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11 results on '"Evans, Michele K."'

1. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

Author

Liang, Jingjing, Le, Thu H, Edwards, Digna R Velez, Tayo, Bamidele O, Gaulton, Kyle J, Smith, Jennifer A, Lu, Yingchang, Jensen, Richard A, Chen, Guanjie, Yanek, Lisa R, Schwander, Karen, Tajuddin, Salman M, Sofer, Tamar, Kim, Wonji, Kayima, James, McKenzie, Colin A, Fox, Ervin, Nalls, Michael A, Young, J Hunter, Sun, Yan V, Lane, Jacqueline M, Cechova, Sylvia, Zhou, Jie, Tang, Hua, Fornage, Myriam, Musani, Solomon K, Wang, Heming, Lee, Juyoung, Adeyemo, Adebowale, Dreisbach, Albert W, Forrester, Terrence, Chu, Pei-Lun, Cappola, Anne, Evans, Michele K, Morrison, Alanna C, Martin, Lisa W, Wiggins, Kerri L, Hui, Qin, Zhao, Wei, Jackson, Rebecca D, Ware, Erin B, Faul, Jessica D, Reiner, Alex P, Bray, Michael, Denny, Joshua C, Mosley, Thomas H, Palmas, Walter, Guo, Xiuqing, Papanicolaou, George J, Penman, Alan D, Polak, Joseph F, Rice, Kenneth, Taylor, Ken D, Boerwinkle, Eric, Bottinger, Erwin P, Liu, Kiang, Risch, Neil, Hunt, Steven C, Kooperberg, Charles, Zonderman, Alan B, Laurie, Cathy C, Becker, Diane M, Cai, Jianwen, Loos, Ruth JF, Psaty, Bruce M, Weir, David R, Kardia, Sharon LR, Arnett, Donna K, Won, Sungho, Edwards, Todd L, Redline, Susan, Cooper, Richard S, Rao, DC, Rotter, Jerome I, Rotimi, Charles, Levy, Daniel, Chakravarti, Aravinda, Zhu, Xiaofeng, and Franceschini, Nora

Subjects
Animals, Humans, Mice, Hypertension, Cadherins, Membrane Proteins, Case-Control Studies, Blood Pressure, Multifactorial Inheritance, Polymorphism, Single Nucleotide, African Americans, Female, Male, Basic Helix-Loop-Helix Transcription Factors, Genome-Wide Association Study, Genetic Loci, Kidney Disease, Cardiovascular, Human Genome, Genetics, Biotechnology, Clinical Research, 2.1 Biological and endogenous factors, Developmental Biology
Abstract

Hypertension is a leading cause of global disease, mortality, and disability. While individuals of African descent suffer a disproportionate burden of hypertension and its complications, they have been underrepresented in genetic studies. To identify novel susceptibility loci for blood pressure and hypertension in people of African ancestry, we performed both single and multiple-trait genome-wide association analyses. We analyzed 21 genome-wide association studies comprised of 31,968 individuals of African ancestry, and validated our results with additional 54,395 individuals from multi-ethnic studies. These analyses identified nine loci with eleven independent variants which reached genome-wide significance (P < 1.25×10-8) for either systolic and diastolic blood pressure, hypertension, or for combined traits. Single-trait analyses identified two loci (TARID/TCF21 and LLPH/TMBIM4) and multiple-trait analyses identified one novel locus (FRMD3) for blood pressure. At these three loci, as well as at GRP20/CDH17, associated variants had alleles common only in African-ancestry populations. Functional annotation showed enrichment for genes expressed in immune and kidney cells, as well as in heart and vascular cells/tissues. Experiments driven by these findings and using angiotensin-II induced hypertension in mice showed altered kidney mRNA expression of six genes, suggesting their potential role in hypertension. Our study provides new evidence for genes related to hypertension susceptibility, and the need to study African-ancestry populations in order to identify biologic factors contributing to hypertension.

