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Items: 43

1.

Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder.

Chapman NH, Bernier RA, Webb SJ, Munson J, Blue EM, Chen DH, Heigham E, Raskind WH, Wijsman EM.

Hum Genet. 2018 Oct;137(10):807-815. doi: 10.1007/s00439-018-1939-3. Epub 2018 Oct 1.

2.

Increasing Metacognitive Capacity by Disrupting Implicit Leader Prototypes.

Brooks B, Chapman NH.

New Dir Stud Leadersh. 2018 Sep;2018(159):53-64. doi: 10.1002/yd.20297.

PMID:
29864235
3.

Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease.

Blue EE, Yu CE, Thornton TA, Chapman NH, Kernfeld E, Jiang N, Shively KM, Buckingham KJ, Marvin CT, Bamshad MJ, Bird TD, Wijsman EM.

Genes Brain Behav. 2018 Jul;17(6):e12429. doi: 10.1111/gbb.12429. Epub 2017 Nov 20.

4.

Methylation Profiling RIN3 and MEF2C Identifies Epigenetic Marks Associated with Sporadic Early Onset Alzheimer's Disease.

Boden KA, Barber IS, Clement N, Patel T, Guetta-Baranes T, Brookes KJ, Chappell S, Craigon J, Chapman NH; ARUK Consortium, Morgan K, Seymour GB, Bottley A.

J Alzheimers Dis Rep. 2017 Sep 13;1(1):97-108. doi: 10.3233/ADR-170015.

5.

Corrigendum: Genetic improvement of tomato by targeted control of fruit softening.

Uluisik S, Chapman NH, Smith R, Poole M, Adams G, Gillis RB, Besong TM, Sheldon J, Stiegelmeyer S, Perez L, Samsulrizal N, Wang D, Fisk ID, Yang N, Baxter C, Rickett D, Fray R, Blanco-Ulate B, Powell AL, Harding SE, Craigon J, Rose JK, Fich EA, Sun L, Domozych DS, Fraser PD, Tucker GA, Grierson D, Seymour GB.

Nat Biotechnol. 2016 Oct 11;34(10):1072. doi: 10.1038/nbt1016-1072d. No abstract available.

PMID:
27727231
6.

Genetic improvement of tomato by targeted control of fruit softening.

Uluisik S, Chapman NH, Smith R, Poole M, Adams G, Gillis RB, Besong TM, Sheldon J, Stiegelmeyer S, Perez L, Samsulrizal N, Wang D, Fisk ID, Yang N, Baxter C, Rickett D, Fray R, Blanco-Ulate B, Powell AL, Harding SE, Craigon J, Rose JK, Fich EA, Sun L, Domozych DS, Fraser PD, Tucker GA, Grierson D, Seymour GB.

Nat Biotechnol. 2016 Sep;34(9):950-2. doi: 10.1038/nbt.3602. Epub 2016 Jul 25.

PMID:
27454737
7.

A DEMETER-like DNA demethylase governs tomato fruit ripening.

Liu R, How-Kit A, Stammitti L, Teyssier E, Rolin D, Mortain-Bertrand A, Halle S, Liu M, Kong J, Wu C, Degraeve-Guibault C, Chapman NH, Maucourt M, Hodgman TC, Tost J, Bouzayen M, Hong Y, Seymour GB, Giovannoni JJ, Gallusci P.

Proc Natl Acad Sci U S A. 2015 Aug 25;112(34):10804-9. doi: 10.1073/pnas.1503362112. Epub 2015 Aug 10.

8.

PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers.

Nato AQ Jr, Chapman NH, Sohi HK, Nguyen HD, Brkanac Z, Wijsman EM.

Bioinformatics. 2015 Dec 1;31(23):3790-8. doi: 10.1093/bioinformatics/btv444. Epub 2015 Jul 30.

9.

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.

Chapman NH, Nato AQ Jr, Bernier R, Ankenman K, Sohi H, Munson J, Patowary A, Archer M, Blue EM, Webb SJ, Coon H, Raskind WH, Brkanac Z, Wijsman EM.

Hum Genet. 2015 Oct;134(10):1055-68. doi: 10.1007/s00439-015-1585-y. Epub 2015 Jul 24.

10.

Fruit development and ripening.

Seymour GB, Ƙstergaard L, Chapman NH, Knapp S, Martin C.

Annu Rev Plant Biol. 2013;64:219-41. doi: 10.1146/annurev-arplant-050312-120057. Epub 2013 Feb 4. Review.

PMID:
23394500
11.

Network inference analysis identifies an APRR2-like gene linked to pigment accumulation in tomato and pepper fruits.

