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Items: 26

1.

Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.

Harold D, Connolly S, Riley BP, Kendler KS, McCarthy SE, McCombie WR, Richards A, Owen MJ, O'Donovan MC, Walters J; Wellcome Trust Case Control Consortium 2; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Donohoe G, Gill M, Corvin A, Morris DW.

Am J Med Genet B Neuropsychiatr Genet. 2019 Apr;180(3):223-231. doi: 10.1002/ajmg.b.32716. Epub 2019 Feb 23.

PMID:
30801977
2.

Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes.

Staples J, Maxwell EK, Gosalia N, Gonzaga-Jauregui C, Snyder C, Hawes A, Penn J, Ulloa R, Bai X, Lopez AE, Van Hout CV, O'Dushlaine C, Teslovich TM, McCarthy SE, Balasubramanian S, Kirchner HL, Leader JB, Murray MF, Ledbetter DH, Shuldiner AR, Yancoupolos GD, Dewey FE, Carey DJ, Overton JD, Baras A, Habegger L, Reid JG.

Am J Hum Genet. 2018 May 3;102(5):874-889. doi: 10.1016/j.ajhg.2018.03.012.

3.

Reflections on Combining the Bonfils Intubation Endoscope, the Macintosh Videolaryngocope, and the Difficult Airway.

McCarthy SE, Cooper RM.

Anesth Analg. 2018 Jul;127(1):304. doi: 10.1213/ANE.0000000000003327. No abstract available.

PMID:
29677067
4.

Altered DNA methylation associated with a translocation linked to major mental illness.

McCartney DL, Walker RM, Morris SW, Anderson SM, Duff BJ, Marioni RE, Millar JK, McCarthy SE, Ryan NM, Lawrie SM, Watson AR, Blackwood DHR, Thomson PA, McIntosh AM, McCombie WR, Porteous DJ, Evans KL.

NPJ Schizophr. 2018 Mar 19;4(1):5. doi: 10.1038/s41537-018-0047-7.

5.

The Hippo pathway effector YAP is an essential regulator of ductal progenitor patterning in the mouse submandibular gland.

Szymaniak AD, Mi R, McCarthy SE, Gower AC, Reynolds TL, Mingueneau M, Kukuruzinska M, Varelas X.

Elife. 2017 May 11;6. pii: e23499. doi: 10.7554/eLife.23499.

6.

Online patient safety education programme for junior doctors: is it worthwhile?

McCarthy SE, O'Boyle CA, O'Shaughnessy A, Walsh G.

Ir J Med Sci. 2016 Feb;185(1):51-8. doi: 10.1007/s11845-014-1218-9. Epub 2014 Nov 4.

PMID:
25366816
7.

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.

McCarthy SE, Gillis J, Kramer M, Lihm J, Yoon S, Berstein Y, Mistry M, Pavlidis P, Solomon R, Ghiban E, Antoniou E, Kelleher E, O'Brien C, Donohoe G, Gill M, Morris DW, McCombie WR, Corvin A.

Mol Psychiatry. 2014 Jun;19(6):652-8. doi: 10.1038/mp.2014.29. Epub 2014 Apr 29.

8.

Unlocking the treasure trove: from genes to schizophrenia biology.

McCarthy SE, McCombie WR, Corvin A.

Schizophr Bull. 2014 May;40(3):492-6. doi: 10.1093/schbul/sbu042. Epub 2014 Mar 27. Review.

9.

Genomic variability of monkeypox virus among humans, Democratic Republic of the Congo.

Kugelman JR, Johnston SC, Mulembakani PM, Kisalu N, Lee MS, Koroleva G, McCarthy SE, Gestole MC, Wolfe ND, Fair JN, Schneider BS, Wright LL, Huggins J, Whitehouse CA, Wemakoy EO, Muyembe-Tamfum JJ, Hensley LE, Palacios GF, Rimoin AW.

Emerg Infect Dis. 2014 Feb;20(2):232-9. doi: 10.3201/eid2002.130118.

10.

Ebola virus genome plasticity as a marker of its passaging history: a comparison of in vitro passaging to non-human primate infection.

Kugelman JR, Lee MS, Rossi CA, McCarthy SE, Radoshitzky SR, Dye JM, Hensley LE, Honko A, Kuhn JH, Jahrling PB, Warren TK, Whitehouse CA, Bavari S, Palacios G.

PLoS One. 2012;7(11):e50316. doi: 10.1371/journal.pone.0050316. Epub 2012 Nov 28.

11.

Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.

Nord AS, Roeb W, Dickel DE, Walsh T, Kusenda M, O'Connor KL, Malhotra D, McCarthy SE, Stray SM, Taylor SM, Sebat J; STAART Psychopharmacology Network, King B, King MC, McClellan JM.

Eur J Hum Genet. 2011 Jun;19(6):727-31. doi: 10.1038/ejhg.2011.24. Epub 2011 Mar 30.

12.

Non-symbolic arithmetic abilities and mathematics achievement in the first year of formal schooling.

Gilmore CK, McCarthy SE, Spelke ES.

Cognition. 2010 Jun;115(3):394-406. doi: 10.1016/j.cognition.2010.02.002. Epub 2010 Mar 27.

13.

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.

