Gagnon D - Search Results

1

Image reconstruction algorithm for a rotating slat collimator.

Zeng GL, Gagnon D, Matthews CG, Kolthammer JA, Radachy JD, Hawkins WG. Zeng GL, et al. Among authors: gagnon d. Med Phys. 2002 Jul;29(7):1406-12. doi: 10.1118/1.1485057. Med Phys. 2002. PMID: 12148720

2

3D RBI-EM reconstruction with spherically-symmetric basis function for SPECT rotating slat collimator.

Wang W, Hawkins W, Gagnon D. Wang W, et al. Among authors: gagnon d. Phys Med Biol. 2004 Jun 7;49(11):2273-92. doi: 10.1088/0031-9155/49/11/011. Phys Med Biol. 2004. PMID: 15248577

3

Image reconstruction algorithm for a spinning strip CZT SPECT camera with a parallel slat collimator and small pixels.

Zeng GL, Gagnon D. Zeng GL, et al. Among authors: gagnon d. Med Phys. 2004 Dec;31(12):3461-73. doi: 10.1118/1.1813873. Med Phys. 2004. PMID: 15651629

4

CdZnTe strip detector SPECT imaging with a slit collimator.

Zheng GL, Gagnon D. Zheng GL, et al. Among authors: gagnon d. Phys Med Biol. 2004 Jun 7;49(11):2257-71. doi: 10.1088/0031-9155/49/11/010. Phys Med Biol. 2004. PMID: 15248576

5

Patient-dependent count-rate adaptive normalization for PET detector efficiency with delayed-window coincidence events.

Niu X, Ye H, Xia T, Asma E, Winkler M, Gagnon D, Wang W. Niu X, et al. Among authors: gagnon d. Phys Med Biol. 2015 Jul 7;60(13):5241-59. doi: 10.1088/0031-9155/60/13/5241. Epub 2015 Jun 18. Phys Med Biol. 2015. PMID: 26086713

6

Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmission.

Gouw LG, Castañeda MA, McKenna CK, Digre KB, Pulst SM, Perlman S, Lee MS, Gomez C, Fischbeck K, Gagnon D, Storey E, Bird T, Jeri FR, Ptácek LJ. Gouw LG, et al. Among authors: gagnon d. Hum Mol Genet. 1998 Mar;7(3):525-32. doi: 10.1093/hmg/7.3.525. Hum Mol Genet. 1998. PMID: 9467013

7

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.

Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, Ronen GM, Bjerre I, Quattlebaum T, Murphy JV, McHarg ML, Gagnon D, Rosales TO, Peiffer A, Anderson VE, Leppert M. Singh NA, et al. Among authors: gagnon d. Nat Genet. 1998 Jan;18(1):25-9. doi: 10.1038/ng0198-25. Nat Genet. 1998. PMID: 9425895

8

Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2.

Oldridge M, Lunt PW, Zackai EH, McDonald-McGinn DM, Muenke M, Moloney DM, Twigg SR, Heath JK, Howard TD, Hoganson G, Gagnon DM, Jabs EW, Wilkie AO. Oldridge M, et al. Among authors: gagnon dm. Hum Mol Genet. 1997 Jan;6(1):137-43. doi: 10.1093/hmg/6.1.137. Hum Mol Genet. 1997. PMID: 9002682

9

Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.

Pegoraro E, Marks H, Garcia CA, Crawford T, Mancias P, Connolly AM, Fanin M, Martinello F, Trevisan CP, Angelini C, Stella A, Scavina M, Munk RL, Servidei S, Bönnemann CC, Bertorini T, Acsadi G, Thompson CE, Gagnon D, Hoganson G, Carver V, Zimmerman RA, Hoffman EP. Pegoraro E, et al. Among authors: gagnon d. Neurology. 1998 Jul;51(1):101-10. doi: 10.1212/wnl.51.1.101. Neurology. 1998. PMID: 9674786

10

Clinical correlates of diagnostic certainty in children and youths with Autistic Disorder.

Rødgaard EM, Rodríguez-Herreros B, Zeribi A, Jensen K, Courchesne V, Douard E, Gagnon D, Huguet G, Jacquemont S, Mottron L. Rødgaard EM, et al. Among authors: gagnon d. Mol Autism. 2024 Apr 3;15(1):15. doi: 10.1186/s13229-024-00592-7. Mol Autism. 2024. PMID: 38570867 Free PMC article.

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