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Phase 1–2 Trial of AAVS3 Gene Therapy in Patients with Hemophilia B

The New England journal of medicine, 2022-07, Vol.387 (3), p.237-247

2022

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Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients

The Journal of clinical investigation, 2008-09, Vol.118 (9), p.3143-3150

2008

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Factor IX Expression within the Normal Range Prevents Spontaneous Bleeds Requiring Treatment Following FLT180a Gene Therapy in Patients with Severe Hemophilia B: Long-Term Follow-up Study of the B-Amaze Program

Blood, 2021-11, Vol.138 (Supplement 1), p.3967-3967

2021

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Opportunistic offering of self-sampling to non-attenders within the English cervical screening programme: a pragmatic, multicentre, implementation feasibility trial with randomly allocated cluster intervention start dates (YouScreen)

EClinicalMedicine, 2024-07, Vol.73, p.102672, Article 102672

2024

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Speech and Language Therapy, The Judicial System and Pakistan

Foundation University Journal of Rehabilitation Sciences, 2023-07, Vol.3 (2), p.36-37

2023

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The impact of a gynecology breast clinic and curriculum on the management of breast disease following residency

Primary care update for Ob/Gyns, 1999-11, Vol.6 (6), p.197-201

1999

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Evaluation of the activity of ertapenem against gonococcal isolates exhibiting a range of susceptibilities to cefixime

Journal of antimicrobial chemotherapy, 2014-06, Vol.69 (6), p.1568-1571

2014

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Pain Management Considerations in Patients With Opioid Use Disorder Requiring Critical Care

Journal of clinical pharmacology, 2022-04, Vol.62 (4), p.449-462

2022

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An evaluation of gentamicin susceptibility of Neisseria gonorrhoeae isolates in Europe

Journal of antimicrobial chemotherapy, 2011-03, Vol.66 (3), p.592-595

2011

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Targeted gene panel sequencing of liquid and tissue biopsies reveals actionable genomic alterations in Ghanaian metastatic breast cancer cases

Translational oncology, 2024-11, Vol.49, p.102100, Article 102100

2024

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Genetic diversity of blaTEM alleles, antimicrobial susceptibility and molecular epidemiological characteristics of penicillinase-producing Neisseria gonorrhoeae from England and Wales

Journal of antimicrobial chemotherapy, 2015-12, Vol.70 (12), p.3238-3243

2015

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Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition (vol 50, pg 572, 2018)

NATURE GENETICS, 2018-09, Vol.50 (9), p.1342

2018

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Genetic diversity of bla sub(TEM) alleles, antimicrobial susceptibility and molecular epidemiological characteristics of penicillinase-producing Neisseria gonorrhoeae from England and Wales

Journal of antimicrobial chemotherapy, 2015-12, Vol.70 (12), p.3238-3243

2015

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Genetic diversity of bla^sub TEM^ alleles, antimicrobial susceptibility and molecular epidemiological characteristics of penicillinase-producing Neisseria gonorrhoeae from England and Wales

Journal of antimicrobial chemotherapy, 2015-12, Vol.70 (12), p.3238

2015

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Genetic diversity of bla TEM alleles, antimicrobial susceptibility and molecular epidemiological characteristics of penicillinase-producing Neisseria gonorrhoeae from England and Wales

Journal of antimicrobial chemotherapy, 2015-08, p.dkv260

2015

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Ten years of external quality assessment (EQA) of Neisseria gonorrhoeae antimicrobial susceptibility testing in Europe elucidate high reliability of data

BMC infectious diseases, 2019-03, Vol.19 (1), p.281-281, Article 281

2019

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Genetic diversity of bla(TEM) alleles, antimicrobial susceptibility and molecular epidemiological characteristics of penicillinase-producing Neisseria gonorrhoeae from England and Wales

Journal of antimicrobial chemotherapy, 2015, Vol.70 (12), p.3238

2015

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Frequency and correlates of culture-positive infection with Neisseria gonorrhoeae in England: a review of sentinel surveillance data

Sexually transmitted infections, 2015-06, Vol.91 (4), p.287-293

2015

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Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Nature genetics, 2016-11, Vol.48 (12), p.1591-1591

2016

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Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Nature genetics, 2016-08, Vol.48 (8), p.970-970

2016

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Phase 1–2 Trial of AAVS3 Gene Therapy in Patients with Hemophilia B

Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients

Factor IX Expression within the Normal Range Prevents Spontaneous Bleeds Requiring Treatment Following FLT180a Gene Therapy in Patients with Severe Hemophilia B: Long-Term Follow-up Study of the B-Amaze Program

STIMULATE-ICP-Delphi (Symptoms, Trajectory, Inequalities and Management: Understanding Long-COVID to Address and Transform Existing Integrated Care Pathways Delphi): Study protocol

Long Covid active case finding study protocol: A co-produced community-based pilot within the STIMULATE-ICP study (Symptoms, Trajectory, Inequalities and Management: Understanding Long-COVID to Address and Transform Existing Integrated Care Pathways)

A Phase I Study Evaluating the Safety and Persistence of Allorestricted WT1-TCR Gene Modified Autologous T Cells in Patients with High-Risk Myeloid Malignancies Unsuitable for Allogeneic Stem Cell Transplantation

Opportunistic offering of self-sampling to non-attenders within the English cervical screening programme: a pragmatic, multicentre, implementation feasibility trial with randomly allocated cluster intervention start dates (YouScreen)

Speech and Language Therapy, The Judicial System and Pakistan

The impact of a gynecology breast clinic and curriculum on the management of breast disease following residency

Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition

Evaluation of the activity of ertapenem against gonococcal isolates exhibiting a range of susceptibilities to cefixime

Pain Management Considerations in Patients With Opioid Use Disorder Requiring Critical Care

An evaluation of gentamicin susceptibility of Neisseria gonorrhoeae isolates in Europe

Targeted gene panel sequencing of liquid and tissue biopsies reveals actionable genomic alterations in Ghanaian metastatic breast cancer cases

Genetic diversity of blaTEM alleles, antimicrobial susceptibility and molecular epidemiological characteristics of penicillinase-producing Neisseria gonorrhoeae from England and Wales

Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition

Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition (vol 50, pg 572, 2018)

Genetic diversity of bla sub(TEM) alleles, antimicrobial susceptibility and molecular epidemiological characteristics of penicillinase-producing Neisseria gonorrhoeae from England and Wales

Genetic diversity of bla^sub TEM^ alleles, antimicrobial susceptibility and molecular epidemiological characteristics of penicillinase-producing Neisseria gonorrhoeae from England and Wales

Genetic diversity of bla TEM alleles, antimicrobial susceptibility and molecular epidemiological characteristics of penicillinase-producing Neisseria gonorrhoeae from England and Wales

Ten years of external quality assessment (EQA) of Neisseria gonorrhoeae antimicrobial susceptibility testing in Europe elucidate high reliability of data

Genetic diversity of bla(TEM) alleles, antimicrobial susceptibility and molecular epidemiological characteristics of penicillinase-producing Neisseria gonorrhoeae from England and Wales

Frequency and correlates of culture-positive infection with Neisseria gonorrhoeae in England: a review of sentinel surveillance data

Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

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