Girirajan S, Rosenfeld JA, Cooper GM, Antonacci F, Siswara P, Itsara A, Vives L, Walsh T, McCarthy SE, Baker C, Mefford HC, Kidd JM, Browning SR, Browning BL, Dickel DE, Levy DL, Ballif BC, Platky K, Farber DM, Gowans GC, Wetherbee JJ, Asamoah A, Weaver DD, Mark PR, Dickerson J, Garg BP, Ellingwood SA, Smith R, Banks VC, Smith W, McDonald MT, Hoo JJ, French BN, Hudson C, Johnson JP, Ozmore JR, Moeschler JB, Surti U, Escobar LF, El-Khechen D, Gorski JL, Kussmann J, Salbert B, Lacassie Y, Biser A, McDonald-McGinn DM, Zackai EH, Deardorff MA, Shaikh TH, Haan E, Friend KL, Fichera M, Romano C, Gécz J, DeLisi LE, Sebat J, King MC, Shaffer LG, Eichler EE.

Nat Genet. 2010 Mar;42(3):203-9. doi: 10.1038/ng.534. Epub 2010 Feb 14.

14.

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders.

Sebat J, Levy DL, McCarthy SE.

Trends Genet. 2009 Dec;25(12):528-35. doi: 10.1016/j.tig.2009.10.004. Epub 2009 Oct 31. Review.

15.

Microduplications of 16p11.2 are associated with schizophrenia.

McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, Zackai EH, Kaplan P, Ganesh J, Krantz ID, Spinner NB, Roccanova P, Bhandari A, Pavon K, Lakshmi B, Leotta A, Kendall J, Lee YH, Vacic V, Gary S, Iakoucheva LM, Crow TJ, Christian SL, Lieberman JA, Stroup TS, Lehtimäki T, Puura K, Haldeman-Englert C, Pearl J, Goodell M, Willour VL, Derosse P, Steele J, Kassem L, Wolff J, Chitkara N, McMahon FJ, Malhotra AK, Potash JB, Schulze TG, Nöthen MM, Cichon S, Rietschel M, Leibenluft E, Kustanovich V, Lajonchere CM, Sutcliffe JS, Skuse D, Gill M, Gallagher L, Mendell NR; Wellcome Trust Case Control Consortium, Craddock N, Owen MJ, O'Donovan MC, Shaikh TH, Susser E, Delisi LE, Sullivan PF, Deutsch CK, Rapoport J, Levy DL, King MC, Sebat J.

Nat Genet. 2009 Nov;41(11):1223-7. doi: 10.1038/ng.474. Epub 2009 Oct 25.

16.

The YPLGVG sequence of the Nipah virus matrix protein is required for budding.

Patch JR, Han Z, McCarthy SE, Yan L, Wang LF, Harty RN, Broder CC.

Virol J. 2008 Nov 10;5:137. doi: 10.1186/1743-422X-5-137.

17.

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.

Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM, Nord AS, Kusenda M, Malhotra D, Bhandari A, Stray SM, Rippey CF, Roccanova P, Makarov V, Lakshmi B, Findling RL, Sikich L, Stromberg T, Merriman B, Gogtay N, Butler P, Eckstrand K, Noory L, Gochman P, Long R, Chen Z, Davis S, Baker C, Eichler EE, Meltzer PS, Nelson SF, Singleton AB, Lee MK, Rapoport JL, King MC, Sebat J.

Science. 2008 Apr 25;320(5875):539-43. doi: 10.1126/science.1155174. Epub 2008 Mar 27.

18.

Herpes compunctorum: cutaneous herpes simplex virus infection complicating tattooing.

Marshall CS, Murphy F, McCarthy SE, Cheng AC.

Med J Aust. 2007 Nov 19;187(10):598. No abstract available.

PMID:
18021059
19.

Role for amino acids 212KLR214 of Ebola virus VP40 in assembly and budding.

McCarthy SE, Johnson RF, Zhang YA, Sunyer JO, Harty RN.

J Virol. 2007 Oct;81(20):11452-60. Epub 2007 Aug 15.

20.

Symbolic arithmetic knowledge without instruction.

Gilmore CK, McCarthy SE, Spelke ES.

Nature. 2007 May 31;447(7144):589-91.

PMID:
17538620
21.

A luciferase-based budding assay for Ebola virus.

McCarthy SE, Licata JM, Harty RN.

J Virol Methods. 2006 Oct;137(1):115-9. Epub 2006 Jul 11.

PMID:
16837071
22.

Ebola virus VP35-VP40 interaction is sufficient for packaging 3E-5E minigenome RNA into virus-like particles.

Johnson RF, McCarthy SE, Godlewski PJ, Harty RN.

J Virol. 2006 Jun;80(11):5135-44.

23.

Use of MALDI-TOF mass spectrometry in a 51-mutation test for cystic fibrosis: evidence that 3199del6 is a disease-causing mutation.

Buyse IM, McCarthy SE, Lurix P, Pace RP, Vo D, Bartlett GA, Schmitt ES, Ward PA, Oermann C, Eng CM, Roa BB.

Genet Med. 2004 Sep-Oct;6(5):426-30.

PMID:
15371908
24.

Medline do you know?

Maccabee SL, McCarthy SE.

Ohio State Med J. 1975 Mar;71(3):199-200. No abstract available.

PMID:
1124191
25.

MEDLINE do you know?

Maccabee SL, McCarthy SE.

J Fla Med Assoc. 1974 Nov;61(11):826-7. No abstract available.

PMID:
4425519
26.

Evaluation of MEDLINE service by user survey.

McCarthy SE, Maccabee SS, Freng CC.

Bull Med Libr Assoc. 1974 Oct;62(4):367-73.

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