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Items: 1 to 50 of 117

1.

Discovery and cross-validation of peripheral blood and renal biopsy gene expression signatures from ethnically diverse kidney transplant populations.

Ventura CG, Whisenant T, Gelbart T, David DSR, Agena F, Salomon DR, David-Neto E, Kurian SM.

Am J Transplant. 2019 Jun 1. doi: 10.1111/ajt.15482. [Epub ahead of print]

PMID:
31152474
2.

Precision medicine for suicidality: from universality to subtypes and personalization.

Niculescu AB, Le-Niculescu H, Levey DF, Phalen PL, Dainton HL, Roseberry K, Niculescu EM, Niezer JO, Williams A, Graham DL, Jones TJ, Venugopal V, Ballew A, Yard M, Gelbart T, Kurian SM, Shekhar A, Schork NJ, Sandusky GE, Salomon DR.

Mol Psychiatry. 2017 Sep;22(9):1250-1273. doi: 10.1038/mp.2017.128. Epub 2017 Aug 15.

3.

Orthogonal Comparison of Molecular Signatures of Kidney Transplants With Subclinical and Clinical Acute Rejection: Equivalent Performance Is Agnostic to Both Technology and Platform.

Kurian SM, Velazquez E, Thompson R, Whisenant T, Rose S, Riley N, Harrison F, Gelbart T, Friedewald JJ, Charette J, Brietigam S, Peysakhovich J, First MR, Abecassis MM, Salomon DR.

Am J Transplant. 2017 Aug;17(8):2103-2116. doi: 10.1111/ajt.14224. Epub 2017 Apr 3.

4.

Peripheral Blood Cell Gene Expression Diagnostic for Identifying Symptomatic Transthyretin Amyloidosis Patients: Male and Female Specific Signatures.

Kurian SM, Novais M, Whisenant T, Gelbart T, Buxbaum JN, Kelly JW, Coelho T, Salomon DR.

Theranostics. 2016 Jul 18;6(11):1792-809. doi: 10.7150/thno.14584. eCollection 2016.

5.

Genome-wide expression profiling in the peripheral blood of patients with fibromyalgia.

Jones KD, Gelbart T, Whisenant TC, Waalen J, Mondala TS, Iklé DN, Salomon DR, Bennett RM, Kurian SM.

Clin Exp Rheumatol. 2016 Mar-Apr;34(2 Suppl 96):S89-98. Epub 2016 Feb 12.

6.

Towards understanding and predicting suicidality in women: biomarkers and clinical risk assessment.

Levey DF, Niculescu EM, Le-Niculescu H, Dainton HL, Phalen PL, Ladd TB, Weber H, Belanger E, Graham DL, Khan FN, Vanipenta NP, Stage EC, Ballew A, Yard M, Gelbart T, Shekhar A, Schork NJ, Kurian SM, Sandusky GE, Salomon DR, Niculescu AB.

Mol Psychiatry. 2016 Jun;21(6):768-85. doi: 10.1038/mp.2016.31. Epub 2016 Apr 5.

PMID:
27046645
7.

Gene Expression in Biopsies of Acute Rejection and Interstitial Fibrosis/Tubular Atrophy Reveals Highly Shared Mechanisms That Correlate With Worse Long-Term Outcomes.

Modena BD, Kurian SM, Gaber LW, Waalen J, Su AI, Gelbart T, Mondala TS, Head SR, Papp S, Heilman R, Friedewald JJ, Flechner SM, Marsh CL, Sung RS, Shidban H, Chan L, Abecassis MM, Salomon DR.

Am J Transplant. 2016 Jul;16(7):1982-98. doi: 10.1111/ajt.13728. Epub 2016 Mar 15.

8.

Understanding and predicting suicidality using a combined genomic and clinical risk assessment approach.

Niculescu AB, Levey DF, Phalen PL, Le-Niculescu H, Dainton HD, Jain N, Belanger E, James A, George S, Weber H, Graham DL, Schweitzer R, Ladd TB, Learman R, Niculescu EM, Vanipenta NP, Khan FN, Mullen J, Shankar G, Cook S, Humbert C, Ballew A, Yard M, Gelbart T, Shekhar A, Schork NJ, Kurian SM, Sandusky GE, Salomon DR.

Mol Psychiatry. 2015 Nov;20(11):1266-85. doi: 10.1038/mp.2015.112. Epub 2015 Aug 18.

9.

Molecular classifiers for acute kidney transplant rejection in peripheral blood by whole genome gene expression profiling.

Kurian SM, Williams AN, Gelbart T, Campbell D, Mondala TS, Head SR, Horvath S, Gaber L, Thompson R, Whisenant T, Lin W, Langfelder P, Robison EH, Schaffer RL, Fisher JS, Friedewald J, Flechner SM, Chan LK, Wiseman AC, Shidban H, Mendez R, Heilman R, Abecassis MM, Marsh CL, Salomon DR.

