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2. Survey of the training needs of genetic assistants supports the creation of genetic assistant training programs.

3. U.S. Efforts in Support of Examinations at Fukushima Daiichi - November 2022 Meeting Notes and Information Request Status

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

6. U.S. Efforts in Support of Examinations at Fukushima Daiichi - November 2021 Meeting Notes with Updated Information Requests

8. Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network

9. U.S. Effort Support to Examinations at Fukushima - November 2019 Meeting Notes with Updated Information Requests

10. Intercontinental collaboration in clinical trials for children and adolescents with cancer—A systematic review by ACCELERATE

11. U.S. Efforts in Support of Examinations at Fukushima Daiichi - 2019 Evaluations

12. Effects of foot orthoses on the biomechanics of the lower extremities in adults with and without musculoskeletal disorders during functional tasks: A systematic review

15. De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

17. Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy

19. A Rapidly Progressive Case of Ectopic Adrenocorticotropic Hormone (ACTH) Syndrome

23. One is the loneliest number: genotypic matchmaking using the electronic health record

24. Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification

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

30. Fresh water skin disease in dolphins: a case definition based on pathology and environmental factors in Australia

31. Three-dimensional Medipix--a new generation of x-ray detectors

32. US Efforts in Support of Examinations at Fukushima Daiichi – 2016 Evaluations

34. Application of broad-spectrum, sequence-based pathogen identification in an urban population.

35. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

37. De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

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

44. Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy

47. Reactor Safety Gap Evaluation of Accident Tolerant Components and Severe Accident Analysis

48. De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Callosum, Axon, Cardiac, Ocular, and Genital Defects

49. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

50. Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned from ClinGen and eMERGE

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