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For: Morales J, Welter D, Bowler EH, Cerezo M, Harris LW, McMahon AC, Hall P, Junkins HA, Milano A, Hastings E, Malangone C, Buniello A, Burdett T, Flicek P, Parkinson H, Cunningham F, Hindorff LA, MacArthur JAL. A standardized framework for representation of ancestry data in genomics studies, with application to the NHGRI-EBI GWAS Catalog. Genome Biol 2018;19:21. [PMID: 29448949 DOI: 10.1186/s13059-018-1396-2] [Cited by in Crossref: 105] [Cited by in F6Publishing: 111] [Article Influence: 26.3] [Reference Citation Analysis]
Number Citing Articles
1 Ghosh S, Nehme R, Barrett LE. Greater genetic diversity is needed in human pluripotent stem cell models. Nat Commun 2022;13:7301. [PMID: 36435871 DOI: 10.1038/s41467-022-34940-z] [Reference Citation Analysis]
2 Ni H, Jordan E, Cao J, Kinnamon DD, Gottlieb SS, Hofmeyer M, Jimenez J, Judge DP, Kransdorf E, Morris AA, Owens A, Shah P, Tang WHW, Wang J, Hershberger RE. Knowledge of Genome Sequencing and Trust in Medical Researchers Among Patients of Different Racial and Ethnic Groups With Idiopathic Dilated Cardiomyopathy. JAMA Cardiol 2022. [DOI: 10.1001/jamacardio.2022.4132] [Reference Citation Analysis]
3 Trinidad MG, Ryan KA, Krenz CD, Roberts JS, Mcguire AL, De Vries R, Zikmund-fisher BJ, Kardia S, Marsh E, Forman J, Kent M, Wilborn D, Spector-bagdady K. “Extremely slow and capricious”: A qualitative exploration of genetic researcher priorities in selecting shared data resources. Genetics in Medicine 2022. [DOI: 10.1016/j.gim.2022.09.003] [Reference Citation Analysis]
4 Asbury K, Mcbride T, Bawn R. Can genomic research make a useful contribution to social policy? R Soc open sci 2022;9. [DOI: 10.1098/rsos.220873] [Reference Citation Analysis]
5 Chappell K, Ait Tayeb AEK, Colle R, Bouligand J, El-asmar K, Gressier F, Trabado S, David DJ, Feve B, Becquemont L, Corruble E, Verstuyft C. The association of ARRB1 polymorphisms with response to antidepressant treatment in depressed patients. Front Pharmacol 2022;13. [DOI: 10.3389/fphar.2022.974570] [Reference Citation Analysis]
6 Wojcik GL. By their powers combined, global initiative joins forces for genomic research. Cell 2022. [DOI: 10.1016/j.cell.2022.10.010] [Reference Citation Analysis]
7 Mattei LH, Robb L, Banning K, Polan RM, Cote ML. Enrollment of Individuals From Racial and Ethnic Minority Groups in Gynecologic Cancer Precision Oncology Trials. Obstetrics & Gynecology 2022;140:654-661. [DOI: 10.1097/aog.0000000000004917] [Reference Citation Analysis]
8 Bastarache L, Delozier S, Pandit A, He J, Lewis A, Annis AC, Lefaive J, Denny JC, Carroll RJ, Hughey JJ, Zawistowski M, Peterson JF. The Phenotype-Genotype Reference Map: Improving biobank data science through replication.. [DOI: 10.1101/2022.09.07.506932] [Reference Citation Analysis]
9 Jacobs BM, Peter M, Giovannoni G, Noyce AJ, Morris HR, Dobson R. Towards a global view of multiple sclerosis genetics. Nat Rev Neurol 2022. [PMID: 36075979 DOI: 10.1038/s41582-022-00704-y] [Reference Citation Analysis]
10 Ferolito B, do Valle IF, Gerlovin H, Costa L, Casas JP, Gaziano JM, Gagnon DR, Begoli E, Barabási AL, Cho K. Visualizing novel connections and genetic similarities across diseases using a network-medicine based approach. Sci Rep 2022;12:14914. [PMID: 36050444 DOI: 10.1038/s41598-022-19244-y] [Reference Citation Analysis]
