Robert Evans Ferrell

Robert Evans Ferrell's AcademicInfluence.com Rankings

Biology

#5080

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#7471

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Molecular Biology

#432

World Rank

#441

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Genetics

#442

World Rank

#510

Historical Rank

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Biology

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Robert Evans Ferrell's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. (2000) (1616)
Deficiency of subsarcolemmal mitochondria in obesity and type 2 diabetes. (2005) (847)
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm (2008) (765)
Estimating African American admixture proportions by use of population-specific alleles. (1998) (758)
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema (2000) (636)
Lymphatic endothelial reprogramming of vascular endothelial cells by the Prox‐1 homeobox transcription factor (2002) (631)
A model for gene therapy of human hereditary lymphedema (2001) (590)
Defective valves and abnormal mural cell recruitment underlie lymphatic vascular failure in lymphedema distichiasis (2004) (551)
Susceptibility genes for age-related maculopathy on chromosome 10q26. (2005) (476)
A regulatory polymorphism of the monoamine oxidase-A gene may be associated with variability in aggression, impulsivity, and central nervous system serotonergic responsivity (2000) (458)
Genetic variation in components of dopamine neurotransmission impacts ventral striatal reactivity associated with impulsivity (2009) (418)
Genetic variation in human NPY expression affects stress response and emotion (2008) (407)
Allelic Variation in the Serotonin Transporter Promoter Affects Onset of Paroxetine Treatment Response in Late-Life Depression (2000) (395)
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD (1998) (393)
A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation. (2001) (391)
Ethnic-affiliation estimation by use of population-specific DNA markers. (1997) (378)
Association and linkage analyses of RGS4 polymorphisms in schizophrenia. (2002) (372)
Effects of exercise on mitochondrial content and function in aging human skeletal muscle. (2006) (356)
Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas (2002) (336)
Molecular epidemiology of vitamin D receptor gene variants. (2000) (316)
A4POE*4-associated Alzheimer's disease risk is modified by α1–antichymotrypsin polymorphism (1995) (316)
A novel measure of genetic distance for highly polymorphic tandem repeat loci. (1995) (312)
Distribution of the four founding lineage haplotypes in Native Americans suggests a single wave of migration for the New World. (1995) (294)
Effects of age, gender, and myostatin genotype on the hypertrophic response to heavy resistance strength training. (2000) (291)
Aggression and anger-related traits associated with a polymorphism of the tryptophan hydroxylase gene (1999) (282)
Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk (2008) (280)
Multilocus Genetic Profile for Dopamine Signaling Predicts Ventral Striatum Reactivity (2011) (278)
Relation of apolipoprotein E phenotype to myocardial infarction and mortality from coronary artery disease. (1993) (268)
Ancestral proportions and admixture dynamics in geographically defined African Americans living in South Carolina. (2001) (262)
Interpretation of Genetic Association Studies: Markers with Replicated Highly Significant Odds Ratios May Be Poor Classifiers (2009) (257)
Population structure in admixed populations: effect of admixture dynamics on the pattern of linkage disequilibrium. (2001) (252)
Truncating mutations in FOXC2 cause multiple lymphedema syndromes. (2001) (250)
Hereditary lymphedema: evidence for linkage and genetic heterogeneity. (1998) (250)
The heritability of otitis media: a twin and triplet study. (1999) (249)
Familial renal cell carcinoma with a 3;11 chromosome translocation limited to tumor cells. (1982) (247)
A regulatory variant of the human tryptophan hydroxylase-2 gene biases amygdala reactivity (2005) (245)
Genome-wide linkage analyses of systolic blood pressure using highly discordant siblings. (1999) (242)
Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis (2002) (241)
Nephropathy in type 1 diabetes: a manifestation of insulin resistance and multiple genetic susceptibilities? Further evidence from the Pittsburgh Epidemiology of Diabetes Complication Study. (2002) (235)
Expressed hypervariable polymorphism of apolipoprotein (a). (1991) (231)
Caucasian genes in American blacks: new data. (1992) (226)
Association of interleukin-15 protein and interleukin-15 receptor genetic variation with resistance exercise training responses. (2004) (221)
Divergent Effects of Genetic Variation in Endocannabinoid Signaling on Human Threat- and Reward-Related Brain Function (2009) (218)
Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions. (2004) (214)
Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP). (2002) (202)
Myostatin Gene Expression is Reduced in Humans with Heavy-Resistance Strength Training: A Brief Communication (2003) (198)
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm (2010) (197)
Effects of weight loss and physical activity on skeletal muscle mitochondrial function in obesity. (2005) (195)
Functional polymorphism in the matrix metalloproteinase-9 promoter as a potential risk factor for intracranial aneurysm. (1999) (194)
Insulin Resistance Is Associated With Higher Intramyocellular Triglycerides in Type I but Not Type II Myocytes Concomitant With Higher Ceramide Content (2009) (194)
Admixture mapping of an allele affecting interleukin 6 soluble receptor and interleukin 6 levels. (2007) (185)
Positional genomic analysis identifies the beta(2)-adrenergic receptor gene as a susceptibility locus for human hypertension. (2000) (181)
Diabetes among Mexican Americans in Starr County, Texas. (1983) (175)
Individual admixture estimates: disease associations and individual risk of diabetes and gallbladder disease among Mexican-Americans in Starr County, Texas. (1986) (175)
Differential distribution of allelic variants in cytokine genes among African Americans and White Americans. (2004) (172)
Ethnic variation in vitamin D-binding protein (GC): a review of isoelectric focusing studies in human populations (1986) (172)
A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2. (2000) (171)
CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses. (2006) (169)
Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy. (2005) (167)
Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations. (1995) (165)
Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin. (1990) (160)
Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. (2012) (158)
Familial cavernous angiomas: natural history and genetic study over a 5-year period. (1982) (158)
Allelic variants of aromatase and the androgen and estrogen receptors: toward a multigenic model of prostate cancer risk. (2001) (157)
A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathy (2002) (155)
A full genome scan for age-related maculopathy. (2000) (155)
Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation. (1981) (150)
The epidemiology of quantitative ultrasound: A review of the relationships with bone mass, osteoporosis and fracture risk (2005) (150)
Vitamin D receptor genotype is associated with fat-free mass and sarcopenia in elderly men. (2004) (149)
Effects of HTR1A C(-1019)G on amygdala reactivity and trait anxiety. (2009) (148)
Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regions. (2001) (147)
On the inheritance of abdominal aortic aneurysm. (1991) (142)
Relationship of prevalence of non‐insulin‐dependent diabetes mellitus to Amerindian admixture in the Mexican Americans of San Antonio, Texas (1986) (142)
Risk for Depression During Interferon-Alpha Treatment Is Affected by the Serotonin Transporter Polymorphism (2009) (138)
Neuroticism is not associated with the serotonin transporter (5-HTTLPR) polymorphism (1999) (136)
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci (2017) (135)
GJC2 missense mutations cause human lymphedema. (2010) (135)
Association of FKBP5 polymorphisms with suicidal events in the Treatment of Resistant Depression in Adolescents (TORDIA) study. (2010) (135)
mtDNA variation indicates Mongolia may have been the source for the founding population for the New World. (1996) (134)
Molecular Anatomy of an Intracranial Aneurysm: Coordinated Expression of Genes Involved in Wound Healing and Tissue Remodeling (2001) (134)
Ambulatory blood pressure after acute exercise in older men with essential hypertension. (2000) (131)
Apolipoprotein E polymorphism: A new genetic marker of hip fracture risk--The Study of Osteoporotic Fractures. (1999) (131)
Exclusion of mutations in the gene for type III collagen (COL3A1) as a common cause of intracranial aneurysms or cervical artery dissections (1993) (131)
VO2 max is associated with ACE genotype in postmenopausal women. (1998) (131)
Influence of age, sex, and strength training on human muscle gene expression determined by microarray. (2002) (130)
Effects of polymorphisms in apolipoproteins E, A-IV, and H on quantitative traits related to risk for cardiovascular disease. (1991) (130)
Human transferrin polymorphism. (1987) (125)
Spinocerebellar ataxia: Variable age of onset and linkage to human leukocyte antigen in a large kindred (1988) (123)
Human novelty-seeking personality traits and dopamine D4 receptor polymorphisms: a twin and genetic association study. (1998) (123)
Fluoxetine-related death in a child with cytochrome P-450 2D6 genetic deficiency. (2000) (122)
Memory performance and the apolipoprotein E polymorphism in a community sample of middle-aged adults. (2000) (121)
Determinants of premenopausal bone mineral density: The interplay of genetic and lifestyle factors (1996) (120)
APO E gene and gene-environment effects on plasma lipoprotein-lipid levels. (2000) (120)
Frequent sequence variation in the human myostatin (GDF8) gene as a marker for analysis of muscle-related phenotypes. (1999) (118)
Comprehensive transcript analysis in small quantities of mRNA by SAGE-lite. (1999) (118)
The PANE1 gene encodes a novel human minor histocompatibility antigen that is selectively expressed in B-lymphoid cells and B-CLL. (2006) (118)
The gender-specific apolipoprotein E genotype influence on the distribution of lipids and apolipoproteins in the population of Rochester, MN. I. Pleiotropic effects on means and variances. (1991) (116)
Apo E allele frequencies in younger (age 42–50) vs older (age 65–90) women (1993) (115)
Factors associated with calcium absorption efficiency in pre- and perimenopausal women. (2000) (115)
Abdominal aortic aneurysm: results of a family study. (1991) (113)
Androgen receptor CAG repeat polymorphism is associated with fat-free mass in men. (2005) (113)
Muscle strength response to strength training is influenced by insulin-like growth factor 1 genotype in older adults. (2005) (113)
Characteristics of skeletal muscle mitochondrial biogenesis induced by moderate-intensity exercise and weight loss in obesity. (2007) (112)
Socio-economic status covaries with central nervous system serotonergic responsivity as a function of allelic variation in the serotonin transporter gene-linked polymorphic region (2004) (112)
Exercise training-induced blood pressure and plasma lipid improvements in hypertensives may be genotype dependent. (1999) (111)
The Brain-Derived Neurotrophic Factor Val66Met Polymorphism Moderates an Effect of Physical Activity on Working Memory Performance (2013) (109)
