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For: Green ED, Gunter C, Biesecker LG, Di Francesco V, Easter CL, Feingold EA, Felsenfeld AL, Kaufman DJ, Ostrander EA, Pavan WJ, Phillippy AM, Wise AL, Dayal JG, Kish BJ, Mandich A, Wellington CR, Wetterstrand KA, Bates SA, Leja D, Vasquez S, Gahl WA, Graham BJ, Kastner DL, Liu P, Rodriguez LL, Solomon BD, Bonham VL, Brody LC, Hutter CM, Manolio TA. Strategic vision for improving human health at The Forefront of Genomics. Nature 2020;586:683-92. [PMID: 33116284 DOI: 10.1038/s41586-020-2817-4] [Cited by in Crossref: 111] [Cited by in F6Publishing: 114] [Article Influence: 55.5] [Reference Citation Analysis]
Number Citing Articles
1 Lokhande HA. Bioinformatics Analysis of miRNA Sequencing Data. Methods in Molecular Biology 2023. [DOI: 10.1007/978-1-0716-2823-2_16] [Reference Citation Analysis]
2 Premzl M. Revised eutherian gene collections. BMC Genom Data 2022;23:56. [DOI: 10.1186/s12863-022-01071-9] [Reference Citation Analysis]
3 Assidi M, Buhmeida A, Budowle B. Medicine and health of 21st Century: Not just a high biotech-driven solution. npj Genom Med 2022;7:67. [DOI: 10.1038/s41525-022-00336-7] [Reference Citation Analysis]
4 Gerussi A, Scaravaglio M, Cristoferi L, Verda D, Milani C, De Bernardi E, Ippolito D, Asselta R, Invernizzi P, Kather JN, Carbone M. Artificial intelligence for precision medicine in autoimmune liver disease. Front Immunol 2022;13. [DOI: 10.3389/fimmu.2022.966329] [Reference Citation Analysis]
5 Lin W. Translating Genetic Discovery into a Mechanistic Understanding of Pediatric Movement Disorders: Lessons from Genetic Dystonias and Related Disorders. Advanced Genetics 2022. [DOI: 10.1002/ggn2.202200018] [Reference Citation Analysis]
6 Little ID, Koehly LM, Gunter C. Understanding changes in genetic literacy over time and in genetic research participants. The American Journal of Human Genetics 2022. [DOI: 10.1016/j.ajhg.2022.11.005] [Reference Citation Analysis]
7 Wen Y, Jacobson PA, Oetting WS, Pereira C, Brown JT. Knowledge and attitudes of incoming pharmacy students toward pharmacogenomics and survey reliability. Pharmacogenomics 2022. [DOI: 10.2217/pgs-2022-0094] [Reference Citation Analysis]
8 Lo RS, Cromie GA, Tang M, Teng K, Owens K, Sirr A, Kutz JN, Mclaughlin RN, Morizono H, Caldovic L, Mew NA, Gropman A, Dudley AM. The functional impact of 1,570 SNP-accessible missense variants in humanOTC.. [DOI: 10.1101/2022.10.26.513893] [Reference Citation Analysis]
9 Bhat V, Adzhubei IA, Fife JD, Lebo M, Cassa CA. Informing variant assessment using structured evidence from prior classifications (PS1, PM5, and PVS1 sequence variant interpretation criteria). Genetics in Medicine 2022. [DOI: 10.1016/j.gim.2022.09.009] [Reference Citation Analysis]
10 Bidzimou MK, Landstrom AP. From diagnostic testing to precision medicine: the evolving role of genomics in cardiac channelopathies and cardiomyopathies in children. Curr Opin Genet Dev 2022;76:101978. [PMID: 36058060 DOI: 10.1016/j.gde.2022.101978] [Reference Citation Analysis]
11 Greiner A, Mehdi H, Cevan C, Gutmann R, London B. Additional Evidence Implicating GPD1L in the Pathogenesis of Brugada Syndrome in A Large Multi-generational Family.. [DOI: 10.1101/2022.09.17.22280058] [Reference Citation Analysis]
12 Francis BM, Sundaram A, Manavalan RK, Peng WK, Zhang H, Ponraj JS, Chander Dhanabalan S. Two-dimensional nanostructures based ‘-onics’ and ‘-omics’ in personalized medicine. Nanophotonics 2022;0. [DOI: 10.1515/nanoph-2022-0439] [Reference Citation Analysis]