11 Atkinson EG, Dalvie S, Pichkar Y, Kalungi A, Majara L, Stevenson A, Abebe T, Akena D, Alemayehu M, Ashaba FK, Atwoli L, Baker M, Chibnik LB, Creanza N, Daly MJ, Fekadu A, Gelaye B, Gichuru S, Injera WE, James R, Kariuki SM, Kigen G, Koen N, Koenen KC, Koenig Z, Kwobah E, Kyebuzibwa J, Musinguzi H, Mwema RM, Neale BM, Newman CP, Newton CRJC, Ongeri L, Ramachandran S, Ramesar R, Shiferaw W, Stein DJ, Stroud RE, Teferra S, Yohannes MT, Zingela Z, Martin AR; NeuroGAP-Psychosis Study Team. Genetic structure correlates with ethnolinguistic diversity in eastern and southern Africa. Am J Hum Genet 2022;109:1667-79. [PMID: 36055213 DOI: 10.1016/j.ajhg.2022.07.013] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Nguyen AB, Cavallari LH, Rossi JS, Stouffer GA, Lee CR. Evaluation of race and ethnicity disparities in outcome studies of CYP2C19 genotype-guided antiplatelet therapy. Front Cardiovasc Med 2022;9. [DOI: 10.3389/fcvm.2022.991646] [Reference Citation Analysis]
13 Huang QQ, Sallah N, Dunca D, Trivedi B, Hunt KA, Hodgson S, Lambert SA, Arciero E, Wright J, Griffiths C, Trembath RC, Hemingway H, Inouye M, Finer S, van Heel DA, Lumbers RT, Martin HC, Kuchenbaecker K. Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals. Nat Commun 2022;13:4664. [PMID: 35945198 DOI: 10.1038/s41467-022-32095-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
14 Karczewski KJ, Solomonson M, Chao KR, Goodrich JK, Tiao G, Lu W, Riley-gillis BM, Tsai EA, Kim HI, Zheng X, Rahimov F, Esmaeeli S, Grundstad AJ, Reppell M, Waring J, Jacob H, Sexton D, Bronson PG, Chen X, Hu X, Goldstein JI, King D, Vittal C, Poterba T, Palmer DS, Churchhouse C, Howrigan DP, Zhou W, Watts NA, Nguyen K, Nguyen H, Mason C, Farnham C, Tolonen C, Gauthier LD, Gupta N, Macarthur DG, Rehm HL, Seed C, Philippakis AA, Daly MJ, Davis JW, Runz H, Miller MR, Neale BM. Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes. Cell Genomics 2022. [DOI: 10.1016/j.xgen.2022.100168] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
15 Chappell K, Colle R, Ait Tayeb AEK, Bouligand J, El-Asmar K, Deflesselle E, Fève B, Becquemont L, Corruble E, Verstuyft C. The ERICH3 rs11580409 polymorphism is associated with 6-month antidepressant response in depressed patients. Prog Neuropsychopharmacol Biol Psychiatry 2022;119:110608. [PMID: 35878676 DOI: 10.1016/j.pnpbp.2022.110608] [Reference Citation Analysis]
16 Hayhurst J, Buniello A, Harris L, Mosaku A, Chang C, Gignoux CR, Hatzikotoulas K, Karim MA, Lambert SA, Lyon M, Mcmahon A, Okada Y, Pirastu N, Rayner NW, Schwartzentruber J, Vaughan R, Verma S, Wilder SP, Cunningham F, Hindorff L, Wiley K, Parkinson H, Barroso I. A community driven GWAS summary statistics standard.. [DOI: 10.1101/2022.07.15.500230] [Reference Citation Analysis]
17 Zheng Y, Joyce B, Hwang SJ, Ma J, Liu L, Allen N, Krefman A, Wang J, Gao T, Nannini D, Zhang H, Jacobs DR Jr, Gross M, Fornage M, Lewis CE, Schreiner PJ, Sidney S, Chen D, Greenland P, Levy D, Hou L, Lloyd-Jones D. Association of Cardiovascular Health Through Young Adulthood With Genome-Wide DNA Methylation Patterns in Midlife: The CARDIA Study. Circulation 2022;:101161CIRCULATIONAHA121055484. [PMID: 35652342 DOI: 10.1161/CIRCULATIONAHA.121.055484] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
