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Blood|December 16, 2006
Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)Takashi Akasaka, Theodore Balasas, Lisa J Russell, et al.
Early Human Development|December 1, 2025
Universal maternal testing for group B streptococcus in late pregnancy: process outcomes and alongside qualitative study for the GBS3 trialJane P Daniels, Kate F Walker, Lucy Bradshaw, et al.
BMJ Open|June 17, 2025
Routine testing for group B streptococcus in pregnancy: protocol for a UK cluster randomised trial (GBS3)Jane Daniels, Kate Walker, Lucy Bradshaw, et al.
Plos Genetics|April 14, 2020
A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver diseaseConnor A Emdin, Mary E Haas, Amit V Khera, et al.
Plos Genetics|April 6, 2021
Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver diseaseConnor A Emdin, Mary E Haas, Amit V Khera, et al.
Oncogene|October 24, 2018
BMI1 is a therapeutic target in recurrent medulloblastomaDavid Bakhshinyan, Chitra Venugopal, Ashley A Adile, et al.
Frontiers in Nutrition|November 29, 2023
A multi-center prospective study of plant-based nutritional support in adult community-based patients at risk of disease-related malnutritionMarta Delsoglio, Corbin Griffen, Rakshan Syed, et al.
Nature Biotechnology|May 2, 2025
The TransEuro open-label trial of human fetal ventral mesencephalic transplantation in patients with moderate Parkinson's diseaseRoger A Barker, Nicholas P Lao-Kaim, Natalie Valle Guzman, et al.
Blood|July 11, 2024
Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predispositionJiarna R Zerella, Claire C Homan, Peer Arts, et al.
Blood Advances|March 26, 2020
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AMLAnna L Brown, Peer Arts, Catherine L Carmichael, et al.
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