Am J Transplant. 2014 May;14(5):1164-72. doi: 10.1111/ajt.12671. Epub 2014 Apr 11.

10.

Hemolytic anemia associated with a novel heterozygote mutation 1183A in the PK-LR gene (PK- Jordan).

Karadsheh NS, Gelbart T, Naffa RG.

Int J Lab Hematol. 2014 Aug;36(4):e66-8. doi: 10.1111/ijlh.12174. Epub 2013 Dec 12. No abstract available.

PMID:
24330591
11.

RNA purification and expression analysis using microarrays and RNA deep sequencing.

Head SR, Mondala T, Gelbart T, Ordoukhanian P, Chappel R, Hernandez G, Salomon DR.

Methods Mol Biol. 2013;1034:385-403. doi: 10.1007/978-1-62703-493-7_25.

PMID:
23775753
12.

Polymorphisms and mutations of human TMPRSS6 in iron deficiency anemia.

Beutler E, Van Geet C, te Loo DM, Gelbart T, Crain K, Truksa J, Lee PL.

Blood Cells Mol Dis. 2010 Jan 15;44(1):16-21. doi: 10.1016/j.bcmd.2009.09.001. Epub 2009 Oct 8.

13.

Suppression of the hepcidin-encoding gene Hamp permits iron overload in mice lacking both hemojuvelin and matriptase-2/TMPRSS6.

Truksa J, Gelbart T, Peng H, Beutler E, Beutler B, Lee P.

Br J Haematol. 2009 Nov;147(4):571-81. doi: 10.1111/j.1365-2141.2009.07873.x. Epub 2009 Sep 8.

PMID:
19751239
14.

Fatal kernicterus in a girl deficient in glucose-6-phosphate dehydrogenase: a paradigm of synergistic heterozygosity.

Zangen S, Kidron D, Gelbart T, Roy-Chowdhury N, Wang X, Kaplan M.

J Pediatr. 2009 Apr;154(4):616-9. doi: 10.1016/j.jpeds.2008.10.049.

PMID:
19324225
15.

The anemia of ageing is not associated with increased plasma hepcidin levels.

Lee P, Gelbart T, Waalen J, Beutler E.

Blood Cells Mol Dis. 2008 Nov-Dec;41(3):252-4. doi: 10.1016/j.bcmd.2008.06.005. Epub 2008 Aug 3.

PMID:
18676162
16.

The serine protease TMPRSS6 is required to sense iron deficiency.

Du X, She E, Gelbart T, Truksa J, Lee P, Xia Y, Khovananth K, Mudd S, Mann N, Moresco EM, Beutler E, Beutler B.

Science. 2008 May 23;320(5879):1088-92. doi: 10.1126/science.1157121. Epub 2008 May 1.

17.
18.

Screening for hemochromatosis by measuring ferritin levels: a more effective approach.

Waalen J, Felitti VJ, Gelbart T, Beutler E.

Blood. 2008 Apr 1;111(7):3373-6. Epub 2007 Nov 19.

19.

Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to gamma-glutamylcysteine synthetase deficiency in a patient of Moroccan origin.

Mañú Pereira M, Gelbart T, Ristoff E, Crain KC, Bergua JM, López Lafuente A, Kalko SG, García Mateos E, Beutler E, Vives Corrons JL.

Haematologica. 2007 Nov;92(11):e102-5.

20.

Soluble transferrin receptor-1 levels in mice do not affect iron absorption.

Flanagan JM, Peng H, Wang L, Gelbart T, Lee P, Johnson Sasu B, Beutler E.

Acta Haematol. 2006;116(4):249-54.

PMID:
17119325
21.

Helicobacter pylori infection and HFE hemochromatosis.

Beutler E, Gelbart T.

Blood Cells Mol Dis. 2006 Nov-Dec;37(3):188-91. Epub 2006 Sep 25.

PMID:
16996754
22.

Hematologically important mutations: Gaucher disease.

Beutler E, Gelbart T, Scott CR.

Blood Cells Mol Dis. 2005 Nov-Dec;35(3):355-64. Epub 2005 Sep 26. Review. No abstract available.

PMID:
16185900
23.

Chronic inflammation does not appear to modify the homozygous hereditary hemochromatosis phenotype.

Beutler E, Waalen J, Gelbart T.

Blood Cells Mol Dis. 2005 Nov-Dec;35(3):326-7. Epub 2005 Sep 9.

PMID:
16154780
24.

Relationship between molecular variants and clinical manifestions in twelve glucose-6-phosphate dehydrogenase-deficient patients in Jordan.

Karadsheh NS, Gelbart T, Schulten HJ, Efferth T, Awidi A.

Acta Haematol. 2005;114(2):125-6. No abstract available.

PMID:
16103639
25.

Regulation of hepcidin transcription by interleukin-1 and interleukin-6.

Lee P, Peng H, Gelbart T, Wang L, Beutler E.

Proc Natl Acad Sci U S A. 2005 Feb 8;102(6):1906-10. Epub 2005 Jan 31.