The 5-HTTPR Polymorphism Confers Liability to a Combined Phenotype of Psychotic and Aggressive Behavior in Alzheimer Disease (2001) (109)
The Gardner syndrome. Significance of ocular features. (1984) (109)
Prospective Analysis of Mannose-Binding Lectin Genotypes and Coronary Artery Disease in American Indians: The Strong Heart Study (2004) (108)
Two DNA polymorphisms in the lipoprotein lipase gene and their associations with factors related to cardiovascular disease. (1993) (108)
Salivary testosterone and a trinucleotide (CAG) length polymorphism in the androgen receptor gene predict amygdala reactivity in men (2010) (106)
Genetic studies of human apolipoproteins. V. A novel rapid procedure to screen apolipoprotein E polymorphism. (1988) (106)
mtDNA variation in the Yanomami: evidence for additional New World founding lineages. (1996) (105)
APOE*4-associated Alzheimer's disease risk is modified by alpha 1-antichymotrypsin polymorphism. (1995) (104)
HGF and MET mutations in primary and secondary lymphedema. (2008) (103)
Vitamin D Receptor Gene Polymorphisms, Bone Turnover, and Rates of Bone Loss in Older African‐American Women (1997) (102)
C2 and CFB Genes in Age-Related Maculopathy and Joint Action with CFH and LOC387715 Genes (2008) (102)
Linkage and association of adrenergic and dopamine receptor genes in the distal portion of the long arm of chromosome 5 with systolic blood pressure variation. (1998) (99)
The 5-HTTPR*S/*L polymorphism and aggressive behavior in Alzheimer disease. (2001) (99)
Connexin 47 Mutations Increase Risk for Secondary Lymphedema Following Breast Cancer Treatment (2012) (98)
Racial differences in the relation between uncoupling protein genes and resting energy expenditure. (2002) (98)
Bleomycin hydrolase is associated with risk of sporadic Alzheimer's disease (1998) (95)
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts (2016) (94)
The influence of macrophage migration inhibitory factor gene polymorphisms on outcome from community‐acquired pneumonia (2009) (93)
Ultrasound screening of first-degree relatives of patients with an abdominal aortic aneurysm. (1991) (93)
A population genetic study of six VNTR loci in three ethnically defined populations. (1991) (92)
Apolipoprotein E genotype and exercise training-induced increases in plasma high-density lipoprotein (HDL)- and HDL2-cholesterol levels in overweight men. (1999) (92)
Estimates of African, European and Native American Ancestry in Afro-Caribbean Men on the Island of Tobago (2006) (91)
Recent progress in understanding the genetic susceptibility to osteoporosis (1999) (90)
Role of Monocyte-Acquired Hemozoin in Suppression of Macrophage Migration Inhibitory Factor in Children with Severe Malarial Anemia (2006) (90)
Haplotypes of IL-10 promoter variants are associated with susceptibility to severe malarial anemia and functional changes in IL-10 production (2008) (90)
Sequence variation in hypoxia-inducible factor 1alpha (HIF1A): association with maximal oxygen consumption. (2003) (90)
Alpha-1-antitrypsin deficiency in aneurysmal disease. (1996) (89)
CNTF genotype is associated with muscular strength and quality in humans across the adult age span. (2001) (88)
Haptoglobin Genotype (2008) (88)
Genetic association studies between Alzheimer's disease and two polymorphisms in the low density lipoprotein receptor-related protein gene (1998) (87)
Changes in high-density lipoprotein-cholesterol subfractions with exercise training may be dependent on cholesteryl ester transfer protein (CETP) genotype. (2002) (86)
C-Reactive Protein Genotypes Affect Baseline, but not Exercise Training–Induced Changes, in C-Reactive Protein Levels (2004) (86)
An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma (2004) (86)
Characteristics of polymorphism at a VNTR locus 3' to the apolipoprotein B gene in five human populations. (1992) (85)
The gender-specific apolipoprotein E genotype influence on the distribution of plasma lipids and apolipoproteins in the population of Rochester, Minnesota. II. Regression relationships with concomitants. (1992) (85)
A progressive early onset cataract gene maps to human chromosome 17q24 (1995) (84)
Impact of apolipoprotein E polymorphism in determining interindividual variation in total cholesterol and low density lipoprotein cholesterol in Hispanics and non-Hispanic whites. (1993) (83)
Conservation of human chromosome 13 polymorphic microsatellite (CA)n repeats in chimpanzees. (1994) (83)
High-density lipoprotein-cholesterol, its subfractions, and responses to exercise training are dependent on endothelial lipase genotype. (2003) (83)
Intra‐ and inter‐population diversity at short tandem repeat loci in diverse populations of the world (1995) (82)
Genetic studies of human apolipoproteins. VI. Common polymorphism of apolipoprotein E in blacks. (1989) (82)
Decreased STAT1 expression by promoter methylation in squamous cell carcinogenesis. (2007) (82)
Molecular regulation of lymphangiogenesis and targets for tissue oedema. (2001) (81)
Polymorphic variation in the dopamine D4 receptor predicts delay discounting as a function of childhood socioeconomic status: evidence for differential susceptibility. (2013) (81)
Mitochondrial DNA variation is an indicator of austronesian influence in Island Melanesia. (1999) (80)
Associations between serotonin transporter gene promoter region (5-HTTLPR) polymorphism and gaze bias for emotional information. (2011) (80)
The gender-specific apolipoprotein E genotype influence on the distribution of plasma lipids and apolipoproteins in the population of Rochester, MN. III. Correlations and covariances. (1994) (80)
Linkage of atypical vitelliform macular dystrophy (VMD-1) to the soluble glutamate pyruvate transaminase (GPT1) locus. (1983) (79)
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. (2012) (79)
VEGFR3 gene structure, regulatory region, and sequence polymorphisms. (2001) (79)
Influence of serotonin-transporter-linked promoter region polymorphism on platelet activation in geriatric depression. (2001) (78)
Characterization of a dinucleotide repeat in the 92 kDa type IV collagenase gene (CLG4B), localization of CLG4B to chromosome 20 and the role of CLG4B in aortic aneurysmal disease (1995) (77)
Disparate Distribution of 16 Candidate Single Nucleotide Polymorphisms Among Racial and Ethnic Groups of Pediatric Heart Transplant Patients (2006) (77)
Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas (1979) (77)
Genetic studies of human apolipoproteins. IV. Structural heterogeneity of apolipoprotein H (beta 2-glycoprotein I). (1988) (76)
Allelic Variation in the Serotonin Transporter Gene-Linked Polymorphic Region (5-HTTLPR) and Cardiovascular Reactivity in Young Adult Male and Female Twins of European-American Descent (2003) (75)
Microsatellite data support an early population expansion in Africa. (1997) (74)
Catechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease (2005) (74)
Brain-Derived Neurotrophic Factor Serum Levels and Genotype: Association with Depression during Interferon-α Treatment (2013) (74)
Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males. (2004) (74)
Genome-Wide Linkage Analysis Reveals Evidence of Multiple Regions That Influence Variation in Plasma Lipid and Apolipoprotein Levels Associated With Risk of Coronary Heart Disease (2001) (74)
MIF (macrophage migration inhibitory factor) promoter polymorphisms and susceptibility to severe malarial anemia. (2009) (72)
Preliminary Localization of a Gene for Autosomal Dominant Hypoparathyroidism to Chromosome 3ql3 (1994) (71)
Central nervous system serotonergic responsivity and aggressive disposition in men (2002) (71)
A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration. (1995) (71)
Genetics and epidemiology of gallbladder disease in New World native peoples. (1984) (70)
Functional single nucleotide polymorphism haplotypes in the human equilibrative nucleoside transporter 1 (2006) (69)
A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10 (1994) (69)
Variants in toll-like receptor 1 and 4 genes are associated with Chlamydia trachomatis among women with pelvic inflammatory disease. (2012) (69)
Androgen receptor CAG repeat polymorphism is associated with cognitive function in older men (2003) (69)
Polymorphisms of interleukin (IL)-1α, IL-1β, IL-6, IL-10, and IL-18 and the risk of ovarian cancer (2004) (68)
The socio-economic status of communities predicts variation in brain serotonergic responsivity (2004) (68)
Variation in the BDNF Gene Interacts With Age to Predict Mortality in a Prospective, Longitudinal Cohort with Severe TBI (2015) (67)
Paired box mutations in familial and sporadic aniridia predicts truncated aniridia proteins. (1994) (66)
Genetic studies of human apolipoproteins. X. The effect of the apolipoprotein E polymorphism on quantitative levels of lipoproteins in Nigerian blacks. (1989) (66)
Case–control study of risk factors for breast cancer in Nigerian women (2006) (66)
High‐Density Association Study of 383 Candidate Genes for Volumetric BMD at the Femoral Neck and Lumbar Spine Among Older Men (2009) (66)
Comparative Gene Expression Analysis of Ovarian Carcinoma and Normal Ovarian Epithelium by Serial Analysis of Gene Expression (2005) (65)
Genetic studies of human apolipoproteins (1989) (64)
Candidate gene analysis in primary lymphedema. (2008) (64)
The MAOA promoter polymorphism, disruptive behavior disorders, and early onset substance use disorder: gene–environment interaction (2007) (64)
Association between allelic variants in cytokine genes and preeclampsia. (2005) (64)
Insulin-like growth factor-2 genotype, fat-free mass, and muscle performance across the adult life span. (2004) (64)
Polymorphisms in the CRP gene moderate an association between depressive symptoms and circulating levels of C-reactive protein (2010) (63)
Association of the serotonin transporter gene-linked polymorphic region (5-HTTLPR) genotype with depression in elderly persons after hip fracture. (2005) (63)
Human Choline Transporter Gene Variation Is Associated with Corticolimbic Reactivity and Autonomic-Cholinergic Function (2006) (63)
Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteria. (1980) (63)
Gallbladder disease epidemiology in Mexican Americans in Starr County, Texas. (1985) (63)
'Unique' alleles in admixed populations: a strategy for determining 'hereditary' population differences of disease frequencies. (1991) (63)
Polymorphism of the Serotonin Transporter (2001) (63)
Phenotypic effects of apolipoprotein structural variation on lipid profiles: II. Apolipoprotein A‐IV and quantitative lipid measures in the healthy women study (1989) (62)
Frequent allelic loss and homozygous deletion in chromosome band 8p23 in oral cancer (1999) (62)
The four founding lineage hypothesis for the New World: a critical reevaluation. (1996) (62)
Apolipoprotein E Gene Polymorphism and Bone Loss: Estrogen Status Modifies the Influence of Apolipoprotein E on Bone Loss (2000) (62)
Identification of functional single nucleotide polymorphism haplotypes in the cytidine deaminase promoter (2006) (62)
PER2 rs2304672 Polymorphism Moderates Circadian-Relevant Reward Circuitry Activity in Adolescents (2012) (62)
A Common Promoter Variant in the Cytochrome P450c17α (CYP17) Gene Is Associated with Bioavailable Testosterone Levels and Bone Size in Men (2001) (60)
Report of the committee on the genetic constitution of chromosome 5. (1988) (60)
Genetics of the Lp lipoprotein in Japanese‐Americans (1985) (60)
Variable expressivity of autosomal dominant anterior segment mesenchymal dysgenesis in six generations. (1982) (60)
Haptoglobin Genotype and Renal Function Decline in Type 1 Diabetes (2009) (59)
