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    Results: 1 to 50 of 52

    1.

    The genetic architecture of lipoprotein subclasses in Gullah-speaking African American families enriched for type 2 diabetes: The sea islands genetic African American registry (project SuGAR).

    Divers J, Sale MM, Lu L, Chen WM, Lok KH, Spruil IJ, Fernandes JK, Langefeld CD, Garvey WT.

    J Lipid Res. 2009 Sep 25. [Epub ahead of print]PMID: 19783527 [PubMed - as supplied by publisher]Related articlesFree article

    2.

    Planning and executing a genome wide association study (GWAS).

    Sale MM, Mychaleckyj JC, Chen WM.

    Methods Mol Biol. 2009;590:403-18.PMID: 19763518 [PubMed - in process]Related articles

    3.

    Variants in intron 13 of the ELMO1 gene are associated with diabetic nephropathy in African Americans.

    Leak TS, Perlegas PS, Smith SG, Keene KL, Hicks PJ, Langefeld CD, Mychaleckyj JC, Rich SS, Kirk JK, Freedman BI, Bowden DW, Sale MM.

    Ann Hum Genet. 2009 Mar;73(2):152-9. Epub 2009 Jan 23.PMID: 19183347 [PubMed - indexed for MEDLINE]Related articles

    4.

    Predictive genomics of cardioembolic stroke.

    Ramoni RB, Himes BE, Sale MM, Furie KL, Ramoni MF.

    Stroke. 2009 Mar;40(3 Suppl):S67-70. Epub 2008 Dec 8.PMID: 19064790 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Genome-wide linkage scan in Gullah-speaking African American families with type 2 diabetes: the Sea Islands Genetic African American Registry (Project SuGAR).

    Sale MM, Lu L, Spruill IJ, Fernandes JK, Lok KH, Divers J, Langefeld CD, Garvey WT.

    Diabetes. 2009 Jan;58(1):260-7. Epub 2008 Oct 3.PMID: 18835935 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease.

    Keene KL, Mychaleckyj JC, Leak TS, Smith SG, Perlegas PS, Divers J, Langefeld CD, Freedman BI, Bowden DW, Sale MM.

    Hum Genet. 2008 Sep;124(2):147-54. Epub 2008 Jul 25. Erratum in: Hum Genet. 2008 Sep;124(2):197-8. PMID: 18654799 [PubMed - indexed for MEDLINE]Related articles

    7.

    Association analysis of the ephrin-B2 gene in African-Americans with end-stage renal disease.

    Hicks PJ, Staten JL, Palmer ND, Langefeld CD, Ziegler JT, Keene KL, Sale MM, Bowden DW, Freedman BI.

    Am J Nephrol. 2008;28(6):914-20. Epub 2008 Jun 26.PMID: 18580054 [PubMed - indexed for MEDLINE]Related articles

    8.

    Evaluation of a SNP map of 6q24-27 confirms diabetic nephropathy loci and identifies novel associations in type 2 diabetes patients with nephropathy from an African-American population.

    Leak TS, Mychaleckyj JC, Smith SG, Keene KL, Gordon CJ, Hicks PJ, Freedman BI, Bowden DW, Sale MM.

    Hum Genet. 2008 Aug;124(1):63-71. Epub 2008 Jun 17.PMID: 18560894 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Adiposity gain during childhood, ACE I/D polymorphisms and metabolic outcomes.

    Ponsonby AL, Blizzard L, Pezic A, Cochrane JA, Ellis JA, Morley R, Dickinson JL, Sale MM, Richards SM, Dwyer T.

    Obesity (Silver Spring). 2008 Sep;16(9):2141-7.PMID: 18551123 [PubMed - indexed for MEDLINE]Related articles

    10.

    Association between birth weight and adolescent systolic blood pressure in a caucasian birth cohort differs according to skin type, CRH promoter or 11beta-HSD2 genotype.

    Dwyer T, Blizzard L, Patterson B, Ponsonby AL, Martin K, Quinn S, Sale MM, Richards SM, Morley R, Rich S, Dickinson JL.

