Header Logo

Connection

Katherine Johnson to Middle Aged

This is a "connection" page, showing publications Katherine Johnson has written about Middle Aged.
Connection Strength

0.245
  1. 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.
    View in: PubMed
    Score: 0.044
  2. Johnson K, De Ridder W, T?pf A, Bertoli M, Phillips L, De Jonghe P, Baets J, Deconinck T, Rakocevic Stojanovic V, Peric S, Durmus H, Jamal-Omidi S, Nafissi S, Mongini T, Lusakowska A, Busby M, Miller J, Norwood F, Hudson J, Barresi R, Lek M, MacArthur DG, Straub V. Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population. J Neurol Neurosurg Psychiatry. 2019 04; 90(4):490-493.
    View in: PubMed
    Score: 0.043
  3. Johnson K, T?pf A, Bertoli M, Phillips L, Claeys KG, Stojanovic VR, Peric S, Hahn A, Maddison P, Akay E, Bastian AE, Lusakowska A, Kostera-Pruszczyk A, Lek M, Xu L, MacArthur DG, Straub V. Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness. Orphanet J Rare Dis. 2017 11 17; 12(1):173.
    View in: PubMed
    Score: 0.042
  4. Johnson KM, Fledderjohann J. Revisiting "her" infertility: medicalized embodiment, self-identification and distress. Soc Sci Med. 2012 Sep; 75(5):883-91.
    View in: PubMed
    Score: 0.028
  5. K?lbel H, Roos A, van der Ven PFM, Evangelista T, Nolte K, Johnson K, T?pf A, Wilson M, Kress W, Sickmann A, Straub V, Kollipara L, Weis J, F?rst DO, Schara U. First clinical and myopathological description of a myofibrillar myopathy with congenital onset and homozygous mutation in FLNC. Hum Mutat. 2020 09; 41(9):1600-1614.
    View in: PubMed
    Score: 0.012
  6. Modest AM, Johnson KM, Karumanchi SA, Resetkova N, Young BC, Fox MP, Wise LA, Hacker MR. Risk of ischemic placental disease is increased following in vitro fertilization with oocyte donation: a retrospective cohort study. J Assist Reprod Genet. 2019 Sep; 36(9):1917-1926.
    View in: PubMed
    Score: 0.012
  7. Mul K, Lemmers RJLF, Kriek M, van der Vliet PJ, van den Boogaard ML, Badrising UA, Graham JM, Lin AE, Brand H, Moore SA, Johnson K, Evangelista T, T?pf A, Straub V, Kapetanovic Garc?a S, Sacconi S, Tawil R, Tapscott SJ, Voermans NC, van Engelen BGM, Horlings CGC, Shaw ND, van der Maarel SM. FSHD type 2 and Bosma arhinia microphthalmia syndrome: Two faces of the same mutation. Neurology. 2018 08 07; 91(6):e562-e570.
    View in: PubMed
    Score: 0.011
  8. ?stergaard ST, Johnson K, Stojkovic T, Krag T, De Ridder W, De Jonghe P, Baets J, Claeys KG, Fern?ndez-Torr?n R, Phillips L, Topf A, Colomer J, Nafissi S, Jamal-Omidi S, Bouchet-Seraphin C, Leturcq F, MacArthur DG, Lek M, Xu L, Nelson I, Straub V, Vissing J. Limb girdle muscular dystrophy due to mutations in POMT2. J Neurol Neurosurg Psychiatry. 2018 05; 89(5):506-512.
    View in: PubMed
    Score: 0.010
  9. 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.
    View in: PubMed
    Score: 0.010
  10. Greil AL, Slauson-Blevins KS, Shreffler KM, Johnson KM, Lowry MH, Burch AR, McQuillan J. Decline in ethical concerns about reproductive technologies among a representative sample of US women. Public Underst Sci. 2017 10; 26(7):789-805.
    View in: PubMed
    Score: 0.009
  11. Greil AL, McQuillan J, Shreffler KM, Johnson KM, Slauson-Blevins KS. Race-ethnicity and medical services for infertility: stratified reproduction in a population-based sample of U.S. women. J Health Soc Behav. 2011 Dec; 52(4):493-509.
    View in: PubMed
    Score: 0.007
  12. Greil AL, Johnson KM, McQuillan J, Lacy N. Are prior pregnancy outcomes relevant for models of fertility-specific distress or infertility helpseeking? Hum Fertil (Camb). 2011 Sep; 14(3):160-6.
    View in: PubMed
    Score: 0.007
  13. Greil A, McQuillan J, Benjamins M, Johnson DR, Johnson KM, Heinz CR. Specifying the effects of religion on medical helpseeking: the case of infertility. Soc Sci Med. 2010 Aug; 71(4):734-42.
    View in: PubMed
    Score: 0.006
  14. King M, McKeown E, Warner J, Ramsay A, Johnson K, Cort C, Wright L, Blizard R, Davidson O. Mental health and quality of life of gay men and lesbians in England and Wales: controlled, cross-sectional study. Br J Psychiatry. 2003 Dec; 183:552-8.
    View in: PubMed
    Score: 0.004
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.