Paroxetine: population pharmacokinetic analysis in late-life depression using sparse concentration sampling. (2006) (59)
Microsatellite instability in oral cancer (1995) (59)
NADPH oxidase p22phox gene variants are associated with systemic oxidative stress biomarker responses to exercise training. (2005) (58)
Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21. (1985) (58)
Loss of heterozygosity of the short arm of chromosomes 3 and 9 in oral cancer (1996) (58)
Genetic Polymorphisms Impact the Risk of Acute Rejection in Pediatric Heart Transplantation: A Multi-Institutional Study (2008) (58)
Genome-wide linkage analyses for hypertension genes in two ethnically and geographically diverse populations. (2003) (57)
Genetic markers for ancestry are correlated with body composition traits in older African Americans (2007) (57)
Phenotypic effects of apolipoprotein structural variation on lipid profiles. III. Contribution of apolipoprotein E phenotype to prediction of total cholesterol, apolipoprotein B, and low density lipoprotein cholesterol in the healthy women study. (1990) (57)
Vitamin D Receptor Translation Initiation Codon Polymorphism and Markers of Osteoporotic Risk in Older African-American Women (1999) (56)
The association of bone mineral density with estrogen receptor gene polymorphisms. (2006) (56)
Association of pre-eclampsia with common coding sequence variations in the lipoprotein lipase gene. (1999) (56)
Obesity gene variant and elite endurance performance. (2001) (56)
Craniosynostosis with autosomal dominant transmission in New Zealand white rabbits. (1996) (56)
Moderate Physical Activity is Associated with Higher Bone Mineral Density in Postmenopausal Women (2001) (56)
Dispersion of human Y chromosome haplotypes based on five microsatellites in global populations. (1996) (56)
ASSOCIATION OF FCγ RECEPTOR IIA (CD32) POLYMORPHISM WITH MALARIAL ANEMIA AND HIGH-DENSITY PARASITEMIA IN INFANTS AND YOUNG CHILDREN (2006) (55)
The relationship between risk factor levels and presence of coronary artery calcification is dependent on apolipoprotein E genotype. (1999) (55)
Somatic mutation and functional polymorphism of a novel regulatory element in the HGF gene promoter causes its aberrant expression in human breast cancer. (2009) (55)
Reported early family environment covaries with menarcheal age as a function of polymorphic variation in estrogen receptor-α (2011) (55)
The insertion/deletion polymorphism of the ACE gene is related to insulin sensitivity in overweight women. (2001) (55)
Genetic studies of human apolipoproteins. VII. Population distribution of polymorphisms of apolipoproteins A-I, A-II, A-IV, C-II, E, and H in Nigeria. (1988) (54)
Correlates of Quantitative Ultrasound in the Women’s Healthy Lifestyle Project (1999) (54)
Serotonin Receptor 2A (HTR2A) Gene Polymorphisms Are Associated with Blood Pressure, Central Adiposity, and the Metabolic Syndrome. (2007) (54)
Segregation distortion of the CTG repeats at the myotonic dystrophy locus. (1996) (53)
The effect of trimethoprim on CYP2C8 mediated rosiglitazone metabolism in human liver microsomes and healthy subjects. (2005) (53)
Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers. (1990) (53)
Association between body fat response to exercise training and multilocus ADR genotypes. (2004) (53)
Heart Rate Variability Is Associated With Polymorphic Variation in the Choline Transporter Gene (2005) (53)
Two discrete regions of deletion at 7q in uterine leiomyomas (1997) (52)
Aromatase gene (CYP 19) polymorphisms and endogenous androgen concentrations in a multiracial/multiethnic, multisite study of women at midlife. (2006) (52)
Genetic studies of human apolipoproteins. I. Polymorphism of apolipoprotein A-IV. (1987) (52)
Candidate Gene Analysis of Femoral Neck Trabecular and Cortical Volumetric Bone Mineral Density in Older Men (2009) (52)
The genetic component of middle ear disease in the first 5 years of life. (2004) (52)
Mitochondrial versus nuclear admixture estimates demonstrate a past history of directional mating. (1997) (52)
DRD4 Polymorphism Moderates the Effect of Alcohol Consumption on Social Bonding (2012) (51)
Association Between NIDDM, RH Blood Group, and Haptoglobin Phenotype: Results from the San Antonio Heart Study (1986) (51)
Genetic studies of human apolipoproteins. XVI. APOE polymorphism and cholesterol levels in the Mayans of the Yucatan Peninsula, Mexico (1991) (51)
Ethnicity determination by names among the Aymara of Chile and Bolivia. (1989) (51)
Genetic variation in the New World: Ancient teeth, bone, and tissue as sources of DNA (1994) (50)
Distribution and evolution of CTG repeats at the myotonin protein kinase gene in human populations. (1996) (50)
Evidence supporting a role for the calcium‐sensing receptor in Alzheimer disease (2009) (49)
Boron-Doped Diamond Microelectrodes Reveal Reduced Serotonin Uptake Rates in Lymphocytes from Adult Rhesus Monkeys Carrying the Short Allele of the 5-HTTLPR. (2010) (49)
Characterization of the lipid-binding properties and lipoprotein lipase inhibition of a novel apolipoprotein C-III variant Ala23Thr. (2000) (49)
On the role of vitamin D binding globulin in glucose homeostasis: Results from the San Luis Valley diabetes study (1989) (49)
Genotype-environment interaction: apolipoprotein E (ApoE) gene effects and age as an index of time and spatial context in the human. (1996) (49)
Interleukin-6 (IL6) genotype is associated with fat-free mass in men but not women. (2003) (48)
Variability within α- and β-adrenoreceptor genes as a predictor of cardiovascular function at rest and in response to mental challenge (2002) (48)
The AVPR1A Gene and Substance Use Disorders: Association, Replication, and Functional Evidence (2011) (48)
Gene and gene by sex associations with initial sensitivity to nicotine in nonsmokers (2008) (48)
Mapping X-linked ophthalmic diseases. Provisional assignment of the locus for choroideremia to Xq13-q24. (1985) (47)
Polymorphic variability in the interleukin (IL)-1beta promoter conditions susceptibility to severe malarial anemia and functional changes in IL-1beta production. (2008) (47)
Molecular and cytogenetic analysis of chromosome 7 in uterine leiomyomas (1995) (47)
Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome. (1982) (47)
Labile Anger During Interferon Alfa Treatment is Associated With a Polymorphism in Tumor Necrosis Factor &agr; (2010) (47)
C174T polymorphism in the CNTF receptor gene is associated with fat-free mass in men and women. (2003) (46)
A tale of two genotypes: consistency between two high-throughput genotyping centers. (2002) (46)
Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2. (1980) (46)
Human adaptive evolution at Myostatin (GDF8), a regulator of muscle growth. (2006) (46)
A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium. (1988) (46)
Specific genetic markers of endurance performance and VO2max. (2001) (46)
Relation of type 2 diabetes to individual admixture and candidate gene polymorphisms in the Hispanic American population of San Luis Valley, Colorado (2004) (46)
Complex adaptive systems and human health: the influence of common genotypes of the apolipoprotein E (ApoE) gene polymorphism and age on the relational order within a field of lipid metabolism traits (2000) (46)
Comprehensive Analysis of HLA-G: Implications for Recurrent Spontaneous Abortion (2010) (45)
Influence of promoter region variants of insulin-like growth factor pathway genes on the strength-training response of muscle phenotypes in older adults. (2007) (45)
The next stage: molecular epidemiology. (1997) (45)
Association of the ACTN3 Genotype and Physical Functioning With Age in Older Adults (2008) (45)
Association of 8p23 Deletions with Poor Survival in Head and Neck Cancer (2001) (45)
Glycosylated hemoglobin determination from capillary blood samples. Utility in an epidemiologic survey of diabetes. (1984) (44)
Influence of the interleukin-6 -174 G/C gene polymorphism on exercise training-induced changes in glucose tolerance indexes. (2004) (44)
A Genome-Wide Association Study of Chronic Otitis Media with Effusion and Recurrent Otitis Media Identifies a Novel Susceptibility Locus on Chromosome 2 (2013) (43)
Lymphedema-distichiasis syndrome and FOXC2 gene mutation. (2002) (43)
Exercise training, NADPH oxidase p22phox gene polymorphisms, and hypertension. (2009) (43)
Polymorphisms of interleukin (IL)-1alpha, IL-1beta, IL-6, IL-10, and IL-18 and the risk of ovarian cancer. (2004) (43)
4G/5G plasminogen activator inhibitor-1 polymorphisms and haplotypes are associated with pneumonia. (2007) (43)
Variants of SLC6A4 in depression risk following severe TBI (2013) (43)
Description of a dinucleotide repeat polymorphism in the human elastin gene and its use to confirm assignment of the gene to chromosome 7 (1993) (42)
Research Perspectives in Inherited Lymphatic Disease (2002) (42)
Chromosome 8q24 variants are associated with prostate cancer risk in a high risk population of African ancestry (2011) (42)
Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions (2009) (42)
ACE insertion/deletion polymorphism and submaximal exercise hemodynamics in postmenopausal women. (2002) (42)
COMT val158Met and executive control: a test of the benefit of specific deficits to translational research. (2007) (42)
Association of the ACTN3 genotype and physical functioning with age in older adults. (2008) (41)
Genetic studies of human apolipoproteins. XVIII. Apolipoprotein polymorphisms in Australian Aborigines. (1991) (41)
The frequency in Japanese of genetic variants of 22 proteins (1977) (41)
Role of common genetic polymorphisms in the LDL receptor gene in affecting plasma cholesterol levels in the general population. (1994) (41)
Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels (2003) (41)
A common promotor variant in the cytochrome P450c17alpha (CYP17) gene is associated with bioavailability testosterone levels and bone size in men. (2001) (41)
Melanopsin Gene Variations Interact With Season to Predict Sleep Onset and Chronotype (2012) (41)
Polymorphism of the serotonin transporter: implications for the use of selective serotonin reuptake inhibitors. (2001) (40)
Leptin receptor Gln223Arg polymorphism and breast cancer risk in Nigerian women: A case control study (2008) (40)
Lipoprotein subclass and particle size differences in Afro-Caribbeans, African Americans, and white Americans: associations with hepatic lipase gene variation. (2006) (40)
Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA (2007) (40)
A locus for renal malformations including vesico-ureteric reflux on chromosome 13q33-34. (2006) (39)
Association of the peroxisome proliferator-activated receptor gamma gene with type 2 diabetes mellitus varies by physical activity among non-Hispanic whites from Colorado. (2007) (39)
The stepwise mutation model: an experimental evaluation utilizing hemoglobin variants. (1980) (39)
Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females. (2004) (39)
IL28B polymorphism is associated with both side effects and clearance of hepatitis C during interferon-alpha therapy. (2011) (39)
Familial nephrotic syndrome: clinical spectrum and linkage to chromosome 19q13. (2000) (39)
The Multinational Andean Genetic and Health Program. IX. Gene frequencies and rare variants of 20 serum proteins and erythrocyte enzymes in the Aymara of Chile. (1980) (39)
Three novel aniridia mutations in the human PAX6 gene (1995) (38)
Trinucleotide repeat length variation in the human ribosomal protein L14 gene (RPL14): localization to 3p21.3 and loss of heterozygosity in lung and oral cancers. (1998) (38)
A novel mutation in the apolipoprotein E gene (APOE*4 Pittsburgh) is associated with the risk of late-onset Alzheimer's disease (1999) (38)
