PubRank

Stephen S Rich

Author PubWeight™ 300.72‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. Nat Genet 2009 16.53
2 Gut microbiomes of Malawian twin pairs discordant for kwashiorkor. Science 2013 6.98
3 Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat Genet 2011 6.36
4 Robust relationship inference in genome-wide association studies. Bioinformatics 2010 5.57
5 Loss-of-function mutations in APOC3, triglycerides, and coronary disease. N Engl J Med 2014 5.47
6 Inactivating mutations in NPC1L1 and protection from coronary heart disease. N Engl J Med 2014 4.94
7 Early-onset stroke and vasculopathy associated with mutations in ADA2. N Engl J Med 2014 4.70
8 High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nat Genet 2012 4.46
9 Pervasive sharing of genetic effects in autoimmune disease. PLoS Genet 2011 4.42
10 Genetics of type 1A diabetes. N Engl J Med 2009 3.18
11 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes. Diabetes 2009 3.16
12 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. PLoS Genet 2011 3.07
13 Imputing amino acid polymorphisms in human leukocyte antigens. PLoS One 2013 3.07
14 The landscape of recombination in African Americans. Nature 2011 3.06
15 Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat Genet 2011 3.03
16 A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. Lancet Neurol 2007 2.99
17 Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet 2013 2.92
18 Candidate gene association resource (CARe): design, methods, and proof of concept. Circ Cardiovasc Genet 2010 2.91
19 Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans. J Clin Endocrinol Metab 2008 2.87
20 Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families. Diabetes 2005 2.85
21 Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium. PLoS One 2013 2.65
22 Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. Nat Genet 2013 2.60
23 Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke. Ann Neurol 2009 2.55
24 Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. Am J Hum Genet 2012 2.53
25 Genetic epidemiology of insulin resistance and visceral adiposity. The IRAS Family Study design and methods. Ann Epidemiol 2003 2.51
26 A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3. Diabetes 2008 2.51
27 Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and randomised trials. Lancet 2011 2.35
28 Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. PLoS Genet 2011 2.33
29 Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium. Diabetes 2009 2.02
30 A genome scan for diabetic nephropathy in African Americans. Kidney Int 2004 2.00
31 The Ischemic Stroke Genetics Study (ISGS) Protocol. BMC Neurol 2003 1.98
32 Pericardial and visceral adipose tissues measured volumetrically with computed tomography are highly associated in type 2 diabetic families. Invest Radiol 2005 1.98
33 Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. Am J Hum Genet 2012 1.96
34 Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus. Am J Hum Genet 2002 1.93
35 Variants of the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in an African-American population enriched for nephropathy. Diabetes 2007 1.86
36 Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nat Genet 2013 1.83
37 Relationship between albuminuria and cardiovascular disease in Type 2 diabetes. J Am Soc Nephrol 2005 1.82
38 The Siblings With Ischemic Stroke Study (SWISS) protocol. BMC Med Genet 2002 1.82
39 Confirmation of genetic associations at ELMO1 in the GoKinD collection supports its role as a susceptibility gene in diabetic nephropathy. Diabetes 2009 1.80
40 Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study. Am J Respir Crit Care Med 2014 1.80
41 Genetics of type 1 diabetes: what's next? Diabetes 2010 1.80
42 Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes. Stroke 2013 1.80
43 Negligible impact of rare autoimmune-locus coding-region variants on missing heritability. Nature 2013 1.79
44 Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND). Diabetes 2007 1.79
45 Heritability of carotid artery intima-medial thickness in type 2 diabetes. Stroke 2002 1.78
46 Genetic linkage and association of Fcgamma receptor IIIA (CD16A) on chromosome 1q23 with human systemic lupus erythematosus. Arthritis Rheum 2002 1.71
47 A generalized family-based association test for dichotomous traits. Am J Hum Genet 2009 1.70
48 Cellular basis of diabetic nephropathy: 1. Study design and renal structural-functional relationships in patients with long-standing type 1 diabetes. Diabetes 2002 1.70
49 Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project. Blood 2013 1.69
