PubMed

Cell adhesion molecule 1: a novel risk factor for venous thrombosis.

Hasstedt SJ, Bezemer ID, Callas PW, Vossen CY, Trotman W, Hebbel RP, Demers C, Rosendaal FR, Bovill EG.

Blood. 2009 Oct 1;114(14):3084-91. Epub 2009 Jul 30.PMID: 19643986 [PubMed - in process]Related articlesFree article

A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22.

Butterfield RJ, Ramachandran D, Hasstedt SJ, Otterud BE, Leppert MF, Swoboda KJ, Flanigan KM.

Neuromuscul Disord. 2009 Apr;19(4):279-87. Epub 2009 Mar 21.PMID: 19318250 [PubMed - indexed for MEDLINE]Related articles

Genome-wide linkage and admixture mapping of type 2 diabetes in African American families from the American Diabetes Association GENNID (Genetics of NIDDM) Study Cohort.

Elbein SC, Das SK, Hallman DM, Hanis CL, Hasstedt SJ.

Diabetes. 2009 Jan;58(1):268-74. Epub 2008 Oct 7.PMID: 18840782 [PubMed - indexed for MEDLINE]Related articlesFree article

Type 2 diabetes susceptibility genes on chromosome 1q21-24.

Hasstedt SJ, Chu WS, Das SK, Wang H, Elbein SC.

Ann Hum Genet. 2008 Mar;72(Pt 2):163-9.PMID: 18269685 [PubMed - indexed for MEDLINE]Related articles

Exclusion of the alpha2 subunit of platelet-activating factor acetylhydrolase 1b (PAFAH1B2) as a prothrombotic gene in a protein C-deficient kindred and population-based case-control sample.

Hasstedt SJ, Scott BT, Rosendaal FR, Callas PW, Vossen CY, Long GL, Bovill EG.

Thromb Haemost. 2007 Sep;98(3):587-92.PMID: 17849047 [PubMed - indexed for MEDLINE]Related articles

A genetic basis for the interrelation of coagulation factors.

Vossen CY, Callas PW, Hasstedt SJ, Long GL, Rosendaal FR, Bovill EG.

J Thromb Haemost. 2007 Sep;5(9):1930-5.PMID: 17723132 [PubMed - indexed for MEDLINE]Related articles

Transcription factor 7-like 2 polymorphisms and type 2 diabetes, glucose homeostasis traits and gene expression in US participants of European and African descent.

Elbein SC, Chu WS, Das SK, Yao-Borengasser A, Hasstedt SJ, Wang H, Rasouli N, Kern PA.

Diabetologia. 2007 Aug;50(8):1621-30. Epub 2007 Jun 20.PMID: 17579832 [PubMed - indexed for MEDLINE]Related articles

Linkage analysis for three coagulation factors clustering on chromosome 13q34: factor VII, factor X and protein Z.

Vossen CY, Hasstedt SJ, Demers C, Rosendaal FR, Bovill EG.

J Thromb Haemost. 2007 Jun;5(6):1325-7. No abstract available. PMID: 17403098 [PubMed - indexed for MEDLINE]Related articles

Meta-analysis of genome-wide linkage studies of quantitative lipid traits in families ascertained for type 2 diabetes.

Malhotra A, Elbein SC, Ng MC, Duggirala R, Arya R, Imperatore G, Adeyemo A, Pollin TI, Hsueh WC, Chan JC, Rotimi C, Hanson RL, Hasstedt SJ, Wolford JK.

Diabetes. 2007 Mar;56(3):890-6.PMID: 17327462 [PubMed - indexed for MEDLINE]Related articlesFree article

Polymorphisms in the glucokinase-associated, dual-specificity phosphatase 12 (DUSP12) gene under chromosome 1q21 linkage peak are associated with type 2 diabetes.

Das SK, Chu WS, Hale TC, Wang X, Craig RL, Wang H, Shuldiner AR, Froguel P, Deloukas P, McCarthy MI, Zeggini E, Hasstedt SJ, Elbein SC.

Diabetes. 2006 Sep;55(9):2631-9.PMID: 16936214 [PubMed - indexed for MEDLINE]Related articlesFree article

A genome search for genetic determinants of markers of protein C activation.

Vossen CY, Hasstedt SJ, Scott BT, Rosendaal FR, Bovill EG.

J Thromb Haemost. 2006 Mar;4(3):706-8. No abstract available. PMID: 16460468 [PubMed - indexed for MEDLINE]Related articles

Sodium bicarbonate cotransporter polymorphisms are associated with baseline and 10-year follow-up blood pressures.