The association between vitamin D receptor gene polymorphisms and bone mineral density at the spine, hip and whole-body in premenopausal women (2005) (38)
Farnesyl diphosphate synthase: a novel genotype association with bone mineral density in elderly women. (2007) (38)
Haptoglobin genotype and functional outcome after aneurysmal subarachnoid hemorrhage. (2014) (38)
The St. Lawrence Island Eskimos: genetic variation and genetic distance. (1981) (37)
Variation in the human lectin‐like oxidized low‐density lipoprotein receptor 1 (LOX‐1) gene is associated with plasma soluble LOX‐1 levels (2008) (37)
Resolution of the two loci for autosomal dominant aniridia, AN1 and AN2, to a single locus on chromosome 11p13. (1992) (37)
The Khatri Sikh Diabetes Study (SDS): Study Design, Methodology, Sample Collection, and Initial Results (2006) (36)
Serotonin transporter promoter polymorphism in African Americans : allele frequencies and implications for treatment. (2003) (36)
Association Analysis of WNT10B With Bone Mass and Structure Among Individuals of African Ancestry (2009) (36)
Multi-institutional prostate cancer study of genetic susceptibility in populations of African descent. (2011) (36)
Genetic studies of human apolipoproteins: XII. Population genetics of apolipoproteins in Papua New Guinea (1990) (35)
Identifying genetic susceptibilities to diabetes-related complications among individuals at low risk of complications: An application of tree-structured survival analysis. (2006) (35)
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1). (1994) (35)
Genetic Variation in α2HS-Glycoprotein Is Related to Calcaneal Broadband Ultrasound Attenuation in Older Women (1998) (35)
A preliminary study on T-786C endothelial nitric oxide synthase gene and renal hemodynamic and blood pressure responses to dietary sodium. (2007) (35)
Albumin Yanomama‐2, a ‘private’ polymorphism of serum albumin (1974) (35)
Blood Pressure Response to Strength Training May Be Influenced by Angiotensinogen A–20C and Angiotensin II Type I Receptor A1166C Genotypes in Older Men and Women (2005) (35)
Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men (2011) (35)
Genomic analysis of immediate/early response to shear stress in human coronary artery endothelial cells. (2002) (35)
Amino acid sequence of sheep carbonic anhydrase C. (1974) (35)
TOMM40 poly-T repeat lengths, age of onset and psychosis risk in Alzheimer disease (2011) (35)
Genetic studies of low-abundance human plasma proteins. V. Evidence for a second orosomucoid structural locus (ORM2) expressed in plasma. (1987) (34)
Genetic characterization of American and Western Samoans. (1994) (34)
Apolipoprotein A-IV polymorphism, and its role in determining variation in lipoprotein-lipid, glucose and insulin levels in normal and non-insulin-dependent diabetic individuals. (1991) (34)
A macrophage migration inhibitory factor promoter polymorphism is associated with high-density parasitemia in children with malaria (2006) (34)
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family (2002) (33)
Genetic differentiation in Dogrib Indians: serum protein and erythrocyte enzyme variation. (1983) (33)
Association between amygdala reactivity and a dopamine transporter gene polymorphism (2014) (33)
Relationship of a 5-HT transporter functional polymorphism to 5-HT1A receptor binding in healthy women (2005) (32)
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas. (1989) (32)
Exercise-induced changes in insulin action are associated with ACE gene polymorphisms in older adults. (2002) (32)
Haplotypes of the monoamine oxidase genes and the risk for substance use disorders (2004) (32)
Three novel activating mutations in the calcium-sensing receptor responsible for autosomal dominant hypocalcemia. (2000) (32)
A discordant sibship analysis between beta-NGF and neurofibromatosis. (1985) (31)
Association of FCgamma receptor IIA (CD32) polymorphism with malarial anemia and high-density parasitemia in infants and young children. (2006) (31)
Steroid sulfatase gene variation and DHEA responsiveness to resistance exercise in MERET. (2004) (31)
Role of angiotensin converting enzyme genotype in sodium sensitivity in older hypertensives. (2001) (31)
Association of Lipoprotein Lipase Gene Variation with the Physiological Components of the Insulin-Resistance Syndrome in the Population of the San Luis Valley, Colorado (1993) (31)
Lipoprotein lipase gene variation is associated with adipose tissue lipoprotein lipase activity, and lipoprotein lipid and glucose concentrations in overweight postmenopausal women (2000) (31)
Association of serotonin-1A and 2A receptor promoter polymorphisms with depressive symptoms and functional recovery in elderly persons after hip fracture. (2008) (31)
Age of onset in hereditary lymphedema. (2003) (31)
No association between ACE I/D polymorphism and cardiovascular hemodynamics during exercise in young women. (2005) (31)
Adenylate Cyclase 7 Is Implicated in the Biology of Depression and Modulation of Affective Neural Circuitry (2012) (30)
RNASEL and RNASEL‐inhibitor variation and prostate cancer risk in Afro‐Caribbeans (2008) (30)
Identification of a novel 5-base pair deletion in calcineurin B (PPP3R1) promoter region and its association with left ventricular hypertrophy. (2005) (30)
Mitochondrial 16S rRNA sequence diversity of hominoids. (2001) (30)
The C161-->T polymorphism in peroxisome proliferator-activated receptor gamma, but not P12A, is associated with insulin resistance in Hispanic and non-Hispanic white women: evidence for another functional variant in peroxisome proliferator-activated receptor gamma. (2005) (30)
eNOS T-786C genotype, physical activity, and peak forearm blood flow in females. (2003) (30)
Evaluation of 15 Functional Candidate Genes for Association with Chronic Otitis Media with Effusion and/or Recurrent Otitis Media (COME/ROM) (2011) (29)
The Aymara of Western Bolivia. IV. Gene frequencies for eight blood groups and 19 protein and erythrocyte enzyme systems. (1978) (29)
Cytochrome P450 1B1 Val432Leu polymorphism and breast cancer risk in Nigerian women: a case control study (2009) (29)
Peripheral retinopathy in offspring of carriers of Norrie disease gene mutations. Possible transplacental effect of abnormal Norrin. (1996) (29)
Genetic studies of low abundance human plasma proteins. II. Population genetics of coagulation factor XIIIB. (1986) (29)
Vitamin D receptor FokI genotype influences bone mineral density response to strength training, but not aerobic training (2005) (28)
Racial variation in toll-like receptor variants among women with pelvic inflammatory disease. (2013) (28)
Does age, sex, or ACE genotype affect glucose and insulin responses to strength training? (2002) (28)
Host and environmental interactions in diabetes mellitus. (1986) (28)
Effects of apolipoprotein E genotype on dietary-induced changes in high-density lipoprotein cholesterol in obese postmenopausal women. (2002) (27)
Serotonin Transporter Promoter Polymorphism in African Americans (2003) (27)
Associations between dietary factors and serum lipids by apolipoprotein E polymorphism. (1996) (27)
Variability within alpha- and beta-adrenoreceptor genes as a predictor of cardiovascular function at rest and in response to mental challenge. (2002) (27)
Association of KIBRA rs17070145 polymorphism and episodic memory in individuals with severe TBI (2012) (27)
DNA polymorphisms of the apolipoprotein AI/CIII/AIV gene cluster influence plasma cholesterol and triglyceride levels in the Mayans of the Yucatán Peninsula, Mexico. (1991) (27)
5‐HTTLPR genotype potentiates the effects of war zone stressors on the emergence of PTSD, depressive and anxiety symptoms in soldiers deployed to iraq (2015) (27)
Population genetics of alpha-1-antitrypsin polymorphism in US whites, US blacks and African blacks. (1991) (27)
Estimation of the frequency of isoform–genotype discrepancies at the apolipoprotein E locus in heterozygotes for the isoforms (1992) (27)
ApoA-IV Polymorphism Associated With Myocardial Infarction in Obese NIDDM Patients: The San Luis Valley Diabetes Study (1994) (27)
Identification of genetic alterations related to chemoresistance in epithelial ovarian cancer. (2003) (27)
Genetic variants in major histocompatibility complex-linked genes associate with pediatric liver transplant rejection. (2008) (26)
Population Genetic Characteristics of the D1S80 locus in seven human populations (1994) (26)
Wilms tumor with aniridia/iris dysplasia and apparently normal chromosomes (1982) (26)
Angiotensinogen M235T polymorphism associates with exercise hemodynamics in postmenopausal women. (2002) (26)
Genetic studies of human apolipoproteins. XV. An overview of IEF immunoblotting methods to screen apolipoprotein polymorphisms. (1990) (26)
The PPARγ Pro12Ala Polymorphism Is Not Associated with Body Mass Index or Waist Circumference among Hispanics from Colorado (2007) (26)
Serotonin transporter triallelic genotype and response to citalopram and risperidone in dementia with behavioral symptoms (2010) (26)
X Chromosome-Linked IRAK-1 Polymorphism Is a Strong Predictor of Multiple Organ Failure and Mortality Postinjury (2014) (26)
Haptoglobin genotype and cerebrovascular disease incidence in type 1 diabetes (2014) (25)
The Serotonin Transporter: Sequence Variation in Macaca fascicularis and its Relationship to Dominance (2007) (25)
Allele sharing at six VNTR loci and genetic distances among three ethnically defined human populations (1992) (25)
Genetic studies of human apolipoproteins. XVII: Population genetics of apolipoprotein polymorphisms in American Samoa. (1991) (25)
Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24. (2003) (25)
The frequency in Japanese of genetic variants of 22 proteins (1977) (25)
Absence of Mutation in the β- and γ-Synuclein Genes in Familial Autosomal Dominant Parkinson's Disease (1998) (25)
Cytochrome P4501A1 genetic polymorphisms and breast cancer risk in Nigerian women (2005) (24)
African American hypertensive nephropathy maps to a new locus on chromosome 9q31-q32. (2003) (24)
A syndrome of microcephaly and retinal pigmentary abnormalities without mental retardation in a family with coincidental autosomal dominant hyperreflexia. (1984) (24)
Alcohol dependence, disinhibited behavior and variation in the prodynorphin gene (2011) (24)
Research Perspectives in Inherited Lymphatic Disease (2008) (24)
A Novel Functional Variant in the Stem Cell Growth Factor Promoter Protects against Severe Malarial Anemia (2009) (24)
A genetic linkage study of familial breast-ovarian cancer. (1989) (24)
Interleukin-6 genotype is associated with high-density lipoprotein cholesterol responses to exercise training. (2005) (24)
Racial disparities and sex-based outcomes differences after severe injury. (2012) (24)
Preeclampsia Risk and Angiotensinogen Polymorphisms M235T and AGT -217 in African American and Caucasian Women (2008) (24)
NOS3 gene polymorphisms and exercise hemodynamics in postmenopausal women. (2006) (23)
ELAC2 and prostate cancer risk in Afro-Caribbeans of Tobago (2002) (23)
OXTR polymorphism predicts social relationships through its effects on social temperament. (2015) (23)
AKAP10 (I646V) functional polymorphism predicts heart rate and heart rate variability in apparently healthy, middle-aged European-Americans. (2009) (23)
Tumor necrosis factor-alpha gene polymorphisms are associated with severity of acute graft-versus-host disease following matched unrelated donor bone marrow transplantation in children: a Pediatric Blood and Marrow Transplant Consortium study. (2010) (23)
Quantitative effects of the apolipoprotein E polymorphism in a biracial sample of 9-10-year-old girls. (1996) (23)
