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3. OXR1 maintains the retromer to delay brain aging under dietary restriction

5. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

6. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

7. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

9. Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

10. Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

11. Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma

12. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

13. Improving access to exome sequencing in a medically underserved population through the Texome Project

14. De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features

16. De novo variants in DENND5B cause a neurodevelopmental disorder

17. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

18. Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development

19. Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies

20. Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care

21. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

22. A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins

23. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

24. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

25. De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

26. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

29. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

32. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

34. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

36. Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability.

47. Daam2 phosphorylation by CK2α negatively regulates Wnt activity during white matter development and injury.

48. Safeguarding gene drive experiments in the laboratory: Multiple stringent confinement strategies should be used whenever possible

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