    Arch Dis Child. 2008 Sep;93(9):760-7. Epub 2008 May 2.PMID: 18456686 [PubMed - indexed for MEDLINE]Related articles

    11.

    Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies.

    Lewis JP, Palmer ND, Hicks PJ, Sale MM, Langefeld CD, Freedman BI, Divers J, Bowden DW.

    Diabetes. 2008 Aug;57(8):2220-5. Epub 2008 Apr 28.PMID: 18443202 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Comprehensive evaluation of the estrogen receptor alpha gene reveals further evidence for association with type 2 diabetes enriched for nephropathy in an African American population.

    Keene KL, Mychaleckyj JC, Smith SG, Leak TS, Perlegas PS, Langefeld CD, Herrington DM, Freedman BI, Rich SS, Bowden DW, Sale MM.

    Hum Genet. 2008 May;123(4):333-41. Epub 2008 Feb 28.PMID: 18305958 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Association of the distal region of the ectonucleotide pyrophosphatase/phosphodiesterase 1 gene with type 2 diabetes in an African-American population enriched for nephropathy.

    Keene KL, Mychaleckyj JC, Smith SG, Leak TS, Perlegas PS, Langefeld CD, Freedman BI, Rich SS, Bowden DW, Sale MM.

    Diabetes. 2008 Apr;57(4):1057-62. Epub 2008 Jan 9.PMID: 18184924 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population.

    Leak TS, Keene KL, Langefeld CD, Gallagher CJ, Mychaleckyj JC, Freedman BI, Bowden DW, Rich SS, Sale MM.

    Mol Genet Metab. 2007 Sep-Oct;92(1-2):145-50. Epub 2007 Jul 6.PMID: 17618154 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Variants of the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in an African-American population enriched for nephropathy.

    Sale MM, Smith SG, Mychaleckyj JC, Keene KL, Langefeld CD, Leak TS, Hicks PJ, Bowden DW, Rich SS, Freedman BI.

    Diabetes. 2007 Oct;56(10):2638-42. Epub 2007 Jun 29.PMID: 17601994 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Association of the estrogen receptor-alpha gene with the metabolic syndrome and its component traits in African-American families: the Insulin Resistance Atherosclerosis Family Study.

    Gallagher CJ, Langefeld CD, Gordon CJ, Campbell JK, Mychaleckyj JC, Bryer-Ash M, Rich SS, Bowden DW, Sale MM.

    Diabetes. 2007 Aug;56(8):2135-41. Epub 2007 May 18. Erratum in: Diabetes. 2007 Oct;56(10):2650. Mychalecky, Josyf C [corrected to Mychaleckyj, Josyf C]. PMID: 17513703 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    The uncoupling protein 1 gene, UCP1, is expressed in mammalian islet cells and associated with acute insulin response to glucose in African American families from the IRAS Family Study.

    Sale MM, Hsu FC, Palmer ND, Gordon CJ, Keene KL, Borgerink HM, Sharma AJ, Bergman RN, Taylor KD, Saad MF, Norris JM.

    BMC Endocr Disord. 2007 Mar 30;7:1.PMID: 17397545 [PubMed]Related articlesFree article

    18.

    Genetic contributions to type 2 diabetes: recent insights.

    Sale MM, Rich SS.

    Expert Rev Mol Diagn. 2007 Mar;7(2):207-17. Review.PMID: 17331067 [PubMed - indexed for MEDLINE]Related articles

    19.

    Investigation of the estrogen receptor-alpha gene with type 2 diabetes and/or nephropathy in African-American and European-American populations.

    Gallagher CJ, Keene KL, Mychaleckyj JC, Langefeld CD, Hirschhorn JN, Henderson BE, Gordon CJ, Freedman BI, Rich SS, Bowden DW, Sale MM.

    Diabetes. 2007 Mar;56(3):675-84.PMID: 17327435 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    A leucine repeat in the carnosinase gene CNDP1 is associated with diabetic end-stage renal disease in European Americans.

