Physician

Pediatric Endocrinology

Dr. Sarah Orton, MD

Sarah Orton, MD is an expert in the field of Pediatric Endocrinology. Sarah Orton is also a published doctor. She has 35 paper published. The most recent paper is: Vitamin D metabolic pathway genes and risk of multiple sclerosis in Canadians.

Publications

MHC transmission: insights into gender bias in MS susceptibility.
Revisiting the T-cell receptor alpha/delta locus and possible associations with multiple sclerosis.
Follow-up investigation of 12 proposed linkage regions in multiple sclerosis.
Age of puberty and the risk of multiple sclerosis: a population based study.
A genome scan in a single pedigree with a high prevalence of multiple sclerosis.
Sex ratio of multiple sclerosis and clinical phenotype.
Multiple sclerosis susceptibility and the X chromosome.
Parent-of-origin effects in MS: observations from avuncular pairs.
A first stage genome-wide screen for regions shared identical-by-descent in Hutterite families with multiple sclerosis.
Effect of immigration on multiple sclerosis sex ratio in Canada: the Canadian Collaborative Study.
Association of UV radiation with multiple sclerosis prevalence and sex ratio in France.
No effect of APOE and PVRL2 on the clinical outcome of multiple sclerosis.
Parental transmission of MS in a population-based Canadian cohort.
The role of hereditary spastic paraplegia related genes in multiple sclerosis. A study of disease susceptibility and clinical outcome.
Parent-of-origin effect in multiple sclerosis: observations from interracial matings.
Vitamin D metabolic pathway genes and risk of multiple sclerosis in Canadians.
Heritability of serum vitamin D concentrations: twin studies.
Mother-child blood group incompatibility and the risk of multiple sclerosis.
Congenital abnormalities and multiple sclerosis.
A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution.
Parent-of-origin effects at the major histocompatibility complex in multiple sclerosis.
Childhood cow''s milk allergy and the risk of multiple sclerosis: a population based study.
Variants in ST8SIA1 do not play a major role in susceptibility to multiple sclerosis in Canadian families.
Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility.
Expression of the multiple sclerosis-associated MHC class II Allele HLA-DRB1*1501 is regulated by vitamin D.
No effect of birth weight on the risk of multiple sclerosis. A population-based study.
Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis.
No effect of preterm birth on the risk of multiple sclerosis: a population based study.
Methylation of class II transactivator gene promoter IV is not associated with susceptibility to multiple sclerosis.
Analysis of 45 candidate genes for disease modifying activity in multiple sclerosis.
Parental non-inherited HLA resistance alleles do not confer protection against multiple sclerosis.
Parental transmission of HLA-DRB1*15 in multiple sclerosis.
The inheritance of resistance alleles in multiple sclerosis.
Sex ratio of multiple sclerosis in Canada: a longitudinal study.

Doctors Specialties

Pediatric Endocrinology

Accepted Insurances

Education

New York Presbyterian Hospital
University of Maryland

Hospital

NewYork-Presbyterian/Weill Cornell

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