| Year |
Citation |
Score |
| 2023 |
Zhang X, Brody JA, Graff M, Highland HM, Chami N, Xu H, Wang Z, Ferrier K, Chittoor G, Josyula NS, Li X, Li Z, Allison MA, Becker DM, Bielak LF, ... ... Carlson CS, et al. WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. Medrxiv : the Preprint Server For Health Sciences. PMID 37662265 DOI: 10.1101/2023.08.21.23293271 |
0.331 |
|
| 2023 |
Rajabli F, Benchek P, Tosto G, Kushch N, Sha J, Bazemore K, Zhu C, Lee WP, Haut J, Hamilton-Nelson KL, Wheeler NR, Zhao Y, Farrell JJ, Grunin MA, Leung YY, ... ... Carlson CS, et al. Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences. PMID 37461624 DOI: 10.1101/2023.07.06.23292311 |
0.328 |
|
| 2020 |
Hu Y, Graff M, Haessler J, Buyske S, Bien SA, Tao R, Highland HM, Nishimura KK, Zubair N, Lu Y, Verbanck M, Hilliard AT, Klarin D, Damrauer SM, Ho YL, ... ... Carlson CS, et al. Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. Plos Genetics. 16: e1008684. PMID 32226016 DOI: 10.1371/journal.pgen.1008684 |
0.307 |
|
| 2019 |
Bien SA, Su YR, Conti DV, Harrison TA, Qu C, Guo X, Lu Y, Albanes D, Auer PL, Banbury BL, Berndt SI, Bézieau S, Brenner H, Buchanan DD, Caan BJ, ... ... Carlson CS, et al. Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. Human Genetics. PMID 31254090 DOI: 10.1007/S00439-019-02030-8 |
0.36 |
|
| 2019 |
Wojcik GL, Graff M, Nishimura KK, Tao R, Haessler J, Gignoux CR, Highland HM, Patel YM, Sorokin EP, Avery CL, Belbin GM, Bien SA, Cheng I, Cullina S, Hodonsky CJ, ... ... Carlson CS, et al. Genetic analyses of diverse populations improves discovery for complex traits. Nature. PMID 31217584 DOI: 10.1038/S41586-019-1310-4 |
0.399 |
|
| 2019 |
Bien SA, Su YR, Conti DV, Harrison TA, Qu C, Guo X, Lu Y, Albanes D, Auer PL, Banbury BL, Berndt SI, Bézieau S, Brenner H, Buchanan DD, Caan BJ, ... ... Carlson CS, et al. Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. Human Genetics. PMID 30820706 DOI: 10.1007/S00439-019-01989-8 |
0.327 |
|
| 2018 |
Mayer SE, Weiss NS, Chubak J, Doody DR, Carlson CS, Makar KW, Wurscher MA, Malone KE. CYP2D6-inhibiting medication use and inherited CYP2D6 variation in relation to adverse breast cancer outcomes after tamoxifen therapy. Cancer Causes & Control : Ccc. PMID 30542984 DOI: 10.1007/S10552-018-1117-X |
0.313 |
|
| 2018 |
Wojcik GL, Fuchsberger C, Taliun D, Welch R, Martin AR, Shringarpure S, Carlson CS, Abecasis G, Kang HM, Boehnke M, Bustamante CD, Gignoux CR, Kenny EE. Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies. G3 (Bethesda, Md.). PMID 30131328 DOI: 10.1534/G3.118.200502 |
0.408 |
|
| 2018 |
Schmit SL, Edlund CK, Schumacher FR, Gong J, Harrison TA, Huyghe JR, Qu C, Melas M, Van Den Berg DJ, Wang H, Tring S, Plummer SJ, Albanes D, Alonso MH, Amos CI, ... ... Carlson CS, et al. Novel Common Genetic Susceptibility Loci for Colorectal Cancer. Journal of the National Cancer Institute. PMID 29917119 DOI: 10.1093/Jnci/Djy099 |
0.317 |
|
| 2018 |
Kocarnik JM, Richard M, Graff M, Haessler J, Bien S, Carlson C, Carty CL, Reiner AP, Avery CL, Ballantyne CM, LaCroix AZ, Assimes TL, Barbalic M, Pankratz N, Tang W, et al. Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study. Human Molecular Genetics. PMID 29878111 DOI: 10.1093/Hmg/Ddy211 |
0.366 |
|
| 2017 |
Gong J, Nishimura KK, Fernandez-Rhodes L, Haessler J, Bien S, Graff M, Lim U, Lu Y, Gross M, Fornage M, Yoneyama S, Isasi CR, Buzkova P, Daviglus M, Lin DY, ... ... Carlson CS, et al. Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI. International Journal of Obesity (2005). PMID 29381148 DOI: 10.1038/Ijo.2017.304 |
0.352 |
|
| 2017 |
Lombardo KA, Coffey DG, Morales AJ, Carlson CS, Towlerton AMH, Gerdts SE, Nkrumah FK, Neequaye J, Biggar RJ, Orem J, Casper C, Mbulaiteye SM, Bhatia KG, Warren EH. High-throughput sequencing of the B-cell receptor in African Burkitt lymphoma reveals clues to pathogenesis. Blood Advances. 1: 535-544. PMID 29296973 DOI: 10.1182/Bloodadvances.2016000794 |
0.315 |
|
| 2017 |
Bien SA, Auer PL, Harrison TA, Qu C, Connolly CM, Greenside PG, Chen S, Berndt SI, Bézieau S, Kang HM, Huyghe J, Brenner H, Casey G, Chan AT, Hopper JL, ... ... Carlson CS, et al. Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data. Plos One. 12: e0186518. PMID 29161273 DOI: 10.1371/Journal.Pone.0186518 |
0.406 |
|
| 2017 |
Bien SA, Pankow JS, Haessler J, Lu Y, Pankratz N, Rohde RR, Tamuno A, Carlson CS, Schumacher FR, Bůžková P, Daviglus ML, Lim U, Fornage M, Fernandez-Rhodes L, Avilés-Santa L, et al. Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium. Diabetologia. PMID 29038867 DOI: 10.1007/S00125-017-4476-Z |
0.338 |
|
| 2017 |
Bien SA, Pankow JS, Haessler J, Lu YN, Pankratz N, Rohde RR, Tamuno A, Carlson CS, Schumacher FR, Bůžková P, Daviglus ML, Lim U, Fornage M, Fernandez-Rhodes L, Avilés-Santa L, et al. Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium. Diabetologia. PMID 28905132 DOI: 10.1007/S00125-017-4405-1 |
0.389 |
|
| 2017 |
Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Carlson CS, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916 |
0.403 |
|
| 2017 |
Emerson RO, DeWitt WS, Vignali M, Gravley J, Hu JK, Osborne EJ, Desmarais C, Klinger M, Carlson CS, Hansen JA, Rieder M, Robins HS. Immunosequencing identifies signatures of cytomegalovirus exposure history and HLA-mediated effects on the T cell repertoire. Nature Genetics. PMID 28369038 DOI: 10.1038/Ng.3822 |
