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Karen Knapp

university of exeter

31H指数
191论文数
3.0K被引数
收录论文 28
发表时间
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Professional challenges faced by student radiographers during COVID-19COVID-19期间放射学学生面临的职业挑战
err2025-06-11
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errJ.P. McNulty; M. Zanardo; C. Buissink; R. DeCoster; W. Hennessy; K. Knapp; B. Kraus; L. Lanca; S. Lewis; B. Mahlaola Tintswalo; M. McEntee; D. O'Leary; H. Precht; T. Starc; L.A. Rainford
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Bone Mineral Density, Bone Biomarkers, and Joints in Acute, Post, and Long COVID-19: A Systematic Review
err2024-10-30
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errAlghamdi, Fahad; Mokbel, Kinan; Meertens, Robert; Obotiba, Abasiama Dick; Alharbi, Mansour; Knapp, Karen M.; Strain, William David
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Hemochromatosis Genetic Variants and Musculoskeletal Outcomes: 11.5-Year Follow-Up in the UK Biobank Cohort Study
err2023-07-18
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errBanfield, Lucy R.; Knapp, Karen M.; Pilling, Luke C.; Melzer, David; Atkins, Janice L.
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Vegan and Omnivorous High Protein Diets Support Comparable Daily Myofibrillar Protein Synthesis Rates and Skeletal Muscle Hypertrophy in Young Adults纯素和杂食性高蛋白饮食支持年轻人的每日肌原纤维蛋白合成率和骨骼肌肥大
err2023-06-01
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errMonteyne, Alistair J.; Coelho, Mariana O. C.; Murton, Andrew J.; Abdelrahman, Doaa R.; Blackwell, Jamie R.; Koscien, Christopher P.; Knapp, Karen M.; Fulford, Jonathan; Finnigan, Tim J. A.; Dirks, Marlou L.; Stephens, Francis B.; Wall, Benjamin T.
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Histones: coming of age in Mendelian genetic disorders
err2023-01-23
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PREAI
errKnapp, Karen; Naik, Nihar; Ray, Sankalita; van Haaften, Gijs; Bicknell, Louise S.
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The principles and effectiveness of X-ray scatter correction software for diagnostic X-ray imaging: A scoping review
err2023-01-01
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errSayed, Mohammad; Knapp, Karen M.; Fulford, Jon; Heales, Christine; Alqahtani, Saeed J.
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The biomechanics of metaphyseal cone augmentation in revision knee replacement
err2022-07-01
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errHu, Jingrui; Gundry, Michael; Zheng, Keke; Zhong, Jingxiao; Hourigan, Patrick; Meakin, Judith R.; Winlove, C. Peter; Toms, Andrew D.; Knapp, Karen M.; Chen, Junning
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Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome
err2022-04-01
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errTessadori, Federico; Duran, Karen; Knapp, Karen; Fellner, Matthias; Smithson, Sarah; Meireles, Ana Beleza; Elting, Mariet W.; Waisfisz, Quinten; O'Donnell-Luria, Anne; Nowak, Catherine; Douglas, Jessica; Ronan, Anne; Brunet, Theresa; Kotzaeridou, Urania; Svihovec, Shayna; Saenz, Margarita S.; Thiffault, Isabelle; Del Viso, Florencia; Devine, Patrick; Rego, Shannon; Tenney, Jessica; van Haeringen, Arie; Ruivenkamp, Claudia A. L.; Koene, Saskia; Robertson, Stephen P.; Deshpande, Charulata; Pfundt, Rolph; Verbeek, Nienke; van de Kamp, Jiddeke M.; Weiss, Janneke M. M.; Ruiz, Anna; Gabau, Elisabeth; Banne, Ehud; Pepler, Alexander; Bottani, Armand; Laurent, Sacha; Guipponi, Michel; Bijlsma, Emilia; Bruel, Ange-Line; Sorlin, Arthur; Willis, Mary; Powis, Zoe; Smol, Thomas; Vincent-Delorme, Catherine; Baralle, Diana; Colin, Estelle; Revencu, Nicole; Calpena, Eduardo; Wilkie, Andrew O. M.; Chopra, Maya; Cormier-Daire, Valerie; Keren, Boris; Afenjar, Alexandra; Niceta, Marcello; Terracciano, Alessandra; Specchio, Nicola; Tartaglia, Marco; Rio, Marlene; Barcia, Giulia; Rondeau, Sophie; Colson, Cindy; Bakkers, Jeroen; Mace, Peter D.; Bicknell, Louise S.; van Haaften, Gijs
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In vivo Measurement of Intraosseous Vascular Haemodynamic Markers in Human Bone Tissue Utilising Near Infrared Spectroscopy
err2021-09-24
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errMeertens, Robert; Knapp, Karen M.; Strain, William David; Casanova, Francesco; Ball, Susan; Fulford, Jon; Thorn, Clare
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MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency
err2021-03-02
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errKnapp, Karen M.; Jenkins, Danielle E.; Sullivan, Rosie; Harms, Frederike L.; von Elsner, Leonie; Ockeloen, Charlotte W.; de Munnik, Sonja; Bongers, Ernie M. H. F.; Murray, Jennie; Pachter, Nicholas; Denecke, Jonas; Kutsche, Kerstin; Bicknell, Louise S.
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Pathogenic variants causing ABL1 malformation syndrome cluster in a myristoyl-binding pocket and increase tyrosine kinase activity
err2020-11-22
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errBlakes, Alexander J. M.; Gaul, Emily; Lam, Wayne; Shannon, Nora; Knapp, Karen M.; Bicknell, Louise S.; Jackson, Meremaihi R.; Wade, Emma M.; Robertson, Stephen; White, Susan M.; Heller, Raoul; Chase, Andrew; Baralle, Diana; Douglas, Andrew G. L.
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Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome
err2019-11-29
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errKnapp, Karen M.; Sullivan, Rosie; Murray, Jennie; Gimenez, Gregory; Arn, Pamela; D'Souza, Precilla; Gezdirici, Alper; Wilson, William G.; Jackson, Andrew P.; Ferreira, Carlos; Bicknell, Louise S.
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