    Freedman BI, Hicks PJ, Sale MM, Pierson ED, Langefeld CD, Rich SS, Xu J, McDonough C, Janssen B, Yard BA, van der Woude FJ, Bowden DW.

    Nephrol Dial Transplant. 2007 Apr;22(4):1131-5. Epub 2007 Jan 5.PMID: 17205963 [PubMed - indexed for MEDLINE]Related articlesFree article

    21.

    Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity.

    Dickinson JL, Sale MM, Passmore A, FitzGerald LM, Wheatley CM, Burdon KP, Craig JE, Tengtrisorn S, Carden SM, Maclean H, Mackey DA.

    Clin Experiment Ophthalmol. 2006 Sep-Oct;34(7):682-8.PMID: 16970763 [PubMed - indexed for MEDLINE]Related articles

    22.

    Genetic susceptibility contributes to renal and cardiovascular complications of type 2 diabetes mellitus.

    Freedman BI, Bowden DW, Sale MM, Langefeld CD, Rich SS.

    Hypertension. 2006 Jul;48(1):8-13. Epub 2006 May 30. Review. No abstract available. PMID: 16735643 [PubMed - indexed for MEDLINE]Related articlesFree article

    23.

    Genetic determinants of the metabolic syndrome.

    Sale MM, Woods J, Freedman BI.

    Curr Hypertens Rep. 2006 Apr;8(1):16-22. Review.PMID: 16600155 [PubMed - indexed for MEDLINE]Related articles

    24.

    Confirmation of the adult-onset primary open angle glaucoma locus GLC1B at 2cen-q13 in an Australian family.

    Charlesworth JC, Stankovich JM, Mackey DA, Craig JE, Haybittel M, Westmore RN, Sale MM.

    Ophthalmologica. 2006;220(1):23-30.PMID: 16374045 [PubMed - indexed for MEDLINE]Related articles

    25.

    Genetic determinants of albuminuria and renal disease in diabetes mellitus.

    Sale MM, Freedman BI.

    Nephrol Dial Transplant. 2006 Jan;21(1):13-6. Epub 2005 Oct 18. Review. No abstract available. PMID: 16234290 [PubMed - indexed for MEDLINE]Related articlesFree article

    26.

    Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree.

    Charlesworth JC, Dyer TD, Stankovich JM, Blangero J, Mackey DA, Craig JE, Green CM, Foote SJ, Baird PN, Sale MM.

    Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3723-9.PMID: 16186355 [PubMed - indexed for MEDLINE]Related articlesFree article

    27.

    Association of the mu-opioid receptor gene with type 2 diabetes mellitus in an African American population.

    Gallagher CJ, Gordon CJ, Langefeld CD, Mychaleckyj JC, Freedman BI, Rich SS, Bowden DW, Sale MM.

    Mol Genet Metab. 2006 Jan;87(1):54-60. Epub 2005 Sep 2.PMID: 16140553 [PubMed - indexed for MEDLINE]Related articles

    28.

    Loci contributing to adult height and body mass index in African American families ascertained for type 2 diabetes.

    Sale MM, Freedman BI, Hicks PJ, Williams AH, Langefeld CD, Gallagher CJ, Bowden DW, Rich SS.

    Ann Hum Genet. 2005 Sep;69(Pt 5):517-27.PMID: 16138910 [PubMed - indexed for MEDLINE]Related articles

    29.

    Genome-wide scans for heritability of fasting serum insulin and glucose concentrations in hypertensive families.

    Freedman BI, Rich SS, Sale MM, Heiss G, Djoussé L, Pankow JS, Province MA, Rao DC, Lewis CE, Chen YD, Beck SR; HyperGEN Investigators.

    Diabetologia. 2005 Apr;48(4):661-8. Epub 2005 Mar 4. Erratum in: Diabetologia. 2005 Aug;48(8):1678. PMID: 15747111 [PubMed - indexed for MEDLINE]Related articles

    30.

    A genome scan for all-cause end-stage renal disease in African Americans.