0.31 |
|
| 2016 |
Carlson CS. Ethnicity: Diversity is future for genetic analysis. Nature. 540: 341. PMID 27974770 DOI: 10.1038/540341D |
0.335 |
|
| 2016 |
Bien SA, Wojcik GL, Zubair N, Gignoux CR, Martin AR, Kocarnik JM, Martin LW, Buyske S, Haessler J, Walker RW, Cheng I, Graff M, Xia L, Franceschini N, Matise T, ... ... Carlson CS, et al. Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array. Plos One. 11: e0167758. PMID 27973554 DOI: 10.1371/Journal.Pone.0167758 |
0.411 |
|
| 2016 |
Yoneyama S, Yao J, Guo X, Fernandez-Rhodes L, Lim U, Boston J, Buzková P, Carlson CS, Cheng I, Cochran B, Cooper R, Ehret G, Fornage M, Gong J, Gross M, et al. Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations. International Journal of Obesity (2005). PMID 27867202 DOI: 10.1038/Ijo.2016.207 |
0.39 |
|
| 2016 |
Franceschini N, Carty CL, Lu Y, Tao R, Sung YJ, Manichaikul A, Haessler J, Fornage M, Schwander K, Zubair N, Bien S, Hindorff LA, Guo X, Bielinski SJ, Ehret G, ... ... Carlson CS, et al. Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans. Plos One. 11: e0164132. PMID 27736895 DOI: 10.1371/Journal.Pone.0164132 |
0.358 |
|
| 2016 |
Du M, Jiao S, Bien SA, Gala M, Abecasis G, Bezieau S, Brenner H, Butterbach K, Caan BJ, Carlson CS, Casey G, Chang-Claude J, Conti DV, Curtis KR, Duggan D, et al. Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants. Plos One. 11: e0157521. PMID 27379672 DOI: 10.1371/Journal.Pone.0157521 |
0.434 |
|
| 2016 |
Lessard S, Manning AK, Low-Kam C, Auer PL, Giri A, Graff M, Schurmann C, Yaghootkar H, Luan J, Esko T, Karaderi T, ... ... Carlson C, et al. Testing the Role of Predicted Gene Knockouts in Human Anthropometric Trait Variation. Human Molecular Genetics. PMID 26908616 DOI: 10.1093/Hmg/Ddw055 |
0.371 |
|
| 2016 |
Kan M, Auer PL, Wang GT, Bucasas KL, Hooker S, Rodriguez A, Li B, Ellis J, Adrienne Cupples L, Ida Chen YD, Dupuis J, Fox CS, Gross MD, Smith JD, Heard-Costa N, ... ... Carlson C, et al. Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project. European Journal of Human Genetics : Ejhg. PMID 26757982 DOI: 10.1038/Ejhg.2015.272 |
0.437 |
|
| 2016 |
Guenthoer J, Chai X, Makar KW, Carlson CS, Bakkar R, King IB, Kang H, Thompson B, Li CI, Hsu L, Cook LS, Porter PL. Abstract C56: Relationship of ancestry and breast cancer subtypes in Hispanic women from New Mexico and Washington State Cancer Epidemiology, Biomarkers & Prevention. 25. DOI: 10.1158/1538-7755.Disp15-C56 |
0.376 |
|
| 2016 |
Santiago-Torres M, Tapsoba JDD, Kratz M, Lampe JW, Breymeyer KL, Levy L, Song X, Villaseñor A, Wang C, Carlson C, Neuhouser ML. Abstract A68: Does genetic ancestry influence the metabolic response to a traditional Mexican versus U.S. diet? A randomized crossover feeding trial among first and second generation women of Mexican descent Cancer Epidemiology, Biomarkers & Prevention. 25. DOI: 10.1158/1538-7755.Disp15-A68 |
0.341 |
|
| 2016 |
Bien SA, Harrison TA, Auer PL, Qu F, Huyghe J, Banbury B, Greenside P, Abecasis GR, Berndt SI, Bézieau S, Brenner H, Casey G, Chan AT, Chang-Claude J, Chen S, ... ... Carlson C, et al. Abstract 4489: Using functional data from Roadmap Epigenomics to inform analysis of rare variants linked to gene expression in a large colorectal cancer study Cancer Research. 76: 4489-4489. DOI: 10.1158/1538-7445.Am2016-4489 |
0.388 |
|
| 2015 |
Dean J, Emerson RO, Vignali M, Sherwood AM, Rieder MJ, Carlson CS, Robins HS. Annotation of pseudogenic gene segments by massively parallel sequencing of rearranged lymphocyte receptor loci. Genome Medicine. 7: 123. PMID 26596423 DOI: 10.1186/S13073-015-0238-Z |
0.317 |
|
| 2015 |
Schumacher FR, Schmit SL, Jiao S, Edlund CK, Wang H, Zhang B, Hsu L, Huang SC, Fischer CP, Harju JF, Idos GE, Lejbkowicz F, Manion FJ, McDonnell K, McNeil CE, ... ... Carlson CS, et al. Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nature Communications. 6: 8739. PMID 26498495 DOI: 10.1038/Ncomms9739 |
0.388 |
|
| 2015 |
Zheng HF, Forgetta V, Hsu YH, Estrada K, Rosello-Diez A, Leo PJ, Dahia CL, Park-Min KH, Tobias JH, Kooperberg C, Kleinman A, Styrkarsdottir U, Liu CT, Uggla C, Evans DS, ... ... Carlson C, et al. Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture. Nature. PMID 26367794 DOI: 10.1038/Nature14878 |
0.401 |
|
| 2015 |
Schumacher FR, Schmit SL, Jiao S, Edlund CK, Wang H, Zhang B, Hsu L, Huang SC, Fischer CP, Harju JF, Idos GE, Lejbkowicz F, Manion FJ, McDonnell K, McNeil CE, ... ... Carlson CS, et al. Genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nature Communications. 6: 7138. PMID 26151821 DOI: 10.1038/Ncomms8138 |
0.418 |
|
| 2015 |
Auer PL, Nalls M, Meschia JF, Worrall BB, Longstreth WT, Seshadri S, Kooperberg C, Burger KM, Carlson CS, Carty CL, Chen WM, Cupples LA, DeStefano AL, Fornage M, Hardy J, et al. Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project. Jama Neurology. 72: 781-8. PMID 25961151 DOI: 10.1001/Jamaneurol.2015.0582 |
0.329 |
|
| 2015 |
Kocarnik JM, Park SL, Han J, Dumitrescu L, Cheng I, Wilkens LR, Schumacher FR, Kolonel L, Carlson CS, Crawford DC, Goodloe RJ, Dilks HH, Baker P, Richardson D, Matise TC, et al. Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study. Plos One. 10: e0120491. PMID 25789475 DOI: 10.1371/Journal.Pone.0120491 |
0.331 |
|
| 2015 |
Nan H, Hutter CM, Lin Y, Jacobs EJ, Ulrich CM, White E, Baron JA, Berndt SI, Brenner H, Butterbach K, Caan BJ, Campbell PT, Carlson CS, Casey G, Chang-Claude J, et al. Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants. Jama. 313: 1133-42. PMID 25781442 DOI: 10.1001/Jama.2015.1815 |
0.345 |
|
| 2015 |
Wang LS, Naj AC, Graham RR, Crane PK, Kunkle BW, Cruchaga C, Murcia JD, Cannon-Albright L, Baldwin CT, Zetterberg H, Blennow K, Kukull WA, Faber KM, Schupf N, Norton MC, ... ... Carlson CS, et al. Rarity of the Alzheimer disease-protective APP A673T variant in the United States. Jama Neurology. 72: 209-16. PMID 25531812 DOI: 10.1001/Jamaneurol.2014.2157 |
0.309 |
|
| 2015 |
Do R, Stitziel NO, Won HH, Jørgensen AB, Duga S, Angelica Merlini P, Kiezun A, Farrall M, Goel A, Zuk O, Guella I, Asselta R, Lange LA, Peloso GM, Auer PL, ... ... Carlson CS, et al. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Nature. 518: 102-6. PMID 25487149 DOI: 10.1038/Nature13917 |
0.334 |
|
| 2015 |
Crosslin DR, Carrell DS, Burt A, Kim DS, Underwood JG, Hanna DS, Comstock BA, Baldwin E, de Andrade M, Kullo IJ, Tromp G, Kuivaniemi H, Borthwick KM, McCarty CA, Peissig PL, ... ... Carlson CS, et al. Genetic variation in the HLA region is associated with susceptibility to herpes zoster. Genes and Immunity. 16: 1-7. PMID 25297839 DOI: 10.1038/Gene.2014.51 |
0.406 |
|
| 2015 |
Schick UM, Auer PL, Bis JC, Lin H, Wei P, Pankratz N, Lange LA, Brody J, Stitziel NO, Kim DS, Carlson CS, Fornage M, Haessler J, Hsu L, Jackson RD, et al. Association of exome sequences with plasma C-reactive protein levels in >9000 participants. Human Molecular Genetics. 24: 559-71. PMID 25187575 DOI: 10.1093/Hmg/Ddu450 |
0.434 |
|
| 2014 |
Rosse SA, Auer PL, Carlson CS. Functional annotation of putative regulatory elements at cancer susceptibility Loci. Cancer Informatics. 13: 5-17. PMID 25288875 DOI: 10.4137/Cin.S13789 |
0.449 |
|
| 2014 |
Naj AC, Jun G, Reitz C, Kunkle BW, Perry W, Park YS, Beecham GW, Rajbhandary RA, Hamilton-Nelson KL, Wang LS, Kauwe JS, Huentelman MJ, Myers AJ, Bird TD, Boeve BF, ... ... Carlson CS, et al. Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. Jama Neurology. 71: 1394-404. PMID 25199842 DOI: 10.1001/Jamaneurol.2014.1491 |
0.358 |
|
| 2014 |
Du M, Zhang X, Hoffmeister M, Schoen RE, Baron JA, Berndt SI, Brenner H, Carlson CS, Casey G, Chan AT, Curtis KR, Duggan D, Gauderman WJ, Giovannucci EL, Gong J, et al. No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 23: 2971-6. PMID 25192705 DOI: 10.1158/1055-9965.Epi-14-0893 |
0.3 |
|
| 2014 |
Du M, Auer PL, Jiao S, Haessler J, Altshuler D, Boerwinkle E, Carlson CS, Carty CL, Chen YD, Curtis K, Franceschini N, Hsu L, Jackson R, Lange LA, Lettre G, et al. Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans. Human Molecular Genetics. 23: 6607-15. PMID 25027330 DOI: 10.1093/Hmg/Ddu361 |
0.438 |
|
| 2014 |
Carty CL, Bhattacharjee S, Haessler J, Cheng I, Hindorff LA, Aroda V, Carlson CS, Hsu CN, Wilkens L, Liu S, Selvin E, Jackson R, North KE, Peters U, Pankow JS, et al. Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology study. Circulation. Cardiovascular Genetics. 7: 505-13. PMID 25023634 DOI: 10.1161/Circgenetics.113.000386 |
0.345 |
|
| 2014 |
Auer PL, Teumer A, Schick U, O'Shaughnessy A, Lo KS, Chami N, Carlson C, de Denus S, Dubé MP, Haessler J, Jackson RD, Kooperberg C, Perreault LP, Nauck M, Peters U, et al. Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. Nature Genetics. 46: 629-34. PMID 24777453 DOI: 10.1038/Ng.2962 |
0.383 |
|
| 2014 |
Figueiredo JC, Hsu L, Hutter CM, Lin Y, Campbell PT, Baron JA, Berndt SI, Jiao S, Casey G, Fortini B, Chan AT, Cotterchio M, Lemire M, Gallinger S, Harrison TA, ... ... Carlson CS, et al. Genome-wide diet-gene interaction analyses for risk of colorectal cancer. Plos Genetics. 10: e1004228. PMID 24743840 DOI: 10.1371/Journal.Pgen.1004228 |
0.401 |
|
| 2014 |
Lim U, Kocarnik JM, Bush WS, Matise TC, Caberto C, Park SL, Carlson CS, Deelman E, Duggan D, Fesinmeyer M, Haiman CA, Henderson BE, Hindorff LA, Kolonel LN, Peters U, et al. Pleiotropy of cancer susceptibility variants on the risk of non-Hodgkin lymphoma: the PAGE consortium. Plos One. 9: e89791. PMID 24598796 DOI: 10.1371/Journal.Pone.0089791 |
0.419 |
|
| 2014 |
Jiao S, Peters U, Berndt S, Brenner H, Butterbach K, Caan BJ, Carlson CS, Chan AT, Chang-Claude J, Chanock S, Curtis KR, Duggan D, Gong J, Harrison TA, Hayes RB, et al. Estimating the heritability of colorectal cancer. Human Molecular Genetics. 23: 3898-905. PMID 24562164 DOI: 10.1093/Hmg/Ddu087 |
0.337 |
|
| 2014 |
Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang ZZ, Bizon C, Lange EM, Smith JD, Turner EH, Jun G, Kang HM, Peloso G, Auer P, Li KP, ... ... Carlson CS, et al. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. American Journal of Human Genetics. 94: 233-45. PMID 24507775 DOI: 10.1016/J.Ajhg.2014.01.010 |
0.388 |
|
| 2014 |
Peloso GM, Auer PL, Bis JC, Voorman A, Morrison AC, Stitziel NO, Brody JA, Khetarpal SA, Crosby JR, Fornage M, Isaacs A, Jakobsdottir J, Feitosa MF, Davies G, Huffman JE, ... ... Carlson C, et al. Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. American Journal of Human Genetics. 94: 223-32. PMID 24507774 DOI: 10.1016/J.Ajhg.2014.01.009 |
