Published in Front Public Health on August 06, 2014
Preservation of retinal structure and function after cilioretinal artery occlusion: a case report. Int Med Case Rep J (2016) 0.75
Genetic Influences on Plasma Homocysteine Levels in African Americans and Yoruba Nigerians. J Alzheimers Dis (2015) 0.75
The Impact of Homocysteine, Vitamin B12, and Vitamin D Levels on Functional Outcome after First-Ever Ischaemic Stroke. Biomed Res Int (2017) 0.75
LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics (2010) 13.54
Homocysteine and cardiovascular disease: evidence on causality from a meta-analysis. BMJ (2002) 7.14
Robust relationship inference in genome-wide association studies. Bioinformatics (2010) 5.57
Vitamin status and intake as primary determinants of homocysteinemia in an elderly population. JAMA (1993) 5.21
Quality control and quality assurance in genotypic data for genome-wide association studies. Genet Epidemiol (2010) 4.83
Clinical practice. Vitamin B12 deficiency. N Engl J Med (2013) 4.58
Genome-wide association study of hematological and biochemical traits in a Japanese population. Nat Genet (2010) 4.36
High prevalence of cobalamin deficiency in elderly outpatients. J Am Geriatr Soc (1992) 3.12
Common variants of FUT2 are associated with plasma vitamin B12 levels. Nat Genet (2008) 2.07
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1. Nat Genet (1999) 1.96
Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations. Am J Hum Genet (2009) 1.87
Idiopathic chronic megaloblastic anemia in children. Acta Paediatr Suppl (1960) 1.83
Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia. Nat Genet (2003) 1.71
New insights into erythropoiesis: the roles of folate, vitamin B12, and iron. Annu Rev Nutr (2004) 1.71
Biomarkers of vitamin B-12 status in NHANES: a roundtable summary. Am J Clin Nutr (2011) 1.43
Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway. Hum Mol Genet (2009) 1.33
Blood folate levels: the latest NHANES results. NCHS Data Brief (2008) 1.32
Vitamin Intervention for Stroke Prevention (VISP) trial: rationale and design. Neuroepidemiology (2001) 1.21
Molecular dissection of the intrinsic factor-vitamin B12 receptor, cubilin, discloses regions important for membrane association and ligand binding. J Biol Chem (1999) 1.21
Update: effects of antioxidant and non-antioxidant vitamin supplementation on immune function. Nutr Rev (2007) 1.18
Human HTm4 is a hematopoietic cell cycle regulator. J Clin Invest (2002) 1.15
Bioinformatic and genetic association analysis of microRNA target sites in one-carbon metabolism genes. PLoS One (2011) 1.14
Screening for cobalamin deficiency in geriatric outpatients: prevalence and influence of synthetic cobalamin intake. J Am Geriatr Soc (2002) 1.09
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets. PLoS Genet (2013) 1.04
Vitamin B6 status, deficiency and its consequences--an overview. Nutr Hosp (2007) 1.03
Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men. Hum Mol Genet (2012) 1.02
Polymorphisms in 1-carbon metabolism, epigenetics and folate-related pathologies. J Nutrigenet Nutrigenomics (2012) 1.01
Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis. Pharmacogenet Genomics (2012) 1.00
Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia. Psychiatr Genet (2012) 0.98
Performance of the serum cobalamin assay for diagnosis of cobalamin deficiency. Am J Med Sci (1994) 0.95
Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk. Neurology (2011) 0.94
Common SNPs in myelin transcription factor 1-like (MYT1L): association with major depressive disorder in the Chinese Han population. PLoS One (2010) 0.92
The neurology of folic acid deficiency. Handb Clin Neurol (2014) 0.91
Association study of myelin transcription factor 1-like polymorphisms with schizophrenia in Han Chinese population. Genes Brain Behav (2011) 0.91
Alkaline phosphatase is increased in both brain and plasma in Alzheimer's disease. Neurodegener Dis (2011) 0.89
Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage. Am J Hum Genet (1995) 0.87
A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption). PLoS One (2013) 0.86
Identification of rare copy number variants in high burden schizophrenia families. Am J Med Genet B Neuropsychiatr Genet (2013) 0.83
An exon 53 frameshift mutation in CUBN abrogates cubam function and causes Imerslund-Gräsbeck syndrome in dogs. Mol Genet Metab (2013) 0.82
Vitamin intervention for stroke prevention. J Neurol Sci (2002) 0.81
B-vitamin status and intake in European adolescents. A review of the literature. Nutr Hosp (2006) 0.80
Vitamins and stroke: the homocysteine hypothesis still in doubt. Neurologist (2008) 0.80
Newly diagnosed dementia and increased risk of hemorrhagic stroke: A nationwide population-based study. Curr Alzheimer Res (2014) 0.80
Vitamin B12 and folate deficiency: should we use a different cutoff value for hematologic disorders? Int J Lab Hematol (2013) 0.79
Genetic defects in folate and cobalamin pathways affecting the brain. Clin Chem Lab Med (2013) 0.79
Serum folate but not vitamin B-12 concentrations are positively associated with cognitive test scores in children aged 6-16 years. J Nutr (2013) 0.79
[Familiar selective vitamin B12 malabsorption with proteinuria. A pernicious anemia-like syndrome]. Nord Med (1960) 0.77