Hunt SC, Xin Y, Wu LL, Cawthon RM, Coon H, Hasstedt SJ, Hopkins PN.

Hypertension. 2006 Mar;47(3):532-6. Epub 2005 Dec 19.PMID: 16365189 [PubMed - indexed for MEDLINE]Related articlesFree article

Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides.

Coon H, Xin Y, Hopkins PN, Cawthon RM, Hasstedt SJ, Hunt SC.

Hum Genet. 2005 Sep;117(5):444-51. Epub 2005 Jun 16.PMID: 15959806 [PubMed - indexed for MEDLINE]Related articles

The power to detect genetic linkage for quantitative traits in the Utah CEPH pedigrees.

Malhotra A, Cromer K, Leppert MF, Hasstedt SJ.

J Hum Genet. 2005;50(2):69-75. Epub 2005 Jan 29.PMID: 15682273 [PubMed - indexed for MEDLINE]Related articles

Calsquestrin 1 (CASQ1) gene polymorphisms under chromosome 1q21 linkage peak are associated with type 2 diabetes in Northern European Caucasians.

Das SK, Chu W, Zhang Z, Hasstedt SJ, Elbein SC.

Diabetes. 2004 Dec;53(12):3300-6.PMID: 15561963 [PubMed - indexed for MEDLINE]Related articlesFree article

Model-fitting and linkage analysis of sodium-lithium countertransport.

Hasstedt SJ, Camp NJ, Hopkins PN, Coon H, McKinney JT, Cawthon RM, Hunt SC.

Eur J Hum Genet. 2004 Dec;12(12):1055-61.PMID: 15383825 [PubMed - indexed for MEDLINE]Related articlesFree article

Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees.

Hunt SC, Coon H, Hasstedt SJ, Cawthon RM, Camp NJ, Wu LL, Hopkins PN.

Am J Hypertens. 2004 Jun;17(6):511-5.PMID: 15177524 [PubMed - indexed for MEDLINE]Related articles

Genome scan of venous thrombosis in a pedigree with protein C deficiency.

Hasstedt SJ, Scott BT, Callas PW, Vossen CY, Rosendaal FR, Long GL, Bovill EG.

J Thromb Haemost. 2004 Jun;2(6):868-73.PMID: 15140118 [PubMed - indexed for MEDLINE]Related articles

Heritability of plasma concentrations of clotting factors and measures of a prethrombotic state in a protein C-deficient family.

Vossen CY, Hasstedt SJ, Rosendaal FR, Callas PW, Bauer KA, Broze GJ, Hoogendoorn H, Long GL, Scott BT, Bovill EG.

J Thromb Haemost. 2004 Feb;2(2):242-7.PMID: 14995985 [PubMed - indexed for MEDLINE]Related articles

Linkage and association mapping of a chromosome 1q21-q24 type 2 diabetes susceptibility locus in northern European Caucasians.

Das SK, Hasstedt SJ, Zhang Z, Elbein SC.

Diabetes. 2004 Feb;53(2):492-9.PMID: 14747303 [PubMed - indexed for MEDLINE]Related articlesFree article

Uncoupling protein-2 polymorphisms in type 2 diabetes, obesity, and insulin secretion.

Wang H, Chu WS, Lu T, Hasstedt SJ, Kern PA, Elbein SC.

Am J Physiol Endocrinol Metab. 2004 Jan;286(1):E1-7. Epub 2003 Aug 12.PMID: 12915397 [PubMed - indexed for MEDLINE]Related articlesFree article

Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended utah pedigrees.

Camp NJ, Hopkins PN, Hasstedt SJ, Coon H, Malhotra A, Cawthon RM, Hunt SC.

Hypertension. 2003 Sep;42(3):322-8. Epub 2003 Jul 21.PMID: 12874090 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular screening and association studies of retinoid-related orphan receptor gamma (RORC): a positional and functional candidate for type 2 diabetes.

Wang H, Chu W, Das SK, Zheng Z, Hasstedt SJ, Elbein SC.

Mol Genet Metab. 2003 Jul;79(3):176-82.PMID: 12855222 [PubMed - indexed for MEDLINE]Related articles

Further evidence for the role of genes on chromosome 2 and chromosome 5 in the inheritance of pulmonary function.

Malhotra A, Peiffer AP, Ryujin DT, Elsner T, Kanner RE, Leppert MF, Hasstedt SJ.