    Freedman BI, Bowden DW, Rich SS, Valis CJ, Sale MM, Hicks PJ, Langefeld CD.

    Nephrol Dial Transplant. 2005 Apr;20(4):712-8. Epub 2005 Feb 8.PMID: 15701670 [PubMed - indexed for MEDLINE]Related articlesFree article

    31.

    A genome scan for ESRD in black families enriched for nondiabetic nephropathy.

    Freedman BI, Langefeld CD, Rich SS, Valis CJ, Sale MM, Williams AH, Brown WM, Beck SR, Hicks PJ, Bowden DW.

    J Am Soc Nephrol. 2004 Oct;15(10):2719-27.PMID: 15466277 [PubMed - indexed for MEDLINE]Related articlesFree article

    32.

    A genome scan for diabetic nephropathy in African Americans.

    Bowden DW, Colicigno CJ, Langefeld CD, Sale MM, Williams A, Anderson PJ, Rich SS, Freedman BI.

    Kidney Int. 2004 Oct;66(4):1517-26.PMID: 15458446 [PubMed - indexed for MEDLINE]Related articles

    33.

    A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance.

    Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM.

    J Med Genet. 2004 Aug;41(8):e106. No abstract available. Erratum in: J Med Genet. 2005 Mar;42(3):288. J Med Genet. 2008 Apr;45(4):256. PMID: 15286166 [PubMed - indexed for MEDLINE]Related articlesFree article

    34.

    Does the addition of information on genotype improve prediction of the risk of melanoma and nonmelanoma skin cancer beyond that obtained from skin phenotype?

    Dwyer T, Stankovich JM, Blizzard L, FitzGerald LM, Dickinson JL, Reilly A, Williamson J, Ashbolt R, Berwick M, Sale MM.

    Am J Epidemiol. 2004 May 1;159(9):826-33.PMID: 15105175 [PubMed - indexed for MEDLINE]Related articlesFree article

    35.

    A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q.

    Sale MM, Freedman BI, Langefeld CD, Williams AH, Hicks PJ, Colicigno CJ, Beck SR, Brown WM, Rich SS, Bowden DW.

    Diabetes. 2004 Mar;53(3):830-7.PMID: 14988270 [PubMed - indexed for MEDLINE]Related articlesFree article

    36.

    Trends in diabetes management practices of patients from an Australian insulin-treated diabetes register.

    Sale MM, Hazelwood K, Zimmet PZ, Shaw JE, Stankovich JM, Greenaway TM, Dwyer T.

    Diabet Med. 2004 Feb;21(2):165-70.PMID: 14984452 [PubMed - indexed for MEDLINE]Related articles

    37.

    Investigation of crystallin genes in familial cataract, and report of two disease associated mutations.

    Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM.

    Br J Ophthalmol. 2004 Jan;88(1):79-83.PMID: 14693780 [PubMed - indexed for MEDLINE]Related articlesFree article

    38.

    Investigation of albinism genes in congenital esotropia.

    Burdon KP, Wilkinson RM, Barbour JM, Dickinson JL, Stankovich JM, Mackey DA, Sale MM.

    Mol Vis. 2003 Dec 16;9:710-4.PMID: 14685142 [PubMed - indexed for MEDLINE]Related articlesFree article

    39.

    Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

    Burdon KP, McKay JD, Sale MM, Russell-Eggitt IM, Mackey DA, Wirth MG, Elder JE, Nicoll A, Clarke MP, FitzGerald LM, Stankovich JM, Shaw MA, Sharma S, Gajovic S, Gruss P, Ross S, Thomas P, Voss AK, Thomas T, Gécz J, Craig JE.

    Am J Hum Genet. 2003 Nov;73(5):1120-30. Epub 2003 Oct 16.PMID: 14564667 [PubMed - indexed for MEDLINE]Related articlesFree article

    40.

    Evidence for a novel type 1 diabetes susceptibility locus on chromosome 8.

    Sale MM, FitzGerald LM, Charlesworth JC, Bowden DW, Rich SS.