13 Lau-Min KS, McKenna D, Asher SB, Bardakjian T, Wollack C, Bleznuck J, Biros D, Anantharajah A, Clark DF, Condit C, Ebrahimzadeh JE, Long JM, Powers J, Raper A, Schoenbaum A, Feldman M, Steinfeld L, Tuteja S, VanZandbergen C, Domchek SM, Ritchie MD, Landgraf J, Chen J, Nathanson KL. Impact of integrating genomic data into the electronic health record on genetics care delivery. Genet Med 2022:S1098-3600(22)00900-5. [PMID: 36107166 DOI: 10.1016/j.gim.2022.08.009] [Reference Citation Analysis]
14 Little ID, Koehly LM, Gunter C. Understanding changes in genetic literacy over time and in genetic research participants.. [DOI: 10.1101/2022.09.12.507568] [Reference Citation Analysis]
15 Hollister BM, Schopp EM, Telaak SH, Buscetta AJ, Dolwick AP, Fortney CJ, Bonham VL, Persky S. Educational considerations based on medical student use of polygenic risk information and apparent race in a simulated consultation. Genet Med 2022:S1098-3600(22)00895-4. [PMID: 36053286 DOI: 10.1016/j.gim.2022.08.004] [Reference Citation Analysis]
16 Zheng M, Allington G, Vilarinho S. Genomic medicine for liver disease. Hepatology 2022;76:860-8. [PMID: 35076957 DOI: 10.1002/hep.32364] [Reference Citation Analysis]
17 Hanchard NA, Choudhury A. 1000 Genomes Project phase 4: The gift that keeps on giving. Cell 2022;185:3286-3289. [DOI: 10.1016/j.cell.2022.08.001] [Reference Citation Analysis]
18 Puddester R, Pike A, Maddigan J, Farrell A. Nurses’ Knowledge, Attitudes, Confidence, and Practices with Genetics and Genomics: A Theory-Informed Integrative Review Protocol. JPM 2022;12:1358. [DOI: 10.3390/jpm12091358] [Reference Citation Analysis]
19 Wei M. Impact of Genomics on the Future of Healthcare. HSET 2022;11:22-26. [DOI: 10.54097/hset.v11i.1262] [Reference Citation Analysis]
20 Groenendyk JW, Greenland P, Khan SS. Incremental Value of Polygenic Risk Scores in Primary Prevention of Coronary Heart Disease: A Review. JAMA Intern Med 2022. [PMID: 35994254 DOI: 10.1001/jamainternmed.2022.3171] [Reference Citation Analysis]
21 Young JL, Halley MC, Anguiano B, Fernandez L, Bernstein JA, Wheeler MT, Tabor HK; Undiagnosed Diseases Network Consortium. Beyond race: Recruitment of diverse participants in clinical genomics research for rare disease. Front Genet 2022;13:949422. [DOI: 10.3389/fgene.2022.949422] [Reference Citation Analysis]
22 Sperber NR, Cragun D, Roberts MC, Bendz LM, Ince P, Gonzales S, Haga SB, Wu RR, Petry NJ, Ramsey L, Uber R. A Mixed-Methods Protocol to Identify Best Practices for Implementing Pharmacogenetic Testing in Clinical Settings. JPM 2022;12:1313. [DOI: 10.3390/jpm12081313] [Reference Citation Analysis]
23 Blee AM, Li B, Pecen T, Meiler J, Nagel ZD, Capra JA, Chazin WJ. An Active Learning Framework Improves Tumor Variant Interpretation. Cancer Res 2022;82:2704-15. [PMID: 35687855 DOI: 10.1158/0008-5472.CAN-21-3798] [Reference Citation Analysis]
24 Roberts MC, Foss KS, Henderson GE, Powell SN, Saylor KW, Weck KE, Milko LV. Public Interest in Population Genetic Screening for Cancer Risk. Front Genet 2022;13:886640. [DOI: 10.3389/fgene.2022.886640] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
25 Shen EC, Srinivasan S, Passero LE, Allen CG, Dixon M, Foss K, Halliburton B, Milko LV, Smit AK, Carlson R, Roberts MC. Barriers and Facilitators for Population Genetic Screening in Healthy Populations: A Systematic Review. Front Genet 2022;13:865384. [DOI: 10.3389/fgene.2022.865384] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