0.356 |
|
| 2014 |
Chen CT, Liu CT, Chen GK, Andrews JS, Arnold AM, Dreyfus J, Franceschini N, Garcia ME, Kerr KF, Li G, Lohman KK, Musani SK, Nalls MA, Raffel LJ, Smith J, ... ... Carlson CS, et al. Meta-analysis of loci associated with age at natural menopause in African-American women. Human Molecular Genetics. 23: 3327-42. PMID 24493794 DOI: 10.1093/Hmg/Ddu041 |
0.634 |
|
| 2014 |
Logsdon BA, Dai JY, Auer PL, Johnsen JM, Ganesh SK, Smith NL, Wilson JG, Tracy RP, Lange LA, Jiao S, Rich SS, Lettre G, Carlson CS, Jackson RD, O'Donnell CJ, et al. A variational Bayes discrete mixture test for rare variant association. Genetic Epidemiology. 38: 21-30. PMID 24482836 DOI: 10.1002/Gepi.21772 |
0.384 |
|
| 2014 |
Carlson CS, Garfall AL, Meng W, Daber R, Zhang B, Hershberg U, Cohen AD, Vogl DT, Brendan W, Carroll M, Stadtmauer EA, Prak EL. Detection of the Malignant B Cell Clone in Multiple Myeloma Via High Throughput Sequencing Is Robust to Significant Levels of Somatic Hypermutation Blood. 124: 3413-3413. DOI: 10.1182/Blood.V124.21.3413.3413 |
0.31 |
|
| 2013 |
Gong J, Schumacher F, Lim U, Hindorff LA, Haessler J, Buyske S, Carlson CS, Rosse S, Bůžková P, Fornage M, Gross M, Pankratz N, Pankow JS, Schreiner PJ, Cooper R, et al. Fine Mapping and Identification of BMI Loci in African Americans. American Journal of Human Genetics. 93: 661-71. PMID 24094743 DOI: 10.1016/J.Ajhg.2013.08.012 |
0.444 |
|
| 2013 |
Carlson CS, Matise TC, North KE, Haiman CA, Fesinmeyer MD, Buyske S, Schumacher FR, Peters U, Franceschini N, Ritchie MD, Duggan DJ, Spencer KL, Dumitrescu L, Eaton CB, Thomas F, et al. Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study. Plos Biology. 11: e1001661. PMID 24068893 DOI: 10.1371/Journal.Pbio.1001661 |
0.401 |
|
| 2013 |
Abbenhardt C, Poole EM, Kulmacz RJ, Xiao L, Curtin K, Galbraith RL, Duggan D, Hsu L, Makar KW, Caan BJ, Koepl L, Owen RW, Scherer D, Carlson CS, et al. Phospholipase A2G1B polymorphisms and risk of colorectal neoplasia. International Journal of Molecular Epidemiology and Genetics. 4: 140-9. PMID 24046806 |
0.327 |
|
| 2013 |
Makar KW, Poole EM, Resler AJ, Seufert B, Curtin K, Kleinstein SE, Duggan D, Kulmacz RJ, Hsu L, Whitton J, Carlson CS, Rimorin CF, Caan BJ, Baron JA, Potter JD, et al. COX-1 (PTGS1) and COX-2 (PTGS2) polymorphisms, NSAID interactions, and risk of colon and rectal cancers in two independent populations. Cancer Causes & Control : Ccc. 24: 2059-75. PMID 24022467 DOI: 10.1007/S10552-013-0282-1 |
0.343 |
|
| 2013 |
Liu CT, Monda KL, Taylor KC, Lange L, Demerath EW, Palmas W, Wojczynski MK, Ellis JC, Vitolins MZ, Liu S, Papanicolaou GJ, Irvin MR, Xue L, Griffin PJ, Nalls MA, ... ... Carlson CS, et al. Genome-wide association of body fat distribution in African ancestry populations suggests new loci. Plos Genetics. 9: e1003681. PMID 23966867 DOI: 10.1371/Journal.Pgen.1003681 |
0.425 |
|
| 2013 |
Duan Q, Liu EY, Auer PL, Zhang G, Lange EM, Jun G, Bizon C, Jiao S, Buyske S, Franceschini N, Carlson CS, Hsu L, Reiner AP, Peters U, Haessler J, et al. Imputation of coding variants in African Americans: better performance using data from the exome sequencing project. Bioinformatics (Oxford, England). 29: 2744-9. PMID 23956302 DOI: 10.1093/Bioinformatics/Btt477 |
0.342 |
|
| 2013 |
Fesinmeyer MD, North KE, Ritchie MD, Lim U, Franceschini N, Wilkens LR, Gross MD, Bůžková P, Glenn K, Quibrera PM, Fernández-Rhodes L, Li Q, Fowke JH, Li R, Carlson CS, et al. Genetic risk factors for BMI and obesity in an ethnically diverse population: results from the population architecture using genomics and epidemiology (PAGE) study. Obesity (Silver Spring, Md.). 21: 835-46. PMID 23712987 DOI: 10.1002/Oby.20268 |
0.603 |
|
| 2013 |
Johnsen JM, Auer PL, Morrison AC, Jiao S, Wei P, Haessler J, Fox K, McGee SR, Smith JD, Carlson CS, Smith N, Boerwinkle E, Kooperberg C, Nickerson DA, Rich SS, et al. Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project. Blood. 122: 590-7. PMID 23690449 DOI: 10.1182/Blood-2013-02-485094 |
0.357 |
|
| 2013 |
Demerath EW, Liu CT, Franceschini N, Chen G, Palmer JR, Smith EN, Chen CT, Ambrosone CB, Arnold AM, Bandera EV, Berenson GS, Bernstein L, Britton A, Cappola AR, Carlson CS, et al. Genome-wide association study of age at menarche in African-American women. Human Molecular Genetics. 22: 3329-46. PMID 23599027 DOI: 10.1093/Hmg/Ddt181 |
0.648 |
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| 2013 |
Monda KL, Chen GK, Taylor KC, Palmer C, Edwards TL, Lange LA, Ng MC, Adeyemo AA, Allison MA, Bielak LF, Chen G, Graff M, Irvin MR, Rhie SK, Li G, ... ... Carlson CS, et al. A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry. Nature Genetics. 45: 690-6. PMID 23583978 DOI: 10.1038/Ng.2608 |
0.421 |
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| 2013 |
Carty CL, Spencer KL, Setiawan VW, Fernandez-Rhodes L, Malinowski J, Buyske S, Young A, Jorgensen NW, Cheng I, Carlson CS, Brown-Gentry K, Goodloe R, Park A, Parikh NI, Henderson B, et al. Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study. Human Reproduction (Oxford, England). 28: 1695-706. PMID 23508249 DOI: 10.1093/Humrep/Det071 |
0.408 |
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| 2013 |