26.

Molecular characterization of a third case of human atransferrinemia.

Knisely AS, Gelbart T, Beutler E.

Blood. 2004 Oct 15;104(8):2607. No abstract available.

PMID:
15466165
27.

The IL-6- and lipopolysaccharide-induced transcription of hepcidin in HFE-, transferrin receptor 2-, and beta 2-microglobulin-deficient hepatocytes.

Lee P, Peng H, Gelbart T, Beutler E.

Proc Natl Acad Sci U S A. 2004 Jun 22;101(25):9263-5. Epub 2004 Jun 10.

28.

Genotypic and phenotypic heterogeneity of African Americans with primary iron overload.

Barton JC, Acton RT, Rivers CA, Bertoli LF, Gelbart T, West C, Beutler E.

Blood Cells Mol Dis. 2003 Nov-Dec;31(3):310-9.

PMID:
14636644
29.

Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans.

Beutler E, Barton JC, Felitti VJ, Gelbart T, West C, Lee PL, Waalen J, Vulpe C.

Blood Cells Mol Dis. 2003 Nov-Dec;31(3):305-9.

PMID:
14636643
30.

Polymorphisms in the human homologue of the drosophila Indy (I'm not dead yet) gene.

Lee P, Ho N, Gelbart T, Beutler E.

Mech Ageing Dev. 2003 Aug-Sep;124(8-9):897-902.

PMID:
14499494
31.

Penetrance of hemochromatosis.

Waalen J, Felitti V, Gelbart T, Ho NJ, Beutler E.

Blood Cells Mol Dis. 2002 Nov-Dec;29(3):418-32.

PMID:
12678056
32.
33.

Seeking candidate mutations that affect iron homeostasis.

Lee P, Gelbart T, West C, Halloran C, Beutler E.

Blood Cells Mol Dis. 2002 Nov-Dec;29(3):471-87.

PMID:
12547238
34.

Juvenile hemochromatosis in the southeastern United States: a report of seven cases in two kinships.

Barton JC, Rao SV, Pereira NM, Gelbart T, Beutler E, Rivers CA, Acton RT.

Blood Cells Mol Dis. 2002 Jul-Aug;29(1):104-15.

PMID:
12482411
35.

Polymorphisms in iron-responsive binding protein 2 and lack of association with sporadic Parkinson's disease.

Lee PL, Gelbart T, West C, Halloran C, Sipe JC, Beutler E.

Mov Disord. 2002 Nov;17(6):1302-4.

PMID:
12465072
36.

Haptoglobin polymorphism and iron homeostasis.

Beutler E, Gelbart T, Lee P.

Clin Chem. 2002 Dec;48(12):2232-5.

37.

Prevalence of coronary heart disease associated with HFE mutations in adults attending a health appraisal center.

Waalen J, Felitti V, Gelbart T, Ho NJ, Beutler E.

Am J Med. 2002 Oct 15;113(6):472-9.

PMID:
12427496
38.

Disruption of a novel regulatory element in the erythroid-specific promoter of the human PKLR gene causes severe pyruvate kinase deficiency.

van Wijk R, van Solinge WW, Nerlov C, Beutler E, Gelbart T, Rijksen G, Nielsen FC.

Blood. 2003 Feb 15;101(4):1596-602. Epub 2002 Sep 26.

PMID:
12393511
39.
40.
41.
42.

Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene.

Waalen J, Felitti V, Gelbart T, Ho NJ, Beutler E.

Mayo Clin Proc. 2002 Jun;77(6):522-30.

PMID:
12059121
44.

A previously undescribed nonsense mutation of the HFE gene.

Beutler E, Griffin MJ, Gelbart T, West C.

Clin Genet. 2002 Jan;61(1):40-2.

PMID:
11903354
45.

Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.

Beutler E, Felitti VJ, Koziol JA, Ho NJ, Gelbart T.

Lancet. 2002 Jan 19;359(9302):211-8.

PMID:
11812557
47.

Synergy between TLR2 and TLR4: a safety mechanism.

Beutler E, Gelbart T, West C.

Blood Cells Mol Dis. 2001 Jul-Aug;27(4):728-30.

PMID:
11778656
48.

Genetics of iron storage and hemochromatosis.

Beutler E, Felitti V, Gelbart T, Ho N.

Drug Metab Dispos. 2001 Apr;29(4 Pt 2):495-9.

PMID:
11259339
49.

Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studies.

Corrons JL, Alvarez R, Pujades A, Zarza R, Oliva E, Lasheras G, Callis M, Ribes A, Gelbart T, Beutler E.

Br J Haematol. 2001 Feb;112(2):475-82. Review.

PMID:
11167850
50.

Three Gaucher-disease-producing mutations in a patient with Gaucher disease: mechanism and diagnostic implications.

Beutler E, Liebman H, Gelbart T, Stefanski E.

Acta Haematol. 2000;104(2-3):103-5.

PMID:
11154983

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