Published in Atherosclerosis on July 01, 2003
Lipoprotein(a): an elusive cardiovascular risk factor. Arterioscler Thromb Vasc Biol (2004) 1.48
Relationship of oxidized phospholipids on apolipoprotein B-100 particles to race/ethnicity, apolipoprotein(a) isoform size, and cardiovascular risk factors: results from the Dallas Heart Study. Circulation (2009) 1.16
Lipoprotein(a) levels, apo(a) isoform size, and coronary heart disease risk in the Framingham Offspring Study. J Lipid Res (2011) 1.00
Lipoprotein(a): genotype-phenotype relationship and impact on atherogenic risk. Metab Syndr Relat Disord (2011) 0.85
Structure, function, and genetics of lipoprotein (a). J Lipid Res (2016) 0.83
Lipoprotein (a) as a cause of cardiovascular disease: insights from epidemiology, genetics, and biology. J Lipid Res (2016) 0.83
The apolipoprotein(a) gene: linkage disequilibria at three loci differs in African Americans and Caucasians. Atherosclerosis (2008) 0.82
Relook at lipoprotein (A): independent risk factor of coronary artery disease in north Indian population. Indian Heart J (2014) 0.81
Lipoprotein (a): a Unique Independent Risk Factor for Coronary Artery Disease. Indian J Clin Biochem (2015) 0.79
Lipoprotein ratios as surrogate markers for insulin resistance in South indians with normoglycemic nondiabetic acute coronary syndrome. ISRN Endocrinol (2014) 0.78
Ethnicity and lipoprotein(a) polymorphism in Native Mexican populations. Ann Hum Biol (2006) 0.75
Lipoprotein(a) and lipid profiles of patients awaiting coronary artery bypass graft; a cross sectional study. BMC Cardiovasc Disord (2016) 0.75
Fibroblast growth factor 23 (FGF23) predicts progression of chronic kidney disease: the Mild to Moderate Kidney Disease (MMKD) Study. J Am Soc Nephrol (2007) 4.59
Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy. Nat Genet (2004) 2.40
MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. Nat Genet (2008) 2.24
Association between the UGT1A1*28 allele, bilirubin levels, and coronary heart disease in the Framingham Heart Study. Circulation (2006) 2.18
Adaptations to climate-mediated selective pressures in humans. PLoS Genet (2011) 2.15
Colloquium paper: human adaptations to diet, subsistence, and ecoregion are due to subtle shifts in allele frequency. Proc Natl Acad Sci U S A (2010) 1.97
TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. Am J Hum Genet (2011) 1.65
Uniparental disomy (UPD) other than 15: phenotypes and bibliography updated. Am J Med Genet A (2005) 1.54
Effect of supervised progressive resistance-exercise training protocol on insulin sensitivity, glycemia, lipids, and body composition in Asian Indians with type 2 diabetes. Diabetes Care (2008) 1.54
Association of polymorphisms of the apolipoprotein(a) gene with lipoprotein(a) levels and myocardial infarction. Circulation (2003) 1.49
Clinical and genetic features in a family with CADASIL and high lipoprotein (a) values. J Neurol (2010) 1.40
Low incidence of mutations in EGFR kinase domain in Caucasian patients with head and neck squamous cell carcinoma. Eur J Cancer (2005) 1.35
Longitudinal cohort study on the effectiveness of lipid apheresis treatment to reduce high lipoprotein(a) levels and prevent major adverse coronary events. Nat Clin Pract Cardiovasc Med (2009) 1.31
GJB2 mutations in keratitis-ichthyosis-deafness syndrome including its fatal form. Am J Med Genet A (2005) 1.29
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle. Hum Mol Genet (2005) 1.26
INSIG2 polymorphism is neither associated with BMI nor with phenotypes of lipoprotein metabolism. Obesity (Silver Spring) (2008) 1.24
APOC3 promoter polymorphisms C-482T and T-455C are associated with the metabolic syndrome. Arch Med Res (2007) 1.22