Preliminary report: Vitamin D receptor and aromatase gene interaction and bone mass in older African-American women (2003) (23)
Smoking and reverse cholesterol transport: evidence for gene‐environment interaction (1989) (23)
Sequence variation in the primate dopamine transporter gene and its relationship to social dominance. (2007) (23)
Phenotypic effects of apolipoprotein structural variation on lipid profiles. I. APO H and quantitative lipid measures in the healthy women study (1989) (22)
Polymorphisms in the platelet-specific collagen receptor GP6 are associated with risk of nonfatal myocardial infarction in Caucasians. (2011) (22)
Nucleotide sequence comparison of a chromosome rearrangement on human chromosome 12 and the corresponding ape chromosomes (2004) (22)
Amino acid sequence of rabbit carbonic anhydrase II. (1978) (22)
Apolipoprotein A-IV genetic polymorphism and its impact on quantitative traits in normoglycemic and non-insulin-dependent diabetic Hispanics from the San Luis Valley, Colorado. (1992) (22)
Association between common alleles of the low-density lipoprotein receptor gene region and interindividual variation in plasma lipid and apolipoprotein levels in a population-based sample from Rochester, Minnesota (1996) (22)
Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19 (2011) (22)
A dietary and behavioral intervention designed to lower coronary heart disease. Risk factors are unaffected by variation at the APOE gene locus. (1997) (22)
Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers (2004) (21)
Criteria to detect minimal expressivity within families with autosomal dominant aniridia. (1992) (21)
Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3. (1998) (21)
Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease. (1998) (21)
The BDNF Val66Met polymorphism does not moderate the effect of self-reported physical activity on depressive symptoms in midlife (2014) (21)
Variable number of tandem repeat (VNTR) polymorphism at locus D17S5 (YNZ22) in four ethnically defined human populations (1992) (21)
X‐linked exudative vitreoretinopathy caused by an arginine to leucine substitution (R121L) in the Norrie disease protein (1996) (21)
FABP2 genotype is associated with insulin sensitivity in older women. (2001) (21)
Familial rheumatoid arthritis: a kindred identified through a proband with seronegative juvenile arthritis includes members with seropositive, adult-onset disease. (1982) (21)
DNA “fingerprints” and paternity ascertainment in chimpanzees (Pan troglodytes) (1990) (21)
DNA “fingerprinting” and the genetic management of a captive chimpanzee population (Pan troglodytes) (1991) (20)
Multiple restriction fragment length polymorphisms of the human epidermal growth factor receptor gene. (1988) (20)
Problems Associated with Layer Charge Characterization of 2:1 Phyllosilicates (1994) (20)
Two common polymorphisms in the APO A‐IV coding gene: Their evolution and linkage disequilibrium (1992) (20)
The Brain-Derived Neurotrophic Factor Val 66 Met Polymorphism Moderates an Effect of Physical Activity on Working Memory Performance (2013) (20)
Phenotypic effects of apolipoprotein structural variation on lipid profiles. IV. Apolipoprotein polymorphisms in a small group of black women from the Healthy Women Study (1989) (20)
The high mobility group I-C gene (HMGI-C): polymorphism and genetic localization (1996) (20)
Genetic studies of human apolipoproteins. III. Polymorphism of apolipoprotein C-II. (1988) (20)
Gene Polymorphisms Impact the Risk of Rejection With Hemodynamic Compromise: A Multicenter Study (2011) (20)
The frequency in Japanese of genetic variants of 22 proteins III. Phosphoglucomutase‐1, phosphoglucomutase‐2, 6‐phosphogluconate dehydrogenase, adenylate kinase, and adenosine deaminase (1977) (20)
No association of psychosis in Alzheimer disease with neurodegenerative pathway genes (2011) (20)
Genome-Wide Linkage Scan to Identify Loci Associated with Type 2 Diabetes and Blood Lipid Phenotypes in the Sikh Diabetes Study (2011) (20)
Renin-angiotensin system genes and exercise training-induced changes in sodium excretion in African American hypertensives. (2006) (19)
Restriction analysis of the structural alpha-L-fucosidase gene and its linkage to fucosidosis. (1988) (19)
Catalase levels in patients with aniridia and/or Wilms' tumor: utility and limitations. (1981) (19)
The Haptoglobin 1 Allele Correlates With White Matter Hyperintensities in Middle-Aged Adults With Type 1 Diabetes (2014) (19)
The frequency of "rare" protein variants in Marshall islanders and other Micronesians. (1976) (19)
Variation of p53 mutational spectra between carcinoma of the upper and lower respiratory tract. (1995) (19)
A simplified method for screening the apolipoprotein E polymorphism. (1991) (19)
Comparison of five tandem repeat loci between humans and chimpanzees. (1992) (19)
Evidence for linkage of Charcot-Marie-Tooth neuropathy (CMT1) to apolipoprotein A2 (Apo-A2). (1988) (19)
Functional Characterization of Genetic Variation in the Frizzled 1 (FZD1) Promoter and Association With Bone Phenotypes: More to the LRP5 Story? (2009) (19)
The peroxisome proliferator-activated receptor gamma coactivator-1 alpha gene (PGC-1alpha) is not associated with type 2 diabetes mellitus or body mass index among Hispanic and non Hispanic Whites from Colorado. (2007) (19)
The impact of the apolipoprotein E polymorphism on the lipoprotein profile in insulin-dependent diabetes: the Pittsburgh Epidemiology of Diabetes Complications Study IX. (1992) (19)
The role of the apolipoprotein E polymorphism in the prediction of coronary artery disease age of onset (1997) (18)
Steroid-resistant nephrotic syndrome and congenital anomalies of kidneys: evidence of locus on chromosome 13q. (2003) (18)
Genomic structure and genetic mapping of the human neutral cysteine protease bleomycin hydrolase. (1997) (18)
Monozygotic twins concordant for probable Alzheimer disease and increased platelet membrane fluidity. (1988) (18)
Calcitonin gene polymorphism CALCA‐624 (T/C) and ovarian cancer (2005) (18)
Erratum: APOE*4–associated Alzheimer's disease risk is modified by α1–antichymotrypsin polymorphism (1995) (18)
Genetic studies of human apolipoproteins. IX. Apolipoprotein D polymorphism and its relation to serum lipoprotein lipid levels. (1989) (17)
C-reactive protein genotype affects exercise training-induced changes in insulin sensitivity. (2006) (17)
Differential serotonin transport is linked to the rh5-HTTLPR in peripheral blood cells (2012) (17)
APOE genotype affects black-white responses of high-density lipoprotein cholesterol subspecies to aerobic exercise training. (2008) (17)
Genetic studies of human apolipoproteins. XI. The effect of the apolipoprotein C-II polymorphism on lipoprotein levels in Nigerian blacks. (1989) (17)
??2- AND ??3-ADRENERGIC RECEPTOR POLYMORPHISMS AND EXERCISE HEMODYNAMICS IN POSTMENOPAUSAL WOMEN (2001) (17)
Simple tandem repeat (TTTA)n polymorphism in CYP19 (aromatase) gene and breast cancer risk in Nigerian women (2006) (17)
Genetic diversity and evolution of the human leptin locus tetranucleotide repeat (2002) (17)
Multi-institutional Study of Outcomes After Pediatric Heart Transplantation: Candidate Gene Polymorphism Analysis of ABCC2. (2014) (17)
Peroxisome Proliferator-Activated Receptor-γ Polymorphism, Body Mass and Prostate Cancer Risk: Evidence for Gene-Environment Interaction (2006) (17)
A Hierarchical Factor Model of Executive Functions in Adolescents: Evidence of Gene-Environment Interplay (2014) (17)
Chimpanzee apolipoprotein H (β2-glycoprotein I): report on the gene structure, a common polymorphism, and a high prevalence of antiphospholipid antibodies (2001) (16)
Genetic studies of low abundance human plasma proteins. III. Polymorphism of the C1R subcomponent of the first complement component. (1986) (16)
Molecular basis of a unique African Variant (A‐IV 5) of human apolipoprotein A‐IV and its significance in lipid metabolism (1992) (16)
Genetic studies of Type 2 (non-insulin-dependent) diabetes mellitus: lack of association with seven genetic markers (1989) (16)
Inter- and intrafamilial variability in premature pubarche and polycystic ovary syndrome. (2002) (16)
Systematic association studies of mitochondrial DNA variations in schizophrenia: focus on the ND5 gene. (2008) (16)
Atypical vitelliform macular dystrophy in a 5-generation family. (1984) (16)
CFH , ELOVL 4 , PLEKHA 1 and LOC 387715 genes and susceptibility to age-related maculopathy : AREDS and CHS cohorts and meta-analyses (2006) (16)
Gender‐specific nonrandom association between the α1‐antichymotrypsin and apolipoprotein E polymorphisms in the general population and its implication for the risk of Alzheimer's disease (1997) (16)
Highly polymorphic apolipoprotein A-IV locus in the baboon. (1990) (16)
Genetic variation at twentythree microsatellite loci in sixteen human populations (2008) (16)
Genetic and other factors determining mannose-binding lectin levels in American Indians: the Strong Heart Study (2009) (15)
Hypervariable polymorphism of APO(a) in blacks and whites as reflected by phenotyping. (1994) (15)
Linkage of DNA markers to cystic fibrosis in 26 families. (1986) (15)
Enhanced B Cell Alloantigen Presentation and Its Epigenetic Dysregulation in Liver Transplant Rejection (2016) (15)
Normal CAG repeat variation at the DRPLA locus in world populations. (1995) (15)
Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach (2012) (15)
mtDNA D-loop 6-bp deletion found in the Chilean Aymara: not a unique marker for Chibcha-speaking Amerindians. (1995) (15)
A common deletion polymorphism in the apolipoprotein A4 gene and its significance in lipid metabolism. (1994) (15)
Cross-sectional analysis of Toll-like receptor variants and bacterial vaginosis in African–American women with pelvic inflammatory disease (2014) (15)
Familial pheochromocytoma due to mutant von Hippel-Lindau disease gene. (1997) (15)
Correlates of lipoprotein(a) levels in a biracial cohort of young girls: the NHLBI Growth and Health Study. (1999) (15)
Glucose Level, Acculturation, and Glycosylated Hemoglobin: An Example of Biocultural Interaction (1990) (14)
Anterior segment mesenchymal dysgenesis: probable linkage to the MNS blood group on chromosome 4. (1982) (14)
Genetic variation in two bone‐related proteins: Is there an association with bone mineral density or skeletal size in postmenopausal women? (1992) (14)
Physical activity, hormone replacement therapy and plasma lipoprotein-lipid levels in postmenopausal women. (2003) (14)
The blacks of Panama: their genetic diversity as assessed by 15 inherited biochemical systems. (1978) (14)
Variants of the Adenosine A2A Receptor Gene Are Protective against Proliferative Diabetic Retinopathy in Patients with Type 1 Diabetes (2010) (14)
Genetic studies of human apolipoproteins. XX. Genetic polymorphism of apolipoprotein J and its impact on quantitative lipid traits in normolipidemic subjects. (1991) (14)
Genetic studies of low-abundance human plasma proteins (1988) (14)
Evolution of Carbonic Anhydrase in Primates and Other Mammals (1976) (13)
Selected genetic polymorphisms and plasma coagulation factor VII changes with exercise training. (2004) (13)
Genetic studies of low-abundance human plasma proteins. VI. Polymorphism of hemopexin. (1987) (13)
War Zone Stress Interacts With the 5-HTTLPR Polymorphism to Predict the Development of Sustained Attention for Negative Emotion Stimuli in Soldiers Returning From Iraq (2013) (13)
Genetic components of variations of red cell glycolytic intermediates at two altitudes among the South American Aymara. (1983) (13)
