| Year |
Citation |
Score |
| 2024 |
de Vries PS, Reventun P, Brown MR, Heath AS, Huffman JE, Le NQ, Bebo A, Brody JA, Temprano-Sagrera G, Raffield LM, Ozel AB, Thibord F, Jain D, Lewis JP, Rodriguez BAT, ... ... Morrison A, et al. A genetic association study of circulating coagulation Factor VIII and von Willebrand Factor levels. Blood. PMID 38320121 DOI: 10.1182/blood.2023021452 |
0.445 |
|
| 2024 |
Alkis T, Luo X, Wall K, Brody J, Bartz T, Chang PP, Norby FL, Hoogeveen RC, Morrison AC, Ballantyne CM, Coresh J, Boerwinkle E, Psaty BM, Shah AM, Yu B. A polygenic risk score of atrial fibrillation improves prediction of lifetime risk for heart failure. Esc Heart Failure. PMID 38258344 DOI: 10.1002/ehf2.14665 |
0.377 |
|
| 2023 |
Armstrong ND, Srinivasasainagendra V, Ammous F, Assimes TL, Beitelshees AL, Brody J, Cade BE, Ida Chen YD, Chen H, de Vries PS, Floyd JS, Franceschini N, Guo X, Hellwege JN, House JS, ... ... Morrison AC, et al. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program. Frontiers in Genetics. 14: 1278215. PMID 38162683 DOI: 10.3389/fgene.2023.1278215 |
0.329 |
|
| 2023 |
de Las Fuentes L, Schwander KL, Brown MR, Bentley AR, Winkler TW, Sung YJ, Munroe PB, Miller CL, Aschard H, Aslibekyan S, Bartz TM, Bielak LF, Chai JF, Cheng CY, Dorajoo R, ... ... Morrison AC, et al. Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci. Frontiers in Genetics. 14: 1235337. PMID 38028628 DOI: 10.3389/fgene.2023.1235337 |
0.432 |
|
| 2023 |
Li X, Chen H, Selvaraj MS, Van Buren E, Zhou H, Wang Y, Sun R, McCaw ZR, Yu Z, Arnett DK, Bis JC, Blangero J, Boerwinkle E, Bowden DW, Brody JA, ... ... Morrison AC, et al. A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. Biorxiv : the Preprint Server For Biology. PMID 37961350 DOI: 10.1101/2023.10.30.564764 |
0.485 |
|
| 2023 |
Wang Y, Selvaraj MS, Li X, Li Z, Holdcraft JA, Arnett DK, Bis JC, Blangero J, Boerwinkle E, Bowden DW, Cade BE, Carlson JC, Carson AP, Chen YI, Curran JE, ... ... Morrison AC, et al. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. American Journal of Human Genetics. 110: 1704-1717. PMID 37802043 DOI: 10.1016/j.ajhg.2023.09.003 |
0.497 |
|
| 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, ... ... Morrison AC, 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 |
0.482 |
|
| 2023 |
van de Vegte YJ, Eppinga RN, van der Ende MY, Hagemeijer YP, Mahendran Y, Salfati E, Smith AV, Tan VY, Arking DE, Ntalla I, Appel EV, Schurmann C, Brody JA, Rueedi R, Polasek O, ... ... Morrison AC, et al. Genetic insights into resting heart rate and its role in cardiovascular disease. Nature Communications. 14: 4646. PMID 37532724 DOI: 10.1038/s41467-023-39521-2 |
0.313 |
|
| 2023 |
Wang Y, Selvaraj MS, Li X, Li Z, Holdcraft JA, Arnett DK, Bis JC, Blangero J, Boerwinkle E, Bowden DW, Cade BE, Carlson JC, Carson AP, Chen YI, Curran JE, ... ... Morrison AC, et al. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study. Medrxiv : the Preprint Server For Health Sciences. PMID 37425772 DOI: 10.1101/2023.06.28.23291966 |
0.503 |
|
| 2023 |
Huffman JE, Nicolas J, Hahn J, Heath AS, Raffield LM, Yanek LR, Brody JA, Thibord F, Almasy L, Bartz TM, Bielak LF, Bowler RP, Carrasquilla GD, Chasman DI, Chen MH, ... ... Morrison AC, et al. Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. Medrxiv : the Preprint Server For Health Sciences. PMID 37398003 DOI: 10.1101/2023.06.07.23291095 |
0.407 |
|
| 2023 |
Feofanova EV, Brown MR, Alkis T, Manuel AM, Li X, Tahir UA, Li Z, Mendez KM, Kelly RS, Qi Q, Chen H, Larson MG, Lemaitre RN, Morrison AC, Grieser C, et al. Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations. Nature Communications. 14: 3111. PMID 37253714 DOI: 10.1038/s41467-023-38800-2 |
0.357 |
|
| 2023 |
Wang N, Yu B, Jun G, Qi Q, Durazo-Arvizu RA, Lindstrom S, Morrison AC, Kaplan RC, Boerwinkle E, Chen H. StocSum: stochastic summary statistics for whole genome sequencing studies. Biorxiv : the Preprint Server For Biology. PMID 37066281 DOI: 10.1101/2023.04.06.535886 |
0.476 |
|
| 2023 |
Seyerle AA, Laurie CA, Coombes BJ, Jain D, Conomos MP, Brody J, Chen MH, Gogarten SM, Beutel KM, Gupta N, Heckbert SR, Jackson RD, Johnson AD, Ko D, Manson JE, ... ... Morrison AC, et al. Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program. Circulation. Genomic and Precision Medicine. e003532. PMID 36960714 DOI: 10.1161/CIRCGEN.121.003532 |
0.457 |
|
| 2023 |
Shrine N, Izquierdo AG, Chen J, Packer R, Hall RJ, Guyatt AL, Batini C, Thompson RJ, Pavuluri C, Malik V, Hobbs BD, Moll M, Kim W, Tal-Singer R, Bakke P, ... ... Morrison AC, et al. Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Nature Genetics. 55: 410-422. PMID 36914875 DOI: 10.1038/s41588-023-01314-0 |
0.322 |
|
| 2023 |
Westerman KE, Walker ME, Gaynor SM, Wesse J, DiCorpo D, Ma J, Alonso A, Aslibekyan S, Baldridge AS, Bertoni AG, Biggs ML, Brody JA, Chen YI, Dupuis J, Goodarzi MO, ... ... Morrison AC, et al. Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits. Diabetes. PMID 36791419 DOI: 10.2337/db22-0851 |
0.496 |
|
| 2023 |
Dron JS, Patel AP, Zhang Y, Jurgens SJ, Maamari DJ, Wang M, Boerwinkle E, Morrison AC, de Vries PS, Fornage M, Hou L, Lloyd-Jones DM, Psaty BM, Tracy RP, Bis JC, et al. Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease. Jama Cardiology. PMID 36723951 DOI: 10.1001/jamacardio.2022.5271 |
0.39 |
|
| 2022 |
Li X, Quick C, Zhou H, Gaynor SM, Liu Y, Chen H, Selvaraj MS, Sun R, Dey R, Arnett DK, Bielak LF, Bis JC, Blangero J, Boerwinkle E, Bowden DW, ... ... Morrison AC, et al. Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies. Nature Genetics. PMID 36564505 DOI: 10.1038/s41588-022-01225-6 |
0.461 |
|
| 2022 |
Wheeler MM, Stilp AM, Rao S, Halldórsson BV, Beyter D, Wen J, Mihkaylova AV, McHugh CP, Lane J, Jiang MZ, Raffield LM, Jun G, Sedlazeck FJ, Metcalf G, Yao Y, ... ... Morrison AC, et al. Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program. Nature Communications. 13: 7592. PMID 36481753 DOI: 10.1038/s41467-022-35354-7 |
0.5 |
|
| 2022 |
Saunders GRB, Wang X, Chen F, Jang SK, Liu M, Wang C, Gao S, Jiang Y, Khunsriraksakul C, Otto JM, Addison C, Akiyama M, Albert CM, Aliev F, Alonso A, ... ... Morrison AC, et al. Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature. PMID 36477530 DOI: 10.1038/s41586-022-05477-4 |
0.472 |
|
| 2022 |
Aragam KG, Jiang T, Goel A, Kanoni S, Wolford BN, Atri DS, Weeks EM, Wang M, Hindy G, Zhou W, Grace C, Roselli C, Marston NA, Kamanu FK, Surakka I, ... ... Morrison AC, et al. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. Nature Genetics. 54: 1803-1815. PMID 36474045 DOI: 10.1038/s41588-022-01233-6 |
0.479 |
|
| 2022 |
Pan Y, Sun X, Mi X, Huang Z, Hsu Y, Hixson JE, Munzy D, Metcalf G, Franceschini N, Tin A, Köttgen A, Francis M, Brody JA, Kestenbaum B, Sitlani CM, ... ... Morrison AC, et al. Whole-Exome Sequencing Study Identifies Four Novel Gene Loci Associated with Diabetic Kidney Disease. Human Molecular Genetics. PMID 36444934 DOI: 10.1093/hmg/ddac290 |
0.496 |
|
| 2022 |
Li Z, Li X, Zhou H, Gaynor SM, Selvaraj MS, Arapoglou T, Quick C, Liu Y, Chen H, Sun R, Dey R, Arnett DK, Auer PL, Bielak LF, Bis JC, ... ... Morrison AC, et al. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies. Nature Methods. PMID 36303018 DOI: 10.1038/s41592-022-01640-x |
0.497 |
|
| 2022 |
Selvaraj MS, Li X, Li Z, Pampana A, Zhang DY, Park J, Aslibekyan S, Bis JC, Brody JA, Cade BE, Chuang LM, Chung RH, Curran JE, de Las Fuentes L, de Vries PS, ... ... Morrison AC, et al. Whole genome sequence analysis of blood lipid levels in >66,000 individuals. Nature Communications. 13: 5995. PMID 36220816 DOI: 10.1038/s41467-022-33510-7 |
0.477 |
|
| 2022 |
Halford JL, Morrill VN, Choi SH, Jurgens SJ, Melloni G, Marston NA, Weng LC, Nauffal V, Hall AW, Gunn S, Austin-Tse CA, Pirruccello JP, Khurshid S, Rehm HL, Benjamin EJ, ... ... Morrison AC, et al. Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes. Nature Communications. 13: 5767. PMID 36180445 DOI: 10.1038/s41467-022-33534-z |
0.383 |
|
| 2022 |
Young WJ, Lahrouchi N, Isaacs A, Duong T, Foco L, Ahmed F, Brody JA, Salman R, Noordam R, Benjamins JW, Haessler J, Lyytikäinen LP, Repetto L, Concas MP, van den Berg ME, ... ... Morrison AC, et al. Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. Nature Communications. 13: 5144. PMID 36050321 DOI: 10.1038/s41467-022-32821-z |
0.467 |
|
| 2022 |
Halford JL, Morrill VN, Choi SH, Jurgens SJ, Melloni G, Marston NA, Weng LC, Nauffal V, Hall AW, Gunn S, Austin-Tse CA, Pirruccello JP, Khurshid S, Rehm HL, Benjamin EJ, ... ... Morrison AC, et al. Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes. Nature Communications. 13: 5106. PMID 36042188 DOI: 10.1038/s41467-022-32009-5 |
0.45 |
|
| 2022 |
Ramdas S, Judd J, Graham SE, Kanoni S, Wang Y, Surakka I, Wenz B, Clarke SL, Chesi A, Wells A, Bhatti KF, Vedantam S, Winkler TW, Locke AE, Marouli E, ... ... Morrison AC, et al. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids. American Journal of Human Genetics. 109: 1366-1387. PMID 35931049 DOI: 10.1016/j.ajhg.2022.06.012 |
0.324 |
|
| 2022 |
DiCorpo D, Gaynor SM, Russell EM, Westerman KE, Raffield LM, Majarian TD, Wu P, Sarnowski C, Highland HM, Jackson A, Hasbani NR, de Vries PS, Brody JA, Hidalgo B, Guo X, ... ... Morrison AC, et al. Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program. Communications Biology. 5: 756. PMID 35902682 DOI: 10.1038/s42003-022-03702-4 |
0.467 |
|
| 2022 |
Kim W, Hecker J, Barr RG, Boerwinkle E, Cade B, Correa A, Dupuis J, Gharib SA, Lange L, London SJ, Morrison AC, O'Connor GT, Oelsner E, Psaty BM, Vasan RS, et al. Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data. Human Molecular Genetics. PMID 35766891 DOI: 10.1093/hmg/ddac117 |
0.448 |
|
| 2022 |
Kurniansyah N, Goodman MO, Kelly TN, Elfassy T, Wiggins KL, Bis JC, Guo X, Palmas W, Taylor KD, Lin HJ, Haessler J, Gao Y, Shimbo D, Smith JA, Yu B, ... ... Morrison AC, et al. A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood. Nature Communications. 13: 3549. PMID 35729114 DOI: 10.1038/s41467-022-31080-2 |
0.318 |
|
| 2022 |
