Below are the most recent publications written about "Genetic Variation" by people in Profiles.
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Bendall EE, Fitzsimmons WJ, Valvano WD, Truscon R, Self WH, Halasa N, Chappell JD, Zhu Y, Safdar B, Ginde AA, Peltan ID, Gaglani M, Columbus C, Shapiro NI, Gibbs KW, Hager DN, Prekker ME, Mohamed A, Johnson NJ, Steingrub JS, Khan A, Duggal A, Wilson JG, Qadir N, Busse LW, Kwon JH, Exline MC, Vaughn IA, Mosier JM, Harris ES, Dawood FS, Ma KC, Surie D, Monto AS, Martin ET, Lauring AS. Genomic Surveillance of Human Metapneumovirus in the United States, 2010-2025. J Infect Dis. 2026 Sep 23; 234(3):e556-e565.
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Tran TCG, Than TT, Lai TNH, Le HD, Nguyen TT, Vu ND, Ngo NBA, Nguyen HT, Nguyen PA, Goonewardene K, Ambagala A, Le VP. Emergence of Non-Hemadsorbing African Swine Fever Virus Genotype II Variants and the Evolution of a Vaccine-Derived Strain in Vietnam. Viruses. 2026 May 26; 18(6).
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Popkin-Hall ZR, Carey-Ewend K, Aghakhanian F, Oriero EC, Seth MD, Kashamuka MM, Ngasala B, Ali IM, Mukomena ES, Mandara CI, Kharabora O, Sendor R, Simkin A, Amambua-Ngwa A, Tshefu A, Fola AA, Ishengoma DS, Bailey JA, Parr JB, Lin JT, Juliano JJ. Population genomics of Plasmodium malariae from 4 African countries. JCI Insight. 2026 06 22; 11(12).
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Hop PJ, Kooyman M, Kenna BJ, Zwamborn RAJ, van Eijk KR, Wang Y, van Dijk CH, Bekema E, van Rheenen W, Beele P, van Vugt JJFA, Khleifat AA, Iacoangeli A, Cooper-Knock J, Smith BN, Topp S, van der Kooi AJ, Fominykh V, Drory V, Lerner Y, Shovman Y, Rowe DB, Williams KL, McLaughlin RL, Hurt J, Huang Y, Chen CY, Tsai E, Runz H, Aronica E, Groen EJN, van Es MA, Pasterkamp RJ, Farhan SMK, Garton FC, McRae AF, McCombe PA, Henderson RD, Fan D, Šlachtová L, Høyer H, Nishimura AL, Cauchi RJ, Brylev L, Rogelj B, Koritnik B, Zidar J, Salas T, Mora Pardina JS, Gotkine M, Povedano M, Corcia P, Vourc'h P, Couratier P, Weber M, Kiernan MC, Pamphlett R, Blair IP, de Carvalho M, Ba?ak NA, Ingre C, Andersen PM, Zinman L, Rogaeva E, MacKenzie IR, Dupre N, Rouleau GA, Traynor BJ, Ticozzi N, Chiò A, Silani V, Hardiman O, Phatnani H, Harms MB, Dalgard CL, Glass JD, Landers JE, Van Damme P, Morrison KE, Shaw PJ, Shaw CE, Al-Chalabi A, van den Berg LH, Kenna KP, Veldink JH. Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. Nat Genet. 2026 Apr; 58(4):717-725.
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Morris GP, Harder AM, Healey AL, McLaughlin CM, Rifkin JL, Cruet-Burgos C, Jenkins JW, Shu S, Spiekerman JJ, VanGessel CJ, Agnew E, Audebert A, Barry K, Baxter I, Beurier G, Boston LB, Boyles RE, Brady SM, Bunting V, Chaparro JM, Courtney C, Dembele JSB, Deshpande S, Diatta C, Eck N, Eveland AL, Faye JM, Flowers D, Fonceka D, Gano B, de Gracia Coquerel M, Goodstein D, Grimwood J, Hudson ME, Kholova J, Johnson K, Johnson KK, Kawa D, Kouressy M, Kresovich S, Lee S, Lemaux PG, Lowery R, Luquet D, Maina F, Mamidi S, McKay JK, Michael TP, Mindaye TT, Mullet J, Ozersky P, Plott C, Prenni JE, Pressoir G, Rami JF, Rife TW, Saxton J, Sine B, Sreedasyam A, Talag J, Teme N, Tuinstra MR, Vadez V, Vogel JP, Walstead R, Wang J, Webber J, Williams M, Xu Y, Mockler TC, Lasky JR, Rice BR, Schmutz J, Shakoor N, Lovell JT. A sorghum pangenome reference improves global crop trait discovery. Nature. 2026 Apr; 652(8112):1245-1253.