18 Martschenko DO, Young JL. Precision Medicine Needs to Think Outside the Box. Front Genet 2022;13:795992. [PMID: 35559033 DOI: 10.3389/fgene.2022.795992] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Adebamowo CA, Adeyemo A, Ashaye A, Akpa OM, Chikowore T, Choudhury A, Fakim YJ, Fatumo S, Hanchard N, Hauser M, Mitchell B, Mulder N, Ofori-Acquah SF, Owolabi M, Ramsay M, Tayo B, VasanthKumar AB, Zhang Y, Adebamowo SN. Polygenic risk scores for CARDINAL study. Nat Genet 2022. [PMID: 35513726 DOI: 10.1038/s41588-022-01074-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Rashed WM, Adel F, Rezk MA, Basiouny L, Rezk AA, Abdel-razek AH. MicroRNA childhood cancer catalog (M3Cs): a resource for translational bioinformatics toward health informatics in pediatric cancer. Database 2022;2022. [DOI: 10.1093/database/baac013] [Reference Citation Analysis]
21 Horowitz JE, Kosmicki JA, Damask A, Sharma D, Roberts GHL, Justice AE, Banerjee N, Coignet MV, Yadav A, Leader JB, Marcketta A, Park DS, Lanche R, Maxwell E, Knight SC, Bai X, Guturu H, Sun D, Baltzell A, Kury FSP, Backman JD, Girshick AR, O'Dushlaine C, McCurdy SR, Partha R, Mansfield AJ, Turissini DA, Li AH, Zhang M, Mbatchou J, Watanabe K, Gurski L, McCarthy SE, Kang HM, Dobbyn L, Stahl E, Verma A, Sirugo G, Ritchie MD, Jones M, Balasubramanian S, Siminovitch K, Salerno WJ, Shuldiner AR, Rader DJ, Mirshahi T, Locke AE, Marchini J, Overton JD, Carey DJ, Habegger L, Cantor MN, Rand KA, Hong EL, Reid JG, Ball CA, Baras A, Abecasis GR, Ferreira MAR; Regeneron Genetics Center. Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease. Nat Genet 2022. [PMID: 35241825 DOI: 10.1038/s41588-021-01006-7] [Cited by in Crossref: 17] [Cited by in F6Publishing: 22] [Article Influence: 17.0] [Reference Citation Analysis]
22 Khasim A, Subramanian V, Ajith KM, Shajahan TK. Structure of Protein Interaction Network Associated With Alzheimer’s Disease Using Graphlet Based Techniques. Nonlinear Dynamics and Applications 2022. [DOI: 10.1007/978-3-030-99792-2_42] [Reference Citation Analysis]
23 Mesaros M, Lenz S, Lim W, Brown J, Drury L, Roggenbuck J. Investigating the Genetic Profile of the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia (ALS-FTD) Continuum in Patients of Diverse Race, Ethnicity and Ancestry. Genes 2022;13:76. [DOI: 10.3390/genes13010076] [Reference Citation Analysis]
24 Pal T. Diversity in cancer genomics research is a matter of equity and scientific discovery. Genet Med 2021:S1098-3600(21)05396-X. [PMID: 34906472 DOI: 10.1016/j.gim.2021.11.016] [Reference Citation Analysis]
25 Polygenic Risk Score Task Force of the International Common Disease Alliance. Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps. Nat Med 2021;27:1876-84. [PMID: 34782789 DOI: 10.1038/s41591-021-01549-6] [Cited by in Crossref: 65] [Cited by in F6Publishing: 72] [Article Influence: 65.0] [Reference Citation Analysis]
26 Mountjoy E, Schmidt EM, Carmona M, Schwartzentruber J, Peat G, Miranda A, Fumis L, Hayhurst J, Buniello A, Karim MA, Wright D, Hercules A, Papa E, Fauman EB, Barrett JC, Todd JA, Ochoa D, Dunham I, Ghoussaini M. An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci. Nat Genet 2021;53:1527-33. [PMID: 34711957 DOI: 10.1038/s41588-021-00945-5] [Cited by in Crossref: 41] [Cited by in F6Publishing: 45] [Article Influence: 41.0] [Reference Citation Analysis]
27 McMahon A, Lewis E, Buniello A, Cerezo M, Hall P, Sollis E, Parkinson H, Hindorff LA, Harris LW, MacArthur JAL. Sequencing-based genome-wide association studies reporting standards. Cell Genom 2021;1:100005. [PMID: 34870259 DOI: 10.1016/j.xgen.2021.100005] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