26 Le Tourneau C, Perret C, Hackshaw A, Blay JY, Nabholz C, Geissler J, Do T, von Meyenn M, Dienstmann R. An Approach to Solving the Complex Clinicogenomic Data Landscape in Precision Oncology: Learnings From the Design of WAYFIND-R, a Global Precision Oncology Registry. JCO Precis Oncol 2022;6:e2200019. [PMID: 35939770 DOI: 10.1200/PO.22.00019] [Reference Citation Analysis]
27 Dolan DD, Lee SS, Cho MK. Three decades of ethical, legal, and social implications research: Looking back to chart a path forward. Cell Genomics 2022;2:100150. [DOI: 10.1016/j.xgen.2022.100150] [Reference Citation Analysis]
28 Shim JK, Bentz M, Vasquez E, Jeske M, Saperstein A, Fullerton SM, Foti N, McMahon C, Lee SS. Strategies of inclusion: The tradeoffs of pursuing "baked in" diversity through place-based recruitment. Soc Sci Med 2022;306:115132. [PMID: 35728460 DOI: 10.1016/j.socscimed.2022.115132] [Reference Citation Analysis]
29 Hanchard NA, Chahrour M, de Vries J. Tailored community engagement to address the genetics diversity gap. Med (N Y) 2022;3:369-70. [PMID: 35690058 DOI: 10.1016/j.medj.2022.05.010] [Reference Citation Analysis]
30 Murray MF, Khoury MJ, Abul-Husn NS. Addressing the routine failure to clinically identify monogenic cases of common disease. Genome Med 2022;14:60. [PMID: 35672798 DOI: 10.1186/s13073-022-01062-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
31 Bhat V, Adzhubei IA, Fife JD, Lebo M, Cassa CA. Resolving Discordant Variant Classifications using Clinical Guideline Evidence.. [DOI: 10.1101/2022.05.16.22275073] [Reference Citation Analysis]
32 Iregbu K, Dramowski A, Milton R, Nsutebu E, Howie SRC, Chakraborty M, Lavoie PM, Costelloe CE, Ghazal P. Global health systems' data science approach for precision diagnosis of sepsis in early life. Lancet Infect Dis 2022;22:e143-52. [PMID: 34914924 DOI: 10.1016/S1473-3099(21)00645-9] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
33 Borle K, Kopac N, Dragojlovic N, Rodriguez Llorian E, Friedman JM, Elliott AM, Lynd LD; GenCOUNSEL Study. Where is genetic medicine headed? Exploring the perspectives of Canadian genetic professionals on future trends using the Delphi method. Eur J Hum Genet 2022;30:496-504. [PMID: 35031678 DOI: 10.1038/s41431-021-01017-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
34 Makarious MB, Leonard HL, Vitale D, Iwaki H, Sargent L, Dadu A, Violich I, Hutchins E, Saffo D, Bandres-Ciga S, Kim JJ, Song Y, Maleknia M, Bookman M, Nojopranoto W, Campbell RH, Hashemi SH, Botia JA, Carter JF, Craig DW, Van Keuren-Jensen K, Morris HR, Hardy JA, Blauwendraat C, Singleton AB, Faghri F, Nalls MA. Multi-modality machine learning predicting Parkinson's disease. NPJ Parkinsons Dis 2022;8:35. [PMID: 35365675 DOI: 10.1038/s41531-022-00288-w] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
35 Merrill BD, Carter MM, Olm MR, Dahan D, Tripathi S, Spencer SP, Yu B, Jain S, Neff N, Jha AR, Sonnenburg ED, Sonnenburg JL. Ultra-deep Sequencing of Hadza Hunter-Gatherers Recovers Vanishing Microbes.. [DOI: 10.1101/2022.03.30.486478] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
36 Halley MC, Smith HS, Ashley EA, Goldenberg AJ, Tabor HK. A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States. Nat Genet. [DOI: 10.1038/s41588-022-01027-w] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
37 Luo L, Gribskov M, Wang S. Bibliometric review of ATAC-Seq and its application in gene expression. Brief Bioinform 2022:bbac061. [PMID: 35255493 DOI: 10.1093/bib/bbac061] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