Published
2017

2. Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium

Author

Ng, Maggie CY, Graff, Mariaelisa, Lu, Yingchang, Justice, Anne E, Mudgal, Poorva, Liu, Ching-Ti, Young, Kristin, Yanek, Lisa R, Feitosa, Mary F, Wojczynski, Mary K, Rand, Kristin, Brody, Jennifer A, Cade, Brian E, Dimitrov, Latchezar, Duan, Qing, Guo, Xiuqing, Lange, Leslie A, Nalls, Michael A, Okut, Hayrettin, Tajuddin, Salman M, Tayo, Bamidele O, Vedantam, Sailaja, Bradfield, Jonathan P, Chen, Guanjie, Chen, Wei-Min, Chesi, Alessandra, Irvin, Marguerite R, Padhukasahasram, Badri, Smith, Jennifer A, Zheng, Wei, Allison, Matthew A, Ambrosone, Christine B, Bandera, Elisa V, Bartz, Traci M, Berndt, Sonja I, Bernstein, Leslie, Blot, William J, Bottinger, Erwin P, Carpten, John, Chanock, Stephen J, Chen, Yii-Der Ida, Conti, David V, Cooper, Richard S, Fornage, Myriam, Freedman, Barry I, Garcia, Melissa, Goodman, Phyllis J, Hsu, Yu-Han H, Hu, Jennifer, Huff, Chad D, Ingles, Sue A, John, Esther M, Kittles, Rick, Klein, Eric, Li, Jin, McKnight, Barbara, Nayak, Uma, Nemesure, Barbara, Ogunniyi, Adesola, Olshan, Andrew, Press, Michael F, Rohde, Rebecca, Rybicki, Benjamin A, Salako, Babatunde, Sanderson, Maureen, Shao, Yaming, Siscovick, David S, Stanford, Janet L, Stevens, Victoria L, Stram, Alex, Strom, Sara S, Vaidya, Dhananjay, Witte, John S, Yao, Jie, Zhu, Xiaofeng, Ziegler, Regina G, Zonderman, Alan B, Adeyemo, Adebowale, Ambs, Stefan, Cushman, Mary, Faul, Jessica D, Hakonarson, Hakon, Levin, Albert M, Nathanson, Katherine L, Ware, Erin B, Weir, David R, Zhao, Wei, Zhi, Degui, Arnett, Donna K, Grant, Struan FA, Kardia, Sharon LR, Oloapde, Olufunmilayo I, Rao, DC, Rotimi, Charles N, Sale, Michele M, Williams, L Keoki, Zemel, Babette S, Becker, Diane M, Borecki, Ingrid B, and Evans, Michele K

Subjects
Biological Sciences, Genetics, Human Genome, Aetiology, 2.1 Biological and endogenous factors, Adiposity, Anthropometry, Black People, Body Mass Index, Chromosome Mapping, Female, Gene Frequency, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Linkage Disequilibrium, Male, Obesity, Polymorphism, Single Nucleotide, Serine Endopeptidases, Transcription Factor 7-Like 2 Protein, Waist-Hip Ratio, White People, Bone Mineral Density in Childhood Study (BMDCS) Group, Developmental Biology
Abstract

Genome-wide association studies (GWAS) have identified >300 loci associated with measures of adiposity including body mass index (BMI) and waist-to-hip ratio (adjusted for BMI, WHRadjBMI), but few have been identified through screening of the African ancestry genomes. We performed large scale meta-analyses and replications in up to 52,895 individuals for BMI and up to 23,095 individuals for WHRadjBMI from the African Ancestry Anthropometry Genetics Consortium (AAAGC) using 1000 Genomes phase 1 imputed GWAS to improve coverage of both common and low frequency variants in the low linkage disequilibrium African ancestry genomes. In the sex-combined analyses, we identified one novel locus (TCF7L2/HABP2) for WHRadjBMI and eight previously established loci at P < 5×10-8: seven for BMI, and one for WHRadjBMI in African ancestry individuals. An additional novel locus (SPRYD7/DLEU2) was identified for WHRadjBMI when combined with European GWAS. In the sex-stratified analyses, we identified three novel loci for BMI (INTS10/LPL and MLC1 in men, IRX4/IRX2 in women) and four for WHRadjBMI (SSX2IP, CASC8, PDE3B and ZDHHC1/HSD11B2 in women) in individuals of African ancestry or both African and European ancestry. For four of the novel variants, the minor allele frequency was low (

Published
2017

3. Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes.

Author

Ng, Maggie CY, Shriner, Daniel, Chen, Brian H, Li, Jiang, Chen, Wei-Min, Guo, Xiuqing, Liu, Jiankang, Bielinski, Suzette J, Yanek, Lisa R, Nalls, Michael A, Comeau, Mary E, Rasmussen-Torvik, Laura J, Jensen, Richard A, Evans, Daniel S, Sun, Yan V, An, Ping, Patel, Sanjay R, Lu, Yingchang, Long, Jirong, Armstrong, Loren L, Wagenknecht, Lynne, Yang, Lingyao, Snively, Beverly M, Palmer, Nicholette D, Mudgal, Poorva, Langefeld, Carl D, Keene, Keith L, Freedman, Barry I, Mychaleckyj, Josyf C, Nayak, Uma, Raffel, Leslie J, Goodarzi, Mark O, Chen, Y-D Ida, Taylor, Herman A, Correa, Adolfo, Sims, Mario, Couper, David, Pankow, James S, Boerwinkle, Eric, Adeyemo, Adebowale, Doumatey, Ayo, Chen, Guanjie, Mathias, Rasika A, Vaidya, Dhananjay, Singleton, Andrew B, Zonderman, Alan B, Igo, Robert P, Sedor, John R, FIND Consortium, Kabagambe, Edmond K, Siscovick, David S, McKnight, Barbara, Rice, Kenneth, Liu, Yongmei, Hsueh, Wen-Chi, Zhao, Wei, Bielak, Lawrence F, Kraja, Aldi, Province, Michael A, Bottinger, Erwin P, Gottesman, Omri, Cai, Qiuyin, Zheng, Wei, Blot, William J, Lowe, William L, Pacheco, Jennifer A, Crawford, Dana C, eMERGE Consortium, DIAGRAM Consortium, Grundberg, Elin, MuTHER Consortium, Rich, Stephen S, Hayes, M Geoffrey, Shu, Xiao-Ou, Loos, Ruth JF, Borecki, Ingrid B, Peyser, Patricia A, Cummings, Steven R, Psaty, Bruce M, Fornage, Myriam, Iyengar, Sudha K, Evans, Michele K, Becker, Diane M, Kao, WH Linda, Wilson, James G, Rotter, Jerome I, Sale, Michèle M, Liu, Simin, Rotimi, Charles N, Bowden, Donald W, and MEta-analysis of type 2 DIabetes in African Americans Consortium

Subjects
FIND Consortium, eMERGE Consortium, DIAGRAM Consortium, MuTHER Consortium, MEta-analysis of type 2 DIabetes in African Americans Consortium, Humans, Diabetes Mellitus, Type 2, HMGA2 Protein, HLA-B27 Antigen, Polymorphism, Single Nucleotide, African Americans, Mutant Chimeric Proteins, KCNQ1 Potassium Channel, Genome-Wide Association Study, Transcription Factor 7-Like 2 Protein, Human Genome, Diabetes, Genetics, 2.1 Biological and endogenous factors, Metabolic and endocrine, Developmental Biology
Abstract

Type 2 diabetes (T2D) is more prevalent in African Americans than in Europeans. However, little is known about the genetic risk in African Americans despite the recent identification of more than 70 T2D loci primarily by genome-wide association studies (GWAS) in individuals of European ancestry. In order to investigate the genetic architecture of T2D in African Americans, the MEta-analysis of type 2 DIabetes in African Americans (MEDIA) Consortium examined 17 GWAS on T2D comprising 8,284 cases and 15,543 controls in African Americans in stage 1 analysis. Single nucleotide polymorphisms (SNPs) association analysis was conducted in each study under the additive model after adjustment for age, sex, study site, and principal components. Meta-analysis of approximately 2.6 million genotyped and imputed SNPs in all studies was conducted using an inverse variance-weighted fixed effect model. Replications were performed to follow up 21 loci in up to 6,061 cases and 5,483 controls in African Americans, and 8,130 cases and 38,987 controls of European ancestry. We identified three known loci (TCF7L2, HMGA2 and KCNQ1) and two novel loci (HLA-B and INS-IGF2) at genome-wide significance (4.15 × 10(-94)

Published
2014

4. Genome-wide association of body fat distribution in African ancestry populations suggests new loci.

Author

Liu, Ching-Ti, Monda, Keri L, Taylor, Kira C, Lange, Leslie, Demerath, Ellen W, Palmas, Walter, Wojczynski, Mary K, Ellis, Jaclyn C, Vitolins, Mara Z, Liu, Simin, Papanicolaou, George J, Irvin, Marguerite R, Xue, Luting, Griffin, Paula J, Nalls, Michael A, Adeyemo, Adebowale, Liu, Jiankang, Li, Guo, Ruiz-Narvaez, Edward A, Chen, Wei-Min, Chen, Fang, Henderson, Brian E, Millikan, Robert C, Ambrosone, Christine B, Strom, Sara S, Guo, Xiuqing, Andrews, Jeanette S, Sun, Yan V, Mosley, Thomas H, Yanek, Lisa R, Shriner, Daniel, Haritunians, Talin, Rotter, Jerome I, Speliotes, Elizabeth K, Smith, Megan, Rosenberg, Lynn, Mychaleckyj, Josyf, Nayak, Uma, Spruill, Ida, Garvey, W Timothy, Pettaway, Curtis, Nyante, Sarah, Bandera, Elisa V, Britton, Angela F, Zonderman, Alan B, Rasmussen-Torvik, Laura J, Chen, Yii-Der Ida, Ding, Jingzhong, Lohman, Kurt, Kritchevsky, Stephen B, Zhao, Wei, Peyser, Patricia A, Kardia, Sharon LR, Kabagambe, Edmond, Broeckel, Ulrich, Chen, Guanjie, Zhou, Jie, Wassertheil-Smoller, Sylvia, Neuhouser, Marian L, Rampersaud, Evadnie, Psaty, Bruce, Kooperberg, Charles, Manson, Joann E, Kuller, Lewis H, Ochs-Balcom, Heather M, Johnson, Karen C, Sucheston, Lara, Ordovas, Jose M, Palmer, Julie R, Haiman, Christopher A, McKnight, Barbara, Howard, Barbara V, Becker, Diane M, Bielak, Lawrence F, Liu, Yongmei, Allison, Matthew A, Grant, Struan FA, Burke, Gregory L, Patel, Sanjay R, Schreiner, Pamela J, Borecki, Ingrid B, Evans, Michele K, Taylor, Herman, Sale, Michele M, Howard, Virginia, Carlson, Christopher S, Rotimi, Charles N, Cushman, Mary, Harris, Tamara B, Reiner, Alexander P, Cupples, L Adrienne, North, Kari E, and Fox, Caroline S

Subjects
Humans, Obesity, Waist-Hip Ratio, Polymorphism, Single Nucleotide, African Continental Ancestry Group, European Continental Ancestry Group, Female, Male, Adiposity, Body Fat Distribution, Genome-Wide Association Study, Genetic Loci, Polymorphism, Single Nucleotide, Developmental Biology, Genetics
Abstract

Central obesity, measured by waist circumference (WC) or waist-hip ratio (WHR), is a marker of body fat distribution. Although obesity disproportionately affects minority populations, few studies have conducted genome-wide association study (GWAS) of fat distribution among those of predominantly African ancestry (AA). We performed GWAS of WC and WHR, adjusted and unadjusted for BMI, in up to 33,591 and 27,350 AA individuals, respectively. We identified loci associated with fat distribution in AA individuals using meta-analyses of GWA results for WC and WHR (stage 1). Overall, 25 SNPs with single genomic control (GC)-corrected p-values

Published
2013

5. A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans.

Author

Qayyum, Rehan, Snively, Beverly M, Ziv, Elad, Nalls, Michael A, Liu, Yongmei, Tang, Weihong, Yanek, Lisa R, Lange, Leslie, Evans, Michele K, Ganesh, Santhi, Austin, Melissa A, Lettre, Guillaume, Becker, Diane M, Zonderman, Alan B, Singleton, Andrew B, Harris, Tamara B, Mohler, Emile R, Logsdon, Benjamin A, Kooperberg, Charles, Folsom, Aaron R, Wilson, James G, Becker, Lewis C, and Reiner, Alexander P