The ATGL gene is associated with free fatty acids, triglycerides, and type 2 diabetes. Diabetes (2006) 1.22
Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model. Hum Mutat (2010) 1.20
Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea. Am J Hum Genet (2009) 1.15
Afamin and apolipoprotein A-IV: novel protein markers for ovarian cancer. Cancer Epidemiol Biomarkers Prev (2009) 1.15
Correlations of C-reactive protein levels with anthropometric profile, percentage of body fat and lipids in healthy adolescents and young adults in urban North India. Atherosclerosis (2003) 1.13
Evidence of functional modulation of the MEKK/JNK/cJun signaling cascade by the low density lipoprotein receptor-related protein (LRP). J Biol Chem (2002) 1.12
Loss of dermatan-4-sulfotransferase 1 function results in adducted thumb-clubfoot syndrome. Am J Hum Genet (2009) 1.09
Dyslipidemia in Asian Indians: determinants and significance. J Assoc Physicians India (2004) 1.08
TNF-alpha gene polymorphism and TNF-alpha levels in obese Asian Indians with obstructive sleep apnea. Respir Med (2008) 1.07
Simple anthropometric measures identify fasting hyperinsulinemia and clustering of cardiovascular risk factors in Asian Indian adolescents. Metabolism (2006) 1.06
CXCR7 mediated Giα independent activation of ERK and Akt promotes cell survival and chemotaxis in T cells. Cell Immunol (2011) 1.05
Heterogeneous phenotypes of insulin resistance and its implications for defining metabolic syndrome in Asian Indian adolescents. Atherosclerosis (2005) 1.02
Hyperhomocysteinemia, and low intakes of folic acid and vitamin B12 in urban North India. Eur J Nutr (2002) 1.01
Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris. Eur J Hum Genet (2006) 0.99
Apolipoprotein E gene polymorphisms in patients with premature myocardial infarction: a case-controlled study in Asian Indians in North India. Ann Clin Biochem (2003) 0.99
Adiponectin, insulin resistance, and C-reactive protein in postpubertal Asian Indian adolescents. Metabolism (2004) 0.98
Yellow teeth, seizures, and mental retardation: a less severe case of Kohlschütter-Tönz syndrome. Am J Med Genet A (2006) 0.97
Increased serum lipoprotein(a) concentrations and low molecular weight phenotypes of apolipoprotein(a) are associated with symptomatic peripheral arterial disease. Clin Chem (2007) 0.96
Apolipoprotein E polymorphism in cerebrovascular & coronary heart diseases. Indian J Med Res (2010) 0.95
Measurement of plasma hydroperoxide concentration by FOX-1 assay in conjunction with triphenylphosphine. Clin Chim Acta (2003) 0.95
Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman. Am J Med Genet A (2008) 0.95
Prevalence of dyslipidemic risk factors in hemodialysis and CAPD patients. Kidney Int Suppl (2003) 0.94
Association between subclinical inflammation & fasting insulin in urban young adult north Indian males. Indian J Med Res (2006) 0.93
Differential expression of RDC1/CXCR7 in the human placenta. J Clin Immunol (2008) 0.93
The 342-kb deletion in GJB6 is not present in patients with non-syndromic hearing loss from Austria. Hum Mutat (2003) 0.93
Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations--phenotypic spectrum and frequencies of GJB2 mutations in Austria. Hum Genet (2002) 0.92
Diagnostic significance of nested polymerase chain reaction for sensitive detection of Pneumocystis jirovecii in respiratory clinical specimens. Diagn Microbiol Infect Dis (2009) 0.92
Distribution of CCR5delta32, CCR2-64I and SDF1-3'A and plasma levels of SDF-1 in HIV-1 seronegative North Indians. J Clin Virol (2007) 0.91
Nonalcoholic fatty liver disease is associated with subclinical atherosclerosis independent of obesity and metabolic syndrome in Asian Indians. Atherosclerosis (2012) 0.91