50 Genome-wide scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND). Diabetes 2007 1.61
51 Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project. Am J Hum Genet 2012 1.60
52 Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study. Am J Hum Genet 2001 1.59
53 ImmunoChip study implicates antigen presentation to T cells in narcolepsy. PLoS Genet 2013 1.55
54 Bicc1 is a genetic determinant of osteoblastogenesis and bone mineral density. J Clin Invest 2014 1.53
55 Population structure of Hispanics in the United States: the multi-ethnic study of atherosclerosis. PLoS Genet 2012 1.53
56 Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. PLoS Genet 2012 1.52
57 Exome sequencing in suspected monogenic dyslipidemias. Circ Cardiovasc Genet 2015 1.51
58 Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. Am J Respir Crit Care Med 2012 1.49
59 Heritability of GFR and albuminuria in Caucasians with type 2 diabetes mellitus. Am J Kidney Dis 2004 1.47
60 Functional IL6R 358Ala allele impairs classical IL-6 receptor signaling and influences risk of diverse inflammatory diseases. PLoS Genet 2013 1.47
61 Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci. Stroke 2011 1.45
62 Chronic and recurrent otitis media: a genome scan for susceptibility loci. Am J Hum Genet 2004 1.44
63 Tests for genetic interactions in type 1 diabetes: linkage and stratification analyses of 4,422 affected sib-pairs. Diabetes 2011 1.44
64 A genome-wide linkage scan for genes controlling variation in renal function estimated by serum cystatin C levels in extended families with type 2 diabetes. Diabetes 2006 1.43
65 Coincident linkage of type 2 diabetes, metabolic syndrome, and measures of cardiovascular disease in a genome scan of the diabetes heart study. Diabetes 2006 1.39
66 Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic stroke. Ann Neurol 2005 1.36
67 Identification of a locus for maturity-onset diabetes of the young on chromosome 8p23. Diabetes 2004 1.34
68 A leucine repeat in the carnosinase gene CNDP1 is associated with diabetic end-stage renal disease in European Americans. Nephrol Dial Transplant 2007 1.33
69 A genome-wide search for quantitative trait loci contributing to variation in seasonal pollen reactivity. J Allergy Clin Immunol 2006 1.32
70 A genome scan for ESRD in black families enriched for nondiabetic nephropathy. J Am Soc Nephrol 2004 1.30
71 Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry. Nat Genet 2011 1.30
72 Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure. J Allergy Clin Immunol 2003 1.27
73 A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q. Diabetes 2004 1.26
74 Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. Diabetes 2003 1.24
75 Association of the distal region of the ectonucleotide pyrophosphatase/phosphodiesterase 1 gene with type 2 diabetes in an African-American population enriched for nephropathy. Diabetes 2008 1.22
76 A genome-wide scan of pulmonary function measures in the National Heart, Lung, and Blood Institute Family Heart Study. Am J Respir Crit Care Med 2003 1.19
77 Genetic mapping of disposition index and acute insulin response loci on chromosome 11q. The Insulin Resistance Atherosclerosis Study (IRAS) Family Study. Diabetes 2006 1.19
78 Calcified atherosclerotic plaque and bone mineral density in type 2 diabetes: the diabetes heart study. Bone 2007 1.18
79 Fine-scale patterns of population stratification confound rare variant association tests. PLoS One 2013 1.18
80 Mutations at the BLK locus linked to maturity onset diabetes of the young and beta-cell dysfunction. Proc Natl Acad Sci U S A 2009 1.17
81 Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study. Diabetes 2004 1.14
82 Interobserver agreement in the trial of org 10172 in acute stroke treatment classification of stroke based on retrospective medical record review. J Stroke Cerebrovasc Dis 2007 1.14
83 Circulating and dietary omega-3 and omega-6 polyunsaturated fatty acids and incidence of CVD in the Multi-Ethnic Study of Atherosclerosis. J Am Heart Assoc 2013 1.14
84 Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. Circ Cardiovasc Genet 2013 1.12
85 Genetic susceptibility to ischemic stroke. Nat Rev Neurol 2011 1.12
86 Sex differences in stroke severity, symptoms, and deficits after first-ever ischemic stroke. J Stroke Cerebrovasc Dis 2007 1.10
87 Association of the estrogen receptor-alpha gene with the metabolic syndrome and its component traits in African-American families: the Insulin Resistance Atherosclerosis Family Study. Diabetes 2007 1.10
88 Analysis of family- and population-based samples in cohort genome-wide association studies. Hum Genet 2011 1.09
