Robert Evans Ferrell
#101,262
Most Influential Person Now
Robert Evans Ferrell's AcademicInfluence.com Rankings
Robert Evans Ferrellbiology Degrees
Biology
#5080
World Rank
#7471
Historical Rank
Molecular Biology
#432
World Rank
#441
Historical Rank
Genetics
#442
World Rank
#510
Historical Rank

Download Badge
Biology
Why Is Robert Evans Ferrell Influential?
(Suggest an Edit or Addition)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)
This paper list is powered by the following services:
What Schools Are Affiliated With Robert Evans Ferrell?
Robert Evans Ferrell is affiliated with the following schools: