A 3D basicranial shape-based assessment of local and continental northwest European ancestry among 5th to 9th century CE Anglo-Saxons von Plomp, Kimberly A., Dobney, Keith, Collard, Mark

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The composition of the founding population of Iceland: A new perspective from 3D analyses of basicranial shape von Plomp, Kimberly A, Gestsdóttir, Hildur, Dobney, Keith, Price, Neil, Collard, Mark

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On the Nature of Oxygen-Containing Surface Groups on Carbon Nanofibers and Their Role for Platinum DepositionAn XPS and Titration Study von Plomp, A. J, Su, D. S, Jong, K. P. de, Bitter, J. H

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3D shape analyses of extant primate and fossil hominin vertebrae support the ancestral shape hypothesis for intervertebral disc herniation von Plomp, Kimberly A, Dobney, Keith, Weston, Darlene A, Strand Viðarsdóttir, Una, Collard, Mark

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Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolv... von Velde, Hedwig M., Vaseghi-Shanjani, Maryam, Smits, Jeroen J., Ramakrishnan, Gayatri, Oostrik, Jaap, Wesdorp, Mieke, Astuti, Galuh, Yntema, Helger G., Hoefsloot, Lies, Lanting, Cris P., Huynen, Martijn A., Lehman, Anna, Turvey, Stuart E., Pennings, Ronald J. E., Kremer, Hannie

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Development, behaviour and sensory processing in Marshall–Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes von Mulder, P. A., Balkom, I. D. C., Landlust, A. M., Priolo, M., Menke, L. A., Acero, I. H., Alkuraya, F. S., Arias, P., Bernardini, L., Bijlsma, E. K., Cole, T., Coubes, C., Dapia, I., Davies, S., Di Donato, N., Elcioglu, N. H., Fahrner, J. A., Foster, A., González, N. G., Huber, I., Iascone, M., Kaiser, A.‐S., Kamath, A., Kooblall, K., Lapunzina, P., Liebelt, J., Lynch, S. A., Maas, S. M., Mammì, C., Mathijssen, I. B., McKee, S., Mirzaa, G. M., Montgomery, T., Neubauer, D., Neumann, T. E., Pintomalli, L., Pisanti, M. A., Plomp, A. S., Price, S., Salter, C., Santos‐Simarro, F., Sarda, P., Schanze, D., Segovia, M., Shaw‐Smith, C., Smithson, S., Suri, M., Tatton‐Brown, K., Tenorio, J., Thakker, R. V., Valdez, R. M., Van Haeringen, A., Van Hagen, J. M., Zenker, M., Zollino, M., Dunn, W. W., Piening, S., Hennekam, R. C.

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Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant von Smits, Jeroen J., de Bruijn, Suzanne E., Lanting, Cornelis P., Oostrik, Jaap, O’Gorman, Luke, Mantere, Tuomo, Cremers, Frans P. M., Roosing, Susanne, Yntema, Helger G., de Vrieze, Erik, Derks, Ronny, Hoischen, Alexander, Pegge, Sjoert A. H., Neveling, Kornelia, Pennings, Ronald J. E., Kremer, Hannie

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Catalysts based on platinum–tin and platinum–gallium in close contact for the selective hydrogenation of cinnamaldehyde von Plomp, A.J., van Asten, D.M.P., van der Eerden, A.M.J., Mäki-Arvela, P., Murzin, D.Yu, de Jong, K.P., Bitter, J.H.

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Pathogenic neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq von Koster, R., Brandão, R. D., Tserpelis, D., van Roozendaal, C. E. P., van Oosterhoud, C. N., Claes, K. B. M., Paulussen, A. D. C., Sinnema, M., Vreeburg, M., van der Schoot, V., Stumpel, C. T. R. M., Broen, M. P. G., Spruijt, L., Jongmans, M. C. J., Lesnik Oberstein, S. A. J., Plomp, A. S., Misra-Isrie, M., Duijkers, F. A., Louwers, M. J., Szklarczyk, R., Derks, K. W. J., Brunner, H. G., van den Wijngaard, A., van Geel, M., Blok, M. J.

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Mixed ancestry of Europeans who settled Iceland and Greenland: 3D geometric-morphometric analyses of cranial base shape von Plomp, Kimberly A., Dobney, Keith, Gestsdóttir, Hildur, Collard, Mark

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Behaviour in Our Bones: How Human Behaviour Influences Skeletal Morphology von Hirst, Cara S, Gilmour, Rebecca J, Cardoso, Francisca Alves, Plomp, Kimberly A

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Mutations in ABCC6 cause pseudoxanthoma elasticum von Bergen, Arthur A.B, Plomp, Astrid S, Schuurman, Ellen J, Terry, Sharon, Breuning, Martijn, Dauwerse, Hans, Swart, Jaap, Kool, Marcel, van Soest, Simone, Baas, Frank, ten Brink, Jacoline B, de Jong, Paulus T.V.M

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A novel lamin A/C mutation in a Dutch family with premature atherosclerosis von Weterings, A.A.W, van Rijsingen, I.A.W, Plomp, A.S, Zwinderman, A.H, Lekanne Deprez, R.H, Mannens, M.M, van den Bergh Weerman, M.A, van der Wal, A.C, Pinto-Sietsma, S.J

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Spondylolysis and spinal adaptations for bipedalism: The overshoot hypothesis von Plomp, Kimberly A, Dobney, Keith, Collard, Mark

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Spondylolysis and spinal adaptations for bipedalism von Plomp, Kimberly A, Dobney, Keith, Collard, Mark

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The changing shape of palaeopathology: The contribution of skeletal shape analyses to investigations of pathological conditions von Gilmour, Rebecca J., Plomp, Kimberly A.

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Incidence, predictability, and pathogenesis of amiodarone-induced thyrotoxicosis and hypothyroidism von Trip, Mieke D., Wiersinga, Wilmar, Plomp, Theo A.

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The ancestral shape hypothesis: an evolutionary explanation for the occurrence of intervertebral disc herniation in humans von Plomp, Kimberly A, Viðarsdóttir, Una Strand, Weston, Darlene A, Dobney, Keith, Collard, Mark

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Development of Refractive Errors—What Can We Learn From Inherited Retinal Dystrophies? von Hendriks, Michelle, Verhoeven, Virginie J.M., Buitendijk, Gabriëlle H.S., Polling, Jan Roelof, Meester-Smoor, Magda A., Hofman, Albert, van Huet, Ramon A., Klevering, B. Jeroen, Bax, Nathalie M., Lambertus, Stanley, Klaver, Caroline C.W., Hoyng, Carel B., Oomen, Clasien J., van Zelst-Stams, Wendy A., Cremers, Frans P., Plomp, Astrid S., van Schooneveld, Mary J., van Genderen, Mies M., Schuil, José, Boonstra, F. Nienke, Schlingemann, Reinier O., Bergen, Arthur A., Pierrache, Laurence, Meester-Smoor, Magda, van den Born, L. Ingeborgh, Boon, Camiel J., Pott, Jan W.R., van Leeuwen, Redmer, Kroes, Hester Y, de Jong-Hesse, Yvonne, Kamermans, Maarten, Ingeborgh van den Born, L., Klaver, Caroline C.W.

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Vertebral morphology influences the development of Schmorl's nodes in the lower thoracic vertebrae von Plomp, Kimberly A., Roberts, Charlotte A., Viðarsdóttir, Una Strand

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