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1. Influence of surface relaxations on atomic-resolution imaging of a charge density wave material

2. Activating the fluorescence of a Ni(II) complex by energy transfer

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

4. Bipolar single-molecule electroluminescence and electrofluorochromism

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

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

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

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

9. Thermally-induced magnetic order from glassiness in elemental neodymium

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

11. Creating tunable and coupled Rashba-type quantum dots atom-by-atom

12. De novo variants in DENND5B cause a neurodevelopmental disorder

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

14. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

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

16. Plasmon-driven motion of an individual molecule

17. Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases.

18. Lethal neonatal respiratory failure due to biallelic variants in BBS1 and monoallelic variant in TTC21

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

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

24. Quantifying Exchange Forces of a Non-Collinear Magnetic Structure on the Atomic Scale

25. Self-induced spin glass state in elemental and crystalline neodymium

26. Anisotropic two-dimensional screening at the surface of black phosphorus

27. Designer quantum states of matter created atom-by-atom

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

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

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

38. An orbitally derived single-atom magnetic memory

39. Design and performance of an ultra-high vacuum spin-polarized scanning tunneling microscope operating at 30 mK and in a vector magnetic field

40. Revealing the correlation between real-space structure and chiral magnetic order at the atomic scale

41. Sensing Noncollinear Magnetism at the Atomic Scale Combining Magnetic Exchange and Spin-Polarized Imaging

42. De novo variants in DENND5B cause a neurodevelopmental disorder

43. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

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

45. Adsorption and STM imaging of tetracyanoethylene on Ag(001): An ab-initio study

46. Absence of superconductivity in ultra-thin layers of FeSe synthesized on a topological insulator

47. Visualizing improved spin coupling in molecular magnets

48. Single-layer MoS$_2$ on Au(111): band gap renormalization and substrate interaction

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