Scott, Hamish S.

Modifiers of epigenetic reprogramming show paternal effects in the mouse

Chong, S., Vickaryous, N., Ashe, A., Zamudio, N., Youngson, N., Hemley, S., Stopka, T., Skoultchi, A., Matthews, J., Scott, H. S., et al. (2007) · Nature Genetics

Epigenetics and DNA MethylationGenetic Syndromes and Imprinting

Cited by 166

Genomic subtyping and therapeutic targeting of acute erythroleukemia

Iacobucci, I., Wen, J., Meggendorfer, M., Choi, J. K., Shi, L., Pounds, S. B., Carmichael, C. L., Masih, K. E., Morris, S. M., Lindsley, R. C., et al. (2019) · Nature Genetics

Acute Myeloid Leukemia ResearchAcute Lymphoblastic Leukemia research

Cited by 155

ARMC5 Mutations Are Common in Familial Bilateral Macronodular Adrenal Hyperplasia

Gagliardi, L., Schreiber, A. W., Hahn, C. N., Feng, J., Cranston, T., Boon, H., Hotu, C., Oftedal, B. E., Cutfield, R., Adelson, D. L., et al. (2014) · The Journal of Clinical Endocrinology & Metabolism

Adrenal and Paraganglionic TumorsAdrenal Hormones and Disorders

Cited by 121

The mutational burden of therapy-related myeloid neoplasms is similar to primary myelodysplastic syndrome but has a distinctive distribution

Singhal, D., Wee, L. Y. A., Kutyna, M. M., Chhetri, R., Geoghegan, J., Schreiber, A. W., Feng, J., Wang, P. P.-S., Babic, M., Parker, W. T., et al. (2019) · Leukemia

Acute Myeloid Leukemia ResearchMultiple and Secondary Primary Cancers

Cited by 62

Molecular Defects in Sanfilippo Syndrome Type A

Blanch, L., Weber, B., Guo, X.-H., Scott, H. S., & Hopwood, J. J. (1997) · Human Molecular Genetics

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 62

Evidence-based risk stratification of myeloid neoplasms harboring TP53 mutations

Shah, M. V., Hung, K., Baranwal, A., Kutyna, M. M., Al-Kali, A., Toop, C., Greipp, P., Brown, A., Shah, S., Khanna, S., et al. (2025) · Blood Advances

Acute Myeloid Leukemia ResearchChronic Myeloid Leukemia Treatments

Cited by 23

Circular RNAs accumulate in ageing human placental tissue and in stillbirth, leading to DNA damage and cellular senescence

Arthurs, A. L., Jackson, M. R., McCullough, D., Scott, H. S., Barnett, C. P., Webb, S. T., Smith, M. D., Jankovic-Karasoulos, T., Dekker, G. A., & Roberts, C. T. (2024) · American Journal of Obstetrics and Gynecology

Circular RNAs in diseasesTelomeres, Telomerase, and Senescence

Cited by 6