Katherine Johnson to Phenotype
This is a "connection" page, showing publications Katherine Johnson has written about Phenotype.
Connection Strength
0.205
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Johnson K, Bertoli M, Phillips L, T?pf A, Van den Bergh P, Vissing J, Witting N, Nafissi S, Jamal-Omidi S, Lusakowska A, Kostera-Pruszczyk A, Potulska-Chromik A, Deconinck N, Wallgren-Pettersson C, Strang-Karlsson S, Colomer J, Claeys KG, De Ridder W, Baets J, von der Hagen M, Fern?ndez-Torr?n R, Zulaica Ijurco M, Espinal Valencia JB, Hahn A, Durmus H, Willis T, Xu L, Valkanas E, Mullen TE, Lek M, MacArthur DG, Straub V. Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness. Skelet Muscle. 2018 07 30; 8(1):23.
Score: 0.106
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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.
Score: 0.045
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Becker LL, Dafsari HS, Schallner J, Abdin D, Seifert M, Petit F, Smol T, Bok L, Rodan L, Krapels I, Spranger S, Weschke B, Johnson K, Straub V, Kaindl AM, Di Donato N, von der Hagen M, Cirak S. The clinical-phenotype continuum in DYNC1H1-related disorders-genomic profiling and proposal for a novel classification. J Hum Genet. 2020 Nov; 65(11):1003-1017.
Score: 0.030
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Peric S, Glumac JN, T?pf A, Savic-Pavicevic D, Phillips L, Johnson K, Cassop-Thompson M, Xu L, Bertoli M, Lek M, MacArthur D, Brku?anin M, Milenkovic S, Ra?ic VM, Banko B, Maksimovic R, Lochm?ller H, Stojanovic VR, Straub V. A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population. Eur J Hum Genet. 2017 05; 25(5):572-581.
Score: 0.024