89 Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions. Am J Hum Genet 2011 1.09
90 A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage. Arthritis Rheum 2004 1.09
91 A genome scan for all-cause end-stage renal disease in African Americans. Nephrol Dial Transplant 2005 1.08
92 Id3 is a novel atheroprotective factor containing a functionally significant single-nucleotide polymorphism associated with intima-media thickness in humans. Circ Res 2010 1.07
93 Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study. Arch Otolaryngol Head Neck Surg 2006 1.07
94 Association of a 62 Variants Type 2 Diabetes Genetic Risk Score With Markers of Subclinical Atherosclerosis: A Transethnic, Multicenter Study. Circ Cardiovasc Genet 2015 1.07
95 Familial clustering for features of the metabolic syndrome: the National Heart, Lung, and Blood Institute (NHLBI) Family Heart Study. Diabetes Care 2006 1.06
96 Links between insulin resistance, adenosine A2B receptors, and inflammatory markers in mice and humans. Diabetes 2011 1.06
97 Age-stratified heritability estimation in the Framingham Heart Study families. BMC Genet 2003 1.04
98 An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes. Kidney Int 2011 1.04
99 Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study. Diab Vasc Dis Res 2008 1.03
100 Apolipoprotein E genotype, cardiovascular biomarkers and risk of stroke: systematic review and meta-analysis of 14,015 stroke cases and pooled analysis of primary biomarker data from up to 60,883 individuals. Int J Epidemiol 2013 1.03
101 Association of protein tyrosine phosphatase 1B gene polymorphisms with type 2 diabetes. Diabetes 2004 1.02
102 The impact of pedigree structure on heritability estimates for pulse pressure in three studies. Hum Hered 2005 1.02
103 A genome-wide scan for urinary albumin excretion in hypertensive families. Hypertension 2003 1.02
104 Biomarkers of dairy fatty acids and risk of cardiovascular disease in the Multi-ethnic Study of Atherosclerosis. J Am Heart Assoc 2013 1.01
105 Common genetic variation, residential proximity to traffic exposure, and left ventricular mass: the multi-ethnic study of atherosclerosis. Environ Health Perspect 2010 1.00
106 Cellular basis of diabetic nephropathy: II. The transforming growth factor-beta system and diabetic nephropathy lesions in type 1 diabetes. Diabetes 2002 1.00
107 Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset. Hum Mol Genet 2013 1.00
108 Variants of the CD40 gene but not of the CD40L gene are associated with coronary artery calcification in the Diabetes Heart Study (DHS). Am Heart J 2006 1.00
109 Evidence of gene-gene interaction and age-at-diagnosis effects in type 1 diabetes. Diabetes 2012 1.00
110 Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations. PLoS One 2012 0.99
111 Next generation sequencing reveals the association of DRB3*02:02 with type 1 diabetes. Diabetes 2013 0.98
112 Association of SCARB1 variants with subclinical atherosclerosis and incident cardiovascular disease: the multi-ethnic study of atherosclerosis. Arterioscler Thromb Vasc Biol 2012 0.98
113 Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project. PLoS One 2012 0.98
114 A genome-wide association study of chronic otitis media with effusion and recurrent otitis media identifies a novel susceptibility locus on chromosome 2. J Assoc Res Otolaryngol 2013 0.97
115 APOM and high-density lipoprotein cholesterol are associated with lung function and per cent emphysema. Eur Respir J 2013 0.97
116 Linkage heterogeneity of end-stage renal disease on human chromosome 10. Kidney Int 2002 0.97
117 Candidate gene polymorphisms for ischemic stroke. Stroke 2009 0.96
118 Heritability and expression of C-reactive protein in type 2 diabetes in the Diabetes Heart Study. Ann Hum Genet 2006 0.95
119 Genetic modifiers of the age at diagnosis of diabetes (MODY3) in carriers of hepatocyte nuclear factor-1alpha mutations map to chromosomes 5p15, 9q22, and 14q24. Diabetes 2003 0.94
120 T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study. J Am Soc Nephrol 2005 0.94
121 Association of the tissue kallikrein gene promoter with ESRD and hypertension. Kidney Int 2002 0.94
122 Genetic ancestry and lower extremity peripheral artery disease in the Multi-Ethnic Study of Atherosclerosis. Vasc Med 2010 0.94
123 Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity. Hum Genet 2012 0.93
124 Structural genomic variation in ischemic stroke. Neurogenetics 2008 0.93
125 Diabetic nephropathy is associated with gene expression levels of oxidative phosphorylation and related pathways. Diabetes 2006 0.92
