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2. Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndrome.

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

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

5. Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposis

6. IgG4‐related disease: Association with a rare gene variant expressed in cytotoxic T cells

7. IRF2BPL Is Associated with Neurological Phenotypes

8. Neurodegeneration as the presenting symptom in 2 adults with xeroderma pigmentosum complementation group F.

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

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

11. Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

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

13. An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

14. Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

15. Variability of Care Practices for Extremely Early Deliveries.

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

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

20. Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes

21. A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative

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

23. IRF2BPL Is Associated with Neurological Phenotypes

24. Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases

25. MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome

26. Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency

27. Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma

29. Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndrome

31. Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

34. The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases

36. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

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

40. Correction to:An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (Genetics in Medicine, (2021), 23, 4, (740-750), 10.1038/s41436-020-01027-3)

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

43. Adult diagnosis of congenital serine biosynthesis defect: A treatable cause of progressive neuropathy

44. Anti-interleukin-12 antibody for active Crohn's disease

45. Code Blue Events in the Neonatal and Pediatric Intensive Care Units at a Tertiary Care Children's Hospital.

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

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