38 Jeske M, Vasquez E, Fullerton SM, Saperstein A, Bentz M, Foti N, Shim JK, Lee SS. Beyond inclusion: Enacting team equity in precision medicine research. PLoS One 2022;17:e0263750. [PMID: 35130331 DOI: 10.1371/journal.pone.0263750] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
39 Tendi EA, Guarnaccia M, Morello G, Cavallaro S. The Utility of Genomic Testing for Hyperphenylalaninemia. J Clin Med 2022;11:1061. [PMID: 35207333 DOI: 10.3390/jcm11041061] [Reference Citation Analysis]
40 Schwab ME, Brown JEH, Lianoglou B, Jin C, Conroy PC, Gallagher RC, Harmatz P, Mackenzie TC. Fetal therapies and trials for lysosomal storage diseases: a survey of attitudes of parents and patients. Orphanet J Rare Dis 2022;17. [DOI: 10.1186/s13023-022-02178-z] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
41 Constantinescu A, Mitchell RE, Zheng J, Bull CJ, Timpson NJ, Amulic B, Vincent EE, Hughes DA. A framework for research into continental ancestry groups of the UK Biobank. Hum Genomics 2022;16. [DOI: 10.1186/s40246-022-00380-5] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
42 Rodriguez-Flores JL, Messai-Badji R, Robay A, Temanni R, Syed N, Markovic M, Al-Khayat E, Qafoud F, Nawaz Z, Badii R, Al-Sarraj Y, Mbarek H, Al-Muftah W, Alvi M, Rostami MR, Cruzado JCM, Mezey JG, Shakaki AA, Malek JA, Greenblatt MB, Fakhro KA, Machaca K, Al-Nabet A, Afifi N, Brooks A, Ismail SI, Althani A, Crystal RG. The QChip1 knowledgebase and microarray for precision medicine in Qatar. NPJ Genom Med 2022;7:3. [PMID: 35046417 DOI: 10.1038/s41525-021-00270-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
43 Park Y, West RA, Pathmendra P, Favier B, Stoeger T, Capes-Davis A, Cabanac G, Labbé C, Byrne JA. Identification of human gene research articles with wrongly identified nucleotide sequences. Life Sci Alliance 2022;5:e202101203. [PMID: 35022248 DOI: 10.26508/lsa.202101203] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
44 Duong D, Waikel RL, Hu P, Tekendo-Ngongang C, Solomon BD. Neural network classifiers for images of genetic conditions with cutaneous manifestations. HGG Adv 2022;3:100053. [PMID: 35047844 DOI: 10.1016/j.xhgg.2021.100053] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
45 Schatz MC, Philippakis AA, Afgan E, Banks E, Carey VJ, Carroll RJ, Culotti A, Ellrott K, Goecks J, Grossman RL, Hall IM, Hansen KD, Lawson J, Leek JT, Luria AO, Mosher S, Morgan M, Nekrutenko A, O'Connor BD, Osborn K, Paten B, Patterson C, Tan FJ, Taylor CO, Vessio J, Waldron L, Wang T, Wuichet K. Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space. Cell Genom 2022;2:100085. [PMID: 35199087 DOI: 10.1016/j.xgen.2021.100085] [Cited by in Crossref: 11] [Cited by in F6Publishing: 13] [Article Influence: 11.0] [Reference Citation Analysis]
46 Tanveer A, Yadav K, Dwivedi S, Gupta S, Yadav PK, Yadav D. Overview of healthcare biotechnology. Biotechnology in Healthcare, Volume 1 2022. [DOI: 10.1016/b978-0-323-89837-9.00003-6] [Reference Citation Analysis]
47 Awotunde JB, Adeniyi EA, Ajamu GJ, Balogun GB, Taofeek-ibrahim FA. Explainable Artificial Intelligence in Genomic Sequence for Healthcare Systems Prediction. Connected e-Health 2022. [DOI: 10.1007/978-3-030-97929-4_19] [Reference Citation Analysis]
48 Hurtado C. Medicina de precisión: conceptos, aplicaciones y proyecciones. Revista Médica Clínica Las Condes 2022;33:7-16. [DOI: 10.1016/j.rmclc.2022.01.002] [Reference Citation Analysis]