Am J Respir Crit Care Med. 2003 Sep 1;168(5):556-61. Epub 2003 Jun 5.PMID: 12791583 [PubMed - indexed for MEDLINE]Related articlesFree article

Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat.

Hunt SC, Hasstedt SJ, Coon H, Camp NJ, Cawthon RM, Wu LL, Hopkins PN.

Kidney Int. 2002 Oct;62(4):1143-8.PMID: 12234284 [PubMed - indexed for MEDLINE]Related articlesFree article

Liver pyruvate kinase polymorphisms are associated with type 2 diabetes in northern European Caucasians.

Wang H, Chu W, Das SK, Ren Q, Hasstedt SJ, Elbein SC.

Diabetes. 2002 Sep;51(9):2861-5.PMID: 12196482 [PubMed - indexed for MEDLINE]Related articlesFree article

Characterization of the human prostaglandin H synthase 1 gene (PTGS1): exclusion by genetic linkage analysis as a second modifier gene in familial thrombosis.

Scott BT, Hasstedt SJ, Bovill EG, Callas PW, Valliere JE, Wang L, Wu KK, Long GL.

Blood Coagul Fibrinolysis. 2002 Sep;13(6):519-31.PMID: 12192304 [PubMed - indexed for MEDLINE]Related articles

Mutation screening and association of human retinoid X receptor gamma variation with lipid levels in familial type 2 diabetes.

Wang H, Chu W, Hemphill C, Hasstedt SJ, Elbein SC.

Mol Genet Metab. 2002 May;76(1):14-22.PMID: 12175776 [PubMed - indexed for MEDLINE]Related articles

Evaluation of apolipoprotein A-II as a positional candidate gene for familial Type II diabetes, altered lipid concentrations, and insulin resistance.

Elbein SC, Chu W, Ren Q, Wang H, Hemphill C, Hasstedt SJ.

Diabetologia. 2002 Jul;45(7):1026-33. Epub 2002 May 8.PMID: 12136402 [PubMed - indexed for MEDLINE]Related articles

Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians.

Elbein SC, Chu W, Ren Q, Hemphill C, Schay J, Cox NJ, Hanis CL, Hasstedt SJ.

J Clin Endocrinol Metab. 2002 Feb;87(2):650-4.PMID: 11836299 [PubMed - indexed for MEDLINE]Related articlesFree article

Quantitative trait linkage analysis of lipid-related traits in familial type 2 diabetes: evidence for linkage of triglyceride levels to chromosome 19q.

Elbein SC, Hasstedt SJ.

Diabetes. 2002 Feb;51(2):528-35.PMID: 11812765 [PubMed - indexed for MEDLINE]Related articlesFree article

Role of common sequence variants in insulin secretion in familial type 2 diabetic kindreds: the sulfonylurea receptor, glucokinase, and hepatocyte nuclear factor 1alpha genes.

Elbein SC, Sun J, Scroggin E, Teng K, Hasstedt SJ.

Diabetes Care. 2001 Mar;24(3):472-8.PMID: 11289470 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred.

Scott BT, Bovill EG, Callas PW, Hasstedt SJ, Leppert MF, Valliere JE, Varvil TS, Long GL.

Thromb Haemost. 2001 Jan;85(1):82-7.PMID: 11204593 [PubMed - indexed for MEDLINE]Related articles

Effect of the peroxisome proliferator-activated receptor-gamma 2 pro(12)ala variant on obesity, glucose homeostasis, and blood pressure in members of familial type 2 diabetic kindreds.

Hasstedt SJ, Ren QF, Teng K, Elbein SC.

J Clin Endocrinol Metab. 2001 Feb;86(2):536-41.PMID: 11158005 [PubMed - indexed for MEDLINE]Related articlesFree article

The G20210A prothrombin polymorphism is not associated with increased thromboembolic risk in a large protein C deficient kindred.

Bovill EG, Hasstedt SJ, Callas PW, Valliere JE, Scott BT, Bauer KA, Long GL.

Thromb Haemost. 2000 Mar;83(3):366-70.PMID: 10744139 [PubMed - indexed for MEDLINE]Related articles

Hereditary thrombophilia as a model for multigenic disease.

Bovill EG, Hasstedt SJ, Leppert MF, Long GL.

Thromb Haemost. 1999 Aug;82(2):662-6. Review. No abstract available. PMID: 10605765 [PubMed - indexed for MEDLINE]Related articles

A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians.

Elbein SC, Hoffman MD, Teng K, Leppert MF, Hasstedt SJ.

