Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 195

1.

Changes in parent motivation predicts changes in body mass index z-score (zBMI) and dietary intake among preschoolers enrolled in a family-based obesity intervention.

Van Allen J, Kuhl ES, Filigno SS, Clifford LM, Connor JM, Stark LJ.

J Pediatr Psychol. 2014 Oct;39(9):1028-37. doi: 10.1093/jpepsy/jsu052. Epub 2014 Jul 12.

2.

Would you dope? A general population test of the Goldman dilemma.

Connor JM, Mazanov J.

Br J Sports Med. 2009 Oct;43(11):871-2. doi: 10.1136/bjsm.2009.057596. Epub 2009 Feb 11.

PMID:
19211586
3.

Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1.

Kaplan FS, Xu M, Seemann P, Connor JM, Glaser DL, Carroll L, Delai P, Fastnacht-Urban E, Forman SJ, Gillessen-Kaesbach G, Hoover-Fong J, Köster B, Pauli RM, Reardon W, Zaidi SA, Zasloff M, Morhart R, Mundlos S, Groppe J, Shore EM.

Hum Mutat. 2009 Mar;30(3):379-90. doi: 10.1002/humu.20868.

4.

Response to "Mutations of the NOGGIN and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al.

Kaplan FS, Xu M, Feldman G, Brown M, Cho TJ, Choi IH, Connor JM, Delai PL, Economides AN, Glaser DL, Groppe J, Katagiri T, Le Merrer M, Morhart R, Ravazzolo R, Rogers JG, Smith R, Triffitt JT, Urtizberea JA, Zasloff M, Shore EM.

Genet Couns. 2008;19(3):357-9; author reply 361-3. No abstract available.

PMID:
18990993
6.

Circulating angiogenic factors in early pregnancy and the risk of preeclampsia, intrauterine growth restriction, spontaneous preterm birth, and stillbirth.

Smith GC, Crossley JA, Aitken DA, Jenkins N, Lyall F, Cameron AD, Connor JM, Dobbie R.

Obstet Gynecol. 2007 Jun;109(6):1316-24.

PMID:
17540803
7.

Demystification of Chester porphyria: a nonsense mutation in the Porphobilinogen Deaminase gene.

Poblete-Gutiérrez P, Wiederholt T, Martinez-Mir A, Merk HF, Connor JM, Christiano AM, Frank J.

Physiol Res. 2006;55 Suppl 2:S137-44.

8.

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.

Shore EM, Xu M, Feldman GJ, Fenstermacher DA, Cho TJ, Choi IH, Connor JM, Delai P, Glaser DL, LeMerrer M, Morhart R, Rogers JG, Smith R, Triffitt JT, Urtizberea JA, Zasloff M, Brown MA, Kaplan FS.

Nat Genet. 2006 May;38(5):525-7. Epub 2006 Apr 23. Erratum in: Nat Genet. 2007 Feb;39(2):276. FOP International Research Consortium [removed]; Cho, Tae-Joon [added]; Choi, In Ho [added]; Connor, J Michael [added]; Delai, Patricia [added]; Glaser, David L [added]; LeMerrer, Martine [added]; Morhart, Rolf [added]; Rogers, John G [added]; Smith, Roger.

PMID:
16642017
9.

Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins.

Johnson D, Morrison N, Grant L, Turner T, Fantes J, Connor JM, Murday V.

J Med Genet. 2006 Mar;43(3):280-4. Epub 2005 Aug 23.

10.

The relation of age, gender, ethnicity, and risk behaviors to self-esteem among students in nonmainstream schools.

Connor JM, Poyrazli S, Ferrer-Wreder L, Grahame KM.

Adolescence. 2004 Fall;39(155):457-73.

PMID:
15673223
11.

First-trimester placentation and the risk of antepartum stillbirth.

Smith GC, Crossley JA, Aitken DA, Pell JP, Cameron AD, Connor JM, Dobbie R.

JAMA. 2004 Nov 10;292(18):2249-54.

PMID:
15536112
12.

First-trimester combined ultrasound and biochemical screening for Down syndrome in routine clinical practice.

Stenhouse EJ, Crossley JA, Aitken DA, Brogan K, Cameron AD, Connor JM.

Prenat Diagn. 2004 Oct;24(10):774-80.

PMID:
15503268
13.

Relationship of the platelet glycoprotein PlA and fibrinogen T/G+1689 polymorphisms with peripheral arterial disease and ischaemic heart disease.

Smith FB, Connor JM, Lee AJ, Cooke A, Lowe GD, Rumley A, Fowkes FG.

Thromb Res. 2003;112(4):209-16. Review.

PMID:
14987913
14.

Fenceline contact of beef calves with their dams at weaning reduces the negative effects of separation on behavior and growth rate.