28 Huang YN, Peng K, Popejoy AB, Hu J, Nowicki TS, Gold SM, Quintana-Murci L, Fuentes-Guajardo M, Shugay M, Greiff V, Burkhardt AM, Alachkar H, Mangul S. Ancestral diversity is limited in published T cell receptor sequencing studies. Immunity 2021;54:2177-9. [PMID: 34644550 DOI: 10.1016/j.immuni.2021.09.015] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Barroso I. The importance of increasing population diversity in genetic studies of type 2 diabetes and related glycaemic traits. Diabetologia 2021;64:2653-64. [PMID: 34595549 DOI: 10.1007/s00125-021-05575-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 Macarthur JA, Buniello A, Harris LW, Hayhurst J, Mcmahon A, Sollis E, Cerezo M, Hall P, Lewis E, Whetzel PL, Bahcall OG, Barroso I, Carroll RJ, Inouye M, Manolio TA, Rich SS, Hindorff LA, Wiley K, Parkinson H. Workshop proceedings: GWAS summary statistics standards and sharing. Cell Genomics 2021;1:100004. [DOI: 10.1016/j.xgen.2021.100004] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 8.0] [Reference Citation Analysis]
31 Esdaille AR, Ibilibor C, Holmes A 2nd, Palmer NR, Murphy AB. Access and Representation: A Narrative Review of the Disparities in Access to Clinical Trials and Precision Oncology in Black men with Prostate Cancer. Urology 2021:S0090-4295(21)00893-1. [PMID: 34582887 DOI: 10.1016/j.urology.2021.09.004] [Reference Citation Analysis]
32 Rashed WM, Adel F, Rezk MA, Basiouny L, Rezk AA, Abdel-razek AH. MicroRNA childhood Cancer Catalog (M3Cs): A Resource for Translational Bioinformatics Toward Health Informatics in Pediatric Cancer.. [DOI: 10.1101/2021.07.26.452794] [Reference Citation Analysis]
33 Magavern EF, Gurdasani D, Ng FL, Lee SS. Health equality, race and pharmacogenomics. Br J Clin Pharmacol 2021. [PMID: 34251046 DOI: 10.1111/bcp.14983] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
34 Sousa JA, Mendonça MI, Serrão M, Borges S, Henriques E, Freitas S, Tentem M, Santos M, Freitas P, Ferreira A, Guerra G, Drumond A, Palma Reis R. Epicardial Adipose Tissue: The Genetics Behind an Emerging Cardiovascular Risk Marker. Clin Med Insights Cardiol 2021;15:11795468211029244. [PMID: 34276231 DOI: 10.1177/11795468211029244] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
35 Han X, Steven K, Qassim A, Marshall HN, Bean C, Tremeer M, An J, Siggs OM, Gharahkhani P, Craig JE, Hewitt AW, Trzaskowski M, MacGregor S. Automated AI labeling of optic nerve head enables insights into cross-ancestry glaucoma risk and genetic discovery in >280,000 images from UKB and CLSA. Am J Hum Genet 2021;108:1204-16. [PMID: 34077762 DOI: 10.1016/j.ajhg.2021.05.005] [Cited by in Crossref: 12] [Cited by in F6Publishing: 5] [Article Influence: 12.0] [Reference Citation Analysis]
36 Huang QQ, Sallah N, Dunca D, Trivedi B, Hunt KA, Hodgson S, Lambert SA, Arciero E, Wright J, Griffiths C, Trembath RC, Hemingway H, Inouye M, Finer S, van Heel DA, Lumbers T, Martin HC, Kuchenbaecker K, Genes & Health Research team. Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistanis and Bangladeshis.. [DOI: 10.1101/2021.06.22.21259323] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