Subjects
Blood Platelets, Humans, Platelet Count, Platelet Aggregation, Genotype, Polymorphism, Single Nucleotide, Adult, Aged, Middle Aged, African Americans, Female, Male, Genome-Wide Association Study, Polymorphism, Single Nucleotide, Genetics, Developmental Biology
Abstract

Several genetic variants associated with platelet count and mean platelet volume (MPV) were recently reported in people of European ancestry. In this meta-analysis of 7 genome-wide association studies (GWAS) enrolling African Americans, our aim was to identify novel genetic variants associated with platelet count and MPV. For all cohorts, GWAS analysis was performed using additive models after adjusting for age, sex, and population stratification. For both platelet phenotypes, meta-analyses were conducted using inverse-variance weighted fixed-effect models. Platelet aggregation assays in whole blood were performed in the participants of the GeneSTAR cohort. Genetic variants in ten independent regions were associated with platelet count (N = 16,388) with p

Published
2012

6. Genetic association for renal traits among participants of African ancestry reveals new loci for renal function.

Author

Liu, Ching-Ti, Garnaas, Maija K, Tin, Adrienne, Kottgen, Anna, Franceschini, Nora, Peralta, Carmen A, de Boer, Ian H, Lu, Xiaoning, Atkinson, Elizabeth, Ding, Jingzhong, Nalls, Michael, Shriner, Daniel, Coresh, Josef, Kutlar, Abdullah, Bibbins-Domingo, Kirsten, Siscovick, David, Akylbekova, Ermeg, Wyatt, Sharon, Astor, Brad, Mychaleckjy, Josef, Li, Man, Reilly, Muredach P, Townsend, Raymond R, Adeyemo, Adebowale, Zonderman, Alan B, de Andrade, Mariza, Turner, Stephen T, Mosley, Thomas H, Harris, Tamara B, CKDGen Consortium, Rotimi, Charles N, Liu, Yongmei, Kardia, Sharon LR, Evans, Michele K, Shlipak, Michael G, Kramer, Holly, Flessner, Michael F, Dreisbach, Albert W, Goessling, Wolfram, Cupples, L Adrienne, Kao, W Linda, and Fox, Caroline S

Subjects
CKDGen Consortium, Kidney, Animals, Zebrafish, Humans, Kidney Failure, Chronic, Adaptor Proteins, Signal Transducing, Adaptor Proteins, Vesicular Transport, Neoplasm Proteins, Glomerular Filtration Rate, Phenotype, Polymorphism, Single Nucleotide, Adult, Aged, Middle Aged, African Continental Ancestry Group, Female, Male, KCNQ1 Potassium Channel, Genome-Wide Association Study, Gene Knockdown Techniques, Genetic Loci, Genetic Association Studies, Kidney Disease, Clinical Research, Genetics, Renal and urogenital, Developmental Biology
Abstract

Chronic kidney disease (CKD) is an increasing global public health concern, particularly among populations of African ancestry. We performed an interrogation of known renal loci, genome-wide association (GWA), and IBC candidate-gene SNP association analyses in African Americans from the CARe Renal Consortium. In up to 8,110 participants, we performed meta-analyses of GWA and IBC array data for estimated glomerular filtration rate (eGFR), CKD (eGFR 30 mg/g) and interrogated the 250 kb flanking region around 24 SNPs previously identified in European Ancestry renal GWAS analyses. Findings were replicated in up to 4,358 African Americans. To assess function, individually identified genes were knocked down in zebrafish embryos by morpholino antisense oligonucleotides. Expression of kidney-specific genes was assessed by in situ hybridization, and glomerular filtration was evaluated by dextran clearance. Overall, 23 of 24 previously identified SNPs had direction-consistent associations with eGFR in African Americans, 2 of which achieved nominal significance (UMOD, PIP5K1B). Interrogation of the flanking regions uncovered 24 new index SNPs in African Americans, 12 of which were replicated (UMOD, ANXA9, GCKR, TFDP2, DAB2, VEGFA, ATXN2, GATM, SLC22A2, TMEM60, SLC6A13, and BCAS3). In addition, we identified 3 suggestive loci at DOK6 (p-value = 5.3×10(-7)) and FNDC1 (p-value = 3.0×10(-7)) for UACR, and KCNQ1 with eGFR (p = 3.6×10(-6)). Morpholino knockdown of kcnq1 in the zebrafish resulted in abnormal kidney development and filtration capacity. We identified several SNPs in association with eGFR in African Ancestry individuals, as well as 3 suggestive loci for UACR and eGFR. Functional genetic studies support a role for kcnq1 in glomerular development in zebrafish.