Pan Y, Bradley G, Pyke K, Ball G, Lu C, Fray R, Marshall A, Jayasuta S, Baxter C, van Wijk R, Boyden L, Cade R, Chapman NH, Fraser PD, Hodgman C, Seymour GB.

Plant Physiol. 2013 Mar;161(3):1476-85. doi: 10.1104/pp.112.212654. Epub 2013 Jan 4.

12.

Regulation of ripening and opportunities for control in tomato and other fruits.

Seymour GB, Chapman NH, Chew BL, Rose JK.

Plant Biotechnol J. 2013 Apr;11(3):269-78. doi: 10.1111/j.1467-7652.2012.00738.x. Epub 2012 Sep 7. Review.

13.

High-resolution mapping of a fruit firmness-related quantitative trait locus in tomato reveals epistatic interactions associated with a complex combinatorial locus.

Chapman NH, Bonnet J, Grivet L, Lynn J, Graham N, Smith R, Sun G, Walley PG, Poole M, Causse M, King GJ, Baxter C, Seymour GB.

Plant Physiol. 2012 Aug;159(4):1644-57. doi: 10.1104/pp.112.200634. Epub 2012 Jun 8.

14.

Identification of rare variants from exome sequence in a large pedigree with autism.

Marchani EE, Chapman NH, Cheung CY, Ankenman K, Stanaway IB, Coon HH, Nickerson D, Bernier R, Brkanac Z, Wijsman EM.

Hum Hered. 2012;74(3-4):153-64. doi: 10.1159/000346560. Epub 2013 Apr 11.

15.

Clinicians adopting evidence based guidelines: a case study with thromboprophylaxis.

Chapman NH, Lazar SP, Fry M, Lassere MN, Chong BH.

BMC Health Serv Res. 2011 Sep 28;11:240. doi: 10.1186/1472-6963-11-240.

16.

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.

Chapman NH, Estes A, Munson J, Bernier R, Webb SJ, Rothstein JH, Minshew NJ, Dawson G, Schellenberg GD, Wijsman EM.

Hum Genet. 2011 Jan;129(1):59-70. doi: 10.1007/s00439-010-0899-z. Epub 2010 Oct 21.

17.

Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates.

Sieh W, Choi Y, Chapman NH, Craig UK, Steinbart EJ, Rothstein JH, Oyanagi K, Garruto RM, Bird TD, Galasko DR, Schellenberg GD, Wijsman EM.

Hum Mol Genet. 2009 Oct 1;18(19):3725-38. doi: 10.1093/hmg/ddp300. Epub 2009 Jun 30.

18.

Venous thromboembolism - management in general practice.

Chapman NH, Brighton T, Harris MF, Caplan GA, Braithwaite J, Chong BH.

Aust Fam Physician. 2009 Jan-Feb;38(1-2):36-40. Review.

19.

The identification of candidate genes associated with Pch2 eyespot resistance in wheat using cDNA-AFLP.

Chapman NH, Burt C, Nicholson P.

Theor Appl Genet. 2009 Apr;118(6):1045-57. doi: 10.1007/s00122-009-0961-1. Epub 2009 Jan 28.

PMID:
19183860
20.

Homoeologous gene silencing in tissue cultured wheat callus.

Bottley A, Chapman NH, Koebner RM.

BMC Genet. 2008 Oct 17;9:65. doi: 10.1186/1471-2156-9-65.

21.

Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.

Brkanac Z, Chapman NH, Igo RP Jr, Matsushita MM, Nielsen K, Berninger VW, Wijsman EM, Raskind WH.

Behav Genet. 2008 Sep;38(5):462-75. doi: 10.1007/s10519-008-9215-2. Epub 2008 Jul 8.

22.

The development of PCR-based markers for the selection of eyespot resistance genes Pch1 and Pch2.

Chapman NH, Burt C, Dong H, Nicholson P.

Theor Appl Genet. 2008 Aug;117(3):425-33. doi: 10.1007/s00122-008-0786-3. Epub 2008 May 16.

PMID:
18483719
23.

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.

Brkanac Z, Chapman NH, Matsushita MM, Chun L, Nielsen K, Cochrane E, Berninger VW, Wijsman EM, Raskind WH.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):556-60.

PMID:
17450541
24.

Segregation analysis of a complex quantitative trait: approaches for identifying influential data points.

Igo RP Jr, Chapman NH, Wijsman EM.

Hum Hered. 2006;61(2):80-6. Epub 2006 May 5.

PMID:
16679774
25.

Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.

Igo RP Jr, Chapman NH, Berninger VW, Matsushita M, Brkanac Z, Rothstein JH, Holzman T, Nielsen K, Raskind WH, Wijsman EM.

Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):15-27.

26.

A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.

Raskind WH, Igo RP, Chapman NH, Berninger VW, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Brown M, Wijsman EM.

Mol Psychiatry. 2005 Jul;10(7):699-711.

PMID:
15753956
27.

Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.

Chapman NH, Igo RP, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Berninger VW, Wijsman EM, Raskind WH.

Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):67-75.

PMID:
15389770
28.

Assignment of SOD3 to human chromosome band 4p15.3-->p15.1 with somatic cell and radiation hybrid mapping, linkage mapping, and fluorescent in-situ hybridization.

Stern LF, Chapman NH, Wijsman EM, Altherr MR, Rosen DR.

Cytogenet Genome Res. 2003;101(2):178. No abstract available.

PMID:
14619883
29.

A model for the length of tracts of identity by descent in finite random mating populations.

Chapman NH, Thompson EA.

Theor Popul Biol. 2003 Sep;64(2):141-50.

PMID:
12948676
30.

Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding.

Chapman NH, Raskind WH, Thomson JB, Berninger VW, Wijsman EM.

Am J Med Genet B Neuropsychiatr Genet. 2003 Aug 15;121B(1):60-70.

PMID:
12898577
31.
32.

Introduction: linkage analyses in the Hutterites.

Chapman NH, Wijsman EM.

Genet Epidemiol. 2001;21 Suppl 1:S222-3. No abstract available.

PMID:
11858132
33.

The importance of connections: joining components of the Hutterite pedigree.

Chapman NH, Leutenegger AL, Badzioch MD, Bogdan M, Conlon EM, Daw EW, Gagnon F, Li N, Maia JM, Wijsman EM, Thompson EA.

Genet Epidemiol. 2001;21 Suppl 1:S230-5.

PMID:
11793674
34.

TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of Guam.

Poorkaj P, Tsuang D, Wijsman E, Steinbart E, Garruto RM, Craig UK, Chapman NH, Anderson L, Bird TD, Plato CC, Perl DP, Weiderholt W, Galasko D, Schellenberg GD.

Arch Neurol. 2001 Nov;58(11):1871-8.

PMID:
11708997
35.

Linkage disequilibrium mapping: the role of population history, size, and structure.

Chapman NH, Thompson EA.

Adv Genet. 2001;42:413-37. Review.

PMID:
11037333
36.

Linkage of hereditary distal myopathy with desmin accumulation to 2q.

Saavedra-Matiz CA, Chapman NH, Wijsman EM, Horowitz SH, Rosen DR.

Hum Hered. 2000 May-Jun;50(3):166-70.

PMID:
10686494
37.

A randomized trial of 72- versus 24-hour intravenous tubing set changes in newborns receiving lipid therapy.

Matlow AG, Kitai I, Kirpalani H, Chapman NH, Corey M, Perlman M, Pencharz P, Jewell S, Phillips-Gordon C, Summerbell R, Ford-Jones EL.

Infect Control Hosp Epidemiol. 1999 Jul;20(7):487-93.

PMID:
10432161
38.

Born to clot: the European burden.

Rees DC, Chapman NH, Webster MT, Guerreiro JF, Rochette J, Clegg JB.

Br J Haematol. 1999 May;105(2):564-6.

PMID:
10233439
39.

Genome screens using linkage disequilibrium tests: optimal marker characteristics and feasibility.

Chapman NH, Wijsman EM.

Am J Hum Genet. 1998 Dec;63(6):1872-85. Erratum in: Am J Hum Genet 1999 Jan;64(1):334.

40.

Global distribution of the CCR5 gene 32-basepair deletion.

Martinson JJ, Chapman NH, Rees DC, Liu YT, Clegg JB.

Nat Genet. 1997 May;16(1):100-3.

PMID:
9140404
41.

Segregation and linkage analysis of a quantitative versus a qualitative trait in large pedigrees.

Graham J, Chapman NH, Goddard KA, Goode EL, Wijsman EM, Jarvik GP.

Genet Epidemiol. 1997;14(6):999-1004.

PMID:
9433614
42.

Differences in Lp[a] concentrations and apo[a] polymorphs between black and white Americans.

Marcovina SM, Albers JJ, Wijsman E, Zhang Z, Chapman NH, Kennedy H.

J Lipid Res. 1996 Dec;37(12):2569-85.

43.

Evaluation of genetic and environmental effects using GEE and APM methods.

Bull SB, Chapman NH, Greenwood CM, Darlington GA.

Genet Epidemiol. 1995;12(6):729-34.

PMID:
8788000

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