126 Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect. Diabetes Care 2002 0.92
127 Genome-wide association analysis of ischemic stroke in young adults. G3 (Bethesda) 2011 0.92
128 A variational Bayes discrete mixture test for rare variant association. Genet Epidemiol 2014 0.92
129 Comprehensive evaluation of the estrogen receptor alpha gene reveals further evidence for association with type 2 diabetes enriched for nephropathy in an African American population. Hum Genet 2008 0.91
130 Associations between genetic variants in the ACE, AGT, AGTR1 and AGTR2 genes and renal function in the Multi-ethnic Study of Atherosclerosis. Am J Nephrol 2010 0.91
131 Association of integrin alpha2 gene variants with ischemic stroke. J Cereb Blood Flow Metab 2007 0.91
132 Age-stratified QTL genome scan analyses for anthropometric measures. BMC Genet 2003 0.91
133 A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma. Hum Genet 2003 0.91
134 Human lipoxygenase pathway gene variation and association with markers of subclinical atherosclerosis in the diabetes heart study. Mediators Inflamm 2010 0.91
135 Genetic susceptibility contributes to renal and cardiovascular complications of type 2 diabetes mellitus. Hypertension 2006 0.90
136 Family-based association analysis confirms the role of the chromosome 9q21.32 locus in the susceptibility of diabetic nephropathy. PLoS One 2013 0.90
137 IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations. Stroke 2007 0.90
138 Early progression of diabetic nephropathy correlates with methylglyoxal-derived advanced glycation end products. Diabetes Care 2013 0.90
139 Investigation of the estrogen receptor-alpha gene with type 2 diabetes and/or nephropathy in African-American and European-American populations. Diabetes 2007 0.90
140 Association of scavenger receptor class B type I polymorphisms with subclinical atherosclerosis: the Multi-Ethnic Study of Atherosclerosis. Circ Cardiovasc Genet 2009 0.90
141 Insulin sensitivity and insulin clearance are heritable and have strong genetic correlation in Mexican Americans. Obesity (Silver Spring) 2014 0.89
142 A method for gene-based pathway analysis using genomewide association study summary statistics reveals nine new type 1 diabetes associations. Genet Epidemiol 2014 0.89
143 Gene expression differences in skin fibroblasts in identical twins discordant for type 1 diabetes. Diabetes 2012 0.89
144 DNA Methylation of the Aryl Hydrocarbon Receptor Repressor Associations With Cigarette Smoking and Subclinical Atherosclerosis. Circ Cardiovasc Genet 2015 0.89
145 Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population. Mol Genet Metab 2007 0.89
146 Genetic analysis of the GLUT10 glucose transporter (SLC2A10) polymorphisms in Caucasian American type 2 diabetes. BMC Med Genet 2005 0.88
147 Association of alpha2-Heremans-Schmid glycoprotein polymorphisms with subclinical atherosclerosis. J Clin Endocrinol Metab 2006 0.88
148 Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis. PLoS One 2011 0.87
149 Evaluation of 15 functional candidate genes for association with chronic otitis media with effusion and/or recurrent otitis media (COME/ROM). PLoS One 2011 0.86
150 Significant linkage at chromosome 19q for otitis media with effusion and/or recurrent otitis media (COME/ROM). BMC Med Genet 2011 0.86
151 Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations-significant evidence for linkage on chromosome 4q in African Americans: the Family Investigation of Nephropathy and Diabetes Research Group. Diabetes Metab Res Rev 2009 0.86
152 APOE genotype modifies the association between plasma omega-3 fatty acids and plasma lipids in the Multi-Ethnic Study of Atherosclerosis (MESA). Atherosclerosis 2013 0.85
153 Genetics of glucose homeostasis: implications for insulin resistance and metabolic syndrome. Arterioscler Thromb Vasc Biol 2012 0.85
154 5. Genetics of allergic disease. J Allergy Clin Immunol 2008 0.85
155 NOTCH3 variants and risk of ischemic stroke. PLoS One 2013 0.84
156 Evaluation of genetic variation and association in the matrix metalloproteinase 9 (MMP9) gene in ESRD patients. Am J Kidney Dis 2003 0.84
157 Quantitative trait loci on chromosome 8q24 for pancreatic beta-cell function and 7q11 for insulin sensitivity in obese nondiabetic white and black families: evidence from genome-wide linkage scans in the NHLBI Hypertension Genetic Epidemiology Network (HyperGEN) study. Diabetes 2006 0.84
158 Examination of candidate chromosomal regions for type 2 diabetes reveals a susceptibility locus on human chromosome 8p23.1. Diabetes 2004 0.84
159 Prevalence of nephropathy in black patients with type 2 diabetes mellitus. Am J Nephrol 2002 0.83
