Kearney H - Search Results

1

Riggs ER, Andersen EF, Kantarci S, Kearney H, Patel A, Raca G, Ritter DI, South ST, Thorland EC, Pineda-Alvarez D, Aradhya S, Martin CL. Riggs ER, et al. Among authors: kearney h. Genet Med. 2023 Aug;25(8):100869. doi: 10.1016/j.gim.2023.100869. Epub 2023 Jun 1. Genet Med. 2023. PMID: 37261438 No abstract available.

2

Mutational analysis of the Drosophila DNA repair and recombination gene mei-9.

Yildiz O, Kearney H, Kramer BC, Sekelsky JJ. Yildiz O, et al. Among authors: kearney h. Genetics. 2004 May;167(1):263-73. doi: 10.1534/genetics.167.1.263. Genetics. 2004. PMID: 15166153 Free PMC article.

3

Meiotic recombination involving heterozygous large insertions in Saccharomyces cerevisiae: formation and repair of large, unpaired DNA loops.

Kearney HM, Kirkpatrick DT, Gerton JL, Petes TD. Kearney HM, et al. Genetics. 2001 Aug;158(4):1457-76. doi: 10.1093/genetics/158.4.1457. Genetics. 2001. PMID: 11514439 Free PMC article.

4

Clinical experience with array CGH: case presentations from nine months of practice.

Poss AF, Goldenberg PC, Rehder CW, Kearney HM, Melvin EC, Koeberl DD, McDonald MT. Poss AF, et al. Am J Med Genet A. 2006 Oct 1;140(19):2050-6. doi: 10.1002/ajmg.a.31417. Am J Med Genet A. 2006. PMID: 16906557

5

REC, Drosophila MCM8, drives formation of meiotic crossovers.

Blanton HL, Radford SJ, McMahan S, Kearney HM, Ibrahim JG, Sekelsky J. Blanton HL, et al. PLoS Genet. 2005 Sep;1(3):e40. doi: 10.1371/journal.pgen.0010040. PLoS Genet. 2005. PMID: 16189551 Free PMC article.

6

Alleles of the yeast Pms1 mismatch-repair gene that differentially affect recombination- and replication-related processes.

Welz-Voegele C, Stone JE, Tran PT, Kearney HM, Liskay RM, Petes TD, Jinks-Robertson S. Welz-Voegele C, et al. Genetics. 2002 Nov;162(3):1131-45. doi: 10.1093/genetics/162.3.1131. Genetics. 2002. PMID: 12454061 Free PMC article.

7

American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities.

Kearney HM, South ST, Wolff DJ, Lamb A, Hamosh A, Rao KW; Working Group of the American College of Medical Genetics. Kearney HM, et al. Genet Med. 2011 Jul;13(7):676-9. doi: 10.1097/GIM.0b013e31822272ac. Genet Med. 2011. PMID: 21681105 Free article.

8

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.

Kearney HM, Thorland EC, Brown KK, Quintero-Rivera F, South ST; Working Group of the American College of Medical Genetics Laboratory Quality Assurance Committee. Kearney HM, et al. Genet Med. 2011 Jul;13(7):680-5. doi: 10.1097/GIM.0b013e3182217a3a. Genet Med. 2011. PMID: 21681106 Free article.

9

Towards an evidence-based process for the clinical interpretation of copy number variation.

Riggs ER, Church DM, Hanson K, Horner VL, Kaminsky EB, Kuhn RM, Wain KE, Williams ES, Aradhya S, Kearney HM, Ledbetter DH, South ST, Thorland EC, Martin CL. Riggs ER, et al. Among authors: kearney hm. Clin Genet. 2012 May;81(5):403-12. doi: 10.1111/j.1399-0004.2011.01818.x. Epub 2011 Dec 13. Clin Genet. 2012. PMID: 22097934 Free PMC article. Review.

10

ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.

South ST, Lee C, Lamb AN, Higgins AW, Kearney HM; Working Group for the American College of Medical Genetics and Genomics Laboratory Quality Assurance Committee. South ST, et al. Genet Med. 2013 Nov;15(11):901-9. doi: 10.1038/gim.2013.129. Epub 2013 Sep 26. Genet Med. 2013. PMID: 24071793 Free article.

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