37 Karczewski KJ, Solomonson M, Chao KR, Goodrich JK, Tiao G, Lu W, Riley-gillis BM, Tsai EA, Kim HI, Zheng X, Rahimov F, Esmaeeli S, Grundstad AJ, Reppell M, Waring J, Jacob H, Sexton D, Bronson PG, Chen X, Hu X, Goldstein JI, King D, Vittal C, Poterba T, Palmer DS, Churchhouse C, Howrigan DP, Zhou W, Watts NA, Nguyen K, Nguyen H, Mason C, Farnham C, Tolonen C, Gauthier LD, Gupta N, Macarthur DG, Rehm HL, Seed C, Philippakis AA, Daly MJ, Davis JW, Runz H, Miller MR, Neale BM. Systematic single-variant and gene-based association testing of thousands of phenotypes in 426,370 UK Biobank exomes.. [DOI: 10.1101/2021.06.19.21259117] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 12.0] [Reference Citation Analysis]
38 Victor S, Chew A, Falconer S. Pro12Ala polymorphism of peroxisome proliferator activated receptor gamma 2 may be associated with adverse neurodevelopment in European preterm babies. Brain Behav 2021;11:e2256. [PMID: 34152086 DOI: 10.1002/brb3.2256] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
39 Atkinson EG, Dalvie S, Pichkar Y, Kalungi A, Majara L, Stevenson A, Abebe T, Akena D, Alemayehu M, Ashaba FK, Atwoli L, Baker M, Chibnik LB, Creanza N, Daly MJ, Fekadu A, Gelaye B, Gichuru S, Injera WE, James R, Kariuki SM, Kigen G, Koen N, Koenen KC, Koenig Z, Kwobah E, Kyebuzibwa J, Musinguzi H, Mwema RM, Neale BM, Newman CP, Newton CR, Ongeri L, Ramachandran S, Ramesar R, Shiferaw W, Stein DJ, Stroud RE, Teferra S, Yohannes MT, Zingela Z, Martin AR, NeuroGAP-Psychosis Study Team. Genetic structure correlates with ethnolinguistic diversity in eastern and southern Africa.. [DOI: 10.1101/2021.05.19.444732] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
40 Hershberger RE, Cowan J, Jordan E, Kinnamon DD. The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy. Circ Res 2021;128:1514-32. [PMID: 33983834 DOI: 10.1161/CIRCRESAHA.121.318157] [Cited by in Crossref: 17] [Cited by in F6Publishing: 20] [Article Influence: 17.0] [Reference Citation Analysis]
41 Miga KH, Wang T. The Need for a Human Pangenome Reference Sequence. Annu Rev Genomics Hum Genet 2021;22:81-102. [PMID: 33929893 DOI: 10.1146/annurev-genom-120120-081921] [Cited by in Crossref: 32] [Cited by in F6Publishing: 33] [Article Influence: 32.0] [Reference Citation Analysis]
42 Dehghani N, Bras J, Guerreiro R. How understudied populations have contributed to our understanding of Alzheimer's disease genetics. Brain 2021;144:1067-81. [PMID: 33889936 DOI: 10.1093/brain/awab028] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
43 Lambert SA, Gil L, Jupp S, Ritchie SC, Xu Y, Buniello A, McMahon A, Abraham G, Chapman M, Parkinson H, Danesh J, MacArthur JAL, Inouye M. The Polygenic Score Catalog as an open database for reproducibility and systematic evaluation. Nat Genet 2021;53:420-5. [PMID: 33692568 DOI: 10.1038/s41588-021-00783-5] [Cited by in Crossref: 115] [Cited by in F6Publishing: 127] [Article Influence: 115.0] [Reference Citation Analysis]
44 Heilbron K, Mozaffari SV, Vacic V, Yue P, Wang W, Shi J, Jubb AM, Pitts SJ, Wang X. Advancing drug discovery using the power of the human genome. J Pathol 2021;254:418-29. [PMID: 33748968 DOI: 10.1002/path.5664] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
45 Hamdi Y, Zass L, Othman H, Radouani F, Allali I, Hanachi M, Okeke CJ, Chaouch M, Tendwa MB, Samtal C, Mohamed Sallam R, Alsayed N, Turkson M, Ahmed S, Benkahla A, Romdhane L, Souiai O, Tastan Bishop Ö, Ghedira K, Mohamed Fadlelmola F, Mulder N, Kamal Kassim S. Human OMICs and Computational Biology Research in Africa: Current Challenges and Prospects. OMICS 2021;25:213-33. [PMID: 33794662 DOI: 10.1089/omi.2021.0004] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