Spencer KL, Malinowski J, Carty CL, Franceschini N, Fernández-Rhodes L, Young A, Cheng I, Ritchie MD, Haiman CA, Wilkens L, Chunyuanwu, Matise TC, Carlson CS, Brennan K, Park A, et al. Genetic variation and reproductive timing: African American women from the Population Architecture using Genomics and Epidemiology (PAGE) Study. Plos One. 8: e55258. PMID 23424626 DOI: 10.1371/Journal.Pone.0055258 |
0.493 |
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| 2013 |
Chen CT, McDavid AN, Kahsai OJ, Zebari AS, Carlson CS. Efficient identification of rare variants in large populations: deep re-sequencing the CRP locus in the CARDIA study. Nucleic Acids Research. 41: e85. PMID 23408856 DOI: 10.1093/Nar/Gkt092 |
0.642 |
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| 2013 |
Kleinstein SE, Heath L, Makar KW, Poole EM, Seufert BL, Slattery ML, Xiao L, Duggan DJ, Hsu L, Curtin K, Koepl L, Muehling J, Taverna D, Caan BJ, Carlson CS, et al. Genetic variation in the lipoxygenase pathway and risk of colorectal neoplasia. Genes, Chromosomes & Cancer. 52: 437-49. PMID 23404351 DOI: 10.1002/Gcc.22042 |
0.423 |
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| 2013 |
Crosslin DR, McDavid A, Weston N, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E, Kho A, Hayes MG, Ritchie MD, Saip A, Crawford DC, ... ... Carlson CS, et al. Genetic variation associated with circulating monocyte count in the eMERGE Network. Human Molecular Genetics. 22: 2119-27. PMID 23314186 DOI: 10.1093/Hmg/Ddt010 |
0.393 |
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| 2013 |
Graff M, Gordon-Larsen P, Lim U, Fowke JH, Love SA, Fesinmeyer M, Wilkens LR, Vertilus S, Ritchie MD, Prentice RL, Pankow J, Monroe K, Manson JE, Le Marchand L, Kuller LH, ... ... Carlson CS, et al. The influence of obesity-related single nucleotide polymorphisms on BMI across the life course: the PAGE study. Diabetes. 62: 1763-7. PMID 23300277 DOI: 10.2337/Db12-0863 |
0.34 |
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| 2013 |
Peters U, Jiao S, Schumacher FR, Hutter CM, Aragaki AK, Baron JA, Berndt SI, Bézieau S, Brenner H, Butterbach K, Caan BJ, Campbell PT, Carlson CS, Casey G, Chan AT, et al. Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. Gastroenterology. 144: 799-807.e24. PMID 23266556 DOI: 10.1053/J.Gastro.2012.12.020 |
0.325 |
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| 2013 |
Carlson CS, Mark K, Wall DA, Schultz KR, Bunin N, Kalos M, Cindy D, Williamson D, Julie G, Borowitz MJ, Grupp SA. Striking Predictive Power For Relapse and Decreased Survival Associated With Detectable Minimal Residual Disease by IGH VDJ Deep Sequencing Of Bone Marrow Pre- and Post-Allogeneic Transplant In Children With B-Lineage ALL: A Subanalysis Of The COG ASCT0431/PBMTC ONC051 Study Blood. 122: 919-919. DOI: 10.1182/Blood.V122.21.919.919 |
0.317 |
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| 2013 |
Robins H, Carlson CS. Reduction Of Immune Repertoire Diversity Through DNA Sequence Constraints At VDJ Junctions Blood. 122: 4944-4944. DOI: 10.1182/Blood.V122.21.4944.4944 |
0.342 |
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| 2013 |
Rieder MJ, Williamson D, Sherwood A, Emerson RO, Desmarais C, Chung M, Robins H, Carlson CS. Frequency Of Gene Usage and Copy Number Variation Within The Rearranged Immunoglobin Heavy-Chain Variable Locus Based On Immune Repertoire Sequencing Blood. 122: 3486-3486. DOI: 10.1182/Blood.V122.21.3486.3486 |
0.329 |
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| 2013 |
Sherwood A, Robins H, Carlson CS, Rieder M. Annotation Of Pseudogenous Gene Segments By Massively Parallel Sequencing Of Rearranged Lymphocyte Receptor Loci Blood. 122: 3480-3480. DOI: 10.1182/Blood.V122.21.3480.3480 |
0.329 |
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| 2013 |
Carlson CS, Howie B, Garfall AL, Prak EL. All Clones Are Not Equal: Somatic Hypermutation Significantly Enhances The Utility Of Tumor Tagging Rearrangements At IG Light Chain Loci In B Cell Malignancy Blood. 122: 1376-1376. DOI: 10.1182/Blood.V122.21.1376.1376 |
0.317 |
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| 2012 |
Jiao S, Hsu L, Berndt S, Bézieau S, Brenner H, Buchanan D, Caan BJ, Campbell PT, Carlson CS, Casey G, Chan AT, Chang-Claude J, Chanock S, Conti DV, Curtis KR, et al. Genome-wide search for gene-gene interactions in colorectal cancer. Plos One. 7: e52535. PMID 23300701 DOI: 10.1371/Journal.Pone.0052535 |
0.33 |
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| 2012 |
Rasmussen-Torvik LJ, Pacheco JA, Wilke RA, Thompson WK, Ritchie MD, Kho AN, Muthalagu A, Hayes MG, Armstrong LL, Scheftner DA, Wilkins JT, Zuvich RL, Crosslin D, Roden DM, Denny JC, ... ... Carlson CS, et al. High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE. Clinical and Translational Science. 5: 394-9. PMID 23067351 DOI: 10.1111/J.1752-8062.2012.00446.X |
0.347 |
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| 2012 |
Liu EY, Buyske S, Aragaki AK, Peters U, Boerwinkle E, Carlson C, Carty C, Crawford DC, Haessler J, Hindorff LA, Marchand LL, Manolio TA, Matise T, Wang W, Kooperberg C, et al. Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative. Genetic Epidemiology. 36: 107-17. PMID 22851474 DOI: 10.1002/Gepi.21603 |