    Diabetes. 2002 Dec;51 Suppl 3:S316-9.PMID: 12475769 [PubMed - indexed for MEDLINE]Related articlesFree article

    41.

    Investigation of chromosome 2q in osteoarthritis of the hand: no significant linkage in a Tasmanian population.

    Stankovich J, Sale MM, Cooley HM, Bahlo M, Reilly A, Dickinson JL, Jones G.

    Ann Rheum Dis. 2002 Dec;61(12):1081-4.PMID: 12429539 [PubMed - indexed for MEDLINE]Related articlesFree article

    42.

    Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene.

    Sale MM, Craig JE, Charlesworth JC, FitzGerald LM, Hanson IM, Dickinson JL, Matthews SJ, Heyningen Vv V, Fingert JH, Mackey DA.

    Hum Mutat. 2002 Oct;20(4):322.PMID: 12325030 [PubMed - indexed for MEDLINE]Related articles

    43.

    Retinopathy of prematurity: recent advances in our understanding.

    Wheatley CM, Dickinson JL, Mackey DA, Craig JE, Sale MM.

    Arch Dis Child Fetal Neonatal Ed. 2002 Sep;87(2):F78-82. Review.PMID: 12193510 [PubMed - indexed for MEDLINE]Related articlesFree article

    44.

    Retinopathy of prematurity: recent advances in our understanding.

    Wheatley CM, Dickinson JL, Mackey DA, Craig JE, Sale MM.

    Br J Ophthalmol. 2002 Jun;86(6):696-700. Review.PMID: 12034695 [PubMed - indexed for MEDLINE]Related articlesFree article

    45.

    Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis.

    Rubio JP, Bahlo M, Butzkueven H, van Der Mei IA, Sale MM, Dickinson JL, Groom P, Johnson LJ, Simmons RD, Tait B, Varney M, Taylor B, Dwyer T, Williamson R, Gough NM, Kilpatrick TJ, Speed TP, Foote SJ.

    Am J Hum Genet. 2002 May;70(5):1125-37. Epub 2002 Mar 29.PMID: 11923913 [PubMed - indexed for MEDLINE]Related articlesFree article

    46.

    Using genetic advances to investigate diabetes in Tasmania.

    Dwyer T, Sale MM, Stankovich JM, Hazelwood KF, Mulcahy N.

    Diabetes Technol Ther. 2001 Winter;3(4):641-6. No abstract available. PMID: 11911178 [PubMed - indexed for MEDLINE]Related articles

    47.

    Investigation of the prevalence of the myocilin Q368STOP mutation in Ugandan glaucoma patients.

    Sale MM, FitzGerald LM, Kagame K, Erdmann I, Craig JE, Dickinson JL, Cooper RL.

    Ophthalmic Genet. 2002 Mar;23(1):67-9. No abstract available. PMID: 11910561 [PubMed - indexed for MEDLINE]Related articles

    48.

    Laboratory methods in ophthalmic genetics: obtaining DNA from patients.

    Dickinson JL, Sale MM, Craig JE, Mackey DA.

    Ophthalmic Genet. 2001 Mar;22(1):49-60. Review.PMID: 11262650 [PubMed - indexed for MEDLINE]Related articles

    49.

    Association of autoimmune thyroid disease with microsatellite markers for the thyrotropin receptor gene and CTLA-4 in Japanese patients.

    Akamizu T, Sale MM, Rich SS, Hiratani H, Noh JY, Kanamoto N, Saijo M, Miyamoto Y, Saito Y, Nakao K, Bowden DW.

    Thyroid. 2000 Oct;10(10):851-8.PMID: 11081251 [PubMed - indexed for MEDLINE]Related articles

    50.

    Analysis of the HNF4 alpha gene in Caucasian type II diabetic nephropathic patients.

    Price JA, Fossey SC, Sale MM, Brewer CS, Freedman BI, Wuerth JP, Bowden DW.

    Diabetologia. 2000 Mar;43(3):364-72.PMID: 10768098 [PubMed - indexed for MEDLINE]Related articles

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