46 Tamm G, Kreegipuu K, Harro J. Platelet MAO activity and COMT Val158Met genotype interaction predicts visual working memory updating efficiency. Behav Brain Res 2021;407:113255. [PMID: 33745984 DOI: 10.1016/j.bbr.2021.113255] [Reference Citation Analysis]
47 Wand H, Lambert SA, Tamburro C, Iacocca MA, O’sullivan JW, Sillari C, Kullo IJ, Rowley R, Dron JS, Brockman D, Venner E, Mccarthy MI, Antoniou AC, Easton DF, Hegele RA, Khera AV, Chatterjee N, Kooperberg C, Edwards K, Vlessis K, Kinnear K, Danesh JN, Parkinson H, Ramos EM, Roberts MC, Ormond KE, Khoury MJ, Janssens ACJW, Goddard KAB, Kraft P, Macarthur JAL, Inouye M, Wojcik GL. Improving reporting standards for polygenic scores in risk prediction studies. Nature 2021;591:211-9. [DOI: 10.1038/s41586-021-03243-6] [Cited by in Crossref: 121] [Cited by in F6Publishing: 126] [Article Influence: 121.0] [Reference Citation Analysis]
48 McCall MK, Connolly M, Nugent B, Conley YP, Bender CM, Rosenzweig MQ. Symptom Experience, Management, and Outcomes According to Race and Social Determinants Including Genomics, Epigenomics, and Metabolomics (SEMOARS + GEM): an Explanatory Model for Breast Cancer Treatment Disparity. J Cancer Educ 2020;35:428-40. [PMID: 31392599 DOI: 10.1007/s13187-019-01571-w] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 8.0] [Reference Citation Analysis]
49 Majara L, Kalungi A, Koen N, Zar H, Stein DJ, Kinyanda E, Atkinson EG, Martin AR. Low generalizability of polygenic scores in African populations due to genetic and environmental diversity.. [DOI: 10.1101/2021.01.12.426453] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 16.0] [Reference Citation Analysis]
50 Mann SP, Treit PV, Geyer PE, Omenn GS, Mann M. Ethical Principles, Constraints and Opportunities in Clinical Proteomics. Mol Cell Proteomics 2021;:100046. [PMID: 33453411 DOI: 10.1016/j.mcpro.2021.100046] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 10.0] [Reference Citation Analysis]
51 Lewis DD, Cropp CD. The Impact of African Ancestry on Prostate Cancer Disparities in the Era of Precision Medicine. Genes (Basel) 2020;11:E1471. [PMID: 33302594 DOI: 10.3390/genes11121471] [Cited by in Crossref: 9] [Cited by in F6Publishing: 12] [Article Influence: 4.5] [Reference Citation Analysis]
52 Gupta H, Chandratre K, Sinha S, Huang T, Wu X, Cui J, Zhang MQ, Wang SM. Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition. BMC Genomics 2020;21:842. [PMID: 33256598 DOI: 10.1186/s12864-020-07222-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
53 Geoffroy E, Gregga I, Wheeler HE. Population-Matched Transcriptome Prediction Increases TWAS Discovery and Replication Rate. iScience 2020;23:101850. [PMID: 33313492 DOI: 10.1016/j.isci.2020.101850] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
54 Fonseca L, Sena BF, Crossley N, Lopez-Jaramillo C, Koenen K, Freimer NB, Bressan RA, Belangero SI, Santoro ML, Gadelha A. Diversity matters: opportunities in the study of the genetics of psychotic disorders in low- and middle-income countries in Latin America. Braz J Psychiatry 2020:S1516-44462020005038202. [PMID: 33237255 DOI: 10.1590/1516-4446-2020-1240] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
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