić, Ana D.; ...; Pekić, Sandra R. | Article | 21aM21a |
| 2019 | Mendelian Randomization and mediation analysis of leukocyte telomere length and risk of lung and head and neck cancers | Kachuri, Linda; ...; Stojsic, Jelena M | Article | 21a+M21a+ |
| 2019 | PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights | Johnstone, Devon L; ...; Tarailo-Graovac, Maja; ...; (broj, koautora 53) | Article | 21a+M21a+ |
| 2024 | The ROMA trial: 7 years of trial activities and the development of the ROMA trial network | Gaudino, Mario; ...; Milojevic, Milan | Article | 21aM21a |
