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1961 1
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1988 5
1989 5
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1993 2
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1995 5
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82 results

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Page 1
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.
Carss KJ, Arno G, Erwood M, Stephens J, Sanchis-Juan A, Hull S, Megy K, Grozeva D, Dewhurst E, Malka S, Plagnol V, Penkett C, Stirrups K, Rizzo R, Wright G, Josifova D, Bitner-Glindzicz M, Scott RH, Clement E, Allen L, Armstrong R, Brady AF, Carmichael J, Chitre M, Henderson RHH, Hurst J, MacLaren RE, Murphy E, Paterson J, Rosser E, Thompson DA, Wakeling E, Ouwehand WH, Michaelides M, Moore AT; NIHR-BioResource Rare Diseases Consortium; Webster AR, Raymond FL. Carss KJ, et al. Am J Hum Genet. 2017 Jan 5;100(1):75-90. doi: 10.1016/j.ajhg.2016.12.003. Epub 2016 Dec 29. Am J Hum Genet. 2017. PMID: 28041643 Free PMC article.
ECT seizure monitoring.
Kramer BA, Pollock VG, Schneider LS, Gray GE. Kramer BA, et al. Among authors: pollock vg. Biol Psychiatry. 1989 Dec;26(8):848-50. doi: 10.1016/0006-3223(89)90126-1. Biol Psychiatry. 1989. PMID: 2590696 No abstract available.
Quantitative, waking EEG research on depression.
Pollock VE, Schneider LS. Pollock VE, et al. Biol Psychiatry. 1990 Apr 1;27(7):757-80. doi: 10.1016/0006-3223(90)90591-o. Biol Psychiatry. 1990. PMID: 2183880 Review.
Meta-analysis in literature reviews.
Pollock VE. Pollock VE. Biol Psychiatry. 1993 Sep 15;34(6):345-7. doi: 10.1016/0006-3223(93)90177-f. Biol Psychiatry. 1993. PMID: 8218600 No abstract available.
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
Gorman KM, Meyer E, Grozeva D, Spinelli E, McTague A, Sanchis-Juan A, Carss KJ, Bryant E, Reich A, Schneider AL, Pressler RM, Simpson MA, Debelle GD, Wassmer E, Morton J, Sieciechowicz D, Jan-Kamsteeg E, Paciorkowski AR, King MD, Cross JH, Poduri A, Mefford HC, Scheffer IE, Haack TB, McCullagh G; Deciphering Developmental Disorders Study; UK10K Consortium; NIHR BioResource; Millichap JJ, Carvill GL, Clayton-Smith J, Maher ER, Raymond FL, Kurian MA. Gorman KM, et al. Am J Hum Genet. 2019 May 2;104(5):948-956. doi: 10.1016/j.ajhg.2019.03.005. Epub 2019 Apr 11. Am J Hum Genet. 2019. PMID: 30982612 Free PMC article.
De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures.
Ito Y, Carss KJ, Duarte ST, Hartley T, Keren B, Kurian MA, Marey I, Charles P, Mendonça C, Nava C, Pfundt R, Sanchis-Juan A, van Bokhoven H, van Essen A, van Ravenswaaij-Arts C; NIHR BioResource; Care4Rare Canada Consortium; Boycott KM, Kernohan KD, Dyack S, Raymond FL. Ito Y, et al. Am J Hum Genet. 2018 Jul 5;103(1):144-153. doi: 10.1016/j.ajhg.2018.06.001. Epub 2018 Jun 28. Am J Hum Genet. 2018. PMID: 29961568 Free PMC article.
Further analysis of a meta-analysis.
Schneider LS, Pollock V, Lyness S. Schneider LS, et al. Among authors: pollock v. J Am Geriatr Soc. 1991 Apr;39(4):441-2. doi: 10.1111/j.1532-5415.1991.tb02922.x. J Am Geriatr Soc. 1991. PMID: 1672700 No abstract available.
Use of meta-analysis for testing theory.
Miller N, Pollock VE. Miller N, et al. Among authors: pollock ve. Eval Health Prof. 1995 Dec;18(4):370-92. doi: 10.1177/016327879501800403. Eval Health Prof. 1995. PMID: 10153163 Review.
P300 topography in Alzheimer's disease.
Holt LE, Raine A, Pa G, Schneider LS, Henderson VW, Pollock VE. Holt LE, et al. Among authors: pollock ve. Psychophysiology. 1995 May;32(3):257-65. doi: 10.1111/j.1469-8986.1995.tb02954.x. Psychophysiology. 1995. PMID: 7784534
82 results