160 Association of the mu-opioid receptor gene with type 2 diabetes mellitus in an African American population. Mol Genet Metab 2005 0.83
161 Amyotrophic lateral sclerosis: an emerging era of collaborative gene discovery. PLoS One 2007 0.83
162 Nephropathy in siblings of African Americans with overt type 2 diabetic nephropathy. Am J Kidney Dis 2002 0.82
163 A hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples. BMC Genomics 2014 0.82
164 Air pollution and percent emphysema identified by computed tomography in the Multi-Ethnic study of Atherosclerosis. Environ Health Perspect 2014 0.82
165 Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Circ Cardiovasc Genet 2014 0.81
166 DNA structural variants as genetic risk factors for the long QT syndrome. J Am Coll Cardiol 2011 0.81
167 Association of protein tyrosine phosphatase-N1 polymorphisms with coronary calcified plaque in the Diabetes Heart Study. Diabetes 2006 0.81
168 Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetes. Am J Kidney Dis 2008 0.81
169 Saturated fat intake modulates the association between an obesity genetic risk score and body mass index in two US populations. J Acad Nutr Diet 2014 0.81
170 Future translational applications from the contemporary genomics era: a scientific statement from the American Heart Association. Circulation 2015 0.81
171 Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat Genet 2016 0.81
172 A genome-wide association study of chronic obstructive pulmonary disease in Hispanics. Ann Am Thorac Soc 2015 0.81
173 Genetic contributions to type 2 diabetes: recent insights. Expert Rev Mol Diagn 2007 0.80
174 Cellular basis of diabetic nephropathy: IV. Antioxidant enzyme mRNA expression levels in skin fibroblasts of type 1 diabetic sibling pairs. Nephrol Dial Transplant 2006 0.80
175 Recent developments in genome and exome-wide analyses of plasma lipids. Curr Opin Lipidol 2015 0.80
176 Whole genome association studies of neuropsychiatric disease: An emerging era of collaborative genetic discovery. Neuropsychiatr Dis Treat 2007 0.79
177 Association study of autoimmune thyroid disease at 5q23-q33 in Japanese patients. J Hum Genet 2003 0.79
178 Detection of diabetic nephropathy from advanced glycation endproducts (AGEs) differs in plasma and urine, and is dependent on the method of preparation. Amino Acids 2013 0.79
179 A review of genetics, arterial stiffness, and blood pressure in African Americans. J Cardiovasc Transl Res 2012 0.79
180 Validity of the family-based association test for copy number variant data in the case of non-linear intensity-genotype relationship. Genet Epidemiol 2012 0.79
181 A functional polymorphism in the lymphotoxin-alpha gene is associated with carotid artery wall thickness: the Diabetes Heart Study. Eur J Cardiovasc Prev Rehabil 2006 0.79
182 P-selectin gene haplotype associations with albuminuria in the Diabetes Heart Study. Kidney Int 2005 0.78
183 Building Momentum: Taking on the Real “Issues” of Diabetes Care! Diabetes Care 2016 0.78
184 Planning genetic studies and human stroke: sample size estimates based on family history data. Neurology 2002 0.78
185 Chromosome 7p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy. BMC Med Genet 2010 0.77
186 Diabetes: Still a geneticist's nightmare. Nature 2016 0.77
187 Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA). Ann Noninvasive Electrocardiol 2013 0.77
188 Evidence for a novel type 1 diabetes susceptibility locus on chromosome 8. Diabetes 2002 0.77
189 Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. Am J Hum Genet 2016 0.76
190 No association of 9p21 with arterial elasticity and retinal microvascular findings. Atherosclerosis 2013 0.76
191 Cellular basis of diabetic nephropathy: V. Endoglin expression levels and diabetic nephropathy risk in patients with Type 1 diabetes. J Diabetes Complications 2009 0.76
192 Identifying variants that contribute to linkage for dichotomous and quantitative traits in extended pedigrees. BMC Proc 2011 0.75
193 Sex differences in stroke evaluations in the Ischemic Stroke Genetics Study. J Stroke Cerebrovasc Dis 2007 0.75
194 Proband race/ethnicity affects pedigree completion rate in a genetic study of ischemic stroke. J Stroke Cerebrovasc Dis 2008 0.75
195 GENOME-WIDE INTERACTION WITH SELECTED TYPE 2 DIABETES LOCI REVEALS NOVEL LOCI FOR TYPE 2 DIABETES IN AFRICAN AMERICANS. Pac Symp Biocomput 2016 0.75
196 Genome-Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent. Mol Nutr Food Res 2017 0.75
197 Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat Genet 2016 0.75
198 Autoimmunity: insights from human genomics. Curr Opin Immunol 2012 0.75