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American Journal of Obstetrics & Gynecology MFM|November 20, 2023
Placenta accreta spectrum care infrastructure: an evidence-based review of needed resources supporting placenta accreta spectrum careGarrett D Fitzgerald, J M Newton, Lamia Atasi, et al.
Clinical Endocrinology|September 24, 2021
SDHC phaeochromocytoma and paraganglioma: A UK-wide case seriesSophie T Williams, Prodromos Chatzikyriakou, Paul V Carroll, et al.
Cancer Cell|May 16, 2018
Molecular, Pathological, Radiological, and Immune Profiling of Non-brainstem Pediatric High-Grade Glioma from the HERBY Phase II Randomized TrialAlan Mackay, Anna Burford, Valeria Molinari, et al.
Ebiomedicine|September 15, 2024
Circulating inflammatory and immune response proteins and endometrial cancer risk: a nested case-control study and Mendelian randomization analysesSabrina E Wang, Vivian Viallon, Matthew Lee, et al.
Molecular Cancer Therapeutics|November 8, 2006
Mutation analysis of 24 known cancer genes in the NCI-60 cell line setOgechi N Ikediobi, Helen Davies, Graham Bignell, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 14, 2025
WUSCHEL-D1 upregulation enhances grain number by inducing formation of multiovary-producing florets in wheatAdam Schoen, Guilherme V Yoshikawa, Parva Kumar Sharma, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.
American Journal of Human Genetics|January 20, 2007
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 tremorPatrick S Tarpey, F Lucy Raymond, Sarah O'Meara, et al.
Genes, Chromosomes & Cancer|September 22, 2005
Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adultsGraham Bignell, Raffaella Smith, Chris Hunter, et al.
Cancer Research|April 19, 2006
A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapyChris Hunter, Raffaella Smith, Daniel P Cahill, et al.
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