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6. Spectrum of germline pathogenic variants using a targeted next generation sequencing panel and genotype-phenotype correlations in patients with suspected hereditary breast cancer at an academic medical centre in Pakistan

8. Outcomes of locally advanced gastric and gastroesophageal adenocarcinoma cancers treated with neoadjuvant FLOT in a tertiary care hospital in Pakistan.

9. Innovations in Artificial Intelligence-Driven Breast Cancer Survival Prediction: A Narrative Review.

14. Overall Survival and the Impact of Albumin-bilirubin Grade in Patients with Advanced Hepatocellular Carcinoma: Data from a Tertiary Care Hospital in a Lower-middle-income Country.

22. Healthcare professionals’ perceptions of implementing a decision support intervention for cascade screening for beta-thalassemia in Pakistan

31. Additional file 1 of Spectrum of germline pathogenic variants using a targeted next generation sequencing panel and genotype-phenotype correlations in patients with suspected hereditary breast cancer at an academic medical centre in Pakistan

32. Additional file 2 of Spectrum of germline pathogenic variants using a targeted next generation sequencing panel and genotype-phenotype correlations in patients with suspected hereditary breast cancer at an academic medical centre in Pakistan

35. Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration

36. Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation Amelogenesis imperfecta

41. Mutations in microcephalin cause aberrant regulation of chromosome condensation

42. Protein-truncating mutations in ASPM cause variable reduction in brain size

43. Identification of microcephalin, a protein implicated in determining the size of the human brain

46. Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter

48. Decision making on antenatal screening results: A comparative Q‐method study of women from two Chinese cities.

49. A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration

50. Transforming Health in One Hundred Days: Key Achievements.

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