Lipoprotein(a)- and low-density lipoprotein-derived cholesterol in nephrotic syndrome: Impact on lipid-lowering therapy? Kidney Int (2004) 0.91
Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers-Danlos syndrome. Hum Mol Genet (2013) 0.91
A new, X-linked endothelial corneal dystrophy. Am J Ophthalmol (2006) 0.90
Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein. Nucleus (2010) 0.89
The phenotype of early-onset retinal degeneration in persons with RDH12 mutations. Invest Ophthalmol Vis Sci (2007) 0.89
A common nonsense mutation in the repetitive Kringle IV-2 domain of human apolipoprotein(a) results in a truncated protein and low plasma Lp(a). Hum Mutat (2004) 0.88
Tracing genetic history of modern humans using X-chromosome lineages. Hum Genet (2007) 0.88
Ala/Ala genotype of Pro12Ala polymorphism in the peroxisome proliferator-activated receptor-γ2 gene is associated with obesity and insulin resistance in Asian Indians. Diabetes Technol Ther (2012) 0.88
Cross-neutralizing activity of human anti-V3 monoclonal antibodies derived from non-B clade HIV-1 infected individuals. Virology (2013) 0.87
Obstructive sleep apnoea correlates with C-reactive protein in obese Asian Indians. Nutr Metab Cardiovasc Dis (2008) 0.87
C-reactive protein and dietary nutrients in urban Asian Indian adolescents and young adults. Nutrition (2006) 0.87
Association of peroxisome proliferator activated receptor-γ gene with non-alcoholic fatty liver disease in Asian Indians residing in north India. Gene (2012) 0.87
Antiretroviral drug resistance mutations in the reverse transcriptase gene of HIV-1 isolates from Northern Indian patients: a follow-up study. Arch Virol (2010) 0.86
Long-term suppression of HIV-1C virus production in human peripheral blood mononuclear cells by LTR heterochromatization with a short double-stranded RNA. J Antimicrob Chemother (2013) 0.86
Proton magnetic resonance spectroscopy and biochemical investigation of type 2 diabetes mellitus in Asian Indians: observation of high muscle lipids and C-reactive protein levels. Magn Reson Imaging (2008) 0.85
Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation. Eur J Hum Genet (2013) 0.85
Genetics of the Lp(a)/apo(a) system in an autochthonous Black African population from the Gabon. Eur J Hum Genet (2006) 0.85
Urinary hydrogen peroxide: a probable marker of oxidative stress in malignancy. Clin Chim Acta (2003) 0.85
"Essentially" pure trisomy 3q27 --> qter: further delineation of the partial trisomy 3q phenotype. Am J Med Genet A (2009) 0.84
Lipoprotein (a) downregulates lysosomal acid lipase and induces interleukin-6 in human blood monocytes. Biochim Biophys Acta (2003) 0.84
Phenotypic variability of a deletion and duplication 6q16.1 → q21 due to a paternal balanced ins(7;6)(p15;q16.1q21). Am J Med Genet A (2010) 0.84
Association of the Myostatin gene with obesity, abdominal obesity and low lean body mass and in non-diabetic Asian Indians in north India. PLoS One (2012) 0.83
Efficient neutralization of primary isolates by the plasma from HIV-1 infected Indian children. Viral Immunol (2011) 0.83
Polymorphism in apolipoprotein E among migraineurs and tension-type headache subjects. J Headache Pain (2009) 0.83
The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome. Eur J Hum Genet (2002) 0.83
Identification of insulin resistance in Asian Indian adolescents: classification and regression tree (CART) and logistic regression based classification rules. Clin Endocrinol (Oxf) (2008) 0.83
Polymorphic variants in DC-SIGN, DC-SIGNR and SDF-1 in high risk seronegative and HIV-1 patients in Northern Asian Indians. J Clin Virol (2008) 0.82
Vitamin D rescues impaired Mycobacterium tuberculosis-mediated tumor necrosis factor release in macrophages of HIV-seropositive individuals through an enhanced Toll-like receptor signaling pathway in vitro. Infect Immun (2012) 0.82