Blood pressure interacts with APOE ε4 to predict memory performance in a midlife sample. (2015) (13)
Genetic association and differential expression of PITX2 with acute appendicitis (2018) (13)
Polymorphic variation in choline transporter gene (CHT1) is associated with early, subclinical measures of carotid atherosclerosis in humans (2012) (13)
AMPD1 gene polymorphism and the vasodilatory response to ischemia. (2006) (13)
Beta2- and beta3-adrenergic receptor polymorphisms and exercise hemodynamics in postmenopausal women. (2004) (13)
Hypertension and sources of blood pressure variability among Mexican-Americans in Starr County, Texas. (1985) (13)
Biochemical markers in a species endangered by introgression: The red wolf (1980) (13)
Genetic polymorphism and fertility parameters in the Aymara of Chile and Bolivia (1986) (12)
Nonsense mutation in the homeobox region of the aniridia gene (1994) (12)
Gene diversity of chimpanzee ABO blood group genes elucidated from intron 6 sequences. (2000) (12)
Renal function and genetic polymorphisms in pediatric heart transplant recipients. (2012) (12)
Gene diversity of chimpanzee ABO blood group genes elucidated from exon 7 sequences. (2000) (12)
Differential rates of evolution in the carbonic anhydrase isozymes of catarrhine primates (1972) (12)
A genetic linkage study in 15 families of individuals with von Recklinghausen neurofibromatosis. (1985) (12)
Wilms tumor with aniridia/iris dysplasia and apparently normal chromosomes. (1982) (12)
Correlation of paternity index with probability of exclusion and efficiency criteria of genetic markers for paternity testing. (1982) (12)
Genetic variation in the Aleuts of the Pribilof Islands and the Eskimos of Kodiak Island. (1988) (12)
Biochemical and genetic identity of alpha‐keto acid reductase and cytoplasmic malate dehydrogenase from human erythrocytes (1988) (12)
EVOLUTION OF THE CARBONIC ANHYDRASE ISOZYMES (1975) (12)
Gene and gene-product variation in the apolipoprotein A-I/C-III/A-IV cluster in the Dogrib Indians of the Northwest Territories. (1989) (12)
Influence of apolipoprotein E genotype variation on the means, variances, and correlations of plasma lipids and apolipoproteins in children (1999) (11)
The frequency in Japanese of genetic variants of 22 proteins: IV. Acid phosphatase, NADP‐isocitrate dehydrogenase, peptidase A, peptidase B and phosphohexose isomerase (1978) (11)
Comparison of ultrasonographic and digital cervical evaluation. (1986) (11)
A family study of the hemoglobin polymorphism in Macaca fascicularis (1980) (11)
Genetic structure of five susceptibility gene regions for coronary artery disease: disequilibria within and among regions (1998) (11)
Association of genetic polymorphisms and risk of late post-transplantation infection in pediatric heart recipients. (2010) (11)
The relationship between ciliary neurotrophic factor (CNTF) genotype and motor unit physiology: preliminary studies (2005) (11)
Apolipoprotein H polymorphism and serum lipoprotein and apolipoprotein levels in two Asian populations. (1993) (11)
Apolipoprotein H (beta-2-glycoprotein I) polymorphism in Asians. (1992) (11)
Genetic studies of low‐abundance human plasma proteins: X. Coagulation factor XIIIB variants in blacks (1989) (11)
Genome-wide linkage study of erythrocyte sodium-lithium countertransport. (2005) (11)
Isoelectric focusing of superoxide dismutase: report of the unique SOD A*2 allele in a US white population. (1988) (11)
Genotypic Variation and Phenotypic Characterization of Granzyme B Gene Polymorphisms (2009) (11)
Hepatic lipase gene -514C>T variant is associated with exercise training-induced changes in VLDL and HDL by lipoprotein lipase. (2011) (11)
Genetics of the apolipoproteins and the contribution of allelic variation to quantitative variation in lipid and lipoprotein levels in the population (1992) (10)
The Nubians of Kom Ombo: serum and red cell protein types. (1978) (10)
Ciliary neurotrophic factor (CNTF) genotype and body composition (2004) (10)
A sensitive immunoblotting technique to identify thyroxin-binding globulin protein heterogeneity after isoelectric focusing (1986) (10)
Nuclear receptor coactivator-3 alleles are associated with serum bioavailable testosterone, insulin-like growth factor-1, and vertebral bone mass in men. (2006) (10)
Alpha2-HS glycoprotein phenotypes and quantitative hormone and bone measures in postmenopausal women (1990) (10)
Genetic studies of human apolipoproteins. II. A rapid one‐dimensional isoelectric focusing technique to characterize apolipoproteins A‐I, A‐II, A‐IV and C‐II of unfractionated plasma (1987) (10)
Immunoglobulin allotypes in Southwest Asia: Populations at the Crossroads (2008) (10)
C 2 and CFB Genes in Age-Related Maculopathy and Joint Action with CFH and LOC 387715 Genes (2008) (9)
Sex linkage of muscle creatine kinase in Harris’ hawks (1987) (9)
Re: Genetic effect of α1-antichymotrypsin on the risk of Alzheimer disease (1997) (9)
Association of SLC34A2 variation and sodium-lithium countertransport activity in humans and baboons. (2009) (9)
Apolipoprotein E Polymorphism Among the Indian Populations and its Comparison with Other Asian Populations (2001) (9)
Linkage relationships of the gene for the beta subunit of nerve growth factor (NGFB) with other chromosome 1 marker loci. (1985) (9)
Exclusion of atypical vitelliform macular dystrophy from 8q24.3 and from other known macular degenerative loci. (1997) (9)
The Heritability of Otitis Media (1999) (8)
Association of a Pvull RFLP at the lipoprotein lipase locus with fasting insulin levels in Hispanic men (1993) (8)
Hemopexin: a unique genetic polymorphism in populations of African ancestry. (1993) (8)
Genetic studies of low-abundance human plasma proteins. XIII. Population genetics of C1R complement subcomponent and description of new variants. (1989) (8)
Serotonin Transporter Promoter Polymorphism in (2003) (8)
An RFLP for glycoprotein A (MN) is in linkage disequilibrium with MN and Ss. (1988) (8)
Management of preterm premature rupture of membranes. (1983) (8)
Genetic testing considerations for oral medicine. (2002) (8)
Dinucleotide repeat polymorphism in the human aniridia (PAX6) gene. (1993) (8)
Genetic polymorphisms in southwest Alaskan Eskimos. (1991) (8)
C 174 T polymorphism in the CNTF receptor gene is associated with fat-free mass in men and women (2003) (8)
Clinial genetic variation at enzyme loci in bald eagles (Haliaeetus leucocephalus) from the western United States (1985) (7)
Novel HLA-DP region susceptibility loci associated with severe acute GvHD (2017) (7)
GENETIC STUDIES OF LOW‐ABUNDANCE HUMAN PLASMA PROTEINS: VII. HETEROGENEITY OF THE C1, SUBCOMPONENT OF THE FIRST COMPLEMENT COMPONENT (1987) (7)
A population genetic study in the Ochamchir region, Abkhazia, SSR. (1985) (7)
Association between NEDD4L gene and sodium lithium countertransport. (2011) (7)
Vitamin D receptor and aromatase gene interaction and bone mass in older African-American women. (2003) (7)
Brown adipose tissue function in short-chain acyl-CoA dehydrogenase deficient mice. (2010) (7)
Circulating Interleukin-6 concentration covaries inversely with self-reported sleep duration as a function of polymorphic variation in the glucocorticoid receptor (2019) (7)
Paternity exclusion in primates: Two strategies (1979) (7)
Genetic studies of human apolipoproteins. XIII. Quantitative polymorphism of apolipoprotein C-III in the Mayans of the Yucatán Peninsula. (1990) (7)
ANGIOTENSINOGEN M235T POLYMORPHISM AND EXERCISE HEMODYNAMICS IN POSTMENOPAUSAL WOMEN (2001) (7)
Genetic studies of low-abundance human plasma proteins. I. Microheterogeneity of zinc-α2-glycoprotein in biological fluids (1986) (7)
Identification of a Novel Mutation Combination in Factor XIII Deficiency: Genetic Update to the First Reported Case in the United States (2006) (6)
•1-Acid Glycoprotein in Late-Life Depression: Relationship to Medical Burden and Genetics (2003) (6)
Plasma lipoprotein(a) distribution and its correlates among Samoans. (2000) (6)
Effect of chronic altitude hypoxia on hematologic and glycolytic parameters. (1982) (6)
Intratribal Genetic Differentiation as Assessed through Electrophoresis (1990) (6)
Two new alleles in the tetranucleotide repeat polymorphism at the lipoprotein lipase (LPL) locus (1992) (6)
Peroxisome proliferator-activated receptor-gamma polymorphism, body mass and prostate cancer risk: evidence for gene-environment interaction. (2006) (6)
Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
The holoacardius acephalus twin: prenatal diagnosis. (1986) (6)
Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
Genetic studies of low-abundance human plasma proteins. IV. Improved typing of alpha-1 acid glycoprotein (orosomucoid) by isoelectric focusing and immunoblotting. (1987) (5)
A regulatory variant of the human tryptophan hydroxylase-2 gene biases amygdala reactivity (2005) (5)
Genetic heterogeneity of aniridia: negative linkage data. (1980) (5)
Purification of a carboxypeptidase B-like enzyme from the starfish Dermasterias imbricata. (1975) (5)
Apolipoprotein E polymorphism and preclinical carotid artery disease in untreated hypertensive men (2006) (5)
Obesity: choosing genetic approaches from a mixed menu. (1993) (5)
The aminoterminal sequence of Dendrostomum pyroides hemerythrin (1971) (5)
Indirect association of DAT1 genotype with executive function through white matter volume in orbitofrontal cortex (2015) (5)
Association Between the Dopamine Receptor D5 Gene and the Liability to Substance Dependence in Males: A Replication (2001) (5)
Abstracts of workshop presentations pp. 948-967 (1989) (5)
Genetic studies of human apolipoproteins: XIV. A simple agarose isoelectric focusing gel method for apolipoprotein E phenotyping (1990) (5)
Substitution of lysine for threonine at position 100 in human carbonic anhydrase Id Michigan. (1973) (5)
Independent and combined influence of AGTR1 variants and aerobic exercise on oxidative stress in hypertensives (2009) (5)
Genetic studies of low abundance human plasma proteins. VIII. Inherited structural variation in antithrombin III. (1988) (5)
Molecular studies of the genetics of non–insulin‐dependent diabetes mellitus (1993) (5)
An electrophoretic study of glycolytic enzymes in a human population living at high altitude: the Aymara of northern Chile and western Bolivia (1981) (5)
Mannose binding lectin genotypes are not associated with increased risk of unexplained recurrent pregnancy loss (2013) (5)
Biochemical genetics of the culex pipiens complex—II. Hexokinase (1980) (5)
MICROARRAY ANALYSIS OF MUSCLE GENE EXPRESSION: INFLUENCE OF AGE, SEX, AND STRENGTH TRAINING (2002) (5)
ACE INSERTION/DELETION POLYMORPHISM AND SUBMAXIMAL EXERCISE CARDIOVASCULAR HEMODYNAMICS IN POSTMENOPAUSAL WOMEN (2001) (5)
The -93T/G LPL Promoter Polymorphism Is Associated With Lower Third-Trimester Triglycerides in Pregnant African American Women (2015) (5)
2,3-Diphosphoglycerate and night vision. (1981) (4)
Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes. (1987) (4)
Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
The Chilean Aymara and their Reproductive Patterns (1990) (4)
Autosomal dominant cone-rod dystrophy: a linkage study with 17 biochemical and serological markers. (1981) (4)
A linkage study of protein-coding loci in Macaca mulatta and Macaca fascicularis. (1985) (4)
Effect of Metabolic Acidosis on Hydrogen Ion Excretion in a Pigtail Macaque with Erythrocyte Carbonic Anhydrase I Deficiency 1 (1981) (4)
Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
A linkage study of multiple endocrine neoplasia type IIa. (1985) (4)
Reduction to homozygosity at the SIS/PDGF-2 locus in human mesenchymal tumors. (1988) (4)