0.415 |
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| 2012 |
Reding KW, Carlson CS, Kahsai O, Chen CC, McDavid A, Doody DR, Chen C, Ornelas I, Lowe K, Bernstein L, Weiss L, McDonald JA, Simon MS, Strom B, Marchbanks PA, et al. Examination of ancestral informative markers and self-reported race with tumor characteristics of breast cancer among Black and White women. Breast Cancer Research and Treatment. 134: 801-9. PMID 22648732 DOI: 10.1007/S10549-012-2099-0 |
0.552 |
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| 2012 |
Buyske S, Wu Y, Carty CL, Cheng I, Assimes TL, Dumitrescu L, Hindorff LA, Mitchell S, Ambite JL, Boerwinkle E, Buzkova P, Carlson CS, Cochran B, Duggan D, Eaton CB, et al. Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study. Plos One. 7: e35651. PMID 22539988 DOI: 10.1371/Journal.Pone.0035651 |
0.434 |
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| 2012 |
Reding KW, Chen C, Lowe K, Doody DR, Carlson CS, Chen CT, Houck J, Weiss LK, Marchbanks PA, Bernstein L, Spirtas R, McDonald JA, Strom BL, Burkman RT, Simon MS, et al. Estrogen-related genes and their contribution to racial differences in breast cancer risk. Cancer Causes & Control : Ccc. 23: 671-81. PMID 22418777 DOI: 10.1007/S10552-012-9925-X |
0.58 |
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| 2012 |
Poole EM, Curtin K, Hsu L, Duggan DJ, Makar KW, Xiao L, Carlson CS, Caan BJ, Potter JD, Slattery ML, Ulrich CM. Genetic variability in IL23R and risk of colorectal adenoma and colorectal cancer. Cancer Epidemiology. 36: e104-10. PMID 22154103 DOI: 10.1016/J.Canep.2011.11.001 |
0.401 |
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| 2012 |
Chen CT, Fernández-Rhodes L, Brzyski RG, Carlson CS, Chen Z, Heiss G, North KE, Woods NF, Rajkovic A, Kooperberg C, Franceschini N. Replication of loci influencing ages at menarche and menopause in Hispanic women: the Women's Health Initiative SHARe Study. Human Molecular Genetics. 21: 1419-32. PMID 22131368 DOI: 10.1093/Hmg/Ddr570 |
0.617 |
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| 2012 |
Kho AN, Hayes MG, Rasmussen-Torvik L, Pacheco JA, Thompson WK, Armstrong LL, Denny JC, Peissig PL, Miller AW, Wei WQ, Bielinski SJ, Chute CG, Leibson CL, Jarvik GP, Crosslin DR, ... Carlson CS, et al. Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study. Journal of the American Medical Informatics Association : Jamia. 19: 212-8. PMID 22101970 DOI: 10.1136/Amiajnl-2011-000439 |
0.346 |
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| 2012 |
Crosslin DR, McDavid A, Weston N, Nelson SC, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E, Kho A, Hayes MG, Pretel S, Saip A, ... ... Carlson CS, et al. Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network. Human Genetics. 131: 639-52. PMID 22037903 DOI: 10.1007/S00439-011-1103-9 |
0.424 |
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| 2012 |
Peters U, Hutter CM, Hsu L, Schumacher FR, Conti DV, Carlson CS, Edlund CK, Haile RW, Gallinger S, Zanke BW, Lemire M, Rangrej J, Vijayaraghavan R, Chan AT, Hazra A, et al. Meta-analysis of new genome-wide association studies of colorectal cancer risk. Human Genetics. 131: 217-34. PMID 21761138 DOI: 10.1007/S00439-011-1055-0 |
0.43 |
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| 2012 |
Heath LM, Makar KW, Resler AJ, Seufert BL, Poole EM, Kleinstein SE, Mandel H, Whitton J, Carlson CS, Potter JD, Ulrich CM. Abstract 36: Genetic variability in MRP4 (ABCC4), ibuprofen use, and colorectal cancer risk in the Colon Cancer Family Registry. Cancer Epidemiology Biomarkers & Prevention. 21: 36-36. DOI: 10.1158/1055-9965.Gwas-36 |
0.405 |
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| 2012 |
Fesinmeyer MD, North KE, Ritchie MD, Lim U, Franceschini N, Wilkens LR, Gross MD, Bůžková P, Glenn K, Quibrera PM, Fernández-Rhodes L, Li Q, Fowke JH, Li R, Carlson CS, et al. Genetic Risk Factors for BMI and Obesity in an Ethnically Diverse Population: Results From the Population Architecture Using Genomics and Epidemiology (PAGE) Study Obesity. DOI: 10.1038/Oby.2012.158 |
0.359 |
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| 2011 |
Zuvich RL, Armstrong LL, Bielinski SJ, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes MG, Jarvik GP, Jiang L, Kullo IJ, Li R, et al. Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality. Genetic Epidemiology. 35: 887-98. PMID 22125226 DOI: 10.1002/Gepi.20639 |
0.363 |
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| 2011 |
Matise TC, Ambite JL, Buyske S, Carlson CS, Cole SA, Crawford DC, Haiman CA, Heiss G, Kooperberg C, Marchand LL, Manolio TA, North KE, Peters U, Ritchie MD, Hindorff LA, et al. The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study. American Journal of Epidemiology. 174: 849-59. PMID 21836165 DOI: 10.1093/Aje/Kwr160 |
0.364 |
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| 2011 |
Dumitrescu L, Carty CL, Taylor K, Schumacher FR, Hindorff LA, Ambite JL, Anderson G, Best LG, Brown-Gentry K, B?žková P, Carlson CS, Cochran B, Cole SA, Devereux RB, Duggan D, et al. Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study. Plos Genetics. 7: e1002138. PMID 21738485 DOI: 10.1371/Journal.Pgen.1002138 |
0.312 |
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| 2011 |
