Below are the most recent publications written about "Phenotype" by people in Profiles.
-
Voronina EN, Sokolova EA, Tromenschleger IN, Mishukova OV, Fedorets VA, Khlistun IV, Savenkov OA, Saprikin OI, Buyanova MD, Filippova IM, Glukhova MA, Rogaev EI, Zhohova LV, Manakhov AD, Smirnova NV. Two Bacillus PGPB Strains in Wheat and Soybean: Wheat Growth Promotion Without Detectable Rhizosphere Microbiome Restructuring. Int J Mol Sci. 2026 Sep 03; 27(17).
-
Gill ME, Jogdand A, Schissel C, Ong MS, Barmettler S, Farmer JR. Advances in the Phenotyping and Management of Common Variable Immunodeficiency. Immunol Allergy Clin North Am. 2026 Nov; 46(4):699-721.
-
Prince N, Chen J, Kaur R, Syphurs C, Hoch A, Angelidou A, McEnaney K, Chawes B, Bæk O, Wang T, Brustad N, Levy O, Diray-Arce J, Pichichero M, Lasky-Su JA. Plasma metabolomics in infancy reveals early signatures of a stringently-defined otitis-prone phenotype. Pediatr Allergy Immunol. 2026 Aug; 37(8):e70428.
-
Fluri R, Coll-Tané M, Brunet T, Cogne B, Conrad S, Nizon M, Nicita F, Travaglini L, Novelli A, Glissmeyer M, Peterson A, Buchan JG, Serber D, Meier K, Gärtner J, Diegmann S, Pingault V, Attie-Bitach T, Courtin T, Schneider MC, Hung W, Sahai I, O'Grady L, Steindl K, Mehta SG, Depienne C, Heron D, Keren B, Heide S, McKee S, Laccone F, Dyer LM, Melver C, Motter C, Jones WD, Wilson ZT, Vats D, Huß K, Zweier C, Sticht H, Gregor A. De novo variants in LDB1 are linked to distinct neurodevelopmental phenotypes determined by variant location and differing pathomechanisms. Am J Hum Genet. 2026 Jul 02; 113(7):1543-1557.
-
Bledsoe JR, Ferry JA, Li J, Sassoon A, Stonhill MA, Siegele B, Liang X, Dalton J, Mochel MC, Ivashkevich Y, Johari V, Sadigh S, Selove W, Sood S, Ward N, Woda B, Degar B, Feraco AM, Rowe J, Davies K, Al-Ibraheemi A, Amador C, Kovach AE, Fleming MD, Harris MH, Tsai HK. Recurrent SWI/SNF Deficiency Defines a Subset of Peripheral T-Cell Lymphoma With Distinct Clinicopathologic Features. Mod Pathol. 2026 07; 39(7):101015.
-
Guertin TM, Sisson C, Gargiulo RM, Macrorie O, Pease EL, Garth HE, Vriens J, De Clercq K, Mager J, Tremblay KD. Onset of embryonic and placental defects coincide in 19 of 22 novel mid-gestation lethal murine knockout lines. Development. 2026 05 15; 153(10).
-
Fleck RC, Gorodyna O, Zhou H, Bryant H, Gadjeva M, Shea AE. Emerging pathogens in urinary tract infections: virulence and phenotypic characterization of Pseudomonas aeruginosa strains. mSphere. 2026 Jun 30; 11(6):e0015126.
-
Robles-Bolivar P, Bächinger D, Bose A, Ramirez K, Brown A, Juliano AF, Lopez-Escamez JA, Kujawa SG, Liu ES, Amr SS, Rauch SD, Eckhard AH, Chari DA. Association of PHEX Gene Dosage With Meniere Disease and Related Audiovestibular Phenotypes in X-Linked Hypophosphatemia. JAMA Otolaryngol Head Neck Surg. 2026 05 01; 152(5):452-464.
-
Dumas A, Hokayem J, Goodman G, Venkatasubramanian K, Chai P. Smartphone-Based Digital Phenotyping Across Health Conditions: Scoping Review. J Med Internet Res. 2026 Mar 24; 28:e84146.
-
Galambos NS, Crocker OJ, Schneider BK, Allerton KS, Gross KE, Schneider AE, Lynch J, Yukselen O, Kucukural A, Conine CC. tRNA-derived RNA processing in sperm transmits non-genetically inherited phenotypes to offspring in C. elegans. Nat Commun. 2026 Mar 15; 17(1).