Biochemical genetics of the Culex pipiens complex—III. α-glycerophosphate dehydrogenase (1981) (4)
Hematocrit and hemoglobin, ATP and DPG concentrations in Andean man: the interaction of altitude and trace metals with glycolytic and hematologic parameters in man. (1981) (4)
Clinal genetic variation at enzyme loci in bald eagles (Haliaeetus leucocephalus) from the western United States. (1985) (4)
TREATMENT TRIAL AND LONG-TERM FOLLOW-UP EVALUATION AMONG COMORBID YOUTH WITH MAJOR DEPRESSION AND A CANNABIS USE DISORDER. (2012) (4)
Regional association-based fine-mapping for sodium-lithium countertransport on chromosome 10. (2008) (4)
726 AUTOSOMAL DOMINANT ANTERIOR SEGMENT DYSGENESIS WITH VARIABLE EXPRESSIVITY: PROBABLE LINKAGE TO MNS BLOOD GROUP ON CHROMOSOME 4 (1981) (4)
The IL-10 -819T polymorphism is associated with increased susceptibility to severe sepsis (2003) (4)
The reduction of aromatic alpha-keto acids by cytoplasmic malate dehydrogenase and lactate dehydrogenase (1987) (4)
Application of molecular techniques to the study of human physiological variation (1989) (3)
X-linked familial exudative vitreoretinopathy caused by an arginine to leucine substitution in exon 3 of the Norrie gene (1994) (3)
Structural studies on Dendrostomum pyroides hemerythrin. (1971) (3)
Impact of pro-domain stability of matrix metalloproteinase-8 on the outcome of sepsis (2011) (3)
Abdominal aortic aneurysm aaa association with alpha 1 antitrypsin haptoglobin and type iii collagen (1991) (3)
Alpha-1-antitrypsin (PI) and vitamin-D binding globulin (GC) phenotypes in rheumatoid arthritis: absence of an association. (1989) (3)
Genetic studies of low-abundance human plasma proteins. XI. Linkage analysis and population genetics of the C1S subcomponent of the first complement component. (1989) (3)
MATRIX METALLOPROTEINASE (MMP)-8 IS CRITICAL In A MURINE MODEL OF SEPSIS As Well As IN PATIENTS WITH COMMUNITY- ACQUIRED PNEUMONIA (CAP)-ASSOCIATED SEPSIS (2010) (3)
Heat stability of Clostridium tartarivorum ferredoxin: Application of structure predicting models (1976) (3)
Association between SLC20A1 and sodium-lithium countertransport. (2011) (3)
Zhou et al. reply (2009) (3)
Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
Restriction fragment length polymorphism of the human insulin gene region among type II diabetic Mexican-Americans and Tunisians. (1986) (3)
Autosomal dominant ophthalmologic disorders and linkage. (1982) (3)
Apolipoprotein E Polymorphism In Two Populations Of Andhra Pradesh (1999) (3)
The SPINK1 N34S mutation is not associated with Type 2 diabetes mellitus in a population of the USA (2005) (3)
Serotonin Transporter Genotype Linked to Adolescent Substance Use Treatment Outcome through Externalizing Behavior (2014) (3)
Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred (2017) (3)
Leptin receptor Gln 223 Arg polymorphism and breast cancer risk in Nigerian women : A case control study (2008) (3)
In the Company of Generals: The World War I Diary of Pierpont L. Stackpole (2009) (3)
Genetic studies of low abundance human plasma proteins VIII. Inherited structural variation in antithrombin III (1988) (3)
PPARα gene polymorphisms modulate the association between physical activity and cardiometabolic risk. (2014) (3)
Biochemical genetics of the Culex pipiens complex. I. 6-phosphogluconate dehydrogenase (1980) (3)
Erratum: Association and linkage analyses of RGS4 polymosphisms in schizophrenia (Human Molecular Genetics (2002) vol. 11 (1373-1380)) (2003) (3)
Variation of p 53 Mutational Spectra between Carcinoma of the Upper and Lower Respiratory Tract (2005) (3)
Genetic variation in an urban population of Aedes aegypti (Diptera: Culicidae). (1984) (3)
Genetic Effect of Two APOA Repeat Polymorphisms (Kringle 4 and Pentanucleotide Repeats) on Plasma Lp(a) Levels in American Samoans (2001) (3)
Genetic variation in the apolipoproteins C-II and C-III. (1988) (2)
VEGFR3 gene structure, regulatory region, and sequence polymorphisms (2001) (2)
Possible heterogeneity in the phosphoglycolate phosphatase (PGP)-haptoglobin alpha (HPA) linkage. (1984) (2)
Haplotype structure and linkage disequilibrium in 26 worldwide populations. (2002) (2)
X-linked, polymorphic genetic variation of thyroxin-binding globulin (TBG) in baboons and screening of additional primates (1984) (2)
Genetic analysis of childhood sarcoma. (1989) (2)
Potential information in family studies of linkage. (1979) (2)
Genetic studies of low-abundance human plasma proteins. IX. A new allele at the complement subcomponent C1R structural locus. (1988) (2)
Genetic markers of fibrinolytic responses of older persons to exercise training. (2006) (2)
Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
Characterization of a new variant of human red cell carbonic anhydrase I, CA if London (Glu-102→Lys) (1973) (2)
Immunoglobulin (Gm and Km) allotypes in the Aymara of Chile and Bolivia. (1985) (2)
Genetic polymorphism of apolipoprotein A-IV in the chimpanzee: common deletion of a conserved 12-nucleotide tandem repeat. (1994) (2)
59: TNF-α and TNF Receptor Superfamily Member 1B Polymorphisms Predict Risk of Acute GVHD Following Matched Unrelated Donor BMT in Children (2008) (2)
Genes, Enzymes and Hypoxia (1978) (2)
EVOLUTION OF ABO BLOOD GROUP GENES (1995) (2)
Characterization of a new variant of human red cell carbonic anhydrase I, CA If London (Glu-102 leads to Lys). (1973) (2)
Polymorphic variability in the IL-1 β promoter conditions susceptibility to severe malarial anemia and functional changes in IL-1 β production (2009) (2)
ESR 1 polymorphism is associated with plasma lipid and apolipoprotein levels in Caucasians of the Rochester Family Heart Study (2008) (2)
The C174T polymorphism in the CNTF receptor (CNTFR) gene is associated with fat free mass in men and women (2003) (1)
Reply to Reed (1992) (1)
Three F XIIIA gene loci? (1989) (1)
Cloning and Sequencing of the Rabbit FGFR2 cDN A (2000) (1)
Influence of age, sex, and strength training on human skeletal muscle gene expression determined by cDNA microarrays (2002) (1)
Interaction of apolipoprotein E genotype and dietary cholesterol in determining plasma cholesterol levels. (1992) (1)
Re: Genetic effect of alpha 1-antichymotrypsin on the risk of Alzheimer disease. (1997) (1)
Red Cell Carbonic Anhydrase I Determined by Enzyme‐Linked Immunosorbent Assay in Patients with Renal Tubular Acidosis (1984) (1)
Protein Phosphatase 3 (PPP3R1) Gene Polymorphism Influences Muscle Volume Response To Strength Training: 872 Board #94 10:30 AM ??? 12:00 PM (2005) (1)
Insulin-like growth factor-2 ( IGF2 ) genotype, fat-free mass, and muscle performance across the adult life span (2004) (1)
IV and with ACE gene polymorphisms in older adults Exercise-induced changes in insulin action are associated (2002) (1)
Hereditary Disorders of the Lymphatic System and Varicose Veins (2013) (1)
Aspects of lymphatic biology and disease: Panel discussion (2002) (1)
A method for inferring evolutionary relationships among haplotypes, exemplified by haplotypes at the monoamine oxidase locus (2004) (1)
Properties of Dendrostomum pyroides hemerythrin. (1970) (1)
Erythrocyte phosphoglucomutase: A family study of a PGM1 deficient allele (2004) (1)
VITAMIN D RECEPTOR GENOTYPE AND INSULIN SENSITIVITY IN POSTMENOPAUSAL WOMEN OF VARIOUS PHYSICAL ACTIVITY LEVELS (2002) (1)
Reply to Baer. (1993) (1)
814 Genetics of Intracranial Aneurysms II: Alterations in the Regulatory Sequence of Collagenase Type IV (2001) (1)
The analysis of hidden electrophoretic variation: Interspecific electrophoretic differentiation and amino acid divergence (2005) (1)
NO ASSOCIATION BETWEEN ACE INSERTION/DELETION POLYMORPHISM AND MAXIMAL EXERCISE CARDIOVASCULAR HEMODYNAMICS IN YOUNG WOMEN (2002) (1)
Molecular and cytogenetic analysis of chromosome 7 in uterine leiomyoma (1994) (1)
Deletion and mutational inactivation of the cyclin-dependent kinase-4 inhibitor gene (p16) in oral carcinoma (1994) (1)
Mechanisms of Beneficial Effects of Physical Activity on Atherosclerosis and Coronary Heart Disease Hepatic lipase gene-514 C T variant is associated with exercise training-induced changes in VLDL and HDL by lipoprotein lipase (2011) (1)
Retinal hemorrhage and vacuum extraction delivery. (1986) (1)
TNFα -238A Allele Identifies Patients Who Develop Both Acute and Chronic GVHD After Matched Unrelated Donor Transplant in Children: A Pediatric Blood and Marrow Transplant Consortium Study (2012) (0)
Estrogens, Genetic Polymorphisms and Breast Cancer Risk (2004) (0)
Impact of Common Type 2 Diabetes Risk Polymorphisms in Asian Indian Sikhs : Gene-Gene Interaction May Improve Risk Prediction (2007) (0)
An Alternative Transcript of the PANE1 Gene Encodes a Minor Histocompatibility Antigen That Is Selectively Expressed in Resting CD19+ Cells and B-CLL. (2005) (0)
COMT polymorphism and seven-year change in cognitive function in a biracial sample of older adults: Findings from the health ABC study (2009) (0)
A Three-Day Seismic Experiment in an Urban Setting: An Introduction to Seismology for Minority Students (2004) (0)
PERIPHERAL BENZODIAZEPINE RECEPTOR POLYMORPHISMS ARE ASSOCIATED WITH PLASMA DHEA AND CORTISOL RESPONSES TO STRENGTH TRAINING (2002) (0)
APOE E4 ALLELE IS ASSOCIATED WITH LOWER MEMORY SCORES IN MIDDLE-AGED ADULTS (1999) (0)
Genetic studies of human apolipoproteins. XIX. Apolipoproteins E and A-IV phenotyping from whole blood and blood stains. (1991) (0)
Identification and Effects of Novel Promoter Region Haplotypes in the Human Equilibrative Nucleoside Transporter, hENT1. (2004) (0)
ENDOTHELIAL LIPASE GENOTYPE AFFECTS HDL-C SUB-FRACTIONS AND THEIR CHANGES WITH EXERCISE TRAINING (2003) (0)
A linkage study for prelingual deafness (1991) (0)
CETP GENOTYPE AND TRAINING-INDUCED CHANGES IN LDL PARTICLE SIZE (2003) (0)
coagulation factor VII changes with exercise training Selected genetic polymorphisms and plasma (2015) (0)
Over-representation of the APOE*4 allele in autopsy confirmed early- and late-onset sporadic Alzheimer`s disease (1994) (0)
PHYSICAL ACTIVITY HABITS, CANDIDATE GENE POLYMORPHISMS, BODY COMPOSITION, AND PLASMA LIPOPROTEIN-LIPID LEVELS IN POSTMENOPAUSAL WOMEN. (1999) (0)
Influence Of AGTR1 Gene Variants And Aerobic Exercise Training On Angiotensin II And Oxidative Stress: 704 (2008) (0)
Effects of Exercise Training on Plasma Nitric Oxide Metabolite Levels: Association with Common eNOS Gene Polymorphisms: 1836 (2008) (0)
Index by Keyword (1989) (0)
Influence of cytokine and growth factor gene polymorphisms on acute and chronic rejection after pediatric heart transplantation (2003) (0)
Effects of Gene Variation on Exercise-Induced Weight Loss, Body Composition and Fat Distribution in Obese Males : 2498 (2007) (0)
INTERACTIVE EFFECTS OF ENOS T-786C GENE POLYMORPHISM AND CARDIOVASCULAR FITNESS ON FLOW-MEDIATED DILATION IN FEMALES (2003) (0)
HAPLOTYPE-BASED PROSTATE CANCER ASSOCIATION STUDY IN AFRO- CARIBBEANS OF TOBAGO (2010) (0)
Predictive Biomarkers and Personalized Medicine Connexin 47 Mutations Increase Risk for Secondary Lymphedema Following Breast Cancer Treatment (2012) (0)
Chromosome 13 and chromosome 2 (CA)n polymorphisms. (1994) (0)
The logica organica of Jose Vasconcelos (1989) (0)
Autosomal dominant aniridia: Prob phosphatase-1 locus on chromosome (genetic heterogeneity/LIPED computer program/variable expres (2016) (0)
Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
Association of the ELOVL4 Gene With Age–Related Maculopathy (2005) (0)
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS SUBSTITUTION OF LYSINE FOR THREONINE AT POSITION 100 IN HUMAN CARBONIC (2003) (0)
ApoE binds with high affinity to the low density lipoprotein ( LDL ) receptors of the liver and peripheral tissues , chylomicron remnant receptors of the liver (0)
