Peter Hillmen

SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage

Ruth Clifford, Tania Louis, Pauline Robbe et al. · Blood · 2013 · 228 citations

Life Sciences, Genetics, Molecular Genetics +11

Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency

António Almeida, Yoshiko Murakami, D. Mark Layton et al. · Nature Medicine · 2006 · 224 citations

Life Sciences, Genetics, Molecular Biology +16

Eculizumab prevents intravascular hemolysis in patients with paroxysmal nocturnal hemoglobinuria and unmasks low-level extravascular hemolysis occurring through C3 opsonization

Anita Hill, Russell P. Rother, L Arnold et al. · Haematologica · 2010 · 191 citations · Full text

Medicine, Clinical Sciences, Hematology +15

Chronic Lymphocytic Leukemia Therapy Guided by Measurable Residual Disease

Talha Munir, David A. Cairns, Adrian Bloor et al. · New England Journal of Medicine · 2023 · 155 citations · Full text

Medicine, Oncology, Pharmacotherapy +12

Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia

Michael Kirwan, Tom Vulliamy, Anna Marrone et al. · Human Mutation · 2009 · 110 citations

Medicine, Genetics, Molecular Genetics +17