Rennert H - Search Results

1

Avoiding pitfalls in bone marrow engraftment analysis: a case study highlighting the weakness of using buccal cells for determining a patient's constitutional genotype after hematopoietic stem cell transplantation.

Rennert H, Leonard DG, Cushing M, Azurin C, Shore T. Rennert H, et al. Cytotherapy. 2013 Mar;15(3):391-5. doi: 10.1016/j.jcyt.2012.10.011. Epub 2012 Dec 17. Cytotherapy. 2013. PMID: 23253437

2

Novel bcl-2 breakpoints in patients with follicular lymphoma.

Wang YL, Addya K, Edwards RH, Rennert H, Dodson L, Leonard DG, Wilson RB. Wang YL, et al. Among authors: rennert h. Diagn Mol Pathol. 1998 Apr;7(2):85-9. doi: 10.1097/00019606-199804000-00004. Diagn Mol Pathol. 1998. PMID: 9785006

3

Duplications and de novo deletions of the SMNt gene demonstrated by fluorescence-based carrier testing for spinal muscular atrophy.

Chen KL, Wang YL, Rennert H, Joshi I, Mills JK, Leonard DG, Wilson RB. Chen KL, et al. Among authors: rennert h. Am J Med Genet. 1999 Aug 27;85(5):463-9. Am J Med Genet. 1999. PMID: 10405443

4

A novel, non-nested reverse-transcriptase polymerase chain reaction (RT-PCR) test for the detection of the t(15;17) translocation: a comparative study of RT-PCR cytogenetics, and fluorescence In situ hybridization.

Rennert H, Golde T, Wilson RB, Spitalnik SL, Van Deerlin VM, Leonard DG. Rennert H, et al. Mol Diagn. 1999 Sep;4(3):195-209. doi: 10.1016/s1084-8592(99)80023-x. Mol Diagn. 1999. PMID: 10553020

5

Detection of clonal T-cell receptor gamma gene rearrangements using fluorescent-based PCR and automated high-resolution capillary electrophoresis.

Luo V, Lessin SR, Wilson RB, Rennert H, Tozer C, Benoit B, Leonard DG. Luo V, et al. Among authors: rennert h. Mol Diagn. 2001 Sep;6(3):169-79. doi: 10.1054/modi.2001.27056. Mol Diagn. 2001. PMID: 11571710

6

Heteroduplex formation in SMN gene dosage analysis.

Ogino S, Leonard DG, Rennert H, Gao S, Wilson RB. Ogino S, et al. Among authors: rennert h. J Mol Diagn. 2001 Nov;3(4):150-7. doi: 10.1016/S1525-1578(10)60666-6. J Mol Diagn. 2001. PMID: 11687598 Free PMC article.

7

Spinal muscular atrophy genetic testing experience at an academic medical center.

Ogino S, Leonard DG, Rennert H, Wilson RB. Ogino S, et al. Among authors: rennert h. J Mol Diagn. 2002 Feb;4(1):53-8. doi: 10.1016/S1525-1578(10)60680-0. J Mol Diagn. 2002. PMID: 11826188 Free PMC article.

8

Genetic risk assessment in carrier testing for spinal muscular atrophy.

Ogino S, Leonard DG, Rennert H, Ewens WJ, Wilson RB. Ogino S, et al. Among authors: rennert h. Am J Med Genet. 2002 Jul 15;110(4):301-7. doi: 10.1002/ajmg.10425. Am J Med Genet. 2002. PMID: 12116201

9

Multiplex RT-PCR for the detection of leukemia-associated translocations: validation and application to routine molecular diagnostic practice.

Salto-Tellez M, Shelat SG, Benoit B, Rennert H, Carroll M, Leonard DG, Nowell P, Bagg A. Salto-Tellez M, et al. Among authors: rennert h. J Mol Diagn. 2003 Nov;5(4):231-6. doi: 10.1016/S1525-1578(10)60479-5. J Mol Diagn. 2003. PMID: 14573782 Free PMC article.

10

Association of susceptibility alleles in ELAC2/HPC2, RNASEL/HPC1, and MSR1 with prostate cancer severity in European American and African American men.

Rennert H, Zeigler-Johnson CM, Addya K, Finley MJ, Walker AH, Spangler E, Leonard DG, Wein A, Malkowicz SB, Rebbeck TR. Rennert H, et al. Cancer Epidemiol Biomarkers Prev. 2005 Apr;14(4):949-57. doi: 10.1158/1055-9965.EPI-04-0637. Cancer Epidemiol Biomarkers Prev. 2005. PMID: 15824169

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