Meet ApplyKite Twin, the application assistant that learns with you

Meet your Twin, it learns with you

Your Twin learns with you

Launch week codes:30% off annual Pro20% off monthly Pro

Ends in00h00m00s

Sarah Leiter

Has grant

NIHR Academic Clinical Lecturer

University of Cambridge

United Kingdom

Research Interests

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Explore related searches

Professors in United Kingdom

Recent Grants

Grant: Close

Academic Clinical Lectureship

Open Date: 2026-08-01

Close Date:

Grant: Close

Academic Clinical Fellowship

Open Date: 2022-09-01

Close Date: 2026-02-01

Grant: Close

MB/PhD Studentship

Open Date: 2011-09-01

Close Date: 2015-08-01

Articles (17)

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Collaborators (1)

Amos Burke

Professor of Paediatric Oncology and Director

University of Birmingham

UNITED KINGDOM

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Sarah Leiter

Research Interests

Make your next move.

Explore related searches

Recent Grants

Articles (17)

Rapid Whole Genome Sequencing Enhances Pediatric Cancer Diagnosis

Somatic PLCG1 Mutation in a Vascular Tumor of an Infant

Observation of risk perception, knowledge and behaviour related to covid-19 in heart failure patients enrolled on a telecoaching program

Abstract 3493: UltraFast whole genome sequencing enables personalized treatments in childhood cancers

Improving the diagnosis of renal tumours of young people through integrated molecular analysis

Patient passports for rare diseases: results of a pilot study

Developing a Paired Whole Genome Sequencing Service for Children With Cancer

Real‐world experience of paediatric acute promyelocytic leukaemia in the United Kingdom and Ireland

A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumor

Molecular analysis improves the diagnosis of young people with renal tumors

Whole genome sequencing can reproduce all standard-of-care diagnostics for childhood cancer: Results from two national systems

Whole genome sequencing provides practice-changing benefits when performed on consecutive, unselected children with suspected cancer

Benefits for children with suspected cancer from routine whole-genome sequencing

Implementation of preductal and postductal oxygen saturation screening in babies born in a district general hospital

An expanded clinical spectrum of hypoinsulinaemic hypoketotic hypoglycaemia

Routine Whole Genome Sequencing for All Children with Hematological Malignancies Defines a New Standard of Care - Data of the First 152 Cases from the NHS England Genomic Medicine Service

Evaluation of positive pulse oximetry screens outcomes in a district general hospital – how often is the cause cardiac?

Collaborators (1)

Amos Burke

Make your next move.