Published
2011

7. Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

Author

Reiner, Alexander P, Lettre, Guillaume, Nalls, Michael A, Ganesh, Santhi K, Mathias, Rasika, Austin, Melissa A, Dean, Eric, Arepalli, Sampath, Britton, Angela, Chen, Zhao, Couper, David, Curb, J David, Eaton, Charles B, Fornage, Myriam, Grant, Struan FA, Harris, Tamara B, Hernandez, Dena, Kamatini, Naoyuki, Keating, Brendan J, Kubo, Michiaki, LaCroix, Andrea, Lange, Leslie A, Liu, Simin, Lohman, Kurt, Meng, Yan, Mohler, Emile R, Musani, Solomon, Nakamura, Yusuke, O'Donnell, Christopher J, Okada, Yukinori, Palmer, Cameron D, Papanicolaou, George J, Patel, Kushang V, Singleton, Andrew B, Takahashi, Atsushi, Tang, Hua, Taylor, Herman A, Taylor, Kent, Thomson, Cynthia, Yanek, Lisa R, Yang, Lingyao, Ziv, Elad, Zonderman, Alan B, Folsom, Aaron R, Evans, Michele K, Liu, Yongmei, Becker, Diane M, Snively, Beverly M, and Wilson, James G

Subjects
Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 4, Chromosomes, Human, Pair 16, Humans, Microfilament Proteins, Receptors, Cell Surface, Duffy Blood-Group System, Leukocyte Count, Artifacts, Reproducibility of Results, DNA Replication, Phenotype, Polymorphism, Single Nucleotide, African Americans, Asian Continental Ancestry Group, European Continental Ancestry Group, Chemokine CXCL2, Genome-Wide Association Study, Molecular Epidemiology, Genetic Loci, Chromosomes, Human, Pair 1, Pair 4, Pair 16, Receptors, Cell Surface, Polymorphism, Single Nucleotide, Genetics, Developmental Biology
Abstract

Total white blood cell (WBC) and neutrophil counts are lower among individuals of African descent due to the common African-derived "null" variant of the Duffy Antigen Receptor for Chemokines (DARC) gene. Additional common genetic polymorphisms were recently associated with total WBC and WBC sub-type levels in European and Japanese populations. No additional loci that account for WBC variability have been identified in African Americans. In order to address this, we performed a large genome-wide association study (GWAS) of total WBC and cell subtype counts in 16,388 African-American participants from 7 population-based cohorts available in the Continental Origins and Genetic Epidemiology Network. In addition to the DARC locus on chromosome 1q23, we identified two other regions (chromosomes 4q13 and 16q22) associated with WBC in African Americans (P