Freedman ML, Monteiro AN, Gayther SA, Coetzee GA, Risch A, Plass C, Casey G, De Biasi M, Carlson C, Duggan D, James M, Liu P, Tichelaar JW, Vikis HG, You M, et al. Principles for the post-GWAS functional characterization of cancer risk loci. Nature Genetics. 43: 513-8. PMID 21614091 DOI: 10.1038/Ng.840 |
0.485 |
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| 2011 |
Naj AC, Jun G, Beecham GW, Wang LS, Vardarajan BN, Buros J, Gallins PJ, Buxbaum JD, Jarvik GP, Crane PK, Larson EB, Bird TD, Boeve BF, Graff-Radford NR, De Jager PL, ... ... Carlson CS, et al. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nature Genetics. 43: 436-41. PMID 21460841 DOI: 10.1038/Ng.801 |
0.306 |
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| 2011 |
Turner S, Armstrong LL, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes G, Jarvik G, Jiang L, Kullo IJ, Li R, Ling H, et al. Quality control procedures for genome-wide association studies. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit1.19. PMID 21234875 DOI: 10.1002/0471142905.Hg0119S68 |
0.34 |
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| 2011 |
Kleinstein SE, Poole EM, Slattery ML, Xiao L, Duggan D, Hsu L, Makar KW, Curtin K, Koepl L, Muehling J, Taverna D, Caan BJ, Carlson CS, Potter JD, Ulrich CM. Abstract 3761: ALOX5 and FLAP tagSNPs, NSAID use and colorectal neoplasia risk Cancer Research. 71: 3761-3761. DOI: 10.1158/1538-7445.Am2011-3761 |
0.41 |
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| 2011 |
Makar KW, Poole EM, Xiao L, Hsu L, Curtin K, Duggan D, Kleinstein SE, Muehling J, Taverna D, Caan BJ, Carlson CS, Potter JD, Slattery ML, Ulrich CM. Abstract 3756: ALOX12 and ALOX15 tagSNPs, NSAID use, and the risk of colorectal neoplasia Cancer Research. 71: 3756-3756. DOI: 10.1158/1538-7445.Am2011-3756 |
0.417 |
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| 2011 |
Reding KW, Carlson CS, Malone KE, Chen CT, Doody DR, Ornelas I, Chen C, Lowe K, Weiss L, Simon M, Strom B. Abstract A89: Examination of ancestral informative markers and self-reported race with tumor characteristics of breast cancer among black and white women Cancer Epidemiology, Biomarkers & Prevention. 20. DOI: 10.1158/1055-9965.Disp-11-A89 |
0.582 |
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| 2010 |
Shen TH, Tarczy-Hornoch P, Detwiler LT, Cadag E, Carlson CS. Evaluation of probabilistic and logical inference for a SNP annotation system Journal of Biomedical Informatics. 43: 407-418. PMID 20015478 DOI: 10.1016/J.Jbi.2009.12.002 |
0.387 |
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| 2010 |
Abbenhardt C, Poole EM, Xiao L, Slattery ML, Galbraith RL, Duggan D, Hsu L, Makar KW, Kulmacz RJ, Curtin K, Potter JD, Caan B, Koepl L, Coghill AE, Muehling J, ... ... Carlson CS, et al. Abstract 934: Phospholipase A2A polymorphisms and risk of colorectal neoplasia Cancer Research. 70: 934-934. DOI: 10.1158/1538-7445.Am10-934 |
0.425 |
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| 2010 |
Haug U, Poole EM, Xiao L, Slattery ML, Galbraith RL, Duggan D, Hsu L, Makar KW, Peters U, Kulmacz RJ, Curtin K, Potter JD, Caan BJ, Koepl L, Coghill AE, ... ... Carlson CS, et al. Abstract 933: Glutathione peroxidase (GPX) candidate and tagSNPs and risk of colorectal neoplasia Cancer Research. 70: 933-933. DOI: 10.1158/1538-7445.Am10-933 |
0.415 |
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| 2010 |
Poole EM, Xiao L, Galbraith RL, Slattery ML, Duggan D, Coghill AE, Koepl L, Hsu L, Makar KW, Curtin K, Muehling J, Taverna D, Caan BJ, Carlson CS, Peters U, et al. Abstract 927: Interleukin-23 receptor tagSNPs and colorectal neoplasia risk Cancer Research. 70: 927-927. DOI: 10.1158/1538-7445.Am10-927 |
0.44 |
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| 2010 |
Makar KW, Poole EM, Xiao L, Rimorin CF, Galbraith RL, Slattery ML, Duggan D, Kulmacz RJ, Koepl L, Coghill A, Hsu L, Curtain K, Muehling J, Taverna D, Caan BJ, ... ... Carlson CS, et al. Abstract 5710: COX-1 and COX-2 polymorphisms, NSAID use, and the risk of colorectal neoplasia Cancer Research. 70: 5710-5710. DOI: 10.1158/1538-7445.Am10-5710 |
0.409 |
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| 2010 |
Hutter CM, Chen LS, Liu Y, Slattery ML, Carlson CS, Vijayaraghavan R, Taverna D, Duggan D, Curtin K, Berndt SI, Schoen RE, Caan B, Jackson R, Kooperberg CL, LaCroix AZ, et al. Abstract 4733: Gene-set analysis of colon cancer genome-wide association data: Identification of the TGF-beta pathway Cancer Research. 70: 4733-4733. DOI: 10.1158/1538-7445.Am10-4733 |
0.434 |
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| 2009 |
Reiner AP, Gross MD, Carlson CS, Bielinski SJ, Lange LA, Fornage M, Jenny NS, Walston J, Tracy RP, Williams OD, Jacobs DR, Nickerson DA. Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiovascular Health Study. Circulation. Cardiovascular Genetics. 2: 244-54. PMID 20031592 DOI: 10.1161/Circgenetics.108.839506 |
0.322 |
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| 2009 |
Reding KW, Li CI, Weiss NS, Chen C, Carlson CS, Duggan D, Thummel KE, Daling JR, Malone KE. Genetic variation in the progesterone receptor and metabolism pathways and hormone therapy in relation to breast cancer risk American Journal of Epidemiology. 170: 1241-1249. PMID 19846565 DOI: 10.1093/Aje/Kwp298 |
