Hendrickson B - Search Results

1

A GC-wave correction algorithm that improves the analytical performance of aCGH.

Leo A, Walker AM, Lebo MS, Hendrickson B, Scholl T, Akmaev VR. Leo A, et al. Among authors: hendrickson b. J Mol Diagn. 2012 Nov;14(6):550-9. doi: 10.1016/j.jmoldx.2012.06.002. Epub 2012 Aug 23. J Mol Diagn. 2012. PMID: 22922130 Free article.

2

Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72,400 specimens.

Sugarman EA, Nagan N, Zhu H, Akmaev VR, Zhou Z, Rohlfs EM, Flynn K, Hendrickson BC, Scholl T, Sirko-Osadsa DA, Allitto BA. Sugarman EA, et al. Eur J Hum Genet. 2012 Jan;20(1):27-32. doi: 10.1038/ejhg.2011.134. Epub 2011 Aug 3. Eur J Hum Genet. 2012. PMID: 21811307 Free PMC article.

3

A multi-exonic BRCA1 deletion identified in multiple families through single nucleotide polymorphism haplotype pair analysis and gene amplification with widely dispersed primer sets.

Ward BD, Hendrickson BC, Judkins T, Deffenbaugh AM, Leclair B, Ward BE, Scholl T. Ward BD, et al. Among authors: hendrickson bc. J Mol Diagn. 2005 Feb;7(1):139-42. doi: 10.1016/S1525-1578(10)60020-7. J Mol Diagn. 2005. PMID: 15681486 Free PMC article.

4

Two rare novel polymorphisms in the D8S1179 and D13S317 markers and method to mitigate their impact on human identification.

Forrest SW, Kupferschmid TD, Hendrickson BC, Judkins T, Petersen DJ, Scholl T. Forrest SW, et al. Croat Med J. 2004 Aug;45(4):457-60. Croat Med J. 2004. PMID: 15311419 Free article.

5

A biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A--> C is a mutation.

Keaton JC, Nielsen DR, Hendrickson BC, Pyne MT, Scheuer L, Ward BE, Brothman AR, Scholl T. Keaton JC, et al. J Hum Genet. 2003;48(8):399-403. doi: 10.1007/s10038-003-0044-0. J Hum Genet. 2003. PMID: 14513821

6

Single nucleotide polymorphisms in clinical genetic testing: the characterization of the clinical significance of genetic variants and their application in clinical research for BRCA1.

Judkins T, Hendrickson BC, Deffenbaugh AM, Scholl T. Judkins T, et al. Mutat Res. 2005 Jun 3;573(1-2):168-79. doi: 10.1016/j.mrfmmm.2004.07.024. Mutat Res. 2005. PMID: 15829246 Review.

7

Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations.

Judkins T, Hendrickson BC, Deffenbaugh AM, Eliason K, Leclair B, Norton MJ, Ward BE, Pruss D, Scholl T. Judkins T, et al. Among authors: hendrickson bc. Cancer Res. 2005 Nov 1;65(21):10096-103. doi: 10.1158/0008-5472.CAN-05-1241. Cancer Res. 2005. PMID: 16267036

8

Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families.

Hendrickson BC, Judkins T, Ward BD, Eliason K, Deffenbaugh AE, Burbidge LA, Pyne K, Leclair B, Ward BE, Scholl T. Hendrickson BC, et al. Genes Chromosomes Cancer. 2005 Jul;43(3):309-13. doi: 10.1002/gcc.20189. Genes Chromosomes Cancer. 2005. PMID: 15846789

9

The BRCA2 genetic variant IVS7 + 2T-->G is a mutation.

Pyne MT, Brothman AR, Ward B, Pruss D, Hendrickson BC, Scholl T. Pyne MT, et al. Among authors: hendrickson bc. J Hum Genet. 2000;45(6):351-7. doi: 10.1007/s100380070007. J Hum Genet. 2000. PMID: 11185744

10

Differences in SMN1 allele frequencies among ethnic groups within North America.

Hendrickson BC, Donohoe C, Akmaev VR, Sugarman EA, Labrousse P, Boguslavskiy L, Flynn K, Rohlfs EM, Walker A, Allitto B, Sears C, Scholl T. Hendrickson BC, et al. J Med Genet. 2009 Sep;46(9):641-4. doi: 10.1136/jmg.2009.066969. Epub 2009 Jul 21. J Med Genet. 2009. PMID: 19625283 Free PMC article.

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