Lipoprotein(a) as a predictor of cardiovascular disease in a prospectively followed cohort of patients with type 1 diabetes. Diabetes Care (2006) 0.82
Apolipoprotein A-IV is an independent predictor of disease activity in patients with inflammatory bowel disease. Inflamm Bowel Dis (2007) 0.82
Plasma distribution of apoA-IV in patients with coronary artery disease and healthy controls. J Lipid Res (2003) 0.82
Health is wealth: methods to improve attendance in a lifestyle intervention for a largely immigrant Filipino-American sample. J Immigr Minor Health (2012) 0.82
MTHFR (677 and 1298) and IL-6-174 G/C genes in pathogenesis of Alzheimer's and vascular dementia and their epistatic interaction. Neurobiol Aging (2011) 0.81
Distribution and cutoff points of fasting insulin in Asian Indian adolescents and their association with metabolic syndrome. J Assoc Physicians India (2008) 0.81
Novel mutation in the Delta-sterol reductase gene in three Lebanese sibs with Smith-Lemli-Opitz (RSH) syndrome. Am J Med Genet (2002) 0.81
Association of polymorphism in the thermolabile 5, 10-methylene tetrahydrofolate reductase gene and hyperhomocysteinemia with coronary artery disease. Mol Cell Biochem (2007) 0.81
Molecular genetics and structural genomics of the human protein kinase C gene module. Genome Biol (2002) 0.81
Differential response to sustained stimulation by hCG & LH on goat ovarian granulosa cells. Indian J Med Res (2012) 0.80
Study of dihydropteroate synthase (DHPS) gene mutations among isolates of Pneumocystis jiroveci. Indian J Med Res (2008) 0.80
Measurement of urinary hydrogen peroxide by FOX-1 method in conjunction with catalase in diabetes mellitus--a sensitive and specific approach. Clin Chim Acta (2004) 0.80
Neutralization of tier-2 viruses and epitope profiling of plasma antibodies from human immunodeficiency virus type 1 infected donors from India. PLoS One (2012) 0.80
Molecular and structural analysis of metachromatic leukodystrophy patients in Indian population. J Neurol Sci (2010) 0.80
Neutralization potential of the plasma of HIV-1 infected Indian patients in the context of anti-V3 antibody content and antiretroviral therapy. [corrected]. J Microbiol (2012) 0.79
Oxidative damage of plasma proteins and lipids in epidemic dropsy patients: alterations in antioxidant status. Biochim Biophys Acta (2005) 0.79
Cholesterol ester transfer protein and apolipoprotein E gene polymorphisms in hyperlipidemic Asian Indians in North India. Mol Cell Biochem (2011) 0.79
Use of different primer directed sequence amplification by polymerase chain reaction for identification of Pneumocystis jirovecii in clinical samples. Indian J Chest Dis Allied Sci (2008) 0.79
Genotypic variation of Pneumocystis jirovecii isolates in India based on sequence diversity at mitochondrial large subunit rRNA. Int J Med Microbiol (2010) 0.79
Correlation of angiogenic cytokines-leptin and IL-8 in stage, type and presentation of endometriosis. Gynecol Endocrinol (2011) 0.79
Joubert-like syndrome unlinked to known candidate loci. J Pediatr (2004) 0.79
Evaluation of single nucleotide polymorphisms of Pro12Ala in peroxisome proliferator-activated receptor-γ and Gly308Ala in tumor necrosis factor-α genes in obese Asian Indians: a population-based study. Diabetes Metab Syndr Obes (2010) 0.79
Serum folic acid and RFC A80G polymorphism in Alzheimer's disease and vascular dementia. Am J Alzheimers Dis Other Demen (2014) 0.79
CXCL12-CXCR7 signaling activates ERK and Akt pathways in human choriocarcinoma cells. Cell Commun Adhes (2014) 0.78
Envelope diversity, characteristics of V3 region and predicted co-receptor usage of human immunodeficiency viruses infecting north Indians. J Microbiol (2012) 0.78