Year |
Citation |
Score |
2023 |
Shen W, Sellers HL, Choate LA, Stein MI, Tandale PP, Tan J, Setlem R, Sakai Y, Fadra N, Sosa C, McClelland SP, Barnett SS, Rasmussen KJ, Runke CK, Smoley SA, ... ... Kearney HM, et al. Clinical Validation of Tagmentation-Based Genome Sequencing for Germline Disorders. The Journal of Molecular Diagnostics : Jmd. PMID 37088140 DOI: 10.1016/j.jmoldx.2023.04.001 |
0.328 |
|
2021 |
Chen JA, Hou Y, Roskin KM, Arber DA, Bangs CD, Baughn LB, Cherry AM, Ewalt MD, Fire AZ, Fresard L, Kearney HM, Montgomery SB, Ohgami RS, Pearce KE, Pitel BA, et al. Lymphoid blast transformation in an MPN with BCR-JAK2 treated with ruxolitinib: putative mechanisms of resistance. Blood Advances. 5: 3492-3496. PMID 34505882 DOI: 10.1182/bloodadvances.2020004174 |
0.561 |
|
2020 |
Larson DP, Akkari YM, Van Dyke DL, Raca G, Gardner JA, Rehder CW, Kaiser-Rogers KA, Eagle P, Yuhas JA, Gu J, Toydemir RM, Kearney H, Conlin LK, Tang G, Dolan MM, et al. Conventional Cytogenetic Analysis of Hematologic Neoplasms: A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee. Archives of Pathology & Laboratory Medicine. PMID 32886736 DOI: 10.5858/Arpa.2020-0089-Cp |
0.319 |
|
2018 |
Baughn LB, Smoley SA, Aypar U, Pitel BA, Vasmatzis G, Johnson SH, Smadbeck JB, Peterson JF, Geiersbach KB, Dyke DLV, Thorland EC, Ketterling RP, Jenkins RB, Hoppman NL, Kearney HM, et al. 13. Clinical utility of mate pair sequencing to detect diagnostic and prognostic chromosomal rearrangements and copy number changes in patients with acute myeloid leukemia Cancer Genetics and Cytogenetics. 36. DOI: 10.1016/J.Cancergen.2018.04.016 |
0.312 |
|
2016 |
Aypar U, Kearney H, Sukov W, Jenkins R, Hoppman N. Next Generation Cytogenetics: Genome-wide Mate Pair Sequencing for Detection of Structural Rearrangements and Copy Number Variation Cancer Genetics. 209: 234. DOI: 10.1016/J.Cancergen.2016.05.017 |
0.324 |
|
2013 |
Rehder CW, David KL, Hirsch B, Toriello HV, Wilson CM, Kearney HM. American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 150-2. PMID 23328890 DOI: 10.1038/Gim.2012.169 |
0.323 |
|
2011 |
Kearney HM, Thorland EC, Brown KK, Quintero-Rivera F, South ST. American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 680-5. PMID 21681106 DOI: 10.1097/Gim.0B013E3182217A3A |
0.37 |
|
2005 |
Blanton HL, Radford SJ, McMahan S, Kearney HM, Ibrahim JG, Sekelsky J. REC, Drosophila MCM8, drives formation of meiotic crossovers. Plos Genetics. 1: e40. PMID 16189551 DOI: 10.1371/Journal.Pgen.0010040 |
0.427 |
|
2004 |
Yildiz O, Kearney H, Kramer BC, Sekelsky JJ. Mutational analysis of the Drosophila DNA repair and recombination gene mei-9. Genetics. 167: 263-73. PMID 15166153 DOI: 10.1534/Genetics.167.1.263 |
0.446 |
|
2002 |
Welz-Voegele C, Stone JE, Tran PT, Kearney HM, Liskay RM, Petes TD, Jinks-Robertson S. Alleles of the yeast Pms1 mismatch-repair gene that differentially affect recombination- and replication-related processes. Genetics. 162: 1131-45. PMID 12454061 |
0.573 |
|
2001 |
Kearney HM, Kirkpatrick DT, Gerton JL, Petes TD. Meiotic recombination involving heterozygous large insertions in Saccharomyces cerevisiae: formation and repair of large, unpaired DNA loops. Genetics. 158: 1457-76. PMID 11514439 |
0.594 |
|
Show low-probability matches. |