Associate Professor Nigel Clarke PhD, MBChB, FRACP (1966–2015) von Laing, Nigel, North, Kathryn

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Evolution of CAR T-cell immunotherapy in terms of patenting activity von Jürgens, Björn, Clarke, Nigel S.

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Mass Spectrometry in Precision Medicine: Phenotypic Measurements Alongside Pharmacogenomics von Clarke, Nigel J

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Advantages and challenges of mass spectrometry assays for steroid hormones von Stanczyk, Frank Z., Clarke, Nigel J.

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Measurement of Estradiol—Challenges Ahead von Stanczyk, Frank Z, Clarke, Nigel J

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Pattern formation in polymer blend thin films: surface roughening couples to phase separation von Coveney, Sam, Clarke, Nigel

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Congenital Fiber-Type Disproportion von Clarke, Nigel F., MB ChB, PhD, FRACP

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Blockchain patent landscaping: An expert based methodology and search query von Clarke, Nigel S., Jürgens, Björn, Herrero-Solana, Victor

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Predicting structure and property relations in polymeric photovoltaic devices von Buxton, Gavin A., Clarke, Nigel

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Toward a Model for Pattern Formation in Ultrathin-Film Binary Mixtures von Clarke, Nigel

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Periodontitis in Dry Skulls von Clarke, Nigel

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Resilient 3D hierarchical architected metamaterials von Meza, Lucas R., Zelhofer, Alex J., Clarke, Nigel, Mateos, Arturo J., Kochmann, Dennis M., Greer, Julia R.

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A novel mutation expands the genetic and clinical spectrum of MYH7 -related myopathies von Clarke, Nigel F, Amburgey, Kimberly, Teener, James, Camelo-Piragua, Sandra, Kesari, Akanchha, Punetha, Jaya, Waddell, Leigh B, Davis, Mark, Laing, Nigel G, Monnier, Nicole, North, Kathryn N, Hoffman, Eric P, Dowling, James J

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Mapping catheter-related mitral valve injury: a case report von Shergill, Simran, Clarke, Nigel R A

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The relative importance of domain size, domain purity and domain interfaces to the performance of bulk-heterojunction organic photovoltaics von Lyons, Benjamin P., Clarke, Nigel, Groves, Chris

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Metal- and Anion-Binding Supramolecular Gels von Piepenbrock, Marc-Oliver M, Lloyd, Gareth O, Clarke, Nigel, Steed, Jonathan W

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Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia von Oates, Emily C., Rossor, Alexander M., Hafezparast, Majid, Gonzalez, Michael, Speziani, Fiorella, MacArthur, Daniel G., Lek, Monkol, Cottenie, Ellen, Scoto, Mariacristina, Foley, A. Reghan, Hurles, Matthew, Houlden, Henry, Greensmith, Linda, Auer-Grumbach, Michaela, Pieber, Thomas R., Strom, Tim M., Schule, Rebecca, Herrmann, David N., Sowden, Janet E., Acsadi, Gyula, Menezes, Manoj P., Clarke, Nigel F., Züchner, Stephan, Muntoni, Francesco, North, Kathryn N., Reilly, Mary M.

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Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cells von OATES, Emily C, REDDEL, Stephen, RODRIGUEZ, Michael L, GANDOLFO, Luke C, BAHLO, Melanie, HAWKE, Simon H, LAMANDE, Shireen R, CLARKE, Nigel F, NORTH, Kathryn N

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Scalable photonic crystal chips for high sensitivity protein detection von Liang, Feng, Clarke, Nigel, Patel, Parth, Loncar, Marko, Quan, Qimin

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Improving genetic diagnosis in Mendelian disease with transcriptome sequencing von Cummings, Beryl B, Marshall, Jame L, Tukiainen, Taru, Lek, Monkol, Donkervoort, Sandra, Foley, A. Reghan, Bolduc, Veronique, Waddell, Leigh B, Sandaradura, Sarah A, O'Grady, Gina L, Estrella, Elicia, Reddy, Hemakumar M, Zhao, Fengmei, Weisburd, Ben, Karczewski, Konrad J, O'Donnell-Luria, Anne H, Birnbaum, Daniel, Sarkozy, Anna, Hu, Ying, Gonorazky, Hernan, Claeys, Kristi, Joshi, Adam Bournazos, Oates, Emily C, Ghaoui, Roula, Davis, Mark R, Laing, Nigel G, Topf, Ana, Genotype-Tissue Expression (GTEx) Consortium, Kang, Peter B, Beggs, Alan H, North, Kathryn N, Straub, Volker, Dowling, James J, Muntoni, Francesco, Clarke, Nigel F, Cooper, Sandra T, Bönnemann, Carsten G, Guigó Serra, Roderic

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