Concepedia

Author

Kimberly Gilmour

University College LondonORCID

Also Known As

Daniel Greene, Daniel L. Kastner, Gilmour K,, Gilmour, K, Gulrukh Ahsan, Hossein-Ardeschir Ghofrani, Jay Suntharalingam, Jesmina James, K C GILMOUR, K C Gilmour

287

Publications

21.2K

Citations

66

H-Index

124

Concepts

All Affiliations

University College LondonGreat Ormond Street HospitalGreat Ormond Street Hospital for Children NHS Foundation TrustUniversity of CambridgeUniversity of Freiburg
KG

About

Kimberly Gilmour is an author at University College London specializing in medicine, immunology, and autoimmune disease.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

30

44

8.4K

2

Health Sciences

4

4

1.7K

3

Allergy

4

5

415

4

Natural Sciences

1

1

34

5

Public Health

1

1

55

Kimberly Gilmour

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126

Publications

17.8K

Citations

61

H-Index

YearCitations

Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development

Florian Otto, Anders Thornell, Tessa Crompton,

Cell

1997

2.8K

Engineered bacteriophages for treatment of a patient with a disseminated drug-resistant Mycobacterium abscessus

Rebekah M. Dedrick, Carlos A. Guerrero-Bustamante, Rebecca A. Garlena,

Nature Medicine

2019

1.3K

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

Steven J. Howe, Marc R. Mansour, Kerstin Schwarzwaelder,

Journal of Clinical Investigation

2008

1.3K

Molecular remission of infant B-ALL after infusion of universal TALEN gene-edited CAR T cells

Waseem Qasim, Hong Zhan, Sujith Samarasinghe,

Science Translational Medicine

2017

871

Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

H. Bobby Gaspar, Kathryn L. Parsley, Steven J. Howe,

The Lancet

2004

682

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

Keren Carss, Gavin Arno, Marie Erwood,

The American Journal of Human Genetics

2016

463

Outcomes Following Gene Therapy in Patients With Severe Wiskott-Aldrich Syndrome

Salima Hacein-Bey Abina, H. Bobby Gaspar, Johanna Blondeau,

JAMA

2015

374

Genome-edited, donor-derived allogeneic anti-CD19 chimeric antigen receptor T cells in paediatric and adult B-cell acute lymphoblastic leukaemia: results of two phase 1 studies

Reuben Benjamin, Charlotte Graham, Deborah Yallop,

The Lancet

2020

344

The Human Phenotype Ontology in 2024: phenotypes around the world

Michael Gargano, Nicolas Matentzoglu, Ben Coleman,

Nucleic Acids Research

2023

311

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease

Claire Booth, Kimberly Gilmour, Paul Veys,

Blood

2010

309

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