Integrative transcriptomic analysis reveals key drivers of acute peanut allergic reactions
Watson, C. T., Cohain, A. T., Griffin, R. S., Chun, Y., Grishin, A., Hacyznska, H., Hoffman, G. E., Beckmann, N. D., Shah, H., Dawson, P., Henning, A., Wood, R., Burks, A. W., Jones, S. M., Leung, D. Y. M., Sicherer, S., Sampson, H. A., Sharp, A. J., Schadt, E. E., Bunyavanich, S.
Published in Nature communications (05.12.2017)
Published in Nature communications (05.12.2017)
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Journal Article
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
Hannes, F D, Sharp, A J, Mefford, H C, de Ravel, T, Ruivenkamp, C A, Breuning, M H, Fryns, J-P, Devriendt, K, Van Buggenhout, G, Vogels, A, Stewart, H, Hennekam, R C, Cooper, G M, Regan, R, Knight, S J L, Eichler, E E, Vermeesch, J R
Published in Journal of medical genetics (01.04.2009)
Published in Journal of medical genetics (01.04.2009)
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Journal Article
A review of manufacturing flexibility
Beach, R., Muhlemann, A.P., Price, D.H.R., Paterson, A., Sharp, J.A.
Published in European journal of operational research (01.04.2000)
Published in European journal of operational research (01.04.2000)
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Journal Article
The detectability of Wolf–Rayet stars in M33-like spirals up to 30 Mpc
Pledger, J L, Sharp, A J, Sansom, A E
Published in Monthly notices of the Royal Astronomical Society (01.05.2021)
Published in Monthly notices of the Royal Astronomical Society (01.05.2021)
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Journal Article
Estimating advertisers' values for paid search clickthroughs
Laffey, D, Hunka, C, Sharp, J A, Zeng, Z
Published in The Journal of the Operational Research Society (01.03.2009)
Published in The Journal of the Operational Research Society (01.03.2009)
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Journal Article
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome
van Bon, B W M, Mefford, H C, Menten, B, Koolen, D A, Sharp, A J, Nillesen, W M, Innis, J W, de Ravel, T J L, Mercer, C L, Fichera, M, Stewart, H, Connell, L E, Õunap, K, Lachlan, K, Castle, B, Van der Aa, N, van Ravenswaaij, C, Nobrega, M A, Serra-Juhé, C, Simonic, I, de Leeuw, N, Pfundt, R, Bongers, E M, Baker, C, Finnemore, P, Huang, S, Maloney, V K, Crolla, J A, van Kalmthout, M, Elia, M, Vandeweyer, G, Fryns, J P, Janssens, S, Foulds, N, Reitano, S, Smith, K, Parkel, S, Loeys, B, Woods, C G, Oostra, A, Speleman, F, Pereira, A C, Kurg, A, Willatt, L, Knight, S J L, Vermeesch, J R, Romano, C, Barber, J C, Mortier, G, Pérez-Jurado, L A, Kooy, F, Brunner, H G, Eichler, E E, Kleefstra, T, de Vries, B B A
Published in Journal of medical genetics (01.08.2009)
Published in Journal of medical genetics (01.08.2009)
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Journal Article
ORE identifies extreme expression effects enriched for rare variants
Richter, F, Hoffman, G E, Manheimer, K B, Patel, N, Sharp, A J, McKean, D, Morton, S U, DePalma, S, Gorham, J, Kitaygorodksy, A, Porter, G A, Giardini, A, Shen, Y, Chung, W K, Seidman, J G, Seidman, C E, Schadt, E E, Gelb, B D
Published in Bioinformatics (15.10.2019)
Published in Bioinformatics (15.10.2019)
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Journal Article
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
Koolen, D A, Sharp, A J, Hurst, J A, Firth, H V, Knight, S J L, Goldenberg, A, Saugier-Veber, P, Pfundt, R, Vissers, L E L M, Destrée, A, Grisart, B, Rooms, L, Van der Aa, N, Field, M, Hackett, A, Bell, K, Nowaczyk, M J M, Mancini, G M S, Poddighe, P J, Schwartz, C E, Rossi, E, De Gregori, M, Antonacci-Fulton, L L, McLellan, M D, Garrett, J M, Wiechert, M A, Miner, T L, Crosby, S, Ciccone, R, Willatt, L, Rauch, A, Zenker, M, Aradhya, S, Manning, M A, Strom, T M, Wagenstaller, J, Krepischi-Santos, A C, Vianna-Morgante, A M, Rosenberg, C, Price, S M, Stewart, H, Shaw-Smith, C, Brunner, H G, Wilkie, A O M, Veltman, J A, Zuffardi, O, Eichler, E E, de Vries, B B A
Published in Journal of medical genetics (01.11.2008)
Published in Journal of medical genetics (01.11.2008)
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Journal Article
Xp deletions associated with autism in three females
THOMAS, N. S, SHARP, A. J, BROWNE, C. E, SKUSE, D, HARDIE, C, DENNIS, N. R
Published in Human genetics (01.01.1999)
Published in Human genetics (01.01.1999)
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Journal Article
Characterization of the Aspergillus nidulans nmrA gene involved in nitrogen metabolite repression
Andrianopoulos, A. (University of Melbourne, Parkville, Victoria, Australia.), Kourambas, S, Sharp, J.A, Davis, M.A, Hynes, M.J
Published in Journal of Bacteriology (01.04.1998)
Published in Journal of Bacteriology (01.04.1998)
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Journal Article
The role of qualitative methods in production management research
Beach, R., Muhlemann, A.P., Price, D.H.R., Paterson, A., Sharp, J.A.
Published in International journal of production economics (01.12.2001)
Published in International journal of production economics (01.12.2001)
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Journal Article
Segmental Duplications and Copy-Number Variation in the Human Genome
Sharp, Andrew J., Locke, Devin P., McGrath, Sean D., Cheng, Ze, Bailey, Jeffrey A., Vallente, Rhea U., Pertz, Lisa M., Clark, Royden A., Schwartz, Stuart, Segraves, Rick, Oseroff, Vanessa V., Albertson, Donna G., Pinkel, Daniel, Eichler, Evan E.
Published in American journal of human genetics (01.07.2005)
Published in American journal of human genetics (01.07.2005)
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Journal Article
Tumor cells are the source of osteopontin and bone sialoprotein expression in human breast cancer
SHARP, J. A, SUNG, V, SLAVIN, J, THOMPSON, E. W, HENDERSON, M. A
Published in Laboratory investigation (01.07.1999)
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Published in Laboratory investigation (01.07.1999)
Journal Article