Alan M. Pittman
St George's University Of London
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 85 publications
The lipedema common case report form as a research tool: standardizing lipedema data collection.
Journal: Frontiers in global women's health
Published: March 18, 2026
Further characterisation of immortalised human lymphatic endothelial cells to explore their transcriptomic profile and VEGFC response.
Journal: Scientific reports
Published: September 01, 2025
Novel start codon variant in the 5'UTR of LDLR associated with familial hypercholesterolaemia.
Journal: European journal of human genetics : EJHG
Published: February 05, 2025
Variants in LPA are associated with familial hypercholesterolaemia: whole genome sequencing analysis in the 100 000 Genomes Project.
Journal: European journal of preventive cardiology
Published: July 11, 2024
Variants in LPA are associated with Familial Hypercholesterolaemia: whole genome sequencing analysis in the 100,000 Genomes Project.
Journal: European journal of preventive cardiology
Published: July 11, 2024
Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy.
Journal: The Journal of clinical investigation
Published: July 08, 2024
Ex Vivo Host Transcriptomics During Cryptococcus neoformans, Cryptococcus gattii, and Candida albicans Infection of Peripheral Blood Mononuclear Cells From South African Volunteers.
Journal: The Journal of infectious diseases
Published: April 06, 2024
The Intellectual Disability Risk Gene Kdm5b Regulates Long-Term Memory Consolidation in the Hippocampus.
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
Published: February 18, 2024
RNA Therapy for Oncogenic NRAS-Driven Nevi Induces Apoptosis.
Journal: The Journal of investigative dermatology
Published: November 10, 2023
RYR2 Variant and Sudden Death in Patients With Dilated Cardiomyopathy.
Journal: Journal of the American College of Cardiology
Published: September 20, 2023
Inflammatory linear verrucous epidermal nevus should be genotyped to direct treatment and genetic counseling.
Journal: Journal of the American Academy of Dermatology
Published: August 24, 2023
Mosaic BRAF Fusions Are a Recurrent Cause of Congenital Melanocytic Nevi Targetable by MAPK Pathway Inhibition.
Journal: The Journal of investigative dermatology
Published: February 01, 2023
Last Updated: 09/26/2026