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1. Complement genes contribute sex-biased vulnerability in diverse disorders

2. Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

3. Genome-wide association analysis identifies 13 new risk loci for schizophrenia

4. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.

5. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

6. Supplementary Glioma Genes from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

7. Supplementary Information from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

8. Data from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

9. Supplementary Glioma Gene Mutations from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

11. A polygenic resilience score moderates the genetic risk for schizophrenia

12. Prevalence and architecture of de novo mutations in developmental disorders

13. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

14. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

16. Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B.1.1.7

17. Signatures of mutation and selection in the cancer genome

18. Mutations in the BRWD3 gene cause X- linked mental retardation associated with macrocephaly

19. Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause x-linked mental retardation associated with a marfanoid habitus

20. Patterns of somatic mutation in human cancer genomes

21. Mutations in the gene encoding the sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation

22. The zebrafish reference genome sequence and its relationship to the human genome

24. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

25. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

26. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

27. Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

28. Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

29. Genome-wide estimates of inbreeding in unrelated individuals and their association with cognitive ability

30. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

31. A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

32. Common variant at 16p11.2 conferring risk of psychosis

33. Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

34. Genetic comorbidities in Parkinson's disease

35. A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies

36. Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

37. Genome-wide association analysis identifies 13 new risk loci for schizophrenia

38. Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

39. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

40. A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility

41. Lung cancer: Intragenic ERBB2 kinase mutations in tumours

42. Erratum: Corrigendum: The zebrafish reference genome sequence and its relationship to the human genome

43. Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

44. Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

45. GLO1—A novel amplified gene in human cancer

46. A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

47. Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

48. X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

49. Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

50. Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly, Central Obesity, Hypogonadism, Pes Cavus, and Tremor

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