Price EO, Harris JE, Borgward RE, Sween ML, Connor JM.

J Anim Sci. 2003 Jan;81(1):116-21.

PMID:
12597380
15.

Seling v. Young: constitutionally protected but unjust civil commitment for sexually violent predators.

Connor JM.

J Contemp Health Law Policy. 2002 Summer;18(2):511-41. No abstract available.

PMID:
12173446
16.

Combined ultrasound and biochemical screening for Down's syndrome in the first trimester: a Scottish multicentre study.

Crossley JA, Aitken DA, Cameron AD, McBride E, Connor JM.

BJOG. 2002 Jun;109(6):667-76.

17.

Early-pregnancy origins of low birth weight.

Smith GC, Stenhouse EJ, Crossley JA, Aitken DA, Cameron AD, Connor JM.

Nature. 2002 Jun 27;417(6892):916. No abstract available.

PMID:
12087395
18.

Early pregnancy levels of pregnancy-associated plasma protein a and the risk of intrauterine growth restriction, premature birth, preeclampsia, and stillbirth.

Smith GC, Stenhouse EJ, Crossley JA, Aitken DA, Cameron AD, Connor JM.

J Clin Endocrinol Metab. 2002 Apr;87(4):1762-7.

PMID:
11932314
20.

Placental and maternal serum inhibin-A and activin-A levels in Down's syndrome pregnancies.

Dalgliesh GL, Aitken DA, Lyall F, Howatson AG, Connor JM.

Placenta. 2001 Feb-Mar;22(2-3):227-34.

PMID:
11170828
21.

Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP).

Xu MQ, Feldman G, Le Merrer M, Shugart YY, Glaser DL, Urtizberea JA, Fardeau M, Connor JM, Triffitt J, Smith R, Shore EM, Kaplan FS.

Clin Genet. 2000 Oct;58(4):291-8.

PMID:
11076054
22.
23.

Glomerular hyperfiltration, high renin, and low- extracellular volume in high blood pressure.

Harrap SB, Cumming AD, Davies DL, Foy CJ, Fraser R, Kamitani A, Connor JM, Lever AF, Watt GC.

Hypertension. 2000 Apr;35(4):952-7.

PMID:
10775568
24.

Placental synthesis of oestriol in Down's syndrome pregnancies.

Newby D, Aitken DA, Howatson AG, Connor JM.

Placenta. 2000 Mar-Apr;21(2-3):263-7.

PMID:
10736251
25.

Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31.

Feldman G, Li M, Martin S, Urbanek M, Urtizberea JA, Fardeau M, LeMerrer M, Connor JM, Triffitt J, Smith R, Muenke M, Kaplan FS, Shore EM.

Am J Hum Genet. 2000 Jan;66(1):128-35.

26.

Second-trimester pregnancy associated plasma protein-A levels are reduced in Cornelia de Lange syndrome pregnancies.

Aitken DA, Ireland M, Berry E, Crossley JA, Macri JN, Burn J, Connor JM.

Prenat Diagn. 1999 Aug;19(8):706-10.

PMID:
10451512
27.

Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressiva.

Virdi AS, Shore EM, Oreffo RO, Li M, Connor JM, Smith R, Kaplan FS, Triffitt JT.

Calcif Tissue Int. 1999 Sep;65(3):250-5.

PMID:
10441661
28.

Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies.

Morris A, Boyd E, Dhanjal S, Lowther GW, Aitken DA, Young J, Menzies AL, Imrie SJ, Connor JM.

Prenat Diagn. 1999 Jun;19(6):546-51.

PMID:
10416971
29.

Neuroticism and polymorphisms in the serotonin transporter gene.

Deary IJ, Battersby S, Whiteman MC, Connor JM, Fowkes FG, Harmar A.

Psychol Med. 1999 May;29(3):735-9.

PMID:
10405095
30.

Fibrinogen, factor VII and PAI-1 genotypes and the risk of coronary and peripheral atherosclerosis: Edinburgh Artery Study.

Lee AJ, Fowkes FG, Lowe GD, Connor JM, Rumley A.

Thromb Haemost. 1999 Apr;81(4):553-60.

PMID:
10235438
31.

Detection of t(12;21) in childhood acute lymphoblastic leukemia by fluorescence in situ hybridization.

Spathas DH, Stewart J, Singer IO, Theriault A, Bovey M, Connor JM.

Cancer Genet Cytogenet. 1999 Apr;110(1):7-13.

PMID:
10198615
32.

Genetic and environmental influences in the development of multiple primary melanoma.

Burden AD, Newell J, Andrew N, Kavanagh G, Connor JM, MacKie RM.

Arch Dermatol. 1999 Mar;135(3):261-5.

PMID:
10086446
33.

1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis.