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Batté A, Bosch-Guiteras N, Pons C, Ota M, Lopes M, Sharma S, Tellini N, Paltenghi C, Conti M, Kan KT, Ho UL, Wiederkehr M, Barraud J, Ashe M, Aloy P, Liti G, Chabes A, Parts L, van Leeuwen J. The modifiers that cause changes in gene essentiality. Cell Syst. 2026 Apr 15; 17(4):101515.
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Titus MK, Giesbrecht D, Oduor CI, Muthoka K, Niaré K, Crudale R, Fola AA, Hui ST, Kim IE, Tonui PK, Itsura PM, Tonui R, Moormann AM, Loehrer PJ, Brown DR, Orang'o OE, Cu-Uvin S, Ermel AC, Katzenellenbogen RA, Bailey JA. Scalable long-read nanopore HPV16 amplicon-based whole-genome sequencing. Sci Rep. 2025 Oct 07; 15(1):34892.
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Alonso-González A, Jáspez D, Lorenzo-Salazar JM, Ma SF, Strickland E, Mychaleckyj J, Kim JS, Huang Y, Adegunsoye A, Oldham JM, Stewart I, Molyneaux PL, Maher TM, Wain LV, Allen RJ, Gisli Jenkins R, Kropski JA, Yaspan B, Blackwell TS, Zhang D, Garcia CK, Martinez FJ, Noth I, Flores C. Rare variants and survival of patients with idiopathic pulmonary fibrosis: analysis of a multicentre, observational cohort study with independent validation. Lancet Respir Med. 2025 Jun; 13(6):495-504.
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Wang D, Scalici A, Wang Y, Lin H, Pitsillides A, Heard-Costa N, Cruchaga C, Ziegemeier E, Bis JC, Fornage M, Boerwinkle E, De Jager PL, Wijsman E, Dupuis J, Renton AE, Seshadri S, Goate AM, DeStefano AL, Peloso GM. Frequency of variants in Mendelian Alzheimer's disease genes within the Alzheimer's Disease Sequencing Project. J Alzheimers Dis. 2025 Apr; 104(3):841-851.
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Choi SH, Jurgens SJ, Xiao L, Hill MC, Haggerty CM, Sveinbjörnsson G, Morrill VN, Marston NA, Weng LC, Pirruccello JP, Arnar DO, Gudbjartsson DF, Mantineo H, von Falkenhausen AS, Natale A, Tveit A, Geelhoed B, Roselli C, Van Wagoner DR, Darbar D, Haase D, Soliman EZ, Davogustto GE, Jun G, Calkins H, Anderson JL, Brody JA, Halford JL, Barnard J, Hokanson JE, Smith JD, Bis JC, Young K, Johnson LSB, Risch L, Gula LJ, Kwee LC, Chaffin MD, Kühne M, Preuss M, Gupta N, Nafissi NA, Smith NL, Nilsson PM, van der Harst P, Wells QS, Judy RL, Schnabel RB, Johnson R, Smit RAJ, Gabriel S, Knight S, Furukawa T, Blackwell TW, Nauffal V, Wang X, Min YI, Yoneda ZT, Laksman ZWM, Bezzina CR, Alonso A, Psaty BM, Albert CM, Arking DE, Roden DM, Chasman DI, Rader DJ, Conen D, McManus DD, Fatkin D, Benjamin EJ, Boerwinkle E, Marcus GM, Christophersen IE, Smith JG, Roberts JD, Raffield LM, Shoemaker MB, Cho MH, Cutler MJ, Rienstra M, Chung MK, S Olesen M, Sinner MF, Sotoodehnia N, Kirchhof P, Loos RJF, Nazarian S, Mohanty S, Damrauer SM, Kaab S, Heckbert SR, Redline S, Shah SH, Tanaka T, Ebana Y, Holm H, Stefansson K, Ruff CT, Sabatine MS, Lunetta KL, Lubitz SA, Ellinor PT. Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk. Nat Genet. 2025 Mar; 57(3):548-562.