Kelly TN, Sun X, He KY, Brown MR, Taliun SAG, Hellwege JN, Irvin MR, Mi X, Brody JA, Franceschini N, Guo X, Hwang SJ, de Vries PS, Gao Y, Moscati A, ... ... Morrison AC, et al. Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. Hypertension (Dallas, Tex. : 1979). 101161HYPERTENSIONAH. PMID 35652341 DOI: 10.1161/HYPERTENSIONAHA.122.19324 |
0.426 |
|
| 2022 |
Pankratz N, Wei P, Brody JA, Chen MH, Vries PS, Huffman JE, Stimson MR, Auer PL, Boerwinkle E, Cushman M, Maat MPM, Folsom AR, Franco OH, Gibbs RA, Haagenson KK, ... ... Morrison AC, et al. Whole exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. Human Molecular Genetics. PMID 35552711 DOI: 10.1093/hmg/ddac100 |
0.513 |
|
| 2022 |
Nauffal V, Morrill VN, Jurgens SJ, Choi SH, Hall AW, Weng LC, Halford JL, Austin-Tse C, Haggerty CM, Harris SL, Wong EK, Alonso A, Arking DE, Benjamin EJ, Boerwinkle E, ... ... Morrison AC, et al. Monogenic and Polygenic Contributions to QTc Prolongation in the Population. Circulation. PMID 35389749 DOI: 10.1161/CIRCULATIONAHA.121.057261 |
0.523 |
|
| 2022 |
Nakao T, Bick AG, Taub MA, Zekavat SM, Uddin MM, Niroula A, Carty CL, Lane J, Honigberg MC, Weinstock JS, Pampana A, Gibson CJ, Griffin GK, Clarke SL, Bhattacharya R, ... ... Morrison AC, et al. Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential. Science Advances. 8: eabl6579. PMID 35385311 DOI: 10.1126/sciadv.abl6579 |
0.42 |
|
| 2022 |
Temprano-Sagrera G, Sitlani CM, Bone WP, Martin-Bornez M, Voight BF, Morrison AC, Damrauer SM, de Vries PS, Smith NL, Sabater-Lleal M. Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Journal of Thrombosis and Haemostasis : Jth. PMID 35285134 DOI: 10.1111/jth.15698 |
0.322 |
|
| 2022 |
He KY, Kelly TN, Wang H, Liang J, Zhu L, Cade BE, Assimes TL, Becker LC, Beitelshees AL, Bielak LF, Bress AP, Brody JA, Chang YC, Chang YC, de Vries PS, ... ... Morrison AC, et al. Rare coding variants in RCN3 are associated with blood pressure. Bmc Genomics. 23: 148. PMID 35183128 DOI: 10.1186/s12864-022-08356-4 |
0.529 |
|
| 2022 |
Hasbani NR, Ligthart S, Brown MR, Heath AS, Bebo A, Ashley KE, Boerwinkle E, Morrison AC, Folsom AR, Aguilar D, De Vries PS. American Heart Association's Life's Simple 7: Lifestyle Recommendations, Polygenic Risk, and Lifetime Risk of Coronary Heart Disease. Circulation. PMID 35094551 DOI: 10.1161/CIRCULATIONAHA.121.053730 |
0.408 |
|
| 2022 |
DiCorpo D, LeClair J, Cole JB, Sarnowski C, Ahmadizar F, Bielak LF, Blokstra A, Bottinger EP, Chaker L, Chen YI, Chen Y, de Vries PS, Faquih T, Ghanbari M, Gudmundsdottir V, ... ... Morrison AC, et al. Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 individuals Across 13 Cohorts. Diabetes Care. PMID 35085396 DOI: 10.2337/dc21-1395 |
0.345 |
|
| 2021 |
Hindy G, Dornbos P, Chaffin MD, Liu DJ, Wang M, Selvaraj MS, Zhang D, Park J, Aguilar-Salinas CA, Antonacci-Fulton L, Ardissino D, Arnett DK, Aslibekyan S, Atzmon G, Ballantyne CM, ... ... Morrison AC, et al. Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes. American Journal of Human Genetics. PMID 34932938 DOI: 10.1016/j.ajhg.2021.11.021 |
0.476 |
|
| 2021 |
Graham SE, Clarke SL, Wu KH, Kanoni S, Zajac GJM, Ramdas S, Surakka I, Ntalla I, Vedantam S, Winkler TW, Locke AE, Marouli E, Hwang MY, Han S, Narita A, ... ... Morrison AC, et al. The power of genetic diversity in genome-wide association studies of lipids. Nature. PMID 34887591 DOI: 10.1038/s41586-021-04064-3 |
0.387 |
|
| 2021 |
Tapia AL, Rowland BT, Rosen JD, Preuss M, Young K, Graff M, Choquet H, Couper DJ, Buyske S, Bien SA, Jorgenson E, Kooperberg C, Loos RJF, Morrison AC, North KE, et al. Full title: A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping. Genetic Epidemiology. PMID 34779012 DOI: 10.1002/gepi.22436 |
0.401 |
|
| 2021 |
Sun D, Richard M, Musani SK, Sung YJ, Winkler TW, Schwander K, Chai JF, Guo X, Kilpeläinen TO, Vojinovic D, Aschard H, Bartz TM, Bielak LF, Brown MR, Chitrala K, ... ... Morrison AC, et al. Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Hgg Advances. 2. PMID 34734193 DOI: 10.1016/j.xhgg.2020.100013 |
0.489 |
|
| 2021 |
Mikhaylova AV, McHugh CP, Polfus LM, Raffield LM, Boorgula MP, Blackwell TW, Brody JA, Broome J, Chami N, Chen MH, Conomos MP, Cox C, Curran JE, Daya M, Ekunwe L, ... ... Morrison AC, et al. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 34582791 DOI: 10.1016/j.ajhg.2021.08.007 |
0.512 |
|
| 2021 |
Little A, Hu Y, Sun Q, Jain D, Broome J, Chen MH, Thibord F, McHugh C, Surendran P, Blackwell TW, Brody JA, Bhan A, Chami N, Vries PS, Ekunwe L, ... ... Morrison AC, et al. Whole genome sequence analysis of platelet traits in the NHLBI trans-omics for precision medicine initiative. Human Molecular Genetics. PMID 34553764 DOI: 10.1093/hmg/ddab252 |
0.463 |
|
| 2021 |
Sun P, Kumar N, Tin A, Zhao J, Brown MR, Lin Z, Yang ML, Zheng Q, Jia J, Bielak LF, Yu B, Boerwinkle E, Hunker KL, Coresh J, Chen YE, ... ... Morrison AC, et al. Epidemiologic and Genetic Associations of Erythropoietin With Blood Pressure, Hypertension, and Coronary Artery Disease. Hypertension (Dallas, Tex. : 1979). HYPERTENSIONAHA12117. PMID 34488438 DOI: 10.1161/HYPERTENSIONAHA.121.17597 |
0.479 |
|
| 2021 |
Sofer T, Lee J, Kurniansyah N, Jain D, Laurie CA, Gogarten SM, Conomos MP, Heavner B, Hu Y, Kooperberg C, Haessler J, Vasan RS, Cupples LA, Coombes BJ, Seyerle A, ... ... Morrison AC, et al. BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion. Hgg Advances. 2. PMID 34337551 DOI: 10.1016/j.xhgg.2021.100040 |
0.471 |
|
| 2021 |
Ligthart S, Hasbani NR, Ahmadizar F, van Herpt TTW, Leening MJG, Uitterlinden AG, Sijbrands EJG, Morrison AC, Boerwinkle E, Pankow JS, Selvin E, Ikram MA, Kavousi M, de Vries PS, Dehghan A. Genetic susceptibility, obesity, and lifetime risk of type 2 diabetes: The ARIC study and Rotterdam Study. Diabetic Medicine : a Journal of the British Diabetic Association. e14639. PMID 34245042 DOI: 10.1111/dme.14639 |
0.362 |
|
| 2021 |
Sarnowski C, Chen H, Biggs ML, Wassertheil-Smoller S, Bressler J, Irvin MR, Ryan KA, Karasik D, Arnett DK, Cupples LA, Fardo DW, Gogarten SM, Heavner BD, Jain D, Kang HM, ... ... Morrison AC, et al. Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. Plos One. 16: e0253611. PMID 34214102 DOI: 10.1371/journal.pone.0253611 |
0.394 |
|
| 2021 |
Goodrich JK, Singer-Berk M, Son R, Sveden A, Wood J, England E, Cole JB, Weisburd B, Watts N, Caulkins L, Dornbos P, Koesterer R, Zappala Z, Zhang H, Maloney KA, ... ... Morrison AC, et al. Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes. Nature Communications. 12: 3505. PMID 34108472 DOI: 10.1038/s41467-021-23556-4 |
0.457 |
|
| 2021 |
Hu Y, Stilp AM, McHugh CP, Rao S, Jain D, Zheng X, Lane J, Méric de Bellefon S, Raffield LM, Chen MH, Yanek LR, Wheeler M, Yao Y, Ren C, Broome J, ... ... Morrison AC, et al. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics. 108: 1165. PMID 34087167 DOI: 10.1016/j.ajhg.2021.04.015 |
0.417 |
|
| 2021 |
Tortolero GA, Brown MR, Sharma SV, de Oliveira Otto MC, Yamal JM, Aguilar D, Gunther MD, Mofleh DI, Harris RD, John JC, de Vries PS, Ramphul R, Serbo DM, Kiger J, Banerjee D, ... ... Morrison AC, et al. Leveraging a health information exchange for analyses of COVID-19 outcomes including an example application using smoking history and mortality. Plos One. 16: e0247235. PMID 34081724 DOI: 10.1371/journal.pone.0247235 |
0.328 |
|
| 2021 |
Hu Y, Stilp AM, McHugh CP, Rao S, Jai D, Zheng X, Lane J, Méric de Bellefon S, Raffield LM, Chen MH, Yanek LR, Wheeler M, Yao Y, Ren C, Broome J, ... ... Morrison AC, et al. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 33887194 DOI: 10.1016/j.ajhg.2021.04.003 |
0.529 |
|
| 2021 |
Wang H, Noordam R, Cade BE, Schwander K, Winkler TW, Lee J, Sung YJ, Bentley AR, Manning AK, Aschard H, Kilpeläinen TO, Ilkov M, Brown MR, Horimoto AR, Richard M, ... ... Morrison AC, et al. Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure. Molecular Psychiatry. PMID 33859359 DOI: 10.1038/s41380-021-01087-0 |
0.375 |
|
| 2021 |
Natarajan P, Pampana A, Graham SE, Ruotsalainen SE, Perry JA, de Vries PS, Broome JG, Pirruccello JP, Honigberg MC, Aragam K, Wolford B, Brody JA, Antonacci-Fulton L, Arden M, Aslibekyan S, ... ... Morrison AC, et al. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices. Nature Communications. 12: 2182. PMID 33846329 DOI: 10.1038/s41467-021-22339-1 |
0.439 |
|
| 2021 |
Surendran P, Feofanova EV, Lahrouchi N, Ntalla I, Karthikeyan S, Cook J, Chen L, Mifsud B, Yao C, Kraja AT, Cartwright JH, Hellwege JN, Giri A, Tragante V, Thorleifsson G, ... ... Morrison AC, et al. Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Nature Genetics. PMID 33727701 DOI: 10.1038/s41588-021-00832-z |
0.436 |
|
| 2021 |
Taliun D, Harris DN, Kessler MD, Carlson J, Szpiech ZA, Torres R, Taliun SAG, Corvelo A, Gogarten SM, Kang HM, Pitsillides AN, LeFaive J, Lee SB, Tian X, Browning BL, ... ... Morrison AC, et al. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 590: 290-299. PMID 33568819 DOI: 10.1038/s41586-021-03205-y |
0.494 |
|
| 2021 |
Xu H, Schwander K, Brown MR, Wang W, Waken RJ, Boerwinkle E, Cupples LA, de Las Fuentes L, van Heemst D, Osazuwa-Peters O, de Vries PS, van Dijk KW, Sung YJ, Zhang X, Morrison AC, et al. Lifestyle Risk Score: handling missingness of individual lifestyle components in meta-analysis of gene-by-lifestyle interactions. European Journal of Human Genetics : Ejhg. PMID 33500576 DOI: 10.1038/s41431-021-00808-x |
0.408 |
|
| 2021 |
Sun D, Richard MA, Musani SK, Sung YJ, Winkler TW, Schwander K, Chai JF, Guo X, Kilpeläinen TO, Vojinovic D, Aschard H, Bartz TM, Bielak LF, Brown MR, Chitrala K, ... ... Morrison AC, et al. Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits Human Genetics and Genomics Advances. 2: 100013. DOI: 10.1016/j.xhgg.2020.100013 |
0.359 |
|
| 2020 |
Maners J, Gill D, Pankratz N, Laffan MA, Wolberg AS, de Maat MPM, Ligthart S, Tang W, Ward-Caviness CK, Fornage M, Debette S, Dichgans M, McKnight B, Boerwinkle E, ... ... Morrison AC, et al. A Mendelian randomization of γ' and total fibrinogen levels in relation to venous thromboembolism and ischemic stroke. Blood. 136: 3062-3069. PMID 33367543 DOI: 10.1182/blood.2019004781 |
0.38 |
|
| 2020 |