Published
2011

8. Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations

Author

Liang, Jingjing, primary, Le, Thu H., additional, Velez Edwards, Digna R., additional, Tayo, Bamidele O., additional, Gaulton, Kyle J., additional, Smith, Jennifer A., additional, Lu, Yingchang, additional, Jensen, Richard A., additional, Chen, Guanjie, additional, Yanek, Lisa R., additional, Schwander, Karen, additional, Tajuddin, Salman M., additional, Sofer, Tamar, additional, Kim, Wonji, additional, Kayima, James, additional, McKenzie, Colin A., additional, Fox, Ervin, additional, Nalls, Michael A., additional, Young, J. Hunter, additional, Sun, Yan V., additional, Lane, Jacqueline M., additional, Cechova, Sylvia, additional, Zhou, Jie, additional, Tang, Hua, additional, Fornage, Myriam, additional, Musani, Solomon K., additional, Wang, Heming, additional, Lee, Juyoung, additional, Adeyemo, Adebowale, additional, Dreisbach, Albert W., additional, Forrester, Terrence, additional, Chu, Pei-Lun, additional, Cappola, Anne, additional, Evans, Michele K., additional, Morrison, Alanna C., additional, Martin, Lisa W., additional, Wiggins, Kerri L., additional, Hui, Qin, additional, Zhao, Wei, additional, Jackson, Rebecca D., additional, Ware, Erin B., additional, Faul, Jessica D., additional, Reiner, Alex P., additional, Bray, Michael, additional, Denny, Joshua C., additional, Mosley, Thomas H., additional, Palmas, Walter, additional, Guo, Xiuqing, additional, Papanicolaou, George J., additional, Penman, Alan D., additional, Polak, Joseph F., additional, Rice, Kenneth, additional, Taylor, Ken D., additional, Boerwinkle, Eric, additional, Bottinger, Erwin P., additional, Liu, Kiang, additional, Risch, Neil, additional, Hunt, Steven C., additional, Kooperberg, Charles, additional, Zonderman, Alan B., additional, Laurie, Cathy C., additional, Becker, Diane M., additional, Cai, Jianwen, additional, Loos, Ruth J. F., additional, Psaty, Bruce M., additional, Weir, David R., additional, Kardia, Sharon L. R., additional, Arnett, Donna K., additional, Won, Sungho, additional, Edwards, Todd L., additional, Redline, Susan, additional, Cooper, Richard S., additional, Rao, D. C., additional, Rotter, Jerome I., additional, Rotimi, Charles, additional, Levy, Daniel, additional, Chakravarti, Aravinda, additional, Zhu, Xiaofeng, additional, and Franceschini, Nora, additional

Published
2018
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9. Correction: Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry

Author

N'Diaye, Amidou, primary, Chen, Gary K., additional, Palmer, Cameron D., additional, Ge, Bing, additional, Tayo, Bamidele, additional, Mathias, Rasika A., additional, Ding, Jingzhong, additional, Nalls, Michael A., additional, Adeyemo, Adebowale, additional, Adoue, Véronique, additional, Ambrosone, Christine B., additional, Atwood, Larry, additional, Bandera, Elisa V., additional, Becker, Lewis C., additional, Berndt, Sonja I., additional, Bernstein, Leslie, additional, Blot, William J., additional, Boerwinkle, Eric, additional, Britton, Angela, additional, Casey, Graham, additional, Chanock, Stephen J., additional, Demerath, Ellen, additional, Deming, Sandra L., additional, Diver, W. Ryan, additional, Fox, Caroline, additional, Harris, Tamara B., additional, Hernandez, Dena G., additional, Hu, Jennifer J., additional, Ingles, Sue A., additional, John, Esther M., additional, Johnson, Craig, additional, Keating, Brendan, additional, Kittles, Rick A., additional, Kolonel, Laurence N., additional, Kritchevsky, Stephen B., additional, Le Marchand, Loic, additional, Lohman, Kurt, additional, Liu, Jiankang, additional, Millikan, Robert C., additional, Murphy, Adam, additional, Musani, Solomon, additional, Neslund-Dudas, Christine, additional, North, Kari E., additional, Nyante, Sarah, additional, Ogunniyi, Adesola, additional, Ostrander, Elaine A., additional, Papanicolaou, George, additional, Patel, Sanjay, additional, Pettaway, Curtis A., additional, Press, Michael F., additional, Redline, Susan, additional, Rodriguez-Gil, Jorge L., additional, Rotimi, Charles, additional, Rybicki, Benjamin A., additional, Salako, Babatunde, additional, Schreiner, Pamela J., additional, Signorello, Lisa B., additional, Singleton, Andrew B., additional, Stanford, Janet L., additional, Stram, Alex H., additional, Stram, Daniel O., additional, Strom, Sara S., additional, Suktitipat, Bhoom, additional, Thun, Michael J., additional, Witte, John S., additional, Yanek, Lisa R., additional, Ziegler, Regina G., additional, Zheng, Wei, additional, Zhu, Xiaofeng, additional, Zmuda, Joseph M., additional, Zonderman, Alan B., additional, Evans, Michele K., additional, Liu, Yongmei, additional, Becker, Diane M., additional, Cooper, Richard S., additional, Pastinen, Tomi, additional, Henderson, Brian E., additional, Hirschhorn, Joel N., additional, Lettre, Guillaume, additional, and Haiman, Christopher A., additional

