P. Ancliff

发表

Recent advances in the understanding of genetic defects of neutrophil number and function

S. Burns, A. Thrasher, G. Bouma, 2010, British journal of haematology.

Chronic neutropenia: how best to assess severity and approach management?

C. Klein, C. Bellanné-Chantelot, J. Donadieu, 2021, Expert review of hematology.

MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia.

M. Ballmaier, R. Scott, S. Unal, 2018, Blood advances.

GATA2 mutations in sporadic and familial acute myeloid leukaemia patients with CEBPA mutations

J. Fitzgibbon, R. Hills, D. Linch, 2013, British journal of haematology.

Long‐term follow‐up of granulocyte colony‐stimulating factor receptor mutations in patients with severe congenital neutropenia: implications for leukaemogenesis and therapy

D. Linch, R. Liesner, R. Gale, 2003, British journal of haematology.

Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds

Asim Khwaja, Arnold Pizzey, Bradley N Smith, 2009, British journal of haematology.

De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

Henning Gall, Fengyuan Hu, Kevin Rue-Albrecht, 2018, American journal of human genetics.

Notch-1 Mutations Are Secondary Events in Some Patients with T-Cell Acute Lymphoblastic Leukemia

L. Foroni, D. Linch, M. Mansour, 2007, Clinical Cancer Research.

Notch-1Mutations Are Secondary Events in Some Patients with T-Cell Acute Lymphoblastic Leukemia

L. Foroni, D. Linch, M. Mansour, 2007 .

Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies

A. Carrió, J. Dopazo, B. Rodríguez-Santiago, 2019, Journal of Medical Genetics.

Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia

I. Macaulay, N. Potter, P. Van Loo, 2021, Nature Cancer.

Ectopic thymus presenting as a subglottic mass: diagnostic and management dilemmas.

I. Pai, A. Ramsay, P. Ancliff, 2005, International journal of pediatric otorhinolaryngology.

Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia

A. Shakoori, A. Segal, D. Linch, 2012, British journal of haematology.

What is the diagnostic yield of bone marrow aspiration to exclude leukaemia prior to systemic treatment in juvenile idiopathic arthritis?

D. O’Connor, J. Bartram, S. Samarasinghe, 2022, British journal of haematology.

Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease.

D C Linch, R E Gale, D. Linch, 2001, Blood.

Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

Andy G Lynch, Sri V. V. Deevi, Eleanor F. Dewhurst, 2017, Scientific Reports.

Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

Sri V. V. Deevi, Eleanor F. Dewhurst, Courtney E. French, 2017, Scientific Reports.