Diabetes. 1999 May;48(5):1175-82.PMID: 10331426 [PubMed - indexed for MEDLINE]Related articlesFree article

Heritability of pancreatic beta-cell function among nondiabetic members of Caucasian familial type 2 diabetic kindreds.

Elbein SC, Hasstedt SJ, Wegner K, Kahn SE.

J Clin Endocrinol Metab. 1999 Apr;84(4):1398-403.PMID: 10199785 [PubMed - indexed for MEDLINE]Related articlesFree article

Is there a link between African iron overload and the described mutations of the hereditary haemochromatosis gene?

McNamara L, MacPhail AP, Gordeuk VR, Hasstedt SJ, Rouault T.

Br J Haematol. 1998 Sep;102(5):1176-8.PMID: 9753041 [PubMed - indexed for MEDLINE]Related articles

An unknown genetic defect increases venous thrombosis risk, through interaction with protein C deficiency.

Hasstedt SJ, Bovill EG, Callas PW, Long GL.

Am J Hum Genet. 1998 Aug;63(2):569-76.PMID: 9683579 [PubMed - indexed for MEDLINE]Related articlesFree article

Evidence of genetic transmission in African iron overload.

Moyo VM, Mandishona E, Hasstedt SJ, Gangaidzo IT, Gomo ZA, Khumalo H, Saungweme T, Kiire CF, Paterson AC, Bloom P, MacPhail AP, Rouault T, Gordeuk VR.

Blood. 1998 Feb 1;91(3):1076-82.PMID: 9446671 [PubMed - indexed for MEDLINE]Related articlesFree article

Uncoupling protein 2 region on chromosome 11q13 is not linked to markers of obesity in familial type 2 diabetes.

Elbein SC, Leppert M, Hasstedt S.

Diabetes. 1997 Dec;46(12):2105-7. No abstract available. PMID: 9392504 [PubMed - indexed for MEDLINE]Related articles

Recessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genes.

Hasstedt SJ, Hoffman M, Leppert MF, Elbein SC.

Am J Hum Genet. 1997 Sep;61(3):668-77.PMID: 9326333 [PubMed - indexed for MEDLINE]Related articlesFree article

Do non-insulin-dependent diabetes mellitus (NIDDM) and insulin-dependent diabetes mellitus (IDDM) share genetic susceptibility loci? An analysis of putative IDDM susceptibility regions in familial NIDDM.

Elbein SC, Hoffman MD, Mayorga RA, Barrett KL, Leppert M, Hasstedt S.

Metabolism. 1997 Jan;46(1):48-52.PMID: 9005968 [PubMed - indexed for MEDLINE]Related articles

Role of the beta 3-adrenergic receptor locus in obesity and noninsulin-dependent diabetes among members of Caucasian families with a diabetic sibling pair.

Elbein SC, Hoffman M, Barrett K, Wegner K, Miles C, Bachman K, Berkowitz D, Shuldiner AR, Leppert MF, Hasstedt S.

J Clin Endocrinol Metab. 1996 Dec;81(12):4422-7.PMID: 8954053 [PubMed - indexed for MEDLINE]Related articles

Intermediate inheritance of Tourette syndrome, assuming assortative mating.

Hasstedt SJ, Leppert M, Filloux F, van de Wetering BJ, McMahon WM.

Am J Hum Genet. 1995 Sep;57(3):682-9.PMID: 7668298 [PubMed - indexed for MEDLINE]Related articlesFree article

Phenotypic assortative mating in segregation analysis.

Hasstedt SJ.

Genet Epidemiol. 1995;12(2):109-27.PMID: 7607413 [PubMed - indexed for MEDLINE]Related articles

HLA-linked rheumatoid arthritis.

Hasstedt SJ, Clegg DO, Ingles L, Ward RH.

Am J Hum Genet. 1994 Oct;55(4):738-46.PMID: 7942852 [PubMed - indexed for MEDLINE]Related articlesFree article

Tabulations and expectations regarding the genetics of human hypertension.

Williams RR, Hunt SC, Hopkins PN, Hasstedt SJ, Wu LL, Lalouel JM.

Kidney Int Suppl. 1994 Jan;44:S57-64. Review.PMID: 8127035 [PubMed - indexed for MEDLINE]Related articles

Evidence for multiple genes determining sodium transport.

Hasstedt SJ, Hunt SC, Wu LL, Williams RR.

Genet Epidemiol. 1994;11(6):553-68.PMID: 7713395 [PubMed - indexed for MEDLINE]Related articles