Published
2011
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10. Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry

Author

N'Diaye, Amidou, primary, Chen, Gary K., additional, Palmer, Cameron D., additional, Ge, Bing, additional, Tayo, Bamidele, additional, Mathias, Rasika A., additional, Ding, Jingzhong, additional, Nalls, Michael A., additional, Adeyemo, Adebowale, additional, Adoue, Véronique, additional, Ambrosone, Christine B., additional, Atwood, Larry, additional, Bandera, Elisa V., additional, Becker, Lewis C., additional, Berndt, Sonja I., additional, Bernstein, Leslie, additional, Blot, William J., additional, Boerwinkle, Eric, additional, Britton, Angela, additional, Casey, Graham, additional, Chanock, Stephen J., additional, Demerath, Ellen, additional, Deming, Sandra L., additional, Diver, W. Ryan, additional, Fox, Caroline, additional, Harris, Tamara B., additional, Hernandez, Dena G., additional, Hu, Jennifer J., additional, Ingles, Sue A., additional, John, Esther M., additional, Johnson, Craig, additional, Keating, Brendan, additional, Kittles, Rick A., additional, Kolonel, Laurence N., additional, Kritchevsky, Stephen B., additional, Le Marchand, Loic, additional, Lohman, Kurt, additional, Liu, Jiankang, additional, Millikan, Robert C., additional, Murphy, Adam, additional, Musani, Solomon, additional, Neslund-Dudas, Christine, additional, North, Kari E., additional, Nyante, Sarah, additional, Ogunniyi, Adesola, additional, Ostrander, Elaine A., additional, Papanicolaou, George, additional, Patel, Sanjay, additional, Pettaway, Curtis A., additional, Press, Michael F., additional, Redline, Susan, additional, Rodriguez-Gil, Jorge L., additional, Rotimi, Charles, additional, Rybicki, Benjamin A., additional, Salako, Babatunde, additional, Schreiner, Pamela J., additional, Signorello, Lisa B., additional, Singleton, Andrew B., additional, Stanford, Janet L., additional, Stram, Alex H., additional, Stram, Daniel O., additional, Strom, Sara S., additional, Suktitipat, Bhoom, additional, Thun, Michael J., additional, Witte, John S., additional, Yanek, Lisa R., additional, Ziegler, Regina G., additional, Zheng, Wei, additional, Zhu, Xiaofeng, additional, Zmuda, Joseph M., additional, Zonderman, Alan B., additional, Evans, Michele K., additional, Liu, Yongmei, additional, Becker, Diane M., additional, Cooper, Richard S., additional, Pastinen, Tomi, additional, Henderson, Brian E., additional, Hirschhorn, Joel N., additional, Lettre, Guillaume, additional, and Haiman, Christopher A., additional

Published
2011
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11. Genome-Wide Association Studies of the PR Interval in African Americans.

Author

Smith, J. Gustav, Magnani, Jared W., Palmer, Cameron, Meng, Yan A., Soliman, Elsayed Z., Musani, Solomon K., Kerr, Kathleen F., Schnabel, Renate B., Lubitz, Steven A., Sotoodehnia, Nona, Redline, Susan, Pfeufer, Arne, Müller, Martina, Evans, Daniel S., Nalls, Michael A., Yongmei Liu, Newman, Anne B., Zonderman, Alan B., Evans, Michele K., and Deo, Rajat

Subjects
GENOMES, ELECTROCARDIOGRAPHY, ATRIOVENTRICULAR node, ARRHYTHMIA, GENETIC polymorphisms, GENE frequency, META-analysis, AFRICAN Americans, EUROPEANS, DISEASE risk factors
Published
2011
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