Knight SW, Vulliamy TJ, Heiss NS, Matthijs G, Devriendt K, Connor JM, D'Urso M, Poustka A, Mason PJ, Dokal I.

J Med Genet. 1998 Dec;35(12):993-6.

34.

Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation.

Ghaffari SR, Boyd E, Connor JM, Jones AM, Tolmie JL.

J Med Genet. 1998 Oct;35(10):836-40.

35.

A fucosidosis patient with relative longevity and a missense mutation in exon 7 of the alpha-fucosidase gene.

Fleming CJ, Sinclair DU, White EJ, Winchester B, Whiteford ML, Connor JM.

J Inherit Metab Dis. 1998 Aug;21(6):688-9. No abstract available.

PMID:
9762612
36.

CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.

MacKie RM, Andrew N, Lanyon WG, Connor JM.

J Invest Dermatol. 1998 Aug;111(2):269-72.

37.

Human alpha-adducin gene, blood pressure, and sodium metabolism.

Kamitani A, Wong ZY, Fraser R, Davies DL, Connor JM, Foy CJ, Watt GC, Harrap SB.

Hypertension. 1998 Jul;32(1):138-43.

PMID:
9674650
38.

Acute intermittent porphyria: alternative splicing of hydroxymethylbilane synthase mRNA excludes exons 3 and 12.

Ong PM, Lanyon WG, Moore MR, Connor JM.

Mol Cell Probes. 1998 Apr;12(2):63-70.

PMID:
9633040
39.

Prediction of liability to orofacial clefting using genetic and craniofacial data from parents.

Mossey PA, Arngrimsson R, McColl J, Vintiner GM, Connor JM.

J Med Genet. 1998 May;35(5):371-8.

40.

A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation.

Ghaffari SR, Boyd E, Tolmie JL, Crow YJ, Trainer AH, Connor JM.

J Med Genet. 1998 Mar;35(3):225-33.

41.

Identification of two novel mutations in the hydroxymethylbilane synthase gene in three patients from two unrelated families with acute intermittent porphyria.

Ong PM, Lanyon WG, Hift RJ, Halkett J, Cramp CE, Moore MR, Connor JM.

Hum Hered. 1998 Jan-Feb;48(1):24-9.

PMID:
9463797
42.

Biochemical markers of trisomy 21 and the pathophysiology of Down's syndrome pregnancies.

Newby D, Aitken DA, Crossley JA, Howatson AG, Macri JN, Connor JM.

Prenat Diagn. 1997 Oct;17(10):941-51.

PMID:
9358574
43.

Evidence for a familial pregnancy-induced hypertension locus in the eNOS-gene region.

Arngrímsson R, Hayward C, Nadaud S, Baldursdóttir A, Walker JJ, Liston WA, Bjarnadóttir RI, Brock DJ, Geirsson RT, Connor JM, Soubrier F.

Am J Hum Genet. 1997 Aug;61(2):354-62.

44.

Acute intermittent porphyria: the in vitro expression of mutant hydroxymethylbilane synthase.

Ong PM, Lanyon WG, Graham G, Hift RJ, Halkett J, Moore MR, Connor JM.

Mol Cell Probes. 1997 Aug;11(4):293-6.

PMID:
9281416
45.

Screening for Down's syndrome: changes in marker levels and detection rates between first and second trimesters.

Berry E, Aitken DA, Crossley JA, Macri JN, Connor JM.

Br J Obstet Gynaecol. 1997 Jul;104(7):811-7.

PMID:
9236646
46.

The pathophysiology of Down's syndrome pregnancies.

Newby D, Aitken DA, Crossley JA, Howatson AG, Connor JM.

Early Hum Dev. 1996 Dec 30;47 Suppl:S67-8. No abstract available.

PMID:
9031845
47.

Heat-stable and immunoreactive placental alkaline phosphatase in maternal serum from Down's syndrome and trisomy 18 pregnancies.

Aitken DA, Syvertsen BS, Crossley JA, Berry E, Connor JM.

Prenat Diagn. 1996 Nov;16(11):1051-4.

PMID:
8953641
48.

Insulin-dependent diabetes mellitus and prenatal screening results: current experience from a regional screening programme.

Crossley JA, Berry E, Aitken DA, Connor JM.

Prenat Diagn. 1996 Nov;16(11):1039-42.

PMID:
8953638
49.

Fibrodysplasia ossificans progressiva -- lessons from rare maladies.

Connor JM.

N Engl J Med. 1996 Aug 22;335(8):591-3. No abstract available.

PMID:
8678940
50.

Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation.

Gedeon AK, Glass IA, Connor JM, Mulley JC.

Am J Med Genet. 1996 Jul 12;64(1):121-4.

PMID:
8826461

Supplemental Content

Loading ...
Support Center