ACE GENE POLYMORPHISM AND EXERCISE TRAINING-INDUCED CHANGES IN SODIUM EXCRETION IN AFRICAN AMERICAN HYPERTENSIVES (2001) (0)
Estrogen receptor-α genotype is associated with prostate cancer risk among men of African descent (2004) (0)
EFFECT OF APO E POLYMORPHISM ON COAGULATION FACTOR VII RESPONSE TO EXERCISE TRAINING (2002) (0)
A note on the use of HGML LIT literature file numbers (1989) (0)
A general method for visualizing enzymes releasing adenosine or adenosine-5′-monophosphate (1984) (0)
26-OR: Impact of genetic polymorphisms on rejection with hemodynamic compromise – A multi-institutional study (2008) (0)
Heart Disease Variation in Plasma Lipid and Apolipoprotein Levels Associated With Risk of Coronary Genome-Wide Linkage Analysis Reveals Evidence of Multiple Regions That Influence (2001) (0)
The estimate of protein polymorphism in human populations: lack of evidence for overestimation due to post-translational modification (1985) (0)
Calcineurin Gene Variation and Resistance Exercise Training Responses in MERET (2004) (0)
The analysis of nondisjunction in human ovarian teratomas using dna markers (1991) (0)
pDL32b (D12S7) detects a 2-allele PstI polymorphism. (1991) (0)
Panel Discussion on Genes, Environment and Disease (1993) (0)
Brief Communication: Hemopexin A Unique Genetic Polymorphism in Populations of African Ancestery (1993) (0)
MUSCULAR STRENGTH ACROSS THE ADULT LIFE SPAN IS INFLUENCED BY INSULIN-LIKE GROWTH FACTOR-2 (IGF2) GENOTYPE. (2002) (0)
The SPINKI N34S mutation is not associated with type 2 diabetes mellitus in the united states (2003) (0)
Blood Pressure Response to Strength Training May be Influenced by Agiotensinogen (AGT M235T) Genotype in Older Adults (2004) (0)
The gene of an early onset progressive cataract (cerulean cataract) maps to 17q24 (1994) (0)
Disparate genetic polymorphism among ethnic groups in pediatric heart transplantation (2006) (0)
In the Company of Generals (2009) (0)
Specific Genetic Markers of Endurance Performance and &OV0312;o2max (2001) (0)
Trauma, serotonin transporter genotypes, affective dysregulation, and SUD risk (2011) (0)
Analysis of the reported relationship between thyroxin-binding globulin and alpha-1-antitrypsin heterogeneity (1987) (0)
CETP Gene Variation And Cholesterol Response To Resistance Exercise Training In MERET: 877 Board #99 9:00 AM ??? 10:30 AM (2005) (0)
Dinucleotide repeat polymorphism at the HPR locus. (1994) (0)
A Novel Approach To Studying The Impact Of Pro-Domain Stability On Matrix Metalloproteinase Activation (2011) (0)
Androgen Receptor CAG repeat is Associated with Fat Free Mass in Men but not in Women (2004) (0)
30: An integrated genetic-protein analysis of the TNF-family pathway predicts for GVHD (2007) (0)
ASSOCIATION OF FC (cid:1) RECEPTOR IIA (CD32) POLYMORPHISM WITH MALARIAL ANEMIA AND HIGH-DENSITY PARASITEMIA IN INFANTS AND YOUNG CHILDREN (2006) (0)
Referees for volume 30 (1992) (0)
139 Association between Renal Function and Genetic Polymorphisms in Pediatric Heart Transplant Recipients (2012) (0)
P-109: ACE gene polymorphism is associated with exercise training-induced changes in Na+ excretion in african american hypertensives (2003) (0)
intensities in postmenopausal women Cardiovascular hemodynamics with increasing exercise (2015) (0)
Further Explorations in the Genetics of Age-Related Maculopathy (ARM) (2009) (0)
日本人における22種の蛋白質の遺伝的変異体とその頻度-1-ALBUMIN,CERULOPLASMIN,HAPTOGLOBIN,およびTRANSFERRIN(放影研闌-27-) (1978) (0)
weight loss in obesity biogenesis induced by moderate-intensity exercise and Characteristics of skeletal muscle mitochondrial (2015) (0)
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts (2015) (0)
Haptoglobin genotype and renal function decline in t ype 1 diabetes Running title: Haptoglobin genotype and renal functi on in T1D (2009) (0)
older adults influenced by insulin-like growth factor 1 genotype in Muscle strength response to strength training is (2015) (0)
315: The Impact of HLA-G Polymorphism on Acute Rejection in Pediatric Heart Transplant Recipients (2010) (0)
1.P.253 Characterization and in vitro expression of a novel apolipoprotein CIII variant identified in individuals of Mayan Indian origin (1997) (0)
exercise hemodynamics in postmenopausal women Angiotensinogen M235T polymorphism associates with (2013) (0)
responsiveness to resistance exercise in MERET Steroid sulfatase gene variation and DHEA (2013) (0)
EXERCISE-INDUCED IMPROVEMENTS IN INSULIN SENSITIVITY ARE ASSOCIATED WITH ACE GENE POLYMORPHISMS (2002) (0)
Ciliary Neurotrophic Factor (CNTF) GENOTYPE is ASSOCIATED with SKELETAL MUSCLE RESPONSES to STRENGTH TRAINING (2001) (0)
Report of the committee on the genetic constitution of chromosome 5. (1989) (0)
AGE, BIRTH CONTROL, STRENGTH TRAINING HISTORY ASSOCIATED TO LEAN MASS GAIN WITH STRENGTH TRAINING (2002) (0)
INTERACTION OF THE ENOS GENE AND PHYSICAL ACTIVITY LEVEL ON FLOW-MEDIATED VASODILATION (2003) (0)
Vitamin D Receptor FokI Polymorphism, HLA-DQB1 Susceptibility Alleles and Type 1 Diabetes: A Gene-Gene Interaction (2002) (0)
Inactivation of STAT1 by promoter methylation contributes to squamous cell carcinogenesis (2005) (0)
and muscle performance across the adult life span Insulin-like growth factor-2 genotype, fat-free mass, (2015) (0)
Converging classical cytogenetic, molecular cytogenetic, and molecular genetic analyses of oral squamous cell carcinoma (1995) (0)
An improved method for complement subcomponent C1R typing. (1990) (0)
resistance exercise training responses interleukin-15 receptor genetic variation with Association of interleukin-15 protein and (2015) (0)
Molecular Studies of Genetic Distance and Admixture (1994) (0)
Perceived Group Reinforcement Scale (2014) (0)
92-kDa type IV collagenase (CLG4B) in aortic aneurysmal disease and assignment to chromosome 20 (1994) (0)
DOES IGF-II GENOTYPE PREDICT BMI AND BODY FAT IN MEN AND WOMEN ACROSS THE ADULT AGE SPAN? (2001) (0)
HLA-G II GENOTYPE AND LOW LEVELS OF SOLUBLE HLA-G POST-TRANSPLANT ARE ASSOCIATED WITH FIRST YEAR REJECTION POST PEDIATRIC HEART TRANSPLANTATION.: 881 (2010) (0)
A Novel Functional Variant in the Stem Cell Growth Factor ( SCGF ) Promoter (-539 C / T ) Protects Against Severe Malarial Anemia (2009) (0)
Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
Abstract 5726: Association between human herpesvirus 8 infection, inflammation and a polymorphism in the IL-6 signaling receptor in increased prostate cancer risk among men of African descent (2010) (0)
Behavioral genetics of the cynomolgus macaque (2006) (0)
RENAL HEMODYNAMIC AND BLOOD PRESSURE RESPONSE TO DIETARY SODIUM IS ASSOCIATED WITH THE ENOS GENE (2003) (0)
Genetic Epidemiology of Adenocarcinoma of the Colon1 (1985) (0)
postmenopausal women is associated with ACE genotype in 2 max V?o (2015) (0)
11-OR: HLA-G II Genotype and Low Levels of sHLA-G Post-Tx are Associated With First Year Rejection in Pediatric Heart Transplantation (2010) (0)
RESTING BLOOD PRESSURE RESPONSE TO STRENGTH TRAINING MAY DEPEND ON ANGIOTENSINOGEN (-20) GENOTYPE (2001) (0)
Skeletal muscle gene expression in Type II diabetic , obese insulin-resistant , and exercise-trained men (2003) (0)
COLLECTIVE EFFECTS OF ADRENERGIC RECEPTOR (AR) POLYMORPHISMS ARE ASSOCIATED WITH BODY FAT RESPONSE TO TRAINING (2003) (0)
exercise hemodynamics in postmenopausal women ACE insertion/deletion polymorphism and submaximal (2013) (0)
P-170 Aromatase gene haplotypes are associated with cognitive function in a biracial cohort of older adults: The health ABC study (2007) (0)
Calcitonin A Genotype Is Associated with Risk of Acute Graft-Versus-Host Disease Following Allogeneic Bone Marrow Transplantation for Children with Acute Myeloid Leukemia in First Remission. (2005) (0)
IS CILIARY NEUROTROPHIC FACTOR (CNTF) GENOTYPE RELATED TO MOTOR UNIT PHYSIOLOGY DURING SUBMAXIMAL CONTRACTIONS (2001) (0)
Genetic association and differential expression of PITX2 with acute appendicitis (2018) (0)
Identification and Effects of Novel Promoter Region Haplotypes in the Human Cytidine Deaminase Gene. (2004) (0)
Index by Abstract Number (1989) (0)
Linkage of Charcot-Marie-Tooth Neuropathy (HMSN Type I) to Antithrombin III (AT3) Supports Heterogeneity of the Disease (1987) (0)
X-linked Cone Dystrophy (COD I) (2007) (0)
Acknowledgement to referees 2003 (2004) (0)
Does the evolutionary conservation of microsatellite loci imply function (1994) (0)
Refinement and Candidate Gene Screening of the Cerulean Cataract Type 1 Locus on 17q24-q25 (2003) (0)
EFFECTS OF ENOS GENE POLYMORPHISM ON 24-HOUR URINARY NITRIC OXIDE METABOLITE LEVELS AFTER ACUTE EXERCISE (2002) (0)
Application of isozymes to the mapping of inherited ophthalmic disorders. (1983) (0)
RS2383206 and its association with mortality in a cohort of individuals with type 1 diabetes (2009) (0)
stress in human coronary artery endothelial cells Genomic analysis of immediate / early response to shear (2002) (0)
NADPH Oxidase p22phox Gene Polymorphisms and Oxidative Stress Responses to Exercise Training in Pre and Stage 1 Hypertensives (2009) (0)
ASSOCIATION OF HIF1A GENOTYPE WITH MAXIMAL OXYGEN CONSUMPTION BEFORE AND AFTER AEROBIC EXERCISE TRAINING (2003) (0)
Refined localization of an X-linked cone-rod dystrophy (COD1) (1994) (0)
Referees for volume 30 (2004) (0)
LSU Geoscience Alliance to Enhance Minority Participation: Building Partnerships with Minority-Serving Institutions (2004) (0)
532: Genetic Polymorphisms Impact the Risk of Infection in Pediatric Heart Transplantation – A Multi-Center Study (2009) (0)
39-OR: CYTOKINE AND CHEMOKINE GENE POLYMORPHISMS IMPACT ON CMV INFECTION IN LUNG TRANSPLANT RECIPIENTS (2012) (0)
Attention for Negative Emotion Stimuli in Soldiers Returning From Iraq War Zone Stress Interacts With the 5-HTTLPR Polymorphism to Predict the Development of Sustained (2013) (0)
Transfer of Advances in Sciences into Dental Education Genetic Testing Considerations for Oral Medicine (2004) (0)
40-OR: The combination high VEGF/high IL-6 and low IL-10 gene polymorphism impact the risk of acute rejection in pediatric heart transplantation – a multicenter study (2007) (0)
GENETIC EFFECTS ON SODIUM EXCRETION IN HYPERTENSIVE AFRICAN AMERICANS: EFFECTS OF SHORT-TERM EXERCISE TRAINING (2002) (0)
associated with fat-free mass in men Androgen receptor CAG repeat polymorphism is (2015) (0)
COMMON GENETIC POLYMORPHISMS AND PLASMA LIPOPROTEIN LIPID RESPONSES TO EXERCISE TRAINING (2002) (0)
EXERCISE-INDUCED ENHANCEMENTS IN INSULIN ACTION ARE ASSOCIATED WITH ACE GENE POLYMORPHISMS IN OLDER HYPERTENSIVES (2002) (0)
A Functional Polymorphism in the Endothelial Nitric Oxide Synthase Gene is a Risk Factor for Subarachnoid Hemorrhage in Normotensive Patients with Intracranial Aneurysms (2003) (0)
P4-120 The calcium sensing receptor in Alzheimer disease susceptibility (2004) (0)
COMMON GENETIC POLYMORPHISMS AND CHOLESTEROL RESPONSE TO EXERCISE TRAINING (2003) (0)
ASSOCIATION OF THE VITAMIN D RECEPTOR (VDR) FOKI GENOTYPE WITH MUSCLE MASS IN OLDER MEN (2003) (0)
Replication of Association of CFH, Plekha1/LOC387715 and Elovl4 Genes With ARM in the AREDS Cohort (2006) (0)
EFFECTS OF ACE AND APO E GENE POLYMORPHISMS ON EXERCISE TRAINING-INDUCED CHANGES IN NITRIC OXIDE METABOLITES (2001) (0)
Comparative Genomics and Molecular Evolution (2004) (0)
Phenotypic effects of the apolipoprotein e locus in white and black perimenopausal healthy women (1989) (0)
Multifaceted assessment of genetic alterations in oralcancer (1997) (0)
PI‐10 (2006) (0)
314: Genotypic Variation and Phenotypic Characterization of Granzyme B Gene Polymorphisms (2008) (0)
FLT4 (VEGFR3) and Milroy Disease (2016) (0)

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