Neil Warner
University of Toronto
H-index: 31
North America-Canada
Top articles of Neil Warner
“Deficiency in ELF4, X-Linked”: a Monogenic Disease Entity Resembling Behçet’s Syndrome and Inflammatory Bowel Disease
Journal of Clinical Immunology
2024/2
Dinesh Babu Uthaya Kumar
H-Index: 5
Liza Konnikova
H-Index: 11
Neil Warner
H-Index: 21
Alexander Hoischen
H-Index: 56
Chromosomal Numerical Aberrations and Rare Copy Number Variation in Patients with Inflammatory Bowel Disease
Journal of Crohn's and Colitis
2023/1/1
Neil Warner
H-Index: 21
Sophie Hambleton
H-Index: 39
A chromosomal duplication encompassing interleukin-33 causes a novel hyper IgE phenotype characterized by eosinophilic esophagitis and generalized autoimmunity
Gastroenterology
2022/8/1
Platelet VPS16B is dependent on VPS33B expression, as determined in two siblings with arthrogryposis, renal dysfunction, and cholestasis syndrome
Journal of Thrombosis and Haemostasis
2022/7
Ling Li
H-Index: 5
Neil Warner
H-Index: 21
The diverse phenotype of intestinal dysmotility secondary to ACTG2-related disorders
Journal of pediatric gastroenterology and nutrition
2022/5/1
Neil Warner
H-Index: 21
Colonic stenosis caused by transcatheter arterial embolization
Clinical Gastroenterology and Hepatology
2022/4/1
A systematic review of monogenic inflammatory bowel disease
2022/4/1
Neil Warner
H-Index: 21
Mucus sialylation determines intestinal host-commensal homeostasis
Cell
2022/3/31
A184 REPURPOSING DRUGS FOR SPLEEN TYROSINE KINASE (SYK) PEDIATRIC PATIENTS USING HIGH-THROUGHPUT SCREENING
Journal of the Canadian Association of Gastroenterology
2022/3
Author Correction: Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice
Nature Genetics
2022/2
A Machine Learning Approach to Identifying Causal Monogenic Variants in Inflammatory Bowel Disease
Gastro Hep Advances
2022/1/1
Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune Dysregulation
Journal of Crohn's and Colitis
2021/11/1
Human autoinflammatory disease reveals ELF4 as a transcriptional regulator of inflammation
Nature immunology
2021/9
Neil Warner
H-Index: 21
Jie Pan
H-Index: 8
O-15: The Noticeable Diversity in Phenotype of ACTG2-Related Disorders–A Report of 4 Cases and Systematic Review of the Literature
2021/7/1
Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice
Nature genetics
2021/4
Novel CARMIL2 loss-of-function variants are associated with pediatric inflammatory bowel disease
Scientific Reports
2021/3/15
Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn’s Disease
Scientific reports
2021/3/10
Neil Warner
H-Index: 21
A26 A SYSTEMTIC REVIEW OF MONOGENIC INFLAMMATORY BOWEL DISEASE: CLINICAL PHENOTYPE AND GENOTYPE
Journal of the Canadian Association of Gastroenterology
2021/3/1
A167 UNDERSTANDING THE IMPACT OF DOWNSTREAM OF KINASE 4 (DOK4) DAMAGING GENETIC VARIANTS IN THE PATHOGENESIS OF PEDIATRIC INFLAMMATORY BOWEL DISEASE (IBD).
Journal of the Canadian Association of Gastroenterology
2021/3/1
UTILIZATION OF WHOLE EXOME SEQUENCING DATA TO IDENTIFY CLINICALLY RELEVANT PHARMACOGENOMIC VARIANTS IN INFLAMMATORY BOWEL DISEASE
Gastroenterology
2021/2/1
Co-Authors
