Raymond Dalgleish

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 14

Top Venues

Orphanet journal of rare diseases

Human cell

Human mutation

medRxiv : the preprint server for health sciences

University of Leicester

University of London (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Leicester

United Kingdom

Professor :: Department of Genetics and Genome Biology

University of Leicester

United Kingdom

Senior Lecturer :: Department of Genetics

University of Leicester

United Kingdom

Lecturer :: Department of Genetics

National Institutes of Health

United States

Expert Scientist :: Pulmonary Branch, NHLBI

National Institutes of Health

United States

Fogarty International Fellow :: Pulmonary Branch, NHLBI

St Marys Hospital Medical School

United Kingdom

Research Associate :: Department of Biochemistry

Education History

University of London

United Kingdom

PHD

University of Glasgow

United Kingdom

BSC

Publications

Raymond Dalgleish, Dimitra Micha, Andrea Superti-Furga, Fleur S van Dijk, David Owen Sillence
Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification. Orphanet journal of rare diseases 19 (1) (2024)
Raymond Dalgleish
Re: Identification of a family with van der Hoeve's syndrome harboring a novel COL1A1 mutation and generation of patient-derived iPSC lines and CRISPR/Cas9-corrected isogenic iPSCs. Human cell 37 (5) (2024)
Raymond Dalgleish, Dimitra Micha, Andrea Superti-Furga, Fleur S van Dijk, David Owen Sillence
Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification. Orphanet journal of rare diseases 19 (1) (2024)
Raymond Dalgleish, Dimitra Micha, Andrea Superti-Furga, Fleur S van Dijk, David Owen Sillence
Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification. Orphanet journal of rare diseases 19 (1) (2024)
Daniel Danis, Michael J Bamshad, Yasemin Bridges, Pilar Cacheiro, Leigh C Carmody, Jessica Xiao-Ling Chong, Ben Coleman, Raymond Dalgleish, Peter J Freeman, Adam S L Graefe, Tudor Groza, Julius O B Jacobsen, Adam Klocperk, Maaike A A Kusters, Markus S Ladewig, Anthony J Marcello, Teresa Mattina, Christopher John Mungall, Monica C Munoz-Torres, Justin T Reese, Filip Rehburg, Bárbara C S Reis, Catharina Schuetz, Damian Smedley, Timmy Strauß, Jagadish Chandrabose Sundaramurthi, Sylvia Thun, Kyran Wissink, John F Wagstaff, David Zocche, Melissa A Haendel, Peter Nick Robinson
A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discovery. medRxiv : the preprint server for health sciences (2024)
Raymond Dalgleish
Re: Identification of a family with van der Hoeve's syndrome harboring a novel COL1A1 mutation and generation of patient-derived iPSC lines and CRISPR/Cas9-corrected isogenic iPSCs. Human cell (2024)
Daniel Danis, Michael J Bamshad, Yasemin Bridges, Pilar Cacheiro, Leigh C Carmody, Jessica Xiao-Ling Chong, Ben Coleman, Raymond Dalgleish, Peter J Freeman, Adam S L Graefe, Tudor Groza, Julius O B Jacobsen, Adam Klocperk, Maaike A A Kusters, Markus S Ladewig, Anthony J Marcello, Teresa Mattina, Christopher John Mungall, Monica C Munoz-Torres, Justin T Reese, Filip Rehburg, Bárbara C S Reis, Catharina Schuetz, Damian Smedley, Timmy Strauß, Jagadish Chandrabose Sundaramurthi, Sylvia Thun, Kyran Wissink, John F Wagstaff, David Zocche, Melissa A Haendel, Peter Nick Robinson
A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discovery. medRxiv : the preprint server for health sciences (2024)
Raymond Dalgleish
Re: Identification of a family with van der Hoeve's syndrome harboring a novel COL1A1 mutation and generation of patient-derived iPSC lines and CRISPR/Cas9-corrected isogenic iPSCs. Human cell 37 (5) (2024)
Raymond Dalgleish
Re: Long-term evaluation of anabolic and anti-resorptive agents in adults with familial osteoporosis due to pro205ala variant of the col1a1 gene. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 33 (6) (2022)
Nadia Garibaldi, Roberta Besio, Raymond Dalgleish, Simona Villani, Aileen M Barnes, Joan C Marini, Antonella Forlino
Dissecting the phenotypic variability of osteogenesis imperfecta. Disease models & mechanisms 15 (5) (2022)
Elspeth A Bruford, Cristina R Antonescu, Andrew J Carroll, Arul Chinnaiyan, Ian A Cree, Nicholas C P Cross, Raymond Dalgleish, Robert Peter Gale, Christine J Harrison, Rosalind J Hastings, Jean-Loup Huret, Bertil Johansson, Michelle Le Beau, Cristina Mecucci, Fredrik Mertens, Roel G W Verhaak, Felix Mitelman
HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions. Leukemia 35 (11) (2021)
Henning Leske, Raymond Dalgleish, Alexander J F Lazar, Guido Reifenberger, Ian A Cree
A common classification framework for histone sequence alterations in tumours: an expert consensus proposal. The Journal of pathology 254 (2) (2021)
Meng Wang, Keith M Callenberg, Raymond Dalgleish, Alexandre Fedtsov, Naomi K Fox, Peter J Freeman, Kevin B Jacobs, Piotr Kaleta, Andrew J McMurry, Andreas Prlić, Veena Rajaraman, Reece K Hart
hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 Update. Human mutation 39 (12) (2018)
Peter J Freeman, Reece K Hart, Liam J Gretton, Anthony J Brookes, Raymond Dalgleish
VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions. Human mutation 39 (1) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Raymond Dalgleish