49 Boyce RD, Camacho J, Liang W, Wiisanen K, Devine B. Overview of effective pharmacogenomic clinical decision support. Clinical Decision Support for Pharmacogenomic Precision Medicine 2022. [DOI: 10.1016/b978-0-12-824453-1.00010-5] [Reference Citation Analysis]
50 Smith M. Benefits of the incorporation of genomic medicine in clinical practice. Progress in Genomic Medicine 2022. [DOI: 10.1016/b978-0-323-91547-2.00001-4] [Reference Citation Analysis]
51 Lally E, Laurino M. Role of the genetic counselor in pharmacogenomic precision medicine. Clinical Decision Support for Pharmacogenomic Precision Medicine 2022. [DOI: 10.1016/b978-0-12-824453-1.00004-x] [Reference Citation Analysis]
52 Calzone K, Tonkin E. Genomic education and training resources for nursing. Genomic Medicine Skills and Competencies 2022. [DOI: 10.1016/b978-0-323-98383-9.00005-9] [Reference Citation Analysis]
53 Johnston JR, McNally EM. Genetic correction strategies for Duchenne Muscular Dystrophy and their impact on the heart. Prog Pediatr Cardiol 2021;63:101460. [PMID: 34898968 DOI: 10.1016/j.ppedcard.2021.101460] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
54 Byeon YJJ, Islamaj R, Yeganova L, Wilbur WJ, Lu Z, Brody LC, Bonham VL. Evolving use of ancestry, ethnicity, and race in genetics research-A survey spanning seven decades. Am J Hum Genet 2021;108:2215-23. [PMID: 34861173 DOI: 10.1016/j.ajhg.2021.10.008] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
55 Abou Tayoun AN, Fakhro KA, Alsheikh-Ali A, Alkuraya FS. Genomic medicine in the Middle East. Genome Med 2021;13:184. [PMID: 34814937 DOI: 10.1186/s13073-021-01003-9] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
56 Lange KI, Best S, Tsiropoulou S, Berry I, Johnson CA, Blacque OE. Interpreting ciliopathy-associated missense variants of uncertain significance (VUS) in Caenorhabditis elegans. Human Molecular Genetics 2021. [DOI: 10.1093/hmg/ddab344] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
57 Muenke M, Blitzer MG. Become an ambassador to recruit the next generation in genomic medicine. Genet Med 2021:S1098-3600(21)01115-1. [PMID: 34906451 DOI: 10.1016/j.gim.2021.08.001] [Reference Citation Analysis]
58 . The Road to Greater Diversity in the Genomics Workforce. Am J Med Genet A 2021;185:3527-8. [PMID: 34784114 DOI: 10.1002/ajmg.a.61712] [Reference Citation Analysis]
59 Norstad M, Outram S, Brown JEH, Zamora AN, Koenig BA, Risch N, Norton ME, Slavotinek A, Ackerman SL. The difficulties of broad data sharing in genomic medicine: Empirical evidence from diverse participants in prenatal and pediatric clinical genomics research. Genet Med 2021:S1098-3600(21)05349-1. [PMID: 34906477 DOI: 10.1016/j.gim.2021.09.021] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
60 Blee AM, Li B, Pecen T, Meiler J, Nagel ZD, Capra JA, Chazin WJ. An active learning framework improves tumor variant interpretation.. [DOI: 10.1101/2021.11.08.467747] [Reference Citation Analysis]
61 Kamariza M, Crawford L, Jones D, Finucane H. Misuse of the term 'trans-ethnic' in genomics research. Nat Genet 2021;53:1520-1. [PMID: 34741159 DOI: 10.1038/s41588-021-00952-6] [Reference Citation Analysis]
62 Aldrighetti CM, Niemierko A, Van Allen E, Willers H, Kamran SC. Racial and Ethnic Disparities Among Participants in Precision Oncology Clinical Studies. JAMA Netw Open 2021;4:e2133205. [PMID: 34748007 DOI: 10.1001/jamanetworkopen.2021.33205] [Cited by in Crossref: 14] [Cited by in F6Publishing: 18] [Article Influence: 14.0] [Reference Citation Analysis]