Surendran P, Feofanova EV, Lahrouchi N, Ntalla I, Karthikeyan S, Cook J, Chen L, Mifsud B, Yao C, Kraja AT, Cartwright JH, Hellwege JN, Giri A, Tragante V, Thorleifsson G, ... ... Morrison AC, et al. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Nature Genetics. PMID 33230300 DOI: 10.1038/s41588-020-00713-x |
0.535 |
|
| 2020 |
Hahn J, Fu YP, Brown MR, Bis JC, de Vries PS, Feitosa MF, Yanek LR, Weiss S, Giulianini F, Smith AV, Guo X, Bartz TM, Becker DM, Becker LC, Boerwinkle E, ... ... Morrison AC, et al. Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Plos One. 15: e0230035. PMID 33186364 DOI: 10.1371/journal.pone.0230035 |
0.488 |
|
| 2020 |
Zhao X, Qiao D, Yang C, Kasela S, Kim W, Ma Y, Shrine N, Batini C, Sofer T, Taliun SAG, Sakornsakolpat P, Balte PP, Prokopenko D, Yu B, Lange LA, ... ... Morrison AC, et al. Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants. Nature Communications. 11: 5182. PMID 33057025 DOI: 10.1038/s41467-020-18334-7 |
0.304 |
|
| 2020 |
Feofanova EV, Chen H, Dai Y, Jia P, Grove ML, Morrison AC, Qi Q, Daviglus M, Cai J, North KE, Laurie CC, Kaplan RC, Boerwinkle E, Yu B. A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos. American Journal of Human Genetics. PMID 33031748 DOI: 10.1016/j.ajhg.2020.09.003 |
0.509 |
|
| 2020 |
Hillman P, Baker C, Hebert L, Brown M, Hixson J, Ashley-Koch A, Morrison AC, Northrup H, Au KS. Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one-carbon metabolism networks. Molecular Genetics & Genomic Medicine. e1495. PMID 32960507 DOI: 10.1002/Mgg3.1495 |
0.319 |
|
| 2020 |
Wang X, Lim E, Liu CT, Sung YJ, Rao DC, Morrison AC, Boerwinkle E, Manning AK, Chen H. Efficient gene-environment interaction tests for large biobank-scale sequencing studies. Genetic Epidemiology. PMID 32864785 DOI: 10.1002/Gepi.22351 |
0.532 |
|
| 2020 |
Small AM, Huffman JE, Klarin D, Sabater-Lleal M, Lynch JA, Assimes TL, Sun YV, Miller D, Freiberg MS, Morrison AC, Rader DJ, Wilson PWF, Cho K, Tsao PS, Chang KM, et al. Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease. Arteriosclerosis, Thrombosis, and Vascular Biology. ATVBAHA119313847. PMID 32847391 DOI: 10.1161/Atvbaha.119.313847 |
0.337 |
|
| 2020 |
Li X, Li Z, Zhou H, Gaynor SM, Liu Y, Chen H, Sun R, Dey R, Arnett DK, Aslibekyan S, Ballantyne CM, Bielak LF, Blangero J, Boerwinkle E, Bowden DW, ... ... Morrison AC, et al. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale. Nature Genetics. PMID 32839606 DOI: 10.1038/S41588-020-0676-4 |
0.563 |
|
| 2020 |
Maners J, Gill D, Pankratz N, Laffan MA, Wolberg AS, de Maat MPM, Ligthart S, Tang W, Ward-Caviness CK, Fornage M, Debette S, Dichgans M, McKnight B, Boerwinkle E, Smith NL, ... Morrison A, et al. A Mendelian randomization of γ' and total fibrinogen levels on venous thromboembolism and ischemic stroke. Blood. PMID 32722807 DOI: 10.1182/Blood.2019004781 |
0.461 |
|
| 2020 |
Lei Y, Ludorf KL, Yu X, Benjamin RH, Gu X, Lin Y, Finnell RH, Mitchell LE, Musfee FI, Malik S, Canfield MA, Morrison AC, Hobbs CA, Van Zutphen AR, Fisher S, et al. Maternal hypertension-related genotypes and congenital heart defects. American Journal of Hypertension. PMID 32710738 DOI: 10.1093/Ajh/Hpaa116 |
0.329 |
|
| 2020 |
Wang Z, Chen H, Bartz TM, Bielak LF, Chasman DI, Feitosa MF, Franceschini N, Guo X, Lim E, Noordam R, Richard MA, Wang H, Cade B, Cupples LA, de Vries PS, ... ... Morrison AC, et al. Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels. Circulation. Genomic and Precision Medicine. PMID 32510982 DOI: 10.1161/CIRCGEN.119.002772 |
0.447 |
|
| 2020 |
de Las Fuentes L, Sung YJ, Noordam R, Winkler T, Feitosa MF, Schwander K, Bentley AR, Brown MR, Guo X, Manning A, Chasman DI, Aschard H, Bartz TM, Bielak LF, Campbell A, ... ... Morrison AC, et al. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Molecular Psychiatry. PMID 32372009 DOI: 10.1038/S41380-020-0719-3 |
0.542 |
|
| 2020 |
Osazuwa-Peters OL, Waken RJ, Schwander KL, Sung YJ, de Vries PS, Hartz SM, Chasman DI, Morrison AC, Bierut LJ, Xiong C, de Las Fuentes L, Rao DC. Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Genetic Epidemiology. PMID 32227373 DOI: 10.1002/Gepi.22292 |
0.411 |
|
| 2020 |
Shah S, Henry A, Roselli C, Lin H, Sveinbjörnsson G, Fatemifar G, Hedman ÅK, Wilk JB, Morley MP, Chaffin MD, Helgadottir A, Verweij N, Dehghan A, Almgren P, Andersson C, ... ... Morrison AC, et al. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Nature Communications. 11: 163. PMID 31919418 DOI: 10.1038/S41467-019-13690-5 |
0.451 |
|
| 2019 |
Kowalski MH, Qian H, Hou Z, Rosen JD, Tapia AL, Shan Y, Jain D, Argos M, Arnett DK, Avery C, Barnes KC, Becker LC, Bien SA, Bis JC, Blangero J, ... ... Morrison AC, et al. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. Plos Genetics. 15: e1008500. PMID 31869403 DOI: 10.1371/Journal.Pgen.1008500 |
0.572 |
|
| 2019 |
Noordam R, Bos MM, Wang H, Winkler TW, Bentley AR, Kilpeläinen TO, de Vries PS, Sung YJ, Schwander K, Cade BE, Manning A, Aschard H, Brown MR, Chen H, Franceschini N, ... ... Morrison AC, et al. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. Nature Communications. 10: 5121. PMID 31719535 DOI: 10.1038/S41467-019-12958-0 |
0.43 |
|
| 2019 |
Clark DW, Okada Y, Moore KHS, Mason D, Pirastu N, Gandin I, Mattsson H, Barnes CLK, Lin K, Zhao JH, Deelen P, Rohde R, Schurmann C, Guo X, Giulianini F, ... ... Morrison AC, et al. Associations of autozygosity with a broad range of human phenotypes. Nature Communications. 10: 4957. PMID 31673082 DOI: 10.1038/S41467-019-12283-6 |
0.473 |
|
| 2019 |
Sarnowski C, Leong A, Raffield LM, Wu P, de Vries PS, DiCorpo D, Guo X, Xu H, Liu Y, Zheng X, Hu Y, Brody JA, Goodarzi MO, Hidalgo BA, Highland HM, ... ... Morrison AC, et al. Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program. American Journal of Human Genetics. PMID 31564435 DOI: 10.1016/J.Ajhg.2019.08.010 |
0.519 |
|
| 2019 |
Evangelou E, Gao H, Chu C, Ntritsos G, Blakeley P, Butts AR, Pazoki R, Suzuki H, Koskeridis F, Yiorkas AM, Karaman I, Elliott J, Luo Q, Aeschbacher S, Bartz TM, ... ... Morrison AC, et al. New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders. Nature Human Behaviour. PMID 31358974 DOI: 10.1038/S41562-019-0653-Z |
0.345 |
|
| 2019 |
Floyd JS, Bloch KM, Brody JA, Maroteau C, Siddiqui MK, Gregory R, Carr DF, Molokhia M, Liu X, Bis JC, Ahmed A, Liu X, Hallberg P, Yue QY, Magnusson PKE, ... ... Morrison AC, et al. Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing. Plos One. 14: e0218115. PMID 31242253 DOI: 10.1371/Journal.Pone.0218115 |
0.514 |
|
| 2019 |
Sung YJ, de Las Fuentes L, Winkler TW, Chasman DI, Bentley AR, Kraja AT, Ntalla I, Warren HR, Guo X, Schwander K, Manning AK, Brown MR, Aschard H, Feitosa MF, Franceschini N, ... ... Morrison AC, et al. A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Human Molecular Genetics. PMID 31127295 DOI: 10.1093/Hmg/Ddz070 |
0.524 |
|
| 2019 |
Flannick J, Mercader JM, Fuchsberger C, Udler MS, Mahajan A, Wessel J, Teslovich TM, Caulkins L, Koesterer R, Barajas-Olmos F, Blackwell TW, Boerwinkle E, Brody JA, Centeno-Cruz F, Chen L, ... ... Morrison AC, et al. Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. Nature. PMID 31118516 DOI: 10.1038/s41586-019-1231-2 |
0.472 |
|
| 2019 |
Wang Z, Zhu C, Nambi V, Morrison AC, Folsom AR, Ballantyne CM, Boerwinkle E, Yu B. Metabolomic Pattern Predicts Incident Coronary Heart Disease. Arteriosclerosis, Thrombosis, and Vascular Biology. ATVBAHA118312236. PMID 31092011 DOI: 10.1161/Atvbaha.118.312236 |
0.469 |
|
| 2019 |
Ward-Caviness CK, de Vries PS, Wiggins KL, Huffman JE, Yanek LR, Bielak LF, Giulianini F, Guo X, Kleber ME, Kacprowski T, Groß S, Petersman A, Davey Smith G, Hartwig FP, Bowden J, ... Morrison AC, et al. Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease. Plos One. 14: e0216222. PMID 31075152 DOI: 10.1371/Journal.Pone.0216222 |
0.492 |
|
| 2019 |
Li Z, Li X, Liu Y, Shen J, Chen H, Zhou H, Morrison AC, Boerwinkle E, Lin X. Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies. American Journal of Human Genetics. PMID 30982610 DOI: 10.1016/J.Ajhg.2019.03.002 |
0.568 |
|
| 2019 |
Yu B, Flexeder C, McGarrah RW, Wyss A, Morrison AC, North KE, Boerwinkle E, Kastenmüller G, Gieger C, Suhre K, Karrasch S, Peters A, Wagner GR, Michelotti GA, Mohney RP, et al. Metabolomics Identifies Novel Blood Biomarkers of Pulmonary Function and COPD in the General Population. Metabolites. 9. PMID 30939782 DOI: 10.3390/Metabo9040061 |
0.452 |
|
| 2019 |
Bentley AR, Sung YJ, Brown MR, Winkler TW, Kraja AT, Ntalla I, Schwander K, Chasman DI, Lim E, Deng X, Guo X, Liu J, Lu Y, Cheng CY, Sim X, ... ... Morrison AC, et al. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Nature Genetics. 51: 636-648. PMID 30926973 DOI: 10.1038/S41588-019-0378-Y |
0.499 |
|
| 2019 |
Bryant TS, Duggal P, Yu B, Morrison AC, Shafi T, Ehret G, Franceschini N, Boerwinkle E, Coresh J, Tin A. Association of Variants with Blood Pressure in the Atherosclerosis Risk in Communities Study. International Journal of Hypertension. 2019: 2137629. PMID 30906589 DOI: 10.1155/2019/2137629 |
0.56 |
|
| 2019 |
Liu Y, Chen S, Li Z, Morrison AC, Boerwinkle E, Lin X. ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies. American Journal of Human Genetics. 104: 410-421. PMID 30849328 DOI: 10.1016/J.Ajhg.2019.01.002 |
0.471 |
|
| 2019 |
de Vries PS, Brown MR, Bentley AR, Sung YJ, Winkler TW, Ntalla I, Schwander K, Kraja AT, Guo X, Franceschini N, Cheng CY, Sim X, Vojinovic D, Huffman JE, Musani SK, ... ... Morrison AC, et al. Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. American Journal of Epidemiology. PMID 30698716 DOI: 10.1093/Aje/Kwz005 |
0.515 |
|
| 2019 |
He KY, Li X, Kelly TN, Liang J, Cade BE, Assimes TL, Becker LC, Beitelshees AL, Bress AP, Chang YC, Chen YI, de Vries PS, Fox ER, Franceschini N, Furniss A, ... ... Morrison AC, et al. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data. Human Genetics. PMID 30671673 DOI: 10.1007/S00439-019-01975-0 |
0.589 |
|
| 2019 |
Kilpeläinen TO, Bentley AR, Noordam R, Sung YJ, Schwander K, Winkler TW, Jakupović H, Chasman DI, Manning A, Ntalla I, Aschard H, Brown MR, de Las Fuentes L, Franceschini N, Guo X, ... ... Morrison AC, et al. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nature Communications. 10: 376. PMID 30670697 DOI: 10.1038/S41467-018-08008-W |
0.486 |
|
| 2019 |
de Vries PS, Sabater-Lleal M, Huffman JE, Marten J, Song C, Pankratz N, Bartz TM, de Haan HG, Delgado GE, Eicher JD, Martinez-Perez A, Ward-Caviness CK, Brody JA, Chen MH, de Maat MPM, ... ... Morrison AC, et al. A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology. Blood. PMID 30642921 DOI: 10.1182/Blood-2018-05-849240 |
0.528 |
|
| 2019 |
Petty LE, Highland HM, Gamazon ER, Hu H, Karhade M, Chen HH, de Vries PS, Grove ML, Aguilar D, Bell GI, Huff CD, Hanis CL, Doddapaneni H, Munzy DM, Gibbs RA, ... ... Morrison AC, et al. Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample. Human Molecular Genetics. PMID 30624610 DOI: 10.1093/Hmg/Ddy435 |
0.564 |
|
| 2019 |
Maners J, Gill D, Pankratz N, Tang W, Smith NL, Morrison AC, Dehghan A, Vries PSd, Heart Cf. Abstract P106: Genetically Determined Fibrinogen, Gamma Prime Fibrinogen and Risk of Venous Thromboembolism and Ischemic Stroke: Evidence From Mendelian Randomization Circulation. 139. DOI: 10.1161/Circ.139.Suppl_1.P106 |
0.313 |
|
| 2018 |
Chen H, Huffman JE, Brody JA, Wang C, Lee S, Li Z, Gogarten SM, Sofer T, Bielak LF, Bis JC, Blangero J, Bowler RP, Cade BE, Cho MH, Correa A, ... ... Morrison AC, et al. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. American Journal of Human Genetics. PMID 30639324 DOI: 10.1016/J.Ajhg.2018.12.012 |
0.443 |
|
| 2018 |
Sabater-Lleal M, Huffman JE, de Vries PS, Marten J, Mastrangelo MA, Song C, Pankratz N, Ward-Caviness CK, Yanek LR, Trompet S, Delgado GE, Guo X, Bartz TM, Martinez-Perez A, Germain M, ... ... Morrison AC, et al. Genome-Wide Association Trans-Ethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. Circulation. PMID 30586737 DOI: 10.1161/Circulationaha.118.034532 |
0.514 |
|
| 2018 |
Franceschini N, Giambartolomei C, de Vries PS, Finan C, Bis JC, Huntley RP, Lovering RC, Tajuddin SM, Winkler TW, Graff M, Kavousi M, Dale C, Smith AV, Hofer E, van Leeuwen EM, ... ... Morrison AC, et al. GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes. Nature Communications. 9: 5141. PMID 30510157 DOI: 10.1038/S41467-018-07340-5 |
0.525 |
|
| 2018 |
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I, Ng FL, Evangelou M, Witkowska K, Tzanis E, Hellwege JN, ... ... Morrison AC, et al. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics. PMID 30429575 DOI: 10.1038/S41588-018-0297-3 |
0.473 |
|
| 2018 |
Ligthart S, Vaez A, Võsa U, Stathopoulou MG, de Vries PS, Prins BP, Van der Most PJ, Tanaka T, Naderi E, Rose LM, Wu Y, Karlsson R, Barbalic M, Lin H, Pool R, ... ... Morrison AC, et al. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. American Journal of Human Genetics. 103: 691-706. PMID 30388399 DOI: 10.1016/J.Ajhg.2018.09.009 |
0.54 |
|
| 2018 |
Tin A, Li Y, Brody JA, Nutile T, Chu AY, Huffman JE, Yang Q, Chen MH, Robinson-Cohen C, Macé A, Liu J, Demirkan A, Sorice R, Sedaghat S, Swen M, ... ... Morrison A, et al. Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels. Nature Communications. 9: 4228. PMID 30315176 DOI: 10.1038/S41467-018-06620-4 |
0.537 |
|
| 2018 |
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I, Ng FL, Evangelou M, Witkowska K, Tzanis E, Hellwege JN, ... ... Morrison AC, et al. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics. PMID 30224653 DOI: 10.1038/S41588-018-0205-X |
0.485 |
|
| 2018 |
Nandakumar P, Morrison AC, Grove ML, Boerwinkle E, Chakravarti A. Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation. Medicine. 97: e11865. PMID 30113482 DOI: 10.1097/Md.0000000000011865 |
0.461 |
|
| 2018 |
Wyss AB, Sofer T, Lee MK, Terzikhan N, Nguyen JN, Lahousse L, Latourelle JC, Smith AV, Bartz TM, Feitosa MF, Gao W, Ahluwalia TS, Tang W, Oldmeadow C, Duan Q, ... ... Morrison AC, et al. Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Nature Communications. 9: 2976. PMID 30061609 DOI: 10.1038/S41467-018-05369-0 |
0.447 |
|
| 2018 |
Ward-Caviness CK, Huffman JE, Evertt K, Germain M, Van Dongen J, Hill WD, Jhun MA, Brody JA, Ghanbari M, Du L, Roetker NS, de Vries PS, Waldenberger M, Gieger C, Wolf P, ... ... Morrison AC, et al. DNA methylation age is associated with an altered hemostatic profile in a multi-ethnic meta-analysis. Blood. PMID 30042098 DOI: 10.1182/Blood-2018-02-831347 |
0.446 |
|
| 2018 |
Pirastu N, Joshi PK, de Vries PS, Cornelis MC, McKeigue PM, Keum N, Franceschini N, Colombo M, Giovannucci EL, Spiliopoulou A, Franke L, North KE, Kraft P, Morrison AC, Esko T, et al. Author Correction: GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. Nature Communications. 9: 2536. PMID 29959320 DOI: 10.1038/S41467-018-04857-7 |
0.369 |
|
| 2018 |
Lumley T, Brody J, Peloso G, Morrison A, Rice K. FastSKAT: Sequence kernel association tests for very large sets of markers. Genetic Epidemiology. PMID 29932245 DOI: 10.1002/Gepi.22136 |
0.346 |
|
| 2018 |
Feitosa MF, Kraja AT, Chasman DI, Sung YJ, Winkler TW, Ntalla I, Guo X, Franceschini N, Cheng CY, Sim X, Vojinovic D, Marten J, Musani SK, Li C, Bentley AR, ... ... Morrison AC, et al. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Plos One. 13: e0198166. PMID 29912962 DOI: 10.1371/Journal.Pone.0198166 |
0.52 |
|
| 2018 |
Loomis SJ, Li M, Maruthur NM, Baldridge AS, North KE, Mei H, Morrison A, Carson AP, Pankow JS, Boerwinkle E, Scharpf R, Rasmussen-Torvik LJ, Coresh J, Duggal P, Köttgen A, et al. Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study. Diabetes. PMID 29844224 DOI: 10.2337/Db17-1362 |
0.549 |
|
| 2018 |
Macri V, Brody JA, Arking DE, Hucker WJ, Yin X, Lin H, Mills RW, Sinner MF, Lubitz SA, Liu CT, Morrison AC, Alonso A, Li N, Fedorov VV, Janssen PM, et al. Common Coding Variants in Are Associated With the Nav1.8 Late Current and Cardiac Conduction. Circulation. Genomic and Precision Medicine. 11: e001663. PMID 29752399 DOI: 10.1161/CIRCGEN.116.001663 |
0.394 |
|
| 2018 |
Liang J, Le TH, Velez Edwards DR, Tayo BO, Gaulton KJ, Smith JA, Lu Y, Jensen RA, Chen G, Yanek LR, Schwander K, Tajuddin SM, Sofer T, Kim W, Kayima J, ... ... Morrison AC, et al. Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Plos Genetics. 14: e1007345. PMID 29750786 DOI: 10.1371/Journal.Pgen.1007345 |
0.539 |
|
| 2018 |
Feofanova EV, Yu B, Metcalf GA, Liu X, Muzny D, Below JE, Wagenknecht LE, Gibbs RA, Morrison AC, Boerwinkle E. Sequence-Based Analysis of Lipid-Related Metabolites in a Multiethnic Study. Genetics. PMID 29610217 DOI: 10.1534/Genetics.118.300751 |
0.536 |
|
| 2018 |
Roetker NS, Pankow JS, Bressler J, Morrison AC, Boerwinkle E. Prospective Study of Epigenetic Age Acceleration and Incidence of Cardiovascular Disease Outcomes in the ARIC Study (Atherosclerosis Risk in Communities). Circulation. Genomic and Precision Medicine. 11: e001937. PMID 29555670 DOI: 10.1161/CIRCGEN.117.001937 |
0.333 |
|
| 2018 |
Guo L, Akahori H, Harari E, Smith SL, Polavarapu R, Karmali V, Otsuka F, Gannon RL, Braumann RE, Dickinson MH, Gupta A, Jenkins AL, Lipinski MJ, Kim J, Chhour P, ... ... Morrison AC, et al. CD163+ macrophages promote angiogenesis and vascular permeability accompanied by inflammation in atherosclerosis. The Journal of Clinical Investigation. PMID 29457790 DOI: 10.1172/Jci93025 |
0.39 |
|
| 2018 |
Sung YJ, Winkler TW, de Las Fuentes L, Bentley AR, Brown MR, Kraja AT, Schwander K, Ntalla I, Guo X, Franceschini N, Lu Y, Cheng CY, Sim X, Vojinovic D, Marten J, ... ... Morrison AC, et al. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. American Journal of Human Genetics. PMID 29455858 DOI: 10.1016/J.Ajhg.2018.01.015 |
0.581 |
|
| 2018 |
Sanner J, Grove ML, Yu E, Moeller FG, Cron SG, Boerwinkle E, Morrison AC, Frazier L. Effects of Gender-Specific Differences, Inflammatory Response, and Genetic Variation on the Associations Among Depressive Symptoms and the Risk of Major Adverse Coronary Events in Patients With Acute Coronary Syndrome. Biological Research For Nursing. 1099800417751662. PMID 29298497 DOI: 10.1177/1099800417751662 |
0.412 |
|
| 2017 |
Li C, Grove ML, Yu B, Jones BC, Morrison A, Boerwinkle E, Liu X. Genetic variants in microRNA genes and targets associated with cardiovascular disease risk factors in the African-American population. Human Genetics. PMID 29264654 DOI: 10.1007/S00439-017-1858-8 |
0.498 |
|
| 2017 |
Smith JA, Zhao W, Yasutake K, August C, Ratliff SM, Faul JD, Boerwinkle E, Chakravarti A, Diez Roux AV, Gao Y, Griswold ME, Heiss G, Kardia SLR, Morrison AC, Musani SK, et al. Gene-by-Psychosocial Factor Interactions Influence Diastolic Blood Pressure in European and African Ancestry Populations: Meta-Analysis of Four Cohort Studies. International Journal of Environmental Research and Public Health. 14. PMID 29258278 DOI: 10.3390/Ijerph14121596 |
0.567 |
|
| 2017 |
Richard MA, Huan T, Ligthart S, Gondalia R, Jhun MA, Brody JA, Irvin MR, Marioni R, Shen J, Tsai PC, Montasser ME, Jia Y, Syme C, Salfati EL, Boerwinkle E, ... ... Morrison AC, et al. DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation. American Journal of Human Genetics. 101: 888-902. PMID 29198723 DOI: 10.1016/J.Ajhg.2017.09.028 |
0.527 |
|
| 2017 |
Pirastu N, Joshi PK, de Vries PS, Cornelis MC, McKeigue PM, Keum N, Franceschini N, Colombo M, Giovannucci EL, Spiliopoulou A, Franke L, North KE, Kraft P, Morrison AC, Esko T, et al. GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. Nature Communications. 8: 1584. PMID 29146897 DOI: 10.1038/S41467-017-01490-8 |
0.463 |
|
| 2017 |
Liu DJ, Peloso GM, Yu H, Butterworth AS, Wang X, Mahajan A, Saleheen D, Emdin C, Alam D, Alves AC, Amouyel P, Di Angelantonio E, Arveiler D, Assimes TL, Auer PL, ... ... Morrison AC, et al. Exome-wide association study of plasma lipids in >300,000 individuals. Nature Genetics. PMID 29083408 DOI: 10.1038/Ng.3977 |
0.484 |
|
| 2017 |
Brody JA, Morrison AC, Bis JC, O'Connell JR, Brown MR, Huffman JE, Ames DC, Carroll A, Conomos MP, Gabriel S, Gibbs RA, Gogarten SM, Gupta N, Jaquish CE, Johnson AD, et al. Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology. Nature Genetics. 49: 1560-1563. PMID 29074945 DOI: 10.1038/Ng.3968 |
0.45 |
|
| 2017 |
Kraja AT, Cook JP, Warren HR, Surendran P, Liu C, Evangelou E, Manning AK, Grarup N, Drenos F, Sim X, Smith AV, Amin N, Blakemore AIF, Bork-Jensen J, Brandslund I, ... ... Morrison AC, et al. New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals. Circulation. Cardiovascular Genetics. 10. PMID 29030403 DOI: 10.1161/Circgenetics.117.001778 |
0.585 |
|
| 2017 |
Graff M, Emery LS, Justice AE, Parra E, Below JE, Palmer ND, Gao C, Duan Q, Valladares-Salgado A, Cruz M, Morrison AC, Boerwinkle E, Whitsel EA, Kooperberg C, Reiner A, et al. Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos. Lipids in Health and Disease. 16: 200. PMID 29025430 DOI: 10.1186/S12944-017-0591-6 |
0.483 |
|
| 2017 |
Findley TO, Tenpenny JC, O'Byrne MR, Morrison AC, Hixson JE, Northrup H, Au KS. Mutations in folate transporter genes and risk for human myelomeningocele. American Journal of Medical Genetics. Part A. PMID 28948692 DOI: 10.1002/Ajmg.A.38472 |
0.433 |
|
| 2017 |
de Vries PS, Yu B, Feofanova EV, Metcalf GA, Brown MR, Zeighami AL, Liu X, Muzny DM, Gibbs RA, Boerwinkle E, Morrison AC. Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study. Human Molecular Genetics. 26: 3442-3450. PMID 28854705 DOI: 10.1093/Hmg/Ddx266 |
0.525 |
|
| 2017 |
Hildebrandt MAT, Reyes M, Wu X, Pu X, Thompson KA, Ma J, Landstrom AP, Morrison AC, Ater JL. Hypertension Susceptibility Loci are Associated with Anthracycline-related Cardiotoxicity in Long-term Childhood Cancer Survivors. Scientific Reports. 7: 9698. PMID 28851949 DOI: 10.1038/S41598-017-09517-2 |
0.429 |
|
| 2017 |
Wain LV, Vaez A, Jansen R, Joehanes R, van der Most PJ, Erzurumluoglu AM, O'Reilly PF, Cabrera CP, Warren HR, Rose LM, Verwoert GC, Hottenga JJ, Strawbridge RJ, Esko T, Arking DE, ... ... Morrison AC, et al. Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Hypertension (Dallas, Tex. : 1979). PMID 28739976 DOI: 10.1161/Hypertensionaha.117.09438 |
0.431 |
|
| 2017 |
Li M, Maruthur NM, Loomis SJ, Pietzner M, North KE, Mei H, Morrison AC, Friedrich N, Pankow JS, Nauck M, Boerwinkle E, Teumer A, Selvin E, Köttgen A. Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism. Scientific Reports. 7: 2812. PMID 28588231 DOI: 10.1038/S41598-017-02287-X |
0.52 |
|
| 2017 |
Liang J, Le TH, Edwards DRV, Tayo BO, Gaulton KJ, Smith JA, Lu Y, Jensen RA, Chen G, Yanek LR, Schwander K, Tajuddin SM, Sofer T, Kim W, Kayima J, ... ... Morrison AC, et al. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Plos Genetics. 13: e1006728. PMID 28498854 DOI: 10.1371/Journal.Pgen.1006728 |
0.582 |
|
| 2017 |
Wild PS, Felix JF, Schillert A, Teumer A, Chen MH, Leening MJ, Völker U, Großmann V, Brody JA, Irvin MR, Shah SJ, Pramana S, Lieb W, Schmidt R, Stanton AV, ... ... Morrison AC, et al. Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. The Journal of Clinical Investigation. PMID 28394258 DOI: 10.1172/Jci84840 |
0.404 |
|
| 2017 |
Haycock PC, Burgess S, Nounu A, Zheng J, Okoli GN, Bowden J, Wade KH, Timpson NJ, Evans DM, Willeit P, Aviv A, Gaunt TR, Hemani G, Mangino M, ... ... Morrison AC, et al. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study. Jama Oncology. PMID 28241208 DOI: 10.1001/Jamaoncol.2016.5945 |
0.323 |
|
| 2017 |
Nandakumar P, Lee D, Richard MA, Tekola-Ayele F, Tayo BO, Ware E, Sung YJ, Salako B, Ogunniyi A, Gu CC, Grove ML, Fornage M, Kardia S, Rotima C, Cooper RS, ... Morrison AC, et al. Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry. Journal of Hypertension. PMID 28234671 DOI: 10.1097/Hjh.0000000000001319 |
0.432 |
|
| 2017 |
de Vries PS, Sabater-Lleal M, Chasman DI, Trompet S, Ahluwalia TS, Teumer A, Kleber ME, Chen MH, Wang JJ, Attia JR, Marioni RE, Steri M, Weng LC, Pool R, Grossmann V, ... ... Morrison AC, et al. Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. Plos One. 12: e0167742. PMID 28107422 DOI: 10.1371/Journal.Pone.0167742 |
0.377 |
|
| 2017 |
Morrison AC, Huang Z, Yu B, Metcalf G, Liu X, Ballantyne C, Coresh J, Yu F, Muzny D, Feofanova E, Rustagi N, Gibbs R, Boerwinkle E. Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits. American Journal of Human Genetics. PMID 28089252 DOI: 10.1016/J.Ajhg.2016.12.009 |
0.582 |
|
| 2016 |
Yu B, de Vries PS, Metcalf GA, Wang Z, Feofanova EV, Liu X, Muzny DM, Wagenknecht LE, Gibbs RA, Morrison AC, Boerwinkle E. Whole genome sequence analysis of serum amino acid levels. Genome Biology. 17: 237. PMID 27884205 DOI: 10.1186/S13059-016-1106-X |
0.462 |
|
| 2016 |
Shah RH, Northrup H, Hixson JE, Morrison AC, Au KS. Genetic association of the glycine cleavage system genes and myelomeningocele. Birth Defects Research. Part a, Clinical and Molecular Teratology. PMID 27620832 DOI: 10.1002/Bdra.23552 |
0.384 |
|
| 2016 |
Ehret GB, Ferreira T, Chasman DI, Jackson AU, Schmidt EM, Johnson T, Thorleifsson G, Luan J, Donnelly LA, Kanoni S, Petersen AK, Pihur V, Strawbridge RJ, Shungin D, Hughes MF, ... ... Morrison AC, et al. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nature Genetics. PMID 27618452 DOI: 10.1038/Ng.3667 |
0.514 |
|
| 2016 |
Liu C, Kraja AT, Smith JA, Brody JA, Franceschini N, Bis JC, Rice K, Morrison AC, Lu Y, Weiss S, Guo X, Palmas W, Martin LW, Chen YI, Surendran P, et al. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Nature Genetics. PMID 27618448 DOI: 10.1038/Ng.3660 |
0.591 |
|
| 2016 |
Yu B, Li AH, Metcalf GA, Muzny DM, Morrison AC, White S, Mosley TH, Gibbs RA, Boerwinkle E. Loss-of-function variants influence the human serum metabolome. Science Advances. 2: e1600800. PMID 27602404 DOI: 10.1126/Sciadv.1600800 |
0.503 |
|
| 2016 |
Agopian AJ, Hoang TT, Mitchell LE, Morrison AC, Tu D, Nassar N, Canfield MA. Maternal hypertension and risk for hypospadias in offspring. American Journal of Medical Genetics. Part A. PMID 27570224 DOI: 10.1002/Ajmg.A.37947 |
0.351 |
|
| 2016 |
van der Laan SW, Fall T, Soumaré A, Teumer A, Sedaghat S, Baumert J, Zabaneh D, van Setten J, Isgum I, Galesloot TE, Arpegård J, Amouyel P, Trompet S, Waldenberger M, Dörr M, ... ... Morrison AC, et al. Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study. Journal of the American College of Cardiology. 68: 934-45. PMID 27561768 DOI: 10.1016/J.Jacc.2016.05.092 |
0.324 |
|
| 2016 |
Nguyen MP, Lupo PJ, Northrup H, Morrison AC, Cirino PT, Au KS. Maternal gene-micronutrient interactions related to one-carbon metabolism and the risk of myelomeningocele among offspring. Birth Defects Research. Part a, Clinical and Molecular Teratology. PMID 27384413 DOI: 10.1002/Bdra.23538 |
0.306 |
|
| 2016 |
Sung YJ, Winkler TW, Manning AK, Aschard H, Gudnason V, Harris TB, Smith AV, Boerwinkle E, Brown MR, Morrison AC, Fornage M, Lin LA, Richard M, Bartz TM, Psaty BM, et al. An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group. Genetic Epidemiology. PMID 27230302 DOI: 10.1002/Gepi.21978 |
0.516 |
|
| 2016 |
Allen NB, Lloyd-Jones D, Hwang SJ, Rasmussen-Torvik L, Fornage M, Morrison AC, Baldridge AS, Boerwinkle E, Levy D, Cupples LA, Fox CS, Thanassoulis G, Dufresne L, Daviglus M, Johnson AD, et al. Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies. American Heart Journal. 175: 112-20. PMID 27179730 DOI: 10.1016/J.Ahj.2015.12.022 |
0.567 |
|
| 2016 |
Smith JG, Felix JF, Morrison AC, Kalogeropoulos A, Trompet S, Wilk JB, Gidlöf O, Wang X, Morley M, Mendelson M, Joehanes R, Ligthart S, Shan X, Bis JC, Wang YA, et al. Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure. Plos Genetics. 12: e1006034. PMID 27149122 DOI: 10.1371/Journal.Pgen.1006034 |
0.52 |
|
| 2016 |
Khera AV, Won HH, Peloso GM, Lawson KS, Bartz TM, Deng X, van Leeuwen EM, Natarajan P, Emdin CA, Bick AG, Morrison AC, Brody JA, Gupta N, Nomura A, Kessler T, et al. Diagnostic Yield of Sequencing Familial Hypercholesterolemia Genes in Patients with Severe Hypercholesterolemia. Journal of the American College of Cardiology. PMID 27050191 DOI: 10.1016/J.Jacc.2016.03.520 |
0.427 |
|
| 2016 |
van Leeuwen EM, Sabo A, Bis JC, Huffman JE, Manichaikul A, Smith AV, Feitosa MF, Demissie S, Joshi PK, Duan Q, Marten J, van Klinken JB, Surakka I, Nolte IM, Zhang W, ... ... Morrison A, et al. Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels. Journal of Medical Genetics. PMID 27036123 DOI: 10.1136/Jmedgenet-2015-103439 |
0.567 |
|
| 2016 |
Dehghan A, Bis JC, White CC, Smith AV, Morrison AC, Cupples LA, Trompet S, Chasman DI, Lumley T, Völker U, Buckley BM, Ding J, Jensen MK, Folsom AR, Kritchevsky SB, et al. Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium. Plos One. 11: e0144997. PMID 26950853 DOI: 10.1371/Journal.Pone.0144997 |
0.534 |
|
| 2016 |
Ogunwale AN, Morrison AC, Sun W, Dodge RC, Virani SS, Taylor A, Gottesman RF, Yang E, Wei P, McEvoy JW, Heiss G, Boerwinkle E, Ballantyne CM, Nambi V. The impact of multiple single day blood pressure readings on cardiovascular risk estimation: The Atherosclerosis Risk in Communities study. European Journal of Preventive Cardiology. PMID 26869459 DOI: 10.1177/2047487316633549 |
0.451 |
|
| 2016 |
Willems SM, Cornes BK, Brody JA, Morrison AC, Lipovich L, Dauriz M, Chen Y, Liu CT, Rybin DV, Gibbs RA, Muzny D, Pankow JS, Psaty BM, Boerwinkle E, Rotter JI, et al. Association of the IGF1 gene with fasting insulin levels. European Journal of Human Genetics : Ejhg. PMID 26860063 DOI: 10.1038/Ejhg.2016.4 |
0.502 |
|
| 2016 |
Vu KN, Ballantyne CM, Hoogeveen RC, Nambi V, Volcik KA, Boerwinkle E, Morrison AC. Causal Role of Alcohol Consumption in an Improved Lipid Profile: The Atherosclerosis Risk in Communities (ARIC) Study. Plos One. 11: e0148765. PMID 26849558 DOI: 10.1371/Journal.Pone.0148765 |
0.377 |
|
| 2016 |
Pattaro C, Teumer A, Gorski M, Chu AY, Li M, Mijatovic V, Garnaas M, Tin A, Sorice R, Li Y, Taliun D, Olden M, Foster M, Yang Q, Chen MH, ... ... Morrison AC, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nature Communications. 7: 10023. PMID 26831199 DOI: 10.1038/Ncomms10023 |
0.493 |
|
| 2016 |
Allen NB, Lloyd-Jones D, Hwang SJ, Rasmussen-Torvik L, Fornage M, Morrison AC, Baldridge AS, Boerwinkle E, Levy D, Cupples LA, Fox CS, Thanassoulis G, Dufresne L, Daviglus M, Johnson AD, et al. Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies American Heart Journal. 175: 112-120. DOI: 10.1016/j.ahj.2015.12.022 |
0.498 |
|
| 2015 |
van Leeuwen EM, Huffman JE, Bis JC, Isaacs A, Mulder M, Sabo A, Smith AV, Demissie S, Manichaikul A, Brody JA, Feitosa MF, Duan Q, Schraut KE, Navarro P, van Vliet-Ostaptchouk JV, ... ... Morrison AC, et al. Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C. Npj Aging and Mechanisms of Disease. 1: 15011. PMID 28721259 DOI: 10.1038/npjamd.2015.11 |
0.392 |
|
| 2015 |
Lunetta KL, Day FR, Sulem P, Ruth KS, Tung JY, Hinds DA, Esko T, Elks CE, Altmaier E, He C, Huffman JE, Mihailov E, Porcu E, Robino A, Rose LM, ... ... Morrison AC, et al. Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nature Communications. 6: 10257. PMID 26674845 DOI: 10.1038/Ncomms10257 |
0.461 |
|
| 2015 |
Yu B, Pulit SL, Hwang SJ, Brody JA, Amin N, Auer PL, Bis JC, Boerwinkle E, Burke GL, Chakravarti A, Correa A, Dreisbach AW, Franco OH, Ehret GB, Franceschini N, ... ... Morrison AC, et al. Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk. Circulation. Cardiovascular Genetics. PMID 26658788 DOI: 10.1161/Circgenetics.115.001215 |
0.505 |
|
| 2015 |
de Vries PS, Chasman DI, Sabater-Lleal M, Chen MH, Huffman JE, Steri M, Tang W, Teumer A, Marioni RE, Grossmann V, Hottenga JJ, Trompet S, Müller-Nurasyid M, Zhao JH, Brody JA, ... ... Morrison AC, et al. A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Human Molecular Genetics. PMID 26561523 DOI: 10.1093/Hmg/Ddv454 |
0.462 |
|
| 2015 |
Day FR, Ruth KS, Thompson DJ, Lunetta KL, Pervjakova N, Chasman DI, Stolk L, Finucane HK, Sulem P, Bulik-Sullivan B, Esko T, Johnson AD, Elks CE, Franceschini N, He C, ... ... Morrison AC, et al. Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nature Genetics. PMID 26414677 DOI: 10.1097/01.Ogx.0000473766.71624.99 |
0.497 |
|
| 2015 |
Gharib SA, Loth DW, Soler Artigas M, Birkland TP, Wilk JB, Wain LV, Brody J, Obeidat M, Hancock DB, Tang W, Rawal R, Boezen HM, Imboden M, Huffman JE, Lahousse L, ... ... Morrison AC, et al. Integrative Pathway Genomics of Lung Function and Airflow Obstruction. Human Molecular Genetics. PMID 26395457 DOI: 10.1093/Hmg/Ddv378 |
0.385 |
|
| 2015 |
Nikpay M, Goel A, Won HH, Hall LM, Willenborg C, Kanoni S, Saleheen D, Kyriakou T, Nelson CP, Hopewell JC, Webb TR, Zeng L, Dehghan A, Alver M, Armasu SM, ... ... Morrison AC, et al. A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nature Genetics. 47: 1121-30. PMID 26343387 DOI: 10.1038/Ng.3396 |
0.588 |
|
| 2015 |
Lunetta KL, Day FR, Sulem P, Ruth KS, Tung JY, Hinds DA, Esko T, Elks CE, Altmaier E, He C, Huffman JE, Mihailov E, Porcu E, Robino A, Rose LM, ... ... Morrison AC, et al. Rare coding variants and X-linked loci associated with age at menarche. Nature Communications. 6: 7756. PMID 26239645 DOI: 10.1038/Ncomms8756 |
0.548 |
|
| 2015 |
Olfson E, Saccone NL, Johnson EO, Chen LS, Culverhouse R, Doheny K, Foltz SM, Fox L, Gogarten SM, Hartz S, Hetrick K, Laurie CC, Marosy B, Amin N, Arnett D, ... ... Morrison AC, et al. Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans. Molecular Psychiatry. PMID 26239294 DOI: 10.1038/Mp.2015.105 |
0.41 |
|
| 2015 |
Gambin T, Jhangiani SN, Below JE, Campbell IM, Wiszniewski W, Muzny DM, Staples J, Morrison AC, Bainbridge MN, Penney S, McGuire AL, Gibbs RA, Lupski JR, Boerwinkle E. Secondary findings and carrier test frequencies in a large multiethnic sample. Genome Medicine. 7: 54. PMID 26195989 DOI: 10.1186/S13073-015-0171-1 |
0.535 |
|
| 2015 |
Salfati E, Morrison AC, Boerwinkle E, Chakravarti A. Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC). Plos One. 10: e0133031. PMID 26162070 DOI: 10.1371/Journal.Pone.0133031 |
0.591 |
|
| 2015 |
Joshi PK, Esko T, Mattsson H, Eklund N, Gandin I, Nutile T, Jackson AU, Schurmann C, Smith AV, Zhang W, Okada Y, Stančáková A, Faul JD, Zhao W, Bartz TM, ... ... Morrison A, et al. Directional dominance on stature and cognition in diverse human populations. Nature. 523: 459-62. PMID 26131930 DOI: 10.1038/Nature14618 |
0.528 |
|
| 2015 |
Huffman JE, de Vries PS, Morrison AC, Sabater-Lleal M, Kacprowski T, Auer PL, Brody JA, Chasman DI, Chen MH, Guo X, Lin LA, Marioni RE, Müller-Nurasyid M, Yanek LR, Pankratz N, et al. Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF. Blood. 126: e19-29. PMID 26105150 DOI: 10.1182/Blood-2015-02-624551 |
0.56 |
|
| 2015 |
Xu H, Zhang H, Yang W, Yadav R, Morrison AC, Qian M, Devidas M, Liu Y, Perez-Andreu V, Zhao X, Gastier-Foster JM, Lupo PJ, Neale G, Raetz E, Larsen E, et al. Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children. Nature Communications. 6: 7553. PMID 26104880 DOI: 10.1038/Ncomms8553 |
0.46 |
|
| 2015 |
Li AH, Morrison AC, Kovar C, Cupples LA, Brody JA, Polfus LM, Yu B, Metcalf G, Muzny D, Veeraraghavan N, Liu X, Lumley T, Mosley TH, Gibbs RA, Boerwinkle E. Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease. Nature Genetics. 47: 640-2. PMID 25915599 DOI: 10.1038/Ng.3270 |
0.534 |
|
| 2015 |
Yu F, Lu J, Liu X, Gazave E, Chang D, Raj S, Hunter-Zinck H, Blekhman R, Arbiza L, Van Hout C, Morrison A, Johnson AD, Bis J, Cupples LA, Psaty BM, et al. Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions. Plos One. 10: e0121644. PMID 25807536 DOI: 10.1371/Journal.Pone.0121644 |
0.477 |
|
| 2015 |
Wessel J, Chu AY, Willems SM, Wang S, Yaghootkar H, Brody JA, Dauriz M, Hivert MF, Raghavan S, Lipovich L, Hidalgo B, Fox K, Huffman JE, An P, Lu Y, ... ... Morrison AC, et al. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nature Communications. 6: 5897. PMID 25631608 DOI: 10.1038/Ncomms6897 |
0.472 |
|
| 2015 |
Yu B, Li AH, Muzny D, Veeraraghavan N, de Vries PS, Bis JC, Musani SK, Alexander D, Morrison AC, Franco OH, Uitterlinden A, Hofman A, Dehghan A, Wilson JG, Psaty BM, et al. Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine: Levels and Incident Coronary Heart Disease. Circulation. Cardiovascular Genetics. 8: 351-5. PMID 25575548 DOI: 10.1161/Circgenetics.114.000697 |
0.481 |
|
| 2015 |
Shetty PB, Tang H, Feng T, Tayo B, Morrison AC, Kardia SL, Hanis CL, Arnett DK, Hunt SC, Boerwinkle E, Rao DC, Cooper RS, Risch N, Zhu X. Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American families. Circulation. Cardiovascular Genetics. 8: 106-13. PMID 25552592 DOI: 10.1161/Circgenetics.114.000481 |
0.45 |
|
| 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, ... ... Morrison AC, 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 |
0.581 |
|
| 2014 |
Stitziel NO, Won HH, Morrison AC, Peloso GM, Do R, Lange LA, Fontanillas P, Gupta N, Duga S, Goel A, Farrall M, Saleheen D, Ferrario P, König I, et al. Inactivating mutations in NPC1L1 and protection from coronary heart disease. The New England Journal of Medicine. 371: 2072-82. PMID 25390462 DOI: 10.1056/Nejmoa1405386 |
0.417 |
|
| 2014 |
Morrison AC, Bis JC, Hwang SJ, Ehret GB, Lumley T, Rice K, Muzny D, Gibbs RA, Boerwinkle E, Psaty BM, Chakravarti A, Levy D. Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study. Plos One. 9: e109155. PMID 25275628 DOI: 10.1371/Journal.Pone.0109155 |
0.584 |
|
| 2014 |
Tang W, Kowgier M, Loth DW, Soler Artigas M, Joubert BR, Hodge E, Gharib SA, Smith AV, Ruczinski I, Gudnason V, Mathias RA, Harris TB, Hansel NN, Launer LJ, Barnes KC, ... ... Morrison AC, et al. Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function. Plos One. 9: e100776. PMID 24983941 DOI: 10.1371/Journal.Pone.0100776 |
0.425 |
|
| 2014 |
Kraja AT, Chasman DI, North KE, Reiner AP, Yanek LR, Kilpeläinen TO, Smith JA, Dehghan A, Dupuis J, Johnson AD, Feitosa MF, Tekola-Ayele F, Chu AY, Nolte IM, Dastani Z, ... ... Morrison AC, et al. Pleiotropic genes for metabolic syndrome and inflammation. Molecular Genetics and Metabolism. 112: 317-38. PMID 24981077 DOI: 10.1016/J.Ymgme.2014.04.007 |
0.539 |
|
| 2014 |
Ganesh SK, Chasman DI, Larson MG, Guo X, Verwoert G, Bis JC, Gu X, Smith AV, Yang ML, Zhang Y, Ehret G, Rose LM, Hwang SJ, Papanicolau GJ, Sijbrands EJ, ... ... Morrison AC, et al. Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. American Journal of Human Genetics. 95: 49-65. PMID 24975945 DOI: 10.1016/J.Ajhg.2014.06.002 |
0.564 |
|
| 2014 |
Simino J, Shi G, Bis JC, Chasman DI, Ehret GB, Gu X, Guo X, Hwang SJ, Sijbrands E, Smith AV, Verwoert GC, Bragg-Gresham JL, Cadby G, Chen P, Cheng CY, ... ... Morrison AC, et al. Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. American Journal of Human Genetics. 95: 24-38. PMID 24954895 DOI: 10.1016/J.Ajhg.2014.05.010 |
0.52 |
|
| 2014 |
Cornes BK, Brody JA, Nikpoor N, Morrison AC, Dang HC, Ahn BS, Wang S, Dauriz M, Barzilay JI, Dupuis J, Florez JC, Coresh J, Gibbs RA, Kao WH, Liu CT, et al. Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circulation. Cardiovascular Genetics. 7: 374-82. PMID 24951664 DOI: 10.1161/Circgenetics.113.000169 |
0.509 |
|
| 2014 |
Magnani JW, Brody JA, Prins BP, Arking DE, Lin H, Yin X, Liu CT, Morrison AC, Zhang F, Spector TD, Alonso A, Bis JC, Heckbert SR, Lumley T, Sitlani CM, et al. Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Circulation. Cardiovascular Genetics. 7: 365-73. PMID 24951663 DOI: 10.1161/Circgenetics.113.000098 |
0.507 |
|
| 2014 |
London SJ, Gao W, Gharib SA, Hancock DB, Wilk JB, House JS, Gibbs RA, Muzny DM, Lumley T, Franceschini N, North KE, Psaty BM, Kovar CL, Coresh J, Zhou Y, ... ... Morrison AC, et al. ADAM19 and HTR4 variants and pulmonary function: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circulation. Cardiovascular Genetics. 7: 350-8. PMID 24951661 DOI: 10.1161/Circgenetics.113.000066 |
0.437 |
|
| 2014 |
Liu CT, Young KL, Brody JA, Olden M, Wojczynski MK, Heard-Costa N, Li G, Morrison AC, Muzny D, Gibbs RA, Reid JG, Shao Y, Zhou Y, Boerwinkle E, Heiss G, et al. Sequence variation in TMEM18 in association with body mass index: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circulation. Cardiovascular Genetics. 7: 344-9. PMID 24951660 DOI: 10.1161/Circgenetics.13.000067 |
0.491 |
|
| 2014 |
Lin H, Wang M, Brody JA, Bis JC, Dupuis J, Lumley T, McKnight B, Rice KM, Sitlani CM, Reid JG, Bressler J, Liu X, Davis BC, Johnson AD, O'Donnell CJ, ... ... Morrison AC, et al. Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circulation. Cardiovascular Genetics. 7: 335-43. PMID 24951659 DOI: 10.1161/Circgenetics.113.000350 |
0.565 |
|
| 2014 |
Loth DW, Artigas MS, Gharib SA, Wain LV, Franceschini N, Koch B, Pottinger TD, Smith AV, Duan Q, Oldmeadow C, Lee MK, Strachan DP, James AL, Huffman JE, Vitart V, ... ... Morrison AC, et al. Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nature Genetics. 46: 669-77. PMID 24929828 DOI: 10.1038/Ng.3011 |
0.396 |
|
| 2014 |
Yu B, Zheng Y, Alexander D, Morrison AC, Coresh J, Boerwinkle E. Genetic determinants influencing human serum metabolome among African Americans. Plos Genetics. 10: e1004212. PMID 24625756 DOI: 10.1371/Journal.Pgen.1004212 |
0.553 |
|
| 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, 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 |
0.509 |
|
| 2014 |
Lin H, Sinner MF, Brody JA, Arking DE, Lunetta KL, Rienstra M, Lubitz SA, Magnani JW, Sotoodehnia N, McKnight B, McManus DD, Boerwinkle E, Psaty BM, Rotter JI, Bis JC, ... ... Morrison AC, et al. Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 452-7. PMID 24239840 DOI: 10.1016/J.Hrthm.2013.11.012 |
0.584 |
|
| 2013 |
Tang W, Morrison A, Wasserman BA, Folsom AR, Sun W, Campbell S, Kao WH, Boerwinkle E. Association of SERPINA9 gene variants with carotid artery atherosclerosis: the Atherosclerosis Risk in Communities (ARIC) Carotid MRI Study. International Journal of Molecular Epidemiology and Genetics. 4: 258-67. PMID 24319541 |
0.453 |
|
| 2013 |
Polfus LM, Smith JA, Shimmin LC, Bielak LF, Morrison AC, Kardia SL, Peyser PA, Hixson JE. Genome-wide association study of gene by smoking interactions in coronary artery calcification. Plos One. 8: e74642. PMID 24098343 DOI: 10.1371/Journal.Pone.0074642 |
0.443 |
|
| 2013 |
Franceschini N, Fox E, Zhang Z, Edwards TL, Nalls MA, Sung YJ, Tayo BO, Sun YV, Gottesman O, Adeyemo A, Johnson AD, Young JH, Rice K, Duan Q, Chen F, ... ... Morrison AC, et al. Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. American Journal of Human Genetics. 93: 545-54. PMID 23972371 DOI: 10.1016/J.Ajhg.2013.07.010 |
0.578 |
|
| 2013 |
Morrison AC, Voorman A, Johnson AD, Liu X, Yu J, Li A, Muzny D, Yu F, Rice K, Zhu C, Bis J, Heiss G, O'Donnell CJ, Psaty BM, Cupples LA, et al. Whole-genome sequence-based analysis of high-density lipoprotein cholesterol. Nature Genetics. 45: 899-901. PMID 23770607 DOI: 10.1038/Ng.2671 |
0.524 |
|
| 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 |
0.511 |
|
| 2013 |
den Hoed M, Eijgelsheim M, Esko T, Brundel BJ, Peal DS, Evans DM, Nolte IM, Segrè AV, Holm H, Handsaker RE, Westra HJ, Johnson T, Isaacs A, Yang J, Lundby A, ... ... Morrison AC, et al. Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics. 45: 621-31. PMID 23583979 DOI: 10.1038/Ng.2610 |
0.375 |
|
| 2013 |
Johnson AD, Hwang SJ, Voorman A, Morrison A, Peloso GM, Hsu YH, Thanassoulis G, Newton-Cheh C, Rogers IS, Hoffmann U, Freedman JE, Fox CS, Psaty BM, Boerwinkle E, Cupples LA, et al. Resequencing and clinical associations of the 9p21.3 region: a comprehensive investigation in the Framingham heart study. Circulation. 127: 799-810. PMID 23315372 DOI: 10.1161/Circulationaha.112.111559 |
0.556 |
|
| 2013 |
Fox ER, Musani SK, Barbalic M, Lin H, Yu B, Ogunyankin KO, Smith NL, Kutlar A, Glazer NL, Post WS, Paltoo DN, Dries DL, Farlow DN, Duarte CW, Kardia SL, ... ... Morrison AC, et al. Genome-wide association study of cardiac structure and systolic function in African Americans: the Candidate Gene Association Resource (CARe) study. Circulation. Cardiovascular Genetics. 6: 37-46. PMID 23275298 DOI: 10.1161/Circgenetics.111.962365 |
0.48 |
|
| 2013 |
Nguyen KD, Pihur V, Ganesh SK, Rakha A, Cooper RS, Hunt SC, Freedman BI, Coresh J, Kao WH, Morrison AC, Boerwinkle E, Ehret GB, Chakravarti A. Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies. Circulation Research. 112: 318-26. PMID 23149595 DOI: 10.1161/Circresaha.112.276725 |
0.572 |
|
| 2012 |
Hancock DB, Artigas MS, Gharib SA, Henry A, Manichaikul A, Ramasamy A, Loth DW, Imboden M, Koch B, McArdle WL, Smith AV, Smolonska J, Sood A, Tang W, Wilk JB, ... ... Morrison AC, et al. Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. Plos Genetics. 8: e1003098. PMID 23284291 DOI: 10.1371/Journal.Pgen.1003098 |
0.398 |
|
| 2012 |
Spellicy CJ, Northrup H, Fletcher JM, Cirino PT, Dennis M, Morrison AC, Martinez CA, Au KS. Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients. Plos One. 7: e51330. PMID 23227261 DOI: 10.1371/Journal.Pone.0051330 |
0.313 |
|
| 2012 |
Kase BA, Northrup H, Morrison AC, Davidson CM, Goiffon AM, Fletcher JM, Ostermaier KK, Tyerman GH, Au KS. Association of copper-zinc superoxide dismutase (SOD1) and manganese superoxide dismutase (SOD2) genes with nonsyndromic myelomeningocele. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 762-9. PMID 22972774 DOI: 10.1002/Bdra.23065 |
0.419 |
|
| 2012 |
Shetty PB, Tang H, Tayo BO, Morrison AC, Hanis CL, Rao DC, Young JH, Fox ER, Boerwinkle E, Cooper RS, Risch NJ, Zhu X. Variants in CXADR and F2RL1 are associated with blood pressure and obesity in African-Americans in regions identified through admixture mapping. Journal of Hypertension. 30: 1970-6. PMID 22914544 DOI: 10.1097/Hjh.0B013E3283578C80 |
0.563 |
|
| 2012 |
Wilk JB, Shrine NR, Loehr LR, Zhao JH, Manichaikul A, Lopez LM, Smith AV, Heckbert SR, Smolonska J, Tang W, Loth DW, Curjuric I, Hui J, Cho MH, Latourelle JC, ... ... Morrison AC, et al. Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. American Journal of Respiratory and Critical Care Medicine. 186: 622-32. PMID 22837378 DOI: 10.1164/Rccm.201202-0366Oc |
0.448 |
|
| 2012 |
Virani SS, Brautbar A, Lee VV, MacArthur E, Morrison AC, Grove ML, Nambi V, Frazier L, Wilson JM, Willerson JT, Boerwinkle E, Ballantyne CM. Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease. Circulation Journal : Official Journal of the Japanese Circulation Society. 76: 950-6. PMID 22322877 DOI: 10.1253/Circj.Cj-11-1166 |
0.485 |
|
| 2011 |
Soler Artigas M, Loth DW, Wain LV, Gharib SA, Obeidat M, Tang W, Zhai G, Zhao JH, Smith AV, Huffman JE, Albrecht E, Jackson CM, Evans DM, Cadby G, Fornage M, ... ... Morrison AC, et al. Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nature Genetics. 43: 1082-90. PMID 21946350 DOI: 10.1038/Ng.941 |
0.351 |
|
| 2011 |
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, ... ... Morrison AC, et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 478: 103-9. PMID 21909115 DOI: 10.1038/Nature10405 |
0.521 |
|
| 2011 |
Wain LV, Verwoert GC, O'Reilly PF, Shi G, Johnson T, Johnson AD, Bochud M, Rice KM, Henneman P, Smith AV, Ehret GB, Amin N, Larson MG, Mooser V, Hadley D, ... ... Morrison AC, et al. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nature Genetics. 43: 1005-11. PMID 21909110 DOI: 10.1038/Ng.922 |
0.522 |
|
| 2011 |
Zheng X, Morrison AC, Turner ST, Ferrell RE. Association between SLC20A1 and sodium-lithium countertransport. American Journal of Hypertension. 24: 1069-72. PMID 21796222 DOI: 10.1038/Ajh.2011.130 |
0.424 |
|
| 2011 |
Zhu X, Young JH, Fox E, Keating BJ, Franceschini N, Kang S, Tayo B, Adeyemo A, Sun YV, Li Y, Morrison A, Newton-Cheh C, Liu K, Ganesh SK, Kutlar A, et al. Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium. Human Molecular Genetics. 20: 2285-95. PMID 21422096 DOI: 10.1093/Hmg/Ddr113 |
0.518 |
|
| 2011 |
Fox ER, Young JH, Li Y, Dreisbach AW, Keating BJ, Musani SK, Liu K, Morrison AC, Ganesh S, Kutlar A, Ramachandran VS, Polak JF, Fabsitz RR, Dries DL, Farlow DN, et al. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Human Molecular Genetics. 20: 2273-84. PMID 21378095 DOI: 10.1093/Hmg/Ddr092 |
0.494 |
|
| 2011 |
Tran PX, Au KS, Morrison AC, Fletcher JM, Ostermaier KK, Tyerman GH, Northrup H. Association of retinoic acid receptor genes with meningomyelocele. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 39-43. PMID 21254357 DOI: 10.1002/Bdra.20744 |
0.399 |
|
| 2011 |
Shi G, Boerwinkle E, Morrison AC, Gu CC, Chakravarti A, Rao DC. Mining gold dust under the genome wide significance level: a two-stage approach to analysis of GWAS. Genetic Epidemiology. 35: 111-8. PMID 21254218 DOI: 10.1002/Gepi.20556 |
0.504 |
|
| 2011 |
Morrison AC, Ness RB. Sodium intake and cardiovascular disease. Annual Review of Public Health. 32: 71-90. PMID 21219163 DOI: 10.1146/Annurev-Publhealth-031210-101209 |
0.323 |
|
| 2011 |
Zheng X, Morrison AC, Feingold E, Turner ST, Ferrell RE. Association between NEDD4L gene and sodium lithium countertransport. American Journal of Hypertension. 24: 145-8. PMID 21088674 DOI: 10.1038/Ajh.2010.222 |
0.42 |
|
| 2010 |
Morrison AC, Srinivas SK, Elovitz MA, Puschett JB. Genetic variation in solute carrier genes is associated with preeclampsia. American Journal of Obstetrics and Gynecology. 203: 491.e1-491.e13. PMID 20691413 DOI: 10.1016/J.Ajog.2010.06.004 |
0.424 |
|
| 2010 |
O'Byrne MR, Au KS, Morrison AC, Lin JI, Fletcher JM, Ostermaier KK, Tyerman GH, Doebel S, Northrup H. Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele. Birth Defects Research. Part a, Clinical and Molecular Teratology. 88: 689-94. PMID 20683905 DOI: 10.1002/Bdra.20706 |
0.415 |
|
| 2010 |
Eijgelsheim M, Newton-Cheh C, Sotoodehnia N, de Bakker PI, Müller M, Morrison AC, Smith AV, Isaacs A, Sanna S, Dörr M, Navarro P, Fuchsberger C, Nolte IM, de Geus EJ, Estrada K, et al. Genome-wide association analysis identifies multiple loci related to resting heart rate. Human Molecular Genetics. 19: 3885-94. PMID 20639392 DOI: 10.1093/Hmg/Ddq303 |
0.534 |
|
| 2010 |
Smith NL, Felix JF, Morrison AC, Demissie S, Glazer NL, Loehr LR, Cupples LA, Dehghan A, Lumley T, Rosamond WD, Lieb W, Rivadeneira F, Bis JC, Folsom AR, Benjamin E, et al. Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. Circulation. Cardiovascular Genetics. 3: 256-66. PMID 20445134 DOI: 10.1161/Circgenetics.109.895763 |
0.564 |
|
| 2010 |
Morrison AC, Felix JF, Cupples LA, Glazer NL, Loehr LR, Dehghan A, Demissie S, Bis JC, Rosamond WD, Aulchenko YS, Wang YA, Haritunians T, Folsom AR, Rivadeneira F, Benjamin EJ, et al. Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. Circulation. Cardiovascular Genetics. 3: 248-55. PMID 20400778 DOI: 10.1161/Circgenetics.109.895995 |
0.549 |
|
| 2010 |
Srinivas SK, Morrison AC, Andrela CM, Elovitz MA. Allelic variations in angiogenic pathway genes are associated with preeclampsia. American Journal of Obstetrics and Gynecology. 202: 445.e1-11. PMID 20223440 DOI: 10.1016/J.Ajog.2010.01.040 |
0.344 |
|
| 2010 |
Meyer TE, Boerwinkle E, Morrison AC, Volcik KA, Sanderson M, Coker AL, Pankow JS, Folsom AR. Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 19: 558-65. PMID 20142250 DOI: 10.1158/1055-9965.Epi-09-0902 |
0.533 |
|
| 2010 |
Schnabel RB, Baumert J, Barbalic M, Dupuis J, Ellinor PT, Durda P, Dehghan A, Bis JC, Illig T, Morrison AC, Jenny NS, Keaney JF, Gieger C, Tilley C, Yamamoto JF, et al. Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediators. Blood. 115: 5289-99. PMID 20040767 DOI: 10.1182/Blood-2009-05-221382 |
0.525 |
|
| 2010 |
Hancock DB, Eijgelsheim M, Wilk JB, Gharib SA, Loehr LR, Marciante KD, Franceschini N, van Durme YM, Chen TH, Barr RG, Schabath MB, Couper DJ, Brusselle GG, Psaty BM, van Duijn CM, ... ... Morrison AC, et al. Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. Nature Genetics. 42: 45-52. PMID 20010835 DOI: 10.1038/Ng.500 |
0.416 |
|
| 2010 |
Kingah PL, Luu HN, Volcik KA, Morrison AC, Nettleton JA, Boerwinkle E. Association of NOS3 Glu298Asp SNP with hypertension and possible effect modification of dietary fat intake in the ARIC study. Hypertension Research : Official Journal of the Japanese Society of Hypertension. 33: 165-9. PMID 19960019 DOI: 10.1038/Hr.2009.198 |
0.495 |
|
| 2009 |
Rodin AS, Litvinenko A, Klos K, Morrison AC, Woodage T, Coresh J, Boerwinkle E. Use of wrapper algorithms coupled with a random forests classifier for variable selection in large-scale genomic association studies. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 16: 1705-18. PMID 20047492 DOI: 10.1089/Cmb.2008.0037 |
0.523 |
|
| 2009 |
Martinez CA, Northrup H, Lin JI, Morrison AC, Fletcher JM, Tyerman GH, Au KS. Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida. American Journal of Obstetrics and Gynecology. 201: 394.e1-11. PMID 19683694 DOI: 10.1016/J.Ajog.2009.06.042 |
0.387 |
|
| 2009 |
Levy D, Ehret GB, Rice K, Verwoert GC, Launer LJ, Dehghan A, Glazer NL, Morrison AC, Johnson AD, Aspelund T, Aulchenko Y, Lumley T, Köttgen A, Vasan RS, Rivadeneira F, et al. Genome-wide association study of blood pressure and hypertension. Nature Genetics. 41: 677-87. PMID 19430479 DOI: 10.1038/Ng.384 |
0.539 |
|
| 2009 |
Zheng X, Kammerer CM, Cox LA, Morrison A, Turner ST, Ferrell RE. Association of SLC34A2 variation and sodium-lithium countertransport activity in humans and baboons. American Journal of Hypertension. 22: 288-93. PMID 19119262 DOI: 10.1038/Ajh.2008.355 |
0.444 |
|
| 2009 |
Meyer TE, Shiffman D, Morrison AC, Rowland CM, Louie JZ, Bare LA, Ross DA, Arellano AR, Chasman DI, Ridker PM, Pankow JS, Coresh J, Malloy MJ, Kane JP, Ellis SG, et al. GOSR2 Lys67Arg is associated with hypertension in whites. American Journal of Hypertension. 22: 163-8. PMID 19057520 DOI: 10.1038/Ajh.2008.336 |
0.543 |
|
| 2009 |
Srinivas S, Morrison A, Elovitz M. 760: Genetic contribution of the renin-angiotesin system to preeclampsia American Journal of Obstetrics and Gynecology. 201. DOI: 10.1016/J.Ajog.2009.10.777 |
0.337 |
|
| 2009 |
Elovitz MA, Morrison A, Appelby D, Baldwin DA, Macones G, Srinivas S, Jeffcoat MK, Parry S. 464: Targeting genetic variations in gene pathways associated with cervical remodeling American Journal of Obstetrics and Gynecology. 201. DOI: 10.1016/J.Ajog.2009.10.630 |
0.373 |
|
| 2009 |
Srinivas S, Morrison A, Elovitz M. Oral concurrent session 4Diabetes/HTN/medical-surgical complication48: Allelic variations in angiogenic pathway genes are associated with preeclampsia American Journal of Obstetrics and Gynecology. 201. DOI: 10.1016/J.Ajog.2009.10.063 |
0.309 |
|
| 2008 |
Au KS, Tran PX, Tsai CC, O'Byrne MR, Lin JI, Morrison AC, Hampson AW, Cirino P, Fletcher JM, Ostermaier KK, Tyerman GH, Doebel S, Northrup H. Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 692-700. PMID 18937358 DOI: 10.1002/Bdra.20499 |
0.373 |
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| 2008 |
Morrison AC, Bare LA, Luke MM, Pankow JS, Mosley TH, Devlin JJ, Willerson JT, Boerwinkle E. Single nucleotide polymorphisms associated with coronary heart disease predict incident ischemic stroke in the atherosclerosis risk in communities study. Cerebrovascular Diseases (Basel, Switzerland). 26: 420-4. PMID 18799872 DOI: 10.1159/000155637 |
0.491 |
|
| 2008 |
Ehret GB, Morrison AC, O'Connor AA, Grove ML, Baird L, Schwander K, Weder A, Cooper RS, Rao DC, Hunt SC, Boerwinkle E, Chakravarti A. Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program. European Journal of Human Genetics : Ejhg. 16: 1507-11. PMID 18523456 DOI: 10.1038/Ejhg.2008.102 |
0.567 |
|
| 2008 |
Klos KL, Boerwinkle E, Ferrell RE, Turner ST, Morrison AC. ESR1 polymorphism is associated with plasma lipid and apolipoprotein levels in Caucasians of the Rochester Family Heart Study. Journal of Lipid Research. 49: 1701-6. PMID 18450649 DOI: 10.1194/Jlr.M700490-Jlr200 |
0.478 |
|
| 2008 |
Sherva R, Miller MB, Pankow JS, Hunt SC, Boerwinkle E, Mosley TH, Weder AB, Curb JD, Luke A, Morrison AC, Fornage M, Arnett DK. A whole-genome scan for stroke or myocardial infarction in family blood pressure program families. Stroke; a Journal of Cerebral Circulation. 39: 1115-20. PMID 18323513 DOI: 10.1161/Strokeaha.107.490433 |
0.462 |
|
| 2008 |
Morrison AC, Boerwinkle E, Turner ST, Ferrell RE. Regional association-based fine-mapping for sodium-lithium countertransport on chromosome 10. American Journal of Hypertension. 21: 117-21. PMID 18091754 DOI: 10.1038/Ajh.2007.17 |
0.553 |
|
| 2008 |
Martinez CA, Northrup H, Lin J, Morrison A, Fletcher JM, Tyerman G, Au KS. 575: Results of a genetic association study of genes in folate metabolism and spina bifida American Journal of Obstetrics and Gynecology. 199: S167. DOI: 10.1016/J.Ajog.2008.09.605 |
0.39 |
|
| 2007 |
Bare LA, Morrison AC, Rowland CM, Shiffman D, Luke MM, Iakoubova OA, Kane JP, Malloy MJ, Ellis SG, Pankow JS, Willerson JT, Devlin JJ, Boerwinkle E. Five common gene variants identify elevated genetic risk for coronary heart disease. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 9: 682-9. PMID 18073581 DOI: 10.1097/Gim.0B013E318156Fb62 |
0.515 |
|
| 2007 |
Morrison AC, Bare LA, Chambless LE, Ellis SG, Malloy M, Kane JP, Pankow JS, Devlin JJ, Willerson JT, Boerwinkle E. Prediction of coronary heart disease risk using a genetic risk score: the Atherosclerosis Risk in Communities Study. American Journal of Epidemiology. 166: 28-35. PMID 17443022 DOI: 10.1093/Aje/Kwm060 |
0.495 |
|
| 2007 |
Grove ML, Morrison A, Folsom AR, Boerwinkle E, Hoelscher DM, Bray MS. Gene-environment interaction and the GNB3 gene in the Atherosclerosis Risk in Communities Study International Journal of Obesity. 31: 919-926. PMID 17299380 DOI: 10.1038/Sj.Ijo.0803545 |
0.461 |
|
| 2007 |
Greenwood TA, Libiger O, Kardia S, Hanis C, Morrison AC, Gu CC, Rice T, Miller M, Turner ST, Myers RH, Grove J, Hsiao CF, Weder AB, Schork NJ. Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program. Genetic Epidemiology. 31: 195-210. PMID 17266112 DOI: 10.1002/Gepi.20202 |
0.417 |
|
| 2006 |
Chang YP, Kim JD, Schwander K, Rao DC, Miller MB, Weder AB, Cooper RS, Schork NJ, Province MA, Morrison AC, Kardia SL, Quertermous T, Chakravarti A. The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program. European Journal of Human Genetics : Ejhg. 14: 469-77. PMID 16493446 DOI: 10.1038/Sj.Ejhg.5201582 |
0.393 |
|
| 2005 |
Hoogeveen RC, Morrison A, Boerwinkle E, Miles JS, Rhodes CE, Sharrett AR, Ballantyne CM. Plasma MCP-1 level and risk for peripheral arterial disease and incident coronary heart disease: Atherosclerosis Risk in Communities study. Atherosclerosis. 183: 301-7. PMID 16285993 DOI: 10.1016/J.Atherosclerosis.2005.03.007 |
0.47 |
|
| 2005 |
Morrison AC, Boerwinkle E, Turner ST, Ferrell RE. Genome-wide linkage study of erythrocyte sodium-lithium countertransport. American Journal of Hypertension. 18: 653-6. PMID 15882547 DOI: 10.1016/J.Amjhyper.2004.11.030 |
0.488 |
|
| 2004 |
Morrison AC, Cooper R, Hunt S, Lewis CE, Luke A, Mosley TH, Boerwinkle E. Genome scan for hypertension in nonobese African Americans: the National Heart, Lung, and Blood Institute Family Blood Pressure Program. American Journal of Hypertension. 17: 834-8. PMID 15363828 DOI: 10.1016/J.Amjhyper.2004.04.009 |
0.474 |
|
| 2003 |
Morrison AC, Brown A, Kardia SL, Turner ST, Boerwinkle E. Evaluating the context-dependent effect of family history of stroke in a genome scan for hypertension. Stroke; a Journal of Cerebral Circulation. 34: 1170-5. PMID 12714704 DOI: 10.1161/01.Str.0000068780.47411.16 |
0.472 |
|
| 2002 |
Morrison AC, Bray MS, Folsom AR, Boerwinkle E. ADD1 460W allele associated with cardiovascular disease in hypertensive individuals. Hypertension. 39: 1053-7. PMID 12052841 DOI: 10.1161/01.Hyp.0000019128.94483.3A |
0.524 |
|
| 2002 |
Morrison AC, Ballantyne CM, Bray M, Chambless LE, Sharrett AR, Boerwinkle E. LPL polymorphism predicts stroke risk in men. Genetic Epidemiology. 22: 233-42. PMID 11921083 DOI: 10.1002/Gepi.0191 |
0.458 |
|
| 2001 |
Huang Q, Morrison AC, Boerwinkle E. Linkage disequilibrium structure and its impact on the localization of a candidate functional mutation. Genetic Epidemiology. 21: S620-5. PMID 11793750 DOI: 10.1002/Gepi.2001.21.S1.S620 |
0.628 |
|
| 2001 |
Morrison AC, Doris PA, Folsom AR, Nieto FJ, Boerwinkle E. G-protein beta3 subunit and alpha-adducin polymorphisms and risk of subclinical and clinical stroke. Stroke. 32: 822-9. PMID 11283377 DOI: 10.1161/01.Str.32.4.822 |
0.45 |
|
| 2000 |
Morrison AC, Fornage M, Liao D, Boerwinkle E. Parental history of stroke predicts subclinical but not clinical stroke: the Atherosclerosis Risk in Communities Study. Stroke. 31: 2098-102. PMID 10978036 DOI: 10.1161/01.Str.31.9.2098 |
0.42 |
|
| 1999 |
Morrison AC, Brancati FL, Folsom AR, Smith L, Boerwinkle E. β3-adrenergic receptor Trp64Arg polymorphism does not predict incident CHD or carotid intima-media thickness in a community-based sample of whites: The ARIC study Human Genetics. 105: 314-319. PMID 10543398 DOI: 10.1007/S004390051107 |
0.466 |
|
| 1999 |
Morrison A, Brancati F, Folsom A, Smith L, Boerwinkle E. β3-Adrenergic receptor Trp64Arg polymorphism does not predict incident CHD or carotid intima-media thickness in a community-based sample of whites: the ARIC study Human Genetics. 105: 314-319. DOI: 10.1007/s004390051107 |
0.309 |
|
| Show low-probability matches. |