0.375 |
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| 2009 |
Reding KW, Weiss NS, Chen C, Li CI, Carlson CS, Wilkerson HW, Farin FM, Thummel KE, Daling JR, Malone KE. Genetic polymorphisms in the catechol estrogen metabolism pathway and breast cancer risk. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 18: 1461-7. PMID 19383894 DOI: 10.1158/1055-9965.Epi-08-0917 |
0.354 |
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| 2009 |
Shen TH, Carlson CS, Tarczy-Hornoch P. SNPit: A federated data integration system for the purpose of functional SNP annotation Computer Methods and Programs in Biomedicine. 95: 181-189. PMID 19327864 DOI: 10.1016/J.Cmpb.2009.02.010 |
0.365 |
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| 2008 |
Salinas CA, Kwon E, Carlson CS, Koopmeiners JS, Feng Z, Karyadi DM, Ostrander EA, Stanford JL. Multiple independent genetic variants in the 8q24 region are associated with prostate cancer risk. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 17: 1203-13. PMID 18483343 DOI: 10.1158/1055-9965.Epi-07-2811 |
0.405 |
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| 2008 |
Carty CL, Cushman M, Jones D, Lange LA, Hindorff LA, Rice K, Jenny NS, Durda JP, Walston J, Carlson CS, Nickerson D, Tracy RP, Reiner AP. Associations between common fibrinogen gene polymorphisms and cardiovascular disease in older adults. The Cardiovascular Health Study. Thrombosis and Haemostasis. 99: 388-95. PMID 18278190 DOI: 10.1160/Th07-08-0523 |
0.392 |
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| 2007 |
Reiner AP, Carlson CS, Jenny NS, Durda JP, Siscovick DS, Nickerson DA, Tracy RP. USF1 gene variants, cardiovascular risk, and mortality in European Americans: Analysis of two US cohort studies Arteriosclerosis, Thrombosis, and Vascular Biology. 27: 2736-2742. PMID 17885212 DOI: 10.1161/Atvbaha.107.154559 |
0.372 |
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| 2007 |
Hamvas A, Wegner DJ, Carlson CS, Bergmann KR, Trusgnich MA, Fulton L, Kasai Y, An P, Mardis ER, Wilson RK, Cole FS. Comprehensive genetic variant discovery in the surfactant protein B gene. Pediatric Research. 62: 170-5. PMID 17597650 DOI: 10.1203/Pdr.0B013E3180A03232 |
0.412 |
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| 2007 |
Bigler J, Sibert JG, Poole EM, Carlson CS, Potter JD, Ulrich CM. Polymorphisms predicted to alter function in Prostaglandin E2 synthase and Prostaglandin E2 receptors Pharmacogenetics and Genomics. 17: 221-227. PMID 17460551 DOI: 10.1097/Fpc.0B013E3280119D50 |
0.335 |
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| 2007 |
Reiner AP, Carlson CS, Ziv E, Iribarren C, Jaquish CE, Nickerson DA. Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA Study Human Genetics. 121: 565-575. PMID 17356887 DOI: 10.1007/S00439-007-0350-2 |
0.395 |
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| 2006 |
Kelada SN, Checkoway H, Kardia SL, Carlson CS, Costa-Mallen P, Eaton DL, Firestone J, Powers KM, Swanson PD, Franklin GM, Longstreth WT, Weller TS, Afsharinejad Z, Costa LG. 5' and 3' region variability in the dopamine transporter gene (SLC6A3), pesticide exposure and Parkinson's disease risk: a hypothesis-generating study. Human Molecular Genetics. 15: 3055-62. PMID 16963468 DOI: 10.1093/Hmg/Ddl247 |
0.346 |
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| 2006 |
Carlson CS. Agnosticism and equity in genome-wide association studies Nature Genetics. 38: 605-606. PMID 16736010 DOI: 10.1038/Ng0606-605 |
0.392 |
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| 2006 |
Carlson CS, Heagerty PJ, Hatsukami TS, Richter RJ, Ranchalis J, Lewis J, Bacus TJ, McKinstry LA, Schellenberg GD, Rieder M, Nickerson D, Furlong CE, Chait A, Jarvik GP. TagSNP analyses of the PON gene cluster: effects on PON1 activity, LDL oxidative susceptibility, and vascular disease. Journal of Lipid Research. 47: 1014-24. PMID 16474172 DOI: 10.1194/Jlr.M500517-Jlr200 |
0.36 |
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| 2004 |
Livingston RJ, von Niederhausern A, Jegga AG, Crawford DC, Carlson CS, Rieder MJ, Gowrisankar S, Aronow BJ, Weiss RB, Nickerson DA. Pattern of sequence variation across 213 environmental response genes. Genome Research. 14: 1821-31. PMID 15364900 DOI: 10.1101/Gr.2730004 |
0.302 |
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| 2004 |
Crawford DC, Carlson CS, Rieder MJ, Carrington DP, Yi Q, Smith JD, Eberle MA, Kruglyak L, Nickerson DA. Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations. American Journal of Human Genetics. 74: 610-22. PMID 15015130 DOI: 10.1086/382227 |
0.399 |
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| 2004 |
Carlson CS, Eberle MA, Rieder MJ, Yi Q, Kruglyak L, Nickerson DA. Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. American Journal of Human Genetics. 74: 106-20. PMID 14681826 DOI: 10.1086/381000 |
0.404 |
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| 2002 |
Mackelprang R, Carlson CS, Subrahmanyan L, Livingston RJ, Eberle MA, Nickerson DA. Sequence variation in the human T-cell receptor loci Immunological Reviews. 190: 26-39. PMID 12493004 DOI: 10.1034/J.1600-065X.2002.19003.X |
0.339 |
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