63 Millet L, Jeon H, Kim B, Bhoi B, Kim S. Reservoir computing using photon-magnon coupling. Appl Phys Lett 2021;119:182405. [DOI: 10.1063/5.0061429] [Reference Citation Analysis]
64 Herbst K, Juvekar S, Jasseh M, Berhane Y, Chuc NTK, Seeley J, Sankoh O, Clark SJ, Collinson MA. Health and demographic surveillance systems in low- and middle-income countries: history, state of the art and future prospects. Glob Health Action 2021;14:1974676. [PMID: 35377288 DOI: 10.1080/16549716.2021.1974676] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
65 Litvinov DY, Karlov GI, Divashuk MG. Metabolomics for Crop Breeding: General Considerations. Genes (Basel) 2021;12:1602. [PMID: 34680996 DOI: 10.3390/genes12101602] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
66 Solomon BD. Can artificial intelligence save medical genetics? Am J Med Genet A 2021. [PMID: 34633139 DOI: 10.1002/ajmg.a.62538] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
67 Ginsburg G, Penny M, Feero WG, Miller M, Addie S, Beachy SH. The National Academies' Roundtable on Genomics and Precision Health: Where we have been and where we are heading. Am J Hum Genet 2021;108:1817-22. [PMID: 34626581 DOI: 10.1016/j.ajhg.2021.08.015] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
68 Vega DM, Yee LM, McShane LM, Williams PM, Chen L, Vilimas T, Fabrizio D, Funari V, Newberg J, Bruce LK, Chen SJ, Baden J, Carl Barrett J, Beer P, Butler M, Cheng JH, Conroy J, Cyanam D, Eyring K, Garcia E, Green G, Gregersen VR, Hellmann MD, Keefer LA, Lasiter L, Lazar AJ, Li MC, MacConaill LE, Meier K, Mellert H, Pabla S, Pallavajjalla A, Pestano G, Salgado R, Samara R, Sokol ES, Stafford P, Budczies J, Stenzinger A, Tom W, Valkenburg KC, Wang XZ, Weigman V, Xie M, Xie Q, Zehir A, Zhao C, Zhao Y, Stewart MD, Allen J; TMB Consortium. Aligning tumor mutational burden (TMB) quantification across diagnostic platforms: phase II of the Friends of Cancer Research TMB Harmonization Project. Ann Oncol 2021;32:1626-36. [PMID: 34606929 DOI: 10.1016/j.annonc.2021.09.016] [Cited by in Crossref: 27] [Cited by in F6Publishing: 30] [Article Influence: 27.0] [Reference Citation Analysis]
69 Law WK, Yaremych HE, Ferrer RA, Richardson E, Wu YP, Turbitt E. Decision-making about genetic health information among family dyads: a systematic literature review. Health Psychol Rev 2021;:1-18. [PMID: 34546151 DOI: 10.1080/17437199.2021.1980083] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
70 Landi I, Kaji DA, Cotter L, Van Vleck T, Belbin G, Preuss M, Loos RJF, Kenny E, Glicksberg BS, Beckmann ND, O'Reilly P, Schadt EE, Achtyes ED, Buckley PF, Lehrer D, Malaspina DP, McCarroll SA, Rapaport MH, Fanous AH, Pato MT, Pato CN, Bigdeli TB, Nadkarni GN, Charney AW. Prognostic value of polygenic risk scores for adults with psychosis. Nat Med 2021;27:1576-81. [PMID: 34489608 DOI: 10.1038/s41591-021-01475-7] [Cited by in Crossref: 13] [Cited by in F6Publishing: 16] [Article Influence: 13.0] [Reference Citation Analysis]
71 Clarke SL, Assimes TL, Tcheandjieu C. The Propagation of Racial Disparities in Cardiovascular Genomics Research. Circ Genom Precis Med 2021;14:e003178. [PMID: 34461749 DOI: 10.1161/CIRCGEN.121.003178] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
72 Cheung NYC, Fung JLF, Ng YNC, Wong WHS, Chung CCY, Mak CCY, Chung BHY. Perception of personalized medicine, pharmacogenomics, and genetic testing among undergraduates in Hong Kong. Hum Genomics 2021;15:54. [PMID: 34407885 DOI: 10.1186/s40246-021-00353-0] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
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